CN101914555A - Novel genes encoding novel proteolytic enzymes - Google Patents
Novel genes encoding novel proteolytic enzymes Download PDFInfo
- Publication number
- CN101914555A CN101914555A CN2009102513862A CN200910251386A CN101914555A CN 101914555 A CN101914555 A CN 101914555A CN 2009102513862 A CN2009102513862 A CN 2009102513862A CN 200910251386 A CN200910251386 A CN 200910251386A CN 101914555 A CN101914555 A CN 101914555A
- Authority
- CN
- China
- Prior art keywords
- sequence
- protein
- seq
- polynucleotide
- proteolytic enzyme
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 108091005804 Peptidases Proteins 0.000 title claims abstract description 464
- 108090000623 proteins and genes Proteins 0.000 title claims abstract description 323
- 102000035195 Peptidases Human genes 0.000 title abstract description 436
- 229940024999 proteolytic enzymes for treatment of wounds and ulcers Drugs 0.000 title description 4
- 102000004169 proteins and genes Human genes 0.000 claims abstract description 232
- 238000000034 method Methods 0.000 claims abstract description 169
- 102000004190 Enzymes Human genes 0.000 claims abstract description 152
- 108090000790 Enzymes Proteins 0.000 claims abstract description 152
- 241000228245 Aspergillus niger Species 0.000 claims abstract description 143
- 239000004365 Protease Substances 0.000 claims abstract description 65
- 102100037486 Reverse transcriptase/ribonuclease H Human genes 0.000 claims abstract 4
- 108090000765 processed proteins & peptides Proteins 0.000 claims description 336
- 235000018102 proteins Nutrition 0.000 claims description 221
- 102000004196 processed proteins & peptides Human genes 0.000 claims description 194
- 229920001184 polypeptide Polymers 0.000 claims description 176
- 150000007523 nucleic acids Chemical class 0.000 claims description 82
- 108091033319 polynucleotide Proteins 0.000 claims description 81
- 102000040430 polynucleotide Human genes 0.000 claims description 81
- 239000002157 polynucleotide Substances 0.000 claims description 81
- 239000002773 nucleotide Substances 0.000 claims description 80
- 125000003729 nucleotide group Chemical group 0.000 claims description 80
- 102000039446 nucleic acids Human genes 0.000 claims description 73
- 108020004707 nucleic acids Proteins 0.000 claims description 73
- 125000003275 alpha amino acid group Chemical group 0.000 claims description 50
- 239000000523 sample Substances 0.000 claims description 44
- 230000008859 change Effects 0.000 claims description 35
- 230000002779 inactivation Effects 0.000 claims description 32
- 241000233866 Fungi Species 0.000 claims description 27
- 241000228212 Aspergillus Species 0.000 claims description 25
- 238000002360 preparation method Methods 0.000 claims description 24
- 238000003752 polymerase chain reaction Methods 0.000 claims description 21
- 201000002909 Aspergillosis Diseases 0.000 claims description 11
- 208000036641 Aspergillus infections Diseases 0.000 claims description 11
- 230000002950 deficient Effects 0.000 claims description 11
- 102000007056 Recombinant Fusion Proteins Human genes 0.000 claims description 9
- 108010008281 Recombinant Fusion Proteins Proteins 0.000 claims description 9
- 238000003745 diagnosis Methods 0.000 claims description 5
- 230000003321 amplification Effects 0.000 claims description 4
- 239000012472 biological sample Substances 0.000 claims description 4
- 239000001963 growth medium Substances 0.000 claims description 4
- 238000003199 nucleic acid amplification method Methods 0.000 claims description 4
- 230000000694 effects Effects 0.000 abstract description 98
- 239000012634 fragment Substances 0.000 abstract description 52
- 230000014509 gene expression Effects 0.000 abstract description 49
- 238000004519 manufacturing process Methods 0.000 abstract description 45
- 239000002299 complementary DNA Substances 0.000 abstract description 27
- 206010017533 Fungal infection Diseases 0.000 abstract 1
- 208000031888 Mycoses Diseases 0.000 abstract 1
- 108020004414 DNA Proteins 0.000 description 142
- 210000004027 cell Anatomy 0.000 description 138
- 229940088598 enzyme Drugs 0.000 description 126
- 235000001014 amino acid Nutrition 0.000 description 124
- 229940024606 amino acid Drugs 0.000 description 122
- 150000001413 amino acids Chemical class 0.000 description 117
- 239000000758 substrate Substances 0.000 description 87
- 230000006870 function Effects 0.000 description 57
- 235000019419 proteases Nutrition 0.000 description 57
- 230000017854 proteolysis Effects 0.000 description 54
- 239000000047 product Substances 0.000 description 46
- 101710118538 Protease Proteins 0.000 description 45
- 238000006243 chemical reaction Methods 0.000 description 45
- 230000008569 process Effects 0.000 description 45
- 235000013351 cheese Nutrition 0.000 description 43
- 238000006460 hydrolysis reaction Methods 0.000 description 43
- 230000007062 hydrolysis Effects 0.000 description 42
- 238000005520 cutting process Methods 0.000 description 36
- 239000000203 mixture Substances 0.000 description 34
- 238000005516 engineering process Methods 0.000 description 33
- 230000002797 proteolythic effect Effects 0.000 description 32
- 125000000539 amino acid group Chemical group 0.000 description 31
- 238000012545 processing Methods 0.000 description 31
- 108010076119 Caseins Proteins 0.000 description 27
- 102000011632 Caseins Human genes 0.000 description 27
- 239000013615 primer Substances 0.000 description 27
- 239000002987 primer (paints) Substances 0.000 description 27
- 239000000463 material Substances 0.000 description 26
- 235000019640 taste Nutrition 0.000 description 26
- 239000013604 expression vector Substances 0.000 description 22
- 238000009396 hybridization Methods 0.000 description 22
- 235000013305 food Nutrition 0.000 description 21
- 125000001151 peptidyl group Chemical group 0.000 description 21
- 238000004458 analytical method Methods 0.000 description 20
- WHUUTDBJXJRKMK-VKHMYHEASA-N L-glutamic acid Chemical compound OC(=O)[C@@H](N)CCC(O)=O WHUUTDBJXJRKMK-VKHMYHEASA-N 0.000 description 19
- 238000011534 incubation Methods 0.000 description 19
- ONIBWKKTOPOVIA-UHFFFAOYSA-N Proline Natural products OC(=O)C1CCCN1 ONIBWKKTOPOVIA-UHFFFAOYSA-N 0.000 description 18
- 240000004808 Saccharomyces cerevisiae Species 0.000 description 18
- 241000894006 Bacteria Species 0.000 description 17
- 108010006303 Carboxypeptidases Proteins 0.000 description 17
- 102000005367 Carboxypeptidases Human genes 0.000 description 17
- ONIBWKKTOPOVIA-BYPYZUCNSA-N L-Proline Chemical compound OC(=O)[C@@H]1CCCN1 ONIBWKKTOPOVIA-BYPYZUCNSA-N 0.000 description 17
- 230000007246 mechanism Effects 0.000 description 17
- 229960002429 proline Drugs 0.000 description 17
- 230000028327 secretion Effects 0.000 description 17
- 230000014616 translation Effects 0.000 description 17
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 17
- 108090000915 Aminopeptidases Proteins 0.000 description 16
- 102000004400 Aminopeptidases Human genes 0.000 description 16
- 241001465754 Metazoa Species 0.000 description 16
- 108010076504 Protein Sorting Signals Proteins 0.000 description 16
- 235000014680 Saccharomyces cerevisiae Nutrition 0.000 description 16
- 239000002243 precursor Substances 0.000 description 16
- 125000000174 L-prolyl group Chemical group [H]N1C([H])([H])C([H])([H])C([H])([H])[C@@]1([H])C(*)=O 0.000 description 15
- 108091028043 Nucleic acid sequence Proteins 0.000 description 15
- 230000001580 bacterial effect Effects 0.000 description 15
- 230000008901 benefit Effects 0.000 description 15
- 238000002474 experimental method Methods 0.000 description 15
- 239000011347 resin Substances 0.000 description 15
- 229920005989 resin Polymers 0.000 description 15
- 239000000413 hydrolysate Substances 0.000 description 14
- 230000002209 hydrophobic effect Effects 0.000 description 14
- 230000001976 improved effect Effects 0.000 description 14
- 244000005700 microbiome Species 0.000 description 14
- 230000004048 modification Effects 0.000 description 14
- 238000012986 modification Methods 0.000 description 14
- 238000010369 molecular cloning Methods 0.000 description 14
- 238000002703 mutagenesis Methods 0.000 description 14
- 231100000350 mutagenesis Toxicity 0.000 description 14
- 239000002753 trypsin inhibitor Substances 0.000 description 14
- ROHFNLRQFUQHCH-YFKPBYRVSA-N L-leucine Chemical compound CC(C)C[C@H](N)C(O)=O ROHFNLRQFUQHCH-YFKPBYRVSA-N 0.000 description 13
- 239000003112 inhibitor Substances 0.000 description 13
- 235000021247 β-casein Nutrition 0.000 description 13
- 102000005593 Endopeptidases Human genes 0.000 description 12
- 108010059378 Endopeptidases Proteins 0.000 description 12
- 241000283891 Kobus Species 0.000 description 12
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 12
- 230000000295 complement effect Effects 0.000 description 12
- 235000013336 milk Nutrition 0.000 description 12
- 239000008267 milk Substances 0.000 description 12
- 210000004080 milk Anatomy 0.000 description 12
- IFQSXNOEEPCSLW-DKWTVANSSA-N L-cysteine hydrochloride Chemical compound Cl.SC[C@H](N)C(O)=O IFQSXNOEEPCSLW-DKWTVANSSA-N 0.000 description 11
- 229940122618 Trypsin inhibitor Drugs 0.000 description 11
- 101710162629 Trypsin inhibitor Proteins 0.000 description 11
- 239000005018 casein Substances 0.000 description 11
- 239000000796 flavoring agent Substances 0.000 description 11
- 230000003993 interaction Effects 0.000 description 11
- 229960003136 leucine Drugs 0.000 description 11
- 235000005772 leucine Nutrition 0.000 description 11
- 239000003550 marker Substances 0.000 description 11
- -1 polyoxyethylene Polymers 0.000 description 11
- 239000000243 solution Substances 0.000 description 11
- 241001225321 Aspergillus fumigatus Species 0.000 description 10
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 10
- 244000068988 Glycine max Species 0.000 description 10
- 235000010469 Glycine max Nutrition 0.000 description 10
- COLNVLDHVKWLRT-QMMMGPOBSA-N L-phenylalanine Chemical compound OC(=O)[C@@H](N)CC1=CC=CC=C1 COLNVLDHVKWLRT-QMMMGPOBSA-N 0.000 description 10
- ROHFNLRQFUQHCH-UHFFFAOYSA-N Leucine Natural products CC(C)CC(N)C(O)=O ROHFNLRQFUQHCH-UHFFFAOYSA-N 0.000 description 10
- 108091034117 Oligonucleotide Proteins 0.000 description 10
- 108020004511 Recombinant DNA Proteins 0.000 description 10
- 230000004071 biological effect Effects 0.000 description 10
- 238000004422 calculation algorithm Methods 0.000 description 10
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 10
- 235000021240 caseins Nutrition 0.000 description 10
- 238000013016 damping Methods 0.000 description 10
- 235000019634 flavors Nutrition 0.000 description 10
- 239000012530 fluid Substances 0.000 description 10
- 230000002018 overexpression Effects 0.000 description 10
- 238000005406 washing Methods 0.000 description 10
- 108091032973 (ribonucleotides)n+m Proteins 0.000 description 9
- 108010062466 Enzyme Precursors Proteins 0.000 description 9
- 102000010911 Enzyme Precursors Human genes 0.000 description 9
- 102000007544 Whey Proteins Human genes 0.000 description 9
- 108010046377 Whey Proteins Proteins 0.000 description 9
- 229940091771 aspergillus fumigatus Drugs 0.000 description 9
- 210000004899 c-terminal region Anatomy 0.000 description 9
- 239000003054 catalyst Substances 0.000 description 9
- 238000006555 catalytic reaction Methods 0.000 description 9
- 239000003795 chemical substances by application Substances 0.000 description 9
- 150000001875 compounds Chemical class 0.000 description 9
- 230000004927 fusion Effects 0.000 description 9
- 229960002989 glutamic acid Drugs 0.000 description 9
- 230000000968 intestinal effect Effects 0.000 description 9
- 210000002784 stomach Anatomy 0.000 description 9
- 239000000126 substance Substances 0.000 description 9
- 210000001519 tissue Anatomy 0.000 description 9
- 238000013519 translation Methods 0.000 description 9
- 102000018389 Exopeptidases Human genes 0.000 description 8
- 108010091443 Exopeptidases Proteins 0.000 description 8
- 102000012479 Serine Proteases Human genes 0.000 description 8
- 108010022999 Serine Proteases Proteins 0.000 description 8
- 241000700605 Viruses Species 0.000 description 8
- 230000004913 activation Effects 0.000 description 8
- 239000000427 antigen Substances 0.000 description 8
- 108091007433 antigens Proteins 0.000 description 8
- 102000036639 antigens Human genes 0.000 description 8
- 238000013459 approach Methods 0.000 description 8
- 230000008878 coupling Effects 0.000 description 8
- 238000010168 coupling process Methods 0.000 description 8
- 238000005859 coupling reaction Methods 0.000 description 8
- 238000001514 detection method Methods 0.000 description 8
- 239000003814 drug Substances 0.000 description 8
- 238000000855 fermentation Methods 0.000 description 8
- 230000004151 fermentation Effects 0.000 description 8
- 239000003205 fragrance Substances 0.000 description 8
- 230000003053 immunization Effects 0.000 description 8
- 238000002649 immunization Methods 0.000 description 8
- 230000001965 increasing effect Effects 0.000 description 8
- 230000003834 intracellular effect Effects 0.000 description 8
- 239000011159 matrix material Substances 0.000 description 8
- 108020004999 messenger RNA Proteins 0.000 description 8
- 229910021645 metal ion Inorganic materials 0.000 description 8
- 235000015097 nutrients Nutrition 0.000 description 8
- COLNVLDHVKWLRT-UHFFFAOYSA-N phenylalanine Natural products OC(=O)C(N)CC1=CC=CC=C1 COLNVLDHVKWLRT-UHFFFAOYSA-N 0.000 description 8
- 239000013612 plasmid Substances 0.000 description 8
- 230000007306 turnover Effects 0.000 description 8
- MTCFGRXMJLQNBG-REOHCLBHSA-N (2S)-2-Amino-3-hydroxypropansäure Chemical compound OC[C@H](N)C(O)=O MTCFGRXMJLQNBG-REOHCLBHSA-N 0.000 description 7
- 108010016626 Dipeptides Proteins 0.000 description 7
- 239000002585 base Substances 0.000 description 7
- 230000015572 biosynthetic process Effects 0.000 description 7
- 230000008034 disappearance Effects 0.000 description 7
- 230000002255 enzymatic effect Effects 0.000 description 7
- 238000010438 heat treatment Methods 0.000 description 7
- 210000004408 hybridoma Anatomy 0.000 description 7
- 230000005847 immunogenicity Effects 0.000 description 7
- 238000003780 insertion Methods 0.000 description 7
- 230000037431 insertion Effects 0.000 description 7
- 230000007935 neutral effect Effects 0.000 description 7
- 239000011049 pearl Substances 0.000 description 7
- 239000000843 powder Substances 0.000 description 7
- 235000019833 protease Nutrition 0.000 description 7
- 239000003531 protein hydrolysate Substances 0.000 description 7
- 238000012216 screening Methods 0.000 description 7
- 238000001228 spectrum Methods 0.000 description 7
- 239000007858 starting material Substances 0.000 description 7
- 210000003934 vacuole Anatomy 0.000 description 7
- 239000013598 vector Substances 0.000 description 7
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 6
- 229920002307 Dextran Polymers 0.000 description 6
- 238000002965 ELISA Methods 0.000 description 6
- XUJNEKJLAYXESH-REOHCLBHSA-N L-Cysteine Chemical compound SC[C@H](N)C(O)=O XUJNEKJLAYXESH-REOHCLBHSA-N 0.000 description 6
- OUYCCCASQSFEME-QMMMGPOBSA-N L-tyrosine Chemical compound OC(=O)[C@@H](N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-QMMMGPOBSA-N 0.000 description 6
- 108010006035 Metalloproteases Proteins 0.000 description 6
- 102000005741 Metalloproteases Human genes 0.000 description 6
- 108010038807 Oligopeptides Proteins 0.000 description 6
- 102000015636 Oligopeptides Human genes 0.000 description 6
- 108090000787 Subtilisin Proteins 0.000 description 6
- 239000002253 acid Substances 0.000 description 6
- 239000000654 additive Substances 0.000 description 6
- 230000002788 anti-peptide Effects 0.000 description 6
- 229910052799 carbon Inorganic materials 0.000 description 6
- 238000004587 chromatography analysis Methods 0.000 description 6
- 230000006378 damage Effects 0.000 description 6
- 238000013461 design Methods 0.000 description 6
- 230000002068 genetic effect Effects 0.000 description 6
- 230000013595 glycosylation Effects 0.000 description 6
- 238000006206 glycosylation reaction Methods 0.000 description 6
- 238000004128 high performance liquid chromatography Methods 0.000 description 6
- 230000003301 hydrolyzing effect Effects 0.000 description 6
- 238000001727 in vivo Methods 0.000 description 6
- 238000002372 labelling Methods 0.000 description 6
- 239000007788 liquid Substances 0.000 description 6
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 6
- 229930182817 methionine Natural products 0.000 description 6
- 238000005457 optimization Methods 0.000 description 6
- 230000001717 pathogenic effect Effects 0.000 description 6
- 239000012071 phase Substances 0.000 description 6
- 238000000746 purification Methods 0.000 description 6
- 230000002829 reductive effect Effects 0.000 description 6
- 230000001105 regulatory effect Effects 0.000 description 6
- 238000011160 research Methods 0.000 description 6
- 238000000926 separation method Methods 0.000 description 6
- 239000011780 sodium chloride Substances 0.000 description 6
- 238000010561 standard procedure Methods 0.000 description 6
- 239000006228 supernatant Substances 0.000 description 6
- 238000013518 transcription Methods 0.000 description 6
- 230000035897 transcription Effects 0.000 description 6
- 238000011282 treatment Methods 0.000 description 6
- 238000011144 upstream manufacturing Methods 0.000 description 6
- 235000021119 whey protein Nutrition 0.000 description 6
- 239000012138 yeast extract Substances 0.000 description 6
- 241000228197 Aspergillus flavus Species 0.000 description 5
- 102000014914 Carrier Proteins Human genes 0.000 description 5
- 102000053602 DNA Human genes 0.000 description 5
- QNAYBMKLOCPYGJ-REOHCLBHSA-N L-alanine Chemical compound C[C@H](N)C(O)=O QNAYBMKLOCPYGJ-REOHCLBHSA-N 0.000 description 5
- AGPKZVBTJJNPAG-WHFBIAKZSA-N L-isoleucine Chemical compound CC[C@H](C)[C@H](N)C(O)=O AGPKZVBTJJNPAG-WHFBIAKZSA-N 0.000 description 5
- 241000124008 Mammalia Species 0.000 description 5
- 230000000996 additive effect Effects 0.000 description 5
- 239000002671 adjuvant Substances 0.000 description 5
- 238000001042 affinity chromatography Methods 0.000 description 5
- 125000003277 amino group Chemical group 0.000 description 5
- 230000000890 antigenic effect Effects 0.000 description 5
- 235000013405 beer Nutrition 0.000 description 5
- 235000008429 bread Nutrition 0.000 description 5
- 229940041514 candida albicans extract Drugs 0.000 description 5
- 230000015556 catabolic process Effects 0.000 description 5
- 238000012512 characterization method Methods 0.000 description 5
- 238000006731 degradation reaction Methods 0.000 description 5
- 230000001419 dependent effect Effects 0.000 description 5
- 230000029087 digestion Effects 0.000 description 5
- 238000011156 evaluation Methods 0.000 description 5
- 239000000284 extract Substances 0.000 description 5
- 238000013467 fragmentation Methods 0.000 description 5
- 238000006062 fragmentation reaction Methods 0.000 description 5
- 230000002538 fungal effect Effects 0.000 description 5
- 238000002523 gelfiltration Methods 0.000 description 5
- 235000014304 histidine Nutrition 0.000 description 5
- 238000003018 immunoassay Methods 0.000 description 5
- 235000013372 meat Nutrition 0.000 description 5
- 239000002609 medium Substances 0.000 description 5
- 125000001360 methionine group Chemical group N[C@@H](CCSC)C(=O)* 0.000 description 5
- 238000012544 monitoring process Methods 0.000 description 5
- 239000000137 peptide hydrolase inhibitor Substances 0.000 description 5
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 5
- 125000001500 prolyl group Chemical group [H]N1C([H])(C(=O)[*])C([H])([H])C([H])([H])C1([H])[H] 0.000 description 5
- 238000003259 recombinant expression Methods 0.000 description 5
- 108091008146 restriction endonucleases Proteins 0.000 description 5
- 230000005070 ripening Effects 0.000 description 5
- 150000003839 salts Chemical class 0.000 description 5
- 230000003248 secreting effect Effects 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- 235000014347 soups Nutrition 0.000 description 5
- 241000894007 species Species 0.000 description 5
- 239000000725 suspension Substances 0.000 description 5
- 238000012360 testing method Methods 0.000 description 5
- 238000007669 thermal treatment Methods 0.000 description 5
- 238000001890 transfection Methods 0.000 description 5
- 108020004774 Alkaline Phosphatase Proteins 0.000 description 4
- 102000002260 Alkaline Phosphatase Human genes 0.000 description 4
- 101000898643 Candida albicans Vacuolar aspartic protease Proteins 0.000 description 4
- 101000898783 Candida tropicalis Candidapepsin Proteins 0.000 description 4
- 102000008186 Collagen Human genes 0.000 description 4
- 108010035532 Collagen Proteins 0.000 description 4
- 101000898784 Cryphonectria parasitica Endothiapepsin Proteins 0.000 description 4
- 241000196324 Embryophyta Species 0.000 description 4
- 240000004859 Gamochaeta purpurea Species 0.000 description 4
- 239000004471 Glycine Substances 0.000 description 4
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 4
- HNDVDQJCIGZPNO-YFKPBYRVSA-N L-histidine Chemical compound OC(=O)[C@@H](N)CC1=CN=CN1 HNDVDQJCIGZPNO-YFKPBYRVSA-N 0.000 description 4
- FFEARJCKVFRZRR-BYPYZUCNSA-N L-methionine Chemical compound CSCC[C@H](N)C(O)=O FFEARJCKVFRZRR-BYPYZUCNSA-N 0.000 description 4
- AYFVYJQAPQTCCC-GBXIJSLDSA-N L-threonine Chemical compound C[C@@H](O)[C@H](N)C(O)=O AYFVYJQAPQTCCC-GBXIJSLDSA-N 0.000 description 4
- 108700026244 Open Reading Frames Proteins 0.000 description 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
- 101000933133 Rhizopus niveus Rhizopuspepsin-1 Proteins 0.000 description 4
- 101000910082 Rhizopus niveus Rhizopuspepsin-2 Proteins 0.000 description 4
- 101000910079 Rhizopus niveus Rhizopuspepsin-3 Proteins 0.000 description 4
- 101000910086 Rhizopus niveus Rhizopuspepsin-4 Proteins 0.000 description 4
- 101000910088 Rhizopus niveus Rhizopuspepsin-5 Proteins 0.000 description 4
- 101000898773 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) Saccharopepsin Proteins 0.000 description 4
- MTCFGRXMJLQNBG-UHFFFAOYSA-N Serine Natural products OCC(N)C(O)=O MTCFGRXMJLQNBG-UHFFFAOYSA-N 0.000 description 4
- 230000009102 absorption Effects 0.000 description 4
- 238000010521 absorption reaction Methods 0.000 description 4
- 239000008351 acetate buffer Substances 0.000 description 4
- 230000009471 action Effects 0.000 description 4
- 239000003513 alkali Substances 0.000 description 4
- 230000000692 anti-sense effect Effects 0.000 description 4
- 235000019658 bitter taste Nutrition 0.000 description 4
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 4
- 239000000969 carrier Substances 0.000 description 4
- 235000013339 cereals Nutrition 0.000 description 4
- OPTASPLRGRRNAP-UHFFFAOYSA-N cytosine Chemical compound NC=1C=CNC(=O)N=1 OPTASPLRGRRNAP-UHFFFAOYSA-N 0.000 description 4
- 230000004069 differentiation Effects 0.000 description 4
- WQOXQRCZOLPYPM-UHFFFAOYSA-N dimethyl disulfide Chemical compound CSSC WQOXQRCZOLPYPM-UHFFFAOYSA-N 0.000 description 4
- 210000003527 eukaryotic cell Anatomy 0.000 description 4
- 230000012010 growth Effects 0.000 description 4
- HNDVDQJCIGZPNO-UHFFFAOYSA-N histidine Natural products OC(=O)C(N)CC1=CN=CN1 HNDVDQJCIGZPNO-UHFFFAOYSA-N 0.000 description 4
- 230000001939 inductive effect Effects 0.000 description 4
- 238000002347 injection Methods 0.000 description 4
- 239000007924 injection Substances 0.000 description 4
- 108010045069 keyhole-limpet hemocyanin Proteins 0.000 description 4
- 210000004962 mammalian cell Anatomy 0.000 description 4
- 238000005259 measurement Methods 0.000 description 4
- 239000012528 membrane Substances 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 239000000693 micelle Substances 0.000 description 4
- 230000000813 microbial effect Effects 0.000 description 4
- 239000000178 monomer Substances 0.000 description 4
- 101150093025 pepA gene Proteins 0.000 description 4
- 238000001556 precipitation Methods 0.000 description 4
- 230000010076 replication Effects 0.000 description 4
- 210000002966 serum Anatomy 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 238000004885 tandem mass spectrometry Methods 0.000 description 4
- 150000007970 thio esters Chemical class 0.000 description 4
- 231100000419 toxicity Toxicity 0.000 description 4
- 230000001988 toxicity Effects 0.000 description 4
- 230000009466 transformation Effects 0.000 description 4
- 241000701161 unidentified adenovirus Species 0.000 description 4
- 241000701447 unidentified baculovirus Species 0.000 description 4
- 241001430294 unidentified retrovirus Species 0.000 description 4
- NWUYHJFMYQTDRP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;1-ethenyl-2-ethylbenzene;styrene Chemical compound C=CC1=CC=CC=C1.CCC1=CC=CC=C1C=C.C=CC1=CC=CC=C1C=C NWUYHJFMYQTDRP-UHFFFAOYSA-N 0.000 description 3
- RQFCJASXJCIDSX-UHFFFAOYSA-N 14C-Guanosin-5'-monophosphat Natural products C1=2NC(N)=NC(=O)C=2N=CN1C1OC(COP(O)(O)=O)C(O)C1O RQFCJASXJCIDSX-UHFFFAOYSA-N 0.000 description 3
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 3
- QCVGEOXPDFCNHA-UHFFFAOYSA-N 5,5-dimethyl-2,4-dioxo-1,3-oxazolidine-3-carboxamide Chemical compound CC1(C)OC(=O)N(C(N)=O)C1=O QCVGEOXPDFCNHA-UHFFFAOYSA-N 0.000 description 3
- 108010088751 Albumins Proteins 0.000 description 3
- 102000009027 Albumins Human genes 0.000 description 3
- 108010017640 Aspartic Acid Proteases Proteins 0.000 description 3
- 102000004580 Aspartic Acid Proteases Human genes 0.000 description 3
- 108091003079 Bovine Serum Albumin Proteins 0.000 description 3
- 241000282461 Canis lupus Species 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- 102000004860 Dipeptidases Human genes 0.000 description 3
- 108090001081 Dipeptidases Proteins 0.000 description 3
- 102000003779 Dipeptidyl-peptidases and tripeptidyl-peptidases Human genes 0.000 description 3
- 108090000194 Dipeptidyl-peptidases and tripeptidyl-peptidases Proteins 0.000 description 3
- 102000002322 Egg Proteins Human genes 0.000 description 3
- 108010000912 Egg Proteins Proteins 0.000 description 3
- 108010014258 Elastin Proteins 0.000 description 3
- 102000016942 Elastin Human genes 0.000 description 3
- 241000588724 Escherichia coli Species 0.000 description 3
- 108090000371 Esterases Proteins 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- 101710089384 Extracellular protease Proteins 0.000 description 3
- 108010068370 Glutens Proteins 0.000 description 3
- 241000238631 Hexapoda Species 0.000 description 3
- 108010001336 Horseradish Peroxidase Proteins 0.000 description 3
- 102100034349 Integrase Human genes 0.000 description 3
- CKLJMWTZIZZHCS-REOHCLBHSA-N L-aspartic acid Chemical compound OC(=O)[C@@H](N)CC(O)=O CKLJMWTZIZZHCS-REOHCLBHSA-N 0.000 description 3
- 101710163270 Nuclease Proteins 0.000 description 3
- 241000283973 Oryctolagus cuniculus Species 0.000 description 3
- 238000012408 PCR amplification Methods 0.000 description 3
- 206010035226 Plasma cell myeloma Diseases 0.000 description 3
- 108010009736 Protein Hydrolysates Proteins 0.000 description 3
- 108091034057 RNA (poly(A)) Proteins 0.000 description 3
- 102100023152 Scinderin Human genes 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000005862 Whey Substances 0.000 description 3
- 230000002378 acidificating effect Effects 0.000 description 3
- 230000002411 adverse Effects 0.000 description 3
- 230000002152 alkylating effect Effects 0.000 description 3
- 125000003368 amide group Chemical group 0.000 description 3
- 150000001408 amides Chemical class 0.000 description 3
- 108091008324 binding proteins Proteins 0.000 description 3
- 229940098773 bovine serum albumin Drugs 0.000 description 3
- 230000003197 catalytic effect Effects 0.000 description 3
- 239000007795 chemical reaction product Substances 0.000 description 3
- 239000003153 chemical reaction reagent Substances 0.000 description 3
- 238000003776 cleavage reaction Methods 0.000 description 3
- 238000007599 discharging Methods 0.000 description 3
- 238000009826 distribution Methods 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 235000014103 egg white Nutrition 0.000 description 3
- 210000000969 egg white Anatomy 0.000 description 3
- 229920002549 elastin Polymers 0.000 description 3
- 238000000605 extraction Methods 0.000 description 3
- 230000002349 favourable effect Effects 0.000 description 3
- GNBHRKFJIUUOQI-UHFFFAOYSA-N fluorescein Chemical compound O1C(=O)C2=CC=CC=C2C21C1=CC=C(O)C=C1OC1=CC(O)=CC=C21 GNBHRKFJIUUOQI-UHFFFAOYSA-N 0.000 description 3
- 238000005187 foaming Methods 0.000 description 3
- 235000019253 formic acid Nutrition 0.000 description 3
- 238000007429 general method Methods 0.000 description 3
- 235000021312 gluten Nutrition 0.000 description 3
- 230000002163 immunogen Effects 0.000 description 3
- 238000001114 immunoprecipitation Methods 0.000 description 3
- 239000003456 ion exchange resin Substances 0.000 description 3
- 229920003303 ion-exchange polymer Polymers 0.000 description 3
- 150000002500 ions Chemical class 0.000 description 3
- 238000002955 isolation Methods 0.000 description 3
- 229960000310 isoleucine Drugs 0.000 description 3
- 230000035800 maturation Effects 0.000 description 3
- 230000003278 mimic effect Effects 0.000 description 3
- 201000000050 myeloid neoplasm Diseases 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 230000035764 nutrition Effects 0.000 description 3
- 235000016709 nutrition Nutrition 0.000 description 3
- 210000000496 pancreas Anatomy 0.000 description 3
- 230000037361 pathway Effects 0.000 description 3
- OAHKWDDSKCRNFE-UHFFFAOYSA-N phenylmethanesulfonyl chloride Chemical compound ClS(=O)(=O)CC1=CC=CC=C1 OAHKWDDSKCRNFE-UHFFFAOYSA-N 0.000 description 3
- 230000004962 physiological condition Effects 0.000 description 3
- 238000011533 pre-incubation Methods 0.000 description 3
- 230000020978 protein processing Effects 0.000 description 3
- 238000003127 radioimmunoassay Methods 0.000 description 3
- 239000000376 reactant Substances 0.000 description 3
- 230000008521 reorganization Effects 0.000 description 3
- 230000002441 reversible effect Effects 0.000 description 3
- 230000000630 rising effect Effects 0.000 description 3
- 108010073419 scinderin Proteins 0.000 description 3
- 230000007017 scission Effects 0.000 description 3
- 230000035945 sensitivity Effects 0.000 description 3
- 238000010532 solid phase synthesis reaction Methods 0.000 description 3
- 230000028070 sporulation Effects 0.000 description 3
- 238000003153 stable transfection Methods 0.000 description 3
- 238000006467 substitution reaction Methods 0.000 description 3
- 150000003573 thiols Chemical class 0.000 description 3
- 230000002103 transcriptional effect Effects 0.000 description 3
- 238000001262 western blot Methods 0.000 description 3
- 235000021246 κ-casein Nutrition 0.000 description 3
- DIGQNXIGRZPYDK-WKSCXVIASA-N (2R)-6-amino-2-[[2-[[(2S)-2-[[2-[[(2R)-2-[[(2S)-2-[[(2R,3S)-2-[[2-[[(2S)-2-[[2-[[(2S)-2-[[(2S)-2-[[(2R)-2-[[(2S,3S)-2-[[(2R)-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-[[2-[[(2S)-2-[[(2R)-2-[[2-[[2-[[2-[(2-amino-1-hydroxyethylidene)amino]-3-carboxy-1-hydroxypropylidene]amino]-1-hydroxy-3-sulfanylpropylidene]amino]-1-hydroxyethylidene]amino]-1-hydroxy-3-sulfanylpropylidene]amino]-1,3-dihydroxypropylidene]amino]-1-hydroxyethylidene]amino]-1-hydroxypropylidene]amino]-1,3-dihydroxypropylidene]amino]-1,3-dihydroxypropylidene]amino]-1-hydroxy-3-sulfanylpropylidene]amino]-1,3-dihydroxybutylidene]amino]-1-hydroxy-3-sulfanylpropylidene]amino]-1-hydroxypropylidene]amino]-1,3-dihydroxypropylidene]amino]-1-hydroxyethylidene]amino]-1,5-dihydroxy-5-iminopentylidene]amino]-1-hydroxy-3-sulfanylpropylidene]amino]-1,3-dihydroxybutylidene]amino]-1-hydroxy-3-sulfanylpropylidene]amino]-1,3-dihydroxypropylidene]amino]-1-hydroxyethylidene]amino]-1-hydroxy-3-sulfanylpropylidene]amino]-1-hydroxyethylidene]amino]hexanoic acid Chemical compound C[C@@H]([C@@H](C(=N[C@@H](CS)C(=N[C@@H](C)C(=N[C@@H](CO)C(=NCC(=N[C@@H](CCC(=N)O)C(=NC(CS)C(=N[C@H]([C@H](C)O)C(=N[C@H](CS)C(=N[C@H](CO)C(=NCC(=N[C@H](CS)C(=NCC(=N[C@H](CCCCN)C(=O)O)O)O)O)O)O)O)O)O)O)O)O)O)O)N=C([C@H](CS)N=C([C@H](CO)N=C([C@H](CO)N=C([C@H](C)N=C(CN=C([C@H](CO)N=C([C@H](CS)N=C(CN=C(C(CS)N=C(C(CC(=O)O)N=C(CN)O)O)O)O)O)O)O)O)O)O)O)O DIGQNXIGRZPYDK-WKSCXVIASA-N 0.000 description 2
- DSSYKIVIOFKYAU-XCBNKYQSSA-N (R)-camphor Chemical compound C1C[C@@]2(C)C(=O)C[C@@H]1C2(C)C DSSYKIVIOFKYAU-XCBNKYQSSA-N 0.000 description 2
- 125000001917 2,4-dinitrophenyl group Chemical group [H]C1=C([H])C(=C([H])C(=C1*)[N+]([O-])=O)[N+]([O-])=O 0.000 description 2
- TYMLOMAKGOJONV-UHFFFAOYSA-N 4-nitroaniline Chemical compound NC1=CC=C([N+]([O-])=O)C=C1 TYMLOMAKGOJONV-UHFFFAOYSA-N 0.000 description 2
- BTJIUGUIPKRLHP-UHFFFAOYSA-N 4-nitrophenol Chemical class OC1=CC=C([N+]([O-])=O)C=C1 BTJIUGUIPKRLHP-UHFFFAOYSA-N 0.000 description 2
- 229920000936 Agarose Polymers 0.000 description 2
- 101710184263 Alkaline serine protease Proteins 0.000 description 2
- 108700028369 Alleles Proteins 0.000 description 2
- 239000004475 Arginine Substances 0.000 description 2
- 241001513093 Aspergillus awamori Species 0.000 description 2
- 241000351920 Aspergillus nidulans Species 0.000 description 2
- 101100407629 Aspergillus niger pepA gene Proteins 0.000 description 2
- 101100136076 Aspergillus oryzae (strain ATCC 42149 / RIB 40) pel1 gene Proteins 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 241000193830 Bacillus <bacterium> Species 0.000 description 2
- 241000194108 Bacillus licheniformis Species 0.000 description 2
- 108010078791 Carrier Proteins Proteins 0.000 description 2
- 108091026890 Coding region Proteins 0.000 description 2
- 102000029816 Collagenase Human genes 0.000 description 2
- 108060005980 Collagenase Proteins 0.000 description 2
- 108020004635 Complementary DNA Proteins 0.000 description 2
- 229920000742 Cotton Polymers 0.000 description 2
- 241000701022 Cytomegalovirus Species 0.000 description 2
- XPDXVDYUQZHFPV-UHFFFAOYSA-N Dansyl Chloride Chemical compound C1=CC=C2C(N(C)C)=CC=CC2=C1S(Cl)(=O)=O XPDXVDYUQZHFPV-UHFFFAOYSA-N 0.000 description 2
- 241000702421 Dependoparvovirus Species 0.000 description 2
- 101100030911 Dickeya chrysanthemi prtF gene Proteins 0.000 description 2
- 102100031780 Endonuclease Human genes 0.000 description 2
- 108010042407 Endonucleases Proteins 0.000 description 2
- 101000925662 Enterobacteria phage PRD1 Endolysin Proteins 0.000 description 2
- 101710091045 Envelope protein Proteins 0.000 description 2
- PLUBXMRUUVWRLT-UHFFFAOYSA-N Ethyl methanesulfonate Chemical compound CCOS(C)(=O)=O PLUBXMRUUVWRLT-UHFFFAOYSA-N 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- 241000206602 Eukaryota Species 0.000 description 2
- 108050001049 Extracellular proteins Proteins 0.000 description 2
- 241000700662 Fowlpox virus Species 0.000 description 2
- 108010010803 Gelatin Proteins 0.000 description 2
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 2
- WHUUTDBJXJRKMK-UHFFFAOYSA-N Glutamic acid Natural products OC(=O)C(N)CCC(O)=O WHUUTDBJXJRKMK-UHFFFAOYSA-N 0.000 description 2
- 101710154606 Hemagglutinin Proteins 0.000 description 2
- 240000005979 Hordeum vulgare Species 0.000 description 2
- 235000007340 Hordeum vulgare Nutrition 0.000 description 2
- 102000004877 Insulin Human genes 0.000 description 2
- 108090001061 Insulin Proteins 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- AMIMRNSIRUDHCM-UHFFFAOYSA-N Isopropylaldehyde Chemical compound CC(C)C=O AMIMRNSIRUDHCM-UHFFFAOYSA-N 0.000 description 2
- 241001138401 Kluyveromyces lactis Species 0.000 description 2
- ODKSFYDXXFIFQN-BYPYZUCNSA-P L-argininium(2+) Chemical compound NC(=[NH2+])NCCC[C@H]([NH3+])C(O)=O ODKSFYDXXFIFQN-BYPYZUCNSA-P 0.000 description 2
- DCXYFEDJOCDNAF-REOHCLBHSA-N L-asparagine Chemical compound OC(=O)[C@@H](N)CC(N)=O DCXYFEDJOCDNAF-REOHCLBHSA-N 0.000 description 2
- ZDXPYRJPNDTMRX-VKHMYHEASA-N L-glutamine Chemical compound OC(=O)[C@@H](N)CCC(N)=O ZDXPYRJPNDTMRX-VKHMYHEASA-N 0.000 description 2
- QIVBCDIJIAJPQS-VIFPVBQESA-N L-tryptophane Chemical compound C1=CC=C2C(C[C@H](N)C(O)=O)=CNC2=C1 QIVBCDIJIAJPQS-VIFPVBQESA-N 0.000 description 2
- 101100434212 Listeria monocytogenes serovar 1/2a (strain ATCC BAA-679 / EGD-e) actA gene Proteins 0.000 description 2
- 206010027336 Menstruation delayed Diseases 0.000 description 2
- 102000003792 Metallothionein Human genes 0.000 description 2
- 108090000157 Metallothionein Proteins 0.000 description 2
- 102000014171 Milk Proteins Human genes 0.000 description 2
- 108010011756 Milk Proteins Proteins 0.000 description 2
- 108010006519 Molecular Chaperones Proteins 0.000 description 2
- VZUNGTLZRAYYDE-UHFFFAOYSA-N N-methyl-N'-nitro-N-nitrosoguanidine Chemical compound O=NN(C)C(=N)N[N+]([O-])=O VZUNGTLZRAYYDE-UHFFFAOYSA-N 0.000 description 2
- 238000000636 Northern blotting Methods 0.000 description 2
- 240000007594 Oryza sativa Species 0.000 description 2
- 235000007164 Oryza sativa Nutrition 0.000 description 2
- 101710093908 Outer capsid protein VP4 Proteins 0.000 description 2
- 101710135467 Outer capsid protein sigma-1 Proteins 0.000 description 2
- 101150095051 PRTG gene Proteins 0.000 description 2
- 108010084695 Pea Proteins Proteins 0.000 description 2
- 229920002230 Pectic acid Polymers 0.000 description 2
- 102000057297 Pepsin A Human genes 0.000 description 2
- 108090000284 Pepsin A Proteins 0.000 description 2
- 241000276498 Pollachius virens Species 0.000 description 2
- 239000004793 Polystyrene Substances 0.000 description 2
- 108090000708 Proteasome Endopeptidase Complex Proteins 0.000 description 2
- 102000004245 Proteasome Endopeptidase Complex Human genes 0.000 description 2
- 101710176177 Protein A56 Proteins 0.000 description 2
- 101710188315 Protein X Proteins 0.000 description 2
- 241000235525 Rhizomucor pusillus Species 0.000 description 2
- AUNGANRZJHBGPY-SCRDCRAPSA-N Riboflavin Chemical compound OC[C@@H](O)[C@@H](O)[C@@H](O)CN1C=2C=C(C)C(C)=CC=2N=C2C1=NC(=O)NC2=O AUNGANRZJHBGPY-SCRDCRAPSA-N 0.000 description 2
- 241000714474 Rous sarcoma virus Species 0.000 description 2
- 241000293869 Salmonella enterica subsp. enterica serovar Typhimurium Species 0.000 description 2
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 2
- 244000061456 Solanum tuberosum Species 0.000 description 2
- 235000002595 Solanum tuberosum Nutrition 0.000 description 2
- 108010073771 Soybean Proteins Proteins 0.000 description 2
- 241000187747 Streptomyces Species 0.000 description 2
- 241000701093 Suid alphaherpesvirus 1 Species 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- 239000005864 Sulphur Substances 0.000 description 2
- 108020005038 Terminator Codon Proteins 0.000 description 2
- AYFVYJQAPQTCCC-UHFFFAOYSA-N Threonine Natural products CC(O)C(N)C(O)=O AYFVYJQAPQTCCC-UHFFFAOYSA-N 0.000 description 2
- 239000004473 Threonine Substances 0.000 description 2
- 235000021307 Triticum Nutrition 0.000 description 2
- 244000098338 Triticum aestivum Species 0.000 description 2
- QIVBCDIJIAJPQS-UHFFFAOYSA-N Tryptophan Natural products C1=CC=C2C(CC(N)C(O)=O)=CNC2=C1 QIVBCDIJIAJPQS-UHFFFAOYSA-N 0.000 description 2
- 239000006035 Tryptophane Substances 0.000 description 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
- 241000700618 Vaccinia virus Species 0.000 description 2
- 240000008042 Zea mays Species 0.000 description 2
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 2
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 2
- 239000004480 active ingredient Substances 0.000 description 2
- 230000032683 aging Effects 0.000 description 2
- AEMOLEFTQBMNLQ-BKBMJHBISA-M alpha-D-galacturonate Chemical compound O[C@H]1O[C@H](C([O-])=O)[C@H](O)[C@H](O)[C@H]1O AEMOLEFTQBMNLQ-BKBMJHBISA-M 0.000 description 2
- 102000005840 alpha-Galactosidase Human genes 0.000 description 2
- 108010030291 alpha-Galactosidase Proteins 0.000 description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 2
- 230000008485 antagonism Effects 0.000 description 2
- RWZYAGGXGHYGMB-UHFFFAOYSA-N anthranilic acid Chemical compound NC1=CC=CC=C1C(O)=O RWZYAGGXGHYGMB-UHFFFAOYSA-N 0.000 description 2
- 230000005875 antibody response Effects 0.000 description 2
- ODKSFYDXXFIFQN-UHFFFAOYSA-N arginine Natural products OC(=O)C(N)CCCNC(N)=N ODKSFYDXXFIFQN-UHFFFAOYSA-N 0.000 description 2
- 235000003704 aspartic acid Nutrition 0.000 description 2
- 238000003556 assay Methods 0.000 description 2
- OQFSQFPPLPISGP-UHFFFAOYSA-N beta-carboxyaspartic acid Natural products OC(=O)C(N)C(C(O)=O)C(O)=O OQFSQFPPLPISGP-UHFFFAOYSA-N 0.000 description 2
- 230000008827 biological function Effects 0.000 description 2
- 230000033228 biological regulation Effects 0.000 description 2
- 229960000846 camphor Drugs 0.000 description 2
- 238000004113 cell culture Methods 0.000 description 2
- 230000001413 cellular effect Effects 0.000 description 2
- 239000002962 chemical mutagen Substances 0.000 description 2
- 230000002759 chromosomal effect Effects 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- 229960002424 collagenase Drugs 0.000 description 2
- 230000001276 controlling effect Effects 0.000 description 2
- 235000005822 corn Nutrition 0.000 description 2
- GLNDAGDHSLMOKX-UHFFFAOYSA-N coumarin 120 Chemical compound C1=C(N)C=CC2=C1OC(=O)C=C2C GLNDAGDHSLMOKX-UHFFFAOYSA-N 0.000 description 2
- 235000020247 cow milk Nutrition 0.000 description 2
- 125000000151 cysteine group Chemical group N[C@@H](CS)C(=O)* 0.000 description 2
- 230000009849 deactivation Effects 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 230000000593 degrading effect Effects 0.000 description 2
- 230000001066 destructive effect Effects 0.000 description 2
- 239000003599 detergent Substances 0.000 description 2
- 235000021245 dietary protein Nutrition 0.000 description 2
- 230000001079 digestive effect Effects 0.000 description 2
- MUCZHBLJLSDCSD-UHFFFAOYSA-N diisopropyl fluorophosphate Chemical compound CC(C)OP(F)(=O)OC(C)C MUCZHBLJLSDCSD-UHFFFAOYSA-N 0.000 description 2
- 201000010099 disease Diseases 0.000 description 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 2
- 229940079593 drug Drugs 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- 238000004043 dyeing Methods 0.000 description 2
- 230000003246 elastolytic effect Effects 0.000 description 2
- 239000003995 emulsifying agent Substances 0.000 description 2
- 210000002472 endoplasmic reticulum Anatomy 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
- 238000006911 enzymatic reaction Methods 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 229960005051 fluostigmine Drugs 0.000 description 2
- 239000010200 folin Substances 0.000 description 2
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 description 2
- 239000008273 gelatin Substances 0.000 description 2
- 229920000159 gelatin Polymers 0.000 description 2
- 235000019322 gelatine Nutrition 0.000 description 2
- 235000011852 gelatine desserts Nutrition 0.000 description 2
- 238000003209 gene knockout Methods 0.000 description 2
- 102000034238 globular proteins Human genes 0.000 description 2
- 108091005896 globular proteins Proteins 0.000 description 2
- 239000008103 glucose Substances 0.000 description 2
- 235000013922 glutamic acid Nutrition 0.000 description 2
- 239000004220 glutamic acid Substances 0.000 description 2
- ZDXPYRJPNDTMRX-UHFFFAOYSA-N glutamine Natural products OC(=O)C(N)CCC(N)=O ZDXPYRJPNDTMRX-UHFFFAOYSA-N 0.000 description 2
- RWSXRVCMGQZWBV-WDSKDSINSA-N glutathione Chemical compound OC(=O)[C@@H](N)CCC(=O)N[C@@H](CS)C(=O)NCC(O)=O RWSXRVCMGQZWBV-WDSKDSINSA-N 0.000 description 2
- UYTPUPDQBNUYGX-UHFFFAOYSA-N guanine Chemical compound O=C1NC(N)=NC2=C1N=CN2 UYTPUPDQBNUYGX-UHFFFAOYSA-N 0.000 description 2
- RQFCJASXJCIDSX-UUOKFMHZSA-N guanosine 5'-monophosphate Chemical compound C1=2NC(N)=NC(=O)C=2N=CN1[C@@H]1O[C@H](COP(O)(O)=O)[C@@H](O)[C@H]1O RQFCJASXJCIDSX-UUOKFMHZSA-N 0.000 description 2
- 238000002744 homologous recombination Methods 0.000 description 2
- 230000006801 homologous recombination Effects 0.000 description 2
- 210000003917 human chromosome Anatomy 0.000 description 2
- 229910052588 hydroxylapatite Inorganic materials 0.000 description 2
- 230000028993 immune response Effects 0.000 description 2
- 239000003547 immunosorbent Substances 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 238000000338 in vitro Methods 0.000 description 2
- 208000015181 infectious disease Diseases 0.000 description 2
- 210000000936 intestine Anatomy 0.000 description 2
- 238000004255 ion exchange chromatography Methods 0.000 description 2
- 238000005040 ion trap Methods 0.000 description 2
- KQNPFQTWMSNSAP-UHFFFAOYSA-N isobutyric acid Chemical compound CC(C)C(O)=O KQNPFQTWMSNSAP-UHFFFAOYSA-N 0.000 description 2
- AGPKZVBTJJNPAG-UHFFFAOYSA-N isoleucine Natural products CCC(C)C(N)C(O)=O AGPKZVBTJJNPAG-UHFFFAOYSA-N 0.000 description 2
- 238000012417 linear regression Methods 0.000 description 2
- 238000004895 liquid chromatography mass spectrometry Methods 0.000 description 2
- 230000007774 longterm Effects 0.000 description 2
- 230000002101 lytic effect Effects 0.000 description 2
- 230000004060 metabolic process Effects 0.000 description 2
- CKFGINPQOCXMAZ-UHFFFAOYSA-N methanediol Chemical compound OCO CKFGINPQOCXMAZ-UHFFFAOYSA-N 0.000 description 2
- 235000021239 milk protein Nutrition 0.000 description 2
- 235000013923 monosodium glutamate Nutrition 0.000 description 2
- 231100000219 mutagenic Toxicity 0.000 description 2
- 230000003505 mutagenic effect Effects 0.000 description 2
- 230000035772 mutation Effects 0.000 description 2
- AIUKPEQJKQUQKZ-UHFFFAOYSA-N n'-(2,4-dinitrophenyl)ethane-1,2-diamine Chemical compound NCCNC1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O AIUKPEQJKQUQKZ-UHFFFAOYSA-N 0.000 description 2
- 235000018343 nutrient deficiency Nutrition 0.000 description 2
- 230000000050 nutritive effect Effects 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- 230000008520 organization Effects 0.000 description 2
- 230000036961 partial effect Effects 0.000 description 2
- 238000005192 partition Methods 0.000 description 2
- 235000015927 pasta Nutrition 0.000 description 2
- 229920001277 pectin Polymers 0.000 description 2
- 101150040383 pel2 gene Proteins 0.000 description 2
- 101150050446 pelB gene Proteins 0.000 description 2
- XYJRXVWERLGGKC-UHFFFAOYSA-D pentacalcium;hydroxide;triphosphate Chemical compound [OH-].[Ca+2].[Ca+2].[Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O XYJRXVWERLGGKC-UHFFFAOYSA-D 0.000 description 2
- 229940111202 pepsin Drugs 0.000 description 2
- 210000001322 periplasm Anatomy 0.000 description 2
- 238000002823 phage display Methods 0.000 description 2
- 230000008488 polyadenylation Effects 0.000 description 2
- 229920002223 polystyrene Polymers 0.000 description 2
- 244000144977 poultry Species 0.000 description 2
- 235000004252 protein component Nutrition 0.000 description 2
- 230000007065 protein hydrolysis Effects 0.000 description 2
- 101150038570 prtB gene Proteins 0.000 description 2
- 238000010926 purge Methods 0.000 description 2
- 238000010791 quenching Methods 0.000 description 2
- 230000000171 quenching effect Effects 0.000 description 2
- 239000012857 radioactive material Substances 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 102000005962 receptors Human genes 0.000 description 2
- 108020003175 receptors Proteins 0.000 description 2
- 230000006798 recombination Effects 0.000 description 2
- 238000005215 recombination Methods 0.000 description 2
- 230000009711 regulatory function Effects 0.000 description 2
- 230000004044 response Effects 0.000 description 2
- 238000010839 reverse transcription Methods 0.000 description 2
- PYWVYCXTNDRMGF-UHFFFAOYSA-N rhodamine B Chemical compound [Cl-].C=12C=CC(=[N+](CC)CC)C=C2OC2=CC(N(CC)CC)=CC=C2C=1C1=CC=CC=C1C(O)=O PYWVYCXTNDRMGF-UHFFFAOYSA-N 0.000 description 2
- 239000002336 ribonucleotide Substances 0.000 description 2
- 235000009566 rice Nutrition 0.000 description 2
- 238000004062 sedimentation Methods 0.000 description 2
- 238000003375 selectivity assay Methods 0.000 description 2
- 230000035807 sensation Effects 0.000 description 2
- 235000019615 sensations Nutrition 0.000 description 2
- 230000014860 sensory perception of taste Effects 0.000 description 2
- 238000012882 sequential analysis Methods 0.000 description 2
- 230000035939 shock Effects 0.000 description 2
- 238000002741 site-directed mutagenesis Methods 0.000 description 2
- 239000001632 sodium acetate Substances 0.000 description 2
- 235000017281 sodium acetate Nutrition 0.000 description 2
- 210000004988 splenocyte Anatomy 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- 230000014621 translational initiation Effects 0.000 description 2
- 229960004799 tryptophan Drugs 0.000 description 2
- OUYCCCASQSFEME-UHFFFAOYSA-N tyrosine Natural products OC(=O)C(N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-UHFFFAOYSA-N 0.000 description 2
- 238000000108 ultra-filtration Methods 0.000 description 2
- 241000712461 unidentified influenza virus Species 0.000 description 2
- 230000003612 virological effect Effects 0.000 description 2
- 239000003643 water by type Substances 0.000 description 2
- YBJHBAHKTGYVGT-ZKWXMUAHSA-N (+)-Biotin Chemical compound N1C(=O)N[C@@H]2[C@H](CCCCC(=O)O)SC[C@@H]21 YBJHBAHKTGYVGT-ZKWXMUAHSA-N 0.000 description 1
- IVWWFWFVSWOTLP-YVZVNANGSA-N (3'as,4r,7'as)-2,2,2',2'-tetramethylspiro[1,3-dioxolane-4,6'-4,7a-dihydro-3ah-[1,3]dioxolo[4,5-c]pyran]-7'-one Chemical compound C([C@@H]1OC(O[C@@H]1C1=O)(C)C)O[C@]21COC(C)(C)O2 IVWWFWFVSWOTLP-YVZVNANGSA-N 0.000 description 1
- ASWBNKHCZGQVJV-UHFFFAOYSA-N (3-hexadecanoyloxy-2-hydroxypropyl) 2-(trimethylazaniumyl)ethyl phosphate Chemical compound CCCCCCCCCCCCCCCC(=O)OCC(O)COP([O-])(=O)OCC[N+](C)(C)C ASWBNKHCZGQVJV-UHFFFAOYSA-N 0.000 description 1
- NWXMGUDVXFXRIG-WESIUVDSSA-N (4s,4as,5as,6s,12ar)-4-(dimethylamino)-1,6,10,11,12a-pentahydroxy-6-methyl-3,12-dioxo-4,4a,5,5a-tetrahydrotetracene-2-carboxamide Chemical compound C1=CC=C2[C@](O)(C)[C@H]3C[C@H]4[C@H](N(C)C)C(=O)C(C(N)=O)=C(O)[C@@]4(O)C(=O)C3=C(O)C2=C1O NWXMGUDVXFXRIG-WESIUVDSSA-N 0.000 description 1
- 125000006701 (C1-C7) alkyl group Chemical group 0.000 description 1
- SUNMBRGCANLOEG-UHFFFAOYSA-N 1,3-dichloroacetone Chemical class ClCC(=O)CCl SUNMBRGCANLOEG-UHFFFAOYSA-N 0.000 description 1
- LOTKRQAVGJMPNV-UHFFFAOYSA-N 1-fluoro-2,4-dinitrobenzene Chemical compound [O-][N+](=O)C1=CC=C(F)C([N+]([O-])=O)=C1 LOTKRQAVGJMPNV-UHFFFAOYSA-N 0.000 description 1
- NHJVRSWLHSJWIN-UHFFFAOYSA-N 2,4,6-trinitrobenzenesulfonic acid Chemical compound OS(=O)(=O)C1=C([N+]([O-])=O)C=C([N+]([O-])=O)C=C1[N+]([O-])=O NHJVRSWLHSJWIN-UHFFFAOYSA-N 0.000 description 1
- UFBJCMHMOXMLKC-UHFFFAOYSA-N 2,4-dinitrophenol Chemical compound OC1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O UFBJCMHMOXMLKC-UHFFFAOYSA-N 0.000 description 1
- GTACSIONMHMRPD-UHFFFAOYSA-N 2-[4-[2-(benzenesulfonamido)ethylsulfanyl]-2,6-difluorophenoxy]acetamide Chemical compound C1=C(F)C(OCC(=O)N)=C(F)C=C1SCCNS(=O)(=O)C1=CC=CC=C1 GTACSIONMHMRPD-UHFFFAOYSA-N 0.000 description 1
- QKNYBSVHEMOAJP-UHFFFAOYSA-N 2-amino-2-(hydroxymethyl)propane-1,3-diol;hydron;chloride Chemical compound Cl.OCC(N)(CO)CO QKNYBSVHEMOAJP-UHFFFAOYSA-N 0.000 description 1
- 125000000022 2-aminoethyl group Chemical group [H]C([*])([H])C([H])([H])N([H])[H] 0.000 description 1
- LOUORYQQOPCXGD-UHFFFAOYSA-N 2-methylpropan-1-ol Chemical compound CC(C)CO.CC(C)CO LOUORYQQOPCXGD-UHFFFAOYSA-N 0.000 description 1
- 150000005341 2-nitrobenzoic acids Chemical class 0.000 description 1
- AQFATCCHOXBYNK-UHFFFAOYSA-N 2-piperidin-1-ium-1-ylethyl 1-cyclohexylcyclohexane-1-carboxylate;chloride Chemical compound [Cl-].C1CCCCC1(C1CCCCC1)C(=O)OCC[NH+]1CCCCC1 AQFATCCHOXBYNK-UHFFFAOYSA-N 0.000 description 1
- OALHHIHQOFIMEF-UHFFFAOYSA-N 3',6'-dihydroxy-2',4',5',7'-tetraiodo-3h-spiro[2-benzofuran-1,9'-xanthene]-3-one Chemical compound O1C(=O)C2=CC=CC=C2C21C1=CC(I)=C(O)C(I)=C1OC1=C(I)C(O)=C(I)C=C21 OALHHIHQOFIMEF-UHFFFAOYSA-N 0.000 description 1
- 101800000535 3C-like proteinase Proteins 0.000 description 1
- 101800002396 3C-like proteinase nsp5 Proteins 0.000 description 1
- WCKQPPQRFNHPRJ-UHFFFAOYSA-N 4-[[4-(dimethylamino)phenyl]diazenyl]benzoic acid Chemical compound C1=CC(N(C)C)=CC=C1N=NC1=CC=C(C(O)=O)C=C1 WCKQPPQRFNHPRJ-UHFFFAOYSA-N 0.000 description 1
- QWKKYJLAUWFPDB-UHFFFAOYSA-N 4-nitrobenzenesulfonamide Chemical class NS(=O)(=O)C1=CC=C([N+]([O-])=O)C=C1 QWKKYJLAUWFPDB-UHFFFAOYSA-N 0.000 description 1
- SJQRQOKXQKVJGJ-UHFFFAOYSA-N 5-(2-aminoethylamino)naphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(NCCN)=CC=CC2=C1S(O)(=O)=O SJQRQOKXQKVJGJ-UHFFFAOYSA-N 0.000 description 1
- CJIJXIFQYOPWTF-UHFFFAOYSA-N 7-hydroxycoumarin Natural products O1C(=O)C=CC2=CC(O)=CC=C21 CJIJXIFQYOPWTF-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- 239000005541 ACE inhibitor Substances 0.000 description 1
- 208000030507 AIDS Diseases 0.000 description 1
- 108010022752 Acetylcholinesterase Proteins 0.000 description 1
- 102000012440 Acetylcholinesterase Human genes 0.000 description 1
- 241000251468 Actinopterygii Species 0.000 description 1
- 102100032488 Acylamino-acid-releasing enzyme Human genes 0.000 description 1
- 108010061216 Acylaminoacyl-peptidase Proteins 0.000 description 1
- 108010000239 Aequorin Proteins 0.000 description 1
- 229920001817 Agar Polymers 0.000 description 1
- 101710134784 Agnoprotein Proteins 0.000 description 1
- 102100024321 Alkaline phosphatase, placental type Human genes 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 108010032595 Antibody Binding Sites Proteins 0.000 description 1
- 108010011485 Aspartame Proteins 0.000 description 1
- 108091005502 Aspartic proteases Proteins 0.000 description 1
- 102000035101 Aspartic proteases Human genes 0.000 description 1
- 101710130081 Aspergillopepsin-1 Proteins 0.000 description 1
- 101100136075 Aspergillus niger pelB gene Proteins 0.000 description 1
- 240000006439 Aspergillus oryzae Species 0.000 description 1
- 235000002247 Aspergillus oryzae Nutrition 0.000 description 1
- 108090000145 Bacillolysin Proteins 0.000 description 1
- 108010001478 Bacitracin Proteins 0.000 description 1
- 108091005658 Basic proteases Proteins 0.000 description 1
- VGGGPCQERPFHOB-MCIONIFRSA-N Bestatin Chemical compound CC(C)C[C@H](C(O)=O)NC(=O)[C@@H](O)[C@H](N)CC1=CC=CC=C1 VGGGPCQERPFHOB-MCIONIFRSA-N 0.000 description 1
- VGGGPCQERPFHOB-UHFFFAOYSA-N Bestatin Natural products CC(C)CC(C(O)=O)NC(=O)C(O)C(N)CC1=CC=CC=C1 VGGGPCQERPFHOB-UHFFFAOYSA-N 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- 108010017384 Blood Proteins Proteins 0.000 description 1
- 102000004506 Blood Proteins Human genes 0.000 description 1
- 241000283690 Bos taurus Species 0.000 description 1
- 101710202338 Bowman-Birk type trypsin inhibitor Proteins 0.000 description 1
- 240000002791 Brassica napus Species 0.000 description 1
- 235000004977 Brassica sinapistrum Nutrition 0.000 description 1
- ALFRSZISNFQELS-UHFFFAOYSA-M C(CCCCCCCCCCCCCCCCC)(=O)[O-].C(C(O)C)(=O)[Ca+] Chemical compound C(CCCCCCCCCCCCCCCCC)(=O)[O-].C(C(O)C)(=O)[Ca+] ALFRSZISNFQELS-UHFFFAOYSA-M 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- BHPQYMZQTOCNFJ-UHFFFAOYSA-N Calcium cation Chemical compound [Ca+2] BHPQYMZQTOCNFJ-UHFFFAOYSA-N 0.000 description 1
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- 240000006432 Carica papaya Species 0.000 description 1
- 235000009467 Carica papaya Nutrition 0.000 description 1
- 102000003908 Cathepsin D Human genes 0.000 description 1
- 108090000258 Cathepsin D Proteins 0.000 description 1
- 108090000624 Cathepsin L Proteins 0.000 description 1
- 102000004172 Cathepsin L Human genes 0.000 description 1
- 108090000317 Chymotrypsin Proteins 0.000 description 1
- 229940122644 Chymotrypsin inhibitor Drugs 0.000 description 1
- 101710137926 Chymotrypsin inhibitor Proteins 0.000 description 1
- 102100025566 Chymotrypsin-like protease CTRL-1 Human genes 0.000 description 1
- 108091062157 Cis-regulatory element Proteins 0.000 description 1
- 108010065152 Coagulase Proteins 0.000 description 1
- 108091033380 Coding strand Proteins 0.000 description 1
- 241001362614 Crassa Species 0.000 description 1
- 102100034560 Cytosol aminopeptidase Human genes 0.000 description 1
- 102100031007 Cytosolic non-specific dipeptidase Human genes 0.000 description 1
- IGXWBGJHJZYPQS-SSDOTTSWSA-N D-Luciferin Chemical compound OC(=O)[C@H]1CSC(C=2SC3=CC=C(O)C=C3N=2)=N1 IGXWBGJHJZYPQS-SSDOTTSWSA-N 0.000 description 1
- AUNGANRZJHBGPY-UHFFFAOYSA-N D-Lyxoflavin Natural products OCC(O)C(O)C(O)CN1C=2C=C(C)C(C)=CC=2N=C2C1=NC(=O)NC2=O AUNGANRZJHBGPY-UHFFFAOYSA-N 0.000 description 1
- 244000000626 Daucus carota Species 0.000 description 1
- 235000002767 Daucus carota Nutrition 0.000 description 1
- CYCGRDQQIOGCKX-UHFFFAOYSA-N Dehydro-luciferin Natural products OC(=O)C1=CSC(C=2SC3=CC(O)=CC=C3N=2)=N1 CYCGRDQQIOGCKX-UHFFFAOYSA-N 0.000 description 1
- 101100317179 Dictyostelium discoideum vps26 gene Proteins 0.000 description 1
- 229940122858 Elastase inhibitor Drugs 0.000 description 1
- 101100407639 Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) prtB gene Proteins 0.000 description 1
- 108010013369 Enteropeptidase Proteins 0.000 description 1
- 102100029727 Enteropeptidase Human genes 0.000 description 1
- 241000588698 Erwinia Species 0.000 description 1
- 101000867232 Escherichia coli Heat-stable enterotoxin II Proteins 0.000 description 1
- 101710129170 Extensin Proteins 0.000 description 1
- 108010074860 Factor Xa Proteins 0.000 description 1
- 108010028690 Fish Proteins Proteins 0.000 description 1
- BJGNCJDXODQBOB-UHFFFAOYSA-N Fivefly Luciferin Natural products OC(=O)C1CSC(C=2SC3=CC(O)=CC=C3N=2)=N1 BJGNCJDXODQBOB-UHFFFAOYSA-N 0.000 description 1
- 241000710198 Foot-and-mouth disease virus Species 0.000 description 1
- 108010058643 Fungal Proteins Proteins 0.000 description 1
- 108700028146 Genetic Enhancer Elements Proteins 0.000 description 1
- 206010071602 Genetic polymorphism Diseases 0.000 description 1
- 239000004366 Glucose oxidase Substances 0.000 description 1
- 108010015776 Glucose oxidase Proteins 0.000 description 1
- SXRSQZLOMIGNAQ-UHFFFAOYSA-N Glutaraldehyde Chemical compound O=CCCCC=O SXRSQZLOMIGNAQ-UHFFFAOYSA-N 0.000 description 1
- 108010024636 Glutathione Proteins 0.000 description 1
- 108090000288 Glycoproteins Proteins 0.000 description 1
- 102000003886 Glycoproteins Human genes 0.000 description 1
- 108010073032 Grain Proteins Proteins 0.000 description 1
- 102100039620 Granulocyte-macrophage colony-stimulating factor Human genes 0.000 description 1
- 244000020551 Helianthus annuus Species 0.000 description 1
- 235000003222 Helianthus annuus Nutrition 0.000 description 1
- 108010033040 Histones Proteins 0.000 description 1
- 102000009331 Homeodomain Proteins Human genes 0.000 description 1
- 108010048671 Homeodomain Proteins Proteins 0.000 description 1
- 241000282412 Homo Species 0.000 description 1
- 101000856199 Homo sapiens Chymotrypsin-like protease CTRL-1 Proteins 0.000 description 1
- 101000746373 Homo sapiens Granulocyte-macrophage colony-stimulating factor Proteins 0.000 description 1
- 101000661807 Homo sapiens Suppressor of tumorigenicity 14 protein Proteins 0.000 description 1
- 102000004157 Hydrolases Human genes 0.000 description 1
- 108090000604 Hydrolases Proteins 0.000 description 1
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 description 1
- CZGUSIXMZVURDU-JZXHSEFVSA-N Ile(5)-angiotensin II Chemical compound C([C@@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CC=1NC=NC=1)C(=O)N1[C@@H](CCC1)C(=O)N[C@@H](CC=1C=CC=CC=1)C([O-])=O)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(N)=[NH2+])NC(=O)[C@@H]([NH3+])CC([O-])=O)C(C)C)C1=CC=C(O)C=C1 CZGUSIXMZVURDU-JZXHSEFVSA-N 0.000 description 1
- 108060003951 Immunoglobulin Proteins 0.000 description 1
- 102000018071 Immunoglobulin Fc Fragments Human genes 0.000 description 1
- 108010091135 Immunoglobulin Fc Fragments Proteins 0.000 description 1
- 108010021625 Immunoglobulin Fragments Proteins 0.000 description 1
- 102000008394 Immunoglobulin Fragments Human genes 0.000 description 1
- 206010062016 Immunosuppression Diseases 0.000 description 1
- 206010061217 Infestation Diseases 0.000 description 1
- 229930010555 Inosine Natural products 0.000 description 1
- UGQMRVRMYYASKQ-KQYNXXCUSA-N Inosine Chemical compound O[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1N1C2=NC=NC(O)=C2N=C1 UGQMRVRMYYASKQ-KQYNXXCUSA-N 0.000 description 1
- GRSZFWQUAKGDAV-UHFFFAOYSA-N Inosinic acid Natural products OC1C(O)C(COP(O)(O)=O)OC1N1C(NC=NC2=O)=C2N=C1 GRSZFWQUAKGDAV-UHFFFAOYSA-N 0.000 description 1
- 101710203526 Integrase Proteins 0.000 description 1
- 102000004889 Interleukin-6 Human genes 0.000 description 1
- 108090001005 Interleukin-6 Proteins 0.000 description 1
- 241001363655 Jaton Species 0.000 description 1
- 125000000998 L-alanino group Chemical group [H]N([*])[C@](C([H])([H])[H])([H])C(=O)O[H] 0.000 description 1
- 229930182844 L-isoleucine Natural products 0.000 description 1
- 239000004395 L-leucine Substances 0.000 description 1
- 235000019454 L-leucine Nutrition 0.000 description 1
- KDXKERNSBIXSRK-YFKPBYRVSA-N L-lysine Chemical compound NCCCC[C@H](N)C(O)=O KDXKERNSBIXSRK-YFKPBYRVSA-N 0.000 description 1
- FBOZXECLQNJBKD-ZDUSSCGKSA-N L-methotrexate Chemical compound C=1N=C2N=C(N)N=C(N)C2=NC=1CN(C)C1=CC=C(C(=O)N[C@@H](CCC(O)=O)C(O)=O)C=C1 FBOZXECLQNJBKD-ZDUSSCGKSA-N 0.000 description 1
- 108010063045 Lactoferrin Proteins 0.000 description 1
- 102100032241 Lactotransferrin Human genes 0.000 description 1
- 108090001090 Lectins Proteins 0.000 description 1
- 102000004856 Lectins Human genes 0.000 description 1
- 108060001084 Luciferase Proteins 0.000 description 1
- 239000005089 Luciferase Substances 0.000 description 1
- DDWFXDSYGUXRAY-UHFFFAOYSA-N Luciferin Natural products CCc1c(C)c(CC2NC(=O)C(=C2C=C)C)[nH]c1Cc3[nH]c4C(=C5/NC(CC(=O)O)C(C)C5CC(=O)O)CC(=O)c4c3C DDWFXDSYGUXRAY-UHFFFAOYSA-N 0.000 description 1
- 102100033320 Lysosomal Pro-X carboxypeptidase Human genes 0.000 description 1
- 208000030984 MIRAGE syndrome Diseases 0.000 description 1
- 101710141347 Major envelope glycoprotein Proteins 0.000 description 1
- 235000006770 Malva sylvestris Nutrition 0.000 description 1
- 108091027974 Mature messenger RNA Proteins 0.000 description 1
- 108010070551 Meat Proteins Proteins 0.000 description 1
- 240000004658 Medicago sativa Species 0.000 description 1
- 235000017587 Medicago sativa ssp. sativa Nutrition 0.000 description 1
- 108010036176 Melitten Proteins 0.000 description 1
- 108010052285 Membrane Proteins Proteins 0.000 description 1
- 102000018697 Membrane Proteins Human genes 0.000 description 1
- 108030000089 Metallocarboxypeptidases Proteins 0.000 description 1
- 102000006166 Metallocarboxypeptidases Human genes 0.000 description 1
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 description 1
- GMPKIPWJBDOURN-UHFFFAOYSA-N Methoxyamine Chemical compound CON GMPKIPWJBDOURN-UHFFFAOYSA-N 0.000 description 1
- 239000012901 Milli-Q water Substances 0.000 description 1
- 244000038561 Modiola caroliniana Species 0.000 description 1
- 102000005431 Molecular Chaperones Human genes 0.000 description 1
- 108010014251 Muramidase Proteins 0.000 description 1
- 102000016943 Muramidase Human genes 0.000 description 1
- 102100025243 Myeloid cell surface antigen CD33 Human genes 0.000 description 1
- 108010064696 N,O-diacetylmuramidase Proteins 0.000 description 1
- 108010062010 N-Acetylmuramoyl-L-alanine Amidase Proteins 0.000 description 1
- AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 description 1
- XUYPXLNMDZIRQH-LURJTMIESA-N N-acetyl-L-methionine Chemical compound CSCC[C@@H](C(O)=O)NC(C)=O XUYPXLNMDZIRQH-LURJTMIESA-N 0.000 description 1
- RSYYQCDERUOEFI-JTQLQIEISA-N N-benzoyl-L-arginine Chemical compound NC(=N)NCCC[C@@H](C(O)=O)NC(=O)C1=CC=CC=C1 RSYYQCDERUOEFI-JTQLQIEISA-N 0.000 description 1
- 238000005481 NMR spectroscopy Methods 0.000 description 1
- 229930193140 Neomycin Natural products 0.000 description 1
- 241000221961 Neurospora crassa Species 0.000 description 1
- 102000035092 Neutral proteases Human genes 0.000 description 1
- 108091005507 Neutral proteases Proteins 0.000 description 1
- 239000000020 Nitrocellulose Substances 0.000 description 1
- IOVCWXUNBOPUCH-UHFFFAOYSA-N Nitrous acid Chemical compound ON=O IOVCWXUNBOPUCH-UHFFFAOYSA-N 0.000 description 1
- 241000256259 Noctuidae Species 0.000 description 1
- 241001597008 Nomeidae Species 0.000 description 1
- 108091092724 Noncoding DNA Proteins 0.000 description 1
- 241000588701 Pectobacterium carotovorum Species 0.000 description 1
- 108010067902 Peptide Library Proteins 0.000 description 1
- 244000046052 Phaseolus vulgaris Species 0.000 description 1
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 1
- ZPHBZEQOLSRPAK-UHFFFAOYSA-N Phosphoramidon Natural products C=1NC2=CC=CC=C2C=1CC(C(O)=O)NC(=O)C(CC(C)C)NP(O)(=O)OC1OC(C)C(O)C(O)C1O ZPHBZEQOLSRPAK-UHFFFAOYSA-N 0.000 description 1
- 108010004729 Phycoerythrin Proteins 0.000 description 1
- 235000010582 Pisum sativum Nutrition 0.000 description 1
- 108010064851 Plant Proteins Proteins 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 101710124584 Probable DNA-binding protein Proteins 0.000 description 1
- 102000056251 Prolyl Oligopeptidases Human genes 0.000 description 1
- 101710178372 Prolyl endopeptidase Proteins 0.000 description 1
- 108010044159 Proprotein Convertases Proteins 0.000 description 1
- 102000006437 Proprotein Convertases Human genes 0.000 description 1
- 101710180012 Protease 7 Proteins 0.000 description 1
- 229940124158 Protease/peptidase inhibitor Drugs 0.000 description 1
- 102000001253 Protein Kinase Human genes 0.000 description 1
- 108091008109 Pseudogenes Proteins 0.000 description 1
- 102000057361 Pseudogenes Human genes 0.000 description 1
- 101100084022 Pseudomonas aeruginosa (strain ATCC 15692 / DSM 22644 / CIP 104116 / JCM 14847 / LMG 12228 / 1C / PRS 101 / PAO1) lapA gene Proteins 0.000 description 1
- 206010037742 Rabies Diseases 0.000 description 1
- 241000235403 Rhizomucor miehei Species 0.000 description 1
- 238000010847 SEQUEST Methods 0.000 description 1
- 108091058545 Secretory proteins Proteins 0.000 description 1
- 102000040739 Secretory proteins Human genes 0.000 description 1
- 229920002684 Sepharose Polymers 0.000 description 1
- 238000012300 Sequence Analysis Methods 0.000 description 1
- 108030000574 Serine-type carboxypeptidases Proteins 0.000 description 1
- 102000034328 Serine-type carboxypeptidases Human genes 0.000 description 1
- 244000040738 Sesamum orientale Species 0.000 description 1
- DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 1
- 240000003829 Sorghum propinquum Species 0.000 description 1
- 235000011684 Sorghum saccharatum Nutrition 0.000 description 1
- 238000002105 Southern blotting Methods 0.000 description 1
- 108091081024 Start codon Proteins 0.000 description 1
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 1
- 239000012505 Superdex™ Substances 0.000 description 1
- 102100037942 Suppressor of tumorigenicity 14 protein Human genes 0.000 description 1
- 210000001744 T-lymphocyte Anatomy 0.000 description 1
- GKLVYJBZJHMRIY-OUBTZVSYSA-N Technetium-99 Chemical compound [99Tc] GKLVYJBZJHMRIY-OUBTZVSYSA-N 0.000 description 1
- 206010043376 Tetanus Diseases 0.000 description 1
- 108700007696 Tetrahydrofolate Dehydrogenase Proteins 0.000 description 1
- 244000269722 Thea sinensis Species 0.000 description 1
- 108090000190 Thrombin Proteins 0.000 description 1
- 102000006601 Thymidine Kinase Human genes 0.000 description 1
- 108020004440 Thymidine kinase Proteins 0.000 description 1
- YZCKVEUIGOORGS-NJFSPNSNSA-N Tritium Chemical compound [3H] YZCKVEUIGOORGS-NJFSPNSNSA-N 0.000 description 1
- 108090000631 Trypsin Proteins 0.000 description 1
- 102000004142 Trypsin Human genes 0.000 description 1
- 101710112930 Trypsin inhibitor 1 Proteins 0.000 description 1
- 108090000848 Ubiquitin Proteins 0.000 description 1
- 102000044159 Ubiquitin Human genes 0.000 description 1
- ZVNYJIZDIRKMBF-UHFFFAOYSA-N Vesnarinone Chemical compound C1=C(OC)C(OC)=CC=C1C(=O)N1CCN(C=2C=C3CCC(=O)NC3=CC=2)CC1 ZVNYJIZDIRKMBF-UHFFFAOYSA-N 0.000 description 1
- 240000006677 Vicia faba Species 0.000 description 1
- 235000010749 Vicia faba Nutrition 0.000 description 1
- 235000002098 Vicia faba var. major Nutrition 0.000 description 1
- 229930003756 Vitamin B7 Natural products 0.000 description 1
- 235000009754 Vitis X bourquina Nutrition 0.000 description 1
- 235000012333 Vitis X labruscana Nutrition 0.000 description 1
- 240000006365 Vitis vinifera Species 0.000 description 1
- 235000014787 Vitis vinifera Nutrition 0.000 description 1
- 241000282485 Vulpes vulpes Species 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- DGEZNRSVGBDHLK-UHFFFAOYSA-N [1,10]phenanthroline Chemical compound C1=CN=C2C3=NC=CC=C3C=CC2=C1 DGEZNRSVGBDHLK-UHFFFAOYSA-N 0.000 description 1
- 230000002159 abnormal effect Effects 0.000 description 1
- 238000000862 absorption spectrum Methods 0.000 description 1
- 229940022698 acetylcholinesterase Drugs 0.000 description 1
- 125000002252 acyl group Chemical group 0.000 description 1
- 125000004442 acylamino group Chemical group 0.000 description 1
- 230000010933 acylation Effects 0.000 description 1
- 238000005917 acylation reaction Methods 0.000 description 1
- 230000003044 adaptive effect Effects 0.000 description 1
- 101150063416 add gene Proteins 0.000 description 1
- 210000001943 adrenal medulla Anatomy 0.000 description 1
- 238000005377 adsorption chromatography Methods 0.000 description 1
- 238000001261 affinity purification Methods 0.000 description 1
- 239000008272 agar Substances 0.000 description 1
- 239000011543 agarose gel Substances 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 230000000735 allogeneic effect Effects 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- 229910021502 aluminium hydroxide Inorganic materials 0.000 description 1
- 108010052590 amastatin Proteins 0.000 description 1
- QFAADIRHLBXJJS-ZAZJUGBXSA-N amastatin Chemical compound CC(C)C[C@@H](N)[C@H](O)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](C(C)C)C(=O)N[C@H](C(O)=O)CC(O)=O QFAADIRHLBXJJS-ZAZJUGBXSA-N 0.000 description 1
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 1
- 235000011130 ammonium sulphate Nutrition 0.000 description 1
- 229940044094 angiotensin-converting-enzyme inhibitor Drugs 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 238000000137 annealing Methods 0.000 description 1
- 239000003242 anti bacterial agent Substances 0.000 description 1
- 229940088710 antibiotic agent Drugs 0.000 description 1
- 229940019748 antifibrinolytic proteinase inhibitors Drugs 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000000605 aspartame Substances 0.000 description 1
- IAOZJIPTCAWIRG-QWRGUYRKSA-N aspartame Chemical compound OC(=O)C[C@H](N)C(=O)N[C@H](C(=O)OC)CC1=CC=CC=C1 IAOZJIPTCAWIRG-QWRGUYRKSA-N 0.000 description 1
- 229960003438 aspartame Drugs 0.000 description 1
- 235000010357 aspartame Nutrition 0.000 description 1
- 235000019606 astringent taste Nutrition 0.000 description 1
- 229960003071 bacitracin Drugs 0.000 description 1
- 229930184125 bacitracin Natural products 0.000 description 1
- CLKOFPXJLQSYAH-ABRJDSQDSA-N bacitracin A Chemical compound C1SC([C@@H](N)[C@@H](C)CC)=N[C@@H]1C(=O)N[C@@H](CC(C)C)C(=O)N[C@H](CCC(O)=O)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H]1C(=O)N[C@H](CCCN)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@H](CC=2C=CC=CC=2)C(=O)N[C@@H](CC=2N=CNC=2)C(=O)N[C@H](CC(O)=O)C(=O)N[C@@H](CC(N)=O)C(=O)NCCCC1 CLKOFPXJLQSYAH-ABRJDSQDSA-N 0.000 description 1
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 1
- 102000005936 beta-Galactosidase Human genes 0.000 description 1
- 108010005774 beta-Galactosidase Proteins 0.000 description 1
- 235000013361 beverage Nutrition 0.000 description 1
- 230000000975 bioactive effect Effects 0.000 description 1
- 239000013060 biological fluid Substances 0.000 description 1
- 230000036983 biotransformation Effects 0.000 description 1
- 230000002051 biphasic effect Effects 0.000 description 1
- 210000001124 body fluid Anatomy 0.000 description 1
- 239000010839 body fluid Substances 0.000 description 1
- 210000000621 bronchi Anatomy 0.000 description 1
- 239000000872 buffer Substances 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- 229910001424 calcium ion Inorganic materials 0.000 description 1
- 239000001506 calcium phosphate Substances 0.000 description 1
- 229910000389 calcium phosphate Inorganic materials 0.000 description 1
- 235000011010 calcium phosphates Nutrition 0.000 description 1
- OEUVSBXAMBLPES-UHFFFAOYSA-L calcium stearoyl-2-lactylate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC(=O)OC(C)C(=O)OC(C)C([O-])=O.CCCCCCCCCCCCCCCCCC(=O)OC(C)C(=O)OC(C)C([O-])=O OEUVSBXAMBLPES-UHFFFAOYSA-L 0.000 description 1
- 235000010957 calcium stearoyl-2-lactylate Nutrition 0.000 description 1
- 238000004364 calculation method Methods 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 108010067454 caseinomacropeptide Proteins 0.000 description 1
- 238000005277 cation exchange chromatography Methods 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 230000003196 chaotropic effect Effects 0.000 description 1
- BULLHNJGPPOUOX-UHFFFAOYSA-N chloroacetone Chemical compound CC(=O)CCl BULLHNJGPPOUOX-UHFFFAOYSA-N 0.000 description 1
- 210000002987 choroid plexus Anatomy 0.000 description 1
- 239000013611 chromosomal DNA Substances 0.000 description 1
- 210000000349 chromosome Anatomy 0.000 description 1
- 239000003541 chymotrypsin inhibitor Substances 0.000 description 1
- 238000002983 circular dichroism Methods 0.000 description 1
- 239000007979 citrate buffer Substances 0.000 description 1
- 238000005352 clarification Methods 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 238000000975 co-precipitation Methods 0.000 description 1
- 238000005345 coagulation Methods 0.000 description 1
- 230000015271 coagulation Effects 0.000 description 1
- 238000002742 combinatorial mutagenesis Methods 0.000 description 1
- 230000002860 competitive effect Effects 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 239000003636 conditioned culture medium Substances 0.000 description 1
- 235000009508 confectionery Nutrition 0.000 description 1
- 238000012790 confirmation Methods 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 235000015140 cultured milk Nutrition 0.000 description 1
- 230000001120 cytoprotective effect Effects 0.000 description 1
- 229940104302 cytosine Drugs 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000008260 defense mechanism Effects 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 238000012217 deletion Methods 0.000 description 1
- 230000037430 deletion Effects 0.000 description 1
- 238000010612 desalination reaction Methods 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 125000003963 dichloro group Chemical group Cl* 0.000 description 1
- 235000019621 digestibility Nutrition 0.000 description 1
- 229940079919 digestives enzyme preparation Drugs 0.000 description 1
- 102000004419 dihydrofolate reductase Human genes 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- PXEDJBXQKAGXNJ-QTNFYWBSSA-L disodium L-glutamate Chemical compound [Na+].[Na+].[O-]C(=O)[C@@H](N)CCC([O-])=O PXEDJBXQKAGXNJ-QTNFYWBSSA-L 0.000 description 1
- 238000006073 displacement reaction Methods 0.000 description 1
- 238000010494 dissociation reaction Methods 0.000 description 1
- 230000005593 dissociations Effects 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 238000011143 downstream manufacturing Methods 0.000 description 1
- 235000013399 edible fruits Nutrition 0.000 description 1
- 239000012636 effector Substances 0.000 description 1
- 239000003602 elastase inhibitor Substances 0.000 description 1
- 238000004520 electroporation Methods 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 229940066758 endopeptidases Drugs 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 230000007071 enzymatic hydrolysis Effects 0.000 description 1
- 238000006047 enzymatic hydrolysis reaction Methods 0.000 description 1
- 230000009144 enzymatic modification Effects 0.000 description 1
- 238000001976 enzyme digestion Methods 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 230000010429 evolutionary process Effects 0.000 description 1
- 230000005284 excitation Effects 0.000 description 1
- 239000013613 expression plasmid Substances 0.000 description 1
- 210000003746 feather Anatomy 0.000 description 1
- 239000012847 fine chemical Substances 0.000 description 1
- MHMNJMPURVTYEJ-UHFFFAOYSA-N fluorescein-5-isothiocyanate Chemical compound O1C(=O)C2=CC(N=C=S)=CC=C2C21C1=CC=C(O)C=C1OC1=CC(O)=CC=C21 MHMNJMPURVTYEJ-UHFFFAOYSA-N 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 238000004108 freeze drying Methods 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- 230000008014 freezing Effects 0.000 description 1
- 102000037865 fusion proteins Human genes 0.000 description 1
- 108020001507 fusion proteins Proteins 0.000 description 1
- 238000005227 gel permeation chromatography Methods 0.000 description 1
- 238000012239 gene modification Methods 0.000 description 1
- 230000005017 genetic modification Effects 0.000 description 1
- 235000013617 genetically modified food Nutrition 0.000 description 1
- 230000035784 germination Effects 0.000 description 1
- 229940116332 glucose oxidase Drugs 0.000 description 1
- 235000019420 glucose oxidase Nutrition 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- 229940049906 glutamate Drugs 0.000 description 1
- 229930195712 glutamate Natural products 0.000 description 1
- 229960003180 glutathione Drugs 0.000 description 1
- 108010092515 glycyl endopeptidase Proteins 0.000 description 1
- 235000011617 hard cheese Nutrition 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- 239000000185 hemagglutinin Substances 0.000 description 1
- 229920000140 heteropolymer Polymers 0.000 description 1
- 239000012145 high-salt buffer Substances 0.000 description 1
- 150000002411 histidines Chemical class 0.000 description 1
- 229940088597 hormone Drugs 0.000 description 1
- 239000005556 hormone Substances 0.000 description 1
- 230000007412 host metabolism Effects 0.000 description 1
- 235000020256 human milk Nutrition 0.000 description 1
- 210000004251 human milk Anatomy 0.000 description 1
- 244000052637 human pathogen Species 0.000 description 1
- 235000003642 hunger Nutrition 0.000 description 1
- 150000002430 hydrocarbons Chemical group 0.000 description 1
- 125000001165 hydrophobic group Chemical group 0.000 description 1
- 238000004191 hydrophobic interaction chromatography Methods 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- YQYJSBFKSSDGFO-FWAVGLHBSA-N hygromycin A Chemical compound O[C@H]1[C@H](O)[C@H](C(=O)C)O[C@@H]1Oc1ccc(\C=C(/C)C(=O)N[C@@H]2[C@@H]([C@H]3OCO[C@H]3[C@@H](O)[C@@H]2O)O)cc1O YQYJSBFKSSDGFO-FWAVGLHBSA-N 0.000 description 1
- 150000002466 imines Chemical class 0.000 description 1
- 230000003100 immobilizing effect Effects 0.000 description 1
- 102000018358 immunoglobulin Human genes 0.000 description 1
- 230000016784 immunoglobulin production Effects 0.000 description 1
- 230000001506 immunosuppresive effect Effects 0.000 description 1
- 238000007901 in situ hybridization Methods 0.000 description 1
- 230000000415 inactivating effect Effects 0.000 description 1
- 229910052738 indium Inorganic materials 0.000 description 1
- APFVFJFRJDLVQX-UHFFFAOYSA-N indium atom Chemical compound [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 description 1
- 206010022000 influenza Diseases 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 229960003786 inosine Drugs 0.000 description 1
- 230000010354 integration Effects 0.000 description 1
- 230000031891 intestinal absorption Effects 0.000 description 1
- 238000007912 intraperitoneal administration Methods 0.000 description 1
- 201000009085 invasive aspergillosis Diseases 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 238000005304 joining Methods 0.000 description 1
- CSSYQJWUGATIHM-IKGCZBKSSA-N l-phenylalanyl-l-lysyl-l-cysteinyl-l-arginyl-l-arginyl-l-tryptophyl-l-glutaminyl-l-tryptophyl-l-arginyl-l-methionyl-l-lysyl-l-lysyl-l-leucylglycyl-l-alanyl-l-prolyl-l-seryl-l-isoleucyl-l-threonyl-l-cysteinyl-l-valyl-l-arginyl-l-arginyl-l-alanyl-l-phenylal Chemical compound C([C@H](N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CS)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CC=1C2=CC=CC=C2NC=1)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC=1C2=CC=CC=C2NC=1)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)NCC(=O)N[C@@H](C)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CO)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CS)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](C)C(=O)N[C@@H](CC=1C=CC=CC=1)C(O)=O)C1=CC=CC=C1 CSSYQJWUGATIHM-IKGCZBKSSA-N 0.000 description 1
- 101150109249 lacI gene Proteins 0.000 description 1
- 101150066555 lacZ gene Proteins 0.000 description 1
- 235000021242 lactoferrin Nutrition 0.000 description 1
- 229940078795 lactoferrin Drugs 0.000 description 1
- 239000010985 leather Substances 0.000 description 1
- 239000002523 lectin Substances 0.000 description 1
- 125000001909 leucine group Chemical group [H]N(*)C(C(*)=O)C([H])([H])C(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 150000002614 leucines Chemical class 0.000 description 1
- 239000003446 ligand Substances 0.000 description 1
- 238000001294 liquid chromatography-tandem mass spectrometry Methods 0.000 description 1
- 244000144972 livestock Species 0.000 description 1
- HWYHZTIRURJOHG-UHFFFAOYSA-N luminol Chemical compound O=C1NNC(=O)C2=C1C(N)=CC=C2 HWYHZTIRURJOHG-UHFFFAOYSA-N 0.000 description 1
- 210000004072 lung Anatomy 0.000 description 1
- 108010057284 lysosomal Pro-X carboxypeptidase Proteins 0.000 description 1
- 229960000274 lysozyme Drugs 0.000 description 1
- 235000010335 lysozyme Nutrition 0.000 description 1
- 239000004325 lysozyme Substances 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 238000013507 mapping Methods 0.000 description 1
- 238000001819 mass spectrum Methods 0.000 description 1
- 230000001404 mediated effect Effects 0.000 description 1
- 201000001441 melanoma Diseases 0.000 description 1
- VDXZNPDIRNWWCW-UHFFFAOYSA-N melitten Chemical compound NCC(=O)NC(C(C)CC)C(=O)NCC(=O)NC(C)C(=O)NC(C(C)C)C(=O)NC(CC(C)C)C(=O)NC(CCCCN)C(=O)NC(C(C)C)C(=O)NC(CC(C)C)C(=O)NC(C(C)O)C(=O)NC(C(C)O)C(=O)NCC(=O)NC(CC(C)C)C(=O)N1CCCC1C(=O)NC(C)C(=O)NC(CC(C)C)C(=O)NC(C(C)CC)C(=O)NC(CO)C(=O)NC(C(=O)NC(C(C)CC)C(=O)NC(CCCCN)C(=O)NC(CCCNC(N)=N)C(=O)NC(CCCCN)C(=O)NC(CCCNC(N)=N)C(=O)NC(CCC(N)=O)C(=O)NC(CCC(N)=O)C(N)=O)CC1=CNC2=CC=CC=C12 VDXZNPDIRNWWCW-UHFFFAOYSA-N 0.000 description 1
- 230000002503 metabolic effect Effects 0.000 description 1
- 230000031864 metaphase Effects 0.000 description 1
- FJQXCDYVZAHXNS-UHFFFAOYSA-N methadone hydrochloride Chemical compound Cl.C=1C=CC=CC=1C(CC(C)N(C)C)(C(=O)CC)C1=CC=CC=C1 FJQXCDYVZAHXNS-UHFFFAOYSA-N 0.000 description 1
- MYWUZJCMWCOHBA-VIFPVBQESA-N methamphetamine Chemical compound CN[C@@H](C)CC1=CC=CC=C1 MYWUZJCMWCOHBA-VIFPVBQESA-N 0.000 description 1
- 229960000485 methotrexate Drugs 0.000 description 1
- 238000001471 micro-filtration Methods 0.000 description 1
- 108010009355 microbial metalloproteinases Proteins 0.000 description 1
- 238000009629 microbiological culture Methods 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 108091005573 modified proteins Proteins 0.000 description 1
- 102000035118 modified proteins Human genes 0.000 description 1
- LPUQAYUQRXPFSQ-DFWYDOINSA-M monosodium L-glutamate Chemical compound [Na+].[O-]C(=O)[C@@H](N)CCC(O)=O LPUQAYUQRXPFSQ-DFWYDOINSA-M 0.000 description 1
- 239000004570 mortar (masonry) Substances 0.000 description 1
- 108091005763 multidomain proteins Proteins 0.000 description 1
- ZTLGJPIZUOVDMT-UHFFFAOYSA-N n,n-dichlorotriazin-4-amine Chemical compound ClN(Cl)C1=CC=NN=N1 ZTLGJPIZUOVDMT-UHFFFAOYSA-N 0.000 description 1
- 229960004927 neomycin Drugs 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- FEMOMIGRRWSMCU-UHFFFAOYSA-N ninhydrin Chemical compound C1=CC=C2C(=O)C(O)(O)C(=O)C2=C1 FEMOMIGRRWSMCU-UHFFFAOYSA-N 0.000 description 1
- 229920001220 nitrocellulos Polymers 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 231100000957 no side effect Toxicity 0.000 description 1
- 238000003499 nucleic acid array Methods 0.000 description 1
- 239000002777 nucleoside Substances 0.000 description 1
- 125000003835 nucleoside group Chemical group 0.000 description 1
- 210000000056 organ Anatomy 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000005022 packaging material Substances 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 230000003071 parasitic effect Effects 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 235000019702 pea protein Nutrition 0.000 description 1
- 101150035909 pepB gene Proteins 0.000 description 1
- 238000005897 peptide coupling reaction Methods 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 101150009573 phoA gene Proteins 0.000 description 1
- BWSDNRQVTFZQQD-AYVHNPTNSA-N phosphoramidon Chemical compound O([P@@](O)(=O)N[C@H](CC(C)C)C(=O)N[C@H](CC=1[C]2C=CC=CC2=NC=1)C(O)=O)[C@H]1O[C@@H](C)[C@H](O)[C@@H](O)[C@@H]1O BWSDNRQVTFZQQD-AYVHNPTNSA-N 0.000 description 1
- 108010072906 phosphoramidon Proteins 0.000 description 1
- 230000026731 phosphorylation Effects 0.000 description 1
- 238000006366 phosphorylation reaction Methods 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 230000035479 physiological effects, processes and functions Effects 0.000 description 1
- 101150082708 pkiA gene Proteins 0.000 description 1
- 108010031345 placental alkaline phosphatase Proteins 0.000 description 1
- 235000021118 plant-derived protein Nutrition 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 238000007747 plating Methods 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 229920000447 polyanionic polymer Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 239000003910 polypeptide antibiotic agent Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000002203 pretreatment Methods 0.000 description 1
- TVLSRXXIMLFWEO-UHFFFAOYSA-N prochloraz Chemical compound C1=CN=CN1C(=O)N(CCC)CCOC1=C(Cl)C=C(Cl)C=C1Cl TVLSRXXIMLFWEO-UHFFFAOYSA-N 0.000 description 1
- 108010017378 prolyl aminopeptidase Proteins 0.000 description 1
- 230000013777 protein digestion Effects 0.000 description 1
- 230000012846 protein folding Effects 0.000 description 1
- 108060006633 protein kinase Proteins 0.000 description 1
- 230000006920 protein precipitation Effects 0.000 description 1
- 238000001742 protein purification Methods 0.000 description 1
- 238000013138 pruning Methods 0.000 description 1
- 230000002685 pulmonary effect Effects 0.000 description 1
- 235000021251 pulses Nutrition 0.000 description 1
- 238000000197 pyrolysis Methods 0.000 description 1
- 238000012797 qualification Methods 0.000 description 1
- 230000006340 racemization Effects 0.000 description 1
- 230000002285 radioactive effect Effects 0.000 description 1
- 238000009790 rate-determining step (RDS) Methods 0.000 description 1
- 239000012925 reference material Substances 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 230000002787 reinforcement Effects 0.000 description 1
- 238000004153 renaturation Methods 0.000 description 1
- 239000012508 resin bead Substances 0.000 description 1
- 239000002151 riboflavin Substances 0.000 description 1
- 229960002477 riboflavin Drugs 0.000 description 1
- 235000019192 riboflavin Nutrition 0.000 description 1
- 238000007423 screening assay Methods 0.000 description 1
- 230000011218 segmentation Effects 0.000 description 1
- 230000001953 sensory effect Effects 0.000 description 1
- 230000037432 silent mutation Effects 0.000 description 1
- 238000004088 simulation Methods 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000007974 sodium acetate buffer Substances 0.000 description 1
- 239000001509 sodium citrate Substances 0.000 description 1
- NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 description 1
- 229940073490 sodium glutamate Drugs 0.000 description 1
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 description 1
- 235000013322 soy milk Nutrition 0.000 description 1
- 229940001941 soy protein Drugs 0.000 description 1
- 235000019710 soybean protein Nutrition 0.000 description 1
- 238000004611 spectroscopical analysis Methods 0.000 description 1
- 230000004763 spore germination Effects 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 230000037351 starvation Effects 0.000 description 1
- 230000001954 sterilising effect Effects 0.000 description 1
- 238000004659 sterilization and disinfection Methods 0.000 description 1
- 230000035882 stress Effects 0.000 description 1
- 239000003774 sulfhydryl reagent Substances 0.000 description 1
- 239000013595 supernatant sample Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- 230000002123 temporal effect Effects 0.000 description 1
- 238000010257 thawing Methods 0.000 description 1
- 125000003396 thiol group Chemical group [H]S* 0.000 description 1
- 229960004072 thrombin Drugs 0.000 description 1
- 238000004448 titration Methods 0.000 description 1
- 230000000699 topical effect Effects 0.000 description 1
- 231100000167 toxic agent Toxicity 0.000 description 1
- 239000003440 toxic substance Substances 0.000 description 1
- 230000005026 transcription initiation Effects 0.000 description 1
- 238000010361 transduction Methods 0.000 description 1
- 230000026683 transduction Effects 0.000 description 1
- 230000032258 transport Effects 0.000 description 1
- 230000017105 transposition Effects 0.000 description 1
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
- 229910052722 tritium Inorganic materials 0.000 description 1
- 239000012588 trypsin Substances 0.000 description 1
- 230000001810 trypsinlike Effects 0.000 description 1
- 229950009811 ubenimex Drugs 0.000 description 1
- 235000019583 umami taste Nutrition 0.000 description 1
- ORHBXUUXSCNDEV-UHFFFAOYSA-N umbelliferone Chemical compound C1=CC(=O)OC2=CC(O)=CC=C21 ORHBXUUXSCNDEV-UHFFFAOYSA-N 0.000 description 1
- HFTAFOQKODTIJY-UHFFFAOYSA-N umbelliferone Natural products Cc1cc2C=CC(=O)Oc2cc1OCC=CC(C)(C)O HFTAFOQKODTIJY-UHFFFAOYSA-N 0.000 description 1
- 229960005486 vaccine Drugs 0.000 description 1
- 238000001291 vacuum drying Methods 0.000 description 1
- 239000005418 vegetable material Substances 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 238000009423 ventilation Methods 0.000 description 1
- KAKZBPTYRLMSJV-UHFFFAOYSA-N vinyl-ethylene Natural products C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 1
- 230000004304 visual acuity Effects 0.000 description 1
- 239000011735 vitamin B7 Substances 0.000 description 1
- 235000011912 vitamin B7 Nutrition 0.000 description 1
- 239000011800 void material Substances 0.000 description 1
- 238000000207 volumetry Methods 0.000 description 1
- 235000008939 whole milk Nutrition 0.000 description 1
- 210000005253 yeast cell Anatomy 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
Landscapes
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Enzymes And Modification Thereof (AREA)
Abstract
The invention relates to newly identified gene sequences that encode novel proteases obtainable from Aspergillus niger. The invention features the full length gene sequence of the novel genes, their cDNA sequences as well as the full-length functional protein and fragments thereof. The invention also relates to methods of using these enzymes in industrial processes and methods of diagnosing fungal infections. Also included in the invention are cells transformed with DNA according to the invention and cells wherein a protease according to the invention is genetically modified to enhance or reduce its activity and/or level of expression.
Description
Invention field
The present invention relates to new identified polynucleotides sequence, this sequence comprises the gene of coding isolating new proteolytic enzyme from aspergillus niger (Aspergillus niger).The invention describes the full length nucleotide sequence of new gene, the cDNA sequence of complete encoding sequence that comprises new proteolytic enzyme and aminoacid sequence and the fragment and the variant of total length functional protein.The present invention also relates in commercial run, use the method for these enzymes and the method for diagnosis fungi infestation.Comprise equally in the present invention be to use according to polynucleotide cell transformed of the present invention and proteolytic enzyme according to the present invention therein by genetic modification to strengthen or to reduce the cell of its activity and/or expression level.
Background of invention
Proteolytic ferment
Protein can be considered as making up the heteropolymer that piece is formed by the amino acid that connects with peptide bond.Repeating unit in the protein is the center alpha-carbon atom with amino group and carboxylic group.Except that glycine, so-called amino acid side chain has substituted in two remaining α hydrocarbon atoms.Amino acid side chain makes that the center alpha-carbon atom is asymmetric.What usually, find in protein is amino acid whose L-enantiomer.Below term description polytype polyamino acid.Peptide is the amino-acid residue short chain with definite sequence.Although in fact the number for residue does not have maximum value, this term indicates its character mainly to form the chain of determining and not having the fixed three-dimensional conformation by its amino acid usually.The term polypeptide is generally used for longer chain, has definite sequence and length and have suitable length in principle to be folded into three-dimensional structure usually.Protein refers to natural existence and shows the polypeptide of determining three-dimensional structure.If protein is mainly brought into play the function of catalyzed chemical reaction, it is commonly called enzyme so.Proteolytic enzyme is the enzyme of peptide bond hydrolysis in catalysis (many) peptides and the protein.
Under physiological conditions, the hydrolysis of proteolytic enzyme catalysis peptide bond.International biological chemistry and molecular biology association (International Union of Biochemistry andMolecular Biology) (1984) recommend to use the term peptase for peptide bond hydrolysis enzyme hypotype (subclass E.C3.4.).Term protease and peptidohydrolase and peptase be synonym and also can be used for herein.Proteolytic enzyme comprises 2 fermentoids: endopeptidase and exopeptidase, they are the site cutting peptide bonds in protein and continuously from the terminal amino acid of removing of N or C-respectively.Proteolytic enzyme is as the synonym of endopeptidase.Peptide bond can betide under 2-, 3-, 4-peptide, peptide, polypeptide or the proteinic situation.Usually, the amino acid of native peptides and polypeptide is formed and is comprised 20 different amino acid, and this amino acid is showed L-configuration (except that the glycine that does not have chiral centre).Yet the proteolytic activity of proteolytic enzyme is not limited to the peptide that only contains 20 natural amino acids.Also can be cut at the peptide bond between the so-called alpha-non-natural amino acid and at amino acid or the peptide bond between the amino acid analogue modified.Some proteolytic enzyme are accepted the amino acid whose D-conformation of some position really.Usually, the significant stereoselectivity of proteolytic enzyme makes that they are very useful in the process of decomposition.Many proteolytic enzyme are showed interesting secondary activity, as esterase activity, thiolesterase activity and (taking off) lactamase activity.These secondary activity not only are confined to amino acid usually, and susceptible of proof is to be very useful in the bio-transformation in fine chemical field.
Filamentous fungus, eukaryotic microorganisms have special importance many reasons are arranged.If control inadequately, the primary process cost of peptide bond hydrolysis cutting is very big in the protein so, and potential harmful to biology.To proteolysed required restriction be by proteolytic enzyme specificity, by make proteolytic enzyme and substrate intracellular compartmentation, by substrate is modified so that it can be by discrete proteolytic enzyme identification, by by the proenzyme activation with special inhibitor exists or non-existent adjusting and realize by the adjusting that proteinase gene is expressed.In fungi, proteolytic enzyme also relates to other basic cell processes, and this process comprises intracellular protein renewal, processing, transposition, sporulation, sprouting and differentiation.In fact, with Aspergillus nidulans (Aspergillus nidulans) and Neuraspora crassa (Neurospora crassa) model animals as the molecular basis of analytical physiology and growth course scope.Their hereditary property makes and can directly enter biological chemistry and genetics research under nutrient of determining and culture condition.In addition, separated making the morbific fungi of people, livestock and farm crop in a large number, and thought that proteolysis works in their pathogenic (host invades, antagonism host's defense mechanism and/or nutrition in infection).Proteolytic enzyme is also in being usually used in experiment, clinical and commercial run; Microorganism and amicrobic proteolytic enzyme all are widely used in also in the manufacturing of visible foodstuffs industry (cure, brewage, cheese producing, tenderization), tanning industry and bio-decontaminated agent (Aunstrup, 1980).Develop some filamentous fungus, especially aspergillus niger belong to commercial significance as homology or both production hosts of heterologous protein make recently the importance of fungal proteinase recovered (van Brunt, 1986ab).Proteolytic enzyme often causes problem in the protein heterogenous expression of fungi and homology overexpression.Particularly, heterogenous expression is subjected to the obstruction of homologous protein enzyme to the proteolytic degradation of expression product.These commercial benefitss cause studying in great detail that proteolysis spectrum and proteolytic enzyme defective strain make up, and have improved the knowledge of proteolytic enzyme expression and adjusting in relevant these biologies.Just be sought after in filamentous fungus, identifying and eliminating new proteolytic enzyme subsequently.
Microorganism such as fungi are particularly useful in large-scale protein matter is produced.Especially when this protein secreting is in substratum.Proteolytic ferment works in these production processes.On the one hand, concrete usually proteolytic ferment is essential for the correct processing of target protein and production host's metabolism health.On the other hand, proteolytic degradation can significantly reduce the proteinic output of excretory.Bad folding can causing in Secretory Pathway by the intracellular protein enzyme liberating.This may be a special problem to producing heterologous protein.The details of proteolysis process and not exclusively known, this process are responsible for the protein of degrading and shifting from the fungus secretion process.In eukaryote, the degraded of cell protein is realized by proteasome, and is usually directed to the protein that will degrade is carried out the ubiquitin mark.Proteasome also may carry out proteolytic degradation to bad folding secretory protein with the vacuole protein enzyme in fungi.This proteolytic degradation may be in kytoplasm, but can not get rid of the proteolytic enzyme that resides in endoplasmic reticulum.From producing the improved aspect of host's strain, the proteolysis system can be genetically engineered and the improved interesting target of production strain.The additional copy of proteinase gene, the overexpression of some proteolytic enzyme, the gene knockout program of transcribing the modification of control and proteinase gene being lacked can provide more detailed understanding to the function of given proteolytic enzyme.In order to improve the output of homology and heterologous protein, the disappearance of protease-encoding gene is the improved valuable strategy of host's strain.
Eukaryotic microorganisms proteolytic enzyme is summarized by North (1982).More closely, Suarez Rendueles and Wolf (1988) have summarized yeast saccharomyces cerevisiae (S.cerevisiae) proteolytic enzyme and function thereof.
Except that the hydrolysis cutting to key, proteolytic enzyme also can be applicable in the formation of key.The key here comprises that not only peptide and amido linkage also comprise ester bond.Proteolytic enzyme is the cutting of catalysis particular key or forms the thermodynamics that at first depends on this reaction really.Enzyme such as proteolytic enzyme do not influence molecular balance.This balance depends on the special condition that reaction takes place.Under physiological conditions, the thermodynamics of reaction helps the hydrolysis of peptide owing to the zwitterion highly stable structure on thermodynamics that produces.To influence balance, perhaps, perhaps, proteolytic enzyme may be used for peptide bond synthetic purpose by Applied Physics-principles of chemistry by utilizing the kinetic parameter of enzyme reaction by the concentration or the characteristic of control response thing and product.The adding of water mixed organic solvents has reduced the degree of ionization of carboxyl composition, has increased the concentration of reaction available substrate whereby.Often adopt the amino and the carboxylic group of biphasic system, water stand-in (water mimetics), oppositely micelle (reverse micelles), anhydrous medium or modification to increase output with the precipitation that causes product.When the proteolytic enzyme with correct character can utilize, the application of this proteolytic enzyme in synthetic provided the advantage of essence.Because proteolytic enzyme is stereoselectivity and regioselectivity, so the sensitive group on the reactant need not protected usually, and reactant is not required to be optically pure.Because enzymatic synthetic condition is gentle, so can avoid the racemization and the decomposition of unsettled reactant or product.The key between amino acid, other compounds of showing primary amino group, mercapto groups or carboxylic group also can be connected by the proteolytic enzyme of suitable selection.In addition, ester, thiol esters and acid amides can be synthesized by some proteolytic enzyme.Shown proteolytic enzyme display area selectivity in the acylation of list, two-and three-sugar, nucleosides and riboflavin.The problem of stability can be prevented by appropriate formulations under harsh reaction conditions sometimes.Encapsulated and the fixing enzyme of not only having stablized, and make and from reaction culture medium, to reclaim and separates facility.Crosslinked widely, handle or with some polymer such as dextran, polyoxyethylene glycol, poly-imines (polyimines) covering surfaces life-span of extensible biological catalyst in essence with aldehyde.
The natural action of proteolytic enzyme
Traditionally, proteolytic enzyme is regarded as degrading enzyme, and this endonuclease capable is cut into little peptide and/or amino acid with protein, and its renewal that act as digestion nutrient protein or participate in cell protein.In addition, shown that proteolytic enzyme is also playing a key role in the cell processes widely by the mechanism of carrying out selective modification with limited proteolysis, and thereby have basic regulatory function (Holzer and a Tschensche 1979; Holzer and Heinrich, 1980).The specificity of proteolytic enzyme is considered to be closely related with its physiologic function and its expression pattern.As for the function of concrete proteolytic enzyme, its location often is very important; For example, many vacuoles and periplasm protein enzyme participate in protein degradation, and many embrane-associated protein enzymes are in protein processing very important (Suarez Rendueles and Wolf, 1988).The not same-action of the proteolytic enzyme in many cell processes can be divided into 4 main protease functions: 1) protein degradation, 2) (mistakes) activation of translation post-treatment and specified protein, 3) form generation and 4) pathogeny.
Utilizing protein is hydrolysis to nutrient as the obvious effect of proteolytic enzyme in the biology in nutrient source.In fungi, this will comprise the degraded of being carried out in the extracellular by extracellular extensive specific proteolytic enzyme.Protein degradation is also important for the fast updating of cell protein, and makes cell can remove abnormal protein and for its proteinic replenishing of the physiological conditions adaptive change that changes.Normally, avoid degraded at random except that correct target protein, have quite extensive specific proteolytic enzyme and also should carry out extraordinary control in order to protect cell.
Opposite with hydrolysis, the synthetic process that drives by ATP in vivo of polypeptide takes place on rrna.The sequence that final amino acid connects is by being derived from genomic information domination.This process is known as translation.Primary translation product is often long than final function product, and this protein precursor must further be processed by proteolytic enzyme usually after translation.Proteolytic enzyme plays a key role in the final functional protein obtaining in this precursor protein matter maturation.Opposite with reconstruct shape with complete in check protein pruning, proteolytic enzyme also can be very destructive, and polypeptide can be degraded to peptide and amino acid fully.Discharged before needs for fear of proteolytic activity, proteolytic enzyme has been carried out regulation and control widely.Many proteolytic enzyme are that this precursor becomes activatory when needs as the precursor synthetic that is known as proenzyme.This activation always takes place by proteolysis significantly.Except that directly relating to this process, single proteinic selectivity activation and inactivation are well-known by the enzymatic phenomenon of specific protein.
Limited proteoclastic selectivity seems and more directly is present in the interaction of albumen enzyme-substrate.Specificity can be derived from the proteolytic ferment of only discerning the specific amino acids target sequence.On the other hand, it also can be the result that " processing site " selectivity under some condition such as pH, ionic strength or secondary modification exposes, thereby makes the incident of other nonspecific protease catalysis high degree of specificity.The vacuole proenzyme has been provided the example of a back type by limited proteoclastic activation.
Form takes place or differentiation may be defined as modulated a series of incidents, and this incident causes organism to change to another state from a state.Although can not establish the direct relation between proteolytic enzyme and the form result in many cases, present evidence is thought the participation of significant proteolytic enzyme in the fungi form takes place; In observing differentiation protein renewal widely, sporulation and the spore germination, think that proteolytic enzyme participates in normal processes directly, form (Deshpande, 1992) as most advanced and sophisticated branch of mycelia and partition.
Aspergillus species particularly Aspergillus fumigatus (A.fumigatus) and flavus (A.flavus) may be the pathogenic agent (Bodey and Vartivarian, 1989) that is called the numerous disease of aspergillosis in the humans and animals.Think that repeatedly proteolytic enzyme is relevant with the toxicity of Aspergillus fumigatus and flavus, it interrelates as the toxicity that has many researchs with excretory proteolytic enzyme and bacterium.In fact, the people of most of aspergillus infections is characterised in that its pulmonary parenchyma that mainly is made of collagen protein and elastin is by extensively degraded people such as (, 1994) Campbell.Research has concentrated on the supposition of secreted proteolytic enzyme in Aspergillus fumigatus and flavus toxicity and has used, this Aspergillus fumigatus and flavus are main human pathogens, and knownly have elastin lytic activity (elastinolytic) and a Collagenase (collagenic) active people such as (, 1993) Kolattukudy.These elastin cracking (elastinolytic) are active in external demonstration relevant with infectivity to mouse people such as (, 1984) Kothary.Known two kinds of secreted protein enzymes are by Aspergillus fumigatus and immobilizing Aspergillus flavus for Producing, i.e. alkaline serine protease (ALP) and neutral metal proteolytic enzyme (MEP).In Aspergillus fumigatus, with two genes of these proteolytic enzyme of coding separate, characterization and destruction (people such as Reicherd, 1990; People such as Tang, 1992,1993; People such as Jaton-Ogay, 1994).Yet when comparing with the wild-type strain, alp mep double-mutant does not show difference on pathogenic.Therefore, can draw sure conclusion think the secretor type Aspergillus fumigatus proteolytic enzyme of external evaluation for tissue invade be not must the factor people such as (, 1994) Jaton Ogay.Although Aspergillus fumigatus only accounts for the sub-fraction of airborne mould spores, it is the most frequent isolating fungi from lung and partition (people such as Schmitt, 1991).Other explanations of fungitoxicity be can be the parasitic growth that condition (temperature and nutrient) in the segmental bronchus helps Aspergillus fumigatus.As a result, when host's pathogenic defence was slackened by immunosuppression processing and disease such as AIDS, the invasive aspergillosis then can be circumstantial incident.
Known have 4 main proteolytic enzyme kinds, and this kind is named with the major function group of its avtive spot: ' Serine ', ' sulfydryl ' or ' halfcystine ', ' aspartic acid ' or ' carboxyl ' and ' metal ' proteolytic enzyme.The 244th and 248 parts (A.J.Barrett ed, 1994 and 1995) to the detailed visible Enzymology method of current summary (Methodsin Enzymology) of the main kind of these proteolytic enzyme, less important kind and non-classified proteolytic enzyme.
The specificity of proteolytic enzyme
Except that the catalyst mechanism of proteolytic enzyme, other importances of proteolytic ferment are specificitys of proteolytic enzyme.The specificity of proteolytic enzyme shows that this proteolytic enzyme may any substrate of hydrolysis.20 natural amino acids provide a lot of possibilities that constitute peptide.For example can constitute 400 dipeptides and 800 different tripeptides etc. with 20 amino acid people.About longer peptide, possible number will become almost unlimited.Some proteolytic enzyme is only in the unusual special sequence of certain location hydrolysis.The interaction of proteolytic enzyme and peptide substrates can comprise 1 to 10 amino-acid residue of peptide substrates.Have even the residue of more and the interactional substrate of proteolytic enzyme about big protein substrate.Yet, this may be included in avtive spot in conjunction with outside crack (cleft) with the low specific interaction of proteolytic enzyme residue.Usually, specific recognition is defined in linear peptide, and this peptide is in the combination of protease activities site.
Describe substrate and the interactional nomenclature of proteolytic enzyme by Schechter and Berger in proposition in 1967 (Biochem.Biophys.Res.Com., 1967,27,157-162), and be widely used in the document now.In this system, think that the amino-acid residue of peptide substrate combines with so-called sublocus (sub-sites) at avtive spot.As usual, the sublocus on these proteolytic enzyme is called as S (representative sublocus), and corresponding amino-acid residue is called as P (representative peptide).The amino-acid residue of the N-end side of the key that easily splits is numbered P3, P2, P1, and the amino-acid residue of those C-end sides is numbered P3 ', P2 ', P1 '.P1 and P1 ' are the amino-acid residues that is positioned near the key place of easily splitting.Substrate residue around the cleavage site can be numbered up to P8 then.Corresponding sublocus be will combine on the residue complementary proteolytic enzyme with substrate and S3, S2, S1, S1 ', S2 ', S3 ' etc. will be numbered.The preferred property of sublocus has been determined the preferred property of cutting the proteolytic enzyme of some specific aminoacid sequence in special site in the binding site peptide point.The aminoacid sequence of substrate should be consistent with the preferred property of being showed by sublocus.Specificity to some substrate obviously depends on the binding affinity of substrate and the key hydrolysis rate that easily splits subsequently.Therefore, proteolytic enzyme shows that by its kcat/Km ratio this ratio is known as the specificity constant better usually to the specificity of some substrate.In this specificity constant, kcat represents turnover ratio, and Km is a dissociation constant.
Except that participating in catalysis and bonded amino-acid residue, proteolytic enzyme contains many other necessary amino-acid residues.Some residues are crucial in folding, and some residues are kept the total three-dimensional structure of proteolytic enzyme, and some residues may relate to the adjusting of proteolytic activity, and some residues can make proteolytic enzyme be positioned special position.Many proteolytic enzyme contain the binding site of one or more metal ions outside avtive spot.These metal ions often work the constitutionally stable effect that makes.In addition, extensively glycosylation of excretory eukaryotic microorganisms proteolytic enzyme.The glycosylation that N-is connected with O-all has generation.But the glycosylation auxiliary protein folding, can increase solubility, prevent to assemble and stablize mature protein.In addition, glycosylated degree can influence secretion and proteinic water combination.
The adjusting of proteolytic activity
The proteolytic activity of the proteolytic enzyme of a great deal of is subjected to extensively regulating to avoid disadvantageous proteolysis infringement.On some degree, this adjusting betides transcriptional level.For example in fungi, secreted protein enzyme gene transcription is for the carbon and the nitrogenous source sensitivity of outside, and the gene of Codocyte endoproteinase is insensitive.External pH is felt by fungi, and some genes are by pH regulator.In this process, transcriptional protein plays a key role.The proteinic proteolysis process of this instrumentality often is the switch that makes instrumentality protein open or close.
Proteolytic enzyme is carried out intramolecularly and intermolecular adjusting.This means that some amino acid in the proteolytic ferment molecule is necessary for this adjusting.Proteolytic enzyme is generally synthetic with the bigger precursor that is known as proenzyme, non-activity in this precursor catalysis.Usually make the peptide chain of precursor protein kinase inactive extend at the N-terminal of proteolytic enzyme.This precursor is known as preceding protein (pro-protein) better.Many protein by this approach processing will go out from emiocytosis, so they contain a signal sequence (presequence) in addition, thereby the former former form of protein of precursor is synthetic completely.Except that making the proteolytic enzyme non-activity, propetide often is necessary for the mediation effective folding.Examples of proteases comprises serine protease (α crack protein enzyme, subtilisin, aqualysin, prohormone convertase), thiol proteinase (cathepsin L and Crewe proteolytic enzyme), aspartate protease (protease A and cathepsin D) and metalloprotease.In addition, propetide can work in cell traffic individually or with signal peptide.It can promote can promote to stride the transhipment of film with the interaction of cell chaperone or it.The size of the extension that the preceding protein of precursor is former changes the variation that certain degree is arranged in the scope of small peptide and polypeptide, polypeptide wherein can be used as autonomous folding unit and exists.Especially, after the proteolytic enzyme cutting, remain strong proteinase inhibitor even often observe these bigger extensions.Even observe after cutting, but also accessory protein enzyme correct folding of this propetide.Can think the proteic function of this propetide performance molecular chaperone, and the separation of this propetide or extra coexpression may be favourable for the production of proteolytic enzyme.
Proteolytic enzyme in being secreted into substratum and remain on tangible difference on the adjusting level between the intracellular proteolytic enzyme.The proteolytic enzyme that is secreted in the substratum is no longer controlled after activation usually, and is simple relatively on its molecular structure of being made up of a spherical module usually therefore.The pair cell endoproteinase must carry out successive control to avoid the infringement of pair cell.Opposite with the proenzyme of secreted protein enzyme, in complicated adjusting proteolytic enzyme more, very large polypeptide section can be inserted between the signal and proenzyme activation domain of proteolysis module.Structure function studies show that this non-proteolytic enzyme part can interact with macrostructure, film, cofactor, substrate, effector, inhibitor, ionic in participation, and these interact and regulate the active of proteolysis modules or its (they) proenzyme and activate.The non-proteolytic module is showed noticeable change on size and structure.Number of modules can not rely on the proteolysis module and exists.Therefore can think that this module is corresponding to folding autonomous independent structures and functional unit.The value of this module tissue is that the acquisition of new module can give receptor protein new binding specificity, and can cause the noticeable change in its activity, adjusting and the target.Can reorganize by module in order to form new interaction, adjusting, specificity and/or target, the applied molecular biology instrument makes full use of the principle of module tissue protein lytic enzyme.Although this extra module is that N or C-terminal extend usually, also observed big section insertion in the external rings of catalyst structure domain.It is believed that equally in this case the main folding still representative of proteolytic enzyme forms the basic topological framework of functional protein hydrolysis entity, and this insertion can be regarded as the substructure that is folded in proteolysis module surface.
Molecular structure
Organize than the module of larger protein in principle and have universal law in essence.Special in bigger multimode framework, general proteolysis module shows that mean size is 100~400 amino acid.This be secreted into substratum in most of globular preteins lytic enzymes big or small consistent.As discussing in the above, the polypeptide module is a polypeptide fragment, this fragment collapsible and the performance independent community function.Another term of this module is a structural domain.Yet structural domain uses in the situation wider than module.Be often referred to the part of polypeptide chain as used herein nomenclature structure territory, this polypeptide chain has been described general folding topological framework in three-dimensional structure.In a protein, structural domain interacts on multiple degree, but more not extensive than the interaction of the structural element in the structural domain.Other term such as subdomain and folding unit also are used for document.Similarly, can be observed and manyly have same functional especially protein and can have identical structural domain.This structural domain can be discerned from the primary structure that shows some sequence pattern, and this sequence pattern is typical for special structural domain.Typical example be mononucleotide in conjunction with folding, cellulose binding domain, helix turn helix DNA in conjunction with primitive, zinc refer to, EF hand, film anchor.Module refers to that those expections can fold and the structural domain of autonomous performance function.Skilled in the art will recognize that how from other biological or species, this structure and the common available computer software of homologous sequence to be identified special structural domain in primary structure by using.
Although multimode or Multidomain protein can be rendered as a string pearl, observed the assembling of more complicated in fact structure.Under multiple pearl was positioned at situation on the identical polypeptide chain, these pearls were commonly called module or structural domain.When pearl be not positioned at one with identical polypeptide chain on, but when forming set, so the term subunit is used in reference to this pearl by noncovalent interaction.Subunit can be by one or identical genetic transcription, perhaps by different genetic transcriptions.This multimode protein can be changed into proteolysis processing after causing the transcribing of a plurality of subunits.Independent subunit can be made up of a plurality of structural domains.Usually, 100-300 amino acid whose less globular proteins only is made up of a structural domain usually.
The molecular classification of proteolytic ferment
Usually proteolytic enzyme is classified according to its molecular property or according to its functional property.Molecular classification is based on the primary structure of proteolytic enzyme.Proteinic primary structure is represented its aminoacid sequence, and this sequence can be derived from the nucleotide sequence of corresponding gene.Extensively explore similarity in the primary structure and can notice similarity in catalyst mechanism and other character, this in addition may extend into functional property.Term family is used to describe a histone enzyme, these protease-based between its primary structure similarity and show evolutionary relationship.The member who it is believed that such family is by occurring by the evolution of divergence from identical ancestors.In a family, the primary structure meticulousr based on sequence more further marked off subfamily.Classification proteolytic enzyme according to three dimensional fold can comprise secondary structure, tertiary structure and quaternary structure.Usually, the classification on the secondary structure is confined to the content and the general direction of secondary structure element.The similarity of tertiary structure has caused the identification to superfamily or special group.One group of family of common ancestor is thought to have by superfamily or special group, and this is that dimension is folding because they all show common 3-.Usually, tertiary structure is more conservative than primary structure.As a result, the similarity of primary structure does not always reflect similar functional property.In fact, thus functional property is can be basically divergent to cause interesting new property.Quaternary structure is not used for the multiple protein enzyme is classified as yet at present.This may be owing to the preference of structural database for simple globular proteins.Activate, the many proteolysis system of adjusting or complex reaction cascade may be made up of a plurality of structural domains or subunit.Universal law in the structure organization of this protease system can cause novel classification.
According to specific classification
When not having sequence information, proteolytic enzyme has been carried out polytype functional classification.With reference to the classification carried out of catalytic reaction pair enzyme and name be rule in the enzyme nomenclature.This method also is to (enzyme nomenclature (EnzymeNomenclature), 1992Academic Press, cardinal principle Orlando) in the EC numbering of enzyme.In enzyme nomenclature (Enzyme Nomenclature) 1992, can discern two proteinoid enzymes (EC3.4), promptly those exopeptidases (EC 3.4.11-19) and those endopeptidases (EC 3.4.21-24,3.4.99).Endopeptidase is at the peptide chain interior region cutting peptide bonds away from end.Exopeptidase only cuts residue from the end of peptide chain.Exopeptidase in the N-end effect can discharge an amino-acid residue, a dipeptides or a tripeptides, and is called as aminopeptidase (EC3.4.11), dipeptidyl peptidase (EC 3.4.14) and three peptidyl peptases (EC 3.3.14) separately.Begin amino acid whose proteolytic enzyme of peptide processing release from C-terminal and be called as carboxypeptidase (EC3.4.16-18).Peptidyl dipeptidase (EC 3.4.15) is removed a dipeptides from C-terminal.Outward-and interior-peptase become one then and to be pepx (EC 3.4.13), it only specifically cuts dipeptides in its amino acid half point.ω peptase (EC 3.4.19) remove to substitute, cyclisation or the terminal residue that connected by isopeptide bond.
Except the position of proteolytic enzyme cutting peptide chain, for the proteolytic enzyme of each type, can be based on the further differentiation of the characteristic of preferred amino acids residue in the substrate.Usually people can distinguish have widely, medium and narrow specific proteolytic enzyme.Some proteolytic enzyme are simply with the specified protein of their hydrolysis or polypeptide and name, as M-Zyme, collagenase, elastoser.Narrow specificity can be constrained to a special amino acid or special sequence of removing or cut respectively.When proteolytic enzyme showed special preferred property to amino acid of P1 or P1 ' position, this amino acid whose name can be qualification person (qualifier).For example, the prolyl aminopeptidase is removed proline(Pro) (proline(Pro) is the P1 residue) from the N-terminal of peptide.When the key of the imino-side of having cut proline(Pro), used X-Pro or proline(Pro) (proline(Pro) is a P1 ' residue), removed proline(Pro) from C-terminal as proline carboxypeptidase.Prolyl endopeptidase (or Pro-X) cuts in the proline(Pro) back, and proline(Pro) endopeptidase (X-Pro) cuts in the proline(Pro) front.The amino-acid residue of the peptide bond front of easily splitting instigates carboxylic group to the contributive amino-acid residue of peptide bond.The amino-acid residue of the peptide bond back of easily splitting instigates amino group to the contributive amino-acid residue of peptide bond.According to common convention, amino acid chain is from N-terminal (initial) to C-terminal (termination) thereby and is numbered.Endo-protease also shows significantly preferred property for the special amino acid of P1 and P1 ' position, as glycyl endopeptidase, peptide acyl Methionin endopeptidase, glutamy endopeptidase.This exoproteinase can show preferred property to certain group amino acid of sharing some similar part.Such one group of preferred amino acids can comprise hydrophobic amino acid, bulky hydrophobic amino acid, little hydrophobic or only for the amino acid of little amino acid, big positive charge etc. only.Except that preferred property, also there is special preferred or eliminating by the preferred residue of other sublocus on the proteolytic enzyme to P1 and P1 ' residue.These multiple preferably can causing only simultaneously can be satisfied the very specific proteolytic enzyme of multiple sequence in conjunction with needs to those.Usually should be realized that proteolytic enzyme is suitable miscellaneous enzyme.Even very specific proteolytic enzyme also may cut the peptide of the preferred property of this proteolytic enzyme of not deferring to common observation.In addition, should be realized that envrionment conditions such as pH, temperature, ionic strength, water activity, these all can influence the preferred property of proteolytic enzyme whether solvent, competitive substrate or inhibitor.Envrionment conditions not only influences proteolytic enzyme, and influences the approach that protein substrate is presented to proteolytic enzyme.
Classify with catalyst mechanism.
Proteolytic enzyme can segment on the basis of its catalyst mechanism.Need know for above-mentioned classification based on each catalyst mechanism, specificity all causes the further segmentation to each class mechanism.Known have 4 main proteolytic enzyme kinds, and name: serine protease (EC 3.4.21 endopeptidase by the major function group of its avtive spot, EC 3.4.16 carboxypeptidase), sulfydryl or L-Cysteine HCL Anhydrous (EC 3.4.22 endopeptidase, EC 3.4.18 carboxypeptidase), carboxyl or aspartate protease (EC 3.4.23 endopeptidase) and metalloprotease (EC 3.4.24 endopeptidase, EC 3.4.18 carboxypeptidase).Member to each catalytic type of proteolytic enzyme has distinctive inhibitor.These little inhibitor are the amino-acid residue of modified protein enzyme active sites irreversibly.For example, serine protease by with the Phenylmethylsulfonyl chloride (PMSF) and diisopropylfluorophosphate (DFP) inactivation of active ser reaction, yet the Histidine of chloromethyl ketone (chloromethylketone) derivative and catalysis triplet reacts.Phosphoramidon and 1,10 phenanthroline generally suppress metalloprotease.Suppress to be shown as usually aspartate protease by stomach en-.E64 suppresses thiol proteinase specifically.Amastatin and bestatin suppress multiple aminopeptidase.Even in a catalysis kind, also observed the suitable variation of proteolytic enzyme to the susceptibility of inhibitor.To a certain extent, this can be relevant with the specificity of proteolytic enzyme.Under the binding site structure prevented the situation of inhibitor near catalytic site based on mechanism, this proteolytic enzyme was escaped from suppress, and has stoped the evaluation based on inhibiting mechanism type.For example chymotrypsin inhibitor is the strong inhibitor with the active serine protease of chymotrypsin-like, elastase inhibitor suppress elastoser such as serine protease and not with trypsinase or chymotrypsin protein enzyme reaction, 4 acid amides PMSF (APMSF) only suppress to have the specific serine protease of trypsin-like.Broad description to inhibitor purposes in the proteolytic enzyme classification comprises Barret and Salvesen, proteinase inhibitor (Proteinase Inhibitors), Elsevier Amstardam, 1986; Bond and Beynon (eds), proteolytic ferment, a kind of practical methods (Proteolytic Enzymes, A Practical Approach), IRL Press, Oxford, 1989; Enzymology method (Methods in Enzymology), eds E.J.Barret rolled up in 1994 244 and nineteen ninety-fives 248 roll up; E.Shaw, cysteinyl proteolytic enzyme and selectivity inactivation thereof (Cysteinyl proteinase and their selectiveinactivation), Adv Enzymol.63:271-347 (1990).
According to the suitableeest action condition classification
The needs of the catalyst mechanism of proteolytic enzyme and its conformation integrity have determined mainly this proteolytic enzyme can use under which kind of condition.The proteolytic enzyme of finding the suitableeest effect under application conditions is a main challenge.Usually the proteolytic enzyme condition that must act on is not the suitableeest, and has represented the compromise between the optimum condition of the ideal conditions of concrete application and proteolytic enzyme really.Except that the special character of proteolytic enzyme, will be appreciated that the condition that also depends on of presenting of protein substrate, and determined that equally also which kind of condition is the most effective for proteolysis.Comprise as pH dependency, temperature dependency, to the sensitivity of metal ion or dependency, ionic strength, salt concn, solvent compatibility with the specification of using relevant enzyme.Another factor of main importance is the activity specific of proteolytic enzyme.The activity specific of proteolytic enzyme is high more, and the required enzyme of specific transformation is few more.Lower enzyme require means lower cost and lower protein contamination level.
PH is a main parameter of proteolytic enzyme performance in determining to use.Therefore, the pH dependency is the important parameter of classification proteolytic enzyme.The main monoid of recognizing is aspartic protease, neutral protease, Sumizyme MP and high alkaline proteases.The suitableeest pH only mates to a certain degree with proteolysis mechanism, as aspartate protease when being everlasting acidity, show just when, metalloprotease and thiol proteinase are brought into play during to slight alkalinity through the neutral pH of being everlasting the suitablelyyest, and serine protease is active in alkalescence and high alkalinity zone mainly.For each kind is all known exception arranged.In addition, total water activity of system works.The pH of proteolytic enzyme in this scope, to great majority its substrate shows the suitableeest hydrolysis rate in the special environment of proteolytic enzyme under special condition just when being defined as a pH scope.This scope can be narrow, as a pH unit, and a quite wide 3-4 pH unit.Usually pH is just when the characteristic that also depends on protein substrate.Both can be used as turnover ratio and specificity the function of pH and change.For the effect of determining, can away from its just when the time use proteolytic enzyme because the production of undesired peptide has been avoided.Undesired peptide can be as very short peptide or causes the peptide of bitter taste.In addition, narrower specificity can be the reason of selection condition, and this condition departs from the suitableeest condition on about transformation efficiency.Depend on pH, specificity can be narrow, as the special position cutting of before or after special amino acid peptide chain only, or broad, as cutting before or after amino acid whose at a plurality of positions cutting peptide chain or how dissimilar.In fact, the pH dependency can be the important tool of regulating proteolytic activity in application.Under the situation that pH changes during the course, proteolysis can spontaneously stop, and need not further to handle so that the proteolytic enzyme inactivation.In some cases, proteolysis itself can be the driving thing that pH changes.
To the application of proteolytic enzyme very crucial be the stability of its processing and operation.Because proteolytic enzyme stability is influenced by working temperature strongly, so also stability is called thermostability usually.Usually the stability of proteolytic enzyme is presented at how long endoproteinase keeps its proteolytic activity under special condition.Special condition can comprise fermentation condition, at the separation of enzyme and condition, holding conditions, preparation and operation or the application conditions in the processing of downstream.When special condition comprised the temperature of rising, stability was often referred to thermostability.Except that the general reason such as the chemically modified of enzyme deactivation, separate folding, the gathering etc., the subject matter of proteolytic enzyme is that they are easy to carry out from degraded.Especially for the utilization of proteolytic enzyme, temperature is just when the related standards that is the proteolytic enzyme classification.Although different definition is arranged, the most useful commercial definition is in some applications efficient temperature of proteolytic enzyme or temperature range.The proteolytic enzyme productivity is the function of stability and turnover ratio.Temperature in this rising will increase turnover ratio usually, and inactivation will be offset the increase of turnover ratio fast, and finally cause low productivity.The conformational stability of proteolytic enzyme will be determined its service temperature maximum value in the condition of given process.Temperature when proteolytic enzyme loosens its activity conformation is shown as separates folding or fusing point, can determine according to several different methods, as NMR, circular dichroism, spectroscopy, differential scan calorimeter etc.For proteolytic enzyme, separate the folding very big increase of following usually from degradation rate.
In the cryogenic application of needs, proteolytic enzyme can be selected in low high intrinsic activity during to moderate temperature.Because inactivation is low relatively under this condition, so activity can be determined its productivity to a great extent under this condition.Only needing in the process of protease activity in short period, the stability of proteolytic enzyme can be used as the switch that this proteolytic enzyme is closed.In this case, can preferably more unsettled rather than very heat-staple proteolytic enzyme.
Other environmental parameters that can work in selecting suitable proteolytic enzyme can be its susceptibility to salt.With the consistency of metal ion be crucial for some application, this metal ion often is found in the multiple natural materials with low concentration.With regard to metalloprotease, the alternative catalytic metal ion of some ion also reduces or even completely destroy activity especially.In some applications, in order to prevent and the washout of proteolytic enzyme coordinate metal ion, must intentionally add metal ion.Well-known is for enzyme stability and life-span, and dissociating of the calcium of calcium ion to prevent protein bound must be provided.
Most microorganisms show some tolerance that the condition that conforms changes.Result's this biology proteolysis that can produce at least composes and may show similar tolerance.A kind of like this proteolysis spectrum can be covered or only be had by minority the proteolytic enzyme covering of extensive hydrolysis spectrum together by many proteolytic ferments.Consider whole proteolysis spectrums of microorganism, it is highly important that and consider the position.
Location and characterization in the cell of proteolysis process and degraded
From industrial point, have the specific advantage of scale operation power and stress tolerance from the proteolytic enzyme of emiocytosis, this is because they must be survived under the cytoprotective not being subjected to.The leukoprotease of big group can further be subdivided into solubility with membrane-bound.The membrane-bound proteolytic enzyme that is positioned at the film inboard and the outside that comprises.The soluble proteins enzyme can further segment according to the specific cells compartment that they took place in the cell.Because cell shields proteolytic enzyme and environment on some degree, and control intracellular condition because of cell, so intracellular protein is more responsive for big environmental change, and it is just when can be more relevant with condition in the specific cell.The condition of knowing the existing cellular compartment of proteolytic enzyme can show its preferred property.When extracellular protease is no longer needing any adjusting, intracellular protease then often to be subjected to complicated control and adjusting after emiocytosis usually.
About the function of special proteolytic enzyme, its location often is very important; For example, many vacuoles and periplasm protein enzyme participate in protein degradation, and many embrane-associated protein enzymes are important (Suarez Rendeules and Wolf, 1988) in protein processing.
Detailed summary to proteolytic enzyme biological property and evolution has been published in van denHombergh:Thesis Landbouwuniversiteit Wageningen: for improving analysis (An analysis of theproteolytic system in Aspergillus in order to improveprotein production) the ISBN 90-5485-545-2 of protein production to the proteolysis system, herein its integral body is quoted as a reference in Aspergillus.
The proteolytic enzyme problem
To the interested major reason of microbial protease is the relevant expression problem of proteolytic enzyme, and this problem is found in several expressive hosts that are used for biological processing industry.Heterologous host takes this problem on the focus to for the utilization that protein production increases recently by recombinant DNA technology, and this is because it seems that heterologous protein is easilier to be fallen (people such as Archer, 1992 by proteolysis; People such as van den Hormbergh, 1996b).
In yeast saccharomyces cerevisiae, had realized that the participation of proteolytic enzyme problem and several proteolytic enzyme in early days in [20th century] eighties, thereby made the directed gene destruction methods complicated to address this problem.In secretion, protein is exposed in several proteolytic activities that are present in the Secretory Pathway.In addition, in prototroph such as Aspergillus, excretory protein can be exposed in several extracellular protein hydrolytic activities.
The problem of the protein degradation of heterogenous expression has been carried out good proof (van den Hombergh:Thesis LandbouwuniversiteitWageningen: be analysis (An analysis of the proteolytic system in Aspergillus inorder to improve protein product ion) the ISBN 90-5485-545-2 of improvement protein production to the proteolysis system in Aspergillus) in Aspergillus, and has reported the cows milk curds proenzyme, human interferon-alpha-2tPA, GMCSF, IL6, lactoferrin, hen's egg-white lysozyme (lysosyme), pig p1A2, aspergillus niger pectic enzyme (lysase) B, this class problem in the expression of intestinal bacteria (E.coli) enterotoxin B and β-glucoronidase and carrot soft rot Erwinia (Erwinia carotovora) pectate lytic enzyme (pectate lysase) 3.
Proteoclastic problem can solve at the several stages of protein production.Biological processing slip-stick artist can by carry out downstream processing at low temperature, by early stage separated product and proteolytic enzyme or by using proteinase inhibitor to solve the proteolysis problem.These can all cause successfully reducing this problem.Yet problem is not eliminated certainly, and this is because many hydrolysis have taken place in the protein production process in vivo.
Understand proteolysis and how to control in cell, main problem relates to the proteoclastic recognition mechanism of triggering.(allogenic) protein with the proteolysis susceptible on which kind of degree is identified as because of malfolding unusually, if perhaps correct folding not settling because they do not have the place given birth to the special very crucial character of stability is identified as " external source ".The factor of known increase proteolysis speed comprises the adverse circumstance pressure (being the expression of rising, seepage water pressure, toxicant and some heterologous protein of temperature) of nutrient deficiency and multiple other types.In order to handle the relevant expression problem of proteolysis in vivo, as the SOME METHODS that will be described below has proved success.Yet we must keep real " cell of non-proteolytic " firmly in mind and not exist, and this is because participate in many basic metabolism and " house keeper (housekeeping) " reaction by the proteolysis of intracellular protease.Therefore in reducing proteoclastic process, must analyze the genetic background potential secondary action that causes proteolysis to reduce, this secondary action can cause protein production to reduce (reducing or sporulation as growth velocity).
In the filamentous fungus expressive host, destroy proteolytic enzyme
Berka and colleague thereof (1990) have described the clone and the destruction of Aspergillus awamori (A.awamori) pepA gene.Recently, 3 destructive aspartyl proteases in the aspergillus niger have been described.Disrupting agent (disruptant) to main extracellular aspartyl protease and main vacuole aspartyl protease is described.Generated the triple disrupting agents of double sum by reorganization, and checked the proteinic albumen zymogram of aspergillus niger pectic enzyme PELB and expression and secretion, this PELB protein is for the unusual susceptible (people such as van denHombergh, 1995) of proteolytic degradation.The destruction of pepA and pepB causes the activity of extracellular protease to reduce 80% and 6% respectively.In Δ pepE disrupting agent, other (vacuole) protease activity is also owing to the proteolysis cascade to other vacuole protein enzymes is seriously influenced equally.The active PELB external degradation in the extracellular of reducing with minimizing relevant with the improved expression in vivo of pelB (people such as van den Hombergh, 1996f).
Protease-deficient (prt) mutant filamentous fungus
Studied whether protein production is improved in several Aspergillus protease-deficient mutant.Archer and colleague thereof have described the proteolysis that the hen egg white N,O-Diacetylmuramidase reduces in the aspergillus niger prt double-mutant supernatant liquor that is generated by Mattern and colleague (1992) thereof, although and infer that degraded still exists, this degraded has reduced significantly.People (1995) such as Van denHombergh show that the external degradation of aspergillus niger PELB has all reduced in their isolating all 7 prt complementation groups.In fact in prtB, prtF and prtG mutant, do not observe degraded.Recently, in the complementation group (prtA-F) of 6 checks, all show the improvement of pelB genetic expression, and in prtB, prtF and prtG mutant, observed maximum expression level.Except that single mutant, it contains the residual extracellular protein hydrolytic activity of comparing with wild-type activity at 2-80%, by reorganization with take turns mutagenesis by another and generate double-mutant.Through this method, several prt double-mutants have been carried out selecting and further characterization, this shows the further minimizing of comparing the PELB degraded with its parental generation strain.
Without destroying or mutagenesis elimination protease activity, reduce proteolysis and also can realize by relevant proteolytic activity decrement is regulated.This can realize by other adjusting sequences that change promotor or gene hereditarily.As by shown in Fraissinet-Tachet and the colleague (1996) thereof, the extracellular protease of aspergillus niger is all suppressed by the carbon catabolite and the nitrogen metabolism thing suppresses adjusting.Nutritive deficiency also causes the fierce increase of proteolysis speed total in the cell, and this also is applicable to the shortage nutrient but has proteinic cell that it does not need or only need a small amount of nutrition under starvation conditions.Can report proteoclastic minimizing in the expression strategy of high expression level on the substratum that is containing high glucose and ammonium concentration making.Several composing type glycolysis-promotors (gpd and pkiA) are highly expressed under these conditions, and also can be used for driving (allogenic) genetic expression in continuously fermenting.The different proteolytic enzyme of degree influence that the nutrient deficiency type of being forced can change this means that the importance of nutrient condition in given process depends on the proteoclastic type that relates to.Therefore specific proteolysis can be induced by the condition of substrate restriction, and this substrate restriction is through being usually used in many large scale fermentation processes.
The proteolytic enzyme problem can partly be solved by a kind of above-mentioned or multiple strategy now.Yet the residual proteolytic activity of the proteolytic ferment of Jian Dinging has not still constituted the subject matter in this area yet.In order further to reduce disadvantageous proteoclastic level, be starved of in this area new proteolytic enzyme is identified, this proteolytic enzyme is responsible for the proteinic degraded of homology and heterogenous expression.The invention provides the new proteinase gene sequence of this proteins encoded enzyme.In case the primary sequence of known new proteinase gene then can adopt one or more above-mentioned recombinant DNA strategies to produce the mutant that (gene knockout) reduces proteolytic activity.
Although proteolytic enzyme is widely used in most of commercial runs, existing enzyme also has remarkable shortcoming at least a following character.
In the time of in joining animal-feed, existing proteolytic enzyme is not enough to opposing and is present in as the digestive ferment in pig and poultry stomach and intestine (GI) road.
On the other hand, existing available enzyme extrude or granulating in be not enough to resist specific (height) temperature and (height) pressure condition of employing.
Equally, existing enzyme does not have enough activity when pH scope 3-7, and this condition is general in numerous food product, drink product and the GI road most of animals.
According to the another one aspect, the specificity of existing available proteolytic enzyme is very limited, and this causes existing enzyme can not degrade or dissolve some " protease resistant " protein, thereby causes peptide or amino acid to yield poorly.In addition, having new specific proteolytic enzyme makes new peptide to synthesize.
The another one shortcoming of existing available enzyme is its low activity specific.
Therefore obviously existence is to a large amount of needs of proteolytic enzyme for a large amount of application, and this proteolytic enzyme has more resistance to digestive ferment, high temperature and/or pressure, and performance is to the new specificity in its hydrolysis site.The invention provides this kind of enzyme.
Goal of the invention
The object of the invention provides the new polynucleotide of the new proteolytic enzyme of coding.Further purpose provides the proteolytic enzyme of natural and recombinant production and produces the recombinant bacterial strain of these enzymes.This bacterial strain also can be used for quickly or produces traditional tunning with higher output.Another object of the present invention provides defective filamentous fungal strains in producing according to proteolytic enzyme of the present invention.This bacterial strain can be used for more effectively production allos or homologous protein.Same antibody and fusion polypeptide and preparation and use are parts of the present invention according to the method for polynucleotide of the present invention and polypeptide.
Summary of the invention
The invention provides the new polynucleotide of the new proteolytic enzyme of coding.
More specifically, the invention provides polynucleotide, these polynucleotide have (preferably under height stringency condition) with according to being selected from the sequence of SEQ ID NO:1~SEQ ID NO:57 or being selected from the nucleotide sequence of sequence hybridization of the sequence of SEQ ID NO:58~SEQ ID NO:114.Therefore, the invention provides nucleic acid, this nucleic acid with have according to the sequence that is selected from the sequence of SEQ IDNO:1~SEQ ID NO:57 or is selected from the sequence of SEQ ID NO:58~SEQ IDNO:114 about 60%, be preferably 65%, more preferably 70%, be more preferably 75%, 80%, 85%, 90%, 95%, 96%, 97%, 98% or 99% homology.
In an embodiment that is more preferably, the invention provides isolating polynucleotide, these polynucleotide can be preferably in the Aspergillus and obtain preferred especially aspergillus niger from filamentous fungus.
In one embodiment, the invention provides isolating polynucleotide, these polynucleotide comprise the nucleic acid encoding sequence, and this polypeptide has the aminoacid sequence that is selected from SEQ ID NO:115~SEQ IDNO:171 or its function equivalent.
In a further preferred embodiment, the invention provides isolating polynucleotide, this polynucleotide encoding is according at least one functional domain that is selected from the polypeptide of sequence of SEQ ID NO:115~SEQ ID NO:171 or its function equivalent.
In a preferred embodiment, the invention provides according to the proteinase gene that is selected from the sequence of SEQ IDNO:1~SEQ ID NO:57.In yet another aspect, the invention provides polynucleotide, be preferably aspergillus niger proteolytic enzyme or this variant polypeptides or cDNA fragment that coding is selected from SEQ ID NO:115~SEQ ID NO:171.In a preferred embodiment, this cDNA has the sequence that is selected from SEQ ID NO:58~SEQ ID NO:114 or its function equivalent.
Coding also can obtain by following method according to the genomic clone of polypeptide of the present invention, promptly select suitable probe, be used for increasing specifically corresponding to according to the genome area of SEQ ID NO:1~SEQ ID NO:57 or its segmental any one sequence, with this probe under proper condition with suitable biology such as Aspergillus such as aspergillus niger in the genomic dna that obtains hybridize, by as PCR (polymerase chain reaction) amplification purpose fragment after segmental purifying and clone to increasing.
In embodiment preferred further, the invention provides polynucleotide, these polynucleotide comprise the encoding sequence according to genome polynucleotide of the present invention, are preferably the polynucleotide sequence that is selected from SEQ ID NO:58~SEQ ID NO:114.
In another preferred embodiment, the invention provides cDNA, this cDNA can clone in suitable host living beings such as aspergillus niger and express and obtain by the sequence that will be selected from SEQ ID NO:1~SEQ ID NO:57.
Also can in suitable host living beings such as aspergillus niger, clone and express according to a polypeptide of the present invention and obtain by the sequence that will be selected from SEQ ID NO:1~SEQ IDNO:57.
The present invention also relates to comprise according to polynucleotide sequence of the present invention and can be used for increasing or survey primer, probe and segmental carrier according to DNA of the present invention.
In a further preferred embodiment, carrier is provided, wherein functionally be connected with the adjusting sequence according to polynucleotide sequence of the present invention, this adjusting sequence is suitable for amino acid sequence coded and expresses in appropriate host cell such as aspergillus niger or aspergillus oryzae (A.oryzea).The present invention also provides the method for preparation according to polynucleotide of the present invention and carrier.
The present invention also relates to the host cell of recombinant production, this cell contains with good grounds allos of the present invention or homologous polynucleotide.
In one embodiment, the invention provides recombinant host cell, wherein the expression according to proteolytic enzyme of the present invention significantly reduces, and perhaps wherein protease activities reduces, perhaps wherein proteolytic enzyme even inactivation.This recombinant chou is particularly useful for the expression of homology or heterologous protein.
In another embodiment, the invention provides recombinant host cell, wherein the expression according to proteolytic enzyme of the present invention significantly increases, and perhaps wherein protease activities increases.This recombinant chou is particularly useful for the expression of homology or heterologous protein, if become rate-limiting step in this essential proteolysis cutting, maturation is then seriously hindered so.
In another embodiment, the invention provides a kind of host cell of recombinant production, this cell contains with good grounds allos of the present invention and homologous dna, be preferably the protein DNA that coding has signal sequence, and wherein this cell can be produced according to functional protein enzyme of the present invention, be preferably the cell that can make, for example comprise copy number purpose Aspergillus bacterial strain according to gene of the present invention or cDNA increase according to proteolytic enzyme overexpression of the present invention.
In another embodiment, the invention provides a kind of host cell of recombinant production, this cell contains with good grounds allos of the present invention and homologous dna, and wherein this cell can be secreted according to functional protein enzyme of the present invention, be preferably can overexpression and secretion according to the cell of proteolytic enzyme of the present invention, for example comprise the copy number purpose Aspergillus bacterial strain that increases according to gene of the present invention or cDNA.
In another aspect of the present invention, provide the polypeptide of purifying.Polypeptide according to the present invention comprises by the polypeptide according to polynucleotide encoding of the present invention.Especially preferred according to the polypeptide of sequence that is selected from SEQ ID NO:115~SEQ ID NO:171 or its function equivalent.
The present invention also provide can with the antibody of polypeptide reaction according to the present invention.These antibody can be polyclonal, but especially preferred monoclonal antibody.This antibody is particularly useful for purifying polypeptide according to the present invention.
The fused protein that comprises the polypeptide according to the present invention also within the scope of the invention.The present invention also provides the method for preparation according to polypeptide of the present invention.
The invention further relates to by detecting and whether exist, perhaps diagnose aspergillosis by detecting whether to exist according to DNA of the present invention or its fragment or function equivalent according to polypeptide of the present invention or its function equivalent.
The present invention also relates to according to the purposes in the described herein commercial run of proteolytic enzyme of the present invention.
Detailed Description Of The Invention
Polynucleotide
The invention provides the polynucleotide of proteins encoded enzyme, this proteolytic enzyme has aminoacid sequence or its function equivalent that sequence is selected from SEQ ID NO:115~SEQ ID NO:171.The sequence of these genes is passed through the order-checking of the genomic clone that obtains from aspergillus niger is determined.The invention provides the polynucleotide sequence of the encoding gene that comprises these proteolytic enzyme of encoding and global cDNA sequence thereof and its encoding sequence.Therefore, the present invention relates to isolating polynucleotide, these polynucleotide comprise nucleotide sequence that is selected from SEQ ID NO:1~SEQ ID NO:57 or the sequence that is selected from SEQID NO:58~SEQ ID NO:114 or its function equivalent.
More specifically, the present invention relates to isolating polynucleotide, these polynucleotide can be hybridized with the sequence that is selected from the polynucleotide sequence of SEQ ID NO:1~SEQ ID NO:57 or is selected from SEQ ID NO:58~SEQ ID NO:114 under the stringency condition, are preferably under height stringency condition.Advantageously, this polynucleotide can particularly obtain from aspergillus niger from filamentous fungus.More specifically, the present invention relates to isolating polynucleotide, these polynucleotide have the nucleotide sequence that basis is selected from the sequence of SEQ ID NO:1~SEQ ID NO:57 or is selected from the sequence of SEQ ID NO:58~SEQID NO:114.
The present invention also relates to isolating polynucleotide, at least a basis of this polynucleotide encoding is selected from the functional domain of the SEQ ID NO:115~sequence of SEQ ID NO:171 or the polypeptide of its function equivalent.
As used herein, term " gene " and " recombination " refer to can be from the chromosomal DNA isolated nucleic acid molecule, and this molecule comprises the open reading-frame (ORF) of coded protein such as aspergillus niger proteolytic enzyme.Gene can comprise encoding sequence, non-coding sequence, intron and adjusting sequence.In addition, gene refers to as isolated nucleic acid molecule defined here.
The Protocols in Molecular Biology of nucleic acid molecule available standards of the present invention separates with sequence information provided herein, and this nucleic acid molecule is as having the sequence that is selected from SEQ ID NO:1~SEQ IDNO:57 or being selected from the nucleotide sequence of the SEQ ID NO:58~sequence of SEQ ID NO:114 or the nucleic acid molecule of its function equivalent.For example, utilize the nucleotide sequence of the sequence that is selected from SEQID NO:1~SEQ ID NO:57 of all or part or the nucleotide sequence of sequence that is selected from SEQ IDNO:58~SEQ ID NO:114 as hybridization probe, hybridization according to nucleic acid molecule available standards of the present invention separates with clone technology and (as is described in Sambrook, J., Fritsh, E.F. and Maniatis, T., molecular cloning: laboratory manual (Molecular Cloning:A Laboratory Manual), 2
Nd, ed., Cold Spring Harbor Laboratory, Cold Spring HarborLaboratory Press, Cold Spring Harbor, NY, 1989).
In addition, comprising the nucleic acid molecule that all or part is selected from the sequence of SEQ ID NO:1~SEQ ID NO:57 or is selected from the sequence of SEQ ID NO:58~SEQ ID NO:114 can separate by polymerase chain reaction (PCR) with the synthetic Oligonucleolide primers, and this primer is based in the sequence that is selected from SEQ ID NO:1~SEQ ID NO:57 or be selected from the sequence information that contains in the sequence of SEQ ID NO:58~SEQ ID NO:114 and design.
Nucleic acid of the present invention can increase as template and the suitable Oligonucleolide primers pcr amplification technology according to standard with cDNA, mRNA or genomic dna.Kuo Zeng nucleic acid can be cloned in the appropriate carriers and with dna sequence analysis and characterize like this.
In addition, corresponding to or can be prepared by the standard synthetic technology with oligonucleotide according to nucleotide sequence hybridization of the present invention, as utilize automatic dna synthesizer.
In a preferred embodiment, isolated nucleic acid molecule of the present invention comprises the nucleotide sequence shown in the sequence that is selected from SEQID NO:58~SEQ ID NO:114.The sequence of sequence that is selected from SEQID NO:58~SEQ ID NO:114 is corresponding to the coding region of aspergillus niger proteolytic enzyme cDNA.This cDNA comprises the sequence of coding according to the aspergillus niger protease polypeptide of the sequence that is selected from SEQ ID NO:115~SEQ IDNO:171.
In another preferred embodiment, isolated nucleic acid molecule of the present invention comprises and is selected from the sequence of SEQ ID NO:1~SEQ ID NO:57 or is selected from nucleotide sequence or its function equivalent complementary nucleotide sequence shown in the sequence of SEQ ID NO:58~SEQID NO:114.
Enough complementary with another nucleotide sequence complementary nucleic acid molecule and its, thus can hybridize with it, and form stable duplex whereby.
One aspect of the present invention is about isolated nucleic acid molecule, this nucleic acid molecule encoding polypeptide of the present invention or its function equivalent such as bioactive fragment or structural domain, and be enough to be suitable for as the PCR primer so that the fragment of amplified nucleic acid molecule or sudden change as the nucleotide sequence and this nucleic acid molecule of hybridization probe with the nucleic acid molecule of identification code polypeptide of the present invention.
" isolating polynucleotide " or " isolating nucleic acid " are DNA or RNA, this DNA or RNA not with two direct adjacency of encoding sequence, and in the naturally occurring genome of the organism that it was derived from it and this encoding sequence directly in abutting connection with (one at 5 ' end, one at 3 ' end).Thereby in one embodiment, isolating nucleic acid comprises 5 ' non-coding (as the promotor) sequence of some or all and the direct adjacency of encoding sequence.Therefore this term comprises as inserting carrier, the plasmid of self-replicating or the recombinant DNA in virus or prokaryotic organism or the Eukaryotic genomic dna, perhaps as the molecule that is separated (as handled the cDNA or the genomic DNA fragment of generation by PCR or restriction endonuclease) of independence and other sequences.It also comprises a kind of recombinant DNA, this recombinant DNA is the part of the hybrid gene of the extra polypeptide of coding, and this polypeptide does not contain cell material, viral material or culture medium (when being produced by recombinant DNA technology) or precursor or other pharmaceutical chemicals (when chemically synthetic) substantially.In addition, " isolating nucleic acid fragment " be not as a naturally occurring nucleic acid fragment and be not found in the native state.
As used herein, term " polynucleotide " or " nucleic acid molecule " mean and comprise dna molecular (as cDNA or genomic dna) and RNA molecule (as mRNA) and the DNA or the RNA analogue that generate with nucleotide analog.Nucleic acid molecule can be strand or double-stranded, but is preferably double-stranded DNA.Nucleic acid can synthesize with oligonucleotide analogs or derivative (as inosine or thiophosphoric acid Nucleotide).This oligonucleotide can be used for having as preparation the nucleic acid of the nuclease resistance of the base pairing ability of change or increase.
Another embodiment of the invention provides isolated nucleic acid molecule, the coding strand antisense of this nucleic acid molecule and proteolytic enzyme nucleic acid molecule such as proteolytic enzyme nucleic acid molecule.Comprise equally within the scope of the invention be the complementary strand of nucleic acid molecule described herein.
The order-checking mistake
Sequence information mentioned herein should straitly be interpreted as comprising the base that mistake is identified like this.Particular sequence disclosed herein can be advantageously used in particularly separating complete gene the aspergillus niger from filamentous fungus, and this can make it be easy to carry out further sequential analysis conversely and identify the order-checking mistake whereby.
Unless otherwise instructed, all all are to determine with the automated DNA sequenator by determined nucleotide sequence that dna molecular is checked order herein, and all are all predicted by as above determined dna sequence dna is translated by the amino acid sequence of polypeptide of the dna molecule encode of determining herein.Therefore, as known in the art, any dna sequence dna, any nucleotide sequence of being determined by this automated method of determining herein all can contain some mistakes.Generally consistent by the nucleotide sequence that automatic gear is determined at least about 90% with the actual nucleotide sequence of the dna molecular of order-checking, more generally be at least about 95%~at least about 99.9% unanimity.Actual sequence can determine that more accurately this method comprises artificial DNA sequence measurement well known in the art by additive method.As being known in the art equally, compare in the nucleotide sequence of determining one insertion or disappearance with actual sequence and just will cause frameshit in the nucleotide sequence translation, thereby will begin with different fully in this insertion or deletion segment by the amino acid of the dna molecular actual coding that checks order by the aminoacid sequence of the nucleotide sequence coded prediction of determining.
Those skilled in the art can identify this wrong base of identifying and know how to proofread and correct this mistake.
Nucleic acid fragment, probe and primer
A part or a fragment that can only comprise nucleic acid molecule according to nucleic acid molecule of the present invention, this nucleic acid molecule is selected from the sequence of SEQ ID NO:1~SEQ ID NO:57 or is selected from the sequence of SEQID NO:58~SEQ ID NO:114, for example can be used as the segmental fragment of the part of probe or primer or this proteinase gene of encoding.Make it possible to generate be designed for from the nucleotide sequence that proteinase gene and cDNA are determined and identify and/or clone other proteolytic enzyme family member and from the probe and the primer of the proteolytic enzyme homologue of other species.This probe/primer generally comprises the oligonucleotide of basic purifying, this oligonucleotide generally comprise preferred under height stringency condition with a nucleotide sequence at least about 12 or 15, be preferably about 18 or 20, be preferably about 22 or 25, more preferably about 30,35,40,45,50,55,60,65 or 75 or more successive Nucleotide nucleotides sequence column region of hybridizing, nucleotides sequence wherein be listed in the sequence that is selected from SEQ ID NO:1~SEQ ID NO:57 be selected from the sequence of SEQ IDNO:58~SEQ ID NO:114 or its function equivalent in show.
The transcript or the genome proteolytic enzyme sequence that can be used for surveying or homologous protein identical based on the probe of proteolytic enzyme nucleotide sequence as coding in other biological.In preferred embodiments, this probe further comprises the labelling groups that adheres to thereon, can be radio isotope, fluorescent chemicals, enzyme or enzyme cofactor as this labelling groups.This probe also can be used as the part of the diagnostic check test kit of the cell of identifying the expressing protein zymoprotein.
Identity and homology
Term " homology " and " identity per-cent " exchange use herein.For purpose of the present invention, in order to determine the identity per-cent of two aminoacid sequences or two nucleotide sequences, in order to carry out optimum ratio than sequence being compared (, in the sequence of first amino acid or nucleotide sequence, having introduced breach) as right in order to carry out with the optimum ratio of second amino acid or nucleotide sequence.Then amino-acid residue on corresponding amino acid position or the nucleotide position or Nucleotide are compared.When the position in first sequence by with second sequence in when identical amino-acid residue or Nucleotide occupy on the corresponding position, this molecule is same on this position so.Identity per-cent between two sequences is the function (that is the overall number of the number/position of % identity=same position (being the lap position) x100) of the total same position number of sequence.Preferably, these two sequences are isometric.
The technician will know that several different computer softwares can be used for the homology between definite two sequences.For example, the definite available mathematical algorithm of sequence comparison and identity per-cent is realized between two sequences.In a preferred embodiment, identity per-cent between two aminoacid sequences is determined with Needleman and Wunsch (J.Mol.Biol. (48): 444-453 (1970)) algorithm, this algorithm has been incorporated in the GAP program of GCG software package (can obtain from http://www.gcg.com), uses Blossom 62 matrixes or PAM250 matrix and 16,14,12,10,8,6 or 4 breach flexible strategy (gap weight) and 1,2,3,4,5 or 6 length flexible strategy (length weight).The technician is appreciated that all these different parameters will produce slightly different result, but total identity per-cent of two sequences and change indistinctively when using different algorithms.
In the another one embodiment, identity per-cent between two nucleotide sequences is determined with the GAP program in the GCG software package (can obtain from http://www.gcg.com), uses NWSgapdna.CMP matrix and 40,50,60,70 or 80 breach flexible strategy and 1,2,3,4,5 or 6 length flexible strategy.In another embodiment, the identity per-cent of two amino acid or nucleotide sequence is with E.Meyers and W.Miller (CABIOS, 4:11-17 (1989)) algorithm is determined, this algorithm has been incorporated into the ALIGN program (2.0 editions) (can obtain from http://vega/igh.cnrs.fr/bin/align-guess.cgi), uses PAM120 flexible strategy (weight) residue table, notch length point penalty 12 and breach point penalty 4.
Nucleic acid of the present invention and protein sequence can further be used as " search sequence " carrying out the search to public database, thereby as identify other family members or relevant sequence.People such as the available Altschul of this search, the NBLAST of (1990) J.Mol.Biol.215:403-10 and XBLAST program (2.0 editions) are carried out.The BLAST nucleotide search can carry out to obtain and proteolytic enzyme nucleic acid molecule homologous nucleotide sequence of the present invention with NBLAST program, mark=100, word length=12.The BLAST protein search can carry out to obtain and protease protein matter molecule homologous aminoacid sequence of the present invention with XBLAST program, mark=50, word length=3.In order to obtain to be used for the comparison jaggy of comparison purpose, can utilize people such as Altschul (1997) Nucleic Acids Res.25 (17): the Gapped BLAST that describes among the 3389-3402.When utilizing BLAST and Gapped blast program, can use the default parameter of each program (as XBLAST and NBLAST).Referring to http://www.ncbi.nlm.nih.gov.
Hybridization
As used herein, term " hybridization " means describes the condition of hybridizing and washing of being used to, under this condition, be at least about mutually 50%, at least about 60%, at least about 70%, more preferably at least about 80% in addition more preferably at least about 85%~90%, more preferably generally keep the phase mutual cross at least about 95% homologous nucleotide sequence.
A preferred non-limitative example of this hybridization conditions is in 45 ℃ hybridization in the 6X sodium chloride/sodium citrate (SSC), be accompanied by the washing of one or many in 1X SSC, 0.1%SDS, temperature is 50 ℃, preferred 55 ℃, preferred 60 ℃, and be more preferably 65 ℃.
The condition of height stringency comprises as in 68 ℃ of hybridization in 5x SSC/5x Denhardt ' s solution/1.0%SDS, reaches in the washing of room temperature in 0.2x SSC/0.1%SDS.Perhaps, washing can be carried out at 42 ℃.
The technician will know the condition that should use for stringency and height stringency hybridization conditions.Be easy to obtain about the extra guide of this condition from this area, as people such as Sambrook, 1989, molecular cloning: laboratory manual (Molecular Cloning:ALaboratory Manual), Cold Spring Harbor Press, N.Y.; With people (eds.) such as Ausubel, 1995, the current rules of molecular biology (CurrentProtocols in Molecular Biology), (John Wiley ﹠amp; Sons, N.Y.).
Certainly, only with polyadenylic acid sequence (as 3 ' the terminal polyadenylic acid zone of mRNA) or with the polynucleotide of complementary T (or U) residue section hybridization be not included in be used among the present invention specifically with nucleic acid moiety hybridization of the present invention polynucleotide, this is because a kind of like this polynucleotide can be hybridized (as actual what double-stranded cDNA clone that takes up an official post) with any nucleic acid molecule that contains polyadenylic acid section or its complement.
From other biological, obtain the DNA of total length
In general method, can screen the cDNA library that makes up by other biological, as from filamentous fungus, particularly from the Aspergillus species.
For example, aspergillus bacterium can screen homologous proteolytic enzyme polynucleotide by rna blot analysis.To after surveying according to the homeodomain transcription thing of polynucleotide of the present invention, utilize the well-known standard technique of those skilled in the art can be from separating from the RNA of suitable strain construction cDNA library.Perhaps, total genome dna library can screen with the probe with proteolytic enzyme multi-nucleotide hybrid according to the present invention.
For example, the homologous gene sequence can be separated by carrying out PCR, two Oligonucleolide primers that this PCR use designs on described nucleotide sequence basis or the Oligonucleolide primers storehouse of two degeneracys.
The template of reaction can be by mRNA is carried out the cDNA that reverse transcription obtains, and this mRNA prepares from known or conjecture can be expressed bacterial classification according to polynucleotide of the present invention.Can carry out subclone to the PCR product and represent the sequence of nucleotide sequence or its function equivalent of new proteolytic enzyme with the sequence of guaranteeing to increase with checking order.
The PCR fragment can be used to separate the cDNA clone of total length by multiple known method then.For example, can carry out mark and be used to screen phage or clay cDNA library the fragment of amplification.Perhaps, the fragment of mark can be used for screening-gene group library.
Also round pcr can be used for separating full length cDNA sequence from other biological.For example, according to standard program, can be from suitable cell or tissue source isolation of RNA.Available Oligonucleolide primers carries out reverse transcription reaction to cause the synthetic of first chain on RNA, Oligonucleolide primers wherein is specific to 5 ' end of most of institutes amplified fragments.
The RNA/DNA hybrid of gained as a result can be carried out " tailing (tailed) " (as use guanine) with the terminal enzyme (DNA) reaction of standard then, this hybrid can digest with RNase H, and can cause second chain synthetic (as with gathering the cytosine(Cyt) primer) then.Thereby the cDNA sequence of institute amplified fragments upstream can be easy to separate.The summary of useful clone's strategy is referring to as people such as Sambrook, on seeing; People such as Ausubel are on seeing.
Carrier
Another aspect of the present invention is preferably expression vector about carrier, and this carrier contains the nucleic acid of proteins encoded zymoprotein or its function equivalent.As used herein, term " carrier " refers to transport the nucleic acid molecule of another nucleic acid that is connected with it.One class carrier is " plasmid ", and it refers to can connect therein the circular double-stranded DNA ring of extra DNA section.Another kind of carrier is a virus vector, and wherein extra DNA section can connect into viral genome.Some carrier can be in the host cell that they are introduced the self-replicating bacteria carrier and the additive type Mammals carrier of bacterium replication orgin (as have).Other carriers (as non-add type Mammals carrier) will be integrated into the host cell gene group after in being incorporated into host cell, and duplicate with host genome whereby.In addition, some carrier can instruct the expression of gene that operationally is connected with them.This carrier is called " expression vector " herein.Usually, the expression vector that utilizes in recombinant DNA technology often adopts the form of plasmid.Term " plasmid " and " carrier " are used interchangeably herein, and this is because plasmid is the most frequently used form of carrier.Yet the present invention means and comprises other forms of expression vector, as the virus vector (as replication defect type retrovirus, adenovirus (adenoviruses) and adeno associated virus (adeno-associated viruses)) of performance equivalent functions.
Recombinant expression vector of the present invention is to be suitable for comprising nucleic acid of the present invention in the form of host cell inner expression nucleic acid, this means that recombinant expression vector is included in one or more adjusting sequences of selecting on the host cell basis that is used to express, this adjusting sequence is operably connected on the nucleotide sequence that will express.In recombinant expression vector, the meaning that " is operably connected " feeling the pulse with the finger-tip mark nucleotide sequence is so that the mode that nucleotide sequence can be expressed is connected to and regulates on the sequence (as in in-vitro transcription/translation system or in carrier is incorporated into host cell the time, in host cell).Term " adjusting sequence " means and comprises promotor, enhanser and other expression controlling elementss (as polyadenylation signal).This adjusting sequence description is in as Goeddel; Gene expression technique: Enzymology method (Gene Expression Technology:Methods inEnzymology) 185, Academic Press, San Diego, CA (1990).That regulates constitutive expression that sequence comprises that those instruct nucleotide sequence in many type host cells regulates sequence with those (as tissue-specific) of only instructing nucleotide sequence to express in some host cell.The technician should be appreciated that the design of expression vector can be dependent on as factors such as the selection of wanting transformed host cells, desired protein expression levels.Expression vector of the present invention can be incorporated in the host cell to produce protein or the peptide (as protease protein matter, the mutant of protease protein matter, its fragment, variant or function equivalent, fused protein etc.) by described nucleic acid encoding whereby.
Recombinant expression vector of the present invention can be protokaryon or eukaryotic cell endoproteinase protein expression and designs.For example, protease protein matter can be expressed in bacterial cell such as intestinal bacteria, insect cell (using baculovirus (baculovirus) expression vector), yeast cell or mammalian cell.Appropriate host cell is further described in Goeddel, gene expression technique: Enzymology method (Gene Expression Technology:Methods inEnzymology) 185, Academic Press, San Diego, CA (1990).Perhaps, recombinant expression vector can for example be regulated sequence and T7 polysaccharase with the T7 promotor in in-vitro transcription and translation.
Being used for expression vector of the present invention comprises and is derived from chromosomal, additive type and carrier virus, as be derived from bacterial plasmid, phage, yeast episome, yeast chromosomal element, virus as baculovirus, papovavirus (papova viruses), vaccinia virus (vaccinia viruses), adenovirus, fowlpox virus (fowl poxviruses), pseudorabies virus (pseudorabies viruses) and retrovirus, with the carrier that is derived from its combination, be derived from the carrier of plasmid and phage genetic elements as those, as clay and phagemid.
DNA inserts fragment and should be operably connected on the suitable promotor, as phage PL promotor, intestinal bacteria lac, trp and tac promotor, SV40 is early stage and late promoter and retrovirus LTRs promotor etc.Other suitable promotors are that the technician is known.In a specific embodiment, preferably those can instruct the promotor of proteolytic enzyme high level expression in the filamentous fungus.This promotor is known in this field.This expression construct can contain transcription initiation, terminated site and transcribe and is used to the ribosome bind site translated in the zone.The encoding part of the mature transcript of being expressed by construct will comprise translation initiation AUG in the initial of the polypeptide that will translate, and comprise suitable localized terminator codon at its end.
Carrier DNA can be incorporated into protokaryon or eukaryotic cell by the conversion or the rotaring dyeing technology of routine.As used herein, term " conversion " and " transfection " mean the multiple art-recognized technology that exogenous nucleic acid (as DNA) is incorporated into host cell, comprise transfection, transduction, infection, the fat transfection of calcium phosphate or calcium chloride co-precipitation, DEAE-dextran-mediation, the transfection or the electroporation of cation lipid mediation.But transform and the proper method of transfection host cell it in people such as Sambrook (molecular cloning: laboratory manual (Molecular Cloning:ALaboratory Manual), 2
NdEd., Cold Spring HarborLaboratory, Cold Spring Harbor Laboratory Press, ColdSpring Harbor, NY, 1989), people such as Davis, molecular biology basic skills (Basic Methods in Molecular Biology) (1986) and other laboratory manuals.
For the stable transfection of mammalian cell, depend on used expression vector and rotaring dyeing technology, known only have a fraction of cell foreign DNA can be integrated into its genome.In order to identify and select these intasomies, the gene (as antibiotics resistance) with a coding selected marker is incorporated in the host cell with target gene usually.Preferred selected marker comprises that those give medicine such as G418, Totomycin and methotrexate (mark of resistance).The nucleic acid of coding selected marker can be introduced host cell on the carrier identical with the proteins encoded zymoprotein, perhaps can introduce on independent carrier.Can identify (that is: the cell that has inserted the selected marker can be survived, and other cells are then dead) by medicament selection by the nucleic acid stability cells transfected of introducing.
Protein expression is realized with the carrier that contains composing type or inducible promoter in the intestinal bacteria of being everlasting in the prokaryotic organism, and this promotor instructs the expression of fusion or non-fused protein.Fused protein joins many amino acid in the encoded protein matter, as joins the N-terminal of recombinant protein.This fusion vector is generally as three purposes: 1) increase the expression of recombinant protein; 2) solvability of increase recombinant protein; With 3) help purifying recombinant proteins by in affinity purification, serving as part.In fusion expression vector, the contact place that the proteolysis cleavage site merges part and recombinant protein through being everlasting introduces so that behind the fused protein purifying, and recombinant protein can separate from merging part.This kind of enzyme and relevant recognition sequence thereof comprise factor Xa, zymoplasm and enteropeptidase.
As shown, expression vector will preferably contain selected marker.This mark comprises the Tetrahydrofolate dehydrogenase of eukaryotic cell culture or the tsiklomitsin or the amicillin resistance of neomycin resistance and intestinal bacteria and other microbial culture.Suitably host's representative example comprises bacterial cell, as intestinal bacteria, streptomyces (Streptomyces) and Salmonella typhimurium (Salmonella typhimurium); Fungal cell such as yeast; Insect cell such as fruit bat S2 and noctuid Sf9; Zooblast such as CHO, COS and Bowes melanoma; And vegetable cell.The suitable culture medium of above-mentioned host cell and condition are known in this field.
In carrier, preferred pQE70, pQE60 and the PQE-9 of using in the bacterium can be available from Qiagen; PBS carrier, Phagescript carrier, Bluescript vector, pNH8A, pNH16A, pNH18A, pNH46A can be available from Stratagene; With can be available from ptrc99a, pKK223-3, pKK233-3, pDR540, the pRIT5 of Pharmacia.Preferred eukaryotic vector has can be available from PWLNEO, pSV2CAT, pOG44, pZT1 and the pSG of Stratagene; With can be available from PSVK3, pBPV, pMSG and the pSVL of pharmacia.Other appropriate carriers are apparent for the technician.
Comprise that intestinal bacteria lacI and lacZ promotor, T3 and T7 promotor, gpt promotor, λ PR, PL promotor and trp promotor, HSV thymidine kinase promoter, early stage and late period SV40 promotor, retrovirus LTRs promotor are as from Rous sarcoma virus (Rous sarcoma virus) (" RSV ") and metallothionein promoter such as mouse metallothionein(MT)-I promotor being used for known bacterium promotor of the present invention.
The DNA of code book invention polypeptide transcribing in more high eukaryote can increase by insert enhancer sequence in carrier.Enhanser is the cis-acting elements of DNA, and it is long to be generally about 10~300bp, act as the transcriptional activity that increases promotor in given host cell type.The example of enhanser comprises SV40 enhanser, cytomegalovirus (cytomegalovirus) early promoter enhanser, the polyoma enhanser that is positioned at replication orgin side in late period and the adenovirus enhanser of bp100~270 of the late side that is positioned at replication orgin.
For with translated protein in the chamber of endoplasmic reticulum, to pericentral siphon zone or in extracellular environment, secrete, suitable secretion signal can be inserted in the polypeptide expressed.This signal can be endogenous to polypeptide, perhaps they can be allogenic signal.
The formal representation that polypeptide can have been modified as fused protein, and can not only comprise secretion signal, and comprises extra allos functional zone.Thereby, for example can be with an extra amino acid, the N-end that particularly charged amino acid joins polypeptide with improve this polypeptide purifying or in subsequently processing and storage stability and the time length in host cell.Similarly, peptide moiety can be joined in the polypeptide to promote purifying.
According to polypeptide of the present invention
The invention provides a kind of isolated polypeptide, this polypeptide has the aminoacid sequence that is selected from SEQ IDNO:115~SEQ ID NO:171, obtainable or express the obtainable aminoacid sequence of sequence that is selected from SEQ ID NO:1~SEQ ID NO:57 in a preferred embodiment in suitable host by expressing polynucleotide according to the present invention, and by in suitable host, expressing the obtainable aminoacid sequence of polynucleotide sequence that is selected from SEQ ID NO:58~SEQ ID NO:114.Similarly, peptide or the polypeptide that comprises the function equivalent of aforementioned polypeptides is contained among the present invention.Aforementioned polypeptides all is contained in the term " according to polypeptide of the present invention ".
Term " peptide " and " oligopeptides " are considered to synonym (being familiar with as common), and required as situation, and each term all uses with indication interchangeably by two amino acid whose chains of peptide base key link coupled at least.Word " polypeptide " is herein as containing the chain that surpasses 7 amino-acid residues.Oligopeptides herein and peptide molecule formula or sequence all from left to right and in the direction from the N-terminal to the C-terminal are write.Amino acid one-letter code used herein is known in this field, and is found in people's (molecular clonings: laboratory manual (MolecularCloning:A Laboratory Manual), 2 such as Sambrook
Nd, ed., Cold Spring HarborLaboratory, Cold Spring Harbor Laboratory Press, ColdSpring Harbor, NY, 1989) in.
" isolating " polypeptide or protein mean polypeptide or the protein that takes out from its natural surroundings.For example, it is isolating that the polypeptide of the recombinant production of expressing in host cell and protein are considered to purpose according to the present invention, as natural or recombinant polypeptide by many suitable basic purifying of technology, this technology is as at Smith and Johnson, disclosed single stage purification process among the Gene 67:31-40 (1988).
Can reclaim and purifying from the reconstitution cell culture with well-known method according to proteolytic enzyme of the present invention, this method comprises ammonium sulfate or ethanol sedimentation, acid extraction, negatively charged ion or cation-exchange chromatography, phosphorylated cotton chromatography, hydrophobic interaction chromatography, affinity chromatography, hydroxylapatite (hydroxylapatite) chromatography and lectin chromatography.For analysis purposes most preferably high performance liquid chromatography (" HPLC ") be used for purifying.
Polypeptide of the present invention comprises the product of natural purifying, the product of chemosynthesis program and the product of being produced by recombinant technology from protokaryon or eucaryon host, this host comprises as bacterium, yeast, higher plant, insect and mammalian cell.Depend on the host who adopts in the recombinant production process, polypeptide of the present invention can glycosylation or non-glycosylated.In addition, as the result of the process of host mediation, polypeptide of the present invention also can comprise the methionine residues of initial modification in some cases.
In addition, protein according to the present invention can be precursor protein matter such as proenzyme, hybridization protein, as the protein of presequence or the former acquisition of presequence, the perhaps non-mature form of any other type.
Protein fragments
The present invention has also described the biological active fragment according to polypeptide of the present invention.
The biological active fragment of polypeptide of the present invention comprises that the aminoacid sequence that comprises with protease protein matter has sufficient consistence or is derived from the polypeptide of latter's's aminoacid sequence of SEQ ID NO:115~SEQ ID NO:171 sequence (as be selected from) aminoacid sequence, it comprises the amino acid that lacks than full length protein, and shows the biologic activity of at least a corresponding full length protein.Usually, biological active fragment comprises and has at least a protease protein matter active structures territory or primitive.It is 10,25,50,100 or the polypeptide of amino acids more that proteinic biological active fragment of the present invention can be as length.In addition, other biological is learned one or more biologic activity that active part can prepare and assess its polypeptide natural form of the present invention that has by recombinant technology, and wherein proteinic other zones lack.
The present invention has also described the nucleic acid fragment of the biological active fragment of the above-mentioned protease protein matter of encoding.
Fused protein
Protein of the present invention or its function equivalent such as its biologic activity partly can be operatively attached to non-protease polypeptide (as the allogeneic amino acid sequence) and go up to form fused protein.As used herein, " chimeric protein " or " fused protein " of proteolytic enzyme comprise the protease polypeptide that is operably connected on the non-protease polypeptide." protease polypeptide " refers to have corresponding to the polypeptide according to the aminoacid sequence of peptide sequence of the present invention, and " non-protease polypeptide " refers to have the polypeptide corresponding to a proteinic aminoacid sequence, protein wherein substantially not with protein homology according to the present invention, as be different from protein protease protein matter or that be derived from identical or different biology.In a proteolytic enzyme fused protein, protease polypeptide can be corresponding to according to of the present invention proteinic all or part of.In a preferred embodiment, the proteolytic enzyme fused protein comprises at least one according to proteinic biological active fragment of the present invention.In another preferred embodiment, the proteolytic enzyme fused protein comprises at least two according to proteinic biological active fragment of the present invention.In fused protein, term " is operably connected " and means protease protein matter and non-protease protein matter merges mutually to meet the mode of reading frame.Non-protease polypeptide can be fused to the N-end or the C-end of protease polypeptide.
For example, in one embodiment, fused protein GST-proteolytic enzyme fused protein, wherein the proteolytic enzyme sequence is fused to the C-end of GST sequence.This fused protein can promote the purifying of recombinant protein enzyme.In another embodiment, fused protein is a kind of protease protein matter that contains the allos signal sequence at its N-end.In some host cell (as Mammals and yeast host cell), the expression of proteolytic enzyme and/or secretion can increase by using the allos signal sequence.
In another example, the gp67 secretion sequence of baculovirus envelope protein can be used as allos signal sequence (the current rules of molecular biology (Current Protocols inMolecular Biology), people such as Ausubel, eds., John Wiley ﹠amp; Sons, 1992).Other examples of eucaryon allos signal sequence comprise the secretion sequence (Stratagene of mellitin and placental alkaline phosphatase; La Jolla, California).In the another one example, useful protokaryon allos signal sequence comprises phoA secretion signal (people such as Sambrook is on seeing) and a-protein secretion signal (Pharmacia Biotech; Piscataway, New Jersey).
The secretion that signal sequence can be used to promote protein of the present invention or polypeptide with separate.The signal sequence general feature is the core of a hydrophobic amino acid, this core usually in secretion process through one or repeatedly cut incident and from mature protein, excise.The sort signal peptide contains the processing site, and this site makes signal sequence can excise from mature protein through Secretory Pathway the time.Signal sequence instructs proteinic secretion, and as secreting from the eucaryon host that this expression vector transformed, and signal sequence is cut subsequently or simultaneously.This protein can be easy to art-recognized method purifying from the substratum of extracellular then.Perhaps, this signal sequence can be connected on the target protein with the sequence that promotes purifying, as has the sequence of GST structural domain.Thereby, for example the sequence of coded polypeptide can be fused on the flag sequence, as the sequence of encoded peptide, this sequence promotes the purifying of fusion polypeptide.In some embodiment preferred of this respect of the present invention, flag sequence is six Histidine peptides, as the mark that in the pQE carrier, provides (Qiagen, Inc.), wherein many can buying by commodity.For example, as people such as Gentz, described in the Proc.Natl.Acad.Sci.USA 86:821-824 (1989), six Histidines provide the purifying that makes things convenient for to fused protein.The HA mark is another peptide that is used for purifying, and this peptide is corresponding to the epitope that is derived from influenza hemagglutinin protein matter, and this is by as people such as Wilson, and Cell 37:767 (1984) is described.
Preferably, the chimeric or fused protein of proteolytic enzyme of the present invention is by the recombinant DNA technology production of standard.For example, link together to meet the mode of reading frame according to will the encode dna fragmentation of different peptide sequences of routine techniques, for example by the end that adopts blunt end or staggered end connect, adopt restriction enzyme digestion provide suitable end, suitably mend flat sticky end, adopt alkaline phosphatase treatment to avoid the connection of unwanted connection and enzymatic.In another embodiment, fused protein can synthesize by routine techniques, and this technology comprises automatic dna synthesizer.Perhaps, pcr amplification to gene fragment can be implemented with anchor primer, this primer can cause the complementary overhang between two successive gene fragments, it can be annealed subsequently and increase again to generate chimeric gene sequence (referring to as the current rules of molecular biology (Current Protocols in Molecular Biology), people such as Ausubel, John Wiley ﹠amp; Sons:1992).In addition, many expression vectors that merge part of having encoded can be buied (as gst polypeptide) by commodity.The protease-encoding nucleic acid clone can be gone in such expression vector, thereby this fusion part is connected on the protease protein matter to meet the mode of reading frame.
Function equivalent
Term " function equivalent " and " functional variant " are used interchangeably herein.Function equivalent according to DNA of the present invention is the separated DNA fragment of coded polypeptide, and this polypeptide is showed as the special function of defined aspergillus niger proteolytic enzyme herein.According to the function equivalent of polypeptide of the present invention is to show as the polypeptide of at least one function of defined aspergillus niger proteolytic enzyme herein.
Functional protein or polypeptide Equivalent can only contain and a plurality of amino acid whose conservative substituting of the sequence that is selected from SEQ ID NO:115~SEQ IDNO:171, and perhaps non-primary amino acid substitutes, inserts or disappearance.Therefore, non-primary amino acid is can change in the sequence that is selected from SEQ IDNO:115~SEQ ID NO:171 and significantly do not change the residue of biological function.For example, conservative amino-acid residue is estimated should not change especially in protease protein matter of the present invention.In addition, conservative unlikely the suiting of amino acid changes in protease protein matter according to the present invention and other proteolytic enzyme.
Term " conservative substituting " means wherein amino-acid residue substituting with the radical amino acid replacement with similar side chain.These families are as known in the art, and comprise having basic side chain (as Methionin, arginine and Histidine), acid side-chain is (as aspartic acid, L-glutamic acid), uncharged polar side chain is (as glycine, l-asparagine, glutamine, Serine, Threonine, tyrosine, halfcystine), non-polar sidechain is (as L-Ala, Xie Ansuan, leucine, Isoleucine, proline(Pro), phenylalanine, methionine(Met), tryptophane), β-branch side chain is (as Threonine, Xie Ansuan, Isoleucine) and aromatic side chains (as tyrosine, phenylalanine, tryptophane, Histidine) amino acid.
The functional nucleic acid Equivalent generally contains silent mutation or does not change the sudden change of the biological function of coded polypeptide.Therefore, the invention provides the nucleic acid molecule of proteins encoded zymoprotein, this protein contains the change for the nonessential amino-acid residue of concrete biologic activity.This protease protein matter is variant in aminoacid sequence with the sequence that is selected from SEQ ID NO:115~SEQ ID NO:171, but still has kept at least a biologic activity.In one embodiment, isolated nucleic acid molecule comprises the nucleotide sequence of coded protein, wherein this protein comprise with the aminoacid sequence that in the sequence that is selected from SEQ ID NO:115~SEQ ID NO:171, shows at least about 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95%, 96%, 97%, 98%, 99% homology or the basic homologous aminoacid sequence of homologous more.
For example, about the guide of the amino acid replacement that how to prepare the phenotype silence at Bowie, people such as J.U., Science 247:1306-1310 provides in (1990), wherein the author shows two kinds of main methods and is used to study the tolerance of aminoacid sequence to changing.First method depends on evolutionary process, wherein suddenlys change to be accepted by natural selection or discarded.Second method utilizes genetically engineered to change to introduce amino acid at the specific position of cloned genes, and selects or screening is kept functional sequence with evaluation.As author's statement, these researchs disclose protein and have surprising tolerance for amino acid replacement.The author further is presented at which kind of variation of proteinic some position may be allowed.For example, most of hidden amino-acid residues require non-polar sidechains, and seldom the feature of surface side chains is guarded usually.Other this phenotype silences alternative is described in people such as Bowie, sees in the reference of going up and quoting.
Introduce one or more nucleotide substitutions, increase or disappearance in the coding nucleotide sequence of the isolated nucleic acid molecule of coding and the protease protein matter of the protein homology that is selected from SEQ ID NO:115~SEQ ID NO:171 can be by being selected from sequence from SEQ ID NO:1~SEQID NO:57 to basis or the sequence that is selected from SEQ ID NO:58~SEQ ID NO:114 and form, thereby one or more amino acid replacement, disappearance or insertion promptly are incorporated in the encoded protein matter.This sudden change can be introduced by standard techniques, as site-directed mutagenesis and PCR-mediated mutagenesis.
Term " function equivalent " also comprise aspergillus niger protease protein matter directly to homologue (orthologues).The straight of aspergillus niger protease protein matter is the protein that can separate and have similar or identical biologic activity from other strains or species to homologue.Thisly directly can be easy to be accredited as the basic homologous aminoacid sequence of sequence that comprises and be selected from SEQ ID NO:115~SEQ ID NO:171 to homologue.
As defined herein, term " basic homology " refers to that first amino acid or nucleotide sequence contain amino acid or Nucleotide enough or minimum purpose identical or of equal value with second amino acid or nucleotide sequence (as having similar side chain), thereby first has the common structural domain with second amino acid or nucleotide sequence.For example, contain have about 60%, be preferably 65%, more preferably be 70%, more preferably be 75%, 80%, 85%, 90%, 95%, 96%, 97%, 98% 99% or the amino acid or the nucleotide sequence in more conforming common structure territory be defined as enough identical herein.
Equally, encode other proteolytic enzyme family member nucleic acid within the scope of the present invention, this nucleic acid thereby have with the sequence that is selected from SEQ ID NO:1~SEQ ID NO:57 or be selected from the different nucleotide sequence of sequence of SEQ ID NO:58~SEQ ID NO:114.In addition, coding from the nucleic acid of the protease protein matter of other species within the scope of the present invention, this nucleic acid thereby have with the sequence that is selected from SEQ ID NO:1~SEQ ID NO:57 or be selected from the different nucleotide sequence of sequence of SEQ IDNO:58~SEQ ID NO:114.
Can be corresponding to the nucleic acid molecule of the variant (as natural allele variant) of albumen enzyme dna of the present invention and homologue based on it with the homology of disclosed proteolytic enzyme nucleic acid herein and separate, preferably under height stringency hybridization conditions, be used in cDNA disclosed herein or its suitable fragment as hybridization probe according to the hybridization technique of standard.
Except that the naturally occurring allele variant of proteolytic enzyme sequence, the technician will recognize in the nucleotide sequence of the sequence that can be by sudden change variation be incorporated into the sequence that is selected from SEQ ID NO:1~SEQ ID NO:57 or be selected from SEQ ID NO:58~SEQ ID NO:114, cause the variation in the aminoacid sequence of protease protein matter whereby and significantly not change the function of protease protein matter.
In another aspect of the present invention, provide improved protease protein matter.Improved protease protein matter is the protein that wherein at least a biologic activity is improved.This protein can obtain by introduce sudden change randomly on the protease-encoding sequence of all or part, as by saturation mutagenesis, and the mutant of the ground expression of results gained of can recombinating and screen its biologic activity.For example, this area provides the standard test of the enzymic activity that is used to measure proteolytic enzyme, thereby can be easy to select improved protein.
In a preferred embodiment, protease protein matter has according to the aminoacid sequence that is selected from the sequence of SEQ IDNO:115~SEQ ID NO:171.In another embodiment, protease polypeptide with according to the basic homology of aminoacid sequence of the sequence that is selected from SEQ ID NO:115~SEQ ID NO:171 and keep according at least one biologic activity that is selected from the polypeptide of sequence of SEQ ID NO:115~SEQ IDNO:171, but because natural variation or above-mentioned mutagenesis and variant in aminoacid sequence.
In a further preferred embodiment, protease protein matter has by isolating nucleic acid fragment amino acid sequence coded, and this isolating nucleic acid fragment can be preferably hybridized under height stringency hybridization conditions with according to the nucleic acid that is selected from the sequence of SEQ ID NO:1~SEQ ID NO:57 or is selected from the sequence of SEQID NO:58~SEQ ID NO:114.
Therefore, protease protein matter is to comprise with the aminoacid sequence that shows in the sequence that is selected from SEQ ID NO:115~SEQ IDNO:171 to have at least about 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95%, 96%, 97%, 98%, 99% or the protein of the aminoacid sequence of bigger homology, and has kept according at least a functionally active that is selected from the polypeptide of sequence of SEQ ID NO:115~SEQ IDNO:171.
Also can identify according to proteinic function equivalent of the present invention as the protease activity of the combinatorial library of the mutant by the screening proteinic mutant of the present invention such as brachymemma.In one embodiment, various variant library forms by the combinatorial mutagenesis on nucleic acid level.Various variation library can be expressed as independent polypeptide or one group of bigger fused protein (as being used for phage display) thereby one of potential protein sequence is overlapped the degeneracy group by producing as synthetic oligonucleotide mixture enzymatic is connected in the gene order.There are many methods to can be used for from the oligonucleotide sequence of degeneracy, producing the potential variant library of polypeptide of the present invention.The method of synthetic degenerate oligonucleotide is known in the art (referring to as Narang (1983) Tetrahedron39:3; People such as Itakura, (1984) Annu.Rev.Biochem.53:323; People such as Itakura, (1984) Science 198:1056; People such as Ike, (1983) Nucleic Acid Res.11:477).
In addition, the fragment library of the encoding sequence of polypeptide of the present invention can be generated and be used to screen follow-up variant selects diversified polypeptide colony.For example, the segmental library of encoding sequence can form by following method, each molecule only take place under the condition of an about otch (nicking) with nuclease processing target encoding sequence double-stranded PCR fragment, make this double-stranded DNA sex change, make the DNA renaturation can comprise from difference and incise the right double-stranded DNA of justice/antisense is arranged, partly and with the fragment of gained as a result connecting into the expression vector of product by handling with the S1 nuclease from the duplex removal strand of reconstruct to form.By this method, the expression library of the interior segments of the terminal and multiple size of the N-of the target protein that can obtain encoding.
Be known in the art several technology and be used for, and have the gene product of selected character from the cDNA library screening from combinatorial library screening-gene product by the point mutation of truncated mutant preparation.The most widely used technology that is suitable for the big gene library of screening of high throughput analysis generally comprises gene library is cloned in the rf expression vector, transforms suitable cell and express this combination gene under certain condition with the vector library of gained as a result, and active detection has promoted coding is detected the separation of the carrier of gene product to purpose in this condition.A kind of technology that strengthens function mutation body frequency in the library returns whole mutagenesis (recursive ensemblemutagenesis) and (REM) can be used from the proteinic variant of evaluation the present invention (Arkin and Yourvan (1992) Proc.Natl.Acad.Sci.USA89:7811-7815 with this screening assay one; People such as Delgrave, (1993) Protein Engineering 6 (3): 327-331).
Except that the proteinase gene sequence that in the sequence that is selected from SEQ ID NO:1~SEQ ID NO:57, shows, for those skilled in the art, it is evident that in given colony to have the dna sequence dna polymorphism, this polymorphism can cause the variation of aminoacid sequence in the protease protein matter.This genetic polymorphism can be present in from the cell of different groups or because in the cell in the colony of natural allelic variation.Allelic variation also can comprise function equivalent.
Fragment according to polypeptide of the present invention also can comprise the not polynucleotide of encoding function polypeptide.This polynucleotide can be brought into play the function of the primer of probe or PCR reaction.Also available this polynucleotide (gene knockout mutant) when wanting the functionally active of destruction proteolytic enzyme in concrete organism.
No matter according to their encoding functions of nucleic acid of the present invention or non-functional polypeptide, all can be used as hybridization probe or polymerase chain reaction (PCR) primer.The purposes of nucleic acid molecule of the present invention of polypeptide with protease activity of not encoding comprises that in addition (1) is from for example from gene or its allelic mutant of separating the proteins encoded zymoprotein the cDNA library of the organism except that aspergillus niger; (2) to the in situ hybridization (as FISH) of Metaphase Chromosome expansion so that the accurate location of proteinase gene in karyomit(e) to be provided, as be described in people such as Verma, human chromosome: basic fundamental handbook (Human Chromosomes:a Manual of BasicTechniques), Pergamon Press, the method among the New York (1988); (3) whether the rna blot analysis probe that can be used as diagnostic tool with the expression of surveying proteolytic enzyme mRNA in particular organization and/or cell and (4) and primer can exist with the nucleic acid of proteolytic enzyme probe hybridization in given biology (as tissue) sample to analyze.
The present invention comprises the method for the function equivalent that obtains proteinase gene or cDNA equally.This method need obtain the probe of mark, and this probe comprises that coding is according to the isolating nucleic acid or its variant that are selected from the SEQ IDNO:115~sequence of SEQ ID NO:171 or all or part of sequence of its variant; Probe with mark under the condition that nucleic acid fragment in probe and library can be hybridized screens the nucleic acid fragment library, form nucleic acid duplex whereby, and prepare the gene order of total length to obtain the gene relevant with proteinase gene from the nucleic acid fragment of the duplex of any mark.
In one embodiment, proteolytic enzyme nucleic acid of the present invention with in the sequence that is selected from SEQ IDNO:1~SEQ ID NO:57, be selected from SEQ ID NO:58~sequence of SEQ ID NO:114 or the nucleotide sequence of its complement sequence and have at least about 60%, 65%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or bigger homology.
In another preferred embodiment, protease polypeptide of the present invention with have at least about 60%, 65%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or bigger homology at the aminoacid sequence that is selected from SEQID NO:115~SEQ ID NO:171 sequence.
Host cell
In another embodiment, the invention describes the cell that contains nucleic acid of the present invention, as transformed host cells or recombinant host cell." cell transformed " or " cell of reorganization " is to rely on recombinant DNA technology to introduce the cell according to nucleic acid of the present invention to wherein (or in its ancestors).This comprises protokaryon and eukaryotic cell, as bacterium, fungi, yeast etc., especially preferably from the filamentous fungus cell of aspergillus niger particularly.
Can select to regulate the expression of insertion sequence or modify host cell with the processed gene product in specific required mode.This modification to protein (as glycosylation) and processing (as cutting) can promote the suitableeest proteinic function performance.
Multiple host cell has translates the distinctive and specific mechanism of post-treatment and modification to protein and gene product.Can select the technician is familiar with in molecular biology and/or the microbiology field suitable clone or host system to guarantee that the exogenous protein of expressing is carried out required and correct modification and processing.For this purpose, can use the eukaryotic host cell that gene product is carried out correct primary transcript processing, glycosylation and phosphorylation.This host cell is well-known in this area.
Host cell is also including, but not limited to mammal cell line such as CHO, VERO, BHK, HeLa, COS, MDCK, 293,3T3, WI38 and choroid plexus cell system.
If desired, can produce by the clone of stable transfection according to polypeptide of the present invention.Many carriers that are suitable for the stable transfection of mammalian cell are public obtainable, and the method that makes up this clone also is known technology, as described in the people such as Ausubel (on seeing).
Antibody
The present invention has further described specificity in conjunction with the antibody according to protease protein matter of the present invention, as mono-clonal or polyclonal antibody.
As used herein, term " antibody " (Ab) or " monoclonal antibody " (Mab) refer to comprise can the binding proteins specific zymoprotein complete molecule and antibody fragment (as Fab and F (ab ')
2Fragment).Fab and F (ab ')
2Fragment lacks the Fc fragment of complete antibody, can remove quickly in circulation, and can have the non-specific tissue bond lacked than complete antibody people such as (, J.Nucl.Med.24:316-325 (1983)) Wahl.Thereby, preferred these fragments.
Antibody of the present invention can prepare by any of several different methods.For example, expressing protein zymoprotein or the segmental cell of its antigenicity can be applied to animal to induce the production of the serum that contains polyclonal antibody.In a preferable methods, protease protein matter prepared product is prepared with purifying so that it does not contain natural pollutent substantially.This preparation is incorporated in the animal then and has the more active polyclonal antiserum of high specific with production.
In most preferred method, antibody of the present invention is monoclonal antibody (or its protease protein matter binding fragment).This monoclonal antibody can prepare (people such as Kohler, Nature 256:495 (1975) with hybridoma technology; People such as Kohler, Eur.J.Immunol.6:511 (1976); People such as Hammerling, In: monoclonal antibody and T-quadroma (Monoclonal Antibodies and T-Cell Hybridomas), Elsevier, N.Y., pp.563-681 (1981)).Usually, this program comprises with protease protein matter antigen or with protease protein matter express cell animal (being preferably mouse) is carried out immunization.The splenocyte of this mouse extracted and merge with suitable myeloma cell line.Can adopt any suitable myeloma cell line according to the present invention; Yet, preferably adopt parent myeloma cell line (SP
2O), available from American Type Culture Collection (American Type Culture Collection), Rockville, Maryland.After the fusion, the hybridoma of gained as a result optionally is maintained on the HAT substratum, clones by restrictive dilution then, such as by people such as Wands (Gastro-enterology 80:225-232 (1981)) description.To measure clone by the hybridoma that this selection obtains then to identify that secretion can the antigenic antibody of conjugated protein zymoprotein.Usually, this polypeptide can with carrier protein such as KLH coupling, as described in people such as Ausubel, on seeing, mix with adjuvant, and be expelled in the host mammal.
Particularly, multiple host animal can carry out immunization by the injection to target polypeptides.The example of suitable host animal comprises rabbit, mouse, cavy and rat.Depend on host species, multiple adjuvant can be used for increasing immune response, and this adjuvant is including, but not limited to Fu Shi (fully with incomplete), adjuvant mineral glue such as aluminium hydroxide, surfactant such as lysolecithin, polyol, polyanion, peptide, emulsifier, keyhole limpet hemocyanin, dinitrophenol(DNP), BCG (bacille Calmette-Guerin vaccine) and spillikin bacillus (Corybebacterium parvum).Polyclonal antibody is the heterogeneous population of antibody molecule that is derived from the serum of immunization animal.
This antibody can be any immunoglobulin (Ig) kind and the subclass thereof that comprises IgG, IgM, IgE, IgA, IgD.The hybridoma of producing mAb of the present invention can be external or cultivate in vivo.
In case produced, promptly in immunoassay such as western blotting or immunoprecipitation analysis, check polyclone or monoclonal antibody to the specific recognition of protease polypeptide or its function equivalent with standard technique, describe as people such as Ausubel, on seeing.The antibody of binding proteins specific zymoprotein or its function equivalent can be used among the present invention.For example, this antibody can be used in the immunoassay to survey the proteolytic enzyme (as in the aspergillus extract) in pathogenic or the non-pathogenic aspergillus bacterial classification.
Preferably, antibody of the present invention is with the fragment production of protease polypeptide, and the standard that this fragment charged residue occurs with for example high frequency may be shown as has antigenicity.For example, this fragment can generate by the standard round pcr, is cloned into then in the pGEX expression vector people such as (, on seeing) Ausubel.Fused protein can be at expression in escherichia coli then, and carries out purifying with the glutathione agarose affinity matrix, describes as people such as Ausubel, on seeing.If want, can generate several (as two or three) to each protein and merge, and each fusion injectable is gone in two rabbits at least.Antiserum(antisera) can cause by series of injections, generally comprises at least three booster shots.Usually, detect the ability of antiserum(antisera) immunoprecipitation recombinant protein enzyme polypeptide or its function equivalent, and incoherent protein can serve as the specific contrast of immune response.
Perhaps, can adopt described single-chain antibody production technology (United States Patent (USP) 4,946,778 and 4,704,692) to produce the single-chain antibody of protease inhibitor polypeptide or its function equivalent.Generate and the test kit of screening phage display library can be available from as Pharmacia.
In addition, it is visible as U.S. Patent No. 5,223,409 specifically to be suitable for generating and screen the method and the reagent of antibody display libraries; The open text No.WO 92/18619 of PCT; The open text No.WO 91/17271 of PCT; The open text No.WO 20791 of PCT; The open text No.WO 92/20791 of PCT; The open text No.WO 92/15679 of PCT; The open text No.WO 93/01288 of PCT; The open text No.WO 92/01047 of PCT; The open text No.WO 92/09690 of PCT; The open text No.WO 90/02809 of PCT; People such as Fuchs (1991) Bio/Technology 9:1370-1372; People such as Hay (1992) Hum.Antibod.Hybridomas 3:81-85; People such as Huse (1989) Science 246:1275-1281; People such as Griffiths (1993) EMBO J.12:725-734.
The polyclone of binding proteins specific enzyme polypeptide or its function equivalent and monoclonal antibody can be used for as surveying proteinase gene or its as expression at the function equivalent of other bacterial classifications of Aspergillus.
For example, protease polypeptide can be easy to survey in the conventional determining to Aspergillus cell or extract.The example of suitable detection comprises western blotting, ELISA, radioimmunoassay etc. without limitation.
" specifically in conjunction with " meaning refers to antibody recognition and in conjunction with special antigen, as protease polypeptide, but other irrelevant molecules in basic nonrecognition and the debond sample.
Antibody can be by carrying out purifying as the affinity chromatography method, and wherein polypeptide antigen is fixed on the resin.
Can be with resisting the antibody (as monoclonal antibody) of polypeptide of the present invention to be used for, as affinity chromatography or immunoprecipitation with the standard technique isolated polypeptide.In addition, this antibody can be used for surveying protein (as at cell pyrolysis liquid or cell conditioned medium in night) to estimate the degree of enriching and the pattern of expression of polypeptides.Also can be with antibody as the part of Clinical Laboratory program and diagnostic ground is used for monitoring the protein level of cell or tissue, to determine as given therapeutics or the efficient in the aspergillosis diagnosis.
Can promote to survey by making antibody and detectable material coupling.Detectable examples of substances comprises plurality of enzymes, prothetic group, fluorescent material, luminescent material, bioluminescent material and radio active material.The example of suitable enzyme comprises horseradish peroxidase, alkaline phosphatase, beta-galactosidase enzymes or acetylcholinesterase; The example of suitable fluorescent material comprises Umbelliferone, fluorescein, fluorescein isothiocyanate, rhodamine, dichloro three azine amine (dichlorotriazinylamine) fluoresceins, dansyl chloride or phycoerythrin; The example of luminescent material comprises luminol,3-aminophthalic acid cyclic hydrazide; The example of bioluminescent material comprises luciferase, luciferin and aequorin; The example of suitable radio active material comprises
125I,
131I,
35S or
3H.
The preferred epitope that is comprised by antigenic peptide is positioned at proteinic surf zone, as hydrophilic region.The proteinic hydrophobicity profile of the present invention can be used for identifying hydrophilic region.The proteinic antigenic peptide of the present invention comprises the individual successive amino-acid residue of at least 7 (being preferably 10,15,20 or 30) in the aminoacid sequence of the sequence that is selected from SEQ ID NO:115~SEQ IDNO:171, and comprise proteinic epitope, thereby antibody and this protein of anti-this peptide form specific immunocomplex.
The preferred epitope that is comprised by antigenic peptide is positioned at the zone of proteinic surface protein enzyme, as hydrophilic region, hydrophobic region, α zone, β zone, spiral (coil) zone, corner (turn) zone and movable (flexible) zone.
Immunoassay
To carrying out according to the qualitative of polypeptide of the present invention or quantitatively definite available any method well known in the art in the biological sample.Specific polypeptide level provides special advantage in the biological sample for measuring based on antigenic technology.
Wherein, specific recognition is provided by primary antibody (polyclone or monoclonal), but secondary detection system can be utilized fluorescence, enzyme or other secondary antibodies of puting together.As a result, obtained immunocomplex.
Therefore, the invention provides the method whether certain organism of diagnosis has infected aspergillosis, the method includes the steps of:
● the separating bio product that imitate from this doubtful organism that infects aspergillosis,
● this biological sample and antibody according to the present invention are reacted,
● determine whether to form immunocomplex.
Also available urea and neutral detergent extract tissue is used for western blotting or spot/narrow line mensuration with release protein.This technology also can be applicable to body fluid.
Other methods of expressing based on the detection proteinase gene of antibody comprise immunoassay, as enzyme-linked immunosorbent assay (ELISA) and radioimmunoassay (RIA).For example, can will be used as the probe of immunosorbent and enzyme labelling to the special monoclonal antibody of proteolytic enzyme protease protein matter is surveyed with quantitative.The amount that is present in the amount useable linear regression Calculation machine algorithm reference standard preparation of the protease protein matter in the sample calculates.In another ELISA measures, two different monoclonal antibody specifics can be used for surveying protease protein matter at biological fluid.In this was measured, one of antibody was used as immunosorbent and another probe as enzyme labelling.
Above-mentioned technology can be used as " step " or " two steps " mensuration substantially and carries out." one step " measures and comprises protease protein matter is contacted with fixed antibody, and without washing, mixture is contacted with the antibody of mark." two steps " comprises washing before being determined at and making mixture and the antibody of mark contacts.Other ordinary method also can suitably adopt.Usually a kind of composition that will measure system is fixed on the support, makes other compositions of system to contact with this composition whereby, and is easy to remove from sample.
Suitable enzyme labelling comprises as those from the oxydase group, its by with the generation of substrate reactions catalyzing hydrogen peroxide.The concentration of the hydrogen peroxide that the activity of oxydase mark can form by antibody/substrate reactions of measuring by enzyme labelling is measured.
Outside dezymotizing, other suitable marks comprise radio isotope, as iodine (
125I,
121I), carbon (
14C), sulphur (
35S), tritium (
3H), indium (
112In) and technetium (
99mTc), and fluorescent mark, as fluorescein and rhodamine, and vitamin H.
For example, the check compound combines with the specificity of protease polypeptide and can survey the surface in a hole of the polystyrene microtiter plates in this matrix such as 96-hole by reversibly or irreversibly protease polypeptide being fixed on the matrix external.Immobilized polypeptide or other micromolecular methods are well-known in the art.For example, can be by adding the polypeptide (usually) in solution and cover microtiter plate with protease polypeptide with the concentration of 0.05~1mg/ml, in 1-100 μ l volume to each hole, and in room temperature to 37 ℃ with dull and stereotyped incubation 0.1~36 hour.The polypeptide that is not attached on the flat board can be by removing excessive solution from flat board vibration, then water or damping fluid washing dull and stereotyped (once or repeatedly).Usually, polypeptide is contained in water or the damping fluid.Dull and stereotyped with the damping fluid washing that lacks the bonded polypeptide then.In order to block the free protein binding site on the flat board, use the protein that has nothing to do with the bonded polypeptide to seal flat board.For example, the concentration among the 300 μ l Tris-HCl is that the bovine serum albumin (BSA) of 2mg/ml is suitable.Suitable matrix comprises that those contain the matrix of definite cross-linking chemistry material (as plastics substrate, as available from Corning Costar Corp. (Cambridge, polystyrene MA), vinylbenzene or polypropylene-base).If desired, can be with the pearl particle as matrix, as beaded agarose or beaded agarose gel.
Check compound and can survey by multiple method well known in the art according to combining of polypeptide of the present invention.For example, specific antibody can be used in the immunoassay.If desired, antibody can be carried out mark (as fluorescent substance or use radio isotope) and direct detection (referring to as West and McMahon, J.Cell Biol.74:264,1977).Perhaps, secondary antibodies can be used for surveying (as Fc traget antibody partly) in conjunction with anti--AN97 antibody.In another kind of detection method, protease polypeptide is carried out mark and survey this mark (as by using labelled protein enzyme polypeptides such as radio isotope, fluorophore, chromophoric group).In the another one method, but protease polypeptide is as producing with the fused protein of the protein of optical detection such as egfp (this protein can be surveyed under UV-light).In another method, protease polypeptide can covalently be connected to the enzyme with detectable enzymic activity or merge this enzyme such as horseradish peroxidase, alkaline phosphatase, alpha-galactosidase or glucose oxidase with it.The gene of all these enzymes of encoding is all cloned, and is that those skilled in the art can be easy to obtain and use.If desired, fused protein can comprise antigen, and this antigen can be surveyed and measure with polyclone or monoclonal antibody with ordinary method.Suitable antigen comprises enzyme (as horseradish peroxidase, alkaline phosphatase and alpha-galactosidase) and non-enzyme polypeptide (as serum protein such as BSA and sphaeroprotein and milk protein matter such as casein).
Epitope, antigen and immunogen
In yet another aspect, the invention provides peptide or polypeptide, this peptide or polypeptide comprise the part that polypeptide of the present invention has epitope.The epitope of this polypeptide portion is the immunogenicity or the antigenicity epitope of polypeptide of the present invention." immunogenicity epitope " is defined as the proteinic part that can cause antibody response when whole protein is immunogen.It is believed that these immunogenicity epitopes are limited on a few locations of molecule.On the other hand, a zone definitions on the combinative protein molecule of antibody is " an antigenicity epitope ".The number of immunogenicity epitope is usually less than the number of antigenicity epitope in the protein.Referring to as Geysen, people such as H.M., Proc.Natl.Acad.Sci.USA 81:3998-4002 (1984).
As for the selection of peptide with antigenicity epitope or polypeptide (promptly containing the combinative protein molecule of antibody zone), well-known in the art be the short relatively synthetic peptide of simulated albumin matter sequence part can cause usually with by the antiserum(antisera) of the proteins react of partial simulation.Referring to as Sutcliffe, people such as J.G., Science 219:660-666 (1984).The polypeptide that can cause proteins react serum is described as proteinic primary sequence usually, can carry out characterization by one group of simple chemical principle, and the immundominance zone (being the immunogenicity epitope) that both had been not restricted to whole protein also is not restricted to amino or C-terminal.Extremely hydrophobic have 6 or still less the peptide of residue is invalid when inducing and simulateding the antibody of protein bound usually with those; Long soluble peptide, especially those peptides that contain proline residue are effective usually.People such as Sutcliffe are on seeing.For example, according to 18 in 20 peptides of these guides design antibody of having induced with HAI protein or intact virus reaction, this peptide contains 75% 8-39 the residue that has covered influenza virus (influenza virus) hemagglutinin HAI polypeptide chain sequence; Induced precipitated phase to answer proteinic antibody from 12/12 peptide of MuLV polysaccharase with from 18/18 of rabies glycoproteins.
Therefore the peptide of the present invention and the polypeptide of the present invention that have the antigenicity epitope can be used for causing the antibody of specificity in conjunction with polypeptide of the present invention, comprise monoclonal antibody.Thereby, by merging the antibody of secretion and activated protein qualitative response usually of high per-cent part in the hybridoma that obtains with having splenocyte that peptide that antigenicity has an epitope carries out the donor of immunization.See people such as going up Sutcliffe, described at 663 pages.Have the antibody that peptide or polypeptide by the antigenicity epitope cause and can be used for surveying the protein that simulated, and can be used for following the trail of the destiny in a plurality of zones of protein precursor at the antibody of different peptides, this protein precursor has experienced the translation post-treatment.The antibody of peptide and anti-peptide can be used for multiplely qualitatively or quantitatively determining that institute's mimic protein carries out, competition assay for example, even this be because shown small peptide (9 amino acid according to appointment) also can be in immune precipitation determination combination and substitute long peptide.Referring to as Wilson, people such as I.A., Cell 37:767-778 is 777 pages (1984).The antibody of anti-peptide of the present invention also can be used for purifying institute mimic protein, for example adsorption chromatography by carrying out with method well-known in the art.
According to the design of above-mentioned guide have antigenicity epitope peptide of the present invention and polypeptide preferably contains at least 7, more preferably at least 9 and 15~about 30 amino acid whose sequences most preferably from about, this sequence is contained in the amino acid sequence of polypeptide of the present invention.Yet, comprise polypeptide of the present invention the major part aminoacid sequence, contain have an appointment 30~about 50 amino acid or any length and also be considered to have epitope peptide of the present invention and polypeptide until the polypeptide that reaches the whole aminoacid sequences that comprise polypeptide of the present invention, and also can be used for inducing antibody with institute's mimic proteins react.Preferably, select to have the aminoacid sequence of peptide of epitope to be provided at the basic solvability (promptly this sequence comprises hydrophilic relatively residue and preferably avoids highly hydrophobic sequence) in the water solvent; And the sequence that contains proline residue is preferred especially.
Peptide of the present invention and polypeptide with epitope can be produced by the ordinary method of any preparation peptide or polypeptide, and this method comprises the recombination method that utilizes nucleic acid molecule of the present invention.For example, short aminoacid sequence with epitope and long polypeptide fusion should can be served as carrier by long polypeptide, and be used to produce the antibody of anti-peptide in the immunization process in recombinant production and purge process.
Peptide with epitope also currently known methods of available chemosynthesis synthesizes.For example, Houghten has described the simple method of synthetic many peptides, as the peptide of 248 of 10-20mg 13 different residues, this peptide has been represented the segmental monamino acid variant of HAI polypeptide, can be less than in 4 week preparation and characterize (by the ELISA-type in conjunction with research).Houghten,R.A.,Proc.Natl.Acad.Sci.USA?82:5131-5135(1985)。Should " simultaneously a plurality of polypeptide synthetic (Simultaneous MultiplePeptide Synthesis (SMPS) " method be further described in people's such as Houghten (1986) the U.S. Patent No. 4,631,211.In this program, but the independent resin of the multiple peptide of solid phase synthesis be contained in the independent bag with solvent perviousness, thereby make the suitableeest use of realization of the many identical repeating step that comprises in the solid phase method.
Manual program can be carried out 500-1000 or more synthetic simultaneously.People such as Houghten are on seeing, at 5134 pages.
Having epitope peptide of the present invention and polypeptide can be used for inducing antibody according to method well-known in the art.Referring to as people such as Sutcliffe, on seeing; People such as Wilson are on seeing; Chow, people such as M., Proc.Natl.Acad.Sci.USA 82:910-914; And Bittle, people such as F.J., J.Gen.Virol.66:2347-2354 (1985).
Usually, available free peptide carries out immunization to animal; Yet tiring of anti-peptide antibody can be strengthened by making peptide and macromolecular carrier coupling, as keyhole limpet hemocyanin (KLH) or Toxoid,tetanus.For example, the peptide that contains halfcystine can use linker as suitable divinyl imide benzene-N-hydroxy-succinamide ester (MBS) and carrier coupling, and other peptide can be used more generally linking agent such as glutaraldehyde and carrier coupling.
Animal such as rabbit, rat and mouse carry out immunization with free or carrier link coupled peptide, as contain the emulsion of have an appointment 100 μ g peptides or carrier protein and freund's adjuvant by intraperitoneal and/or intradermal injection.Need carry out the reinforcement several times in for example about 2 week at interval and inject to provide the useful of anti-peptide antibody to tire, this antibody can be surveyed by measuring with the free peptide that is adsorbed onto solid surface as ELISA.Tiring of anti-peptide antibody from the animal serum of immunization can increase by the selection of antagonism peptide antibody, as by peptide is adsorbed onto on the solid support, and according to the selected antibody of method wash-out well-known in the art.
Of the present invention have the peptide that immunogenicity has an epitope and identify that according to method well known in the art this peptide is that proteinic those can cause the part of antibody response when complete protein is immunogen.For example, people such as Geysen, 1984, the program of synthesizing hundreds of peptides on solid support is fast simultaneously disclosed on seeing, this peptide has the enough purity in the enzyme-linked immunosorbent assay reaction.Synthetic peptide and antibody are not surveyed its interaction from the support removal then.In this mode, the peptide with desired protein immunogenicity epitope can be identified by those skilled in the art routinely.For example, the important epitope of immunology is located with 7 amino acid whose tolerance range by people such as Geysen in the envelope protein of foot and mouth disease virus (foot-and-mouth virus), this is that by synthetic all 208 six possible peptides overlapping group realizes that this overlapping group has covered whole 213 aminoacid sequences of the present invention.
Further, the U.S. Patent No. 5 of Geysen (1990), 194,392 have described and have surveyed or the general method of definite monomer (amino acid or other compounds) sequence, and this monomer is the homeomorphic thing with its paratope of spy (antigen binding site) complementary epitope (i.e. " mimotope ") of target antibody.More generally, the U.S. Patent No. 4,433,092 of Geysen (1989) has been described and has been surveyed or the method for definite sequence monomer, and this monomer is the topological diagram Equivalent with the ligand-binding site point complementary part of specific objective acceptor.Similarly, Houghten, R.A. wait people's (1996) U.S. Patent No. 5 about the alkylating oligo peptide of mistake, 480,971 disclose group and the library that linear C1-C7-alkyl is crossed alkylating oligopeptides and this peptide, and utilize this oligopeptides group and library to determine that preferred and target recipient molecule bonded crosses the method for the sequence of alkylating oligopeptides.Thereby the present invention has the conventional preparation of also available these methods of non-peptide analogs of the peptide of epitope.
The removal of protease activity or minimizing
The present invention also relates to produce the method for the mutant cell of parental cell, this method comprises destroys or nucleotide sequence or its control sequence of disappearance proteins encoded enzyme the proteolytic enzyme that the production that causes like this is few than parental cell.
Having modification and the inactivation that the structure of strain of the protease activity of minimizing can be routinely expresses necessary nucleotide sequence by the pair cell endoprotease activity realizes.Modify or the nucleotide sequence of inactivation to can be as coding be the crucial proteolytic enzyme or the nucleotide sequence of its part for the display protein enzymic activity, perhaps nucleotide sequence for having regulatory function, it is that proteolytic enzyme is expressed necessary from the encoding sequence of nucleotide sequence.The example of a kind of like this adjusting or control sequence can be promoter sequence or its funtion part, promptly is enough to influence the part that proteolytic enzyme is expressed.Other control sequences that may modify are including, but not limited to leader sequence, polyadenylation sequence, propeptide sequence, signal sequence and termination site.
The modification of nucleotide sequence or inactivation can be finished by the cell that pair cell carries out mutagenesis and selects proteolytic enzyme throughput wherein to reduce or eliminate.Specific or mutagenesis at random can by as use the suitable oligonucleotide of suitable physics or chemical mutagen, use or dna sequence dna carried out the mutagenesis that PCR generates finish.In addition, mutagenesis can be carried out with any combination of these mutagenic compound.Be suitable for the physics of this purpose or the example of chemical mutagen and comprise ultraviolet ray (UV) irradiation, azanol, N-methyl-N '-nitro-N-nitrosoguanidine (MNNG), o-methyl hydroxylamine, nitrous acid, ethylmethane sulfonate (EMS), sodium bisulfite, formic acid and nucleotide analog.When using these medicament medicaments, the mutagenesis generally cell by under suitable condition will mutagenesis when selected mutagenic compound exist is carried out incubation and is carried out, and select to show reduce or do not have a cell that protease activity is expressed.
The modification of proteolytic enzyme production of the present invention or inactivation can be by introducing, substitute or remove one or more Nucleotide and carry out in the nucleotide sequence of transcribing or translate necessary regulatory element at proteins encoded enzyme or its.For example, Nucleotide can be inserted or removes, thereby cause the introducing of terminator codon, the removal of initiator codon or the change of open reading-frame (ORF).This modification or inactivation can be realized by the mutagenesis that site-directed mutagenesis or PCR generate according to method well known in the art.
Can carry out in vivo although modify in principle, promptly direct on the cell of expressing the nucleotide sequence that will modify, the face that is preferably as follows is modified external with demonstrating.
The example of being produced by the selection inactivation or the minimizing of host cell that makes things convenient for approach interrupts based on gene substitution or gene.For example, in the gene interrupt method, will be corresponding to native gene or the segmental nucleotide sequence of target gene at vitro mutagenesis to produce the nucleotide sequence of defective, then this nucleotide sequence is transformed into host cell to produce the gene of defective.By homologous recombination, the defective type nucleotide sequence has substituted native gene or gene fragment.Defective gene or gene fragment be also coded markings preferably, and this mark can be used for selecting transformant, and the gene of proteins encoded enzyme is modified or destroyed in this transformant.
Perhaps, the modification of the nucleotide sequence of code book invention proteolytic enzyme or inactivation can be used with protease-encoding sequence complementary nucleotide sequence by the antisense technology of having established and carry out.More specifically, the proteolytic enzyme production of cell can reduce or eliminate by the nucleotide sequence of introducing with the nucleic acid array complementation of proteins encoded enzyme, and this nucleotide sequence can be transcribed in cell and can be hybridized with the proteolytic enzyme mRNA that produces in the cell.The complementary antisense base sequences can with the condition of proteolytic enzyme mRNA hybridization under, the amount of the proteolytic enzyme of translation has has then reduced or eliminated.
Preferably the cell that will modify according to method of the present invention derives from microorganism, as is suitable for the fungi strain that the desired protein product is produced, and this protein pair cell is a homologous or allogenic.
The invention further relates to the mutant cell of parental cell, this cell comprises the destruction or the disappearance of the nucleotide sequence of proteins encoded enzyme or its control sequence, the proteolytic enzyme that the mutant cell production that causes like this is few than parental cell.
The proteolytic enzyme defective mutant cell of Xing Chenging is used in particular for expressing the host cell of homology and/or heterologous polypeptide like this.Therefore, the invention further relates to the method for production homology or heterologous polypeptide, this method comprises (a) and cultivate mutant cell under the condition that helps polypeptide production; (b) reclaim polypeptide.Term " heterologous polypeptide " is defined as herein for host cell and is the polypeptide of non-natural, has modified therein and changed the natural protein of native sequences or its and express by recombinant DNA technology the operation of host cell has been changed the natural protein that quantity changes under existing situation.
The method that the present invention produces the product do not contain proteolytic enzyme substantially has special importance, particularly Fungal Protein such as enzyme to the production of eucaryon polypeptide.The protease-deficient cell also can be used for being expressed in and has heterologous protein importance or that have pharmacy importance in the foodstuffs industry.
The purposes of proteolytic enzyme in commercial run
The present invention also relates to proteolytic enzyme according to the present invention in the industry of many selections and the purposes in the pharmacy procedure.Although obtained long term experience in these processes, proteolytic enzyme according to the present invention is compared with the enzyme of present use has many significant advantages.Depend on specific application, these advantages can comprise as lower production cost, higher substrate specificity, lower antigenicity, lower adverse side effect, when in suitable microorganism, producing higher output, more suitable pH and temperature range, better end product taste and food grade and suitable aspect etc. the aspect.
In the large-scale industrial application of food or fodder production, proteolytic ferment is generally used for improving following aspect, as the minimizing of the factor of protein solubility, extract output, viscosity or taste, quality, nutritive value, antigenicity or unfavorable nutrition, color or functional and processing aspect such as the raw-material filterability of protein.In these are used, the protein starting material can be the animal or plant source, and example comprises plant protein such as soy-protein, wheat gluten, rapeseed protein, pea protein, alfalfa matter, sunflower protein, broad bean shape soybean protein matter, cotton or til seed protein, corn protein, barley protein, sorghum gluten matter, potato protein, rice protein, coffee protein and be derived from the protein of animal such as milk protein matter (as casein, whey protein), egg white, fish protein, meat protein comprises gelatin, collagen protein, hematoglobin protein (as oxyphorase), hair, the feather and the flesh of fish.
According to an importance of proteolytic enzyme of the present invention is that they have covered and are ideally suited whole just when scope in the pH of multiple application and temperature.The danger that benefit from for example many large scale process 50 degrees centigrade or higher high relatively processing temperature infect with controlling microbial.Several proteolytic enzyme according to the present invention meet this needs, but they do not show thermostability extremely simultaneously, thereby they can stand the trial that extra heat treatment makes enzyme deactivation.The characteristic in back makes the proteolytic activity of the production approach noresidue that obtains end product.Similarly, many feeds and foods prods have slightly acidic pH value, thereby for their processing, acid or be preferred near the proteolytic enzyme of pH neutral.Also meet these needs according to proteolytic enzyme of the present invention.
The specificity of endo-protease defines according to the preferred cutting of the key between the amino group of the residue of the carboxyl of the amino-acid residue of position P1 and position P1 ' respectively usually.This preferred property can be mainly is condition with P1 (as residue positively charged in the trypsinase substrate), P1 ' (as by the hydrophobic residue in the thermophilic sporeformer proteolytic enzyme cutting) or P1 and P2 (as by the specificity cutting of adrenal medulla endo-protease between two positively charged residues).In some cases, farther residue can determine to cut preferred property, as P2 for the suis PEPA A.More known residues are to being cut with negatively influencing; It is well-known that to be proline(Pro) have resistance at the key of position P1 ' for the effect of many proteolytic enzyme.Most of endo-proteases preferably cut at hydrophobic environment or near electronegative residue.For example, industrial obtainable endo-protease such as Quimotrase (from ox pancreas, obtaining) or subtilisin, neutral metal proteolytic enzyme or thermophilic sporeformer proteolytic enzyme (all from the bacillus bacterial classification, obtaining) tend to preference hydrophobic amino acid as-Phe ,-Leu and-Tyr " afterwards " cutting.Other industrial obtainable endo-proteases for preferably-Arg and-Lys after the trypsin of cutting from ox pancreas, obtain) and the preferred papoid (complex mixture of plurality of enzymes comprises the proteolytic enzyme that obtains from papaya) that after-Arg, cuts.On the contrary, the peptide bond that is formed by little residue such as Ala, Gly, Ser, Thre and Ile and Pro is weak substrate (Keil, people such as B; Protein Seq Data Anal (1993) 5:401-407).This state reaches for pharmacy, food and drink, agricultural even chemical industry all has deep meaning.Proteolytic enzyme according to the present invention has been showed the preferred property of uncommon cutting.
Exopeptidase is only acting near the polypeptide chain end.Those effects at free N-end have discharged single amino acids residue (so-called aminopeptidase) or dipeptides or tripeptides (so-called dipeptidyl peptidase and three peptidyl peptases).Those effects at free C-end have discharged single residue (so-called carboxypeptidase) or dipeptides (so-called peptidyl dipeptidase).Carboxypeptidase is divided into 3 groups on the basis of its catalyst mechanism, i.e. serine-type carboxypeptidase, metallocarboxypeptidase and halfcystine type carboxypeptidase.Other exopeptidase is specific (a so-called pepx) or can cut peptide bond (so-called ω peptase) except that those α-carboxyls or alpha-amino group group for dipeptides.Pyroglutamyl peptidase (pyroglutamyl-peptidase) and acyl amino acyl group peptase (acylaminoacyl-peptidase) (, being respectively gene 18 and 45) that the example of this new ω peptase is as identifies in the present invention referring to table 1.
The general example of industrial application comprises the processing to the material of plant or animal-origin, and this application-dependent is in the use of pure endo-protease, and proteolytic enzyme expection according to the present invention therein can be brought into play high performance.These procedure of processings can be at the modification of large quantities of features of the protein component of starting material or (part) purifying.For example, but these procedure of processing specific aims make solvability, filterability, separability, proteins extraction output and the digestibility maximization of product, and toxicity, unfavorable taste and viscosity are minimized.In addition, this processing also can change (or partially purified) proteinic physicochemical characteristic of starting material or purifying.These advantages not only are being suitable for as the processing assistance application endo-protease of the present invention in industry the time, and also are suitable for when being applied in the animal-feed as the organized enzyme composition.Can be applied in the bread industry as bread additive specifically according to endo-protease of the present invention, as postponing the viscosity of the aging of bread or minimizing dough/pasta.Perhaps endo-protease can be used in beer and the wine industry to prevent or unwanted protein wadding is minimized.Perhaps, it can be used in the brewing industry so that the protein extract output optimization of the cereal of preparation wort.In addition, it also can be used as the milk peptizer with fabulous feature and is advantageously used in the diary industry, perhaps makes the quality of multiple milk composition form (texturishing), foaming or sedimentation (setting) feature optimization.Another application in diary industry is that new proteolytic enzyme is in cheese (Enzyme Modified Cheeses) (EMC) the purposes of preparation through enzyme modification.
In addition, can be with multiple proteins substrate handling to obtain the hydrolysate of medical science or non-medical applications with common and other proteolytic ferments combinations according to endo-protease according to the present invention.Endo-protease according to the present invention herein is effective surprisingly in the complete hydrolysis that obtains protein substrate, even the part of protease resistant is complete hydrolysis also, endo-protease also makes the allergenicity of final hydrolysate minimize or effectively suppress the formation of unfavorable taste surprisingly.
More specifically, endo-protease according to the present invention is characterised in that its preferred property in unusual peptide bond scinderin matter, especially as p1 amino acid residue A la, Gly, Ser and Thr, or residue Ile and Pro (Keil, people such as B when P1 or P1 ' position; ProteinSeq Data Anal (1993) 5:401-407).As a result, those have the component of the protein parent material of resistance to dissolve and hydrolysis with endo-protease according to the present invention to hydrolysis with the endo-protease of prior art the time.The non-limitative example of this protease resistant component comprises collagen protein, gelatin and the specific milk composition in the material of so-called extensin in the vegetable material and animal-origin.
Contain trypsin inhibitor in multiple feed such as the soybean.These protein suppress tryptic activity in as the GI-road of pig and poultry.This trypsin inhibition activity causes suboptimal protein digestion in these animals, thereby the refuse that causes increasing produces and poor economical effectiveness.This problem can be partly by solving the high bake soybean.Two kinds of dissimilar trypsin inhibitors in soybean, have been identified, i.e. Bowman-Birk type trypsin inhibitor and Kunitz type trypsin inhibitor.
The present invention provides now for the selectable approach by baking degraded trypsin inhibitor activity, be it provide can near the L-Cysteine HCL Anhydrous (EC 3.4.22, table 1) of the peptide bond place cutting between the leucine 176-aspartic acid 177 of the C-terminal of Kunitz type trypsin inhibitor (such as by Wilson (1988) at CRC CriticalReviews in Biotechnology 8 (3): among the 197-216 summary).This causes the inactivation of this trypsin inhibitor in the soybean.Find surprisingly to satisfy these standards better than the similar enzyme that is derived from other biological by fungi aspergillus niger excretory L-Cysteine HCL Anhydrous.
Proteolytic enzyme also is widely used in the cheese preparation field.In the production of cheese, essential is cheese milk to be solidified so that can separate cheese material such as casein from whey.Several milk Thrombin coagulases, be also referred to as setting accelerator and obtained describing, and comprise (ox) rennin, ox stomach en-, porcine pepsin and microbial enzyme such as Rhizomucor miehei proteolytic enzyme, Rhizomucor pusillus proteolytic enzyme and Cryptonectria parasitica proteolytic enzyme.Rennin can obtain from the ox stomach, but also can pass through as Kluyveromyces lactis (Kluyveromyces lactis) through microorganisms producing.All these enzymes are characterised in that the specificity that has the key of the peptide bond between residue in κ-casein 105 (phenylalanine) and the residue 106 (methionine(Met)) or close this peptide bond.This means that κ-casein is cut open at side-κ-casein and the contact that is called big peptide (glycomacropeptide) big peptide half point (GMP) of sugar that has negative charge by adopt these enzymes in the cheese preparation.When this took place, big peptide was diffused in the whey, and its deliquescent stabilization to casein micelles has been lost, and in case enough κ-caseins obtain hydrolysis, casein micelles promptly begins to solidify.Details for further milk enzymatic coagulation sees that (as D.G.Dalgleish, AdvancedDairy Chemistry volume 1 is seized Elsevier, London, 1992 by the P.F.Fox volume.
Current available setting accelerator makes it possible to obtain the cheese of suitable high yield, yet, will be appreciated that cheese owing to the large volume of producing, the output that the magnitude with 10 increases can constitute basic economical advantage.Subsequently, for setting accelerator huge demand is arranged in this area with (even faint) improved output.
Setting accelerator is characterised in that the substrate specificity that it is high, yet this specificity depends on pH and temperature.In general cheese production process, pH will only become low pH value in the 4.5-5.5 scope from initial pH 6.3, and final value depends on condition used in the cheese production process.Some setting accelerator change more responsive than other for pH.For example Rhizomucorpusillus proteolytic enzyme changes responsive more than rennin for pH.Except that pH, other parameter such as temperature and water-content also can influence the proteolytic enzyme specificity.Well-known most of setting accelerator shows the substrate specificity that changes with the pH that changes, thereby causes producing the proteolytic activity that change latter stage at cheese.Same well-known setting accelerator is variant on the proteoclastic degree of casein; Also show difference in the model peptide that they produce in the proteolysis process.These are the correlative factors in the cheese ripening process, and can influence character such as taste, local flavor and the quality of cheese.In some cases, setting accelerator has caused the formation of detrimental action such as bitter peptides or unfavorable taste.In addition, the variation in the proteolysis specificity can cause the minimizing of output.Well-known a kind of composition stomach en-is an example of proteolytic enzyme in many ox milk-coagulating enzyme preparations, and this proteolytic enzyme is compared with pure rennin and produced lower output and taste effect.In producing new improved cheese quality and taste, still need setting accelerator.This new setting accelerator causes aging relevant taste and the quality characteristics of fast development and cheese, in having provided basic economic interests.
Well-known total free aminoacids is extremely important in taste and local flavor generation.Especially amino acid leucine, phenylalanine, methionine(Met) and Xie Ansuan play an important role in general cheese taste and flavor compound.This total free aminoacids is converted to the actual generation local flavor and compound such as methanediol, dimethyl disulfide, methylpropanoic acid and the methylpropanal of taste by the microbial fermentation that adds in the cheese manufacturing processed.Exopeptidase plays an important role in the generation of total free aminoacids.Yet they are only worked as and have suitable specific endo-protease combination just effectively.Outward-and the appropriate combination of interior-peptase can be used in the cheese preparation, have new and cheese product improved taste characteristics thereby produce.
Enzyme according to the present invention can be used for the protein material in hydrolysis of animal source, as the mixture of full-fat milk, skimming milk, casein, whey protein or casein and whey protein.The mixture of this casein and whey protein can be as similarly ratio is suitable in the human milk.In addition, enzyme mixture according to the present invention can be used for the protein material in hydrolyzing plant source, as barley or other cereals that is used to make beer, soymilk, its enriched material or isolate, corn protein, its enriched material or isolate and rice protein wheat gluten, germination or that do not germinate.
In the field of large-scale industry process, some application only depend on endo-protease, and in other application, the combination of endo-protease and circumscribed proteolytic enzyme is crucial.Depend on general example that simple endo-protease is used and that can bring into play fabulous performance according to proteolytic enzyme of the present invention therein and comprise application as soybean or pea or grain protein processing, this application minimizes viscosity or makes foaminess or other physicochemical characteristic optimizations, bread additive in the bread industry minimizes the viscosity of dough/pasta, the auxiliary extraction output optimization that prevents the protein wadding or make cereal of processing in beer and the wine industry, fodder additives in the biological industry strengthens the microorganism active in intestinal absorption or the adjusting intestines, and the processing in the diary industry is assisted and made solidifying of multiple milk composition, foaming or settling characteristics optimization.In addition, the protein that is derived from milk or soybean or collagen protein is handled to produce so-called protein hydrolyzate with proteolytic enzyme.Although the main outlet of these protein hydrolyzates is baby preparation and the food that is used for the hospitalier, the product that is intended to supply the personnel such as the sportsmen of non-needs of medical treatment or carry out the people of slimming has formed a section that increases fast.In all these are used, protein hydrolyzate provides attracting advantage, as the allergenicity that reduces, the picked-up of promoted gi tract, amino acid needed less chemical depletion as glutamine and halfcystine, at last, during Long-term Storage, there is not protein precipitation in the acidic drinks.If hydrolysate with two and the mixture of tripeptides provide, be all these advantages capable of being combined so.Yet all commercial hydrolysates of buying are all produced by making up several endo-proteases at present.Back one method means proteinic non-homogeneous and incomplete degraded.Required two in order to obtain-and three peptide mixts, comprise multiple two-and the hydrolytic process of the combination of three peptidyl peptases are ideal.Unfortunately, having only minority is known from these enzymes of food grade and industrial acceptable microorganism, and it is obtainable to say nothing of industry.According to the present invention, several height useful two-be can obtain economically with three peptidyl peptases with relative pure state.Preferred those to the substrate that will cut show low optionally two-or three peptidyl peptases, only show that promptly minimum amino-acid residue cuts preferred property.Two of the naturally occurring peptide bond of the preferred high per-cent of those hydrolysis-or the combination of three peptidyl peptases.Although naturally occurring peptide bond is had high activity, to total hydrolysis of total free aminoacids by two-and the characteristic of three peptidyl peptases prevent.Same preferred those optimal activities are at pH 4~8 and show two of enough temperature stabilities-or three peptidyl peptases.Enough temperature stabilities mean and enzyme-to-substrate one are being arised from 50 degrees centigrade of heating after 1 hour, and remaining at least initial hydrolysis is active 40%, preferably at least 60%, more preferably 70~100%.
Although two-or tripeptides or two-and the method for effective production of three peptide mixts be key with availability according to enzyme of the present invention, be generally endo-protease with first enzyme of protein substrate incubation.The endo-protease that preferably has the wide spectrum endopeptidase activity is suitable for this state, as be used for subtilisin (available from the Delvolase of DSM), neutral metal proteolytic enzyme (available from the Neutrase of NOVO) or thermophilic sporeformer proteolytic enzyme (available from the Thermoase of Daiwa Kasei) near neutrallty condition, with stomach en-that is used for acidic conditions or aspergillosis stomach en-(aspergillopepsin) (as the SumizymeAP available from Shin Nikon, Japan).The purpose of first digestion is the heat sink feature of falling of improving solvability, reducing viscosity and minimizing water/protein mixture.In addition, with this pre-treatment of endonuclease enough two for forming-and the initiation site of three peptidyl peptases and quicken two whereby-or the tripeptides forming process be crucial.Selectively, the proteolytic enzyme that makes hydrolysate debitterize flavor with two-or three peptidyl peptases be included in this stage of process or thereafter.
The main purpose of follow-up hydrolysis is the allergenicity of product is minimized or to promote the gi tract picked-up.In the production of this hydrolysate, use two peptidyls-and three peptidyls-peptase have special importance, this is because it provides the effective way of producing hydrolysate.
The place one's entire reliance upon combination of one or more endo-proteases and one or more circumscribed proteolytic enzyme of other application in food and fodder industry.The combination of this endo-protease and circumscribed proteolytic enzyme generally is used for industry to improve as the taste of end product and the aspect of color.It is former because the generation of taste and color mainly depends on the existence of total free aminoacids.Total free aminoacids not only can obtain by circumscribed proteolytic enzyme such as carboxypeptidase and aminopeptidase, and can obtain by peptidyl dipeptidase.If with endo-protease or even two peptidyls-or three peptidyls-peptase combination, carboxypeptidase, aminopeptidase and peptidyl-pepx can generate a large amount of total free aminoacidss in the short period of time so.Yet, in all these processes, should avoid amino acid or even uncontrolled release of non-protein component so that adverse side effect minimize.
Although total free aminoacids can cause many sense of taste equally, these sense of taste are very basic (bitter, sweet, sour and " delicious (umami) "), and feel that the necessary amino acid concentration of these tastes is very high.Although these high threshold values are arranged, total free aminoacids can form main sensation by many local flavor mechanism and enhancement mechanism in low-down concentration range.One of these mechanism comprise total free aminoacids and draw combination in the reaction (Maillard reaction) with sugar in so-called U.S.A.Compare with total free aminoacids, utilize these U.S.As to draw product, can be than the total free aminoacids of record low several magnitude threshold value and develop and inundatory complicated local flavor and aroma system.U.S.A draws product usually in the culinary art of preparation food or feed product, form in the temperature that raises in curing and toasting.In handling, these have produced color and large quantities of fragrance simultaneously.In these reactions, amino group and reducing compound reaction are as the first step and finally cause whole group reaction approach.In food or feed, the aminocompound that comprises mainly is a total free aminoacids, and this amino acid discharges from the protein starting material with the multiple protein enzyme, and required reducing compound mainly refers to reducing sugar.This means in raw-material processing, should avoid the improper release of total free aminoacids and sugar so that unfavorable taste minimizes, and this unfavorable taste can be at subsequently heating steps as generating in jet drying and sterilization.The idea in back has been emphasized once more according to the higher degree of enzyme of the present invention and the benefit of low use cost.
Except that reaction is drawn by U.S.A, also can in envrionment temperature, carry out important chemical transformation to amino acid.The conversion of back one type is that enzyme is dependent, and quite general in the food of fermentation, as beer, cultured milk, cheese ripening and meat and grape wine ripening process.In these fermenting processs, total free aminoacids discharges from used starting material by the proteolytic enzyme that adds or by the hydrolase of proteolysis from used starting material or microorganism introduction.In the ripening stage, the metabolic activity of microorganism changes total free aminoacids in the derivative of the sensory quality with increase.For example, L-leucine, L-Isoleucine and L-Xie Ansuan cause valuable fusel such as amylalcohol and isopropylcarbinol (isobutanol) in beer fermentation.Similar cheese volatile matter such as thiomethyl alcohol and dimethyl disulfide can be traced back to the generation of methionine(Met) in the cheese and methylpropanoic acid and methylpropanal can trace back to Xie Ansuan.Last free amine group glutamatic acid can form strong taste enhancement because the degradation production of itself and RNA is the synergy of so-called 5 '-ribonucleotide.If with 5 '-ribonucleotide as the combination of the proper concn of 5 '-IMP and 5 '-GMP, the detection threshold of the delicious taste that is generated by L-glutamic acid is known to reduce by two orders of magnitude.
In order in all these processes, to obtain clear and definite and accurate taste effect, protein substrate should with interior-and the combination of circumscribed proteolytic enzyme come hydrolysis, wherein and circumscribed proteolytic enzyme at least a, in preferred-and circumscribed proteolytic enzyme both be pure, and preferred selective or preferably discharge preferred amino acids for the amino acid of particular group.Therefore, preferred proteolytic enzyme is characterised in that the highly selective for the aminoacid sequence that can be cut, and this idea makes the enzyme in the Aspergillus that is known as " maturing enzyme " have special importance.
Except that food and fodder industry, proteolytic enzyme also is widely used in chemistry, pharmacy, diagnosis and personal care (personal care) industry.
In personal care (personal care) industry, proteolytic enzyme is used to form peptide, and this peptide joins in the multiple product to improve the aspect as skin feel, gloss or protection.The new tendency that a kind of direct topical application proteolytic enzyme is arranged in addition.Use closely similar ground with the enzyme in the leather industry, the main purpose of a kind of application in back is cleaning, unhairing and softening skin.
In chemistry and pharmaceutical industry, proteolytic enzyme has developed into the valuable instrument of producing expensive batching or intermediate.In these industry, proteolytic enzyme is not only because its hydrolysis ability but also because it is from the ability of the synthetic peptide of natural or alpha-non-natural amino acid and be employed.A kind of selection in back is clearly by being confirmed based on the possibility of amino acid whose structure piece with endo-protease such as the synthetic aspartame of thermophilic sporeformer proteolytic enzyme from it.
Different with the situation of food and fodder industry, may need uncommon reaction conditions although will realize required chemical conversion, the solid of proteolytic enzyme-also think important advantage with regioselectivity.The general example of proteolytic enzyme in this industrial application comprises the use in producing multiple medicine intermediate such as Regular Insulin, microbiotic, feritin and ACE-inhibitor of endo-protease, aminopeptidase and carboxypeptidase.The summary of this application is provided in IndustrialBiotransformations, A.Liese, K.Seelbach, C.Wandrey, Wiley-VCH; ISBN 3-527-30094-5.
Consider required specificity, solid-and regioselectivity, have no side effect and, provide basic advantage according to the improved performance of proteolytic enzyme of the present invention to the tolerance of unusual reaction conditions such as high solvent strength.
From the angle of pharmacy, the reference of the effect of proteolytic enzyme by a great deal of be illustrated in Martindale " The Extra Pharmacopoeia " (PharmaceuticalPress, London, UK).In addition, the vital role of very special proteolytic enzyme is illustrated by the following fact in regulating various biological procedureses, and promptly many hormones are activation after its precursor molecule is by a kind of so very special proteolytic enzyme processing only.Inhibitor activity for this specific protease of some kind has been contained in the exploitation of various novel drugs.Therefore, new the identifying of proteolytic enzyme with the present available sequence provided herein of effective inhibitors.
Whole disclosures of the document that each is quoted herein all are hereby incorporated by.
Table 1
Embodiment
Embodiment 1
Measure proteolytic activity and specificity
The proteolytic enzyme specificity can be studied with multiple peptide substrates.The synthetic substrate is widely used in screening, survey proteolytic ferment to determine enzyme concn, research specificity and to probe into interaction with inhibitor in fermentation, in separation.Peptide P-N-methyl-p-nitroaniline is preferred for measuring protease activity, and this is because can follow this activity continuously and therefore make it possible to carry out kinetic measurement.The absorption that the cutting of peptide P-N-methyl-p-nitroaniline can be measured at 410nm when discharging the 4-N-methyl-p-nitroaniline increases and follows the tracks of.The p-Nitroaniline substrate is generally used for Serine and L-Cysteine HCL Anhydrous.In addition, used peptide thioesters and 7-amino-p-methylcoumarin peptide derivant.The peptide thioesters is highstrung substrate for Serine and metalloprotease, and it has showed high relatively turnover ratio, and this is because thioester bond is easy to cutting than amido linkage.The available sulfhydryl reagent of the cutting of thioesters is as 4,4-dithio pyrimidine (324nm) or 5, and 5-two sulphur two 2-nitrobenzoic acids (405nm) are followed.With respect to amido linkage, the turnover ratio of identical increase has been observed in the cutting of ester bond usually.The most well-known substrate of measuring the esterase activity of proteolytic enzyme is the p-nitrophenol derivative.The release of p-nitrophenol derivative can be dependent on used pH and monitors at different wavelength, and as having used the wavelength of 340nm in the neutral pH left and right sides time, and when surpassing pH 9, monitoring is carried out about 405nm.In addition, the hydrolysis of ester also can be by following with the volumetry of pH-stat equipment.Esterase activity is being carried out under the situation of quantitative measurment, can use pH susceptibility dyestuff.
Perhaps, can be with peptide attached on the fluorescence leavings group.When at suitable wavelength monitor, proteolysis is followed the increase of fluorescence.Normally used is peptidyl 2-phenyl amide and peptidyl 4-methyl-7-tonka-bean base acid amides.For example the release of 7-amino-4-methylcoumarin is measured with the excitation wavelength of 350nm and the radioactive wave progress row of 460nm.7-amino-4-methylcoumarin use advantage as leavings group for (380nm absorptions) of producing look and fluorescence (400nm excites, and 505nm launches) is arranged.When easily splitting the key both sides amino acid must all be arranged, the group of introducing quench fluorescence is useful.The general feature of this substrate is that peptide sequence separates the fluorescence donor groups with acceptor groups, and this receptor group serves as the Quenching of fluorescence agent.Cutting to the peptide bond between quencher group and the fluorophore will cause the essence of fluorescence to increase.Reported that several D-As are right, comprise that anthranilic acid (Abz) is as donor and 2,4-dinitrophenyl (Dnp) is as acceptor, 5-[(2 ' amino-ethyl)-amino]-naphthene sulfonic acid (EDANS) is as donor and 4-[[4 '-(dimethylamino) phenyl] azo]-phenylformic acid (DABCYL) is as acceptor.D-A is right very easily in the Abz/EDDnp representative, and this is that fluorescence has increased with 7~100 the factor, and the absorption spectrum of EDDnp does not change with pH because after complete hydrolysis.In addition, this peptide sequence can contain and reaches 10 residues and do not lose quenching effect.Along with the size increase of connection peptides, the position of the key that easily splits cannot not become specially.Therefore, except that whether definite hydrolysis takes place, also be essential to the additional analysis of product.This can be by analyzing with HPLC and separating the peptide of being produced and determine that segmental aminoacid sequence carries out.In addition, the peptide of digestion is formed and can directly be analyzed by the HPLC/ analytical technique of mass spectrum of combination.
Have the peptide of definite sequence except using, the synthetic peptide library also can be used for studying the specificity of proteolytic enzyme.Peptide is with at random or semirandom mode solid phase synthesis.Reported the preparation of a protease substrate family as people such as Meldal (PNAS USA 91,3314,1994), this preparation starts from H-Lys (Abz)-resin, with peptide resin is extended to 6 amino acid, and makes Tyr (NO2) and this peptide coupling at last.Each resin bead all has unique sequence, and after with protease treatment, the fluorescing owing to discharging the peptide that contains Tyr (NO2) of susceptible.Sequential analysis to the peptide of susceptible will provide proteolytic enzyme specific information.
Protease activity is usually with unit representation.Usually SI units (IU) are defined as that per minute shifts the required enzyme amount of 1 micromole's substrate under the condition of determining.For proteolytic enzyme, IU can relate to the hydrolysis of 1 micromole's peptide bond in the per minute.Yet under the situation of proteolytic enzyme unit, departing from international definition is rule rather than exception.In the pattern peptide of a key of specificity cutting, the calculating of IU is very simple, for can be in a plurality of positions on multiple degree the proteolytic enzyme of scinderin matter substrate, use many unit definition that depart from.Except that used unit definition, any hydrolysising experiment all needs to describe enough conditions that unit is measured of carrying out.This condition comprises as concentration of substrate, enzyme-substrate ratio, pH and temperature.The general mensuration of determining the proteolytic enzyme given activity comprises protein substrate, as oxyphorase, Regular Insulin or the casein of sex change.Under the fixed condition, digest polypeptide in the interval with proteolytic enzyme at a fixed time.Indigested and big polypeptide is precipitated with TCA, and the TCA soluble product is by measuring 220 or the absorption of 280nm or by with Folin reagent (folin reagent), triketohydrindene hydrate, fluoro-2,4-dinitrobenzene/dansyl chloride, titration soluble peptide or TNBS method or fluorescence are usually determined.After hydrolysis the marked product, also can use the peptide substrate that carries out mark with specific dyestuff or fluorophore such as fluorescein.In addition, the lab analysis instrument of available standards adopts the standard amino acid analytical procedure.For understanding the size distribution of the peptide that generates by proteolytic enzyme, can carry out the gel chromatography experiment.In addition, the better resolving power of the model peptide that is generated by proteolytic enzyme can be by adopting inverse technique HPLC to obtain.The degree of protein substrate hydrolysis is typically expressed as degree of hydrolysis or DH.Under the stable situation of hydrolytic process pH, DH can derive from the alkali consumption (enzymically hydrolyse of food protein (Enzymatic Hydrolysis of FoodProtein) in the hydrolysis, J.Adler-Nissen, 1986, Elsevier Applied SciencePublishers LTD.).DH relates to the multiple useful functional property of hydrolysate, as solvability, emulsifying capacity, foaming and froth stability, vibration expansion, organoleptic quality.In addition, taste is an important aspect of hydrolysate food grade.Bitter taste is a subject matter of protein hydrolyzate.The termination of hydrolysis reaction can wait and carry out by change pH, heat inactivation, denaturing agent such as SDS, acetonitrile.
Standard program according to this area is expressed the polypeptide shown in the table 1, and has carried out the purifying to small part.They are to analyze and find to have activity listed in the table 1 according at least a aforesaid method.
Embodiment 2
Directly determining of the Kcat/Km ratio of protease substrate
The synthetic substrate can be used for monitoring enzymic activity, be used for determining enzyme concn, be used for determining to suppress constant or be used to study substrate specificity in purge process.The Kcat/Km determination of ratio has provided the measurement to substrate specificity.It makes it possible to contrast the hydrolysis rate of enzyme of the same race to the different enzymes of the specificity of different substrates or cutting same substrate.This ratio has second order rate constant unit, so be expressed as 1/ (concentration. the time).The substrate that will have the Kcat/Km ratio of 10.5-10.6M-1.sec-1 scope is considered to extraordinary substrate, promptly has good avidity and fast turnover ratio.Yet some have the Kcat/Km value is very specific at the substrate of 10.4M-1.sec-1 scope.
The Kcat/Km ratio can be calculated after determining independent parameter.In this case, Km and Vm can obtain from multiple linear graph (as Hanes or Cornish-Bowden method) neutralization or by non-linear regression method.Known Vm=kcat.Et (wherein Et is final organized enzyme concentration), kcat=Vm/Et so.When product or substrate inhibition generation, perhaps when substrate precipitates with high concentration, promptly can not carry out the Kcat/Km determination of ratio by preceding method.Yet may be able to obtain the exact value of the Kcat/Km ratio of effect first-order condition under, this condition is for when concentration of substrate during well below the Km of estimation.Under these conditions, Michaelis-Menten equation: v=(Vm.S)/(Km+S) become:
V=(Vm.S)/Km, because S<<Km
Or v=(Vm/Km) .S=kobs.S=-dS/dt
Its quadrature is divided into lnS=-kobs.t+lnSo, and wherein So is an initial substrate concentrations, and the concentration of substrate of S when being preset time.This speed and concentration of substrate are proportional.In other words, to observe with kobs be the single order process of single order rate constant to substrate hydrolysis.Because Vm=kcat.Et, so kobs=Vm/Km=(kcat.Et)/Km.
The successive of substrate hydrolysis record is made it possible to determine kobs with graphic representation at lnS in to the figure of time.When if organized enzyme concentration is known, the Kcat/Km ratio can be inferred from kobs simply:
Kcat/Km=kobs/Et
Measuring method: utilize initial substrate concentrations well below the Km that estimates and low enzyme concn so that can write down the hydrolysis of substrate.You will obtain the first order curve that product generates: after the substrate complete hydrolysis, the absorption of product (or flat fluorescent) will make it possible to accurately determine So, and this is because Pt=So.Kobs maybe can select match software from lnS for use to the slope of the figure of time, and (Enzfitter SigmaPlot...) determines.
NB: do not forget the concentration of substrate (S=So-P) that calculates any preset time from production concentration, this is because can not provide correct kobs (dP/dt=kobs.S is integration in an identical manner) with P to temporal mapping.
Perhaps, people can measure successive t1/2 (transformation period) from producing mirage (apparition) curve, and this is because in the single order process:
So t1/2=ln2/kobs=0.693/kobs is kobs=0.693/t1/2
Utilize this method to make it possible to check that you have correct single order decay (equal value of successive t1/2).
Embodiment 3
Proteinase gene in the inactivation aspergillus
The approach that makes the most convenient of proteinase gene inactivation in the Aspergillus genome is gene substitution technique (being also referred to as " a step gene disruption ").The basis of this technology by RothsteinRJ at Meth.Enzymol.101, p202 describes in 1983.This technology is substantially based on the homologous recombination of dna fragmentation that transforms and fungal cell's genomic dna.By double exchange, the gene of inactivation is the dna fragmentation displacement that (partly) transformed transformant.The dna fragmentation of this conversion preferably contains the selected marker to aspergillus niger.Substantially use general Protocols in Molecular Biology to carry out to the operation of DNA and the generation of inactivation construct.At first, isolation of genomic DNA from the aspergillus niger strain, this DNA is used for the inactivation to proteinase gene subsequently.The genomic dna of aspergillus niger can separate with the method for any description, and as by by people such as Graaff (1988) Curr.Genet.13,315-321 is described and well known to a person skilled in the art method.As template, this template is used for polymerase chain reaction (PCR with this genomic dna; People such as Sambrook, (1989) molecular cloning: laboratory manual (Molecular Cloning:A Laboratory Manual), 2
NdEdition, Cold Spring Harbor Laboratory Press, New York) to the amplification in proteinase gene flank zone.This flank zone refers to want the non-coding region of the proteinase gene upstream and downstream of inactivation herein.Each flank zone length preferably surpasses 1.0kb.
The DNA oligonucleotide of two strands is used to cause pcr amplification to each flank zone.For 5 '-flank zone, the upstream dna sequence dna homology of a primer and this proteinase gene encoding sequence starting point.This homology zone is preferably placed at the translation initiation site upstream and surpasses the 1.0kb place.Second primer be positioned at complementation and the reverse DNA sequence homology of proteinase gene encoding sequence in abutting connection with the upstream.
For 3 '-flank zone, primer be positioned at the dna sequence dna homology of this proteinase gene encoding sequence in abutting connection with the downstream.Second primer be preferably placed at complementation and the reverse DNA sequence homology that proteinase gene encoding sequence downstream surpasses the 1.0kb place.
Be included in all primers and with aspergillus niger genome homologous dna sequence dna length should minimum be 15 Nucleotide, preferred length is 18 Nucleotide.Most convenient ground, all primers should contain the recognition site of suitable restriction enzyme with aspergillus niger genome homologous sequence upstream.These extra recognition sites have promoted clone's process.
Primer and aspergillus niger genomic dna well known to a person skilled in the art that being used for PCR under the condition reacts.The annealing temperature of primer can be from calculating with the part of aspergillus niger genome homologous dna sequence dna.The fragment that will contain 5 '-flank zone and 3 '-flank zone is cloned in the carrier that available general Protocols in Molecular Biology breeds in intestinal bacteria.The gene clone that will can be used as selected marker in the aspergillus niger then is between two flank zones.Most convenient ground under the control of marker gene expression promoter in realizing aspergillus niger, is preferably endogenous Aspergillus niger promoter.The direction of insertion of the marker gene preferably direction with initial proteinase gene is identical.Final inactivation fragment contains 5 '-flank zone, preferred marker gene and the 3 '-flank zone under aspergillus niger endogenesis promoter control, and all are all in this direction and orientation.The dna clone of final construct is gone in the carrier that can breed in intestinal bacteria.
The inactivation construct is digested to remove the escherichia coli vector sequence with suitable restriction enzyme, and the inactivation fragment is separated (people such as Sambrook with standard technique, (1989) molecular cloning: laboratory manual (Molecular Cloning:A LaboratoryManual), 2
NdEdition, Cold Spring Harbor Laboratory Press, New York).At last aspergillus niger is transformed with the fragment of inactivation with the method that is described in the document, as use, the method that 293-299 describes by people (1991) Curr.Genet.20 such as Kusters-van Someren.Cell transformed is selected by transformation mixture is coated on the agar plate, and this flat board has selectivity for the growth of the aspergillus niger strain of presentation markup gene.After the Aspergillus strain that transforms being carried out purifying by replica plating, with southern blotting technique the representative number of bacterial strain is analyzed (people such as Sambrook with standard method, (1989) molecular cloning: laboratory manual (Molecular Cloning:ALaboratory Manual), 2
NdEdition, Cold Spring HarborLaboratory Press, New York).Therefore, the mycelial genomic dna of conversion bacterial strain separates with suitable restriction enzyme and digests.Restriction fragment separates with sepharose, and trace is also surveyed with the marker gene fragment of mark on nitrocellulose filter.Hybridization and washing are under the stringency condition.The bacterial strain of restriction fragment that contains the mark of correct length is thought correct.Utilize this method can select to have the Aspergillus niger strain of inactivating protein enzyme gene.
Embodiment 4
With ion exchange chromatography protein isolate enzyme
As the proteolytic enzyme by nucleotide sequence coded a small amount of that provides herein is to contain the expression plasmid of associated dna sequence, transform aspergillus niger strain and this aspergillus niger strain is grown on the suitable substratum with this plasmid and obtain by structure.After the liquid nutrient medium of having collected the cell that does not contain pollution, can be purified to the desirable proteins enzyme.
For with pure substantially isolated in form by the nucleotide sequence coded proteolytic enzyme that is provided, can defer to several strategies.All these strategies all are described in the relevant scientific literature fully (referring to as protein purification handbook (Protein PurificationHandbook), 18-1131-29 Edition AA is as being published by Amersham PharmaciaBiotech, Uppsala, Sweden).Program applicable to purifying protein enzyme from the mixture of complexity provides hereinafter.Existing selectively suitably for required enzyme feature, mensuration is necessary.For proteolytic enzyme, generally produce the synthetic peptide substrates of look as use as described in the embodiment 1.This peptide substrates is optionally for endo-protease, carboxypeptidase, aminopeptidase or ω peptase.Selectivity for specific three peptidyl peptases has been described in embodiment 11.By in relevant synthetic peptide, selecting correct amino-acid residue, can select to have required specific proteolytic enzyme.
Should determine at first whether proteolytic enzyme is secreted in the substratum, depends on the expression system of described production proteolytic enzyme, this proteolytic enzyme can be secreted maybe and can remain in the cell.If proteolytic enzyme is secreted in the fermention medium, the fragment that produces cell or these cells must be removed by centrifugal or filtration, and the limpid or clarifying substratum of gained is the starting point that is further purified.At those proteolytic enzyme is not in the situation of secretor type, must ruptured cell so that can carry out the purifying of proteolytic enzyme.In this case, the most handy rubbing machine of the cellular material of collection grind, levigate with pearl, handle filtration or centrifugal then with ultrasonic degradation or with French crushing apparatus (French press) or Manton-Gaulin homogenizer.At this proteolytic enzyme is under the hydrophobic or membrane-bound situation, must filter or centrifugal before add nonionic detergent so that the proteolytic enzyme dissolving.
After clarification steps, the purification step that can use three phases is to obtain the agnoprotein enzyme of basic pure state.In this three steps all or part of, it is essential adding stain remover.
At first or acquisition phase, with the target protein enzyme separate, partial purification and concentrating.In intermediate purification phase subsequently, the great majority of large quantities of impurity are removed, and in last refining (polishing) stage, the residual impurity of the trace of a large amount of related substanceses is removed and enzyme is dissolved in the suitable damping fluid.Depend on the characteristic and the physical properties of the proteolytic enzyme that obtains, the mode of revising slightly of the enough different proteins bond materials of those skilled in the art's energy makes this three phases optimization and use these stages under the condition of some change.Yet selectivity assay determination in all cases is indispensable, and this is because it will make it possible to the proteolytic activity of purifying is further carried out the successive monitoring.The assay determination that is applicable to this purpose comprises the use of producing the look peptide substrates as previously mentioned.
Catch in the step at first of purifying, the strong ion exchange resin of anionic type is preferred for clarifying the substratum that contains enzyme with desalination.For guaranteeing combining of desirable proteins hydrolytic activity and resin, hanging down substratum and the resin of having checked 3 or 4 different pH values under the conductivity condition.In these checks, resin is used the damping fluid balance usually, and this damping fluid has pH value and the conductivity identical with containing the enzyme substratum.Then this substratum is applied in the post under the pH condition, this condition has shown the abundant combination of permission resin to proteolytic enzyme, does not promptly have required enzymic activity and can trace back in the substratum that flows through.Enzymic activity is with successive salt gradient wash-out from ion exchange resin subsequently, and this gradient originates in the resin level pad and ends to the damping fluid that has wherein added 1 mol NaCl.To contain required active elutriated fraction according to this mensuration and collect and be ready for use on extra purification step.This extra purification step depends on the purity of required enzyme in the fraction of collection: if almost pure state, extra gel-filtration step will prove that it is for enough; If not almost pure state, using hydrophobic interaction resin chromatography after the gel-filtration step so.
Hydrophobic interaction resin chromatography is that the salts contg by the component that at first will collect from ion exchange resin is increased to 4 mol NaCl and is undertaken by removing any precipitation that forms.If the limpid component of gained does not contain required activity as a result, should activity obviously be present in the precipitation so, and can reclaim with pure substantially state.If the limpid component of gained still shows required activity in mensuration as a result, so equally this liquid is applied in the phenyl dextran resin (Pharmacia), this resin is with having identical pH and conductive high-salt buffer balance.If required enzymic activity is attached on the phenyl dextran resin, then should activity carry out following salt-free washing after the wash-out with the salt gradient that reduces continuously, carry out wash-out with chaotropic agent in case of necessity.As the front, will in mensuration, show the step that the component of active gradient is collected and finally carried out gel-filtration.If required enzymic activity debond phenyl dextran resin, many pollutents will be in conjunction with on them, thereby be present in required enzymic activity in the void volume of post before being applied to gel-filtration column, only need extra ultrafiltration step to obtain the more activity of conc forms.Gel-filtration column has not only been removed the pollutent of trace, and enzyme has been brought into when using subsequently in the necessary damping fluid.
Although this method is applicable to that usually according to the separation of proteolytic enzyme of the present invention and purifying, isolation technique is described in embodiment 4 more specifically.In this embodiment, the separation of Aspergillus proteinase is described as using the fixed bacitracin, promptly a kind of known and interactional peptide antibiotic of broad variety proteolytic enzyme selectivity.
Embodiment 5
With affinity chromatography protein isolate enzyme
The another kind of method affinity chromatography of purify small quantities proteolytic enzyme.In order to obtain the proteolytic enzyme of purified form, 100 milliliters cultures are grown in shaking in the bottle of good ventilation.Centrifugal with except that after any insoluble substance, supernatant is applied in 40 milliliters of usefulness, 0.05 mol sodium acetate Ph, 5.0 equilibrated bacitracin-dextran post.Be incorporated on the post proteolytic enzyme with replenished 1MNaCl and 10% (v/v) Virahol the acetate buffer wash-out (J.Appl.Biochem., 1983pp420-428).Active ingredient is collected, distilled water is dialysed and is applied in 20 milliliters of bacitracins-dextran post, and this post still carries out balance with acetate buffer.As preamble, wash-out carries out with the acetate buffer that has replenished NaCl and Virahol.With active ingredient promptly show required active component collect, to 5 mmoles/liter acetate buffer pH5.0 dialyse and concentrate with Amicon PM-10 membrane ultrafiltration then.In order to obtain the proteolytic enzyme of basic pure state, spissated liquid is carried out chromatography on Superdex 75 posts, this post is with 0.05 mol sodium acetate pH 5.0 balances and replenished the NaCl of 0.5 mol.
With the enzyme of purifying the further experiment susceptible of proof molecular weight that carries out on the PAGE whether with the basis of sequence data on predicted consistent.Last confirmation can obtain by the-terminal amino acid analysis of carrying out part.
Embodiment 6
Character from the new L-Cysteine HCL Anhydrous of aspergillus niger
In the present embodiment, as previously described, aspergillus gene nr28 is cloned and in aspergillus niger, cross and express.The enzyme that obtains is carried out purifying and be used for destroying the trypsin inhibition activity of soybean under multiple condition according to the program of describing among the embodiment 4.Papoid and bromeline have been used as the reference material.Bromeline is available from Sigma, and papoid is available from DSM Food Specialities Business Unit Beverage Ingredients, PO Box 1,2600 MA Delft, Holland.
Trypsinase suppresses according to Kakade, M.L., and Rackis, J.J., McGhee, J.E. and Puski, G. (1974): the method for J.Cereal Chemistry 51:376-382 is measured.Substrate N-benzoyl-L-arginine-p-Nitroaniline is degraded to N-benzoyl-L-arginine and p-Nitroaniline as the measurement to tryptic activity.Trypsinase be obtain from British Drug Houses Ltd and be derived from ox pancreas, in every gram product, contain above 0.54Anson unit.
The Kunitz inhibitor of soybean also obtains from Sigma.
Measuring before trypsinase suppresses, trypsin inhibitor with the concentration of 2mg/ml and above-mentioned L-Cysteine HCL Anhydrous in pH 3 preincubation in the 50mM sodium acetate buffer.The ratio of enzyme with zymoprotein and trypsin inhibitor 1: 100 (w/w) added.Albumin is as the negative contrast of enzyme.Remaining tryptic activity is measured after 3 hours at 37 ℃ of incubations.The results are shown in the table 2.
Many kinds of L-Cysteine HCL Anhydrouss of table 2. are to the effect of the Kunitz trypsin inhibitor enzymatic inactivation of soybean.
1 | 2 | 3 | 4 | 5 |
The enzyme of check | Remaining TI activity (%) | Remaining TI activity (%) after the pepsin | Remaining TI activity (%) after 75 ℃ of thermal treatments | Remaining TI activity (%) after 90 ℃ of thermal treatments |
Papoid | 25 | 55 | 78 | 95 |
Bromeline | 30 | 62 | 86 | 99 |
Aspergillus niger | 26 | 26 | 28 | 35 |
Albumin (contrast) | 100 | 100 | 100 | 100 |
TI: trypsin inhibitor activity
In L-Cysteine HCL Anhydrous and trypsin inhibitor preincubation, when existing, stomach en-repeats experiment.The final concentration of stomach en-with 1.3mg/ml added.The results are shown in row 3.
The experiment of having carried out another series is to check thermostability.Before in the preincubation that L-Cysteine HCL Anhydrous is joined with trypsin inhibitor, with these enzymes incubation 5 minutes in 75 and 90 ℃.The results are shown in row 4 and 5.
These results confirm that significantly these new L-Cysteine HCL Anhydrouss from aspergillus niger more have activity than present available L-Cysteine HCL Anhydrous in the trypsin inhibitor inactivation in making animal-feed.
Embodiment 7
Exopeptidase promotes the maturation of cheese and the taste of cheese
Make the aminopeptidase of encoding according to aforesaid method overexpression in aspergillus niger by gene nr 20 and 54 (referring to table 1).The purifying of these enzymes carries out according to the program of describing among the embodiment 4.The activity of the enzyme sample of purifying determines that in the phosphoric acid water damping fluid (50mM) of pH7.2 the p-nitrophenyl sulfonamide derivatives (3mM) that contains many hydrophobic amino acid residues in this damping fluid is as substrate.Substrate by the conversion of aminopeptidase by monitoring because substrate conversion and have the variation of optical density(OD) to determine at 400nm, wherein use do not contain enzyme solution as a reference.Depend on used substrate, active (A) is calculated as the variation of per minute OD, and is expressed as Phe-AP, Leu-AP or Val-AP unit.With normal cheese milk Delvo-tec
TMThe starter culture of DX 31 scopes (DSM Food Specialities Delft, Holland) is inoculated the cheese with acquisition Gouda type, and realizes with the setting accelerator (every liter of cheese milk 50IMCU) of mean dose.In addition, every kind of circumscribed proteolytic enzyme of 25Phe-unit is joined in two kinds of experiment cheese, and contrast does not contain any circumscribed proteolytic enzyme.The cheese preparation parameter that uses is consistent with the program that half hard cheese of two kinds of cheese is used.Between cheese of testing and contrast cheese, reach such degree record in the difference aspect local flavor and the fragrance generation, promptly the cheese of experiment contains its organoleptic character of great majority after 3 week, and contrast cheese has obtained similar evaluation after 6 week.The level of total free aminoacids is shown as the twice height in the cheese of testing after 3 week; It is suitable that the level of 6 week after ripening becomes again.(Milford MA USA) carries out amino acid analysis according to the Picotag method of Waters.
These data declaration products can shift to an earlier date the keeping quality of selling in 3 months and not reducing cheese.The degree of the organ sensation feature of experiment cheese and contrast difference also is to contrast the cheese part omitted and tends to the former cheese taste of bitter taste and be overcome in having the experiment cheese of aminopeptidase.Equally, the quality of also finding cheese is more lubricated on some degree.
Embodiment 8
New specificity by gene 55 encoded protein enzymes
As explained before, some protein is formed as specific amino acid or specific tertiary structure and can tolerate enzymically hydrolyse.In this case, the new specific proteolytic enzyme of available displaying improves the amount of dissolved peptide from protease-resistant protein matter significantly.
Beta-casein is to have very limited tertiary structure but protein with very high-caliber proline residue.Many proteolytic enzyme are had any problem in cutting contains the sequence of proline(Pro), thereby beta-casein produces the hydrolysate that is rich in big protease resistant peptide relatively with common protease hydrolysis.The resistance peptide of back can make hydrolysate have many unfavorable character.For example, these big peptides have relative strong effect for allergenicity and bitter taste as everyone knows.In addition, these peptides have stoped and further have been degraded to total free aminoacids, thereby in some process, the appearance of the protease resistant peptide that these are big equals production loss.The utilizability of the proteolytic enzyme of protease resistant part that therefore, can scinderin matter and use and to become important techniques and economic benefits.
Beta-casein is represented in the cow's milk a kind of of main Caseinum componemt.This protein has carried out sufficient characterization on its aminoacid sequence, and can buy with almost pure form.Similarly, beta-casein provides and be used for the fabulous check substrate studying the enzyme cleavage site and concern between the length of the multiple peptide that enzymic hydrolysis forms.
Although present embodiment proof endo-protease subtilisin has the cutting feature of wide spectrum, very special enzyme has main influence as the adding by the prolyl endo-protease of gene 55 (referring to table 1) coding for the segmental size of the beta-casein that forms.
Having minimum value from cow's milk (freeze dried, salt-free substantially powder) is that the beta-casein of 90% beta-casein obtains from Sigma.From Bacillus licheniformis (B.licheniformis) (
Every gram 560000DU) subtilisin obtains from DSM Food Specialities (Seclin, France).By the proline specific endo-protease of gene 55 coding overexpression and be used in the program of describing among the embodiment 4 and carry out purifying in aspergillus niger.
With the beta-casein powder with the concentration of 10% (w/w) with
Powder is dissolved among the phosphoric acid buffer pH7.0 of 0.1 mol together with the concentration of 0.1% (w/w).In 45 ℃ of shaking baths after the incubation 24 hours, reaction by 90 ℃ with solution heating 15 minutes and stop.In half solution (1ml contains 10 milligrams of beta-caseins), add 100 microlitre proline specific proteases, and make and be reflected at 45 ℃ and proceed other 24 hours.In 90 ℃ again after the thermal shock, with Delvolase
TMAnd Delvolase
TMThe sample of the beta-casein material of both processing of+proline specific endo-protease is analyzed to study accurate peptide size distribution in two kinds of samples with LC/MS equipment.
LC/MS analyzes
To use and P4000 pump (Thermoquest
TM, Breda, Holland) and link coupled use ion trap mass spectrograph (Thermoquest
TM, Breda, Holland) HPLC be used for characterized to the enzymatic protein hydrolysis product that produces by enzyme mixture of the present invention.The peptide of these formation PEPMAP C18 300A (MIC-15-03-C18-PM, LC Packing, Amsterdam, Holland) post and Milli Q water (Millipore, Bedford, MA, the U.S.; Solution A) 0.1% uniting of formic acid gradient in separates, and carries out wash-out with 0.1% formic acid (solution B) in the acetonitrile.This gradient originated in 100% solution A and be reduced to 70% solution B in 45 minute, kept other 5 minutes in back one ratio then.Used volume injected is 50 microlitres, and flow velocity is per minute 50 microlitres, and the temperature maintenance of post is at 30 ℃.The protein concn of the sample of injection is about 50 mcg/ml.
The details of independent peptide obtain with " scanning dependency (scan dependent) " MS/MS algorithm, and this algorithm is the distinctive algorithm of ion trap mass spectrograph.Carry out varifocal (zoom) scanning analysis completely after the scanning analysis to determine the strong ionic electriferous states of great majority in complete quality of scanning scope.MS/MS analyzes the peptide sequence information that a kind of ion in back obtains part subsequently, and this information can be used for using the SEQUEST from Xcalibur Bioworks to use (Thermoquest
TM, Breda, Holland) and carry out database search.Used database is extracted by the OWL.fasta database, and this database can obtain at NCBI (NCBI (National Centre for Biotechnology Informatics)), and it contains the target protein that carries out used application.
By with these technology as method for screening, only have the peptide of quality in about 400~2000 dalton's scopes and be considered to be fit to further analyze with the MS order-checking.
Angiotonin (M=1295.6) is used for adjusting the suitableeest sensitivity of MS pattern and the suitableeest fragmentation in the MS/MS pattern, having carried out the constant of 60 μ g/ml inculcates, the result causes the triple charged kinds of double sum main in the MS pattern, and about 35% the suitableeest collision energy in the MS/MS pattern.
In independent sample with Delvolase digestion, the LC/MS/MS Analysis and Identification cover 40 peptides of a plurality of parts of beta-casein molecule.These peptides account for 79% of total beta-casein sequence together.Peptide can be traced back to the length of the peptide in 2~23 amino-acid residue scopes in the hold-times different on the C18 post.Altogether the peptide of Fa Xianing<15% less than 6 amino acid.Use Delvolase
TMA large amount of identifiable peptides have also been generated with the sample of proline specific protease digestion from beta-casein.These peptides have covered total beta-casein protein sequence>50% together.In this sample, the remarkable homogeneous of the distribution of peptide size, this be because this peptide only in the length range of 2 and 6 residues.This result be presented at contain in the hydrolysate with proline specific protease preparation big by two-, three-to the component of 6AA peptide, this has shown and has been characterised in that the uncommon specific endo-protease obvious advantageous effect of incubation altogether.It is equally clear the endo-protease that is coded in the C-terminal cutting peptide chain of proline residue according to the endo-protease of gene 55 in these experiments.
Embodiment 9
Selectivity discharges specific amino acids and forms to promote local flavor.
Total free aminoacids such as leucine and phenylalanine not only are contained in U.S.A and draw in the reaction, and in numerous food fermentation as the precursor of required fragrance.For promote in food fermentation or in the heating of food, toast or the stage of curing promotes the formation of this fragrance, advantageously add protein hydrolyzate in these products, this hydrolysate contains these specific amino acid of high-caliber relatively free form.In the present embodiment, we have described the production that selectivity is rich in the yeast extract of leucine and phenylalanine.This enrichment is by obtaining to the favourable circumscribed proteolytic enzyme of the release of similar amino acid group is made up the endo-protease that selected amino-acid residue group has a preferred property of cutting.The preferred property of endo-protease should be complementary with the preferred property of used circumscribed proteolytic enzyme.For example our definite aminopeptidase characteristics by gene 20 and 54 (referring to table 1) coding is to have the clear and definite preferred property to the release of leucine and phenylalanine residue, the preferred property of the cutting coupling of this preferred property and thermophilic sporeformer proteolytic enzyme.Carboxypeptidase by gene 23 and 24 codings has preferred property, this preferred property and the preferred property of the tryptic cutting coupling that discharges arginine and leucine residue.Carboxypeptidase by gene 5 codings is characterised in that to have quite unusual preferred property to discharging glycine, and this preferred property can make up with some endo-protease that is present in the papoid.Carboxypeptidase by gene 51 codings can be removed glutaminic acid residue, this and the glutamate specific proteolytic enzyme coupling of being encoded by gene 43.
C180 is known can be at the N-terminal side cutting peptide bonds of big hydrophobic amino acid such as Leu and Phe from the thermophilic sporeformer proteolytic enzyme of endo-protease of Daiwa Kasei KK (Osaka, Japan) (commercial can buy as Thermoase).For the amino acid that will therefore expose discharges from the peptide of new formation, we use the aminopeptidase by gene nr20 and 54 (referring to table 1) coding.These genes are according to aforesaid method overexpression in aspergillus niger, and the purifying of these enzymes carries out according to the program of describing in embodiment 4.
Do not follow for these combinations with enzyme discharge leucines as much as possible and phenylalanine to discharge unfavorable amino acid, obviously should select condition used in the enzymically hydrolyse modestly.In addition, must make endogenous (with may be non-specific) proteolytic enzyme inactivation of yeast self.After many check incubations, designed a flow process, this flow process makes these two kinds of new proteolytic enzyme so that selectivity and validity discharge leucine and phenylalanine from yeast protein surprisingly.
In order to make yeast entogenous proteolytic enzyme inactivation, yeast suspension was placed 5 minutes at 95 degrees centigrade.Then suspension is cooled fast to the temperature that needs, and pH is adjusted to 7.0 with 4N NaOH.With the equal incubation under below the condition simultaneously of yeast, thermophilic sporeformer proteolytic enzyme and a kind of aminopeptidase.After thermal shock, with the pH regulator to 7.0 of 2000 ml yeast suspension, thereafter 680 milligrams Thermoase is added, and after stirring, add the aminopeptidase of purifying.Mixture is centrifugal then in 50 degrees centigrade of incubations 3 hours in stirring.In order to stop all enzymic activitys, with the pH regulator to 4 of supernatant, and in 95 degrees centigrade the other 45 minutes thermal treatment of carrying out.After another time is centrifugal, from supernatant, obtained to be used for the sample of amino acid analysis.Sedimentary or undissolved material is by removing in centrifugal 15 minutes with 3500rpm in Hereaus Megafuge2.0R whizzer.With the supernatant taking-up and with-20 ℃ of freezing placements.
With the supernatant sample after thawing immediately the Picotag method (Milford MA, the U.S.) according to Waters carry out the analysis of aminoacids content.
In amino acid analysis, the value of Trp and Cys is omitted, and the value of Asp and Asn is added up to a value.According to the data that obtained, in the hydrolysate of gained as a result, the ratio between L-Ala and the leucine (21.3: 11.7) is 1: 0.5.The L-Ala of commodity yeast generally is shown as 1: 0.3 to leucic ratio.
In second experiment, prepared the yeast extract that is rich in free glutamic acid.In order to realize this purpose, endo-protease (coded) with the preferred property of cutting and the carboxypeptidase (coded) that can remove these L-glutamic acid that therefore expose have been used by the gene nr 51 in the table 1 by the gene nr 43 in the table 1 at the C-of glutaminic acid residue end.By the endo-protease of gene nr 43 coding and by the carboxypeptidase (referring to table 1) of gene 51 codings according to aforesaid method overexpression in aspergillus niger.The purifying of these enzymes carries out according to the program of describing in embodiment 4.
The basic role of free glutamic acid in many fragrance forming processes fully proved, and thinks MSG, and promptly sodium glutamate is single most important flavour enhancing composition.
In the present embodiment,, will add by the enzyme product of the purifying of gene 43 codings then the pH regulator to 8.0 of the yeast suspension of 200ml heat-shocked, and with mixture 50 degrees centigrade of incubations 4 hours.Then pH is reduced to 5.0, and suspension is centrifugal.In 100 milliliters of supernatant, add gene product by the purifying of gene 51.Carried out 30 minutes in 50 degrees centigrade in the successive pH regulator with the incubation of this carboxypeptidase.After the enzyme incubation being stopped, once more with material centrifugal (on seeing) and obtain sample and be used for amino acid analysis with 95 degrees centigrade thermal treatments in 5 minutes.
According to (on seeing), in the hydrolysate of gained as a result, the ratio between L-Ala and the L-glutamic acid (30.0: 48.7) is 1: 1.6 according to the amino acid no that obtains.Commodity yeast L-Ala generally is shown as 1: 1 to the ratio of L-glutamic acid.
Embodiment 10
The local flavor that is rich in specific amino acid whose yeast is estimated
In order to prove that the protein hydrolyzate that is rich in according to specific amino acids of the present invention can generate specific fragrance, many experiments have been carried out with the yeast of describing among the embodiment in front.For this reason, the major part with these hydrolysates prepares and freeze-drying.With the performance of the powder of gained and the performance (GistexLS is available from DSM Food Specialities, Delft, Holland) of the commodity yeast extract in the standardized mixture compare under several reaction conditionss as a result.This standardized mixture is made up of a kind of hydrolysate, alkali mixture and water.
The alkali mixture contains well-mixed 22 gram Maxarome PlusPowder (the special type yeast extracts with high-content natural nucleotide in mortar, can obtain from DSMFood Specialities equally), 29.2 gram glucose, 9 gram REFEL-F fat (hydrogenant soya-bean oil, acquisition is from Barentz, Hoofddorp, Dutch) and 0.2 gram lactoyl calcium stearate (calcium stearoyl lactylate) (emulsifying agent, acquisition is from Abitec, Northampton, Britain).
All standardized mixtures all contain 5 gram yeast extract powder (promptly being rich in the material of leucine or L-glutamic acid or the yeast extract of commodity), 3 gram alkali mixtures and 3 gram water.Behind thorough mixing, these three kinds of slurries are carried out different heating means, promptly in the reaction bottle, carry out 65 minutes (liquid reactions) in 90-95 degree centigrade, perhaps in vacuum drying oven, carry out drying (vacuum bakeout reaction) at 20 millibars, perhaps in the reaction bottle at opening after the moisture loss, heat 10 minutes (baking reaction) in 120 degrees centigrade in 120 degrees centigrade.
After thermal treatment, all three kinds of products all have supposition at Vandyke brown to the color of black scope almost.Under the situation of vacuum bakeout reaction, only used light upper strata.The taste of heating product is estimated to grind to form thin powder and these powder are dissolved in the concentration of 2% (w/w) by the cake with blackening to carry out in the water that contains 0.6% (w/w) NaCl.Observation to one group of taste experimental subjects is set forth in the table 3.
Table 3
Reference | Leucine | L-glutamic acid | |
Liquid | Meat soup toasts slightly | Cold tea, the slight fragrance of a flower, zymic | Fleshiness soup more, meat, zymic |
Vacuum bakeout | Burnt fried potato | Astringent taste, beans, zymic | Burnt meat soup, zymic |
Baking | Adustion, meat soup, deliciousness | Less baking, the fragrance of a flower, deliciousness | Baking, more fleshiness soup is more delicious |
Embodiment 11
The whey protein hydrolysate of the non-allergenicity that forms with three peptidyl peptases
Can carry out overexpression as described by the dipeptidyl peptidase of gene 19 and 55 codings and by gene 4,9,10,12,26,35,46 and the 50 three peptidyl peptases of encoding, and carry out purifying according to the method that in embodiment 4, provides.Behind purifying, the pH of the enzyme that each is independent is just when determining by any available and technician's known method with temperature stability.In addition, the specificity of each independent enzyme can be used among the embodiment 1 method that outlines and determines.Illustrate in the selectivity experiment below by the displaying of three peptidyl peptases.
Make enzyme by gene 12 coding overexpression and be used in the program of describing among the embodiment 4 and carry out purifying in the aspergillus niger host cell.Being Ala-Ala-Phe-pNA and Ala-Phe-pNA (all from Bachem, Switzerland) with the enzyme that obtains like this and different synthetic product look substrate carries out incubation pH5 and 50 degrees centigrade.Cause the remarkable increase that absorbs at 410nm with the incubation of Ala-Ala-Phe-pNA substrate, with the incubation of Ala-Phe-pNA then not.This observation proves that significantly three peptidyl peptases excise tripeptides, and does not show amino-peptidase activity, and this amino-peptidase activity can cause the unfavorable increase of total free aminoacids.
In addition, by the favourable enzyme stability feature of enzyme demonstration of gene 12 codings, as shown in experiment below.With 4 enzyme samples respectively at 0,40,50 and 60 degree centigrade pH5 incubation 1 hour.Make each enzyme sample and above-mentioned Ala-Ala-Phe-pNA substrate in citrate buffer solution, carry out incubation then, and residual activity can be determined in each independent sample by measuring the increase that absorbs at 410nm in pH 5.0 degree centigrade sample shows 100% activity, and 40 degrees centigrade sample shows 96% residual activity, and 50 degrees centigrade sample shows 92% residual activity, and 60 degrees centigrade sample shows 88% residual activity.
Have in the general method of the hydrolysate of tripeptides at high proportion a production, can with whey protein (WPC 75) with 10 gram protein/liter concentration to dissolve/be suspended in pH be in 8.5 the water medium.For the first time the endo-protease subtilisin of enzyme temperature the region between the heart and the diaphragm and wide spectrum (
Every gram 560000DU is from DSM) carry out.Be that every gram protein enzyme enriched material is that this enzyme of 0.5% after 2 hours, is heat-treated mixture so that used endo-protease inactivation whey predigestion in 60 degrees centigrade with concentration.Add then with temperature regulation to 50 degree centigrade, and with three peptidyl peptases, then whole mixture is carried out incubation up to the level that reaches the tripeptides of wanting.The further procedure of processing of the hydrolysate of Huo Deing depends on specific application like this, but can be in conjunction with microfiltration and centrifugal and follow-up evaporation and spraying drying.
Sequence table
<110>DSM?NV
<120〉the new gene of encoding novel proteolytic enzymes
<130>20095WO
<160>171
<170>PatentIn?version3.1
<210>1
<211>2520
<212>DNA
<213〉aspergillus niger
<400>1
cgcaggcgtc?cgttgcgccg?cgaaaacctg?ccgagtgggc?cgtttaggct?ttgggtctcc 60
ccacgatgta?agcataatca?ttctgtgcct?gagtgtgaat?tctcctgttg?gaggctgcat 120
cttaattctt?aactgcatga?aaagcacttg?ggtgctattt?tctttttcct?ttctttcttt 180
tccgtgttca?tttccattcc?cttgctcttc?ttctttgtgt?cgacatttac?aaatcacatt 240
tttcttatac?tttcttttct?tcacctcgtt?tcttcctatt?cactctctgt?gttcagcatt 300
cgttatcagc?actttatctt?ttgctcgtct?cttttatctt?cacttgtttg?tgcctttcca 360
ctagcaatct?atcgtttgat?ctttctagag?cattgtcttg?attgtgtcat?tctgtcattg 420
actccggcta?tgaaatatta?ttctcaatct?gcctaaaacc?aaattctact?ctatcactac 480
acatttgtat?cacctgatct?ggctgagata?ggagagtccg?gcatctcatc?gtctgcatca 540
gacaattgcg?ataaattcat?tgcttgcacc?tgttattgat?tcttccaagt?tatgcatctc 600
ccacagcgtc?tcgttacagc?agcgtgtctt?tgcgccagtg?ccacggcttt?catcccatac 660
accatcaaac?tcgatacgtc?ggacgacatc?tcagcccgtg?attcattagc?tcgtcgtttc 720
ctgccagtac?caaaaccaag?cgatgctcta?gcagacgatt?ccacctcatc?tgccagcgat 780
gagtccctgt?cactgaacat?caaaaggatt?cccgttcgtc?gtgacaatga?tttcaagatt 840
gtggtagcgg?aaactccctc?ttggtctaac?accgccgctc?tcgatcaaga?tggtagcgac 900
atttcataca?tctctgtcgt?caacattggg?tctgatgaga?aatctatgta?catgttgctc 960
gacacaggcg?gctctgatac?ctgggttttc?ggttccaact?gcacgtccac?accctgcacg 1020
atgcacaata?ccttcggttc?ggacgattct?tcgacccttg?aaatgacatc?ggaagagtgg 1080
agtgtgggct?atggaactgg?gtctgtcagc?ggcttgctag?gaaaagacaa?gctcacgatt 1140
gcaaatgtca?ctgtacgcat?gactttcgga?cttgcttcca?acgcatcgga?taacttcgag 1200
tcgtacccaa?tggacggcat?tctcggtctc?ggtcgaacca?acgatagttc?ctacgacaac 1260
ccaacattca?tggatgccgt?tgcagaaagt?aacgttttca?agtcgaatat?cgttggcttc 1320
gccctttcac?gtagccccgc?caaggatggc?acggtcagct?ttggcactac?tgacaaggac 1380
aagtacaccg?gcgatatcac?ctacaccgat?accgtcggat?cggacagcta?ttggcgcatt 1440
cccgtggacg?atgtctatgt?tggcggcact?tcatgcgatt?tctccaacaa?atcagccatc 1500
atcgataccg?gaacttctta?tgctatgctg?ccttcaagcg?actcgaagac?gctgcacagt 1560
ctcattcccg?gcgccaaatc?ttcggggagc?taccacatta?ttccgtgcaa?cacaactact 1620
aagctacaag?tggcattctc?tggtgtgaat?tacaccatct?cgccgaagga?ctacgtggga 1680
gcaacttcag?gttctggatg?cgtttcgaac?attatcagct?acgacttatt?tggtgatgac 1740
atctggctcc?tgggtgacac?gtttctcaaa?aatgtgtatg?ctgtgtttga?ctacgatgag 1800
ttacgggtcg?gatttgcaga?gcgttcctcg?aacaccacct?ctgcgtcgaa?ctctacgagc 1860
tctggaacaa?gcagcacctc?gggatccact?acaacgggca?gctcaacgac?tacgacgagc 1920
tctgctagct?ctagtagttc?atctgatgct?gaatcaggaa?gtagcatgac?cattcccgct 1980
cctcagtatt?tcttctctgc?tctggcgatt?gcttccttca?tgctttggct?ctagttaacc 2040
gcatcttact?cgacgcctga?acctcgggaa?acatatgcat?tatttacaca?tgctgctgat 2100
ttgtatttgc?atatattctt?cgagcctgga?cggcgtgcgg?gtcatattac?cttacattcg 2160
aagtccttct?ctaatcaatc?aacatttatt?cttactccac?cagttctggc?tcgcaattaa 2220
ccctgtctaa?gaaaaagttg?gtatagaaca?tggcatccac?tacctggaac?attcaaagaa 2280
ccttgtccgg?gatcagtgtg?tatgacttcg?ggtacgattc?tgacatgaca?gttagcgtcc 2340
atcctgagga?ttcatcctga?tctccttacc?tagtatggac?ttatcaaagt?ccttgacgct 2400
attgtaccct?cccacagcca?tcaggatatc?gaaatcggcc?aacagcgact?tcatcacatg 2460
gcgaacaccc?tcctcaccca?tgatactgag?gccccagatc?cagagccggc?cgacgaaaac 2520
<210>2
<211>5001
<212>DNA
<213〉aspergillus niger
<400>2
taggaaaatc?agaggcgaca?atttgctccg?atactggata?agtaccatcg?gtcacgaaat 60
tcagcaccga?ctggcttatg?tcctgctccg?ataccttagc?ggacattatg?ttagtagttc 120
taagcaagag?cccttggttc?ttggtaatcg?gcggatcaaa?aacgtaaaga?agacaaacag 180
aagcgccaca?ctaggctctg?cctccctctt?acagaagatc?tgccaggtat?cgatccacaa 240
agatatacca?aggactccaa?tgcagcagat?cgcaaccgaa?agggaaggcg?agctgtcaac 300
accgccatgt?gacttcaccg?ctcaccgcct?tagctgcgat?gggcaagacc?acgaacgatc 360
tcgctcttcc?ccagggccag?actgaggccg?attatatgat?ttttttcttt?cttttccgtg 420
tgtctcgtct?gctgctatat?tcttattttt?ctgttcggta?aagatacctc?ctaagaatag 480
acacgggttg?tttttttgtg?aattatctgt?tggtgtggtg?ctctctatcg?aaccggaaac 540
ctgaactcca?ctctgaaccg?ttacagttgg?agggtaacct?tcgttcagcg?gccaactgtg 600
tgacctcaaa?attcctgaaa?catcataatc?ggcgtcaagc?agagcccatc?gtgttgtctc 660
agttactatt?gagaagcctg?atacgggcaa?acgcttctcg?atccatgtga?gtcatgcttg 720
taccagccct?gaactccatt?gaataaaaaa?aaagcaagaa?aagagattgc?ccctccgtcg 780
ttttctgtat?taaacatcca?atcctcaacc?ggcagcctta?cattggctgc?cacagatttg 840
tgcctccata?cagcatgctt?cgtggtcttc?gtgatgtcgt?attattacaa?tttgcaatcc 900
ccttgttctt?gctattggta?tttcaaacat?ggaatgggtg?cttttcccgt?ttcaattccc 960
cgcaccctga?acctcaagca?ttgctagctt?ctctaaaatg?aataaaactg?ttatacttgc 1020
ttcctaaaag?tttgcgcttc?tggcctatgg?attactaaca?gcattttaga?ttatcgctac 1080
ggggtgtgat?cacaggattt?ggttctaaat?cacatttcca?gagaccattg?agcaaaatgt 1140
catctactca?aaagagccat?ttcaagctac?tccagaagtt?caaaccggag?tactcgccta 1200
gcgagtttgc?tcagtatgag?tcggagagaa?caggcatgag?ggtagtggtc?attgaccaaa 1260
aaggacccaa?agtcacaggt?tattttgttc?tagccacaga?gattctcgat?gattcaggtg 1320
ctcctcacac?gttggagcac?ttgtgcttta?tgggctcgcg?gaactataga?tataagggct 1380
tccttgacaa?gctagcaaca?cgtgtttatt?cgagcaccaa?tgcctggacg?gccacagacc 1440
acacggccta?caccttggac?acagcaggct?gggaagggtt?cgctcaaatc?ttgcccgtgt 1500
acctagagca?tgttatagct?ccaacactga?cagatgaagg?gtgctatacc?gaagtgcatc 1560
atattgatgg?cgctggagac?gacgctggag?tcgtctactc?ggagatgcag?ggtgtgcaga 1620
ataactctgc?agagttaatc?gatctaaccg?ctcgtcgatt?gacttacccg?catggtgtag 1680
gttttcgcta?cgagacaggc?ggtatgatgg?agcagctccg?cgtcctcacc?gcggaccgta 1740
tccgagcgtt?ccatcgtgag?atgtaccagc?ccaagaactt?atgcctaatc?atcacaggcg 1800
aagtagatca?ccagaacatg?ctggagacct?tggacaagtt?cgaagatact?attctagatg 1860
tcattcccag?tcctgattca?cctttcaaga?ggccgtgggt?agattccaag?caggcgccgc 1920
cattggagaa?gtccattgtc?cagactgtgg?aatttccgga?agaagatgaa?tctttcgggg 1980
agatagaaat?tagattcctc?ggtccggact?gtaccgaccc?tgttcaaagt?gagtgttccg 2040
ctgtcctcat?ttcgaagata?tacttactct?gttatagccg?gggctgtcaa?tgttgcattg 2100
ctgtatctgg?ccggttcatc?tgcttctcta?ttggataaca?tcctggttga?gaaggagcag 2160
ctcgccagtg?ctgtctatta?tgctaccgaa?gatcatccca?gcattgagat?ccgcttcaca 2220
ttaaccagtg?tggagacaga?gaaactcgcg?aaggtagagc?aacggttttt?cgaagtgctc 2280
aaggacgcta?tggagaaaga?tttagacatg?aggtatatca?aggagtgcat?tgaccggcaa 2340
agacggacct?ggaagttctc?taccgaaagc?tccgcctctt?cctttgcgga?gtacgtgatc 2400
tcggattttc?ttttcggaaa?gagagacgga?tcgactatgc?ttgatgttgc?gaccttgcaa 2460
gagtacgacg?tgctggagaa?gtggagtgaa?gaacagtggc?gcagttttat?caaaacatgg 2520
atttctgatg?ccaaccatgt?cactatcctt?ggtgttccgt?ccgttaagat?gtctgacaca 2580
ttaaagaagg?aggaggaagc?tagagtcgca?gagcaaaaga?agcgcttggg?tgatgagggg 2640
ctgaagaagt?tggccgacaa?gctggaaaaa?gctaaagctg?aaaatgacaa?ggagatcccc 2700
aaggagatgc?tggagaggtt?ccaaatccct?ggaatagagt?ctatccattt?cgtggacact 2760
actacagcca?ggtctggtgc?agccctcgat?gccgggcgcc?catcccacaa?ggcgcaaaaa 2820
ctggtggatg?ctgatggctc?tgatctgccc?ttgttcatcc?atttcgagca?tatccccagt 2880
agcttcgtgc?agctctccct?cctcatctcg?gcacaggccg?tacctgtgca?gcttcgtcca 2940
ctgctgtctg?tgtatactga?ggcattcttc?aacctgcctg?tcaaccggaa?cggggaaacc 3000
atcaactttg?agcaggtggt?tgtcgagttg?gaaagggata?ctgttggcta?ctccatggaa 3060
ggagctagaa?gcctaggaaa?ctcggagatg?ttgcggatct?cattccaggt?ggagcttgag 3120
aagtatcaca?cggcgatcgc?atggatccag?gaactttcct?ggaactcgat?tttcgatgtc 3180
gagcgactcc?gagcgattac?cagtcgactg?ctctccgatg?tgcccgattc?caagcgtagt 3240
ggcgacgaca?tgctcgcggc?tgttcatgtg?atggtccact?atgcagcaga?gtctattgtt 3300
cgggctcgga?gcaccttggt?gaaggcgcgt?tatttgaaac?ggatcaagaa?gcaattagca 3360
gaagagccga?agtctgtcgt?tgcgcggatg?gaagaaatca?gagatgcgct?tttccgtttc 3420
gagaacatgc?gagtcttagt?tatcgctgac?ctggagaaac?ttcaaaaccc?tgtgtcagca 3480
tggaaaccat?ttgctgagcg?tttgggtgca?ggtgcccctc?tacagcctat?cacgactaga 3540
agaccgttgc?tcagtgaggc?aggccagaag?ttgggcggta?agtcgtatgt?ggttcctatg 3600
ccgacgattg?attcatcgtt?cgcatatgct?accgcacgtg?gtttggattc?ttatgatgat 3660
ccaagacttc?ctgccttaat?ggttgcaatt?gcatacatga?acgcggttga?gggtcccctc 3720
tgggttgcag?ttcgaggcaa?gggtttggca?tatggcacga?actttgccta?taacattgat 3780
accggattcg?tcaacttcga?cgtttaccgc?tcccccaacg?cccataaagc?cttcgactcc 3840
agcaagcaga?ttgttgagga?tcacctctct?ggtgcgatgc?ccttcgatcc?cttgatgctg 3900
gagggttcca?ttagcagcat?tgtggtaagc?tttgcgaatg?aacagtcgac?aattggtagc 3960
gcagcctcag?gcagtttcat?ccgacaggtg?attcggcgcc?tgcctagcga?ctacaaggag 4020
cgggtgctca?agcaggtgcg?ggctactagc?gttgatgacg?tgaaaggcgc?tctgaaggac 4080
atcattctgc?ctttgtttaa?cccgtccacg?gccaatatcg?tggttacctg?cgctacagtg 4140
cttgaggagg?tttgtcattc?catgaagaaa?ttatgatctt?cttgtgtatc?atttactaac 4200
tgtcggttta?gactatcaag?gaaggtctcc?aggcatcggg?attcacgcct?gcggtgcagc 4260
cactcaaaga?attcgaagat?gactatgggc?tgaaggtcgg?cgatgacgag?gacgaggagt 4320
ccgacgatga?cgacgatgag?tatgaaaccg?gatctgaaga?tgaagatgac?agtgatgaag 4380
acatggagga?tgacgaagat?gatgagtgat?gcaatctata?cgacaacctc?tagacatgac 4440
aagatttatc?tgagccagtt?cctggataac?acctaggtcg?aaagaccagc?tacccctggg 4500
ggcccagata?tgccgacccg?tgtgatctgt?attgttagag?atgtctccaa?ctagcagacg 4560
cgcaatgatt?tttgatgtta?atgatatatc?gtacaacata?agtggttaac?caccacaaat 4620
ctgcacctaa?atcttagttg?tgattatcgg?tacctaccaa?acccgagtaa?acgttgccag 4680
aagtttatga?aaaagctctc?gttcttctta?tttcattgaa?tgttgtaata?aaaagtgcta 4740
gcagatgctt?tcgctatcgg?gcccactact?atgattaacc?tgaagcttag?tctcttaggt 4800
gacataacct?gttctacaca?ggctgccatt?atatttgcaa?cacacagctt?ctatctctga 4860
cctttgtgag?aataatacaa?ttactagaaa?ccccaggaga?tataaataca?ctctactcct 4920
accgaactaa?cacccagatc?gacaaattat?aaaccaaacc?acgtgacaat?atgatatcta 4980
tatatgaata?tgtataaggt?a 5001
<210>3
<211>3850
<212>DNA
<213〉aspergillus niger
<400>3
gcgcggggtt?cctgcatgtc?tttcatggtt?gggaggtata?tgtacatgta?atgccgttgg 60
gttctggata?cccacaataa?agtgtttcta?ctattacttt?tgcattgtta?gactttgaag 120
gctgctctgt?aagggtccat?tccgttggag?tcaaacaacc?gtctgtccgc?gggcatatgt 180
ctcagtctga?ggtgagaact?gcaatataca?ctccaagctt?tctcaatctg?atgcacagat 240
tgcaaacatc?tcccttgctg?tgtggtaaag?tctccctttc?tcggtgaacc?ttcttcgggg 300
tcgcaactga?ttccattgac?cctcaccatc?tgtcgaattg?ttcccgaaag?ctcgcgtcca 360
aataggcttt?acggacgcca?cagctgctcg?aggccatctc?caagggggaa?tgaacaatgg 420
aatggtaagc?cgctaagaaa?ggggaactgt?cggttctggt?cgattggcag?ggtcagggca 480
gtgcttgggc?tgttcctctg?gccctccctt?gcttcaagct?ggccccgatt?tggcagctcg 540
tgaagctcac?cagacattca?gccagccaga?tgactggcac?ctttccgctg?ggcataaatt 600
ggccctggca?gccatgtcat?gccaatcttg?gctccaggac?cagtcattcc?ttttcttgtt 660
cctgtcaaac?agatcaagtc?ctcgaggatg?ggagctcttc?agtggctgtc?catcacggct 720
gctgcggcct?ccgcagtgtc?agccttgacc?ccggagtaag?tatctccaat?catttggaac 780
tggcccatat?tgtgcatagc?taaccagctt?acctgcatag?gcagatgatc?ggtgccccac 840
ggagaaccga?agttatacca?aacccctccg?gtgtatgccc?attgccaggt?ccagccttac 900
aaagaagcgt?cgtctgctga?cacgagaagg?acaccggtct?attctcgacc?tcccaatggt 960
cgtttgacac?tcattctgag?agcacctggt?ggagcttgat?cgacctccaa?tcgggcaaga 1020
ccaccactct?caccgatgat?agcgatatcg?aggagatcat?ctggcttggc?tctgacaatt 1080
ctacgctcct?ctacatcaac?agcaccaacg?cgcaggttcc?cggtggcgtg?gagctgtgga 1140
ttgcggactc?ttctgacttt?gcaaatgcgt?tggttcaggc?ctttaacgat?gcctctgcag 1200
actagtgcta?atcctacttg?gtgcagttac?aaggcagcct?ctctctccgc?cggttttctc 1260
ggcatcaaat?caaccgtgac?agattccggc?gacgtgcatt?tcatccttcg?tggaaagtcc 1320
tatcccaacg?gaacggcata?caatgatcag?ctcgccgaga?cctatcccag?tacagcccgc 1380
atctacgaca?gcatctttgt?gcggcactgg?gacacttacc?tgaccaccgc?ctcccacgct 1440
gtattctccg?gtaccctgca?aagctcgacc?agcgacgacg?gcaatgttca?atatacctct 1500
tcagggggat?tgaccaacct?ggttaaccca?gtcaagggtg?ccgaaagccc?attccctcct 1560
tttggaggca?acgacgacta?tgacctctcg?cctgacggca?aatgggttac?cttcaagagc 1620
aaagcgccag?agctgcctct?tgctaacaac?acggctgcct?atgtctatct?cgtcccacac 1680
gacggctctg?cgactgcctt?tgccgtcaac?ggccctgata?gtcctgcaac?cccggaggga 1740
gttgaaggag?aatccaacaa?tcccgtgttc?tcccctgata?gcgacaaaat?agcgtacttc 1800
caaatggcta?ctaatacata?cgagtcggac?cgcaacgtgc?tatacgtata?ctccatcgcc 1860
gatgacacca?tcactcccct?tgcaaaggac?tgggaccgat?cgcctagctc?cgtgacatgg 1920
gtcgatggag?acaacctcgt?cgtggcaagc?caagatctag?gacgaaccag?acttttcgcc 1980
atcccaggcg?atgcagggga?cgacttcaag?cccacgaact?tcaccgacgg?cggctccgtg 2040
tcggctcaat?acgtcctatc?caactctacc?ctcctcgtca?cgtccagcgc?cttctggaca 2100
agctggagcg?tctacaccgc?cagccctgac?gagggcgtga?tcaacacact?ggcctcagcc 2160
aacgagatcg?accccgagct?tagcggcctt?agttcctccg?actttgaaga?gttctacttt 2220
gacggcaact?ggactaccgt?aagtctatcc?ctccttgccc?ccaccaccac?atcacaaaca 2280
tactaaactc?accgcagctc?caaggatgga?tcacctaccc?ccaagacttc?gactcatcca 2340
agaaataccc?cctcgccttc?ctcatccacg?gcggccccga?agacgcctgg?gcggatgaat 2400
ggaacctgaa?atggcactcc?aaggtcttcg?ccgaccaggg?atacgtcgtc?gtccagccaa 2460
accccacagg?aagcaccggg?ttcggccagc?agctcacaga?cgctatccaa?cttaactgga 2520
gtacgccatt?ccctatcccc?aaactcccct?cttaaacata?cagctaacaa?atgaaataac 2580
agccggcgcc?gcctacgacg?acctaaccaa?agcctggcaa?tacgtgcacg?atacctacga 2640
cttcatcgac?acggacaacg?gcgtcgccgc?gggtcccagc?ttcggcgcgt?tcatgatcac 2700
ctggatccag?ggcgatgact?ttggacgcaa?gttcaaggcg?ctggttagcc?atgatggtcc 2760
gttcattggc?gatgcgtggg?tcgagacgga?tgagttatgg?tttgttgagc?atgaggtgag 2820
tggaccaagc?caaacccccc?ttttctcccc?ttacaccatt?acccctatac?aaatatgatg 2880
attctgaccg?tgtatagttc?aacggcacct?tctggcaagc?gcgcgacgca?ttccacaaca 2940
cggatccatc?cggccccagc?cgcgtcctcg?catacagcac?cccccagctc?gtcatccaca 3000
gtgacaagga?ttatcgcata?cctgtggcaa?atgggattgg?actgtttaat?acgctgcagg 3060
agaggggcgt?gcccagtcgg?tttttgaatt?tcccggatga?ggatcattgg?tatgttcata 3120
cccttttctt?cccccttttt?tctcccatga?ttatgggtgt?tgtggatgct?gatgtagcta 3180
tgtgtgtgtt?tagggtcacc?gggcaagaaa?acagcctcgt?ctggtatcag?caggtgctgg 3240
gatggattaa?tcggtattct?ggggtgggag?ggtcgaatcc?tgatgcgatt?gctttggagg 3300
atacggtgaa?tccggtggtg?gatttgaatc?cttgatcatt?ccctgttgct?cgttactact 3360
agtcagttat?gatcatgttc?tggctgggtc?ccaggataga?tggacggtta?ttactggtcg 3420
ttatattctg?tttgcagtgg?ttactagttg?gtagatcagt?tacgagatga?tgtatgagac 3480
gacagaaaga?cttatgctta?tgttgggagc?tgcttcattt?gtatatcaat?ttattcttgt 3540
agtgattgat?aactaactac?tgtctgactg?tctgtcaacc?gctatactaa?cattatacca 3600
accaaccaac?caatcaaatc?aatttctggt?tctttcttct?cttctgtttc?ttcacctcgc 3660
aactagacca?attcatcaag?gacagggcag?gacaggatct?ggtatctgaa?cggaacaacc 3720
gaaggaaaaa?caaatcatac?acaagctttt?gtacaatcaa?accataagaa?tcagtacagc 3780
tttctctttc?agcctttcca?aatgagagga?aggacagaga?aaatacaaag?atgataccct 3840
agaaacgaaa 3850
<210>4
<211>3139
<212>DNA
<213〉aspergillus niger
<400>4
attgagtagg?ctgcgctctt?tgattctttg?cgaggtacta?aacccaaaca?ggcaattgag 60
atgttcggga?gagaatatgc?ggggatgcta?tgcctgttgc?agggatgatt?atctccacac 120
tagcgcgtta?aaggtttagt?agcctgagat?ggattgccga?tctccgaccg?ggccctgcct 180
cagccccagt?acttgtggaa?cgcgtcgaag?atttacaaca?ccatgccaga?cctaactagg 240
taataaagtt?gcgatgatgg?ggactgccgc?aaggctgtca?atttgggggc?cgaactcagc 300
ctcaacctgg?aaaaattaac?tccgattgtt?ttgatttgat?catgggagat?tacagtctac 360
gtgaaatgag?cttataaaga?acgttggagt?accggctctc?aacctgtctt?gtacctgcaa 420
gctttcctca?attcccttct?atctttctta?aaatcctctc?attagacatc?atgacgaggc 480
agacttctct?cgttcccagg?ctactaacgc?tagcctcact?agctgcactt?tcacaagcag 540
agctaggcaa?gatccaatgg?aaaggatctt?gcaacttgac?cacttatccg?gcattgatct 600
gtggaacact?agacgtgcca?tacgactaca?cggagtcaaa?ttccagcaag?acactgactc 660
tcgacatcgc?caagtggcca?gcgaccaaga?aaccagtctc?ggagcccatc?atatttaact 720
ttggaggacc?tggtgtcaat?tcgttcgagg?gccttgggct?ttatggagag?gaatttcagg 780
cgtaggttgc?agttctgctt?tgataccgca?tcttatgctg?actgacattg?ttctctagta 840
ttcttggagg?tcacaatgat?ttgatagctt?ttaacaaccg?gtttgtcgct?cttctttctt 900
gagctagaaa?catctactaa?cgttgtacct?ttatatagag?gcgttggaaa?caccatcccg 960
ttctcctgct?acagcgatga?cgccacccgt?gaactcgtcg?cccttcaagc?tcctaacgac 1020
ggcagagcgt?ccagcacggc?tttgggagaa?atctgggccc?agaacgcaaa?catcgcacag 1080
gcatgctatg?ctacgaacaa?tcaaactggt?agtcttattg?gaactagctt?tgctgcaagg 1140
gacatcatgc?aggtcgctga?tgcgctcagt?ggaaaggata?gtttggtcaa?ctactggggt 1200
aaatatcacg?gctgaaccga?gtttatactt?ttgctgacaa?tctacacttt?aggattctca 1260
tacggcacta?caatcggtgc?tgttctcgca?gccatgttcc?cggatcgaat?ggggaatgtc 1320
gcgcttgacg?gagtggacaa?ccccagagag?gctctttatg?gatagtgagt?ggcccttgaa 1380
gtttgcccga?tctggtatga?ttcagacagc?taattccttc?cgaaaagcaa?cgcacaagcg 1440
gttgtggacg?tcgacaaagt?tttcgaagga?ttctgcacgg?gctgcatggc?cgcaccggac 1500
ctctgcccta?tcgccaagga?gtacaccagc?gccgccaact?tggaagccgc?aatttacctg 1560
atgctggaaa?acctcaagta?caacccgatt?gccattcccg?aaaccggtgg?aatcgtaact 1620
tggagcgacg?tcaagtcgac?catttttgag?gccatgtacc?tgccaagctc?ttggcccttg 1680
acctctgagc?ttctttacta?cgtgcaaacc?cgcaacacaa?cgatccttgg?caactctgaa 1740
gtatacgaca?ccatcaaatc?ctacggtcaa?tcggcttctt?tgacttcggc?ttccgatgag 1800
gtcggcacgg?ccattacatg?ctccgacaag?catcgatctg?ccaccattaa?agaggtcctc 1860
ccgtacgtca?aagccagaca?ggctctgacc?aagatcggaa?gtgatggctc?ggacggcgac 1920
atgagatgcg?cgcagtggaa?tccgaagatg?ttcgccaagg?agcgctactc?cggtgacttt 1980
gaagtcaaga?cagccaaccc?ggtgttgatt?ctgagcaaca?cttacgatcc?agcgactcct 2040
cttcccgcag?cgaagaacct?gacagagacc?tttgagggaa?gtgtcttgct?cgagcagaac 2100
ggatacggtg?tatgtttata?cttccccttc?tcatcatatc?aaaagtgagc?aagcagctaa 2160
cctactgatg?atagcatact?accctgtcta?tgccatctct?ttgcactgcc?aaggccgtcc 2220
gggcttactt?caccaatggc?acattgcccg?ctgacggaac?gatctgccag?gtggacgtgc 2280
ctctgttcac?gaacttgacc?tacaaggatg?tgtggccgaa?gagtttccaa?cggagcgttg 2340
agtcgaggga?tgatgcgact?atcctcaagg?ctttgatgtc?ggtccgtgat?aagatgtcgc 2400
gacgcaggat?gtggtaagcg?catgctatag?atggggatgt?tgaaaaccca?aagcgatgac 2460
tggataatgt?tcttcatata?atttattctg?tgccgattcc?ggcatacgct?cgtcatgtaa 2520
tagagtttag?ttaatgttgc?aagggattgt?atagtattta?tttgtacacc?aacagcgctt 2580
catggagacc?ggaacttccc?tgagtacaga?atttcccatc?taggctttta?tttaactttg 2640
acaatactca?gtagtttgga?tgtcgatagc?attgaggcaa?gtaccggttg?ttgttttggt 2700
agtggagtga?atcaggactg?tcccacaaca?atccgctgat?ctgaatgttt?gatgtttcga 2760
tctgaggtat?ctgagctgcg?agcctccaaa?tcggcaaccc?catacttcag?ggatattcca 2820
gaacattact?agccttggag?gctttgaggt?ttagctgcag?ggcggtcaaa?ctaattgatt 2880
tctctcaatt?gtcctaccgc?tattgagtga?tctttagtgg?atgagtggaa?cggagaattc 2940
ccggtcggat?aatgcctgca?ttagtattgg?ccaacagagt?attccatcaa?cgactcccgc 3000
gctgacattt?aatccatgca?caccctgaat?tacctcgagc?ttattctcgg?tcctacattt 3060
gatcctctca?tactttccct?tatgtccttg?cccacttgct?ttacagattg?aatccggatc 3120
cttcagcact?cggcagaca 3139
<210>5
<211>2940
<212>DNA
<213〉aspergillus niger
<400>5
atagcagaac?agaacatgta?tcttgtcaac?gaattgattg?atttcagcac?ggaaatgttc 60
aaggcatgga?acaattgctt?ctgacccgga?accgcggatt?gcaaggatgg?atatgtggat 120
cagatggtgt?gaagaagatc?tgtctgttag?catacttcat?aagttccaag?gaggagtaaa 180
tgtggagtca?taagagtaat?atcgaatatc?atagaatggg?gttgtcttgc?taacggtgaa 240
tcggactccg?tcggctctgc?cagcgatcgg?caggtcacgc?gtctgcgtaa?cttggtactt 300
atcttcccag?tcacctaagc?actgttactc?cactcttctc?tctttgacga?taagaagata 360
gcagagactc?ttgataaaaa?gggttgggag?catgctttga?atttcttcac?tccgagagct 420
ttctgtcccc?atctggtctc?ttgttgtccc?cgatgtacta?ctctctctgg?gttgctgcct 480
tggtggccgc?gctgcccgtc?tcccgggccc?agtttgtggc?tccgcccacg?gatctcattc 540
ccaccaaggg?atatctcgac?atccccgtcc?gctacaaaca?ggtccccacc?ggcatttgtg 600
agactgatcc?cagtgtcaag?agcttctccg?gttacgtcga?tgtcgctgag?catgagcaca 660
tcttcttctg?gttcttcgag?gcgcgcaacc?aagatcccac?cgaggctccc?ttgaccgtct 720
ggatcaatgg?aggcatgtct?gaccccggtc?attatttcct?tccaattgct?aaccgttcgt 780
aggtcctggt?tcctcctcca?tgatcggctt?gttccaagag?cacggcccat?gcggcattga 840
cgccaatggc?tccgtctaca?acaaccccta?ctcctggaac?aacgccagca?acatgctcta 900
catcgaccag?cccgtgcaga?ccggcttctc?ctacagcatt?ccggttcccg?gctatgtgga 960
ttcttccaca?gacaatgtta?ttgctctgcc?ctcccccgcc?tgccccgact?atgcagcgga 1020
tatgttctgt?ggcacttact?cctaccccaa?cgtgagcctt?acggctaatt?ccaccgacaa 1080
cgccgccccc?aacttctacc?gcgccctaca?gggttttatg?ggcgcatttc?ctcagtactc 1140
gcgcgaaacc?ttccacttca?ccacggagag?ttatggcggc?cactacgggc?ccgtcttcaa 1200
cgagtacatc?gaggagcaga?acgcccatct?ccagccggga?gccaagaaga?tccaactggg 1260
cagtgtgatg?atcggcaatg?gctggtatga?cccgattatt?caataccagg?cctactacaa 1320
ctttacggta?cactacctgg?tttctgatcc?ttatccttac?agcctggaca?ctaatctatc 1380
tacaggtata?tccgggcaac?acatacgact?acctgccatt?caacaagtcc?atcagctcgc 1440
tgatgtacaa?caacctctat?ggccccggaa?actgcctcga?ccagctctac?gactgcgccg 1500
cccgaggcat?cgacgagatc?tgcagcactg?ccgacgattt?ttgcgccaac?gaggtcgaaa 1560
acgtctacga?catttactcc?ggtcgggatg?agtatgactt?tcgtgaactc?actccggacc 1620
cgttccctta?cgagttctac?gttgactacc?tgaacaaagc?gtccgtgcag?gccgccatcg 1680
gcgcatacat?caattacacg?gagagcaaca?acgctgttgg?actcgccttt?tcgtccaccg 1740
gtgacgacgg?gcgactcatg?aacaccatcc?aggatgtggg?caagctgctc?aaacagggtg 1800
tcacggtggt?catgtacgcc?ggggatgccg?actataactg?caactggctg?ggtggggaag 1860
ccgtgtcgtt?gcaggtcaag?gccgccaact?tcagtagtgc?gggttacacc?aacattgtca 1920
cctcggatgg?agtgacacac?ggccaggtgc?gccaggcggg?gcaatttgcc?tttgtgcgag 1980
tgtatgagag?tggacatgag?gttcccttct?atcaaccctt?gcttgcgctg?gagatgtttg 2040
agcgcgtcat?tggcggcaag?gatgtggcga?cgggaaagat?tcccatctcg?tcgagtttac 2100
agacggtggg?cacgcccaag?agttactacc?gggagggcaa?cagcacgatt?cagtgggagg 2160
tgttggattc?tctggcgacg?tacaacacaa?ccacgaatgc?tccgaacccg?gtgagccgga 2220
ggctgaagcg?gatgggacca?gctttgcggt?ttcagatgta?gatctgaagt?acctgcgatt 2280
gtgcattgaa?gtacattgtt?cagtgcaatt?accgatcatg?gctagctgtg?ccgcccaaag 2340
ggggaagcta?caatctaaac?gccatatctt?tcgatgcaga?caccttacga?gccatgaaat 2400
gccattttat?gatcaggcta?tctactgccg?gtgattttat?gtagtgttgg?aaattttctg 2460
ttcaatcgca?acccaaagga?accaactggc?tgtaaaagac?acaacataac?tcgccagagc 2520
caaactgtgc?gaagatatga?gaagcaaagt?ttaaacgctc?ccaagccatg?gtttccctgt 2580
caagcctcat?tcactctatt?ggcttcagct?gaaagaagag?gataaacatt?caggggtaga 2640
accagacaaa?atctggtctg?gcggggatct?ggtggggacc?cgaatccaag?ttgcgttagt 2700
ttgaggcatg?gatcgacacg?cgacgaacat?gcagtggagg?gccgctatcg?ctgttttgac 2760
tcgacatcgg?accaaaacca?aggaaattcg?tattcatcga?tcgatagttc?ttctcatctg 2820
gcaaggcatg?gatccgtctc?cccacttcag?ccggtacctc?ccggcacaac?aaaaggagca 2880
tggcagcctg?atttcctgcg?ttccaactgt?tcgtcggttg?atctccctga?tcaagtccag 2940
<210>6
<211>4550
<212>DNA
<213〉aspergillus niger
<400>6
tgaaccatca?ggtgggacca?cagagcccac?cgtccagctc?aaggcagctc?tctattcgaa 60
gaaagaggta?ctggatatat?cgggtacttc?tagctccagg?tcgtgaagcg?ttgcgagata 120
cacaaatact?gttggcgatc?gaatgggacg?aacatgtgaa?tgttagcacc?agaagtggat 180
ggtagctacg?aacgatggga?ggcggaggtc?cgagtgtacg?atagagctgt?ggagatagat 240
tcgtatataa?tagagatata?tattcattgc?attgcattgc?tgtggtagaa?aacttgtttt 300
ggatcgcatg?aattgctggc?ctgaatgatc?aggtcagaag?acgccgcagc?tccgccggac 360
aagagccaat?cagagggcgc?caatcggggt?gtccgcccgg?ttcccttttc?agtgtctgtc 420
actgcagctc?gcctgacttc?agttcctttt?ctccttcctc?acggtcctcg?tcattcgccc 480
ctctctgttg?cagtctctct?tgttgggggg?tcttgtgaat?gtcttgcgtc?tggctccaca 540
tccacaaaag?gagcctactg?tctgtcgcta?cgaacaattc?tgttgcgagg?gccgctgcct 600
ctacctccgc?cgcgccgccg?ccgccgtcat?cgccgccgcc?tggttctaat?acttattcgc 660
ctctttatcg?ccccatcacc?aatcccatcg?gatttacttt?gtcgcctgcg?aggtcactag 720
tttctcgcaa?tcctaaattt?cctgcctatc?ggcgctctag?tcgacacttt?tctttgtgcc 780
cggccgctgc?aacgcccggt?gtcaccacga?gcatctgccc?tggtcaggcg?cccgtccgct 840
ctctcagctc?gctcattata?cactctacga?gaccccgtgc?tatacgtatc?cgtaccgacc 900
agatggattt?gaatggagac?gcaggcgcca?agcgcaagcg?cagctccatc?accacacccg 960
ccgaacggcc?cgtaaagcac?cttcgccccg?aatcgagcgc?attgacaccc?ggggattcga 1020
cgcctgccaa?tgggactgta?tacgatgtgg?aggatgatga?agatgcgagt?cgtctgctgc 1080
ctgtagggcc?tgctcaggcc?gactcaccgg?aatggcaagc?taccatagag?gaggttgtga 1140
aaagcgtagt?gtctatccac?ttctgtcaga?cctgctcctt?cgacacggag?ctgtccatga 1200
gtagtcaggc?tactgggttt?gtggtagatg?cagagaatgg?gtacatattg?acaaaccgac 1260
acgtggtttg?cccgggacct?ttctggggat?actgcatctt?tgataaccat?gaggaagtat 1320
gttgtacatt?ccacatgtgg?atcgccttat?gacagtgatg?ctgatttgaa?ttggttacta 1380
gtgcgacgtt?cgtcctgtgt?atcgggaccc?tgttcacgac?tttggaattt?tgaaattcga 1440
cccgaaggct?attcgatata?tgaaattgag?ggaactgaaa?ctgcagccgg?atgcagctaa 1500
agtgggatca?gaaattcgcg?ttgtgggtaa?tgatgcagga?gaaaaactga?gtattctgtc 1560
tggtgtcatt?agtcggctgg?atagaaacgc?gcccgaatac?ggcgatggct?acagtgactt 1620
caatacgaat?tacatccagg?ccgccgcagc?agctagcggt?ggaagttccg?gcagtcctgt 1680
agttaacatt?gatggccatg?cgattgctct?gcaggccggt?ggtcgtgcag?acggtgcagc 1740
gacggattac?ttcctccctc?tggaccgacc?gctacgcgca?ctggaatgca?tccgtcgcgg 1800
agagcctgtc?acgcgtggaa?cgattcagac?gcagtggatc?ttgaagccgt?tcgacgagtg 1860
tcgtcggttg?ggcttgacgc?ctgagtggga?ggcgaccgtg?cgtaaagcag?cgcccacgga 1920
aaccagcatg?ctggtggccg?agatcatcct?gcctgaaggc?ccggcggacg?gaaagctcga 1980
ggaaggagac?gtgctcctgc?aggtcaacgg?ggtgcttctc?acccaattca?tccggttgga 2040
tgacatcctg?gattcgagtg?ttgggcagac?agtgcgtctg?cttgtccaaa?gaggcggtca 2100
gaatgtggag?attgagtgcc?aggttggcga?cctgcatgcc?atcacgcccg?accggttcgt 2160
gacggtggct?ggaggcacgt?tccataacct?gtcttaccag?cagtcgcggc?tgtatgccat 2220
cgctactcgc?ggtgtctacg?tctgcgaggc?tgccggctcc?ttcaaactgg?aaaacacact 2280
gtcaggatgg?atcatcgact?cggtggacaa?gcggcccact?cgcaatctgg?atgagttcgt 2340
ggaggtgatg?cgaacgattc?ccgatcgttc?gcgcgtggtc?atctcgtatc?ggcatattcg 2400
cgatctccac?acccgaggca?ccagcatcgt?ctatatcgat?cgacactggc?accccaagat 2460
gcgactggct?gtgcgcaacg?acgacaccgg?tctgtgggac?ttttcggacc?tcgcggaccc 2520
tatcccagct?cttcctccgg?ttccgaggaa?agccgatttc?attcaactcg?atggtgttag 2580
ccagcctgct?gcggccgaca?ttgtgcgcag?cttcgtacga?gtatcctgta?cgatgcccct 2640
gaagctggac?ggctaccccc?aggccaagaa?gactgggttc?ggattggtcg?tcgatgcaga 2700
gaagggtttg?gtggttgtgt?cgcgagcgat?cgtgccgtac?gacctctgcg?acatcaacgt 2760
cacggtggcc?gactccatca?tcgtgaacgc?taaagtagtt?ttcctgcatc?cgctccaaaa 2820
ctacagcatc?atccagtacg?acccaagcct?ggtgcaggcg?ccggttcaga?gtgccaaact 2880
cgccaccgac?tacatcaagc?agggacagga?cacgatcttt?gtgggattca?accagaactt 2940
ccggattgtc?gtggccaaga?ccgccgtaac?cgacatcacc?actgtttcta?ttccagccaa 3000
cgcgtccgca?ccgcgctacc?gcgcgatcaa?cctggacgcc?atcactgtgg?acaccggact 3060
cagcgggcag?tgttctaacg?gtgtcctgat?tggcgaggac?ggagtggtgc?aggcattgtg 3120
gttgaactat?cttggagaac?gcacatctaa?ttcgcataag?gatgtggaat?accatctagg 3180
atttgcgact?ccatctcttc?ttcctgtcct?gtcgaaggtg?cagcagggag?agatgccgga 3240
attgcggatt?ctgaacatgg?agagctacgt?ggtccagatg?agtcaagctc?gtatcatggg 3300
cgtgtcggag?gaatggatcg?agaaggtgac?gcaagctaac?ccatcgcggc?atcagctctt 3360
catggtgcgc?aaggtcgatt?gcccaccgcc?tgggttcaac?tcagcggccg?acacgttcga 3420
ggagggtgat?atcatcctga?ccttggacgg?acagctgatc?acccgcgtct?cggagttgga 3480
tatcatgtac?gagaaggata?cgctggaagc?cctgattgtt?cgaaatggac?aagaaatgcg 3540
gatccaggtg?ccgactgttc?caacagagga?cctagagact?gaccgtgcgg?tcgtgttctg 3600
tggtgctgtg?ttgcagaaac?cacaccatgc?ggtccgtcag?cagatttcta?agctacacag 3660
cgaagtctac?gtcagcgcaa?gagtatgctc?ctcacccctt?aaccactgcc?atcaagtaac 3720
taaccaccct?atcccttcaa?cagagtcgcg?gatccccctc?ctaccaatac?ggcttggccc 3780
caaccaattt?catcaccgcc?gtaaacggcg?ttccaacccc?gaacctggac?cgcttctccg 3840
aagaagtgag?caaaatcccc?gacaacacat?atttccgcct?acgggcggtg?acattcgaca 3900
atgtgccgtg?ggtagtgacc?gtgaagaaga?acgatcatta?cgtatgccac?aacccctccc 3960
tctttacctc?caccaaattc?agagaatgtg?gagactaaca?caataatctc?cagttcccca 4020
tgtccgagta?tatcaaagac?cagtcccagc?cttccggttg?gcggaccgtg?tctcacgaca 4080
aggataaata?taaagacggc?attgcaccgg?atgctgcgaa?cttgaacccg?gatgctatgg 4140
acgaagggtt?tgatggagtc?agtgatattg?agccggattt?ggagtgattg?aaggcggact 4200
gtatagtatt?ctgtgatgag?catggctgtg?ttagatgtgt?atagcagaca?tggcttggaa 4260
tagtagaaaa?agtgaaaaat?gggaaaatga?tagagattaa?atcggttcgc?atatacgaag 4320
ttgtagatgg?atgtattgtt?tcggatgttt?acgtagtacg?tagtggctac?tctatcgagg 4380
tgtgatgata?gcattagtct?ttgatttgtt?ttcgtcccat?ctgcacatgt?actccgtata 4440
tgagaagtat?gttgctcgac?aacccaagtc?tgaaagtatg?aatgaacgaa?tcgacaacac 4500
acatgaagat?aattttatcc?aagcaaaaga?agccccattt?catcttattt 4550
<210>7
<211>2660
<212>DNA
<213〉aspergillus niger
<400>7
gaatgcgctg?aaaaaaatgc?tgttgatagc?ctaaggtagt?cacccgacgg?gcttgtgatt 60
ggaggaaacc?gcaatgacgc?tggtcccgtg?ccatgagctg?actcagctgg?ctgactcaac 120
gcgtgacttt?ctgcaaaggg?aaggcaccgg?catgtgattg?gtcgccttcc?gttcctgcta 180
tcgaggcgtc?atcgcctaca?gcccatcgag?tacacctcct?cttctctcct?ctctccttcc 240
ttccttcctc?tccatcctct?tctgggtttc?cattgatcac?ccagtagctg?gtattttctg 300
agctacttgc?tttttctatt?ttgatacttt?tgtgtccgta?agttcacttt?atgccctctg 360
acccccccct?tgataacccg?tgctgataag?ctccctgccc?aggtaccgta?ccttccagac 420
cgcaaggtac?ccatcctctg?cctactcatc?ccatcaccat?ctcaattcat?accggccccg 480
tagggtttca?gcaacaatga?gagtccttcc?agctgctatg?ctggttggag?cggccacggc 540
ggccgttcct?cccttccagc?aggtccttgg?aggtaacggt?gccaagcacg?gtgccgacca 600
tgcggccgag?gtccctgcgg?atcacagtgc?cgacgggttc?tccaagccgc?tgcacgcatt 660
ccaggaggaa?ctgaagtctc?tctctgacga?ggctcgtaag?ctttgggatg?aggtggccag 720
cttcttcccg?gagagcatgg?atcagaaccc?tctcttttcc?ctccccaaga?agcacaaccg 780
ccgtcccgac?tcgcactggg?accacatcgt?ccgcggctcc?gacgttcaga?gcgtctgggt 840
cactggtgag?aacggtgaga?aggagcgcga?ggtcgatggc?aagctggaag?cctatgatct 900
cagggtcaag?aagaccgatc?ctggctctct?tggcatcgac?cccggcgtga?agcagtacac 960
cggttatctc?gatgacaacg?agaatgataa?gcatttgttc?tactgtaagc?acaccttggt 1020
tcaagatcac?gctttttata?tgctctggat?atctaacgca?acttagggtt?cttcgagtct 1080
cgcaatgacc?ccgagaatga?tcccgttgtt?ctgtggctga?acggtggccc?tgggtgctct 1140
tccctcaccg?gtctcttcat?ggagcttggc?cctagcagca?tcaacaagaa?gatccagccg 1200
gtctacaatg?actacgcttg?gaactccaac?gcgtccgtga?tcttccttga?ccagcctgtc 1260
aatgtcggtt?actcctacag?taactctgct?gtcagcgaca?cggtcgctgc?tggcaaggac 1320
gtctatgcct?tgcttaccct?cttcttcaaa?caattccccg?agtatgctaa?gcaggacttc 1380
cacattgccg?gtgaatctta?tgctggtcac?tatatccccg?tcttcgcttc?ggagatcctg 1440
tctcacaaga?agcgcaacat?caacctgcag?tccgttctca?ttggcaacgg?tctcaccgac 1500
ggatacaccc?agtacgagta?ctaccgtccc?atggcctgcg?gtgacggcgg?ttacccagct 1560
gtcttggacg?agagctcctg?ccagtccatg?gacaacgctc?ttcctcgctg?ccagtctatg 1620
attgagtctt?gctacagttc?cgagagcgct?tgggtttgtg?tcccggcctc?catctactgt 1680
aacaacgccc?tccttgcccc?ttaccagcgc?actgggcaga?acgtctatga?tgtccgtggt 1740
aagtgcgagg?atagctctaa?cctttgctac?tcggctatgg?gctacgtcag?cgactacctg 1800
aacaagcccg?aagtcatcga?ggctgttggc?gctgaggtca?acggctacga?ctcgtgcaac 1860
tttgacatca?accgcaactt?cctcttccac?ggtgactgga?tgaagcccta?ccaccgcctc 1920
gttccgggac?tcctggagca?gatccctgtc?ttgatctatg?ccggtgatgc?tgatttcatt 1980
tgcaactggc?tgggcaacaa?ggcctggact?gaagccctgg?agtggcccgg?acaggctgaa 2040
tatgcctccg?ctgagctgga?ggatctggtc?attgtcgaca?atgagcacac?gggcaagaag 2100
attggccagg?ttaagtccca?tggcaacttc?accttcatgc?gtctctatgg?tggtggccac 2160
atggtcccga?tggaccagcc?cgagtcgagt?ctcgagttct?tcaaccgctg?gttgggaggt 2220
gaatggttct?aaagacgtgc?taccaccgca?tatagacttt?ctggtcattt?cggtgacact 2280
gcagatatgt?ttcttaacga?tagtttgagc?atgcttgtca?atgcccacta?gtcccgatcc 2340
ttatatgttg?catggtatct?atgagttttg?tcactatagt?gcattataca?tttgtacttc 2400
gtatgagaat?gaatcgatcg?catttacacg?catataaata?gtacccaaac?cgtctggaca 2460
tgaataaggc?ccggccagta?gtttacatac?agtgtagaaa?actaggcgta?cagacgtctc 2520
agtacgtaat?caatggttaa?aaaaaccact?cccatagaag?ccaagccata?agagcctact 2580
catgtagttc?gccactgaac?gcacccgtat?atcgtaaacc?agcagaaaga?gaaaaggaaa 2640
attgaggaaa?ggacgatttg 2660
<210>8
<211>1680
<212>DNA
<213〉aspergillus niger
<400>8
aaaacgtgcg?cactgcaccc?actcgttccg?gctggggtct?agaaatctgg?acggtcccag 60
gcagatcggt?gcctgggcaa?aaccttgata?aaaatagctt?gttcgatctt?gagttagaca 120
gccaattgta?tactcactag?agacacttga?tgattcagtc?tgtgacgtac?gtgcacctcc 180
acactccgtc?gatggattat?gtgtccccgt?gggcacgcgg?agatcgggga?catcagtcga 240
gaaacttgcc?taatctagtg?acaagcagaa?aagtcaaagt?catccgcatg?cgacttgcag 300
atcatctaga?gggatataat?aaagtcgtgc?gtttatgacc?ttgcaggaaa?cgacccgcct 360
cctcctgcct?ctttattatc?gataccctct?gccactagcg?tcgtacatca?cacttcacaa 420
tccattctcc?tctcattcat?catgaagttc?acaaattatc?tcttgacgac?tgcaacgctc 480
gcaagcagtg?tcctagcggc?tcctgctccc?cgcaccggtt?tggaggacag?actccgtgcc 540
cggtcattgc?agcgtcaatc?acatcctctg?gcacctattc?cacttgacac?atccaccaaa 600
gagaattcca?gactcctcga?agccgacgag?aataccaccc?atgttacata?cagcagtaac 660
tgggcgggcg?cagtgcgcga?gcaaccacct?ccgcaaggca?cgtattctgc?cgtgtcggca 720
acctttcgtg?taccagaacc?cacggcgcaa?ggggggagcg?gaacgcaggc?tgggtcggcc 780
tgggtcggga?tagatggcga?cacatacagc?aacgccattc?tacagacagg?agtcgacttc 840
tacgtggaaa?acgggcagac?gtacaacgat?gcctggtatg?agtggtaccc?agactatgca 900
tatgacttcg?acctagatgt?aagcacaggg?gacacgatcg?tcgccaaggt?ggaagccatc 960
tcgccaagtc?aaggtgtagc?cactattgag?aacatatcga?cggggaagaa?ggccacgcag 1020
acgatcagag?ccccagctgc?gacagctacc?cttgccggcc?agaatgccga?ctggatcgtg 1080
gaggatttcc?agtctggcga?ctcaatggtc?gatctggctg?gctttggcga?gatcagcttc 1140
tggggcgtgc?aagcacaagg?aggagggtct?acatggggtg?tagatgatgc?gactattgtc 1200
gaactgaagc?agggcaacga?agtgttgaca?gacgtggagg?tgcaaagtga?ttcggccttt 1260
acggtgaaat?atacgagctg?atgtgatggt?atatggtcgc?atattctcat?ccttcgacta 1320
atctttctcc?ttttggacgg?tgacataatt?tttctggttg?attttgaaaa?tgccttgatg 1380
tatttcggta?gtagttttaa?ggttgatact?tccagcatgc?gggctcggct?attgggagga 1440
accaagaagg?ctatatggcc?ctcgggtatt?cgccgcattc?taaggtcgca?tgccttctcg 1500
gctttcctta?tatatatcta?ctttccattt?ccccaacctc?attcttgatg?cgagaatcta 1560
cccacacata?cagttaatca?tgtcccgtat?ataccaacta?agccgagcat?ttcagcgcag 1620
ccaagttggc?gcgctccggc?cgcgctctct?actacccgct?cggtcatccc?gctgcggctt 1680
<210>9
<211>2590
<212>DNA
<213〉aspergillus niger
<400>9
ttacatgctc?tgtgtgttgg?taaacacgct?gtcacattct?tcatgtcctc?tggattgcac 60
gataacttta?ccgcgtctct?ccaaccggat?tgatgaaact?atcaacaggg?ccccgcatta 120
ttggcataac?cgacattttg?aaaaagtatc?gcgggcgaga?agagagcctt?tttcgacaac 180
aaacgtcggt?ctctttggtt?tgcatcgaga?gacatagata?cagttgaccg?cggcgcgaca 240
ctttttagga?gcgcagagga?cggtttctgc?ggcgatttga?tccgcaggcg?agcaaaggtc 300
taagacacct?ctgtttggaa?ctgcgcaggt?accagaactc?gaaactaatg?cgacattcga 360
gcgacgatga?tatatgtcaa?ctatatcctg?ggacttctgt?ccctcttaca?caccgctgta 420
gccacagctc?ctgattatgt?cgtggtagac?caactgaaca?gcatccccga?cggatggaca 480
aaaggcgcag?ctcccccgcc?atttactccg?atgaagttct?ggttgtcgat?gcatcacgag 540
tacaaggcgg?acttcgagca?gaaagtcatc?gatatctcga?cacccggtca?ccgggattat 600
ggacggcata?tgaaacgcaa?cgatgtcatg?gcctttatgc?gcccatccga?tcaggtctca 660
aagatcatct?tctcttggct?tgagtcggag?catgttccac?caaatgccat?cgaagatcgc 720
ggggattggg?tcgccttcac?agtcccgttg?gcccaagcac?aatcaatgat?gaagaccgat 780
ttttacaact?tccaccacct?ggaaacaaac?acaacccaaa?ttaggaccct?caagtactcc 840
gttcccgagc?aagtcgatgc?tcatctgcaa?atgatccagc?caacgactcg?cttcggccga 900
cctaagacac?aaaccagcct?accgagcctc?atgccagtgt?cggttaacat?tgatgaaata 960
agcgaagact?gcttgacagg?cgtgacgccc?atttgccttc?gccagctcta?tggtttacct 1020
agcaccaagg?caagccccga?ctcgagaaac?gtcctcggaa?tttccggcta?tctggaccag 1080
tacgcgcgct?acagtgacct?cgacgagttt?ctagccgtat?actctccaaa?cagcgtagac 1140
gccgacttct?ccgtagtatc?gatcaacgga?ggccaaaacc?cacaaaactc?acaagaggga 1200
agcacagagg?ccagtctcga?catccaatac?gccctctcca?tggcatttga?cgctaacgcg 1260
actttctaca?ctaccgccgg?acgtgcgcca?tccgtctcag?actcgggtac?ggtgagcacc 1320
gacggctcga?ccaacgagcc?gtatctcgaa?cagctccagt?atctggtggg?tcttccggac 1380
gaggatcttc?ctgcagtgct?tagcacgtct?tacggcgagg?atgagcaaag?tctgccggag 1440
gaatacacag?aagccacgtg?caatttattt?gcccaattag?gtgcacgcgg?ggtctcggtg 1500
atcttcagca?gcggagactc?gggcgtcgga?ggatcgtgtg?tatctaacga?cggaagccag 1560
aggacccgct?ttcagcctat?cttcccggcg?tcgtgcccgt?ttgttacatc?cgtgggtggg 1620
actgagggcg?tcgggccgga?aaaggctgtg?gacttttcga?gtggagggtt?ctccgagcgc 1680
tttgctcgcc?cgtcgtacca?gaatgcgagt?gtggaagcat?accttgcccg?cttaggagat 1740
aaatgggatg?gattgtataa?tccagacgga?cggggtattc?ctgatgtgtc?ggcccaggct 1800
agcaactatg?taatcaggga?ccatgggcaa?tggctacaaa?ctgcgggaac?aaggttagtg 1860
gccctaccaa?gtcaacaatt?gaaaatcaaa?cgagctgata?atattacagt?gctgccgccc 1920
ctgtctttgc?agcagtcatc?tctcgactga?acgctgcacg?tctcgagcag?ggtaaaccta 1980
cactagggtt?tctgaatcct?tggctgtact?cactcgacca?gcaaggattt?acggatattg 2040
tagacggcgg?atcagtgggt?tgtgacgggt?caaatggagg?agctcttgtc?ccgtatgcca 2100
gttggaatgc?caccaaggga?tgggatccgg?ttactgggct?ggggacacct?ctgtatcaga 2160
ctctggagca?gttggcgcag?tctgcttagt?actgcggcgg?gatggcctat?tttgtgtcgt 2220
tgatgttttt?gtcccctaaa?tgtcaacgcc?attaattctt?ctcaagtgcg?attagatttc 2280
gtaaaacaga?agctggacaa?tatgcagaaa?ttagagtaca?aagctggaga?cagaaggtcg 2340
atctccagaa?tttgctaatg?gttgtggtac?tcacgtcagg?gtgctcgagc?acaccagcta 2400
actaccaact?ttacccgtta?attctaccgc?agtagtaatc?tagaaaatac?tagataagct 2460
gatcaagctt?gaaacaaata?agcttaccga?ccgagaccca?tacagcctcg?cagtacaaca 2520
acttactacg?ggtgagacat?cctcacccgt?ccgtaagatc?gaaaggatta?ctatacacgg 2580
agtaagcact 2590
<210>10
<211>3080
<212>DNA
<213〉aspergillus niger
<400>10
ggtacagtag?tgggttttag?tttggatgta?tctggagaca?tcgatgcttg?ttcgccggcg 60
ctaatttggg?gccatcgctt?agggaagaaa?aagaaaggaa?ggatttcatc?tgccgcggca 120
tttttggtca?ggcattggca?atactccaag?cagcttgcca?aagtgagaaa?tgtgcttatg 180
aataatattg?agtaatagtt?aatcaattgt?cttacaggat?aatatgggaa?tagcattggc 240
attgcgtggt?tggcaggcag?catgttgcaa?attgcaacaa?cgcgatcccg?gcgatcgccg 300
tcggactccg?ggtgggaatc?agggttggag?acccattgct?tatcaacaac?agccgacgcc 360
agtcgttctg?gggtgcattt?gcagaatctt?tggacgaatc?agccttttgt?cagtatcggc 420
cggtccgaat?tgacccagct?tgctagccgt?tggagacatg?caatgatgcc?attgtctcgt 480
ccgataagca?agtgcggcca?atccctcgtt?ccttctggct?gtctcagaaa?agttataatg 540
tccgtctcgc?ctgcctagcg?aacaattcga?actctgtgtg?tgttgtccct?ctcaaggtct 600
ccagcatgcg?ttcttccggt?ctctacacag?cactcctgtg?ctccctggcc?gcctcgacca 660
acgcgattgt?ccatgaaaag?ctcgccgcgg?tcccctccgg?ctggcatcat?gtcgaagatg 720
ctggctccga?ccaccagata?agcttgtcga?tcgcgctggc?acgcaagaac?ctcgatcagc 780
ttgaatccaa?gctgaaagac?ttgtcaacac?ctggcgaatc?gcaatacggc?cagtggctgg 840
accaggagga?tgtcgacacg?ctgttcccgg?tggccagcga?caaggctgtg?attaactggc 900
tgcgcagcgc?caacatcacc?catatttccc?gccagggcag?cttggtgaac?tttgcgacca 960
cggtcgataa?ggtgaacaag?cttctcaacg?ccacctttgc?ctactaccaa?agcggctctt 1020
cccagagatt?gcgcacaaca?gagtactcca?tcccggatga?tctggtcgac?tcaatcgacc 1080
tcatctcccc?aacgaccttc?ttcggcaagg?aaaagaccac?tgctggtctg?aaccagcggg 1140
cgcaaaagat?tgacacccat?gtggccaaac?gctccaacag?ctcgtcctgt?gccgatgtca 1200
tcacgctgtc?ctgcctgaag?gagatgtaca?attttggcaa?ctacactccc?agcgcctcgt 1260
cgggcagcaa?gctgggcttc?ggcagcttcc?tgaacgaatc?cgcctcgtat?tctgaccttg 1320
ccaagttcga?gaagctgttt?aacctgccct?cccagagctt?ttccgtggag?ttggtcaacg 1380
gcggtgtcaa?tgatcagaat?caatcgacgg?cttccttgac?cgaggcggac?ctcgatgtgg 1440
aattgctcgt?cggagttgct?catcccctcc?cggtgactga?gttcatcact?tctggcgaac 1500
cgtgagtatt?gaattcctag?acagagcttg?aatcgaagct?aattgtgtag?tcctttcatt 1560
cccgaccccg?atgagccgag?tgccgccgac?aacgagaacg?agccttacct?ccagtactat 1620
gagtaccttc?tctccaagcc?caactcggct?ctgccccaag?tgatttccaa?ctcctatggt 1680
gacgacgaac?aggtacgacc?ccacattccc?ccttccctgt?atgtagatac?taaccggacc 1740
agaccgttcc?agagtactac?gccaagcgag?tctgcaacct?gatcggactt?gttggcctgc 1800
gcggcatcag?tgtcctcgag?tcgtccggtg?acgaaggtac?acttacttcc?cctgtcctat 1860
tccttgcatc?gaaaataccc?taacagcagc?acaggtatcg?gatctggctg?ccgaaccacc 1920
gacggcacca?accgaaccca?attcaacccc?atcttcccgg?ccacctgtcc?ctacgtgact 1980
gccgtgggag?gaacaatgtc?ctatgccccc?gaaatcgcct?gggaagccag?ttccggcgga 2040
ttcagcaact?acttcgagcg?ggcgtggttc?cagaaggaag?ctgtgcagaa?ctacctggcg 2100
caccacatca?ccaacgagac?caagcagtac?tactcgcaat?tcgccaactt?tagcggtcgc 2160
ggatttcctg?acgttgctgc?ccatagcttt?gagccttcgt?gagtccattc?ccagcatcat 2220
gataatacga?aatagggtct?aatgacatct?gcagatatga?ggttatcttc?tacggcgccc 2280
gctacggctc?cggcggtacc?tcagccgcgt?gtcccctttt?ctctgcgcta?gtgggcatgc 2340
tgaacgatgc?tcgtctgcgg?gcgggcaagt?ccacgctggg?tttcttgaac?cccctgctct 2400
atagcaaggg?gtacagagcg?ttgactgatg?tgacgggggg?ccagtcgatc?ggatgcaatg 2460
gcattgatcc?gcagaatgat?gagactgttg?ccggcgcggg?cattatcccg?tgggcgcact 2520
ggaatgccac?ggtcggatgg?gatccggtga?ctggattggg?acttcctgac?tttgagaagt 2580
tgaggcagtt?ggtgctgtcg?ttgtagatgt?atactatata?tatggtatga?gattatgtat 2640
gtgatatgtg?atattatgtg?agagagaatg?gtttagactg?tgcgtcatat?acatggacag 2700
ttcattttct?cattaaacga?gcaccttcat?acggtaagga?cctcagaggt?tcctcccatt 2760
gttatgaccg?cttcccttct?ttctagagat?acatgcttcc?ccaccccgcc?tcaacgcgac 2820
cgtctacgga?caccagtcag?aagaccccaa?caacccacta?ttagtggcta?gtaaggacga 2880
catgcataat?tactccgtga?aacccccgaa?attaagcccg?acaggggcat?agagaaaccg 2940
atccaatcac?ttaacttacc?ccgcttctag?cacggcatag?ggctgagcga?tgcgatggtg 3000
caatggccac?gccgttgccg?attagccgta?gggccagttg?tgaatttccg?ggatcaccct 3060
acaacacatg?cttcatgcgt 3080
<210>11
<211>1890
<212>DNA
<213〉aspergillus niger
<400>11
gaggatgata?gtctgatggc?cattccgctt?gaggcaaagt?gtgccccaat?gtcacgcggt 60
cagctagtct?tctgcaggtc?tgcagttgga?caggggaact?tgagtgctat?tatcgccaag 120
gtgaatgttc?tctaccgctt?tgataccaga?gtgatcgtcc?cttttgccgt?cactcttggt 180
gttgcgaagc?agatgtcgtt?cgtttgcata?tgggagccga?agatccacgc?agggtgcttg 240
aaaagacata?ctgcgatcct?cccgtttcca?agaatgcttg?tacacttgaa?gtttttgtca 300
agatcccccc?gcctggccag?tcccgagcta?agcgaaatga?gctttccctc?aatgctgcag 360
acaggagaca?ccatcgcttt?ggcgccttgg?caccatcagc?caccgtcggt?cctatcatca 420
tcgccctggt?caatagggaa?cgcgtcaatt?gcgtatctgg?gtagtgttat?ctgctcgata 480
ttgcaccggc?agagcaggaa?tcgggattgg?cggatgtaga?gaaaattcag?cttcaaggag 540
gggggaaggg?agacgctgaa?atggtataaa?accacgtcca?attccctacc?agatagccct 600
catccagcag?catcaaaagc?atcttccact?cagactccaa?gcagctccca?gtccctcttc 660
aattcattac?cttccaaaca?tcatcccatc?aagatgaaga?ctactgctct?cttgaccgcc 720
ggcctgctgg?ccaccactgc?tatggccgct?cctctgacgg?ccaagcgcca?ggctgctcgg 780
gccaagcgct?ccacgaaccg?ccagagcaac?cctcccttca?agcctggcac?caacgaggtc 840
ctcgccctta?acggcaccaa?gaatgtggag?tacagctcca?actgggccgg?tgccgtcctc 900
attggcactg?gttacactgc?cgtgaccgcc?gagttcgtcg?tgcccacccc?ctccgtgccc 960
tccggtggct?cgagccgcga?ggagtactgt?gcctccgcct?gggtgggcat?tgacggtgac 1020
acctgtgaca?ctgctatcct?ccagaccggt?gtggactttt?gtgtccaggg?cagcgaggtg 1080
agcttcgatg?cctggtacga?gtggtacccc?gactacgcct?acgacttcag?cggcatctcc 1140
atctcggccg?gtgataccat?caaggtcacc?gtcgatgcca?gcagcgacac?caccggtact 1200
gccacgattg?agaacgtgag?cactggtacc?acggtcaccc?acagcttcac?gggcggtgtt 1260
gatggtgatc?tgtgtgagta?caacgctgag?tggatcgtcg?aggacttcga?ggaggatgac 1320
tccctcgttc?cctttgccga?ctttggcacc?gtgactttca?ccagctgctc?cgctaccaag 1380
gatggttcct?ctgttggccc?tgaggatgct?accatcatcg?acatcgagca?gaatgaggtg 1440
ctgacctccg?tttccgtctc?cagtagcgag?gtcgttgtca?agtacgtcta?agacgttgga 1500
tgtatggggt?tcgggattgt?tgatgccccg?atgggtgtgc?tttcgacggc?aatggtgaga 1560
tgagtgatgg?aaatgagagg?ttggtctttt?ggcccggggc?tagttttctc?ttggtactcc 1620
tgaaaagcca?atagttcaaa?tgtctttatc?ttgttagttt?gatgttatag?tttgccttga 1680
gttgatttaa?ttgaaccaac?gttggatcat?cgtatccctt?agcgcaaata?aaatattacg 1740
tacgcctttt?aaaatattat?gtatgtctgt?taaggttctg?actgttcaga?tttatgtcaa 1800
acaacagcaa?atcattggta?atccaggact?cggggatatg?agcttcagac?attcacccca 1860
ttactgcatg?actatgaccg?tgtctttagc 1890
<210>12
<211>3080
<212>DNA
<213〉aspergillus niger
<400>12
ttgttgtgat?tgctaagaga?catcacattg?ctcatatgag?tttgattgcg?actgttaata 60
ttaatgtccg?actgggagga?aatgagtggc?gttatccagg?cagctgcatg?caatactaca 120
ttcccctcac?gagggaaatc?tggccatctc?ggaaatcaat?ggtgtcatcc?gagttgattc 180
ccctcaataa?tggtcctgat?aagccactat?tgctgcagaa?cgcctatctg?tgccgttagt 240
gcatgcatag?tgtccccagt?tctttttctg?ccgattaatc?tattgccaga?cggactccgt 300
cgcgcttccg?aatgccggga?accgcggcta?agctttgctg?tagctttgct?gcaggaacat 360
ctgcatcttt?caaaatatct?tcagaggagc?cgatcgctga?gtttctcaag?agattagatg 420
aatgttcgta?cttggccgca?atataagctt?catggcggct?tcaaccttcc?atgagaaata 480
agaataaggc?tgccggggat?ggcctcaccg?tgtccctgca?tgcaagggat?gcataatgca 540
ccgtgacctg?ttccaccacg?ccggagcccg?cccgccctcc?gacggcccaa?acccactgca 600
gaatggcttg?attaagttcc?ccttctataa?ctaaccggtt?gttcctcgtc?gttgtctgct 660
ctgctctcca?cccagggtcg?tttttgcttt?tgcctcctta?accatggtcg?ccttttcccg 720
catctcggca?ggcttcgccc?ttgccgcccc?tgccctggcc?agcgtcgtcc?tggagaccgt 780
caagtctgtt?cccagcgact?ggaagctcgt?ggaggctgct?gataccagct?ccacaatttc 840
tttgtccgtt?gctctggcgc?gtcagaacct?ggaccagttg?gaggagaagc?tcctggccgt 900
gtccacccct?ggcaaggaca?cctacggcca?gttcttggat?ctggacgaca?tcaatgagca 960
gtttcctctc?gcagatgacg?ctgctgttgt?ggcttggctg?aagaaggcag?gcgtcaccca 1020
gatccataag?gagggtggtc?tgctgaactt?tgcgaccact?gtgggcacag?ccaaccagct 1080
tctcaacacc?accttctcgg?tgtacaagag?cggatctacc?cagaagctgc?gcacaacgca 1140
atactctgtt?ccggatgagc?tgaccgggtc?cattgatctc?atctcgccga?ctgttttctt 1200
tggaaagtcc?aacgctgcgc?gctcggcggc?cgtgcgtgct?tcgcagacta?ccaaggagac 1260
cagcagaaag?aagagcagta?atgtgtgcga?gtacatcact?ccggattgcc?tcaaagagca 1320
gtatagcatt?gactatacgc?ccgaggcatc?gtcgggaagt?cgtgttgggt?ttggcagttt 1380
cttgaacgag?tcggccttgt?actcggattt?ggatctgttc?acccagtact?ttgacattcc 1440
ccagcagagt?ttcactgttg?agactatcaa?cgggggaatc?aacaaccagg?agaatgatcc 1500
ggatggtgaa?gccgatctcg?atgtccagaa?catcgtgggc?atctcgcatc?ccttgccggt 1560
gacggagtac?attaccggag?gatctccgtg?agtgttccca?aagatgcaat?tgaattaaag 1620
ctaatggttc?agtccattca?ttcccgacgt?cgagactact?accgacgaga?acgagcctta 1680
cctgcagtac?tacgagtatc?tgctggccaa?gaccaacgac?gagctgccac?tggttatcag 1740
caactcgtac?ggcgatgacg?aagatgtaag?catccctgcc?tcccacacaa?atcgcctgct 1800
gacagaatag?accgttccca?ttgcctacgc?cacccgcgta?tgcaacctca?tcggcctgat 1860
gggcacacgt?ggtatctcca?tcctcgagtc?ttccggcgac?tctggtacgt?tgtaccccat 1920
atatattgca?tcaagtcccg?actgacaaat?acaggtgtgg?gcggcgcatg?catgtccaac 1980
gacggcaccg?acaagaccga?attcaccccc?atgttcccag?gaacatgccc?gtacatcacc 2040
gcggtcggcg?gcacccaaga?cgtgcccgaa?gtcgcctggg?tggacagctc?cggcggcttc 2100
agcaactact?tctcgcagcc?gtcgtaccag?tcggatcagg?tggagaccta?cctggacaag 2160
tacatctctg?cctcgacgaa?gaagtactac?gagcagtaca?ccaacttcag?cggtcgcgcg 2220
ttccctgacg?tgtctgcgtt?tgcaggttct?ccttagtatg?tatccatccc?agatgattgt 2280
atggacatct?gctaatgtcc?gacagctacg?aaacttatat?tgatggtcag?ctcggccttg 2340
tggcgggtac?ttctggcgct?agccctgtgt?ttgcggggat?cgtcgcgctg?ctgaacgatg 2400
cccgtctgcg?ggccaacaag?acatccttgg?gcttcctgaa?cccttggctg?tactcgagcg 2460
gctacaagag?cctgaatgac?attaccagtg?gcgaggcagt?gggctgccaa?ggcgatgtgg 2520
agggcgctgg?agtcattcct?tgggcgagct?ggaatgccac?gacgggatgg?gatccggcga 2580
cagggctggg?aacgcctaat?tttgccaagc?tgaaggaggc?ggttcttgcg?ttgtaagcag 2640
gaggatactg?agtggacgtg?cggagtgaag?gatatgtgca?aggcgttaac?ttataatagc 2700
ctgtgtgtgg?actatagaat?catctacagc?ccacaaccaa?ttagcttctg?catagtcacc 2760
acccttaaac?taaggataat?caattgttta?ccgctgtcag?tctcaaatcc?gtcatgtcat 2820
ggaccctgtt?cgatcaactt?gaaacaagct?taatctacca?gcggcggtga?tgaaaccgcc 2880
agcggacact?tgtttcagtt?acccgcaagc?ctgtatccag?tatgcaagcc?ctacttaaac 2940
ccttcaccac?cctgattatt?ctactctctc?tctctctcca?accacaccat?tcttttcttc 3000
attgtgccgg?tcacatccat?tctttacttt?cattctcctc?ccttctcttctcttctctac 3060
ttccccaagt?cactcattat 3080
<210>13
<211>3598
<212>DNA
<213〉aspergillus niger
<400>13
accggagcag?aggaacaagc?ggagaagctg?aaacgtatga?atgctgagta?cgagcaaaag 60
ttccctggct?tgcggtttgt?gtatgttctc?tcagtatacc?caacgacttg?tgttggtctg 120
acatatctcc?ctggcatagt?acttttgtaa?acggtcgcaa?ccgggatgtc?atcatggagg 180
agatgcgtga?gaggattgac?cggggcaatg?ccgatcgtga?ggtggaggag?attatacagg 240
tgagatggct?gtctacccaa?acacggagca?gtgctgacag?ttcgctcctt?taaaggcaat 300
gtgcgatatt?gcaaaggatc?gggcgcggaa?actggagcag?tccgctaaga?tatagttcac 360
atactgcaag?catatattta?aacaatgaat?acccttcgat?ttcagcaggc?gctgcgacat 420
ctccttgctg?aatcgctgct?ttacaagcca?tatttcggtc?catgcgattc?atctatggag 480
cactctgcct?ctgtccggaa?acaatggctg?gtaatctgca?tggaacttgg?tgattccgtt 540
agtataaagt?gaccaactag?tgccggcgaa?ttatgggaag?cctgccttgt?cttacgacgg 600
gacgatcttc?cgtcgaacgc?gtgctaccag?cattttcata?gtatgacggg?tccgtatttg 660
atttactatc?gatggtaaaa?cgcctcctct?atggggtccc?ctagcactcg?gcaggccagc 720
ttgtgagaca?acccgggagg?tcagccatta?ttaggccaat?gagagctggc?aggttggaga 780
ggttgtactt?cgacaatgtt?ggacagccat?gcaacgtcgg?acaatagctt?tgatagggaa 840
tatcctaagg?gcgaaccagg?agggataggg?gtaggtatgg?ctgtatcgat?tagtagtccc 900
tctttcaccc?agaacaaact?ctagtatata?tagtagtaaa?tgttccgcgg?atggccaatg 960
accccaaatc?atctttcatc?ccatccacgc?atgagcaaac?atgcatggtc?tgcgcctagt 1020
atgcagcata?gggacattgc?ctttggttat?cctggcatat?ccggcggctt?cattgcatac 1080
aacttcagca?gccgtggact?tggactccct?tcgtctgacc?tctaactccg?aatacgtcaa 1140
ttctgtccat?gtagacacga?atcgatcagt?cgcagtgtcc?gctgaagaac?attataccga 1200
tacagcagct?cgactggttc?agaacattgt?tcctggagcg?agctttcgtc?tcatcgatga 1260
ccactttgtc?ggcgacaatg?gagttgcaca?tgtatacttc?cgccaaacgc?tccatggtat 1320
tgacattgac?aatgcggatt?tcaatgttaa?tgtctgctcc?ccaattactc?tgttcggaag 1380
gaagcttact?gttacagatt?ggaaaagatg?gactggtctt?gtctttcgga?cattcgttct 1440
tcacaggcgc?gttgccgagc?agccatctgg?acaataccaa?cgttttgagt?ccggaggctg 1500
cacttagagg?agcaagggac?gctatacagc?ttccactgac?tattgacaat?gtttctactg 1560
aagctgcaga?ggggcggaac?gagtacatat?tcagagaggc?agtgggagcg?gtatctgacc 1620
ccaaagctaa?gctagtctac?cttgtcaagc?cagaagggac?tctggcgctc?acctggagga 1680
tagaaacaga?catgtatgag?cactggctac?tgacatacat?tgatgcagag?actaccactg 1740
tccacggcgt?ggttgactat?gtcgcagacg?cgacatatca?agtttagtga?gtggctctcc 1800
ccatcgaata?acgaagctaa?gacaacagtc?cctggggcac?aaacgatcca?gcagaaggac 1860
atcgcaccat?tgtcaccgac?ccctgggacc?tatccgcatc?cgcatacacc?tggataagcg 1920
atggacggga?caactacacc?acaaccagag?gcaacaatgc?catcgcacac?tggaatccga 1980
ccggcggtgg?ctcctatctc?tacaacctac?gtccatccga?ccccaacttg?aatttccaat 2040
ggccatactc?cccaaacatg?tccccacccc?gatcatacat?caacgcctcc?atcgtccaac 2100
tcttctacac?agcaaacgcc?taccacgacc?tcctctatac?actcggcttc?accgaatccg 2160
ctggcaactt?ccaatggaat?aacagcgccc?acggcggccg?agacaaagac?tacgtgatcc 2220
tcaacgcaca?agacggctcc?gggttcagca?acgcaaactt?tgcaacccca?cccgatggta 2280
tccccggccg?tatgcgcatg?tacatctgga?tcgagtctac?tccgtcgcgt?gatggaagtt 2340
ttgacgcggg?cattgtaatt?cacgaataca?ctcacggtgg?taagcatctc?cccagaagat 2400
ggaagtccta?atctaacaaa?ccagtatcca?atcgtctcac?cggcggctcc?cacaacgccg 2460
gatgcctcag?cgccctcgaa?tcgggtggca?tgggcgaagg?ctggggcgac?tttatggcga 2520
cggccatccg?aatcaagccc?aacgatacac?gcacaacgtc?ttacactatg?ggtgcatggg 2580
cagataatga?taaatgtggt?gtccgggact?atccttattc?tacctccttt?actgagaacc 2640
ctttgaacta?tacgagcgtg?aataccatga?acggcgtgca?cgccatcgga?actgtctggg 2700
caaccatgct?atacgaggtc?ttgtggaacc?tcatcgacaa?gtacgggaag?aatgatgggt 2760
cgaggccggt?gtttagaaac?ggggtgccta?cagatggaaa?gtacttgatg?atgaagttgg 2820
tggtggatgg?gatggcactg?taagtgatgc?acagaatagc?ttctttcacc?tttgtaatgt 2880
ccgtggtatc?ctgactaatg?gactgaaggc?aaccatgtaa?tccgaacttc?gtgcaagcca 2940
gggacgcgat?ccttgacgca?gacattgtgt?tgactggcgg?gaagaatcgc?tgtgagatct 3000
ggagggggtt?tgcgaagaga?ggattggggc?aaggagcggc?tcatagtagt?ttaaattgga 3060
tgcggagggg?gagtacactt?cttcctacgg?gatgttagtc?ttgcacaggt?cgttcttggt 3120
gagagatgag?tggagatgcc?tggtttatta?gaataggact?aattatctag?cactaataca 3180
atatcgacag?atctaaacag?taagtataaa?tctataagtt?atcacacgca?taaaccccat 3240
caccccctag?tctacttcga?aacaaacacc?acaccaccaa?catcctcatc?ctcaccaaac 3300
acccctcccc?cgcataagaa?cctaaacaac?agccctcaac?tccatactct?gcgcccccct 3360
cgccacacac?aacaacaacc?cacccacgag?cagactcacc?cccgcgtata?tcgacagcgc 3420
cagaaaccca?tacttctgca?ccagcgcccc?ggaaataggt?atcccagcca?tagcactaca 3480
ctcccagata?agatatgatt?agcaaaatcc?acccttactc?cccaagaaga?tcaattcaaa 3540
ataaatctaa?tgtgcatacc?tcaaagccgt?agcccccata?acaaccccca?ccgccaac 3598
<210>14
<211>2847
<212>DNA
<213〉aspergillus niger
<400>14
cttttggctt?gtgatcttga?ttgctagaga?tgtatatcct?cacggatacc?gccggagtgc 60
gccatttctg?gttaccttct?ctttcccttt?ttgtctcgat?cgtgaggcgg?aacgcaggat 120
gaagacacgg?cttctccatc?gcggcccacc?aaccaacaat?gtccttggac?gcccaactct 180
ccatctactg?gtcattggtc?caatgcagag?actccgtcga?gctcaaatgg?gccggccaac 240
cccgagtcgt?caggggcagc?ggcagcgacg?agctaaatta?gaccactgat?aagacgcgat 300
agtccaaagt?ctgaccgtca?cattgtgcca?ggcagataag?ttgaatcgtg?tgactggatg 360
ttggctaacg?tatggcgtct?ccggaggccc?gacggaccct?gcgcgatcgg?cggtggagcg 420
caatctaagg?acatccgcgc?ctaagatatc?tacccttcag?cagttcagcc?tagccctgca 480
gacttgtcgg?accagtgcta?tcgtgatcgg?cccccacggt?cgaatgagct?cttgtctctt 540
tccgtcagac?cctgccagtt?aatctgctat?ctactccgcg?gtaacatcgt?gcctgtctcc 600
actaaggcag?ggtccagggc?tgtatgtctt?actttgcacc?gagtcggccg?ccggttggct 660
ctgtcttggc?aattgcgaat?atcctcacgg?gcgacggacg?acacggattt?ggacggacat 720
gcggagatct?tcgtcggttt?attcctggaa?gggacatcat?ctccttccat?catgacggct 780
gccatagcgg?ggactctgag?acatttttgc?tctgaagagc?atggtcgact?tggatgatgg 840
aggagttgat?cgaggtcaat?gaggagaggc?ttgcaagtat?aagaagagac?tgctcgacca 900
gcagaatgga?tcttcttgtt?catcaaccaa?gagtccaagg?cttctttgtc?tggttctatc 960
tcttctccga?actctcttgc?ttgacattct?cgtggtcaaa?atggtcgtct?tcagcaaaac 1020
cgctgccctc?gttctgggtc?tgtcctccgc?cgtctctgcg?gcgccggctc?ctactcgcaa 1080
gggcttcacc?atcaaccaga?ttgcccggcc?tgccaacaag?acccgcacca?tcaacctgcc 1140
aggcatgtac?gcccgttccc?tggccaagtt?tggcggtacg?gtgccccaga?gcgtgaagga 1200
ggctgccagc?aagggtagtg?ccgtgaccac?gccccagaac?aatgacgagg?agtacctgac 1260
tcccgtcact?gtcggaaagt?ccaccctcca?tctggacttt?gacaccggat?ctgcagatct 1320
gtaagcttcc?ctgctcgggt?gttcgggcaa?atcgtgacta?acctggacta?gctgggtctt 1380
ctcggacgag?ctcccttcct?cggagcagac?cggtcacgat?ctgtacacgc?ctagctccag 1440
cgcgaccaag?ctgagcggct?acacttggga?catctcctac?ggtgacggca?gctcggccag 1500
cggagacgtg?taccgggata?ctgtcactgt?cggcggtgtc?accaccaaca?agcaggctgt 1560
tgaagcagcc?agcaagatca?gctccgagtt?cgttcagaac?acggccaatg?acggcctttt 1620
gggactggcc?tttagctcca?tcaacactgg?tgagtcaatc?ctacatcagc?cgggttgacc 1680
tacctgctga?ccgatacaca?gtccagccca?aggcgcagac?caccttcttc?gacaccgtca 1740
agtcccagct?ggactctccc?cttttcgccg?tgcagctgaa?gcacgacgcc?cccggtgttt 1800
acgactttgg?ctacatcgat?gactccaagt?acaccggttc?tatcacctac?acggatgccg 1860
atagctccca?gggttactgg?ggcttcagca?ccgacggcta?cagtatcggt?gacggcagct 1920
ccagctccag?cggcttcagc?gccattgctg?gtaagaaccg?ccttcattta?acacacaact 1980
tgtccacctc?tttactaact?agtgtataga?caccggtacc?accctcatcc?tcctcgatga 2040
cgaaatcgtc?tccgcctact?acgagcaggt?ttctggcgct?caggagagcg?aggaagccgg 2100
tggctacgtt?ttctcttgct?cgaccaaccc?ccctgacttc?actgtcgtga?ttggcgacta 2160
caaggccgtt?gttccgggca?agtacatcaa?ctacgctccc?atctcgactg?gcagctccac 2220
ctgctttggc?ggtatccaga?gcaacagcgg?tctgggactg?tccatcctgg?gtgatgtttt 2280
cttgaagagc?cagtacgtgg?tcttcaactc?tgagggccct?aagctgggat?tcgccgctca 2340
ggcttagatt?atccactgaa?gtggagtcta?tgatctgctg?attgatccct?cgacgatgaa 2400
ctacatgtgg?aaatgcatag?cagacgaggg?tgatggtgat?gatgttgatt?tgatgatgac 2460
ccgtacatac?ttgatgaagc?tcggtacata?tgcaaatgtg?actgtatcta?tgtgatgaat 2520
atatgtatcc?atctcatggc?ttttggctat?gagtgcagga?taaacacctg?aaccagtagt 2580
agtactttcc?cacctatatc?tactgcggtg?cctcgtccgg?cccaacatca?ccccagaggt 2640
ggccgcagag?gagtcttata?agatagctac?tatcagttac?aacacctctc?tgacagatgt 2700
gaaggagtac?aataaatcac?cgaaacacaa?attcaactaa?agtcggtaag?taataataat 2760
ttaagaccca?atccacgcaa?tgttaaacta?tctctggtgt?tgaaagatct?ctcccctggc 2820
aacacctagt?tgtgggagaa?ctgtgtt 2847
<210>15
<211>2899
<212>DNA
<213〉aspergillus niger
<400>15
gcccaggtga?agaccggaca?ggaagcggat?aggtacggga?cattttctaa?tctacccgcg 60
atcgggacat?ggctaaccaa?gcatatagac?tcgaattcta?ccggtaaatc?aagtatggga 120
cgtgcatcag?gctggatatc?ggattacgca?aggcgaacag?ggggaccgtt?agctgtatta 180
tcaacatcta?ggctatttca?tattaggaca?acgactgacg?cattgggtat?tccgctgggg 240
tagtcttatc?ggttggggcc?aagtaccttg?tagaactgta?acccacgtta?ataccgccac 300
ttggctgggg?cggtgattta?gcatatgtaa?gctccagttg?gacggctacc?cgagcttccc 360
atgatctaca?ggagtacgtg?tctggctgtc?tgctgcctac?ttggtagaca?ggtcagcgat 420
aggtagatag?gacctgtccg?cagctgttgg?ctagtttggt?aaggcggttg?cgctagtttg 480
aagtaggcag?gcaccgggaa?cctaaggcgg?tcttacatca?tcacccgcgc?tcggattcgc 540
gtgatccgac?catcacgata?aggcctcagg?tagcaaggag?accttccaga?cagctctgaa 600
tgagactcaa?aggtagatat?aatgatggaa?agataggata?gctagatcag?gcttattgta 660
cctgatcgtt?aagagcctag?agaagatgta?cctggaagac?ctggcagcta?caatcacctg 720
gagcgataac?ccgtgacgat?ccccttgcca?aatgacgcag?ccgggctggc?caaccattgg 780
ctgcgacctg?gcaggtcgct?ccgcaaccag?cgccgcccgg?ctccaagtca?cccgcatcac 840
tcttccctac?ccccagacct?cctcttttcc?cttgctatcc?tccatctctt?cttcatcgtt 900
ctttgtctct?atcatcattt?tctattcata?cgtgcatcat?tcagtcgttt?ggcccagtcc 960
atcatatccc?gctgggtagc?cgtttccgcc?gtcgcccatc?atgaagtcag?cctccttgct 1020
cacagcatcc?gtgctgttgg?gctgtgcctc?cgccgaggtt?cacaagctca?agcttaacaa 1080
ggtgcctctg?gaagagcagc?ttgtgagtgt?ggtctttcac?tgctttgttt?tttttagcta 1140
gttagcttca?aagaagctcc?agaaccattc?aaagctgatt?tcgtggtcta?tagtacacgc 1200
ataacatcga?cgcccatgtc?cgcgctctgg?gccagaagta?catgggtatc?cgcccgtcca 1260
tccacaaaga?gctggtcgag?gagaacccta?tcaatgacat?gagccgtcat?gatgttctgg 1320
tggacaactt?cctgaacgca?cagtgtatgg?agataccgtc?ttcttatggc?tgcaactgct 1380
gacccttcct?gccatagact?tctctgagat?cgagctgggt?actccccccc?agaagttcaa 1440
ggttgtcctg?gacactggca?gctcgaacct?ttgggttcct?tcgagcgaat?gcagctctat 1500
cgcctgctac?ctccacaaca?agtatgattc?gtctgcctcc?agtacgtatc?acaagaatgg 1560
cagtgaattc?gccatcaagt?acggctctgg?cagccttagc?ggattcattt?ctcaggacac 1620
cctgaagatt?ggcgacctga?aggtcaaggg?acaggacttc?gctgaggcga?ccaatgagcc 1680
tggccttgcc?tttgccttcg?gccggttcga?tggcattctc?ggcttgggtt?atgacaccat 1740
ctccgtgaac?aagattgttc?ctcccttcta?caacatgctt?gaccagggac?tcctcgacga 1800
gccggtcttt?gccttctacc?ttggagatac?caacaaggag?ggtgacgagt?ccgtggcgac 1860
cttcggtggt?gtcgacaagg?accactacac?cggcgagctg?atcaagattc?ccctccgtcg 1920
caaggcttac?tgggaggttg?agcttgacgc?cattgctctt?ggcgatgatg?ttgctgagat 1980
ggagaacacc?ggtgtcattc?tggacactgg?tacctccctg?attgctctgc?ctgctgacct 2040
ggctgagatg?atgtaagtcg?aattcttcgg?attcctgggt?tgaaaagaaa?tgctgctaac 2100
aaccttctag?caatgctcag?atcggtgcta?agaagggctg?gaccggccag?tacaccgttg 2160
actgcgacaa?gcgctcgtcc?ctgcccgatg?ttactttcac?ccttgccggc?cacaacttca 2220
ccatctcctc?gtatgactac?accttggagg?tgcagggctc?ttgcgtcagt?gccttcatgg 2280
gcatggactt?ccctgagccg?gttggtccct?tggccatttt?gggcgatgcg?ttcctgcgca 2340
agtggtacag?cgtgtatgac?ctgggcaaca?gcgctgttgg?tctggccaag?gccaagtaaa 2400
ttagttctgc?gggttgatgt?ggtatctatg?atgcagctgk?tgctgtcatt?attgcttctt 2460
gtagcttgat?ctatgatttt?tgcagacgaa?cacacgtgat?gttgtgaatg?gttttcctca 2520
tgtttgcagc?ggttgccgga?tagattctag?ggatcttcaa?tggaaagccg?gtgatattat 2580
ttgaccttta?tttgggcact?gagaatcttg?actgtatgaa?atatgatagt?aacaccttaa 2640
acatgaatgc?aaatggcgta?aaccgtgtga?tgcagtcaca?ataaccagca?accgcggtac 2700
cagccgaagt?ctgggccggc?gagtctcgcc?ccgcacaggc?caggcgccaa?acccaagcag 2760
cgctcttggc?agccaagcct?tcttcatcac?gctctcacca?cctcctccat?ccaggctttc 2820
tctctgctcg?gtctttgttt?catcatcctc?ccacgcctgc?ccttctattc?aaccgctctt 2880
cgatcttcat?atccgatcg 2899
<210>16
<211>2738
<212>DNA
<213〉aspergillus niger
<400>16
gaggcatgag?gcatttctga?ggcccgctac?tccgcattct?gcagcatatc?gtctctgcgt 60
aggggaggtc?gaaaccagct?gtaggactcg?gcttcggtgt?atctgtaccg?actgactaga 120
aatcgctcaa?tcgtgtagta?tagctgtctc?tttgttcctc?acaacatgtc?tacgatatgc 180
tattaaaaaa?agcagaagat?ggagtcagag?ccacccggtt?agggccgggc?cgcccgggag 240
gagaacaaaa?tacgggacag?aatctcagtg?atgggggaga?agagagagtg?gcgacctgac 300
aattcacaca?cgacacgaat?aatagccgaa?actaacaaga?taaatcacat?cacatcatga 360
agaagacctg?cgtaatgatg?ataagcaatc?ccaccaataa?tacaatgcca?ttgatagtgg 420
ctgacctgaa?gcaattcggg?gaggagacgc?caagctcgac?gatcaccgga?gcttgaaaga 480
ccaacgagac?aagatgacag?gcccgtcgca?ccacgccact?aactgcccta?acagaaatcg 540
gcctgaatag?tgcgacgagt?gtcccggttc?tgggcctcca?cgataagata?agtcatgggc 600
ttatcgcgtc?atcggcgccg?atctcgcgat?cagctgaaac?caatcattca?atcaatttgc 660
atcacccgac?tgggggcgag?atttcagggc?cagctgaaac?ggtcggctgc?cgagattgtc 720
agtggatgat?gaatgttatg?ctggaagaga?gggggagaat?gacgtctcaa?ttctgggtca 780
cttactagtt?gactagccac?ctagtattta?gctgctagct?agggattcgg?tttaaaagcc 840
tggtggtttc?tctcttcttc?tcgtcatttt?ctcttcatct?catacccatt?cttcaaaact 900
cctccacttt?gatcaattat?cctccatcat?ggctaccaaa?atcaagctca?tccccaatct 960
caactacaag?cgctcaggca?ccaagtccta?cgtgcacttg?atgcgcaagt?accgcttcca 1020
tcccaccaag?cctggtccct?acactctcag?cagctccatc?caacagaccg?gtcgtccgta 1080
cactgaaaag?cccatcgggg?gtcgggccca?tatccggcag?ctggtgcgga?agaagagcac 1140
caccagcgat?gaggttggcg?aggttccggc?cgaagatgtg?cagaacgact?ccatgtatct 1200
ggcgaccgtg?gggatcggaa?ccccggcgca?gaacctgaag?ttggactttg?acactggttc 1260
agctgatctt?tgggtacacc?cccattatga?aagacctaat?atggaaacga?gcgtcactga 1320
cagatgtagg?tctggtccaa?caaactcccc?tcaacccttc?tatccgagaa?caagacccat 1380
gcgatcttcg?actcgtccaa?atcgagcacc?ttcaagacct?tggaaggtga?atcctggcaa 1440
atctcctacg?gagatggatc?ctccgcatca?gggagtgtgg?gcaccgacga?cgtcaacatt 1500
ggcggcgtag?tcgtcaagaa?ccaagccgtt?gagctggcag?agaagatgtc?cagcacattc 1560
gcccaaggcg?aaggggacgg?attgctcggt?ctagcattca?gcaacatcaa?cacggtacag 1620
ccaaagtccg?tgaaaacgcc?cgtcgagaac?atgatcctgc?aggatgacat?tcccaagtcg 1680
gctgagctgt?tcacggccaa?gctggatacc?tggcgggaca?ctgatgacga?gtcgttttac 1740
acctttggct?tcattgacca?ggatctggtg?aagacggcag?gtgaagaggt?ctactacacc 1800
cctgtcgata?acagtcaagg?cttctggcta?ttcaactcga?cctccgcgac?ggtaaatgga 1860
aagaccatta?accggtcggg?taacaccgcc?attgctgata?ccggtacgac?gctggccttg 1920
gtggacgatg?acacgtgtga?ggccatttat?agtgcaattg?acggcgccta?ttatgatcag 1980
gaagtacagg?gctggatcta?tccgaccgat?acggcgcagg?ataagctacc?cactgtgtcg 2040
tttgccgtgg?gtgaaaagca?gttcgtggtg?cagaaggagg?acctggcgtt?ttcggaggcg 2100
aagacgggct?atgtctatgg?aggaatccaa?agtcgtggtg?atatgaccat?ggacatcttg 2160
ggagacacat?ttttgaagag?tatttatgct?gtaagtgcat?tgctgttggc?gttaaggggt 2220
gatatcgaag?ctcactaact?ggattgcaga?tctttgatgt?cgggaacctg?cgctttggag 2280
ccgtccagcg?cgaggagttg?cgccagagcc?tgaagtcgga?gtagacgagt?ggctgaatct 2340
atcatggttt?gatgatgtta?tgtatttgca?tgtcccgttt?ttttggttaa?atcctagtgg 2400
cttttgagcc?ccgaagtatg?tacgcagtaa?atagcagtgc?aatatagtac?tccgtacctt 2460
gttatcagat?gctctggttt?gaagcacaaa?ggaagccatc?agtctcccaa?tcagagcttc 2520
cagcccgccc?cgtccttcca?tttccacaac?ctcagcgcca?tgaaacatgc?catccctgct 2580
cctaccataa?ccgccgcaaa?aagctgcccc?ttccagaaaa?cagcatgttc?cagatccaac 2640
aacgccccgg?caataggatt?tccaatgaga?atgccaagcc?ccgcgaacac?gaaagacatg 2700
cccatccacg?tccccacaac?agccatgtct?ggacacaa 2738
<210>17
<211>2349
<212>DNA
<213〉aspergillus niger
<400>17
cgcgcactaa?ccctccacgt?attccaatat?accaaatctg?cccaaagcgc?cagccagctt 60
cctcaagcct?tgcggtcaga?taaggccctg?tacctagcta?gttgccgctg?ctcccggcgc 120
tgggccaagc?cgtcggacgt?ccgtcccccc?tctttccccc?tcctctcccc?tctccactgg 180
tggaacgatg?tctggctgtt?gccatcgttc?tcagaagcaa?cgccccctgg?atcgggtggc 240
tgtcgtacta?ttgcatgttc?gtccgcgcta?ctaggaaagt?ttttttccca?cccggagtat 300
ccgtgtttag?tccgcgggct?ggctgaccgg?ctagctggcc?gtgccagttg?ggtaaggttc 360
caagggagga?ccttactagg?tagaaacggg?atccaacaat?gaggggaaaa?gggcggatat 420
ggcttgccgg?gggttcattg?cggcctggac?gaagaaaggg?agatgatcac?taatgcaaca 480
caatcttggc?ttgcaaggaa?ttgcgctcca?accagaatgt?ctctgcgtag?ggatgccaat 540
tcgtgcgggc?catgctggat?ggatagtacg?ctgctccact?ctcgctcgac?cttttgcagt 600
ccacaatcgt?ttccccgtat?cgttgggcgg?gggcgttttt?ctgcagctat?ggttgctgct 660
gccccgacgg?tgaacctttc?tgcatccccg?gttttagtcg?attttagttg?gcgggcctgg 720
agattaaact?ccgtcggacg?aagaggagca?gtggtgtcat?cgtcggcgga?ttgcatgcta 780
tcggaagagc?atggaagagg?gaaaacatca?acttcatttg?caaaacgctc?gagcataaat 840
agaggcctgg?attccgccgt?tctggtgtct?tttcttcttc?atccagcatc?gcaagtctct 900
caagcatcgc?ctggttcgtt?cttctcactc?ttccaccacc?agccttgtca?ataagttagc 960
tcttcatctt?ttcgaagaaa?ccaattctcc?aaacgtcaaa?atgaagttct?ctaccatcct 1020
taccggctcc?ctcttcgcca?ctgccgctct?ggctgctcct?ctcactgaga?agcgccgtgc 1080
tcgcaaggag?gcccgcgccg?ctggcaagcg?ccacagcaac?cctccctaca?tccctggttc 1140
cgacaaggag?atcctcaagc?tgaacggcac?ctccaacgag?gattacagct?ccaactgggc 1200
tggtgccgtc?ctgatcggcg?acggctacac?caaggtcact?ggcgagttca?ctgtccccag 1260
tgtctctgct?ggatctagca?gctccagtgg?ctacggcggt?ggctacggct?actacaagaa 1320
caagagacaa?tccgaggagt?actgcgcctc?cgcttgggtt?ggtatcgacg?gtgacacctg 1380
cgagaccgct?attctccaga?ctggtgtcga?cttctgctac?gaggatggcc?agacttccta 1440
cgatgcctgg?tacgagtggt?accccgacta?cgcctacgac?ttcaacgaca?tcaccatctc 1500
cgagggtgac?accatcaagg?tcactgtcga?ggccaccagc?aagagcagcg?gtagcgccac 1560
cgttgagaac?ctgaccactg?gccagtccgt?cacccacacc?ttcagcggca?acgtcgaggg 1620
tgacctttgc?gagaccaacg?ccgagtggat?cgtcgaggac?ttcgagtctg?gtgactctct 1680
tgtggctttc?gctgacttcg?gctccgttac?cttcaccaat?gctgaggcta?ccagcgacgg 1740
ttccactgtc?ggcccctctg?acgctaccgt?tatggacatt?gagcaggatg?gcaccgtcct 1800
caccgagacc?tccgtctctg?gcgacagcgt?cactgtcacc?tacgtttaaa?tgcatctcta 1860
tgcatgagat?atcggtcgct?tcaatgtctt?cgagacgaag?acaaaccctg?gggatgaatg 1920
aaaaaatgag?tgatgagcta?tccggattga?tctgatcttg?ttgagttgtt?aattccgttt 1980
ctgttgatgt?ttttgaatga?ttatacctac?ttttaagtag?aagaaatgga?tgagcgcgtg 2040
catgctgaaa?atgactgtcc?ctgcttatat?tgtagaagat?cttccagaaa?gctgtgctgc 2100
cgatctgaag?atctgaagat?cactagtgag?atctcgcagc?tcggctgtgt?aagtgcattt 2160
gctctgtcga?tcataacttt?gtaaaagctt?gtatgcatag?cagacatctg?tcgattattt 2220
agatgcttcg?atttgatcat?ctttactaga?atccccattc?gagtagagct?tcagagcgtc 2280
gggtggaaat?atcgggtcgt?ggatggtatc?ggagaagtct?cacaacatga?acgaaagatc 2340
cgcggtata 2349
<210>18
<211>1495
<212>DNA
<213〉aspergillus niger
<400>18
tgattgtgca?gacttcctca?tcatcgaagg?agacaacaat?gaaaccccag?ggagacacgg 60
aagcaggaaa?acagactgcg?gccggcgaga?aagacacgat?gtgacgaagg?cttatctcgt 120
gacgccaaga?caatgcgggg?aaagctgccc?ttccaagacc?caactggcct?gcctctttct 180
cattacaacc?tcatcgcctt?gattgacttt?ctggaccttg?gtggcttgga?ggccggtcgc 240
atcgagcttg?ctactcgcta?cttgctttgt?ttcgatgact?ggctttcgtt?gatcgcaaca 300
ttctttcttg?gtatttttgt?agggatagct?agttgcttat?catgggagat?tacggccccg 360
gagtgtcgtc?actcacggca?cagctacctg?gaaatccgcc?tgtctctgaa?acagatcagg 420
atgagatctc?agtacttgta?acgggctttg?gggtaagctt?ccagtgtcca?taccattctc 480
ccaatatcgc?aactcacatg?ttctacagcc?attcaagtct?aatctagtga?acgcctcata 540
tctgatagcc?tcgtccctac?caccctcttt?cacattctca?cctgcatctt?cagacggctc 600
tgatgctgtt?ccccgtcgag?tttcgataaa?tgtccatcct?tcacccatac?ccgttgcata 660
ttcatcggtg?cggacgaccc?tccccgtcat?tctcgatgac?tatgccaaga?cgcacggagg 720
ccgacgccca?gacatcgtca?tacacattgg?catagcagca?atgaggaact?actattccgt 780
ggagacgcag?gctcaccgtg?atgggtatct?gatgtccgac?atcaaaggca?gatccgggta 840
cgaggatggc?gagaagctgt?ggagggagct?cgacttgcca?ctggtgctta?gggctggccc 900
ttcagaggga?cacgcctcgg?agaagaaaca?tctcagcccc?cgtccaccgg?acgaagattt 960
cctagcagca?tggaagacat?tttgccctcc?agaaaccgat?gcgcggatct?ccactgatgc 1020
cggacgttat?ctctgcgagt?tcatcctgta?caccagcttg?gcactggcat?accaggcggg 1080
tgaggatcgc?aatgtcacct?tcttccatgt?tcccgcgtca?tgcttggatg?aggatataga 1140
gacgggcaag?gaggttgccg?tcgcgctaat?caaggctctt?gtgactagct?ggagtgagca 1200
gcagcacagc?gttccctagt?tctgaatgac?tttttcaatc?ttctcggagt?tgtgacattg 1260
catgtcccag?cagttttggt?ttatcggtgg?tcctatctga?gtactatatt?tttttggcaa 1320
tattttgcat?tagtgaatac?atatgggcgc?ctgatgggtt?atgatcgcat?cacacctggc 1380
gccgcataga?ttttgggcat?aaggagtgtt?ggtgtaagat?caccatcaat?ttattactgg 1440
tgttggattt?gtgtagggat?agaaccaata?tagattaaat?tctcacgcca?tacat 1495
<210>19
<211>2501
<212>DNA
<213〉aspergillus niger
<400>19
gcgtcttcgg?caagcggaag?ggaccccgca?aaagctacgc?attgccattg?ttcaggaacc 60
cactaaataa?acacacggac?atgtggtttt?ggctgcccgt?gcgccccgaa?gccgcagccc 120
gaacggaggc?attaaccctg?atgcgtccgt?tgattgttat?ggtcttgtcc?aacataacgg 180
ggaatttctg?accgcacacg?atgccaggca?acccatttta?tcacggctga?gcatgttgat 240
aggtgttgaa?ttcattttcc?gtaggcagac?gtctcctaga?gcaatttctg?ctgtatggca 300
gacattcgtg?accgaaaccg?tctcactcac?ggtctaccat?ggtagttatg?cttcgtacat 360
aagacaagaa?aggaatgcct?tcaatcatgg?caagaaggga?atttggtaat?ttgggtgcta 420
ctgccgtctt?cctttgttgt?gaaccttctc?cattacacac?agtgtccctt?gaaggccccg 480
tatgccttca?tactccgcca?caatagccgc?catcggggct?ttcctgcttt?cgcagcccgt 540
catgggctca?aggcagggaa?aggccccctt?tggctggggt?actcagtcac?ttgctcactt 600
tggtatcaac?ccagaccttg?ggttgcacaa?ccagcagaac?ctcaactccc?tcatttcaca 660
ttcagcgatg?gccactgcgt?tggagacgga?atatgccacc?gtatgaaaag?caccagccct 720
ggctcttagt?cctgatcact?gattgtagac?tcagatccct?attgaccata?acaacgcatc 780
ggctggcact?tatcaaaatc?ggttctgggt?cagcgatgaa?ttctatcagc?ctggcaaccc 840
gatatttgtg?tacgataccg?gggagtcgga?tggcggatcg?atagcccagt?cctacctaac 900
ctccactctc?tccttcttca?gagaattcct?gatcgaattc?aacgccatgg?gaatcgcctg 960
ggagcacaga?tactatggaa?actcgacccc?ggctcccgta?tcctatgaaa?ctccacccga 1020
ggcatggcaa?tacctcacca?ccaagcaggc?gctcgcggac?cttccgtact?ttgctagtaa 1080
ctttagccgc?gagaagtatc?ctgacatgga?cctgacgccg?cagggcacgc?cgtggatcat 1140
ggtgggcggc?tcgtacgcag?ggattcgtgc?tgcattaact?cgcaaggagt?acccagagac 1200
gatattcgca?gccttttcct?catcgtctcc?ggtggaagca?caggtcaata?tgagcgcgta 1260
ttacgaccaa?gtctatcgtg?gcatggttgc?cagcggatgg?accaactgct?cggcagatat 1320
ccacgctgct?ctggaatata?ttgacgatca?actttcggat?gaagatacag?ctacctcggt 1380
caaacaactt?ttcttcggat?ctggcgccga?gaccaactcc?aacggtgatt?tcactgcagc 1440
gctaactgcc?atctacggct?acttccaaag?ttatggtatg?gcgggaggta?ttggaggtct 1500
aggcgcattc?tgcgagtatc?tcgaaattga?tcccaagacg?aacgggacta?caggaccgga 1560
tggccttgcc?cctacgtatg?gcggccagta?tgtcgccgaa?cgatgggccg?catggccaac 1620
ctttctcgag?ctggtcaatc?tgaatatggg?gaccaactgc?gggcctcagg?acgcgtctca 1680
gccaattgac?tgtgactttt?ccaagccata?cggcgatccc?tcggccatca?cttggacttg 1740
gcaatactgc?agcgaatggg?ggttcttcca?ggcgaacaac?gatgggccgc?actcgctggc 1800
ctcgcgatat?cagtcggtgg?aataccagca?agaagtatgt?aaccggcagt?tccccgatgc 1860
agtggacaag?ggactgctgc?ctccgtcgcc?gcgggcggat?gatgtcaacc?aagagtttgg 1920
gggatggacg?atccgcccgt?ccaatgttta?cttcagcgga?ggagaattcg?atccgtggcg 1980
atcattgtcc?attctgtcga?cagaagattt?cgcacctcaa?ggggtggagt?ttacgagcgc 2040
gatcccagcc?tgtggggtgc?agaccaatga?ggacaccgtc?tttggatacg?tcatgcagaa 2100
ctcggaacat?tgctttgact?ttcaagcgac?gccgaccgtg?gggaagttat?cacgcggcat 2160
cttcacatcc?gccttgttgc?aatggctcga?atgttttgga?cagaactcaa?gccaatccag 2220
gtgatctggg?gggccagggg?gtgtgtgggt?gtgtaggtgt?gggtgtgttt?ggttgtgctg 2280
gagcctggag?ccaggataaa?gaagatagga?caaggatgac?tgagtggatc?ctgggatgct 2340
cctacttact?tagaaaggta?cagggcgcgt?cacggcgaag?gtagactcgt?accccagatt 2400
agatgatcaa?cgagaagcct?cggaggtttt?ggatcaacgt?tgggttttag?cgtcacgtcc 2460
aaagtcctgc?atgcaggtgc?cgcttttccc?ttttgggaga?t 2501
<210>20
<211>2660
<212>DNA
<213〉aspergillus niger
<400>20
agagtccgcc?ttgacaatgt?ctaagaaagc?atgctgagcc?ccctccccca?gtgtttatag 60
gtgagtagga?atggagtata?gtgcttgagt?gctttcacgc?tggtaaacgg?acccgctggg 120
cggctagact?gccttgtttt?cggtctagga?accattcaag?attcaacggc?tacaagtcaa 180
gtcagaccat?ctatcaatag?tgcgagatag?cagagagtcg?gaccggagtc?tcacaggcat 240
ccttggcggt?cgaggagtga?tgagttgtgc?gaccagcgcg?tgttccttat?ttaagccgcg 300
cgcgcacctc?tgacgcaacg?gtctcaaagg?ggggtctcac?ctcttgcatg?ttcggctgca 360
ttcaattcga?cctctccgtg?tctgtctagc?atcaccccaa?atcctatcgg?aatagtcctc 420
cggttaagtc?aacattgcaa?atcagtcctt?tcatttttgc?ccagctcagc?gctcggcctt 480
ctgtgaccct?tggagcctga?tcaattgccg?aaaggtgttc?gggcgggtca?gccttggaca 540
gctcatttgc?agtgcagagg?ttcatcagca?tcagctgtac?tacttgactt?cctatcatca 600
ttattgatta?ttatattata?tcctatcttc?tccgccaatc?ttccatcgcc?ggtagttttt 660
cgtagacaac?atgaagctct?caatagctct?tgcactcggc?gcaacggctt?cgacgggggt 720
gttggctgct?gttgtaccgc?agcaagaacc?gctgataacc?ccccaagatc?ccccaactca 780
tcatcatcag?gagaagttct?tgatcgagtt?ggctccttat?cagacgagat?gggttaccga 840
ggaagaaaag?tgggacttaa?aactggtata?gcaacattcc?ccattttatt?actgtcacaa 900
tagcacatct?cactgatcgc?tctgcgaatg?ttccattagg?atggcgtgaa?cttcatcgat 960
attactgaag?aacgaaacac?tgggttctac?ccaacgttgc?atgctggtag?ctatgttcac 1020
tatccgccga?cgatgaagca?tgcggagaag?gtggttcccc?ttctgcgggg?tctctccaag 1080
gacaacatgg?agcaaaacct?caacaaattt?acctcatttc?acactcgcta?ctataggtcg 1140
tccactggta?ttgagtccgc?aaagtggcta?tacagtaggg?tttcggatgt?cattgagcag 1200
tcgggtgcag?cagagtacgg?cgccactgtg?gagcagttcg?ctcactcatg?gggccaattc 1260
agtatcattg?ctcggatccc?aggccagact?aacaaaactg?ttgtcctggg?cgcacatcag 1320
gacagcatca?atcttttcct?cccctccatc?ctagctgcac?ctggtgccga?tgatgacgga 1380
agtggaaccg?tgactatact?cgaagctttg?cgtggtctgc?tgcagtcaga?cgccattgtc 1440
cggggcaacg?cttccaacac?aatcgaattc?cactggtact?cggcagagga?aggtggtatg 1500
cttggttcgc?aagccatatt?ctctcaatat?aagagagata?agcgagacat?caaggcgatg 1560
cttcaacagg?atatgactgg?ttatacccag?ggagctctgg?acgccggtcg?tcaagaagcc 1620
attgggatta?tggttgacta?cgttgatgag?ggactgacac?aattcctcaa?agatgtcact 1680
actgaggtaa?ggtcactccc?gctttccttc?tttgtgagac?atataactaa?cgattgcggt 1740
caaagtattg?tggtattggc?tacatcgaaa?ccagatgtgg?ctacgcctgt?tcggaccaca 1800
cgtccgcaag?caaatatggc?tatcccgcag?ctatggcgac?ggaatccgaa?atggaaaaca 1860
gcaacaagag?gatccacacg?actgatgaca?gcatccggta?tctaagcttc?gatcatatgc 1920
tggagcatgc?gaggttgaca?cttggcttcg?cttacgagct?ggcctttgct?caattctagt 1980
gtccttcatg?attttacgtt?gtaaccgggt?ctagcagata?attctggcta?actagtgagg 2040
cttatatgtg?ttcaggtttc?ctatgtcggt?ttattgtggc?attagacaag?attacagagt 2100
aaccaatact?ccattttgta?atggaataga?tgtctgaggc?ccaagtgttg?gcaaggaacc 2160
ttgcctatat?accacagatt?aatactattg?gctttggtga?ttcaagaata?ggcctatggc 2220
tggactttat?atatgttgac?attctatttt?gtaccggcaa?cagactctaa?cactagcacc 2280
taacaaataa?aacacgtgtg?actcttatgg?gtggcatgat?gatagtctgc?agaatggccc 2340
gataagataa?acgaaggaga?tcctactata?cccgattgag?tcacactagc?ctgaaacaga 2400
aagacggtca?ctccgccggg?gcgatcactt?ccactggctt?caatcttcga?gtcattcctg 2460
cggtctgttt?tctccttgtt?accactccct?ttgcccttca?gatcagatcc?tgaacggaga 2520
aagctcaccc?ttcatactac?ataatattct?acataacttg?cttggactga?attggcgata 2580
ttccgtcggt?cgctcctatc?tatcgcctac?gtcaccagcg?gtgcccctcc?aaggaagacc 2640
ccaccatcag?accttggatc 2660
<210>21
<211>2047
<212>DNA
<213〉aspergillus niger
<400>21
ccgagctata?caaatgcgca?tacaaaaatg?gacagagtta?catttcaacg?ataaacatga 60
atgataagct?tccagcaatg?gcggccaagc?gatatgcaaa?ccgattttag?tacgcattcg 120
gtttatctgt?tatctctctc?ggagtaaact?gtatgctctt?cgccgaaacc?acaaaagtaa 180
gcggggaaac?gtatactacc?aatcaaacac?cccgagatgg?tgactccgaa?cgcagcagac 240
ctatttagat?atatttaggc?atgacaagta?tcaatggatg?acagaaacac?cgagacctgg 300
tacaatctaa?gttgaggaga?gatttgaatc?agaaagcagc?tcgcacattt?catcatgaga 360
actactacgt?cttttgctag?gcttgcattg?gcagtggcct?cagttggtat?tgtctttgct 420
agtccaacaa?aaaataacga?tgggaaactg?gtatatggct?caccagaatc?cgtcggcatg 480
atatccgccc?ctttgcacca?aatggtccaa?aatgttagcg?catatacaca?tgctgccaac 540
tatagcaagt?tctcgtacga?caaagtccat?cccatcgagc?cagggtctgt?taccctggtg 600
gctctcgacg?gtgtcatcgt?cagcgaattt?gccttgggca?agagaaatct?ctacgccgat 660
gtcaacggca?ccaatttacc?tcgatacctg?caggaagaca?ccaccctgga?tacagtctac 720
gatatggcaa?gcctcacgaa?gctgttcacc?acggtagctg?ctttacggga?acttgacgct 780
ggtcgaattg?cgcttaatgt?aactgttgca?acttatatac?cggactttgc?gacgaatggg 840
aaggagaata?ttactatctt?ggagctgttc?acgcatacaa?gcggtttcgc?ttctgatcca 900
tcgccaccac?ttttctctgc?ttattatacg?acgtatgatg?aacgcattaa?agcaattttg 960
acgcaaaaaa?ttatcaatac?ccccggcagc?acatacctct?acttagatct?caactttatg 1020
tcgctgggcc?tcgttatcga?gaccgtaacg?ggacgtgccc?tggatgatct?tatttatgac 1080
ttcaccagac?cgcttgaaat?gacatctacc?ttcttcaacc?gcgggaatat?cgaaggctct 1140
acaccccagt?cacccaacta?cgaccgcaca?gccgtacaag?aatttcagat?cgcagccctc 1200
ggaccctcag?aaccacagcg?tccacaacca?gtgcgcggca?cagttcacga?cgagaacgca 1260
tggtccctag?acggcgtatc?aggtcatgca?ggtctattct?ccactgtgcg?cgatacagcg 1320
acattctgcc?agatgatcct?caacaacggc?acatatgcag?gccaacggat?cctttctcga 1380
acagcggtag?acatgatttt?cacaaacttc?aatgccaggt?ttccggggga?tgctcgtagt 1440
ttagggtttg?agttggatca?gtattctact?gcgggaccga?tggcgagttt?gcaaactgcg 1500
agtcacactg?gatttactgg?gactacgttg?gtgatggata?ggacgtataa?cgccttttgg 1560
ttgcatttta?gtaaccgggt?gcatccgtct?agggcatggt?ctagcaatac?tattgtgaga 1620
gaggctattg?ggtattgggt?tgggaagagc?ttggggttgg?atgttgcgtt?tgctctgttg 1680
taatggttga?gcggaggacg?taccagatgg?gatcctggat?tcattccttc?gatacacttg 1740
tatgtacacg?aggaatgtat?tcgaatgcaa?atacctcata?tattacagaa?tccgcagtat 1800
gaatccggat?aattttgtta?aggcaaatcc?agaaatttct?aaaggttcac?taccataaac 1860
acaaatattc?accattcaat?atggcatgtt?atcatccatt?ctcataaaag?accctcgatc 1920
cggaagaccg?atcctgtcag?ggaattagtc?aaccctctcc?aataaatgca?gcatgaaaga 1980
aatctaccat?gaatcaaccc?cgagccctaa?ataatccgaa?aagatccagt?ctggtgacag 2040
tgcaggg 2047
<210>22
<211>2730
<212>DNA
<213〉aspergillus niger
<400>22
tggccacgcc?atcctcttat?gctctctcta?tccactctct?ccctcagctt?ctctcaacca 60
cttccttacc?catctttcac?cctctcttcc?cctttccccc?tttcaaatct?cttgaccttc 120
aagtctggcg?cgcgtctgga?cagcggctct?tgtgctagag?gtcttaactc?ctaccccgcc 180
ttcctctggc?cttgaccttc?tctgttcctg?aaccaggttc?cctcccggtc?ctctccgccg 240
acgttatccc?cgacattgtg?ctgctcatta?cctccgcccc?caaggtaacg?ggtaagcgaa 300
aagtgcaagg?cccagttggc?taaatttcga?tgactccttg?agcgcgactc?caagtccgct 360
tgggaccgtt?tcctccgctc?cgtcttcggc?aatatctact?actactacta?ttactattac 420
taccccggtc?agccgccgcc?gccgtattac?aagtacccat?cgcctactga?tggtctcctt 480
atcattccgc?ggggagacca?cttccattcc?ctccatggcg?tcctggttgc?tctcgacgct 540
cctttttctg?agcccgtcct?tggtgtcagc?caaatcggcc?gcagactatt?atgttcactc 600
cttgcccggt?gcccccgagg?ggcccttgct?gaagatgcat?gccgggtaag?cttcgctgtc 660
ccggaacggt?ccgcttagca?cctatatact?gacttattgc?ctccacgcgc?agccatattg 720
aggtggatcc?acagaacaat?ggaaatcttt?tcttctggca?ctaccagaat?cgccatattg 780
ccaaccgcca?gcggactgtg?atctggttga?acggtggtcc?cggatgtagt?tccatggacg 840
gcgcgttgat?ggaggtcggt?ccgtatcgcc?tgaaggacaa?tgaaaccttg?acctataatg 900
agggttcctg?ggacgaattc?gccaatttgt?tgttcgtcga?tcagccagtc?ggaaccgggt 960
tcagttatgt?caacacggac?agctatcttc?atgagctcga?tgagatgtcg?gctcagttca 1020
ttgtctttct?ggaagagtgg?ttcagattat?ttccggagta?tgaacgcgat?gatgtatgct 1080
gcaatcacct?atgctgccct?agtcctgcac?cttcacggat?tctgttctaa?catctgcgac 1140
agatctacat?tgccggcgag?tcttacgccg?gtcagcatat?tccatacatc?gccaaagcca 1200
tccaggaacg?gaacaagaac?gttcaaggga?agaccatcgc?ttcgtggaat?ctaaaaggcc 1260
tattgattgg?caatggttgg?atttctccta?atgaacagta?catgtcctac?ttgccctacg 1320
catatgaaga?aggccttatc?aaggaaggca?gccggaccgc?gaaggaactc?gaagttttac 1380
agtcagtctg?taagtccagg?ctggaaactg?gcaagaacaa?ggtccacctc?aacgactgcg 1440
agaaggtcat?gaatgctctg?ttggataaga?cggtcgaaga?caacaaatgt?ctcaacatgt 1500
atgacatccg?ccttcgtgac?accaccgatg?catgcggtat?gaactggccc?accgacctgg 1560
aggacgtgaa?gccctatctg?cagcgggaag?atgtggttaa?agcgcttaac?atcaatccgg 1620
agaagaagtc?tggctgggtg?gagtgttcag?gtgcagtgag?cagcgctttc?aatccgcaaa 1680
agtccccgcc?ctcggttcaa?ctacttcccg?gcttgctgga?atcgggactt?caaatcctcc 1740
ttttcagcgg?agacaaggac?ctgatttgca?accatgttgg?aacggaacag?ctcatcaata 1800
acatgaagtg?gaacggaggc?acgggtttcg?agacctcacc?tggcgtctgg?gctcctcgac 1860
acgactggag?tttcgaaggc?gagccggcgg?gtatctatca?atatgccaga?aacctgactt 1920
acgtgctcat?ctacaacgca?agccatatgg?ttccctacga?ccttcctcgt?cagagccggg 1980
acatgctaga?tcgcttcatg?aatgtcgata?tcgcgagcat?cggaggcagc?cccgccgact 2040
cgcgcattga?cggcgagaag?ctgccccaga?cgtcggtggg?cggccatccc?aacagcaccg 2100
cggcggagga?gcaggagaag?gagaggatca?aggagacgga?atggaaagcc?tacgccaagt 2160
caggcgaagc?cgttctcctc?gtcgtcatta?tcggtgtatt?agtttggggc?ttcttcatct 2220
ggcgcagccg?ccggcgtcac?cagggatacc?ggggcgtctg?gcataaggac?atgagcggaa 2280
gctctgttct?cgagcggttc?cacaacaagc?gcacgggagg?cgcagacgtc?gaagcggggg 2340
atttcgacga?ggcggagctc?gatgaccttc?attctccaga?cctcgaaaga?gaacactacg 2400
ccgtgggcga?ggacagcgac?gaggatgata?tttcacgaca?gcattctcaa?caggcctccc 2460
gagccggggg?cagtcataat?ctatcctagt?tcatctttgg?ttgggtaaac?ttgtgatggt 2520
gtaggtgtat?ggcttgcttg?gggtctttgc?cttttgtttt?tgttttcttg?gccacgaaag 2580
gacgtgcctc?cttatatgtg?catttatcat?tttatctagc?tggctgcctg?gcatcattta 2640
acatttagac?atgaacaaag?tttatgaccg?cttcctgata?catagccagg?cggaaattcc 2700
tcccgtctat?aagccaacag?tctcatccac 2730
<210>23
<211>2660
<212>DNA
<213〉aspergillus niger
<400>23
actttattgc?caagcgaatg?acttcgactt?tcttatttct?gcaacgcgtt?tggccagtta 60
ataatttgct?agactcaact?gattgctcgg?tgccatctta?ccagggatcg?gcaagccgaa 120
aagtacgcta?ttgcacccaa?tctgtaaaga?agacttctcc?aaactccaaa?gtagaacaga 180
cccatcttta?gctttaataa?ctccaatcat?gacgattgga?actatcggaa?aatataatct 240
aagttcaatg?gatctggtcc?gtcgctagaa?tatcggagta?aatgagccca?acccctggcc 300
atcaggttcg?acggaggaat?tcttctggtt?gggtacaaga?ttgacacgat?ccccttggcc 360
gctgaacgtc?actcttccgc?tgtcaaagct?tgttggctga?cttcgatccc?ggatgatgtt 420
tctgatttca?cctgcagtga?cagttgcggc?tgcacttctg?ctgatcaacg?gcgcaggagc 480
aactcaatct?gaacgaagtc?gggctgccgc?tcatttttcc?aaacgtcatc?cgacgtaccg 540
tgctgcgacc?agagcccagt?cgagcaacac?ttccgactac?cgattcttca?ataataggac 600
caagcgtatg?tattacaccg?gccatgaact?ctattcgtcg?ctgacatgtg?gtcatccctg 660
gatagcccac?ttggtggaaa?gcttacccga?tgtgcacttc?gatgttgggg?agatgtactc 720
ggggtcgatc?cctatcgatg?acagcaacaa?tggatctcga?tccctgtttt?atatcttcca 780
acctaagata?ggcgaacctt?cagacgacct?taccatttac?ctcaatggag?ggccaggctg 840
ttcctccgaa?cagggattct?ttcaggaaaa?tggcaggttc?acatggcagc?ctggtaccta 900
tgcacccgtc?atcaacgaat?attcttgggt?caatttgacg?aacatgctat?ggtacgcttc 960
ttcctgagga?ttaaattgga?ggtatgcact?ctgtacattt?tatgagacta?atgtgaataa 1020
attcagggtt?gaccaaccag?tcggaaccgg?attttccgtt?ggaaatgtta?cagccaccaa 1080
cgaagaagag?attgccgccg?attttctcga?cttctttgaa?aagtttgaag?atctatacgg 1140
gataaagaac?tttcgcattt?tcatgaccgg?tgagagctac?gccggtcgct?atgttcccta 1200
tatctcgtcg?gcaatgctag?acaagaacga?caccacgcgt?ttcaatctga?gcggtacgag 1260
ccctgtctac?tcataactac?tacccctata?agcttagttg?actgaaactg?actttttaac 1320
gtccctctag?gagcccttct?ttatgacgcc?tgcatcggcc?aatgggacta?catccaggcc 1380
gaactccctg?cctacccctt?cgtcaagcag?cacgcttcac?tattcaactt?caatcagtcc 1440
tacatgaacg?agcttgaaac?cacctacgaa?gaatgcggct?acaaggccta?cttcgatgag 1500
tactttgcct?ttccaccaag?cggcatccaa?cccccaaaat?acatgaacta?ctccgagtgc 1560
gacatctata?acatgatcta?ctacgaagcc?tataacccga?acccatgctt?caatccctac 1620
cgcgtcattg?atgagtgtcc?acttctctgg?gacgtcctgg?gctggccgac?agacttggca 1680
tacgagcctg?cgcccaccac?atacttcaac?cgtatcgatg?tcaagaaggc?cctgcacgcc 1740
cccatggatg?tggaatggga?gctctgcagc?tacgacctcg?tcttcgctgg?aggcgacgct 1800
gacccgggtc?cggagcagca?aggggatgac?tcacccaacc?ccaccgaggg?tgtcctcccg 1860
cgtgttattg?aggcgaccaa?ccgcgtgctc?attgccaacg?gtgactggga?ctacctgatt 1920
atcaccaacg?gcaccctcct?cgccatccag?aatatgacct?ggaacggcca?gctgggcttc 1980
cagtccgcac?ctgccacacc?gatcgatatt?cagatgcccg?atctccagtg?ggttgagatt 2040
tttgaggccc?aggagggata?tggagggctg?gatggccctc?agggggttat?gggtgtacaa 2100
cattatgagc?gcggtttgat?gtgggcggag?acatatcagt?cggggcataa?gcaggctcag 2160
gatcagggcc?gtgtctcgta?tcgccatctg?cagtggctgt?tggggcaagt?tgagattctt 2220
tagtctcccg?ccttagatat?aattgatatc?acactgtaat?gttccctcca?aaaagcttca 2280
tttattgata?gtttcagtga?attttgttac?ttccagtaac?aactctatta?tggcattccc 2340
tggtttttaa?tgctgcctcc?ttttaccgta?gctacggcta?tgactacata?taacggactg 2400
atttttctat?ctcaacttaa?ctttgtattg?ccccctggat?cctgactaca?gaaaataaat 2460
aattcaaatt?gatatttatt?ggccttttat?tggcagcata?atatctttct?catataagca 2520
cgcgagaaac?ttgttcctca?tcatactata?tttatcccca?cagctgatgc?cgtgattcgg 2580
taatgaagat?ggagattatg?cggattgcgc?acttcataat?caaacatcgt?ataagtgtgt 2640
cagtaatata?tatctataat 2660
<210>24
<211>2800
<212>DNA
<213〉aspergillus niger
<400>24
aatgccgaag?cttgacctga?tacgacttca?aggtatcgtc?accgacaatc?gttatcatca 60
cgctacaggc?ccgcagtttc?cgcttgaatt?cccgcattag?gaaatgagca?tcgcattcct 120
cttcccacga?ggtctctttc?cgagggcagc?cgctgcaaca?tcattgggat?catgcttggt 180
tctcctctcc?catagctgtc?cgcgagcttc?tcattggtac?ctcttcgcta?cctcgttgca 240
tcctattcgc?gcatggcccc?gccagagatg?tttctgcaag?gtcccatcac?cttgccgcgt 300
tgctattccc?cgccctcgag?ttcccgacaa?gttactttgt?gtcagtggct?gagaagcctg 360
gttctgagag?tgtactcaga?caatcatatg?gttccctcca?tgtgctacgt?cgtcctagcg 420
tcgctgcact?acatcatcgt?taggcagcat?ggaactggca?cccgcacata?aagcccccga 480
cacccccatc?gataggctcg?gtgttcgtgc?acgcctgtcc?actggcccct?cccccaaagg 540
cccttcatca?gtatgctgtt?tcgcagtctg?ttgtcgacgg?ctgtcctagc?cgtctcgctg 600
tgcacggata?atgcttcagc?tgctaaacat?ggtcgatttg?gccaaaaagc?tcgcgacgcc 660
atgaacatcg?cgaagcgttc?cgctaacgcc?gtgaaacact?cgttgaagat?ccctgtcgag 720
gactatcagt?tcttgaacaa?caagactaag?cgtatgtatc?tcagttcgat?attgaacgat 780
ggctgatttg?cttccgtcgg?acagcttacc?gcgtggaaag?cctgcctgat?gttcacttcg 840
atctgggcga?gatgtattcc?ggcttggtcc?ctattgagaa?gggcaacgtg?tcacggtccc 900
ttttctttgt?cttccagccc?actattggcg?agcctgtgga?tgagatcacc?atctggctga 960
atggtggccc?tggttgcagt?tcccttgagg?cctttctcca?ggagaatggt?agattcgtgt 1020
ggcagcctgg?aacctaccag?cctgttgaga?acccatactc?gtgggtgaat?ctcaccaatg 1080
ttctgtggta?agtgtgatat?tactggatcg?ctagttgagt?ttacatgggc?ggtatcgacc 1140
taacctattt?tttgtagggt?tgaccaacct?gtgggaacgg?gattctctct?gggtgtccca 1200
accgctacgt?ccgaggagga?gattgctgaa?gactttgtga?agttcttcaa?gaactggcag 1260
cagatctttg?ggatcaaaaa?cttcaagatc?tatgttactg?gagaaagtta?tgcgggccgt 1320
tatgttcctt?acatatccgc?tgctttccta?gatcagaatg?atacagaaca?cttcaaccta 1380
aaaggtgagt?tatacttcac?caaagtaatc?tttaactagg?gcttgtactg?attgtactat 1440
ctaggtgcac?tggcatatga?tccctgtatt?ggtcagtttg?actacgtgca?ggaggaagca 1500
cctgttgttc?cctttgtcca?gaagaacaat?gccctcttca?atttcaatgc?aagctttttg 1560
gcggaactag?agagcatcca?tgagcaatgt?ggatacaagg?atttcatcga?ccagtatcta 1620
gtcttcccag?catccggtgt?ccagccgcca?aaggctatga?actggagcga?tcccacctgt 1680
gatgtttatg?acatcgttaa?taacgccgtc?ctggatccca?acccgtgctt?caacccctac 1740
gaaatcaacg?agatgtgccc?cattctctgg?gacgttcttg?gattccccac?cgaagtcgac 1800
tatctccctg?cgggcgccag?catctacttt?gaccgcgctg?atgttaagcg?tgccatgcac 1860
gctcctaaca?tcacctggtc?cgagtgctcg?gtggagagcg?tctttgtcgg?gggcgacggc 1920
ggtcccgagc?aggagggcga?ctactcggcc?aaccccatcg?agcatgtctt?gccccaggtc 1980
atcgaaggca?ccaaccgagt?tctgatcggt?aacggtgatt?atgacatggt?catccttacc 2040
aacggcaccc?ttctctcgat?ccagaacatg?acatggaatg?gaaagcttgg?attcgacacg 2100
gcccccagca?cccccatcaa?catcgacatc?cctgacctga?tgtacaatga?agtgttcatt 2160
gagaacggct?atgacccaca?aggtggtcag?ggtgtcatgg?gcatccagca?ctatgagcgt 2220
ggtcttatgt?gggctgagac?cttccagagc?ggacacatgc?agccccaatt?ccaacccaga 2280
gtgtcatacc?gtcaccttga?gtggctgctt?ggccggcggg?ataccctgta?aggcgggtag 2340
gctaccacgg?gggacgatgt?cacgatgata?gtcataagtt?atgatctgta?gatacgttgt 2400
atgcgaatgt?acatgaattg?cttttactgg?cagtctctaa?agcaaaattc?atagtagagt 2460
actggcctac?ttaccctcac?ttcccctatc?ttttcaacct?gaagaccgga?agaattgtaa 2520
ctaacaagca?taacgtagct?gatttgaagc?agagcataac?acactctacc?cctcggcact 2580
tctacttatg?acgctatttg?actgctaact?cgggtttaat?cctgaagctg?cagtccaatc 2640
gtacattaaa?ctcaatgtgc?cttgcccagg?aaacgatatt?tgacttatat?gatctgaaaa 2700
tgaacaattg?tccccgagag?agagagagag?agcgagcggt?aaatacttag?caagtcagtc 2760
acgcagtatc?ctccactaat?gccgtaacac?aggaaatgga 2800
<210>25
<211>2165
<212>DNA
<213〉aspergillus niger
<400>25
gaatcaggat?ggaggcccga?cggccatcaa?ccgccgaaca?tccggctgct?cgaccgaatt 60
cggagacatg?gtcggagcta?ggcgggaata?gccgtccaaa?gtcacgatag?gtcgcttgta 120
ctgtgtagaa?gtcagaccct?ttggatccag?cgttcgttgt?gaatggctcc?acgcagcctt 180
tgctttgacc?aatttggggc?tgagtcactt?ggtcgatgat?gactggctat?accagtgcaa 240
agtgtgagca?ccatgcttac?actattgcct?tagcctggcc?gttgaagctg?acatgagagg 300
aacaggcaga?agagaaatgc?tgccttgcct?cttgggggcc?aatttaacct?ccccagactg 360
cggcacatcc?gtcttggact?tgtgcttctt?tgcaacttac?gttataacga?gtctgtgaac 420
aggaaaacag?acgcccggtc?agtcaagatg?aaaggtgcgg?cgctaattcc?tcttgcggcg 480
ggcattcctt?ttgcccatgg?cctgtctctc?cataaacgcg?acgggcctgc?cgtcgttcgt 540
atgcccattg?agcgcaggag?cgcccagtcc?ttgcagaaac?gagattctac?ggtcggtgtg 600
actttgcaga?actgggtatg?ttaagctata?cggccgtgaa?gtatagatca?tgctgacaat 660
cgctaggatg?cgacctatta?cgcagtcaac?ctgacgttag?gaacacctgc?gcaaaaggta 720
tcattagctt?tggacactgg?cagcagcgac?ctctgggtga?acaccggcaa?ctcaacttac 780
tgctcaatcg?acaatctatg?caccccttat?ggcttgtaca?atgccagcga?atcgtctact 840
gtaaagaccg?tgggcacaca?cctcaacgat?acatatgcgg?acggcacaaa?cctttacggt 900
ccttatgtga?ccgataagct?cacgatcggc?aacacaacaa?tcgataatat?gcagtttggg 960
atcgccgagt?caacgactag?taaacgtggg?tgaaccgttt?gtccatgaat?gatcgtcgct 1020
gactaggtct?actataggcg?ggatcgccgg?cgtcggttac?aagatttcga?cctaccaagc 1080
cgagcatgac?gacaaagtct?acgccaacct?ccctcaggcc?ctcgtcgaca?gcggtgccat 1140
taagtctgct?gcgtacagca?tatggctaga?tagtttggag?gcgtcgactg?gctccctcct 1200
tttcggaggt?gtcaatacag?ccaagtacaa?gggcgatctg?cagactcttc?cgatcattcc 1260
tgtgtatggc?aaatactact?ccctcgccat?cgcccttacg?gagctcagcg?ttgcgaccga 1320
ctccaactcc?agtagcttca?ccgacagtct?ccccctctct?gtgtcactcg?atactggcac 1380
caccatgacg?gcactgccca?gcgacctggt?caacaaggtc?tacgatgcgc?tcaacgcaac 1440
ctacgacaag?acatacgaca?tggcctacat?cgactgcgac?actagagagg?cggattacaa 1500
tgtaacatac?agtttctccg?gggcaacgat?caccgtgagc?atgagtgagc?tgattatccc 1560
cgcaacggag?ccggggtggc?ccgacaacac?gtgtgtcttg?ggcctcgtgc?ctagccagcc 1620
gggcgtgaac?ctgctcggtg?atacattcct?gcgcagtgcg?tacgtcgtgt?atgatctcga 1680
gaacaacgaa?atctctctcg?ccaataccaa?tttcaatcca?ggcgacgatg?atatcctcga 1740
aatcggaacg?ggaacgtctg?ctgtgccagg?agccacaccg?gttccctctg?ctgtctcttc 1800
tgcaactgga?aatggactga?tctcgtctgg?caccgcagtg?cccacgctgt?cgggtgtcac 1860
aataactgct?acagccacag?caaccggctc?aaccggcact?ggctctagcg?gtggttcgtc 1920
ggctgaagcc?acgagtactt?cctcggaggg?cgctgcggcg?caagctacga?gcaacccgat 1980
gaacctgctc?ccaggacttg?cgggtatcgg?cctacttctc?gctctgtaac?gcgattgtac 2040
ctactcaaat?agatatcacg?acgagactct?aatgtaataa?tgtggtatac?aataacccca 2100
atatctacat?ttccttaacc?gtaaactgca?tactctacac?caaatccacc?accaaaatac 2160
atacc 2165
<210>26
<211>2800
<212>DNA
<213〉aspergillus niger
<400>26
gcccagccaa?tcataagaaa?cccggtcctg?gcaaggtcttggcggggatg?gtgcaagcca 60
gccaaacaac?cggtttgttg?gacgccctgc?ggtacactga?aatcttgggc?tgttcgacaa 120
aaacaaagca?ggtaacacaa?agatataata?cggcggaatg?ataggatatc?cctgtcgatc 180
agccggacag?gatggcgcta?gtgtcacctc?cagcttcggc?taccctcgca?gcggacccaa 240
tcagcgtccc?tcccagcccc?cgatacagta?atggtatgca?catcgcagtc?ttaatcgcct 300
gcagcggcag?taatgatagt?cctgccggtg?aataataccc?cataacaaac?aaataaataa 360
tactacttat?ctctcctcgt?ccctttcact?ttccctttgc?cgtcttcaat?cccctcatct 420
tggtctcttc?ggcagccttt?caccatgctg?tcgtctctcc?ttagccaggg?agcagccgta 480
tccctcgcgg?tgttgtcgct?gctcccttcg?cctgtagccg?cggagatctt?cgaaaagcta 540
tccggcgtcc?ccaatggtga?gttatagacc?ccaattcttc?attttgagcc?acatactgac 600
gtgattcctt?cgaatactac?caggctggag?atacgccaac?aatcctcaag?gcaacgaggt 660
cattcgcttg?caaatcgccc?ttcagcagca?tgatgtcgct?ggtttcgaac?aagccgtgat 720
ggatatgtcc?acccccggac?acgccgacta?tggaaagcat?ttccgcaccc?acgatgagat 780
gaagcgcatg?ttgctcccca?gcgagactgc?cgtcgactca?gtccgcgact?ggctggaatc 840
cgccggtgtc?cacaatatcc?aggtcgacgc?cgactgggtc?aagttccata?ccaccgtaaa 900
caaggccaat?gccctgctgg?atgccgactt?caagtggtat?gtcagcgacg?ccaagcatat 960
tcgtcgtctg?cgcaccctgc?aatactccat?ccccgacgcc?ctggtctcgc?acatcaacat 1020
gatccagccc?accacccgct?ttggccagat?ccagcccaac?cgtgccacca?tgcgcagcaa 1080
gcccaagcac?gccgatgaga?cattcctcac?cgcagccacc?ctggcccaga?acacctccca 1140
ctgcgactcc?atcatcacac?cgcactgtct?gaagcagctg?tacaacatcg?gtgactacca 1200
ggccgatccc?aagtccggca?gcaagatcgg?ctttgccagc?taccttgagg?aatacgcccg 1260
gtatgccgat?ctcgagaggt?tcgagcagca?cctggctccc?aatgccatcg?gccagaactt 1320
cagcgtcgtc?caattcaacg?gcggcctcaa?cgatcagctt?tcatcgagtg?acagcggcga 1380
agccaacctc?gacctgcagt?acatcctggg?cgtcagcgct?cccgtcccca?tcaccgagta 1440
cagcaccggc?ggacgcggcg?aactagtccc?cgacctgagc?tcccccgacc?ccaacgacaa 1500
cagcaacgag?ccctaccttg?acttccttca?gggaatcctc?aagcttaaca?actccgacct 1560
cccacaagtc?atctctacct?cctacggtga?agacgaacag?gtatgcacct?cacctgaccc 1620
attccatttt?acatccctca?cctctctcaa?ccaaactaac?aacaccaaca?gactatcccc 1680
gtcccctacg?cccgcaccgt?ctgcaacctc?tacgcccaac?tcggcagccg?cggcgtctct 1740
gtaatcttct?ccagcggcga?ctccggcgtc?ggcgccgcct?gcctcaccaa?cgacggcacc 1800
aaccgcacgc?acttccctcc?tcaattcccc?gcctcctgcc?cctgggtaac?ctccgtcggc 1860
gcaacctcca?agacctcccc?cgagcaagcc?gtctccttct?cctccggcgg?cttctccgac 1920
ctctggcccc?gcccctccta?ccaacacgcc?gccgtgcaaa?cctacctcac?caagcacctg 1980
ggcaacaagt?tctcggggct?tttcaacgcc?tccggccgcg?ccttccccga?cgtctccgcg 2040
cagggcgtca?actacgctgt?ttacgacaag?ggcatgcttg?gccagttcga?cgggacgagt 2100
tgctccgcgc?cgacgttcag?tggcgtcatc?gcgttgttga?acgatgcgag?actgagggcc 2160
gggttgcctg?tgatggggtt?cttgaatccg?ttcctgtatg?gtgtcggaag?tgagaagggt 2220
gcgttgaatg?atattgtgaa?cggcgggagt?gtgggttgtg?atgggaggaa?tcggttcggg 2280
ggcacgccta?atggtagtcc?tgttgtgccg?tttgctagtt?ggaatgccac?gaccgggtgg 2340
gatcctgtgt?cggggttggg?aacgccggat?tttgcgaagt?tgaaaggggt?ggcgttgggt 2400
gaggagggtg?gtaattaagt?gtgagatggg?gggaaaggga?ttttcttttc?gatgtgaata 2460
ttaggtgaat?tgtgtggata?attttcatac?ataattaagt?ctgcattggc?agtgataacc 2520
tggaagaaat?gtctaatgag?tgtgatttgt?ttacttatgt?atattgagta?atggaatgta 2580
gatgacttgt?ctttgtactg?tataacgaaa?tgattatttg?agtggagggt?attaaagaac 2640
tataaaatat?atacaaaggt?taacccatgc?agtcgtaacc?cataatgcaa?agctctactc 2700
tatctgtatc?ggtagcagat?aagtgtatgc?aatctatctt?tgttgatgat?gcaatcaagc 2760
gggcacacca?ccagtgccaa?acagctccat?cttgatgcgg 2800
<210>27
<211>2660
<212>DNA
<213〉aspergillus niger
<400>27
ggagacagaa?tacatggaat?tgatgctcaa?caacgacaag?gagctcgcgt?tccgtaatgc 60
caagttcatc?gcttagattg?ggaggatcgg?ccaggtctgt?atataggccg?cgatagaaca 120
cgaaataaat?gatttatgac?tatttgcggg?catgagccct?cacgtagtgt?gctatagacc 180
gtagacttgg?taaacattgc?tatcgatccc?ccccttcgta?tattagtcat?aattcttcct 240
gatgtcaact?ctcaaaacac?agcattccac?agcgttcata?tgatgtcaat?gtctcaatcc 300
ctaacgtttt?gctgaaacag?gtacctcttg?gttatttttc?atatagtagg?aaggtcgccc 360
ttgcatgtgg?tatgagacca?ttggcggcat?ctagcttgaa?tggtactcaa?tatgaccagt 420
agtctccact?tcagcagtgt?gtttgtgata?gccaagacat?cggcagtagt?tcctgcagag 480
cttctacacc?tcttcatctt?cacttcacca?atccactctc?tcactgctca?cttctagttt 540
cgcaacacta?gagaatcatg?tggctctttc?tcgtgtgcag?tatcctgctg?ccacttggag 600
tagtcaacgc?acagtctcaa?tacttcaaca?acaaaaccaa?aggtatacca?catcgcgtca 660
gtttgaatcc?cactaacagc?gctagaattc?gtcgtcaatg?gctctgctat?tccttttgtc 720
gatttcgaca?ttggcgagtc?ctatgcgggc?tacctaccca?acacgccttc?tggaatctcg 780
agtctatact?tctggttctt?tccatcttct?gatcctgatg?cgtctgatga?ggtatgctta 840
tcgccgtctc?atatgcttcg?cacggctaat?aaacagatca?ccgtctggct?gaatggcggc 900
ccaggatgca?gctctctggc?aggcatcatg?ctcgagaacg?gcccctttct?atggcaacct 960
ggtacctacc?gacccgtgcg?caacccttat?gcctggaaca?acctcacaaa?tatggtgtac 1020
attgatcagc?ctgctggaac?gggattctcg?cttggcccgt?ctacggtggt?ctcagaattt 1080
gatgtagcca?gacagtttat?ggacttctgg?aggcggttca?tgaaaacatt?cgatctgcag 1140
aatcgaaaga?tatatctcac?tggcgagagc?tatgcgggcc?agtacatccc?atacatcgcg 1200
tcgcagatgc?ttgaccagga?tgatgatgag?tatttccggg?ttgccggcat?ccagatcaat 1260
gatccctaca?tcaatgagct?gccagttttg?caagatggta?tgcctctgac?acaggttatt 1320
gcttactcct?ctgacattga?tgacttccag?tgcctgcagt?tgcgaccgtc?aatcagcacc 1380
gctccctctt?tccctttaat?gacaccttca?tgagtcaaat?caccaagctt?tccgacgatt 1440
gtggctacac?ttcgtttctt?gacgatgccc?ttacctttcc?accccgttct?caattcccat 1500
cagtgcccta?taatgctagc?tgcaacatct?gggatatcat?aaacaacgct?tctctagctc 1560
tcaacccatg?cttcaaccgc?taccatatcc?ccgacgcctg?ccccaccccc?tggaacccag 1620
tcggcggccc?catcgttgga?cttggtccga?ccaactactt?caaccgcagt?gacgtccaga 1680
aagccatcaa?cgcgtaccca?acggactatt?tcgtctgcaa?ggatggaatc?ttcccgacgg 1740
ccaacggact?ggacacatcc?cctccaagct?ccctgggacc?gctgccgcgc?gtcatcgaac 1800
agaccaacaa?taccatcatt?gcgcacggcc?tgatggattt?cgagctgctg?gcgcagggaa 1860
ccctgatcag?tatccagaat?atgacctgga?atgggaagca?ggggttcgag?cgggagccgg 1920
tggagccgtt?gttcgtgccg?tatggtggat?catcgggagg?aggcgtgctg?ggaacggcac 1980
atacagagcg?tggattgaca?ttttcgacag?tatttagttc?aggacatggt?aggtccatat 2040
ctcagtatgc?gatgcagcgg?gttgctaaca?ggaatagaaa?tcccggaata?tgcaccgggg 2100
gcggcatatc?gccagctgga?gtttttgctg?gggagggttg?cgaatctgtc?ggtgggttga 2160
ccggagacag?caaagagaat?gaagaaaaga?aaaaaaaaaa?aaaaaaacaa?tatgaataat 2220
tgcagacaat?tattgagcag?gtgcagataa?cagagcagaa?tggttgagct?gtcagatcgg 2280
ttgacttttc?ggcaatgaga?tttggggaag?ctagctctga?gattggtcct?ccgccaaagc 2340
tatcgcaatc?atgatccaat?caacactgca?tactaccttg?atcccctcgc?tgtagacccg 2400
tattgccgga?caaacaattg?actagatatg?aactcttgat?tataaaccaa?tcaagacccc 2460
cagtagcgca?tattatcacc?cccatacgtt?catgatcggc?agcctaatcc?gaggtcggat 2520
cgggaattcc?ttcaaactct?gaaaccgcgc?tgggtccacc?ccgcatcttc?acagtaaaaa 2580
tctaagattc?ccctcaatcc?ctgctccatc?tactttcctc?cctctcatac?cacttttgct 2640
ttttgtatag?taaatatcca 2660
<210>28
<211>1540
<212>DNA
<213〉aspergillus niger
<400>28
taaacagaac?taagcaaaag?tccagatctt?gtgtcccctt?cgactaccaa?tcggaacaat 60
aggaattaac?tattagcctg?caactgtctg?caccatcatg?caacccctct?cgttgtgatt 120
gctcctgttt?tacattcccc?gagacatgct?catctagttg?caagccatct?ctaacccacc 180
tgcatgaagg?gtgcagaaac?acgaacagtg?gcgtggtagc?acacactctc?tgcagtactc 240
gatgccaata?tttccaccag?ctgaactaca?atctccgcgt?cagaattaat?atataaccat 300
caccaatacc?ccttacatcc?caactcagca?actacagcaa?tacttacacc?tatcctccac 360
aaccccacaa?ctccacccca?tcatgtccaa?actctccgct?gctatctcca?aggtacttcc 420
ccatatccac?aacacccccc?acaccatccc?tcaaatctaa?caacaataac?aataacctct 480
caccacccca?gctctccctc?tccaccatag?ccaccactct?gctcctcctt?acccccccaa 540
ccaccgccta?cttctacaaa?tatcccgccc?tcttcgtcta?caaagacacc?aactgcaccg 600
atatctcctt?ctcacttgtc?tacccctccc?tgggtaactg?caacggcgga?tactacgact 660
acgcgggctc?attccagatg?ttcaatatcg?atgctgcgta?tacctgtaat?ggcagtgact 720
cgacactgat?gtttgagatg?tataatagct?ccggctcgga?ttgtggagat?gagagtgatt 780
tgttgtttag?acagccggtg?acggaggagt?gtactgttgc?ggatgtggag?agtccggggc 840
cgttggagat?gccggtttgg?tttgagttgg?ggtgtatgta?attgattcgt?tgagtcggta 900
aggagggatg?gacggggggt?tatataggta?gcttggtggg?taagcactat?tggggaattg 960
tggtgggatg?gctggtacta?tgttgttcgg?tgtggggatt?cttgagggtg?ggttagagac 1020
taaagtgagt?tgtctgaggc?agtagtggat?gacttctgct?tctgtgatgc?tggtatgtga 1080
taaagttaat?tacatatgca?aatgtgcaat?catagactga?taggtggaaa?cttgtctact 1140
cgttgagata?tatagttata?ctggaaatgt?tattcatcaa?ggctgaatac?aagtgtaacc 1200
gtgcacagat?tatctttgat?actgtctatg?ggctgtacga?gcgtctctga?ctcctacaat 1260
gagttagcgg?ctgcacatta?ctatgaggac?ctgtgaattc?gacaccaaaa?ataaccagcc 1320
ctgcagccga?ttacatctgc?ctttccatct?attttctgga?gtcaagcagg?tattccaaca 1380
tactcttact?tgcttaatac?accaactttc?atatatctac?ccagaattac?tcaatcgtga 1440
tgtaggcact?ggcaatcata?gtaactatat?ttcgtttcat?tttatttgtt?tgtacaattt 1500
tttttttccg?gtagtttaat?cattccaatc?aaagaattgt 1540
<210>29
<211>2800
<212>DNA
<213〉aspergillus niger
<400>29
acactttctt?cgatgctatg?tcccagccat?ataaggttca?attctccgac?tcaagtgaca 60
gaatcagcta?tacacggttc?actgcttctt?atatagtaca?tgaggattca?ataaagccaa 120
gttcagcaga?gtcttggttc?cagagcttga?atactcggta?gcattccagg?gattgtgggg 180
agacaatcca?ggagcagcag?ccatcatttg?gtgcctgagg?cacacagcac?tgcctcgtct 240
ccactcccaa?tacttaccaa?gtcacccacc?attccttccc?tctttcggcc?tttctctttc 300
tctctctcac?ttctgctctc?gtgcaccact?tttcttccca?ctcacgccat?ccttctccat 360
ccatttcctg?ccaaactttt?gtctgtcatt?ttaggttttt?tgaaggagat?gactcggtga 420
ctactcttca?atcccggcgt?actcaacatc?cataatgcgt?cacctcttat?cactgctggt 480
gcttctgatc?gcatcggccg?ccctggtctc?cgccgtcccc?gccggctcca?ttatcactcc 540
acaaccaccc?gtcgagcccg?ttcaccttct?ctcttcccag?ccctctgatc?cccgaaggcc 600
atggatccgc?ctccgtgact?ggatcatcga?gtccatatgg?ggcatcgaaa?aacccgcatc 660
tcgtcgattc?ccactcaacg?attccccgcg?caatcgctct?cctccctccc?ggattctggc 720
gcgctacggt?agtgacgtcg?tacttcgttt?cagcctgcgc?aatcacgatg?aggccgaggc 780
attggcccag?gctgcagaca?ttctattcct?ggacgtatgg?gcgtctactc?cagcattcgt 840
agatatccga?ctggccgagg?aagtcgtaag?tggttcatcc?ttccgtccat?atctgcccgg 900
ttgactgatg?cctgatccac?tgtgaccctc?gcaacagatt?ccctcattat?tgggcttgct 960
accaaattcc?ctccagaccg?catatactcc?cctaatagac?aacctggcag?agagaatcta 1020
tacgacctat?ccatctaaaa?agccgatagg?acttgaagga?caatctggat?ttgcgtcctc 1080
gagtcgacct?gcgccaaagt?tcggtgacct?ttttttccac?gagtatcagc?ctttgtccgt 1140
cattatcccc?tggatgcggc?tgctggcttc?catgtttcca?tcccatgtgc?gcatgattag 1200
cgttggagta?tcttacgagg?gtcgcgaaat?tcccgccctc?cgactgagcg?caggcagctc 1260
caccgcggcg?tcaggccctc?gtaaaacaat?catcgttacg?ggtggtagcc?atgcccgcga 1320
atggattggc?acctcaaccg?tgaaccatgt?aatgtacacg?ctcattacca?agtatggcaa 1380
atccaaggcc?gttacccgcc?ttctacagga?cttcgactgg?atcatgatcc?ccacgatcaa 1440
tcccgacggc?tatgtttata?cctgggagac?ggaccgacta?tggcgcaaga?atcgacagcg 1500
gaccagccta?cgcttctgtc?ccggaatcga?tcttgaccgc?gcctggggct?tcgaatggga 1560
cggcggtcgg?acccgcgcta?acccttgttc?agaaaactat?gctggagacg?agcccttcga 1620
gggaatggaa?gcacaacaat?tagcacagtg?ggcgctcaac?gagacacaaa?acaacaatgc 1680
cgacatcgtg?agcttccttg?accttcactc?ttactctcaa?acaattctct?accccttctc 1740
ctactcctgc?tcctcgatcc?ctccaacgct?cgagagcctg?gaagagctag?gccttggcct 1800
agccaaggcc?attcggtacg?cgactcacga?aatctacgat?gtcacttctg?cctgcgaagg 1860
catcgtcacg?gccagtgcgg?cagataacaa?ccccgggcgg?ttcttcccca?ttggtggcaa 1920
ctccggtggc?agtgcgttgg?actggtttta?ccaccaagtg?cacgcgactt?attcatacca 1980
gatcaagctt?cgtgatcgcg?gaagctacgg?gttcctcctt?ccgtctgaac?acatcatccc 2040
caccggcaag?gagatctaca?atgttgttct?gaaattggga?tccttcctca?tcggaggcga 2100
ctcatttgac?gtcgattggg?aatcagaact?cttcgatctg?tcaaaggacg?aatccgatct 2160
ggatagccgc?tattcaaaat?ccaatgaccg?ctccccggcg?tatctacaca?acgccaacgg 2220
ccccctgccc?aacattgacg?aagacgaaga?taaggaatgg?gtaatggtgg?aggaagaaga 2280
ctacacagac?gatgacgacg?acgatgatga?tgatgatgaa?gaagaggaag?aggaagagga 2340
agatacatat?tgggccaccg?aacacacata?cgaatttcgg?cgacgacgct?gatgatggac 2400
aaactaatca?accctattta?tatgacaccc?tcgcccatat?actctccttc?tgatgacgat 2460
caataatgac?taatgacggg?tttgcgggag?tgattgacgt?gtttatcatg?ctctgcttct 2520
cgattctttt?tattatttta?gatactgttc?ccttcaggtg?cctatagcct?atagagctta 2580
ggggtattct?ctacataatt?aaatacagag?taattcaatg?aatcgtccta?tcaaataatg 2640
gacccgagta?actaactggt?gtttcattcc?ttccgtactg?tacttaatct?gtaaggaatt 2700
gaaagctaag?cctcataagc?tacttcaccc?cactctttac?ccaggtgcag?tgtatcatga 2760
tcatcgtcat?acattcattc?gttaggtatc?tttccgatgc 2800
<210>30
<211>2380
<212>DNA
<213〉aspergillus niger
<400>30
cccgcctgta?caaggctcat?tgagcgacct?ttatttctat?gaaggcttct?tgcagtgtag 60
agccgctgtt?tagaactcgg?aaataggcgt?gcatagtatg?gacccaatca?acagagttaa 120
tctatttact?ctaacgccta?gcaagcaatc?agtgcccaga?ggaagctaac?ggatggctgg 180
ccaagctgcg?ccagaaacga?aatgagtccg?taataccatc?cctgcatgct?tatctgtatt 240
ctgtgcatgc?atgatgcttt?cctcatgggg?cattacccag?tagtccgaag?acgcaatgtg 300
accatctgac?tgagttttaa?atatactgtc?caagtgcctt?ctgacccggt?ccccgcttga 360
tggcaatcaa?caaaaggtga?atgtgactga?aaggcgcggt?ccagacaaca?ggacttagac 420
tttgttgtga?gactataaaa?ggatctaact?attgcactac?tgaaatcaag?tattctagtc 480
taccattgac?atttctcccc?tttcggtggc?tactcgctca?acatggcttt?cctcaaacgc 540
attctcccgc?tgctggccct?catcttacct?gcagttttca?gtgccacaga?acaggtccct 600
catccgacca?tccagaccat?cccggggaag?tacattgtta?ctttcaagtc?cggcattgac 660
aatgcgaaga?ttgagtctca?tgccgcatgg?gtaacggagc?tccacaggcg?cagcttagaa 720
ggccgcagta?caaccgaaga?tgaccttccc?gccgggatcg?aaagaacgta?cagaattgcc 780
aattttgctg?ggtacgcggg?gtctttcgat?gagaaaacta?tcgaggagat?ccgcaaacat 840
gaccatgttt?gtgtccacgt?atcctagacc?gtatggtttc?gactaattgc?tgtacaggta 900
gcttatgtgg?aacaagatca?ggtctggtat?ctcgatacgc?tagttaccga?aaggcgagct 960
ccttggggac?tggggagcat?ttctcaccgt?ggtgggtcta?gcaccgacta?catctatgat 1020
gacagcgctg?gggagggtac?atacgcttat?gtagtggaca?ccggcatctt?ggctacgcat 1080
aatgagtttg?gtggtcgtgc?tagcctggca?tataatgctg?cagggggtga?gcacgttgat 1140
gatgttggac?atggtacaca?tgtagcaggg?accatcgggg?gcaaaacata?cggggtttcg 1200
aaaaacgctc?acctactgtc?cgtgaaggtg?tttgtaggtg?aatccagctc?gacatcggtc 1260
attctggatg?gcttcaattg?ggccgccaat?gatattgtga?gcaagaaccg?gaccagtaag 1320
gcggcgataa?atatgagtct?tggtatgtgc?gccctctctg?gggatctaat?cccgctaacc 1380
gtgatgcagg?tggaggctac?tcctatgcgt?ttaacaatgc?agttgagaat?gcttttgacg 1440
agggtgtgct?ctcttgtgtt?gccgctggaa?atgagaatgt?aagctctgct?gaactgtcca 1500
ccattgagct?aaatttagac?taatgttttg?cagagagatg?cagcacggac?tagcccggct 1560
tctgcacccg?acgccattac?tgttgccgct?atcaacagaa?gcaatgcccg?tgcgtcattc 1620
tcaaactacg?gctctgtggt?tgacattttt?gccccgggag?agcaagtact?ttctgcatgg 1680
accggctcga?actcggccac?caacacgatc?tccggcacgt?ccatggctac?accccatgtg 1740
acaggtttga?tcctctattt?gatgggcttg?cgggaccttg?ctaccccagc?ggctgcaacg 1800
accgagctca?agaggttggc?tacgcggaat?gctgtcacca?atgtggcggg?tagccccaat 1860
cttctggcct?acaatggaaa?cagcggcgtg?tcaaaagggg?gtagcgatga?tggagatgag 1920
gactaggtgc?gtaacatgag?tgaatatggc?ttagaatagt?ggggatcgga?gagtagacta 1980
gtttatatgc?gaaataaagt?gtgtatcagc?accctggcct?gttcatgtaa?gtcggcattt 2040
tcacttttgc?cgacaccgca?aatatgctgt?gcttgaggct?gttgcctccc?cagccagcct 2100
tcccgagact?gaaactcaca?catccattgg?atgtataaag?ttctgcacat?gcgaaatgcc 2160
gctgccgttt?acctcccgac?gtggtaccgg?accgaaggca?gacacagatc?atggaccgct 2220
ataccgcaca?gacaacttgt?gctccttact?gaaagtacca?ttccacaggt?cattgcagca 2280
tgatgagtga?tgatgtactt?ctccccatca?agaaccactg?gcggtggttg?gaatgaatct 2340
agatcaaaga?gatcaaccgc?ttccccggac?agatcaggcc 2380
<210>31
<211>2441
<212>DNA
<213〉aspergillus niger
<400>31
aaacgacgtt?ttaggtcaat?actgaagtcg?ttgaaaacgc?ttgattcttc?gctatctagg 60
cgcgctcgga?ggagcagttg?aagttacgga?gttcgggtca?cgtgacctcg?actactagta 120
atctactgag?attacgttcc?aacataattt?catcaggaag?aatgcaaagg?ccccagagaa 180
ggagaatttc?acgatcggtg?aaaacgacca?agcagcatca?catttgaatg?aaactacatt 240
gctccgtgtt?tattccgttt?ctctctcttc?tctctatcta?ttgcttctct?ttggctagac 300
ttcaccaact?aattaatgct?tacacgatga?tagctgcatc?cattgaatca?aactgacccc 360
gcaaagctga?ctgaaccaac?ccctccggtg?ctgttgctac?tgccagtttg?aattcaatat 420
cctataaccc?accctgctca?atgatcaccc?ttttgtcggc?cctgttcggc?agcgtagtat 480
atgccgctac?gcagaccgtg?ttagggccag?agggggctga?tccctttacg?gtgtttcgca 540
gcccacactc?accggcattt?tcaattcgca?tccaggagca?gaatgactcg?atctgtgatg 600
ctcgttcacc?ccaattcact?ggttggctcg?acattggccc?gaagcatctt?ttcttttggt 660
attttgaaag?ccagaatgac?cccttccatg?atcccctaac?gctatggatg?actgggggcc 720
caggagactc?gagtatgatt?ggacttttcg?aagaagttgg?cccttgccgg?attaatgagt 780
ttgggaatgg?aacagatcac?aacccctggg?cctggaccaa?gaattcatca?cttctttttg 840
ttgaccagcc?agtcgatgtc?gggttttcct?atatcgatga?gggctatgag?ctgcctcatg 900
actcacgtga?agccgcggtg?gacatgcatc?ggttcttgcg?attattcata?tccgagattt 960
ttcctcacaa?acagttcctt?cccgttcacc?tttccggtga?atcttacgca?gtaagataga 1020
agccgccccc?agaaaaagct?tgctcagtgt?tctaacaatt?accttgtgat?acactgtgta 1080
gggccggtac?attccttatc?tggcgaccca?aatcttggaa?caaaatgaac?tgtataaaga 1140
tagccccagg?ataccgctga?aatcgtgctt?ggtgggtaac?ggattcatgt?cacccaagga 1200
tgcaacgttc?gggtattggg?aaacactgtg?tactactaac?tcaggagtcc?catctcctat 1260
cttcaatgaa?actaggtgcg?atattatggc?ggcgaatatg?ccgcactgta?tggatctata 1320
tgacatatgc?attcaacact?cagaccccgc?gatatgtcat?gcggcccagt?ccgtctgtta 1380
cgatagtgtt?gtagggtagt?atgataacga?ggccggcgct?gatggccgta?acagatttga 1440
tagtgagttg?ttatcatcag?aggctcatgg?ccaaattatt?gctaaggatg?acgacagtca 1500
ctgcaccttg?tgagatcgac?gaaatgtgct?atatcgaagc?ggctctaatt?gagagatatt 1560
tgaattcgcc?atctgtttgg?gaggccctgt?cgccaccgca?acaggttacc?gaatacaaat 1620
tcgtcgctac?ttctgttatt?gatgcatttg?ctcaatcagc?ggacggcatg?gtgtcgagct 1680
cgaagcagat?cgctttctta?ctcgcaaata?atgttgactt?cttagcgtat?caaggcaacc 1740
ttgatctcgc?ctgtaatacg?gctggcaacc?tacgttgggc?gaactcgctt?tcttggaaag 1800
gccagacaga?atttaccgca?aagcccttac?ttccgtgggt?ctcgatcaac?tctgggagcc 1860
aggaacctgt?ggggagtgcg?aaggaaattc?aggtttcggt?cggtgaaggg?acggacgaaa 1920
cgtcacgctt?tgcctttgtg?actgtggaca?acgctggaca?cctggtaagt?caaagtaaaa 1980
ttaggagaga?ggggtttaat?gatccagttg?gctaacgagt?agtgttggta?ctatggtagt 2040
tgccccaaga?tcggccggat?gtagcgcttg?acatgatgat?tcgctggatt?actggggcat 2100
cctttgttta?acaaggaaca?gttgcgggac?tcaaagattt?caaactgacc?tactccttac 2160
cttttatgaa?atgggcccgc?tgcctaggtc?aaacaagggt?gctcgggcaa?acaataccag 2220
ttttggacta?ggggtccgtc?tgctttcatc?agcccttcgt?agcttggact?tttgtccatg 2280
tccctgctgc?ctcggtccat?cacacgcccg?ctccccccat?ttcctttcct?tcccttctct 2340
tttcgttcta?ttatgcttga?gtgcccgatc?ttccctgcat?gctatgccta?tttcagtgta 2400
cgcagtttgg?gtttttgtcc?gaggaagaca?atcatccatg?c 2441
<210>32
<211>3500
<212>DNA
<213〉aspergillus niger
<400>32
gtttgttgtg?gttgttgttt?ggggtcccat?ttgcaatccc?tgaaccggac?cctgtcaatc 60
cctcccaagt?ccctcgttat?cttccgcctt?ttccaccccc?tccacacttt?atttttccat 120
ccatcatctt?ccagtgcctc?aatccaaatc?actgtcgttg?aatatagatt?cgcatctgtt 180
ttccgtacgt?gtatttgttt?actttcggga?gggagattct?cgccgttcat?tccagatttc 240
cgcccgtccg?ccaaggcggc?tgcgcctcca?gccaagccaa?aacctccttg?gatcgccagg 300
tggaaagaat?ccctttcact?cccccgtcga?gtgagtctgt?ctcactgctc?cctccggtcg 360
ttgcgcgcgc?tctctctttc?ctctccacac?ctccagtata?cttcctctgc?gggtgtgtga 420
gagactgcga?cgatccggag?aagaataaaa?ccctccagtg?cagcttaatc?tccggagtga 480
tccgtcatac?atgaccggct?cccgagccaa?gatctcgact?gggtccatcc?agtgaaaggg 540
aactcaatcg?tttgcacttt?tcgtcgctgc?ctgatgctgt?ggaccgaagg?gctctgttga 600
accctgactc?tccggatctc?tcggtgttgt?tttgatgcca?gcacgctcgt?tccacactca 660
cctttaacct?ctcccatcgg?ctgtcttcac?tcgctgacag?caatgcggtt?tctcacttat 720
tccctgccct?tcattgcaag?tgctatctcg?ctctttgggg?tcaatgtaca?aggttagctc 780
ggcgacatcc?ggcgcataga?tttgttctaa?ctggatcaaa?tacagctcga?tcacaagctc 840
caagtgccat?ccgtcatgtg?tcgacgcttg?accagcccac?catcaagaca?ccctcacagc 900
gggtcgatca?ccttgaccac?tttgacatca?ccttcaatat?tcatgacaag?caccagcgga 960
taaagctgga?gctggagccc?aaccatgaca?tcctggcgga?agacgcatcc?gtacagtatc 1020
tcgacgcgga?cgggaacgtg?cgacggcacg?agcccattgc?tccacatgag?cataaggtct 1080
tcaaggggag?gagtctactc?gggcgaggaa?aaggcatgtg?ggatccggtc?ggatgggcgc 1140
ggatctactt?gaagcaggat?ggctcagagc?cactatttga?gggagtcttc?agtatcgacg 1200
gcgacaacca?tcacgttcag?ctgaaatcgg?catacatgga?gaagaaacgc?cccgtggatg 1260
tcgaccttcc?cgactcagcg?actgactata?tgatcttcta?ccgggattcg?gatatggtgc 1320
gtctacatac?ggaactcaag?cggtcgtcgc?tcggatcgac?ctcgtgtcaa?gccgatcagc 1380
tcggcttcaa?cactaacccc?aaccaccctg?tgctacaacc?gtatggccag?gcagagaccg 1440
atacgtgggg?agcaatttca?ttgaactcct?tgtttggact?caacaagcgc?caatccgata 1500
tcggaagtgt?gtctggcaat?gcgggcggag?tcaatctggc?gtcgaccatt?ggtgatactt 1560
cgggctgtcc?gagtacgaag?caagtagctt?tgattggtgt?tgcaacggac?tgcgccttta 1620
ccggctcatt?caacaacgag?actgccgcca?aggaatgggt?catcagtact?gtcaacagcg 1680
cgtccaatgt?ctacgaaaag?tccttcaaca?ttacgattgg?gctgcggaat?ctgactatca 1740
ccgacagctc?atgccccgac?aacccgcccg?cggccacggc?atggaacatg?ccctgctcca 1800
gcggcaatct?cacctcccga?ctggatctgt?tttccaagtg?gcgcggtgag?caatcggatg 1860
acaatgctta?ttggaccctg?atgagcgatt?gcgcgacggg?caacgaggtc?ggactgtcat 1920
ggcttggcca?actctgcaat?agcgatgctt?cttcggatgg?ctcgagcacg?gtcagtggaa 1980
ctaacgtcgt?cgttcggtct?tccggctcgg?attggcagat?ctttgctcat?gaatctggcc 2040
acacctttgg?cgctgtccac?gactgtgact?cccagacctg?cgcggaggat?ctcgaagcct 2100
cgtcccagtg?ctgtccgttg?acctcgagca?cctgcaacgc?caacgggaaa?tacatcatga 2160
atcctacaac?tggaacagac?atcactgcgt?tctcgcaatg?cactatcgga?aatatatgcg 2220
cagccctggg?ccgcaacagc?gttaagtcca?gttgtctctc?cgccaaccgc?gacgtcacca 2280
cctacactgg?cagccagtgc?ggcaacggaa?ttgtcgagtc?cggcgaagac?tgcgattgtg 2340
gcggggaaga?tggttgcggc?gacaacaact?gctgcgacgc?gaagacatgc?aagttcaagt 2400
cgggagctgt?gtgtgatgac?tccaacgaca?gctgctgttc?aagctgccaa?ttctcctcag 2460
ctgggacggt?atgtcgtgcc?agtcgcggcg?actgcgacgt?ggcagagacc?tgcagcggca 2520
actccagtac?ttgtcctacc?gactcgttca?agaaggacgg?cacgagctgc?ggcagcagtg 2580
gctcgggact?tgcctgcgct?agtggccaat?gcaccagccg?cgactaccag?tgccgcagtg 2640
tgatgggcag?tctcctccac?agcaacgaca?cctacgcctg?ttcctccttc?agttcctcct 2700
gcgaactggt?ctgcacctcc?ccgaagatcg?gcacgtgcta?cagcgtcaac?caaaacttcc 2760
tcgacggcac?tccctgcggt?agtggcggct?actgcagcaa?cggcgactgc?aagggccaaa 2820
acgtcgaatc?ctggatcaag?aaccacaaag?gtatcgtcat?tggtgtcgcc?tgcgccgtag 2880
gcgccctgat?ccttttggcc?ctgatgacct?gcatcgtaaa?ccgctgtcgc?cgggctcgcg 2940
cgccaaaacc?cgtcccgcgt?ccagtgcctt?acgggccgtg?gcccggcgct?aggcctcccc 3000
cgccgccgcc?catgaaccag?tggccggcgc?gaggctatca?aggcttaggg?aatgagccgc 3060
cgcccccgta?tccaggtgta?cctggtcagc?cagtaccgca?acatatgcct?ccccaggggc 3120
ggtacgcttg?attgacgaga?cttcttctgt?gcttctttcc?atgcgatata?gtatgcatta 3180
cgattcttgc?agcactagca?ttacaaatgt?gacgattact?tcattgatcc?tttattgacc 3240
ttacattctt?gtcttggagt?ggaggcgtgt?tctagagttt?tggtttgatg?ctgaattgtt 3300
cttttctata?cgggggtctg?ggcgtttcgt?gaattgcagt?acttacaatc?caggggtgca 3360
atccccaggg?ggttggttcg?cgtcttcttt?ccctttcttt?gcccatatta?gacggggccg 3420
tgggatgtat?ggtcggggtc?tgatgtatgt?attcctgccg?tgtataatga?acttttccgt 3480
cataatatat?tgcttcttgt 3500
<210>33
<211>2520
<212>DNA
<213〉aspergillus niger
<400>33
ttgatgcata?atgctttcct?tcagaggtaa?tacttcgagg?acggctatga?agcgtatgcc 60
acatacgatt?ggtatttgac?gatatttgtc?atgctataca?tgaaatttac?atattgtata 120
tagtgtcatg?ggtttgaata?aagacatatc?gatgtatctt?aatagcaggt?caattgatga 180
cgctcttgtt?gctccgacga?aaagcgactg?catcgggccg?atgcgggtcc?agggtcgtcc 240
ttatcaacgc?cccgtcagca?ctaacagttg?acatgtttct?ccaggtcggc?tagaaccgcc 300
ttttcgcgag?aaacgcgtgc?tatcgcgagt?gcagggcaat?tgttgcctag?cagtagctaa 360
agcctgagtt?ccgtgatctt?cacttctact?tcttcttctt?ccctgctccc?aacccattac 420
tctgcacccc?acgcccaaat?gcgtttccta?agcagtgcag?ccctattcgg?cctggcgtat 480
gcctccaccc?aggcggtcct?ccagccagag?gaaccatccg?acttccgtac?attccacagc 540
ccatattccc?cgcaccactc?gatccgcatc?cgccagcaga?atgaatcaat?ctgcgctgcc 600
cattccgccc?aatacaccgg?ctggctcgac?atcggccgta?aacatctctt?cttctggtac 660
tttgagagcc?agaatgaccc?tgccaatgat?cccctcactc?tctggatgac?aggagggcca 720
ggggggtcca?gcatgatcgg?tctgtttgaa?gaagtcgggc?catgtctgat?caatgagtac 780
ggcaatggca?cttactacaa?tccgtggggc?tggtcccgga?actcctccct?actatttgtc 840
gatcagccag?tcgatgtggg?attttcgtac?gtcgatgaag?gagaggacct?gccgggcgat 900
tcgcatcaag?ctgcaattga?catgcatcgg?ttcttgcagt?tgtttgtctc?ggaggttttc 960
ccgcaattgc?agactcttcc?cgttcatctt?tctggtgaat?cgtatgctgt?atgtatcttc 1020
tctaggtcac?ctgagctaag?actaacttcc?acagggtcac?tatgtccctt?acctcggcag 1080
tcagatcgtc?caacagaaca?agctctatcc?cactgagccc?caggtccttc?tgcactcatg 1140
tctcgtaggc?aacggctact?attctcctcg?cgacactacc?tacggctact?gggaaaccct 1200
ctgcaccact?aaccctggag?tccccgagcc?cgtcttcaac?cgaaccagat?gcgacatcat 1260
ggcggccaat?atgccgcgat?gcatggaagt?atccgacgta?tgtgttcgga?accccgatcc 1320
agctatctgc?catgctgcgt?cggaggtatg?ctacgagggc?gtgatcggat?ggtatgatga 1380
cgagtctggt?gaaggtggtc?ggaataggtt?tgatagtgag?ctttgcccca?tccagttgtc 1440
ccctgtcagc?aaatctctgc?aatttactga?tatgaaacag?taaccgctcc?ctgcgccctt 1500
gacggcatat?gctacatcga?ggccgctcgc?atcgagcagt?acctgaacac?acccgcagtt 1560
tgggctgctc?tatcaccacc?caaagaaatc?aaagaataca?aggttacttc?cgacaatgtg 1620
tcgcgcgcat?tcgatctcac?ttcagacacg?atgacgccag?cgtctgagca?agtcgcgttc 1680
ctgcttgcga?atcaggtaca?tttcctggcg?tatcagggca?atctcgatct?ggcgtgtaat 1740
acggcgggta?atctgcgctg?ggcgcattct?ctgccatgga?gaggtcaggt?cgagttcgcg 1800
tcgaaggcgc?tgcggccatg?gagttgggta?gatgtggtat?ctggaaaagg?tggagtggct 1860
ggaacgacga?aggaggtgag?agtgaaggtt?agtgagagta?cggataagga?gtcgaggttt 1920
gcgctagtta?cggttgatgg?ggcgggacat?tttgtgagta?tccctttcgc?cttgtgggat 1980
ccaagtatgc?ggattactaa?tggtctatta?caacttttac?agcttcctca?agatagacct 2040
gatatcgcgt?tggatatgat?ggtgcgctgg?atatccgggg?catcgtttac?tgagtgaagc 2100
atgaatgtcg?cagacgatgg?gataccggca?tatttcacag?gtttggtgta?atatatgtct 2160
tgtagctgtc?ttcagcagta?tttacaatat?gctgctgcct?tctctgattt?gggtataatt 2220
atagtttaac?acaatcaact?gcatcggcag?agatggatgg?gcttgatttc?gcacccgcag 2280
cagcgatgaa?tttccgtcta?accgagcgaa?cggtagcgga?cactaacact?gattgtattt 2340
acaaccctgt?ttctttcctc?ttgatttgag?acagaagtat?gtaagctagg?cgtagtagaa 2400
tacatttgtc?atctacttct?actgagttgc?ataacgtaag?cgactattgg?ccgctacctt 2460
gccccagtta?gttagttagt?agtagtgggt?gccgaagtca?gcacacattt?ttcagccctc 2520
<210>34
<211>1721
<212>DNA
<213〉aspergillus niger
<400>34
attgatacga?ggcgtttgta?ggtggcgttc?ctgaagagga?tctgataccc?actggttttc 60
ccagtgggcc?tatgttttcg?tgatagtttc?ggcatttcta?tccatctagg?aaaattttga 120
tggcacctgc?tagtcgatgt?gcccttcctg?atggagcgat?ctcaaagtgt?caaatttctc 180
ggcgaaacgc?gtctacccct?tctttgggat?aattccctgg?tatgcagcat?tcctgacacg 240
agggattgtt?tgggattccc?cagattccac?gtagcggttg?gcaatgatgc?ttatgatttt 300
ataattctca?tcttgtcctt?tgtcctcggt?gcagtagaga?atcttcactg?cccgatacca 360
atatgacatt?gttactcaac?ttccacgcgc?tctttacagt?cattcttgtt?gccaatcttt 420
caaccagatg?cagcgcactg?ctctctggac?gtgacttttg?ctccacgcca?gcgcccggtg 480
agtcactccg?agcggagcat?aggaggctgt?atgatgtaca?ggcccaacgt?gacagcaccg 540
ccgaggagag?ccgggaggtg?gtgccttgga?ttgaaatcga?gacatggttt?catattgtaa 600
gcagcaatga?agcagcaaac?acagtatcag?acgacatgat?caccagccag?gtccgtcacc 660
attcaacttt?tgacccatgc?ctgcgcaatg?tcgtgttttg?gactaacaag?tcctagcttt 720
cctatcttca?gaaggcatat?gaaagtgcga?ctatcaccta?tcggttggag?ggcataactc 780
gtcacataaa?tgactcgtgg?gcgcgaaatg?atgatgaact?ggggatgaag?aatgccctac 840
gaaggggcaa?ttatggcaca?ttaaatgtct?atttccaaac?agatctccag?gcgtcatccg 900
acgagaattc?tcgggactat?ccaaatgacg?gtaaccgacg?aacagatgtg?tcagatcaat 960
catcatcaac?tgtcctaggc?ttctgtacgt?tgcctgaccc?gagtgtgaat?tccagcagcc 1020
ctcgttccag?ctacatcaag?gatggttgta?acgtgttagc?ggatatcatg?ccgggtggta 1080
gtttagcgca?gtacaacaaa?ggcggcacag?cggttcatga?ggttggccat?tggaatgggc 1140
tgctgcatac?gttcgaaggt?gaatcgtgct?cccctgataa?tgaaggagat?tacattgatg 1200
acaccccgga?gcaatctgag?cctacgagcg?gatgtcccgc?cgagaaagat?tcatgccccg 1260
atcttcctgg?ccttgatgct?attcataatt?ttatggacta?ttcatctgat?gactgttatg 1320
agagttttac?tccagatcaa?gcggagagaa?tgaggagtat?gtggtccgct?atgcgggaag 1380
ggaagtgacg?gacggactcc?aagggtatat?aatttgcaca?tataccagct?atagatagac 1440
aactatggta?gcacgaatat?tgatgtcaac?atcttggtct?ttcaattccg?tgggaattga 1500
ctatcacaat?tcatgaacct?tttgtagaat?ttgtgtattg?gagagcgatt?gatgcaaact 1560
agacactcgt?tcgaaattca?cagctagctg?tcatgtggaa?tgcgaaatca?gatcatcgct 1620
tgcgcttttt?tccacgatct?tcatcgtcca?ggccactttc?cctgtccttt?ttctttgcct 1680
ttgattcgag?ttcgtcccag?tcttcaccac?tctcttcgtc?g 1721
<210>35
<211>3550
<212>DNA
<213〉aspergillus niger
<400>35
cctatcctct?gctccgcccg?gtggagagga?tctattgacg?ctatggttct?tgagcaatgg 60
cgacaagacc?caccagtgga?gataagagga?ccgaaactat?ggcttgttca?aggtctgctt 120
cgataaaccc?ctcatcacga?taaaccaagt?tgggcttact?aacaaggcca?atccttcaac 180
aatctcatcg?cacaacgacc?caaaatccag?caaggcacga?tccaacatac?cctgtaatga 240
caggaaacaa?attatcactc?ctctgggtgc?tgatgcagac?caactcagta?ttccgcgtgg 300
attgtccgac?tccgaagaca?agctttggtg?tctggtgctg?atcgtccgtc?gtggagccac 360
cactagtgga?ttgaattacc?cacacaccca?ctacttatac?tctttacgct?gtctatcatc 420
ttcgtgctga?tcagggggtt?attttcttgc?gctatttggt?ttcccactat?gcttctgttt 480
tgcagggctg?gtcataacaa?tttggtagtt?tgggttgggt?ggcttgttat?ggtcgatgtc 540
ggggaggggt?tcaccgttga?acaatatgct?tgtcgttagg?taggttgaac?tgatgcttgt 600
gttttgtttc?caggcgccct?ggacagcctt?tggctatcag?caatagctca?atagctggtg 660
ttttgctcgg?acgcgggtct?tggtcgggtt?gacccagtgt?gatctacgct?agacgctttc 720
ctgattggcg?atggatgtca?cgcctcttat?cagggtttgg?tgatcatatt?tagcctacat 780
aggcaggttc?ccttccgctg?ggtatggaag?tgcaaacgcc?agcgtatgga?gagtgaagtg 840
atgctagtca?atgggatcag?cagcgttctt?gtcaactagc?atatattccg?acgtttccca 900
ccgttcctga?tgatggcttg?catgccacgc?ttgctctgtc?gctgcgatca?acatgcatgt 960
ctcacttttc?ctactcagtg?ttacggcagc?gtttgccagc?ccaacacccc?ataactatgt 1020
tgttcatgag?cggcgcgatg?cattgcccag?tgtctgggta?gaagaaagcc?ggctggacaa 1080
aggtgcccta?ctgcctatgc?ggatagggct?tactcagtcc?aacctggatc?gtggccatga 1140
tttattgatg?gaggtgtatg?tgttccgact?cctcaccaga?accaagctga?ttgtccaggt 1200
ctcatccaca?atcgtctcgc?tacggaaagc?atctctccag?cgaggaggtg?cacgacctat 1260
ttgccccgtc?gaatgaggcc?gtcgagaccg?tccgaacctg?gattgaatcc?gccggaattg 1320
ctccaagccg?catctcgcaa?tcatacaaca?agcagtggct?acagttcgat?gcccatgcaa 1380
gcgaggttga?gcagcttctg?cagacggaat?actacatcta?cacccatgcc?gacacgggaa 1440
gttcccatgt?gacatgccac?gagtgagtcc?attttctaca?tgccatgaca?ccgctaacca 1500
gttaggtacc?atgtgcccga?aaccatccaa?tcgcacatcg?actacataac?accaggagta 1560
aagatgctgg?aagtgcgcgg?cacgccctcc?aaaaagagag?atgcagagaa?gcgctctctt 1620
ggcagtctgc?ccccaatctt?agcaccacta?ccaatcaata?tcacgaagat?tttcgacgac 1680
ccgctagcac?actgcgatct?ggcggtaacc?ccagactgca?ttcgaggtac?gttcatccat 1740
cccaattcaa?gatttcacgc?taaccgtcta?gccatgtaca?acatcaccaa?aggaacaaca 1800
gccacaaagg?gcaacgagct?cggcatcttc?gaggacctag?gagacatcta?cagccaagat 1860
gacctcaacc?ttttcttcgc?caactttgcc?aggttcgatt?actctccacc?ctcccttaga 1920
cacaactaac?accaccaagc?gacatcccac?agggaaccca?tccaaccctc?gactccatcg 1980
acggcgccac?cgccccaaca?gacgtcacca?acgccggccc?cgaatccgac?ctggacttcc 2040
aaatcgccta?cccaatcatc?tggccccaga?acaccatcct?ctaccaaacc?gacgacccca 2100
actacgaaga?caactacaac?ttcaaaggac?tcctcaacaa?cttcctctac?gccatcgacg 2160
gctcctattg?caacgaaacc?tcctctctag?accctcaata?cccagatccc?tccccaggcg 2220
gctactcctc?ccccaagcaa?tgcggcgtct?acacccccac?aaacgtaatc?tccatctcct 2280
acggcagccc?cgaagccgac?ctccccatcg?cctaccaacg?ccgccaatgc?cacgagttca 2340
tgaaactcgg?ccttcagggc?atcagcgtgg?tcgtcgcatc?gggcgactcc?ggcgtcgcct 2400
ccagcacggg?cacctgcttt?ggcgatgcag?acaacgtctt?cgtcccagat?ttcccagcca 2460
catgtcccta?tctcaccgca?gtaggaggca?catacctccc?cctaggcgca?gacgcagcca 2520
aggaccagga?aatagcagtc?acccgcttcc?cctccggcgg?cggcttcagc?aatatctacg 2580
cccgaccatc?ctaccagaac?cactccgtgg?agacctattt?ctccactacc?agcgacgacc 2640
tcacctaccc?ttactactcc?ggagtaaact?acacagactt?ctccaacaca?gatggggtat 2700
acaaccgcat?cggacgagga?taccccgatg?tttcagctat?cgcagacaat?atcatcatct 2760
acaaccaggg?cgaagcgaca?ctggtgggtg?gtacgtctgc?cgcggcgccg?gcgttcgcgg 2820
ccatgttgac?gcgcattaac?gaggagaggc?tggcgaaggg?gaagtccacg?gtggggtttg 2880
tgaacccggt?gctgtatgaa?catcctgagg?cgtttaggga?tgtgactgtt?gggtcgaatc 2940
ccgggtgtgg?gactgatggg?ttcccggttg?ctggggggtg?ggatccggtg?acggggttgg 3000
ggacgccgcg?gtttgaggat?ttgatggata?tatttgtggg?tgatgattga?tggctgagac 3060
aagatgtggg?aaggtgtaat?gaagatgatc?ctatttaatc?cggtaatcta?ccacacattc 3120
atattactag?tttatagcct?agtcagatat?ataacattgt?actactacta?tagaggcgtg 3180
tgatgcaaat?gctaaaatat?tgatatacta?ttaagcaact?acattatgat?ctaaacttta 3240
cagttcatag?tacagaaagg?ctttgatcag?tcctagttca?ataaaaggta?tagactactc 3300
actacatatt?aaacaccaca?actcgggatg?cttggggtat?agtgatctga?gagtcgcggg 3360
aatgcccaaa?tgctctgttc?gatcatatct?tggttgatgt?catgttggac?gcattatatc 3420
aaaagtcatc?tagcgctttt?ctgaaagttc?tattatgaga?attttgcttg?tttatagcta 3480
gcgggtggat?gattaatttt?gtatgagtga?ttctatagac?gttgatcatt?tccatgattt 3540
agaaactgag 3550
<210>36
<211>2280
<212>DNA
<213〉aspergillus niger
<400>36
ctgcctctca?gcgaaaaccc?caaaaccaaa?catttctaga?tcagacaatc?aattgcggac 60
tgagttccct?gaatggtgga?agatgccata?ctgttagcgg?ggactatttt?tagcatgtca 120
tgacttggtc?ggcgtccgta?catagaaggt?tagcggatgt?cttgatgatc?acacaaaaaa 180
gggataggat?gaaactggat?gtctcactgg?ctatctcatt?tgcccaacag?catcagtcgt 240
tccggcccgc?tagttccacc?acatgtcact?tgtctcggat?tattctcgaa?ggtctggtat 300
ttcaatgttc?cacctggtcg?ctctacataa?atagaccttt?acgccgtttt?gttttcttct 360
tcgttctacg?tcgtttattt?atccaaaatg?gcttccaaga?ccctcctact?cattccggca 420
ctggccacag?ccgctctggg?aagtgtattg?gacctagata?tcaaggttca?aaatggctat 480
gtatgtcaat?gagaagctca?gctccctgag?aaatatctac?taactcggcg?aagaggacta 540
tcgaggtaga?ccttggaacc?ccaggtggcc?cgtttgattt?gatgtacgac?accggatcat 600
caacactctg?ggtgcttgat?agcaattgta?cagatgattg?tccaaatgtt?agcgggttag 660
ttgattcatc?ccaccattcc?ttaagcctac?actaatcacg?agcgccaggt?actcccgaca 720
cggctacaac?ctcacctcta?ctggtgtcaa?cttaggtgtc?aacgacagca?ttgcttacag 780
cggaggcact?gtcagcggct?tcactgccac?ggatattctc?acggttcccg?acaccaacgt 840
ctcatatcgc?cagagctttg?ccgtcattac?cgacagtacc?tgggcggcct?tagcagccga 900
tgggttcatc?ggcctggcat?cgtctaccat?cgcattcaag?aatactacga?cagccgtcga 960
acagatgatg?caggatggac?ttttggatga?acctcgattc?gccatatatg?caggttcagg 1020
ggaatcgacc?gtgaccaacc?ctaatccgga?gaataatggc?gtgttcacct?ttggtggcag 1080
ccatgaggaa?acctatgcgg?acggggaact?gcaatggatg?aagatgctct?ccccctttga 1140
aatatacaaa?acaaatctcc?ttggaattca?gggacacaac?aactccgatg?gccaggccct 1200
gtcaagcgac?gtcctgaact?ggtacggcca?ggttattttc?gataccggta?ggcattttct 1260
accacactgt?tttctttagc?ttgctagact?aatctattca?acgtcgcagg?tgcttcatcg 1320
ataagcattc?ccaacgacca?gattgaggcg?atgtatgccc?taacgccttt?ctcatacgct 1380
gacatctcat?ctggataccg?acctctgtgc?tccgatttca?atgatacatg?gtcgatctct 1440
tttacaatgg?gcttctatgg?cgagggtgtc?accttcaatt?tgaccggtga?tcagctggcc 1500
gtgcctggct?atcaggacga?cgaccactgc?ttccctccct?tcaatccatg?ggacagctac 1560
aacacgatta?ttggtcagca?ttggttgagc?aatttctatg?ctgtattcga?cttcggatca 1620
ttcgacccgg?agacatacga?tatacgtgtt?gggctggctc?ctttgaagaa?ggaatacctg 1680
ccgagcgctt?gacctaagaa?cttctattcg?tgtctttgag?catttagttc?aaacctcttg 1740
ctcggacgtc?aatgtttaag?catgcgtaaa?actatctact?agaagttaat?gttcatcgag 1800
agttcatcgt?ttaaataagc?agcttatctt?cattctttac?agccactata?cgcgacatga 1860
caattgtttt?atgggtcggt?gcgataaagt?ggccatctaa?aggcaatagc?aattaaaata 1920
agccaggaga?tggaacatga?aagaatctta?ctctttgtca?tggcctcatg?caactttggt 1980
gcgggctgtc?ggtgaccctg?tggggcacat?ctccggggag?tggaggccgt?taagcttcgg 2040
acaacattat?ttcttcagct?caaccatgaa?aaggttcggg?gacctgcatg?catcccccaa 2100
gcccgcaagt?ccgcgtcatc?aacaaatatt?gcgaagaaat?ggtacgcttt?agagccatgc 2160
gggctatatt?ttcggttcta?tagattgtta?gatataatta?ttgcttgtcg?aacccagatg 2220
cagcattgat?ctgttataat?cctcatattc?cgcgagtcac?ttgattccgt?gatcaagatt 2280
<210>37
<211>2287
<212>DNA
<213〉aspergillus niger
<400>37
tagttgaagg?aggcttttgg?ctttcttcct?ctttatcttt?cttctgttgt?cagtgattct 60
gatcgcagaa?gatgtgcaca?agatgaagac?cgccccgagt?catctatgga?tactgaagag 120
atggaagaga?tctgacaacc?aaggagtttg?tattatccag?ttccagtttc?atgttttgcc 180
tccgtctgat?agttccacca?aagatactgc?cattttgtat?ccgtagttag?acggagacaa 240
attgacaacg?acagccttgg?gggccaagtt?cagacatact?tccagccgca?cgcatggatg 300
tataccttgt?tgctacgtga?gcgtacgcca?gcttatcgac?ctattttagg?acctgctccc 360
acgtggagat?tctgcagcaa?acgcaggaaa?caaggaccag?aaattcgtca?tcatcgtttc 420
tccttagcaa?tcggctagga?tgtttccctg?ctctcgtatt?tggtctctgc?tcgttgcagc 480
cgccaccgct?agtgctgtac?ccaccagtct?ggccaccacg?cacctgcaat?cggttgactt 540
gcttctgact?cgcagttctt?acgggtttct?tactgacata?gcccttggaa?ctccgggtca 600
gagcctgccg?tatctggttg?actggacctg?gaccggccac?tatgtggtga?ccaccttgtg 660
ctacaacgat?cccaccgcca?cctacgattg?tctcaacgtc?gatcagaaaa?ttttcaacca 720
gactttgtca?tccactttta?tcaaccaaac?tgaccagtat?ggctatcttt?actgggatcc 780
caaccacttc?tactttacgg?agcccgcagc?agccgatgtg?gcgacggaca?tgctgcgcat 840
cggtcccacc?gcggtgaaca?ccaccatcca?agcagccaat?ttcgtcttca?acgagactat 900
tagcgcattc?cctttctcgg?gagtatatgg?actctcacct?gtttttcagg?gtgacaatcg 960
tgagttgttt?ccccaccgtc?ataaaactaa?ttcatgttaa?cacgaatcat?aggatccgtg 1020
caagcgtcct?tctaccaagg?atggaggagc?ggcgcctggc?actctccaat?tgtctctttt 1080
atctactgcc?acgacaatgc?caccaaagcg?gtatgcagtg?gttacgacgg?ccttcagaca 1140
ctaggcggat?acaacacctc?tcacgtccag?ggagatatca?cctggtacga?catcattgtc 1200
acggaggcga?tcaacacgct?ggactttgtc?tatgcgccag?ccgtgattaa?ttattgggcg 1260
ttgaacctca?cgcgcttctc?tatcggagac?gaagagcaag?agctcaacaa?gaccactact 1320
ctggatggaa?agcaagccgc?cgttgccgcg?ttcgaccacg?cttcgtatgg?tcgcggtgcc 1380
ccagtgtctg?tgtacggtta?ccagcgtcta?gtcgagctgg?tcggggcaaa?agccgtcacg 1440
ctttccgatc?ctccaaataa?cggtgagcag?ggattctatc?agttcgattg?ccggaactcg 1500
agtttactgc?caccgctgcg?gtatgagttt?gccgggtcag?agcgggcgtg?ggagattgtg 1560
cccgagaact?atgtggaggt?gctggcgaac?ggaaccaata?agtgcacctt?taatgtacgc 1620
accctgggag?atggagcgat?ggtaatggga?aattttggcg?agacatttgc?cattgataag 1680
tatgtcatgt?ttgactttga?gaagttgcag?gtggggattg?cagacttcgc?gtggtaatgg 1740
tataaggatg?tgtgtttgaa?catgtgcatt?atctcgagtt?tgactgaata?gacggagaat 1800
ccaagaccgt?agatcatgat?gctatctgct?tgattatttt?caatgtctct?agtatgggga 1860
aagtaataca?tgtgataata?tctccaaagt?agtaattaaa?agagaaaact?aatcaccact 1920
agtaattaat?actgcaaata?gcgctgttcc?acattgagac?aaccatataa?taataagtta 1980
gtggatatac?ggaatattag?aggtcatctt?aataccatac?tagtggatac?aaccatccgt 2040
acatacggaa?taggaaggag?gagcgagatg?gtcatcattt?gacactgagc?atactgtgtt 2100
ggcccagtca?agctgttgta?tgggggagct?cctagtgtgc?ccaaggctcc?agcatcttca 2160
ccttccgcaa?cgactttact?tagtttacat?taggtgagcc?tttctgttac?atagttgatt 2220
gaaagcctct?ccccaattgt?cttagcatga?tagaggttac?tcggagaacg?tactaatcag 2280
gaggcca 2287
<210>38
<211>1950
<212>DNA
<213〉aspergillus niger
<400>38
gatctttcta?gagcattgtc?ttgattgtgt?cattctgtca?ttgactccgg?ctatgaaata 60
ttattctcaa?tctgcctaaa?accaaattct?actctatcac?tacacatttg?tatcacctga 120
tctggctgag?ataggagagt?ccggcatctc?atcgtctgca?tcagacaatt?gcgataaatt 180
cattgcttgc?acctgttatt?gattcttcca?agttatgcat?ctcccacagc?gtctcgttac 240
agcagcgtgt?ctttgcgcca?gtgccacggc?tttcatccca?tacaccatca?aactcgatac 300
gtcggacgac?atctcagccc?gtgattcatt?agctcgtcgt?ttcctgccag?taccaaaacc 360
aagcgatgct?ctagcagacg?attccacctc?atctgccagc?gatgagtccc?tgtcactgaa 420
catcaaaagg?attcccgttc?gtcgtgacaa?tgatttcaag?attgtggtag?cggaaactcc 480
ctcttggtct?aacaccgccg?ctctcgatca?agatggtagc?gacatttcat?acatctctgt 540
cgtcaacatt?gggtctgatg?agaaatctat?gtacatgttg?ctcgacacag?gcggctctga 600
tacctgggtt?ttcggttcca?actgcacgtc?cacaccctgc?acgatgcaca?ataccttcgg 660
ttcggacgat?tcttcgaccc?ttgaaatgac?atcggaagag?tggagtgtgg?gctatggaac 720
tgggtctgtc?agcggcttgc?taggaaaaga?caagctcacg?attgcaaatg?tcactgtacg 780
catgactttc?ggacttgctt?ccaacgcatc?ggataacttc?gagtcgtacc?caatggacgg 840
cattctcggt?ctcggtcgaa?ccaacgatag?ttcctacgac?aacccaacat?tcatggatgc 900
cgttgcagaa?agtaacgttt?tcaagtcgaa?tatcgttggc?ttcgcccttt?cacgtagccc 960
cgccaaggat?ggcacggtca?gctttggcac?tactgacaag?gacaagtaca?ccggcgatat 1020
cacctacacc?gataccgtcg?gatcggacag?ctattggcgc?attcccgtgg?acgatgtcta 1080
tgttggcggc?acttcatgcg?atttctccaa?caaatcagcc?atcatcgata?ccggaacttc 1140
ttatgctatg?ctgccttcaa?gcgactcgaa?gacgctgcac?agtctcattc?ccggcgccaa 1200
atcttcgggg?agctaccaca?ttattccgtg?caacacaact?actaagctac?aagtggcatt 1260
ctctggtgtg?aattacacca?tctcgccgaa?ggactacgtg?ggagcaactt?caggttctgg 1320
atgcgtttcg?aacattatca?gctacgactt?atttggtgat?gacatctggc?tcctgggtga 1380
cacgtttctc?aaaaatgtgt?atgctgtgtt?tgactacgat?gagttacggg?tcggatttgc 1440
agagcgttcc?tcgaacacca?cctctgcgtc?gaactctacg?agctctggaa?caagcagcac 1500
ctcgggatcc?actacaacgg?gcagctcaac?gactacgacg?agctctgcta?gctctagtag 1560
ttcatctgat?gctgaatcag?gaagtagcat?gaccattccc?gctcctcagt?atttcttctc 1620
tgctctggcg?attgcttcct?tcatgctttg?gctctagtta?accgcatctt?actcgacgcc 1680
tgaacctcgg?gaaacatatg?cattatttac?acatgctgct?gatttgtatt?tgcatatatt 1740
cttcgagcct?ggacggcgtg?cgggtcatat?taccttacat?tcgaagtcct?tctctaatca 1800
atcaacattt?attcttactc?caccagttct?ggctcgcaat?taaccctgtc?taagaaaaag 1860
ttggtataga?acatggcatc?cactacctgg?aacattcaaa?gaaccttgtc?cgggatcagt 1920
gtgtatgact?tcgggtacga?ttctgacatg 1950
<210>39
<211>2660
<212>DNA
<213〉aspergillus niger
<400>39
accttctggg?gtggattatc?tgaagagatg?aactgccccg?cccaagtgca?agaagatgat 60
gcctgacagt?tgatgcctga?gggatgcttg?tatcaggtga?tcccggctat?ggtggtctaa 120
cccagttggg?ctgaattgac?cacatttagt?tagtgtcagc?cttaaacaga?tgaggctttt 180
cgcatgattc?atttccaagg?aacccaagga?aatggtcaaa?cagcaaagga?ataatgaccc 240
aacagttata?cctagctatg?cagcataaaa?gagaaaaaaa?acttgaactg?atacgagcca 300
tcatgtaacc?tccgtctctg?gctcaattct?ccatccaatc?acaattcttc?caagcaaact 360
tgggattcgc?cgggttctcg?gcaaccctaa?cctctaccag?taaaggttga?tccttccccc 420
acccgatttc?gcatggcttg?gacccctgaa?atatagttcc?tctacgtgcc?tgaatatgga 480
gcacgttatt?cgtctttcag?ggtcttgggg?ccttggcctt?ggggctgcca?agcgggcggc 540
ggagtgtgcc?ccgtggtgcc?ctgttttgag?cttggatgcg?attactatca?tcacttaata 600
agagcaagac?cctgcgtcga?tattgacggt?caatacactg?acctcagaga?accgtcgatg 660
tgcctgattt?cgctccatca?aaatgacgtc?ttctaccttg?cgccttgccg?tcgcgttggc 720
tttgtcaact?tgcagcagtg?ccctatcgag?ccagcgagat?gattcacttg?tggttccatt 780
tccttttggc?aatcttgagg?atgtccatat?tgccaagcgg?gatagctcca?agacagtaga 840
agctcctcta?gtgatatatg?tcagtcagct?ctcccactct?ccatctatgt?catcaactcg 900
acaaccctaa?caatcaacag?ggcgacagct?actggatgaa?cgcctcaatt?ggaacccctg 960
cgcagtcact?aagtttccta?ctagatctta?cgcgctcaag?ggtcgagccc?gcatacaccc 1020
tcgatgagaa?ttacgaatgt?tctgacgatg?aactctgctc?cgaattcggc?ttctacaaac 1080
ccaccgattc?atccacttat?cagcatctca?cctacacaca?gagacacgat?gcaggtgtcg 1140
actactccta?ccttgatacc?ataactcttg?gagatcacgc?aaccgacaat?gtcccactgg 1200
acatgtatct?tttgtcctac?atttcctgtc?agttccccct?ctctccctta?ccaccctatt 1260
tatccatcat?ctgaccattg?tctaaccacc?acatagacag?ctccctcggt?ctctcctccg 1320
tcaacaccag?cttcccctac?atcctggtcg?atcgcggcct?caccacctcc?ccatccttca 1380
gcctaatcgg?cgacaacgga?aacaccacca?cccccagcat?catctttgga?ggcatcaaca 1440
cctccaaatt?caacgggccc?ctgcaagcct?tctccttcgc?agaccacagc?atcaccaaca 1500
atccattcgt?caccgtcgaa?gctgactccc?tccaactaac?caccaacacc?aacgataatt 1560
ccacctaccc?tattccctcc?tccaccccca?tgatgctcag?aaccgaagaa?ctaatcacct 1620
acctccccaa?ctcgaccgtc?caatccctct?acaccgacct?taacataacc?atggacggcg 1680
tgatctccac?ttcaagattc?tacggggtcc?ttccctgcgc?ccgccaggaa?accgaatctc 1740
acacaatctc?tctagccatc?ggcaacatga?ccttctctgt?gtcctgggat?gagctcttcg 1800
tcccgtggac?gcgtgacgga?ctatgcaagt?tcggcattca?ggcccaggat?tcagattaca 1860
aaactcgtgc?ggagctgggt?gttccctttc?tgagacggat?gtatgtcgct?gtggattata 1920
ataatcagtt?tgtgggcgtt?gcgacgctga?aggatgatga?tgatcagaat?ggaggtgaag 1980
atgagattgt?ggagattggc?actgggacgg?cgttgcctag?tgctgtcggg?gattggccgg 2040
ctagtgttac?ggcgtatacg?cctgctgctt?ctacagggac?ggcggctgcg?acgttgacat 2100
tcacgacggc?gacgtctagc?gggggaggtg?tggtgccgac?gggtctatca?gagttgggta 2160
gggcgttttt?ggtgccgggg?gtgctgggga?tggctgtttt?gcaggctgtt?taggttagag 2220
attgtggtac?gattattctg?taggttaaag?atgtatattg?tctgttattg?tacttgatag 2280
cttgatatgt?ataatgaaag?tagtatagtt?tgaatttttg?ttatacacca?cgtgaaccca 2340
ctggaccgtt?gtctactgct?cgcagtgagt?gatatagtgt?agacccgtat?tactagtcat 2400
gtaggaccct?accttgatac?cataacactc?ggagaccacg?caaccgacaa?cgtcccactg 2460
gacatgtacc?ttttgtccta?catttcctgt?cagccccttt?ttgaatgtac?ctacatccct 2520
ctaaactcta?gtactatcac?gaacagcaaa?tgacattcaa?tctattctat?gcatattacc 2580
cttctaacaa?tacccagatt?ctatcaaatc?acgtgaacat?acagccctcc?caagtcacct 2640
gacaaagcgg?acaacaatgc 2660
<210>40
<211>2501
<212>DNA
<213〉aspergillus niger
<400>40
tgattcccaa?atcgcaccag?atgaagttga?atcagtggta?cagtttagcg?ggtggctgtc 60
atgacagaca?gaccctcaaa?ttgaagcaat?ggcagataga?tatggtctcc?agtccaccga 120
ttgaatgcag?ttggagaagt?caatcccccc?ttggaaagcc?cccaacgttg?cgctttctga 180
ccacctgaaa?tctgacaatc?agcaatcctt?cagctcttct?cagcgtctct?tggggccgat 240
ccccatcgga?tgaacacgcc?tcatccctca?ttaggcatgg?ctgagctgca?tgtcagcgga 300
gtcccaacac?ccaaaccaat?cctttagcgc?gcaccgggcc?tgcgaagcca?tcaccatcgc 360
ccgccttgca?gcaatgtgct?ccccggtcgc?attcctttcg?tttcataatc?tcacctccgg 420
ccagcccata?tccttcatct?cgcagctttt?ccctactcct?tcttttcttt?tgctttcttc 480
ccccatcgca?ggctgtttga?atgcctgctg?aagtatccat?ggtatgatgc?gaccgatact 540
tctcccccta?ctgggggtat?ttctgcagac?ctcctcggca?tccaatccct?atgtaatgag 600
ctggtcttcc?caagcctacg?gtccagatgg?cccgtggcag?gccgtatcca?tcgacgtggg 660
cagcaaccag?cagacggtcg?atctttaccc?cggagccaac?tatgctagca?cgatcctgat 720
gagcactctc?tgcacgaaca?aaaccctgtc?atccacctgc?tacgctgccg?aagcaggcac 780
gttcaaccaa?aacacctcca?ccactgccta?caccaccgcc?agctcgtggg?aaacaactta 840
ctgggccgtc?gagggtggaa?gccaagaggc?tgtgctcggc?gatgaggtca?ccttagggtc 900
gtttgtcgtc?cccaatgtga?gcttcgaagc?catctaccag?acctaccaga?cctatcccaa 960
tggcatcgcc?tatcctgtct?cggtcggcag?tctggccctg?gggggtccgt?acttgtcgga 1020
taccgtctcc?aattcgacgg?tcctgaacat?gatcgcagga?tggctttact?cgtccaacga 1080
cattccgtcc?tactcgtacg?gcatgcatat?cgggtcggta?gaccccaaaa?tcccaggctc 1140
cctgatcttg?gggggctacg?ataagagccg?agtgatcgga?gacgtgagtg?cgcagggagt 1200
agtgtcttcg?agtggtcttt?tggaacttga?attaaaggat?attgggctgg?gtgttgcggc 1260
gggttcctct?cccttcagct?tcaacaacga?aagtggcttg?tttctccaaa?gcagtggttc 1320
ggttcaggcc?aagaccgtcc?agattgatcc?aaccaagccc?tacatgtacc?ttccccaggc 1380
gacatgcgat?gccatcacct?ccaccatgcc?gatctccttc?aattccagct?tggggctata 1440
cttctgggac?accacgagcg?atgattatct?gaatatcacg?tcttccgccg?catacctctc 1500
ctttgtgttc?aacatgaatg?gggtcaacaa?caagaacatt?accatcaaga?ttcccttttc 1560
ccagctcaat?cttacgctgc?aagaaccgct?ggtcgatcaa?aacgtcacct?acttcccgtg 1620
cttcctcact?acctccaccc?cggtgctcgg?tcgagccttt?ctccagtccg?cattcgttgg 1680
ggtgaactgg?ttcaacggga?acaactcggg?cacatggttt?ctggcacagg?cccccggccc 1740
gggttacgcc?agtgaagaca?tcacccggat?cgcagtgagt?gacacgtcgc?tttctgcctc 1800
taacggtacc?tgggaagaga?cctgggctac?gtactggggc?atcaaaacat?ccgacaactc 1860
gagcagctcc?aagagtggcc?tgtcttccgg?tgccaaaatt?ggaattggcg?tcggggtggg 1920
tgtcggtgga?gcagtgttga?tcgcagcagg?tatagccatt?gcattctgtc?ttcgccgtcg 1980
ccgcggggcg?agtcaagagg?cggctggaga?gcaacggagg?tcgatgttta?ggggctttgc 2040
ggagctaccg?ggaggtgctc?acagtgaacc?ggcgaaggag?ttggatacga?agatgcataa 2100
gccgccgcag?gaaatgatgg?cttcgcagga?ggtagagcga?tacgagctgg?ggtgatggct 2160
aattctaaat?tttaatatgc?gaagggatcc?ctacaggata?ctacaggata?ccatatacgt 2220
gcgaatataa?tagctagttg?ttccaatatt?atgtatcaag?cttatactgt?ggattaacca 2280
acgacttgtc?tccgatacat?agggtagtac?gtagtcatgg?atccggggtg?tattgtcatt 2340
cagcatgacg?cattgctcaa?gccaaaagta?agctgggcca?gtgtatcacc?catgaaagca 2400
accctctctc?acctctgtac?tgatgacttg?gtggaaattt?ggatcctcgg?aaattgtgat 2460
taacacgtgg?atctagaccc?gaccaggcgg?gagcttggca?t 2501
<210>41
<211>3570
<212>DNA
<213〉aspergillus niger
<400>41
gaaaaggatt?gtccccatgc?ataataggcg?ttccaccacc?tgcatatcca?tacatgcagc 60
ccgagttatg?cgatgtgatc?gggcctggaa?taacatgatc?tccgatctaa?cgggggccca 120
aaaggggcag?ccaagatctg?ctaggcccaa?ccaggctagc?ggcgggccat?ctgaggcggt 180
gatccatttt?gggcgaggaa?aaggcaaaaa?gtggatcggc?gaaaggcaag?ttggagtgtc 240
gggagtttgg?tctcccgccc?cagggccgcg?tattagtcta?gctctctttc?tattcactcg 300
ggccaactcg?tcaactctct?ccctcgcttt?cattcagatt?tcattatttc?tcttacggtc 360
ttgccattct?tgccactttc?ggtccttatt?attgcttttg?atccccagtt?cccttttccc 420
aactgggtgg?cgctcctaca?gaccgacaca?tacctggcgg?actttccttg?cttctggctg 480
tacaccggga?cccgcctcat?acccagtacg?tgttggtcca?tggcaagcct?cctacttggc 540
ctgattacat?cgtcctgaga?gagagagttc?accaaaactc?tcccccaaac?gatgcgtctt 600
acaggtggtg?tcgctgcggc?tctgggcctc?tgcgctgctg?cctccgcttc?tctccatccc 660
catcgttcct?acgagaccca?tgattacttc?gctctacacc?ttgatgaatc?cacctcgccg 720
gccgacgtcg?cccaacgact?aggtgctcgc?cacgaaggcc?ccgtcggaga?attaccctca 780
catcatacct?tctcgatacc?ccgtgaaaac?agtgacgatg?tccatgcgct?gctggatcaa 840
ttgcgcgatc?gtcggaggtt?acgccgccgc?tccggagatg?acgccgctgt?ccttccctcc 900
ttggtcgggc?gagacgaagg?tctaggtggc?attctttggt?ccgagaagct?ggctccccag 960
agaaagctcc?ataaaagagt?gccgccgaca?ggatatgctg?ccagatcgcc?cgtcaacact 1020
cagaatgacc?cccaagcgct?tgcggcgcag?aaacgcattg?cctcggaatt?gggcatcgcg 1080
gaccccatct?tcggcgaaca?atggcatttg?tataatactg?ttcagttggg?ccatgatctt 1140
aacgtgacgg?gtatctggct?ggagggcgtt?acagggcagg?gtgtcacgac?ggctattgtc 1200
gatgacggtt?tggacatgta?cagcaacgat?cttaggccga?actattttgc?ggcgggttct 1260
tatgactata?acgacaaagt?accagagccg?aggccgcgct?tgagcgatga?ccgccacggt 1320
actagatgcg?cgggtgaaat?cggtgcggcg?aagaacgacg?tgtgcggggt?tggtgttgcg 1380
tatgatagtc?gcatcgctgg?tattcggatt?ctctccgcac?ccattgatga?cactgatgag 1440
gctgcggcta?ttaactacgc?ctatcaggag?aacgatatct?actcgtgttc?ctggggtccc 1500
tatgacgatg?gcgccacaat?ggaagccccg?ggcaccctga?tcaagcgggc?catggtcaat 1560
ggtatccaaa?atggtcgtgg?tggaaaaggc?tcggtttttg?tgtttgcggc?tggtaacggt 1620
gccattcatg?acgataactg?taactttgac?ggttacacca?acagtatcta?cagcatcacg 1680
gtgggtgcca?ttgatcggga?gggtaaccat?cctccgtatt?cggaatcctg?ctcggcgcaa 1740
ctggtggttg?cctacagcag?cggcgccagt?gatgcaattc?ataccacgga?cgtcggcaca 1800
gacaagtgct?cgactaccca?tggtggaact?tcggcggccg?gcccgctcgc?tgcgggaacc 1860
gtggcgctgg?ccctcagtgt?gcggccggaa?ctcacctggc?gtgacgttca?gtatttgatg 1920
attgaggcgg?cagtgcctgt?tcatgaagat?gatggaagct?ggcaggacac?taagaacggg 1980
aagaagttca?gccatgactg?gggatatggt?aaggtcgaca?catatacgct?ggtgaaacgg 2040
gcagagacct?gggatctggt?gaagcctcaa?gcctggctcc?attccccctg?gcagcgggtt 2100
gagcatgaga?tcccacaggg?cgagcagggc?ttggctagtt?cgtacgaggt?gacggaggat 2160
atgttgaagg?gagccaacct?ggaacggctg?gagcatgtca?cggtcaccat?gaatgttaac 2220
cacacccgcc?gaggcgatct?cagcgtggag?ttacggagcc?ctgacggtcg?ggtcagtcac 2280
ctcagtacgc?cccggcggcc?agataatcaa?gaggtgggct?atgttgactg?gaccttcatg 2340
agcgttgctc?actggtaagt?aaactttttc?tcggttgtcg?gttcttctgc?taatacatat 2400
ctaggggcga?gtccgggatt?ggcaaatgga?ctgtgattgt?caaggacacc?aatgtcaacg 2460
agcatactgg?gcaattcatc?gattggcgac?tcaacttgtg?gggcgaggcg?attgacggag 2520
ccgagcagcc?tctccacccc?atgcctactg?aacacgatga?cgaccacagc?tatgaggaag 2580
gaaacgtggc?taccacgagc?atcagcgccg?ttcccacgaa?aaccgagctg?cctgacaagc 2640
ccactggtgg?cgttgatcgc?ccggtgaacg?ttaagcctac?aacatccgcg?atgccgaccg 2700
gtagtcttac?agagcccatc?gatgatgaag?aactccagaa?gacccctagt?acagaggcaa 2760
gctcaacacc?aagtccttct?ccgaccaccg?cgtcagatag?tatcctgcct?tccttcttcc 2820
ccacgttcgg?tgcgtcgaag?cggacgcaag?tttggatcta?cgctgcgatc?ggctccatca 2880
ttgtgttctg?cattggcctg?ggcgtctact?tccatgtgca?gcgccgcaaa?cgtattcgcg 2940
acgacagccg?ggatgactac?gatttcgaga?tgatcgagga?cgaggatgag?ctacaggcaa 3000
tgaacggacg?gtcgaaccgt?tcacgtcgcc?ggggtggcga?gctgtacaat?gcttttgcgg 3060
gcgagagcga?tgaggaaccg?ttattcagtg?atgaggatga?tgaaccgtat?cgggatcggg 3120
ggatcagcgg?cgaacaagaa?cgggagggcg?cagatggaga?gcattctcgg?agatgaagtg 3180
cagtagatga?gggttgattt?tatttcggac?agtgtttctt?acttgttgga?tgacctgcgt 3240
tgaacaatat?tcctgctgtg?tatgctgcat?agagaaagcg?tgtatatacc?atgtatgtgt 3300
gcatcatctt?tgatcgggtt?attattcttc?atctgccatg?gtttgtgatc?tccggaatag 3360
taccaaagga?acactaaatt?aagggtcttg?gcgatgacgc?ttcccgtcgc?tgcttttgac 3420
ttcctccgca?tctcgtctct?cctgctgttg?accgcccgcc?aaccaacctc?catctcctca 3480
ctcctcccac?cttaatcttg?ctgtcctgct?tctagagccc?cccagtttaa?tttaaaaacc 3540
ggcttttcct?agctccacgt?attgtacctc 3570
<210>42
<211>1236
<212>DNA
<213〉aspergillus niger
<400>42
aggtcccgga?cagatgacaa?ggctctaaga?ctgtatgtct?cattcagggt?ctagccgtgc 60
ccgctcttat?tggcccggac?gcttcacgcc?gcgattactg?cgcccccgca?tgtctctctc 120
tccgctcgct?atcgatgcgg?tgtttgcccg?ccattgatgg?gaggaatgtc?tcacttcggg 180
cttgtgcttc?gcagatccat?acccctcaat?gacctagtat?agcaaacagg?cgtgatgtca 240
atgattgtgt?ttctattcag?agcatcaggc?ctcccatgtc?tatacctcag?ttatggagcc 300
ttggccgcct?tgggtaggca?aggcctcccg?ggtattctca?ttgccatttc?accgctactg 360
cagcttcaag?tgaagagaaa?gaggggaaag?aaagaatata?agtagcttga?caatctcctg 420
cacgtcctcc?tcttcagctc?acatcaaaca?tctattcttc?actcctcaag?agtaaaccac 480
tactaccaaa?cacaatctca?tctatagctc?acgagtacca?gcatcactca?tctaccacaa 540
tgaagacctt?ctctaccgtc?acctctctcc?tcgctctctt?ctcctcggct?ctggccgcac 600
ccgttgacag?cgctgaagcc?gccggcacca?ccgtctctgt?ctcatacgac?actgcctacg 660
atgtctctgg?agcttccttg?accaccgtct?cctgctcgga?cggtgccaac?ggcctgatca 720
ataagggcta?ctccaacttc?ggctcccttc?cgggcttccc?caagattgga?ggcgccccta 780
ccattgcagg?ctggaactct?cccaactgcg?gcaagtgcta?cgccctgacg?tacaacggcc 840
agacagtcaa?cattctggcc?attgattccg?cacctggtgg?cttcaacatc?gctctggagg 900
ccatgaacac?cctcaccaac?aaccaggccc?agcagctggg?tcgtatcgaa?gctacctata 960
ctgaggtgga?tgtcagtctt?tgcgcataaa?cgccaaacat?tcagcaaatg?cttgggggat 1020
gaattcggcc?atggcaggga?atggttatag?ttggatatga?tttcgggatt?tacgattgat 1080
acgcttattt?gggatacttt?cctttatctt?acctattgtt?aatagcataa?tacggagcat 1140
cacatacgta?catacacata?catcaatata?gtgatatatg?aacttgaata?cagagctttt 1200
tgaaaatgaa?atgagagatt?ctaaggtcgt?atctac 1236
<210>43
<211>1750
<212>DNA
<213〉aspergillus niger
<400>43
gtgaaagata?tcggatagcc?gtagaccctg?aaagattatt?tgagcctaag?ggctcttgca 60
gtgacgctag?caacagcgaa?cccactggga?tccaaaacac?tagatgaagc?tattgtaagc 120
cggaaccctt?ccggcgcccc?acccagctcc?tgcaggggcg?aaaacatgac?tctctaactt 180
aggagaaatc?acagccaagg?cccaagttca?ctgagagacc?gaaatggcgt?gaatttaaat 240
gttgcctttc?gcgcacttta?ctattccctt?gttcctatca?gcagtcactg?cttggcctcc 300
tttctagtga?gcagttccat?tcactttagg?ccccacggct?tcgttacaag?agcagtatgg 360
ctcaaatatt?ctggctttca?ctcttcctgc?ttgtctcttg?ggtcagagcc?gagtccaacc 420
gcaccgaggt?ggacctgatt?ttcccaagaa?atgatacctt?tgcgccaatg?cctttgatgc 480
cggttgtatt?cgccgttcaa?gccccttccg?tcgcccataa?agttaataca?tacatcgagt 540
acggctatta?cccagtaggc?cgtccaaatg?aaacagttat?tggccagacc?gaccatgtgt 600
ccgactcaac?aaacgaaacc?acttatttca?gtgtctctgg?tatcggcaga?acgttcaata 660
ccactggcag?ctgggagctg?ttttggaggc?tgagatggac?caattgttca?atctcagaag 720
actcgagata?ctacaaccaa?tcctacccct?ggatatcctc?cccatacatc?gacggtagcc 780
tcaacatcga?caaggtctat?gagggctttc?actacacagc?atacaatgtc?attgtcgaca 840
gggttacctt?cagcactcgc?gaagatgcta?gccaacccaa?cctcacgacc?ctcaccaata 900
gcgagaactg?cgataaagtc?tcgtctcttg?ctctattgtc?gattgtggac?tccctaagga 960
ttccacccca?gttaccccaa?gaagatattg?ataccgtgtc?aatgtgccca?caactcgccg 1020
atgccaggct?aaattcaact?tcaacttcaa?gcccctgcag?cgttagcatt?agtcccgagg 1080
ttgagtctaa?tatcctggcc?aagatcgcag?acaatgaatg?caataacgca?cttcaccccg 1140
ctgtgagttg?caccactgaa?gaaaccaagg?aaggcagcgc?gagcagccat?gaccacggcc 1200
atgctgtatg?gcttgtcatt?acgctagctt?ttgccttcct?tttctaaagg?atccaatgct 1260
agatgtgctc?gactcaggct?ttgagacagg?tagacaggaa?aacaggcttt?attgtcacgt 1320
cgccagtagg?ggaccatcaa?ccacacatat?gtccctacga?gaccatagct?atcaggaaca 1380
atgtacgggc?tggaactcca?ctcactctta?ggttgtaaat?cccatttctc?aatacatagt 1440
ttgtgagcaa?accacgcttt?tcttgaatca?ttgcatcctc?tttagcttca?attccttacc 1500
cacaaacacg?agaggagcgg?acccgccatt?ccacatagtg?tcttggcagg?gtcgcctctc 1560
caactacaat?gcccaacttc?agaggcccag?actatctctg?ccaagtgcca?aggctggact 1620
caaattacgg?aactctcgga?tgcttgtgcc?atggcttatt?gcttgaaggg?tttggaggtt 1680
tcggtggtta?gcgcccggat?aggcagtaga?acacctccaa?atgaggaatg?cggccgaagg 1740
taggtggggc 1750
<210>44
<211>2030
<212>DNA
<213〉aspergillus niger
<400>44
tggatgccga?gcaaattaat?taactgcgct?tacatggctg?tcctaacaaa?tcccttggca 60
ctcttagcag?tggtgcctgg?atgggacgaa?gccctgggca?tagcttgttc?atcggtaggc 120
cgaaactctc?ttttacgtac?cgtacggcca?atatcagtgt?gaacccgcaa?tttagatact 180
attaacttac?aagtaccctc?acgttatgta?gccgaatgtt?taaaagcgat?ggaccggttt 240
aaagtctccg?ttgtgcgatg?gctgttatta?acttggatta?acttgcaatt?tgcatcaagt 300
aagacgtgct?tctttttgga?tctttttaca?cacattactt?acggcggatg?ctctcgacac 360
tccggatttc?accagggtgg?tgttagtcca?ccatcggact?ccgatgcatc?ttaacatggg 420
tggtcgagat?gtcgccattc?tcagcaggca?ctttgctgtg?acatcctcac?aaagtgttaa 480
tggcgttgtc?tctgggatgg?tatgaggaag?aatgatgcca?tccgtgaaga?gtgtcgactt 540
gatagatact?caacaaaaag?tcatcctata?agtattgggt?tggatctgct?gttcttatca 600
tttcgtctcc?atcccactgc?aatcttcttc?aagacttcaa?agtccatagt?tccaacacac 660
agtcacctct?tcacccagct?tcactaccaa?ccaattcttc?aagaagaagt?tcactgctgc 720
aattgctact?gccattttcg?caagcgttgc?cgtcgcagct?ccccagcgtg?gcctcgaggc 780
ccgcctcaag?gcccgcggca?gcagcaaggg?atcccgaccc?ctccaggcag?ttgctagacc 840
tgcatcaacc?aagaaccaga?ccaacgttga?gtacagctcc?aactggtccg?gtgccgtgct 900
ggtggagcct?ccctctgctg?cagcgaccta?cactgcggtg?accggcacct?tcactgtccc 960
tgagcccacc?ggcaactctg?gaggcagtca?ggctgcatct?gcctgggttg?gtatcgacgg 1020
tgatacctat?ggaaacgcca?ttcttcagac?cggtgttgac?ttcaccgtga?ccgacggaga 1080
ggcctcgttc?gatgcctggt?atgagtggta?cccggattac?gcctacgact?tcagcggcat 1140
cgacatctcg?gcaggcgatg?agattgttgc?cattgtggag?tcctacacct?cgactaccgg 1200
tattgccatt?attgagaaca?agagcaccgg?ccagaaggtg?tccaaggagc?tgtcgtccag 1260
ctccagcctc?ggtggacaga?acgctgagtg?gattgtggaa?ggtaatatga?aacatacatt 1320
cctcattcaa?cattaccaaa?cgctaacgcg?atcttagact?tcgaggaaaa?tggttcgctc 1380
gtcaacctgg?tggactttgg?caccgtcacc?ttcactggtg?ctgttgccaa?ggcggcgggt 1440
ggtgagagtg?ttggacttac?cgatgcgacc?atcatcgaga?ttgaggagaa?tggccaggtt 1500
gtcactgacg?ttaccatcga?cagcgactct?gaggtgacca?tcacctacga?gtaaatttgc 1560
acacgaggcc?tgtcactgtg?actgacggtg?ttgagtgtct?caatacaaag?cgggttgatt 1620
ggtatgcagg?gatgtgatga?tgtgatcagg?tcagcgcttg?atttcaatcg?acgaggcagt 1680
ggagaacgaa?gatgtagata?gttttgattt?ctagtactac?tttgcggggc?ccctgttgaa 1740
tttgagtcat?tcttttgatt?gatcctccgg?aatcatatat?caagtaatgg?tgcagcgtag 1800
ggagtactcc?ataaggcaga?tgaagtacag?gtcttaaaac?ggtatgatcc?agtaagacaa 1860
agcggatctt?gtattccaaa?caatcacgtc?ggtaacatgg?actactactt?tcatctataa 1920
tgtttgtatg?ccagttgtgc?tgcagattat?taatttgtat?aggcattgta?caggtgcgct 1980
acattgttca?gcaagtaaac?gtgattttga?agtccccaag?aacacaaagc 2030
<210>45
<211>3080
<212>DNA
<213〉aspergillus niger
<400>45
cttcggctgc?gtcatgattc?atgcgtcaaa?tcagtggact?cttagtaggt?ggatgtacag 60
cacttatttg?atacttcgag?tgtccgccaa?catccggccg?tctatattct?ataccaatcc 120
acattatgcc?caacgaaact?gtatgctgtg?atttaagcag?aagtgagcaa?agcactgtgt 180
cagctgatct?aatatactat?atgctccgat?taaacccaag?cagtctgcta?ccagggagac 240
taccaggcag?aaagtatctg?gctgcatttg?tcccagtctg?cacaggactc?gctatgttat 300
ggagcagaag?tattgtgcat?ggattccatc?tgtcccacta?gcatgactat?ctcaatatcc 360
accgggtaca?tgatttagcc?ggtatcactc?ccccgtccct?gtagcaaagg?cccgcgcaag 420
aggtgtttcc?agaaagggct?ccacgcttag?caccgttcag?caaattctgc?atcagccgcg 480
gggaaactgc?ggtttgttgc?caggtcgagg?tgcttaaata?ccaccgtctt?ctcgctcgtc 540
agtgctctgc?tcaggcgtcg?ctcagtcaag?ttcagttcaa?gactcaggat?atccgggcag 600
tcctccgcaa?ctatgcgctg?ctccctcatc?tcccttctag?gcctggcggc?catcccggcc 660
cttggaggct?gtcccttcgc?acacactgcg?aacatgggca?ttgataacat?ggtgaaagca 720
cacgctcaca?tgtcccgacc?gttgattgcc?tccaagagca?gcccctcaac?tgttcctacc 780
tcctctagca?ccccttctgt?cgggcagaaa?ggcgtgttca?tgatgaaccg?cattgctcct 840
ggcacatccg?agctctacat?tgccaacaca?gatggcagta?atgaacgccc?actcctctcc 900
aaccccgtct?acgagtacca?tgcctccttc?tccccggatg?tagaatggat?caccttcacc 960
agcgagcgca?atggtgacgg?taactctgac?atctaccgcg?tacggaccaa?cggctccgat 1020
ctccaggaat?tggttgccac?gcctgcagtg?gaagactccg?ttgttatctc?tcccaacggc 1080
cgcctggcag?cctacgtctc?caccgccaac?aacatgaagg?caaacatctg?gatccttgat 1140
cttcagaccg?gcgcgcagtg?gaacctcaca?aatacaccca?ccactgccgc?caactcctcc 1200
ctcatggaga?gctatctccg?tcctgcctgg?tctcctgatg?gcgaatggat?cgccttctct 1260
tcggaccgca?acacccaatg?ggacggacac?ggcgtaccga?ccttcctcgg?ccgcacgggc 1320
tgggagacga?cgcaagaact?ctctctctac?gccatccgtc?ccaatggctc?tgacttccgt 1380
cagatcatct?ccaagccata?ctactctctt?ggatctccga?aatggtcagc?agacggtaaa 1440
cgcatcgtct?actacgaaat?gacccgggaa?gacacctaca?acgcccatcg?tccagaaacc 1500
attaccacag?ccaactcgac?gatcatgtcc?gtagacttcg?agacaggcac?cgatgtgcgc 1560
gtggaagtcg?ccggctccgg?tgtcaagcaa?ttccctcagt?acctggacaa?gaacggcacc 1620
atcgcctaca?ccctcaaagg?cggcaccagc?gagggcttct?acacgaccgc?gggactctac 1680
gtcaacacga?cctcggcgac?cctcaggtcc?ccggcgtggt?ctcccgacgg?caagcaagta 1740
gtctacgaaa?agagcacctg?gagcatccgc?tcggggtaca?agcagctcta?cagctgggac 1800
agtgactggg?actaccgctt?cacggacgtc?ttccctcagg?tctcgcacca?ggagcgcgtc 1860
gccatcacac?agaagcagct?gggcaattcg?tccatcgtga?cgttgaacac?aaccggaggc 1920
gacttgcaac?tcgtctacga?ccccagcacg?gcggactttg?tcagcgatga?cgaaaccaca 1980
ggactgagcg?cttaccagcc?cagctggtca?ccctgcggcg?agtggctcgt?cttcggcgtc 2040
ggattctggt?tcgagacgag?agaagcctca?ggcggatgga?tcgtgcgggc?caccgccaac 2100
gggagctact?cggaggttct?cgtgaacagc?agctactcca?tcaccgagga?tggagccctg 2160
aacagcgggt?tcccgagttt?ctcgccggat?ggcaagaaag?tggtgtatcg?ggtttgggga 2220
gccgacactg?caacctacgg?caacgccagc?gagatcgggc?tgcgggtgct?ggacctcgag 2280
acgcgaaaga?caaccgtcct?aaccacagaa?tgggacaatc?tgccccagtt?ctctcccgat 2340
ggagagctca?tcctattcac?acgcaaaacc?agcacgtaca?attacgatgt?gtgcacgatc 2400
cggccggatg?ggacagatct?ccgcgtgttg?acgagcagcg?gtgctaatga?tgcgcatgcg 2460
gtctggtcgc?aggatggacg?gattatgtgg?tctaccggca?tgtatgggtt?ccggtttgag 2520
tgtgcgctgt?atggtgatac?gttccagccg?tatgggcagg?ttatgattat?ggatgcggat 2580
gggggaaata?agaagttgat?gaccaactcg?atgtgggaag?attcgatgcc?gttgttcttg 2640
ccgagggagg?tactttagtt?ggtggcggga?ggatgctctg?atttttagag?gatatgtgac 2700
gtttgatgta?tgataagaat?tacacaagta?gttttgatca?taacgcgttg?aagaggatga 2760
aaaaaaaccc?ccgttgttcg?acttgatctt?ggcgatccgg?tgtagggttg?ttggacgagc 2820
aggatgtact?gcttaattca?agcaagtttg?ctactccgat?tcagtatgga?ggggcaatta 2880
atgatgacga?tattctgcac?tttctactct?acctactact?tatctgtata?tgaatgagaa 2940
aaaaatagta?tgcaacgaat?atagatcgta?ttgacagaac?ctgtcagaga?gaatgacctc 3000
gatagtcgac?tccatagcat?ttgatctttt?actaacagcg?aaagattccg?gactaactat 3060
ccatatatag?tactcctaca 3080
<210>46
<211>3290
<212>DNA
<213〉aspergillus niger
<400>46
ttccaacttc?ccatgaagtg?atgtagtagt?ctgctaataa?tacctcaaga?tagaatatag 60
tatttactac?ttatcgtcag?ctttgtcgaa?aattcaaagg?tttgtggaag?gccacctcat 120
ccgcacctgt?tgcctacagg?gatagcatcc?tgcgaggtgc?ttatccgctt?atcagcaaag 180
gtggcagggg?gggtaaggct?atcccgggtt?aggaaggccc?gcggcacgat?gcgatccttc 240
cagactagga?agctacctaa?tagggacagt?aagggaccaa?tctcaggact?aaaccgtgca 300
gcctactgaa?tctcaccact?cggacctgat?atttgccttc?ggcttgcagg?ggtatatcat 360
ctcaatatcc?tctagtggac?ggaaactagc?aactagtact?ttgagctgac?tcggccacta 420
taaatatgcg?gtcttatgct?cctcaacgac?aggcaactgc?tctgactacc?aaaatctgag 480
taggactagc?accgttgcga?gctcctcttc?acgataccga?atcttttata?agcaagtggt 540
ccaatatcca?ggtctaacgt?atccatacaa?tgcctccgga?tgcaaaatcg?cctggctacc 600
agcctggtat?ggcagtatta?ccatctaggc?cacatcctgc?caagggaaaa?gccattcgat 660
tcctcctttc?ccttgcattg?gtcgcgtttg?ctattgttca?attatgtggt?aatttccaca 720
aaaataggag?cgttgaacaa?cagcttcaga?gtcaaacact?tgatgatgag?tcctttaaat 780
gggaagatgt?gtgtaaatct?atcacgttgg?gatgtaacgt?tctaacgcac?tctattaggt 840
tactcctacc?aagcaactcg?tataccatcc?atgctttggt?gatcacgaat?gcgctcgctt 900
gtcgcttcca?atgaattgga?accgaactga?tggtgaaggg?tcaaaaattg?ccttggcggt 960
tatcaaactt?cctgccaagg?tacctgtcac?agatgcgcga?tatggtggtg?ccattcttct 1020
gaatccaggt?atgtagagcc?atattgctac?tcttcagcgg?ctgtgctgag?tttcaaatag 1080
gtggtcctgg?tggatccgga?gtgagcatgg?tctttagata?cgggaaagct?atccagacca 1140
tcgtcgactc?cccagaatca?ccaagtgcag?attcagcgag?cggaaagtat?ttcgatgttg 1200
ttagctttga?tccaagaggg?gtcaacaaca?caacacctaa?tttttcctgc?ttccctgacc 1260
ccgcgacgag?gaaagcgtgg?ttactgcagt?cagaggcaga?gggtctactt?gggagttctg 1320
aaggagtctt?cgatactcga?tgggcaaggt?acgaagcttt?tggtatgagc?tgcaatcaac 1380
aaggagtcac?agcgtcaaag?gatggagaat?ggataggaaa?attcatgaat?acggcccccg 1440
tggtggcgga?tatggttgaa?ctcgtagagc?gccatggaga?gtggcgtgaa?cgggaaacag 1500
agcggctact?ttcgacagct?ccgaacactt?tcccagttgg?aacaaacgtt?gacgccgaga 1560
ggataaggct?gcacaaccgt?tggaaaaaag?gggaggagaa?gctgctatac?tggggctttt 1620
cctatgggac?aatcctgggt?tccacgtttg?cggctatgca?gcctcatcgc?ataaaccgtg 1680
ctgtcataga?cggagtctgc?aacgctgatg?attattacgc?cggcaactgg?cttaccaatt 1740
tacaagattc?ggatgcagca?ttcaataaat?ttttcgagta?ctgctacaca?gctggcccat 1800
cagcgtgtcc?gtttgcgctc?ggcggagatc?ccgaagatct?caagtctcgt?tatgagcaga 1860
ttttgaccaa?tcttacatcg?agccctattg?ctgtgtctcc?ttctggaaat?aggggcccag 1920
agataataac?ctatagtgat?gtgaagtcat?tggtcgtgca?agctctctat?gtgcctttga 1980
aattattcga?tttggtggct?aggctattag?ctgagctcga?gcaaggtaac?ggctcttcat 2040
tcgctgactt?gaagtatgaa?gccaaacaat?ggccagtacc?gcctccatgc?gattcctcgt 2100
ccacacaata?caaagtacct?ggcgagagtg?atcaggaggc?cgggaggaat?atcctatgta 2160
cagatggtcc?aggcctcgac?ggaactgcca?aggaggattt?ccggagctac?tggaatatgc 2220
tccggggaca?aagtaaggcg?gttggagatt?tctgggccga?ggttcgcatg?tcgtgtgtca 2280
aactggagac?gcgacctgag?tggcgctatg?atggtaggtc?cgaccaacac?catattatac 2340
acacaatata?agctgacagg?tatgcgtatc?caagggccct?tcgcaggcaa?tacatcgcac 2400
ccattgctgt?ttatcgggaa?tacttatgat?ccagtaacgc?cgctacggaa?gtaagctttg 2460
ttcacctgat?cgtagcagac?tttgaagtac?agactgacgc?ataggcagtg?ctcatacgat 2520
ggcgcgtgga?tttcctgagt?caatcgttct?agagcagaac?tctgtcggag?tgagtacctt 2580
atctgttccc?caacccatat?gcaagatgac?taactgttca?atgtcgcagc?attgcacact 2640
gagtggccca?tccttgtgta?cagcgaaagc?gatacgccag?tatttccaga?ccggagagtt 2700
acctgacccc?ggaactgttt?gccaggtaga?ggagcttccc?tttcgtcttg?ccggatatga 2760
gagaagtcag?gtcatgtcgc?caggtgacac?agaattgatg?tccgccttgc?attcgctgag 2820
cgagttccgc?catctgctag?gcgcgtgaaa?aaggttaaat?aagtgtcgcc?agcgagcgct 2880
gcagttatta?atcctttaca?tcataggagc?tggctagaat?gttaacgatg?cagtttgccc 2940
ctgtatctcg?accaagagca?tgaataacac?attatatcag?caaatgttat?tgagcaaatc 3000
aattattcac?ctgcactcaa?ttcaatttaa?gatctgttgc?ctagactacc?agaattatta 3060
aggcgacctt?atcgaagcat?ttgcagacca?acccctgtcc?atcgtcaggg?gcaagacaga 3120
catttcttct?agaacccgga?tgatgtataa?tcgcggtggg?gaagatcatc?ctaaaccatt 3180
gccccagact?cgcctacctt?aggtaatcca?tacaaatgcc?ggggaaatca?ctgaggtgtt 3240
gttcatcacg?gcgttgaatc?ggcttctgcg?gtattaccac?cataactgta 3290
<210>47
<211>3080
<212>DNA
<213〉aspergillus niger
<400>47
gaaaatcccg?accgttaggc?tacctaatct?gctgtcttta?cccccgttag?cccacttacc 60
cagctttagt?ctctcgaagg?aaaagaaaac?aaagtaatcg?ggagcctata?atattcggcc 120
agaagtgggg?caatcacttc?aaccgttcat?ctgttattga?gttatcaagt?ctgtcaagtt 180
cgtcggagct?ggataaggta?gtcgccatcc?ccatttccgc?tgtgcaatgc?cgcagcgccg 240
aagtgtctgc?agctagctct?attttgttca?gctacgtatc?tgtctcttaa?ccaaatggat 300
gtcgccattc?gcccactaac?aacgccattc?cccacggccg?acggactccg?gcgcaagggc 360
ctgataagcg?ttagctccga?ctccgagtta?gtcatgcggc?ttattacgcg?cccttctccc 420
ctcacgatgt?tgatgctttt?tctggtatct?ctggcataac?tggcaaagat?caggctgtgg 480
tcataagagt?atcattgcct?tcagcttctt?cgccatgttg?agtagtctgc?tgcttggggg 540
tcttctgggt?ctagcgaccg?ctcaatttcc?tcccgagccg?gaaggcatca?ctgtgctcaa 600
gtccaagttg?catgagaatg?tgactatttc?tttcaaagag?gtgtgtgcag?agtatctaga 660
aatagctttt?atgctcgatg?ccgtgctgat?tgtcagcctg?gaatttgcga?aactacgccg 720
ggtgtccgat?cttattcggg?ctatgtacac?cttccccccg?gtttcctttc?cgacgggaca 780
ggagaagtgc?aggattatcc?tatcaacacg?taagccaatc?tcgaaacatt?ggaggatgag 840
caattactga?gcctcaacca?gcttcttttg?gtttttcgaa?gcccgcaaag?atcccagcaa 900
tgcgcctctg?gccatctggc?tcaatggcgg?tccgggtggc?tcgtcgctca?tggggctcct 960
tgaagaatta?ggtccttgtt?ccattgcatc?agactccaag?accacagtcc?tcaatccttg 1020
gagttggaac?aatgaagtca?atcttctatt?ccttgaccag?ccaactcaag?tcggcttctc 1080
atacgatgtc?ccaacaaatg?gcactttggt?tcggactgcg?gacggcgaag?aagagatagt 1140
ttccggtgat?ttctccattg?atgttcccca?gtccaacttc?acccatcatg?ttggtacctt 1200
tgcaagccag?aagcttgcac?agacagctaa?tgggactgca?ttcgcggctc?acgctctatg 1260
gcatttcgcg?caaacctggt?ttttcgagtt?cccacactac?aagccaaacg?atgatcgtgt 1320
cagtctctgg?gctgaaagtt?acggaggcca?ttatggtcca?ggcatctttc?ggttcttcca 1380
acagcagaat?gacaaaatcg?cagaggggac?tgcagaagac?ggtgcacagt?atttgcatct 1440
cgacacgctt?ggcattgtga?acggcttgat?ggatatggtg?atccaagaag?aggcttacat 1500
tacttggcca?tacaataacg?taaggctcgc?cccttcttca?ttcaactcgc?gtaatgccta 1560
attcagttca?gacctacggc?ctcgaaatct?tcgataaacc?cctctacgaa?gaactgatgt 1620
ataactggac?gcatccagga?ggctttcgcg?atcaggccct?cgcctgcgaa?gcggctttga 1680
aagaacgcga?ttccggcttg?cctcactcag?ggaagaatat?ctctgaaatt?tgcggaggcc 1740
ttgcactaga?atggggagat?ggccccatca?cctactacca?caccttcaat?cgcgggtggt 1800
acgacatcgc?ccatcctaag?aacgacccat?tccctgccaa?gcacatgctc?ggatatttga 1860
cgcaggagtc?cgtccttgcc?gctcttgggg?taccagtcaa?tttcacatcg?tcttcgagtg 1920
ccgtggctac?acagttcata?aaaacctttg?atatcgtcca?cggcggcttc?ctggatgcaa 1980
ttggctacct?cctcgacagt?ggtgtaaaag?tacacatgat?gtacggagat?cgtgattacg 2040
cctgcaattg?ggtcgggggc?gaaaaagcca?gccttgcagt?tccgtattcc?cgtatcaccg 2100
aatttgccga?cacgggatac?tccccactcc?ttacgcccga?cgggatcagc?ggcatgaccc 2160
gccagctggg?caactacagc?ttcactcgcg?tcttccaagc?cgggcatgag?gtcccctcct 2220
accagcctgt?cgcggcgtat?gagatcttca?tgcgggcgac?attcaacaaa?gatatcccta 2280
ctggcctctt?ggctgttgat?gacgaattcc?agtcggttgg?acctaaggat?acgtggcata 2340
tcaagaatat?ccctcctatt?atgccaaagc?cgcagtgcta?tgttctaagt?cccggcacgt 2400
gtaccccgga?ggtttgggag?accgttttga?acggatccgc?gacggtaaag?gattggtatg 2460
tcgtggatga?tagcgcgggt?gttgaggacc?acgaggggtt?cagcattctt?ggaggggatg 2520
agttgtagta?gcttagaagt?ctaccggaaa?gccttgctag?ctcttaaaat?acgacacaaa 2580
tagttgagcg?acatagtcta?ctctctcact?tacgaacacg?tgatgaatct?ctccagcaat 2640
aaagtggacc?aatcaattgg?aggaaaatat?atccacgatg?gtcggacggg?ccaacgaaaa 2700
gggccaacta?gcgcccctct?gaggatgatg?gtctagtctg?caggatatga?gattgttcac 2760
atcttatggg?tcttcaactg?cacaaattag?gcggaggtcg?cctcaccgaa?agagacgtaa 2820
gctgcttttt?ggtggattca?ttattagccg?ttatgccatt?tactaaaaca?ccgcagttcc 2880
agatcgcgta?gatggcctca?aagtgttcgc?cagatttgat?tgagggctac?ttcgcccaag 2940
cctatggcct?gtagatgcca?atttcttcaa?tacaaagata?ggcgaaacat?gttgaaaatc 3000
catcatattc?aattaaattt?caaaacatag?cgagacatta?agtattacat?atatttcaat 3060
gaatagagac?ttcttgcaca 3080
<210>48
<211>2520
<212>DNA
<213〉aspergillus niger
<400>48
tctcgcctgc?ctcgaccttc?ctgctatggc?aattctttcc?ccaagctgag?cggttccatc 60
cgcttcccga?ccgccaaact?tatcaacccg?agcgatacgg?agaggggaaa?ggctatcacg 120
gcaatgattg?cgcaactctg?cgataagata?accccatgtt?ttgacgtagc?ctcggccctg 180
tcttctcctc?attattatcc?tccgattccc?ccagggttcc?tgtcttctgc?agaaagtgct 240
ctcggaatcg?aagatgacca?ggtttcaatt?gcttcccctt?gtcgcagggc?tgcttgcccc 300
ttcaattgca?gcccttagca?tcccttcccc?gcagcagatc?ctcgattctc?tcactttcgg 360
agagcacacc?gacggctttt?gtccgctggc?acccaaggtt?gaggttcctg?acgatggttt 420
ctttccagct?ctcaagttcg?tagaagatgc?ctcgttcaag?tcgcgccaag?tcaatcgtct 480
ctccagggcg?gttcaagttc?cgaccgcaat?cgacgactac?atgaaggatc?cctacgacga 540
aaagttcgcc?ccattcctcg?acttccagaa?gctcctgcag?accctctttc?ccctcacgta 600
cgtccccagt?ccccgtcttc?atggctccat?ctaacgcaat?ccagccactc?ctacgcccgc 660
gtagatcaca?tcaaccgatt?tggtctcgtc?ttcaccctca?atggcacaga?tgactcgctc 720
aagcccctgc?tattcaccgc?gcaccaggac?gtcgtgccca?tcaacgaccc?tgccgactgg 780
acctatcccc?ccttcgatgg?ccactacgac?ggcgaatggc?tctggggccg?cggtgccagc 840
gactgcaaga?acgtcctgat?cggtctcatg?tccgttgttg?aagacctact?ctcccaaaag 900
tgggagccaa?cccgcacagt?cgtcctggcc?ttcggattcg?acgaagaatc?ccacggcttc 960
ctcggcgccg?gatccatcgc?caaattcctt?gagaagaaat?acggaccgga?cagcttcgaa 1020
tttatcctcg?acgaaggcgg?catgggcctc?gaagttctag?acgacaacaa?caacggcgtc 1080
gtctacgctc?tccccggcgt?tggcgaaaag?ggcagcatcg?acgttgtgct?cactctggcc 1140
gtaccaggcg?gccacagctc?cgtgccccct?ccacacacgg?gaatcggcat?catcgccgag 1200
atcatctatg?agctagaacg?ccaggacctc?ttcgtccccg?tcctagacac?tcaccacccg 1260
acccgcaaga?tgctcgaatg?ccaagtccgc?cactccccct?cgcaagtcga?accgtggctc 1320
gcctccgccc?tccaatcaag?cgactacatc?tccctagcag?agaaactggc?ctcctcgcgc 1380
ggcgacaagt?tccgcttcat?cctccaaacc?tcccaagcag?cggacatcat?caacggcggc 1440
gtcaaatcca?acgctctccc?cgagaaaatc?aacgccctcg?tcaactaccg?catcgctctg 1500
caccaaaccc?cagacgatat?caagaaccgc?gctgtggaga?tcatctctcc?catcgtcaag 1560
aaatataacc?tctccctcac?ggccttcccg?gaaagcgaca?ccgttgaccc?ctccctcaac 1620
aaccacctca?cccttactac?cctcagcggc?gccctcagtc?ccgccccggt?cagcccaacg 1680
gacatcgaca?ccgacgccgt?ctgggcccgt?ttctcgggcg?tcactcgctc?ggtcttcgaa 1740
tctgtcccta?gtctcgaggg?cagaaaggtc?gtcgtgagcg?gcgacatcat?gaccgggaat 1800
acggatacga?gattctactg?ggctttgtcg?aggaatattt?acaggtggag?tccgtcgagg 1860
gcgggtaaag?cgctgaatat?tcatactgtt?gatgagagga?tcgatattga?tattcatctt 1920
gaggcgatga?tgctgtatta?cggtatgcat?ctctcctttt?atggatactc?ctatcagact 1980
aacttgtatc?tctagatctt?attcgctctt?tcgatggacg?gaccgattca?tctgtcattt 2040
ctgctgcgtc?ggcagctgct?gatgatgaac?ttgctcacga?cgtgctgtga?gtctgtagga 2100
actctcctac?tctttagggt?ggctcaggat?gaatgatggt?tatgaatcat?gtggtctact 2160
gcgccaaaag?ttcatgtctt?tcctggagtt?caacgagaac?cagatctata?tttccacgaa 2220
tagctccagt?atatagccaa?atgcaaccac?gtatttgtct?atcgatctga?cagtctaatt 2280
ctttacctta?tactaggggt?aagaaagggt?aagaaaataa?aataatattt?gcagcggcct 2340
atgaagataa?ttatgtactc?gacgttgccc?aatgcactgt?agcccctctc?cctgtaacag 2400
gagtagccat?aaaagcaaaa?cgaaagtggt?aagaagacgg?gggcaatatc?cctgctttag 2460
caatatacaa?caatagtaac?aatcgagagc?tcaatatgaa?tgtataacga?gtgacctgca 2520
<210>49
<211>2730
<212>DNA
<213〉aspergillus niger
<400>49
tttagttgtg?atctcaatcg?caaatggaca?ggagatgata?ttcatgtcat?aatcagagtg 60
ccatgtcagc?gaccatgtct?tgccaagagt?catcatttcc?ggtaaaaccg?acggaggtaa 120
aaccccggtc?attcactagt?tcgagggagg?gaatagtctc?gcaggtctct?tcttctttct 180
tcctcggggt?ggcggatgga?tcacttcttc?atttgatggt?tgcctgccaa?cgacccactt 240
gactaggttt?cccccttgat?gggattcgtt?ggttttacca?gacagagcct?cttcacagcc 300
cagcgcgtgt?tccgcaaaag?caacagccca?agggtctgaa?ggctgacatt?ggagcgggtc 360
tgacgcagga?tggcttgctg?ttaaaaaaac?tcaggaacag?gccaagacga?agcgaccgcg 420
caaggctgag?cagttctccg?atttccccgt?gcccctcctg?cgcctcccat?gggcgacttt 480
tgatcccaga?tccatcgttt?ctgcaccgac?catataagaa?gctccgcacc?cccaaactcc 540
cctggcaagt?tcctgccccc?aaattacgtg?agacagggaa?ccatcacagc?aacaccatga 600
agagcaccac?tcttctttcc?ttggcctggg?ctgcccagtc?cgcctattcc?ctctctatcc 660
acgagcgcga?tgaacccgct?actcttcagt?tcaactttga?acgtcgtcag?atcgccgacc 720
ggtcccgtcg?gaagcgatcg?acggcctcgg?ccgacctcgt?taacctggta?tgttcccatc 780
ccgagtctca?aatcagggga?attatgacgg?tcgctaatgc?aggtttctag?gctacgaatc 840
ttggctacac?gatgaacctc?acactcggca?ctcccggcca?ggaagtcagt?gtgacgttgg 900
acaccggcag?cagcgatctc?tgggtcaatg?gggccaactc?gtccgtctgc?ccctgtaccg 960
attacggctc?ttacaactca?agcgcttctt?ccacctacac?cttcgtgaac?gatgagtttt 1020
atatccagta?tgtcgacggc?agtgaagcca?caggcgacta?tgtcaacgat?actctaaagt 1080
tctccaatgt?gactttgacg?aactttcaat?ttgccgtcgc?atatgacggc?gactccgagg 1140
gtaagtcttc?gctattccct?cactttcatt?ttacactttg?ctaacggttt?taccatgcag 1200
agggggtcct?cggtatcgga?tacgccagca?atgaagccag?ccaggccacc?gtcggtggtg 1260
gtgaatacac?caacttcccc?gaagccctcg?tcgatcaagg?cgcgatcaac?tggccggcct 1320
acagtctatg?gctcgatgac?ctcgacgaag?gaaaaggcac?cattctgttc?ggcggagtca 1380
acaccgccaa?gtactacggc?agcctgcaga?ccctgcctat?cgtctccatc?gaagacatgt 1440
acgtcgagtt?cgcggtcaac?ctgacggccg?tgcaccttga?gaagaacggc?aactccgtct 1500
cggtcaacaa?cagcgccacg?caattcccca?tccccgccgt?gctggacagc?ggcacggccc 1560
tgacctacat?cccgacctcc?gccgcagcca?gcatctacga?ggccgtcggt?gcccaatacc 1620
tgagcgagta?cgggtacgga?gtgatcgagt?gcgacgtcaa?ggacgaagac?ttcaccttcc 1680
tgttcgactt?tggatccttc?aacatgagcg?ttgacatcag?cgagatgatc?ctcgaggcca 1740
gttccgacat?gaccgacatg?aacgtttgta?cgtttggcct?cgcagtgatc?gaaaatgagg 1800
ccctgctggg?cgataccttc?ctgcgcagcg?catacgtcgt?ctacgatctc?ggaaacaacg 1860
agatctccct?ggccaaggcc?aacttcaacc?ccggcgagga?ccacgtcctg?gagatcggca 1920
ccggatcgga?tgccgtgccc?aaggcgacgg?gggcgacggc?gaccggcgcg?gcagccacat 1980
ccacggcctc?gagcgacaag?tcggacaagg?agagttcggc?tacagtgccg?cgcagccaga 2040
ttgtctcgct?ggtggcggga?gtcttggtcg?gtgttttctt?ggttctgtaa?atatagagat 2100
ttcacgttgc?atgttgatga?tacataccat?agatttgctt?ctaattgccc?cttacatctc 2160
gaaatgtttt?ctgtttttag?cttgatatcc?catcgcttca?ggtttcagat?atggaaatga 2220
aatgaaaatc?ggaatgcaag?atctgatcga?atagttgttt?cactgccgcg?tggctggtcc 2280
gatcggcacg?aagccagtaa?tcgacaacca?atcatacatt?gtgatttcct?gtcaacctcc 2340
ttgcgactac?tactaatttt?atcatatcat?gccgttgtga?cctatcctac?tcggtgtccc 2400
cacaccgatg?atagccaccc?gcgaccggat?aatcggtaac?ctgccaagag?tcgaacggct 2460
ttcctgtgga?aagggtggct?gcaacctgtt?tgtttcagtt?tttgtgttgc?agaattgact 2520
atccttctga?cctgtgaatg?atactgggat?ggtgacgtag?tgaaaatgtt?ggtggagcga 2580
ttaaggtttg?tgcctgtcag?cctcgtcaag?tccatcatca?tgtcttttcc?ggactatcac 2640
ttcctctact?ctgaagtacc?gggactcccc?gccagtattc?gtttcgccaa?tcagagcatt 2700
cgatgtgaac?cggattgaag?agtgcccggt 2730
<210>50
<211>3231
<212>DNA
<213〉aspergillus niger
<400>50
ccgacgcgac?ggcattagtt?cctcgatagc?gtgggaagac?catggagaga?ccggccgata 60
agctgcagag?gagctttctg?tgggctgacc?agtgcctatc?agcaaatgga?cacgcggtga 120
cacccccgca?atcgcaagac?cgcctcgaca?ccgtccatcc?aggcaccatc?gcaacggcaa 180
accagcctct?cctccaatca?aaccatcgat?gtgatattgc?tagcggcggt?gagaacagca 240
ggtcgaatgt?cgcaattaat?tctcgcatcg?tccctcactg?caaggggccc?actaccagag 300
ctctgcggcg?ttgttattta?aatccgttgt?tgggaccttt?cggtcatcag?ccactgtgtc 360
tggtcactat?cgcgctggtt?caacctcaac?atgttggtcc?gtcagcttgc?cctggctctg 420
gccattgcgg?ccttgtccga?tgccattccg?acatccatca?agcatgtcct?gcacgagaaa 480
cgtcacaagc?ccgcatccga?ctgggtgaag?ggtgcgcgcg?ttgagagcga?tgcggtcctg 540
cctatgcgca?ttggccttgc?ccagaacaac?ttggacaagg?gctatgactt?cctgatggaa 600
gtgtgagtca?aaatctacct?tttttatgct?atatgcctag?ttttaggatc?gcaatggatg 660
acctcgaaac?atgctgacat?gagattggcg?cagatcggac?cccaagtctt?ccaaatacgg 720
ccagtactgg?tcggcagacg?aggtgcacga?catcttttcg?ccatccgagg?aggctgttga 780
ggcagtgaga?gaatggcttg?tcgcctctgg?tatccatccg?tcgcgggtgg?tgcactccga 840
caacaagggc?tggctcgcgt?tcgacgccta?cgcccatgaa?gccgagaggc?tgttcatgac 900
ggaattccac?gagcacgaga?gcgaccgaag?tgctaagatc?agggttggat?gcgaccagta 960
agaagattct?tctatcacct?tccatgagta?gctattaatc?ggaatctaga?taccacgtcc 1020
ccgaacacat?ccagaagcac?atcgactaca?ttacccctgg?agtgaagctc?acccaggtcg 1080
tgaagaggac?caacaaagtc?aagcgtgctt?cccaactagc?tcactcttcc?aaggccaagt 1140
ctgctgccca?aggtccgcag?ccactcccca?acaaggccaa?gttcctgcct?gaagacctcc 1200
gcggctgcgg?ttacaacatc?accccctcgt?gtatcaaggc?cttgtatcag?atcccagacg 1260
ctaagacggc?gaccccgaac?aacagcctgg?gtctgtacga?gcagggtgac?tactttgcca 1320
agtccgacct?cgacctcttc?tataaggagt?atgcgccgtg?ggttccccag?ggtacctatc 1380
ccatcccagc?cctgattgat?ggcgccaatt?actcggttcc?ttcctacagc?tccctgaaca 1440
cgggtgaatc?cgacattgac?attgacatgg?cgtgagtcat?ttctgcacct?tgtcatcaga 1500
cccctactga?cgttttgaag?ctactccctg?ctctaccctc?agcaggtgac?cctctaccag 1560
gttgacgacc?agctctacga?accagtcgag?gtcgacacaa?ccaatctgtt?caacaccttc 1620
ctcgacgctc?tcgatggcgt?gagtacagac?ctcgttctca?gtcttaccca?gctaacaccc 1680
ctagtcctac?tgcacctaca?gcgcctacgg?cgagaccggc?gatgacccgt?cgatcgaccc 1740
cgtatacccc?gacacccgcc?ccggcggcta?caaaggtacc?tacctacacc?acctcttccc 1800
catacaatcc?aacctaacac?accaacagga?aagctccagt?gcggcgtcta?taagcccact 1860
aacgtaatca?gcgcctccta?cggccaatcc?gaagccgacc?tccccgtcag?ctacaccaag 1920
cgccaatgca?atgagttcat?gaagctcggt?ctacagggac?actccatcct?cttcgcgtct 1980
ggcgactacg?gcgtcgcgtc?tttcgccggc?gacggtgacg?agaacggctg?tctcggccca 2040
gagggcaaga?tcttcaaccc?ccagtacccc?tccaactgcc?cctacgtcac?ctccgttgga 2100
ggtaccatgc?tgtacggcta?ccagaccgtc?aacgacagcg?agagcgtcat?gcacgttaac 2160
cttggcggaa?ccgcaagtaa?cttcagcact?tctggtggct?tctcgaatta?cttcccccaa 2220
ccggcatatc?agtttgctgc?tgtggagcaa?tacttccagt?ctgcgaacct?gtcgtatccg 2280
tattactcgg?agtttgaggt?cgatgttaac?acgaccaagg?gtctctacaa?taggcttggt 2340
cgtgcttatc?cggatgtctc?ggcgaatgga?gcgcatttcc?gcgcttatat?ggatggatac 2400
gattatcatt?ggtatggatc?gagtttggcg?tcgcctttgt?tcgcgtcggt?tcttactttg 2460
gtgagctttg?tcacccccca?ttactaatta?ttgacacatg?gctgaccgac?ttagctcaac 2520
gaggaacgct?tcgctatcgg?caagggcccc?gtgggattcg?tgaatcccgt?gctttatgct 2580
tatccgcaag?tgctgaacga?tatcactaat?ggtactaatg?ctgggtgtgg?aacttatggg 2640
tttagtgcta?ttgaggggta?agtgctcagt?acttggttct?gtcaggaggg?gtgtgctaat 2700
tgatgactat?agatgggatc?ccgctagtgg?tttgggtacg?cctaactacc?cattgatgaa 2760
ggagctgttc?ctctctttgc?cttaggattg?aacggtgctg?tgtcagaggg?tgataggtgg 2820
tcaagctgtg?tatatatgtc?tgatggggaa?atatttacga?tcataggata?atgtgtcgac 2880
gagcatgaat?ggccaattat?ctcgcctgtc?accgtgaata?aggtcaaatg?tagatcggtt 2940
taatagttca?actacagaga?attcttggat?attgtcaaat?gttgactatt?cgctgtctct 3000
ttatcgtcta?atgtataata?tcatcaaata?acctaaccca?agggatatca?aaaacataag 3060
aaaataataa?accggtacta?tgtgtcgaaa?aaaggaatgt?ttgtgaattt?tttaaaaccg 3120
ttcatacctc?ccgtccatgt?ccaccaaatg?cacagcgctg?gtcgaatccc?tctccgaccg 3180
tgtcgtatag?tcaacggaga?tattcactga?cttggaaatc?ttgctgttgg?t 3231
<210>51
<211>2660
<212>DNA
<213〉aspergillus niger
<400>51
tcctgagcaa?gcagctaccg?gtaatctgag?acctaatcct?ggtaagtgga?tcgagttcat 60
ttacctcatc?atctaacctc?gcttcatgat?tcgcaggcgc?tttccgcgac?tagtcgatgc 120
cagtatccat?ttgcctgcag?atccgatgct?tccaccgacc?accgttactt?ctctccagac 180
ccccatccgg?ctttccgacg?gcctcctctg?catcccctca?caaagcaagc?ggagacctgc 240
ctgaataggg?agagtttttt?caatgagccc?acacgcagtt?acctcgcttc?cgcatgagat 300
gggtccattc?ttgacaatgc?tgcctaatgc?gcagaagggc?cgtcatgcgc?ctggagaact 360
acataaatag?ggaccacgca?tgccccgacg?atgtatgaat?tgttcaaact?tctccgccca 420
agtgagttct?cttttcattc?cattccgaag?ggagaatcac?cagtatgcgg?gttaccacgg 480
caattgcttc?attactactg?gtcggctcgg?ccaccagtct?ccaaaatcct?catcgtcggg 540
ctgttccgcc?ccctctctcg?catcgcagcg?tagcgtctcg?ctccgtgccc?gttgagcgcc 600
gaaccaccga?ctttgagtat?ttgactaaca?agactgcaag?tgcgtgattc?cgttttttaa 660
ctaccgcatt?tatcgttcta?agatcaattg?caggattcct?ggtcaatggc?acaagcatcc 720
ccgaagtcga?tttcgacgtc?ggcgagtcct?acgccggcct?tctccccaat?acgcccactg 780
gcaattctag?cctattcttc?tggttcttcc?cctcgcaaaa?tccagaggcc?agcgatgagg 840
ttagtggtcg?ctctgttttt?tccggtcatg?cgtcagccag?ctaacaatta?acaaagatca 900
ccatctggct?caacggcggc?cccggatgta?gctccctaga?cggcctgctt?caagagaacg 960
gcccattcct?ctggcagcct?ggcacttaca?agcccgttcc?taatccatac?tcatggacca 1020
acctcaccaa?tgtggtttac?atcgaccaac?ccgccggcac?aggcttctcc?ccgggcccct 1080
cgaccgtaaa?taacgaggaa?gacgtggctg?cccagttcaa?cagctggttc?aagcacttcg 1140
tcgacacctt?cgacctgcac?ggccgcaagg?tctacatcac?cggtgaaagc?tacgcgggca 1200
tgtacgtccc?ctacattgcc?gatgccatgc?tgaacgagga?ggatacaacc?tacttcaact 1260
tgaagggtat?ccagatcaac?gacccgtcca?tcaacagcga?ctcggtcatg?atgtactgta 1320
tgtttccctt?catatacctc?cacctccacc?accaccacca?ctaacaacat?cacccaccag 1380
cccccgccgt?ccgccatctg?aaccactaca?acaacatctt?ccagctaaac?tccactttcc 1440
tctcctacat?caacgccaaa?gccgacaagt?gcggctacaa?cgccttcctc?gacaaagcca 1500
tcacctaccc?accccccagt?cccttcccca?ccgcccctga?aatcaccgaa?gactgccaag 1560
tctgggacga?agtcgtcatg?gccgcctacg?acatcaaccc?ctgcttcaat?tactaccacc 1620
tgatcgactt?ctgcccctac?ctctgggacg?tgctcggctt?cccctccctc?gcctccggcc 1680
caaacaacta?cttcaaccgc?tccgacgtcc?agaagatcct?gcacgtccct?ccaacggact 1740
actccgtgtg?ctcggagacc?gtcatcttcg?cgaacggcga?cggcagcgac?cccagctcct 1800
ggggtcccct?acccagcgtc?atcgaacgca?ctaacaacac?tatcatcggc?cacggctggc 1860
tcgattacct?cctcttcttg?aacggctcgc?tcgccacaat?ccagaacatg?acctggaacg 1920
gtaagcaagg?gttccagcgt?cctcccgtgg?aaccgctctt?cgtcccttac?cattatggtc 1980
tggctgagct?gtactggggc?gatgagcctg?acccgtataa?ccttgatgct?ggcgctggat 2040
acctgggtac?agcgcatacc?gagcgcgggt?tgactttcag?ctcggtgtat?ttgtctggtc 2100
atggtaagtt?tattatatcc?ccttggaagc?ggtatgatga?acgttagaga?gtgctgactg 2160
ttgcttcctc?ctcgtgatag?aaatcccgca?gtatgttcct?ggtgcggctt?accgccagtt 2220
ggagttcctg?ctcggtagga?ttagtagtct?ttcggcgaag?gggaactata?cctcttgatt 2280
tcagcggatg?acgacaaaaa?gatgatgagg?aagatgattg?gatgctttca?gatgggaatg 2340
cgtgcatagg?agatgagatg?agatgatgta?tcattgaggt?gtgatgactt?gtacatatgt 2400
agatcggtag?taaaagggat?actataggat?atggtatttg?atgtatcatt?tatgtacacc 2460
acgtggattc?aattgagggg?agcttcaatt?cctggttatt?acttatcata?tttccaacat 2520
gtccgcgtat?aaccggtaac?aactaacggc?ttcatgtttg?tcaagtgact?gtcttggtac 2580
aatactactg?tttctatatt?ctactgttgg?taacttaatc?tggacatatt?ctatatccac 2640
gtacagattc?tcgctagatt 2660
<210>52
<211>3150
<212>DNA
<213〉aspergillus niger
<400>52
ccaatcaacc?acggatgatt?gggttcaggt?cctggaggca?cggagtcgga?ccaagacact 60
aaggtacagc?actagcgaga?caatgtgtta?tcgctattat?tggcaaaatg?gccgcgggat 120
ctcttatgca?gggttcggct?ccatcctccc?ccctcttcct?atccagtcaa?tccgcctcgg 180
ttattgaagg?agatcctgag?ctgtttaact?gacgcctcac?cgatcaggcc?ggaaatggtg 240
gcgggataca?acatcgtttc?cacacaatag?tgcttgtctc?ctgcgatctg?catggcatgc 300
taatctccgc?cagcatgtat?cttctatcca?ctggatatga?attttcctcc?cctcacacca 360
tgtgggcctg?ggggttttcc?ctcaaacttt?gtcgctcatg?taacgatgta?tataaagccc 420
tgaggatggc?atcccccacc?catcggtctt?ttgctgaccg?ttctccttga?agaaattctc 480
gagtggcttg?tggtgcatgt?atagatttaa?tcttcgaggg?ttattaacta?ggtatagctg 540
tgactaagtc?tgtccttgca?ttgaacaaca?caccatgcgt?ggctctcggt?tggtgctctt 600
gttgcccctg?gctgcactta?gttgtgctat?gcccgagaat?gaatggtcat?ctacgataag 660
aaggcagtta?ccaaaagcgt?ccactggcgt?caaatcgata?aaaaccccaa?acaatgtcac 720
tatcaggtat?aaagaaccag?gaaccgaagg?aatttgtgag?acaacacctg?gggtcaaatc 780
atactccgga?tatgtcgatc?tttcgccaga?gtcgcatact?ttcttttggt?ttttcgagtc 840
acgccgtgac?cccgaaaatg?atccagtgac?tctgtggctg?aatggtggcc?ctggaagcga 900
ttccttgatt?gggctttttg?aaggttggcc?aaatatcctg?acggaaaaga?taaaattcag 960
cttgcatgtt?ctgacgcctt?cacaacagag?ttgggtccgt?gtcacatcac?accagagtac 1020
gaatcaatca?tcaatcagta?ctcctggaac?gaggtcacca?atcttctttt?cttgtctcag 1080
cccctcggtg?tgggtatgga?atattgctgc?cttcatacat?cctgagtaca?ttgcttacgg 1140
tcttatctgc?gaagggttct?cttacagtga?aaccgaggcc?gggtccttga?atccatttac 1200
tggagccgtc?gagaacgcct?cctttgctgg?agttcagggt?cgatacccag?ttattgatgc 1260
cactatcatc?ggtaagttgt?ccggtttgac?tctcacctag?cattctcctc?aatgtcctac 1320
tttacagaca?cgaccgatat?cgctgcacgc?gcaacctggg?aggtgcttca?gggcttcctc 1380
agtggcctgt?cgcagctaga?ttccgaagtc?aagtccaagg?agttcaacct?gtggacagag 1440
agttacggag?ggtgagtgca?actttcatac?cagaccgacg?taagctgact?tgatcaagac 1500
actatggacc?agcggtaggt?tgtcttttct?ggttgcacac?atattgatct?aatgaccgaa 1560
gttcttcaat?catttctacg?agcaaaattc?gaagatcgct?agcggggaag?tcaatggcgt 1620
ccaactgaat?tttaactccc?tcgggattat?caacggcatc?attgatgccg?cgattcaggt 1680
acttagaaat?gcagctcgcg?cagaggctgc?ggcctagaag?gacatcgcta?aagtaattaa 1740
taggcagact?actacgcaga?ctttgccgtt?aataatacat?atggaatcaa?agctgtaagt 1800
ttaaatacac?gtacatcgtg?gatttaagat?caaccgtgct?catgcttgct?aggtcaatga 1860
cacagtgtac?aactatatga?agttcgccaa?cacgatgcca?aatggatgcc?aggatcaggt 1920
tgcttcgtgt?aaattgacca?ataggacctc?gctttctgat?tatgctatat?gtacagaagc 1980
agccaatatg?tgcagggaca?atgtcggtga?gtggttctac?tgtttctctg?caggggtgca 2040
atgatgaagg?actttgctaa?gctgtcatgt?acagaagggc?cttactacca?gtttggcggc 2100
cgtggcgtgt?atgatattcg?gcacccctac?aatgtaagtg?gcaaggataa?ggattgtact 2160
ttccgaacag?ggacactgct?catatgtcaa?cgtaggaccc?gaccccgccg?tcctactttg 2220
ttgactacct?caagaaagac?tcagtcatgg?atgctatcgg?cgtggacatt?aactacaccg 2280
agtccagcgg?cgaagtatat?tatgcattcc?agcagaccgg?cgactttgta?tggccgaatt 2340
tcattgagga?cctcgaagag?atcctccaac?tccccgtacg?cgtgtcgttg?atctacggcg 2400
atgccgacta?tatctgtaac?tggttcggcg?gtcaggccat?ctcactcgca?gttaactacc 2460
cccatgcagc?tcagttccgt?gcagcgggat?acacacccat?gacagtagat?ggggtcgaat 2520
acggtgagac?tcgcgagtat?ggcaactttt?cgttcacccg?cgtatatcag?gctgggcacg 2580
aggttccata?ctatcaaccg?atcgcagcgt?tgcagctgtt?caaccgtact?ttatttggat 2640
gggatattgc?agcgggtaca?actcagattt?ggcccgaata?tagcaccaac?gggacatcgc 2700
aggctacaca?cacggagtcg?ttcgtgccac?tgtccacggc?gtcgagtacc?accgtcaatt 2760
aggattgggg?gaaatttttc?cctctttggt?atggctaatg?ctgtgttatc?cattccgata 2820
cttgtccata?acctaaaaga?gtggcacgga?agctttccta?gacatgcttg?ctctagtcaa 2880
cttttatcct?accactgtgt?ggtcctacca?taatgtcatc?ctaaacttat?caggtgtctt 2940
acatcatttt?gcagtgacca?taaaagtcat?gtcatattaa?gtccattacg?gtagttcgta 3000
acttgctgat?ggcttacgta?attgtgcctc?agcaggatgt?cgtgatacgc?tccaaaaccc 3060
aatctgatca?tggatatcca?gcggaataac?acaaaagaaa?aaataaacat?aaccaaccac 3120
caaaatgaca?gaggctaatg?cctggacaac 3150
<210>53
<211>3221
<212>DNA
<213〉aspergillus niger
<400>53
ccatcagctc?ttgttgttat?gttttatgtc?atagtgtaat?gctagcctta?gcgtgcgtgg 60
tgtttgaatt?tcagattggg?catggatacc?tgggcgtctc?gggatggata?ctgggacgtg 120
gtaagatgct?tggaagcgtt?gattttgagt?ttgacaatat?atccctatgt?ttctcttctc 180
cacacccttt?taccgtaatg?cgacagcatt?gtgtagagtg?cattgcctta?attagaacct 240
acgaatcctt?gatttgtata?tgacacccga?tcaccatcga?gccacctaca?tcatggcgcg 300
ctctcagatc?ctccgaacca?aaacagtaat?gtcgatcgtc?gcgcctgaac?caaggctgat 360
tttccctgct?gaagcgtgtc?ataaagtgaa?acatactttg?tagataaact?cggcaattaa 420
ctgccactta?ccccatacat?cgctaccgga?gagtggagcg?agtgcacggc?catcaagtga 480
aactgataac?cggcgatccg?ccggcttatc?ggcgatggcg?ttatcagagg?gaccttagta 540
ggttgcacag?ttcactagta?tttattacta?agtacttcct?tcgccttgct?tattgcccat 600
gattcgtcct?tctctttttc?tttggttaat?tgaactactc?tccatgagag?ttctgtacag 660
gttgagatag?accaaccacc?accaccatgc?cttttccctt?ttcgtccgct?cttctcggct 720
atatcttaac?tacgagcact?actctcacct?ccctagtcgc?aggacagtat?taccctccga 780
cgcctgagga?tctcaccgtt?attcattcgg?agatattccc?tggtgcgagg?atctcctata 840
agcaagtgag?aaatacacca?cccttctcct?caatcccaat?ctaacacccc?atactaatac 900
tatgtgacca?gcccctcggc?atctgcacca?ccaccccctc?cacccccagc?tactccggct 960
acatccacct?ccccccacac?acccttacca?atctctccat?tccaggaatc?agcatctcgc 1020
aaccataccc?tatcaatacc?tttttctggt?actttccttc?ccgccatcac?cacaacaatg 1080
atacatcccc?actcaccatc?tggatgaacg?gcgggcccgg?cggatcctcc?atgattgggc 1140
tatttcaaga?gaacgggcca?tgtactgtga?atacggactc?gaattccacg?gcctataatc 1200
cctggtcgtg?gaatgagtac?gtcgatatgt?tgtatattga?gcagccggtg?cagacgggat 1260
ttagttatga?tgtgttgagg?aatgggacgt?tagatttggt?tagtggggag?atagatgtta 1320
gtattagtga?tggtgagagg?gatggagtag?gacagaatga?gacgtttttg?gtggggacgt 1380
tgccgagtca?ggatgtgcat?gggacggtga?atgggacggt?taatggggga?agggcgcttt 1440
gggttgcgtt?gcaggtttgg?ttgggtgaat?tctctgaata?tgtttcttct?gttgacggga 1500
atggtggtgg?tgatgacagg?gtgagtatat?ggacggagtc?atatggggga?cggtatggac 1560
cggcatacac?ggcgctcttt?caggagatga?atgagaggat?tgagagtggg?gaggtaagca 1620
ccgggaagaa?gatccatttg?gatacgctgg?gcattatcaa?tgggtgtgtg?gatttactcg 1680
tgcaggtccc?ttcgttccct?gagcaggcgt?ataacaatac?gtatgggatc?gagggaatca 1740
atcgcacgct?ctacgaccgg?gctatggata?gttggagcaa?gcctggcggg?tgcagggata 1800
tgatcatcga?gtgtcgcgat?gctggcgagc?tcggagatcc?cctcatgtat?ggcgacaatg 1860
agacggtaaa?tagcatctgc?gaggaggcgt?cggactactg?ttcgcgggag?atcaagagcc 1920
tgtatacgaa?tacctccggg?cgaggatact?acgacatagc?gcatttcacg?ccggatgcag 1980
ctctcgtgcc?ttacttcgtc?gggttcttga?atcgcccatg?ggtgcaaaag?gcacttgggg 2040
tcccggtgaa?ctataccatg?tcgtcagagg?cagtggggaa?cagtttcgcc?tcgacgggcg 2100
attatccgcg?aaatgatccc?cgcggaatga?tcggggatat?tggatacttg?cttgactccg 2160
gtgtcaaggt?ggctatggta?tatggggacc?gggactatgc?ttgtccgtgg?cgcggcgggg 2220
aagatgtcag?cctgctggtg?gagtacgagg?atgcggagaa?gttccgtgct?gctgggtatg 2280
ccgaagtgca?gacgaagtca?tcctacgttg?ggggtctagt?aaggcagtat?gggaacttct 2340
cgttcacgcg?tgtctttcag?gcgggccatg?aggtgccatt?ttatcagccc?gaaacggcgt 2400
atgagatttt?taatcgcgct?cagtttaatt?gggatattgc?gacgggaggc?atttctctgg 2460
agcagaatca?gagctatggg?acggagggac?cgtcgtcaac?gtggcatatc?aaaaacgaag 2520
tgccggagag?ccctgagccg?acgtgctatt?tgttggcgat?ggattcgact?tgtacggatg 2580
agcagaggga?acgggtgctg?agtggggatg?cggtggtgag?ggattgggtt?gttgttgatg 2640
atattgaggc?tgaaagctcg?ttcagcggtg?ttggtgatca?gctggcacag?gtccctttgg 2700
gacattgacg?ttggttgcca?tatgttgaca?gtgttggtgg?atgaaagtga?tatagatgga 2760
taaagttagt?gcataagtgc?atagctgact?aagaatgagc?atcattcata?tatggataag 2820
tctggctagc?tcgatccggc?aagtggccgg?ctgactgcct?aaagtggaag?actggaagcc 2880
ttcagatttc?catcagtcca?tctcaatatc?tccatctggc?ttgtcaaact?cctatatcca 2940
ccggccggac?ccttctatta?ttaacagcgc?cgctatcacc?cggacaatcc?gtatggcatc 3000
acgggttgac?ccctccattg?cggccatcga?accttctcga?accttctatt?ggtcgaccgc 3060
tgcggtcaac?gtcacacgtc?accgcaggct?cacctgaaag?ccgccggcgt?tgcactatac 3120
atcagccctc?gtcctcacac?ctggctttct?ccgctaatcc?tccaagtaca?cccttcactg 3180
tgccttgatg?tcttgaatca?acatctataa?aaactgcatt?a 3221
<210>54
<211>2590
<212>DNA
<213〉aspergillus niger
<400>54
gagtgagtaa?attgatctaa?cggcgtcgcg?ctgacaaaca?tcatagctat?caatcagaaa 60
aagcgaagca?tatttcacat?acgatcggat?agcctaccaa?ggaactgagg?atatacgtac 120
agctttcgct?tggctgacac?gtaaagtcat?ttggtgattt?tggagcgact?ttggatctcc 180
ttccatgtaa?gttataacct?accgcaattc?caaagtatag?ctagtagctg?tcagtcactc 240
aagaacttgc?agcaaggcga?tggcaagaca?aaacaatcga?tggtacggag?tagatagaag 300
acactaaagc?actttcacat?gacactgttg?acatagtgct?tatgctcttt?acactcaaca 360
tgagtcactt?tgataaggtg?atttcgccag?atggtggcat?tattgactcc?tgattggatc 420
caccgataag?gaaccacttt?ttggctggca?atgtactatg?ttattgacag?gcatcgaact 480
tccccaaatc?tcaggctggg?ccgccagcaa?atggcgcggt?tccggactcc?ggcgggggct 540
gacagggcca?accgttggct?gcttgtccct?tgccgccgga?gagcttattt?aactcttgtc 600
tctcctcttc?ccccacaaag?ctcactcagc?actcaaggcc?tcaccgcgcc?atagtcccgc 660
tcttgatcat?ccttagcaaa?acggctgtaa?atcatgagaa?catctactct?tttgctcctc 720
tggagcactg?caggagcagc?tttggcttct?ccgtacccgc?ttcccgactc?gcaagtagtc 780
ttcgccgcgg?atcacgaggt?cccgaataca?cagggcaaac?acgtcgtgga?cgaggccata 840
ctctcggcgc?tgaacgctca?ttctgaccca?gtcgctgcaa?tggtgtctct?acgtcccgaa 900
actgcagctt?ttctagctga?acctcgtctc?ttgcacattc?ggggcgaaga?gaaggcggaa 960
tggatgaccg?aaggcgacaa?gctgcgcctc?cgccaacgcg?gaaagaagtt?catggacatt 1020
accgagcatc?aggacttcta?cgcagagcag?gcgatggctt?cgtttgctgg?ggatcctagt 1080
taatctccct?tttgtcgagg?taattaatac?tgtgttaacg?ccctttagat?cttcccaagc 1140
tgtcccataa?aggtctcgtc?aagccgctgt?tctctcaaat?cgagacggaa?cgaatgcacg 1200
atatcctgca?gcacatgacc?tcctactaca?atcgatacta?cggtgattat?cacggcgaga 1260
tgagctccga?atggctgcac?gactacattg?ctgcggtatc?tccaccccct?acagccacaa 1320
tttttgaaca?tgaacttact?caaccaagat?catctccaaa?tcgcctttcc?gcacccacat 1380
ctctctcgaa?tacttcaccc?atcctttccg?ccaatcttca?attattgcac?gcttcgagcc 1440
taaagttcgc?agcttctccc?aacctttgac?catcattggt?gcgcaccaag?attcggccaa 1500
ttatcttttt?cccctgctgc?ccgcccctgg?cgctgacgat?gactgttccg?gcactgtcag 1560
tatcctcgag?gccttccgcg?ttctggcgga?gaatggctac?acgcccaagg?acgggcctgt 1620
tgaattccat?tggtatgcgg?ctgaagaggc?cgggctactg?ggcagccaag?ccatcgcgcg 1680
gtacaagaag?gagcagggcg?ctaaaattga?tgccatgatg?gagtttgtag?gttcccatca 1740
tccaacggac?ttggaatcac?ttttgacttt?cggttattaa?catctgcata?ggatatgacg 1800
gcttttattg?cccgtaacgc?caccgagacc?atcgggtttg?ttgcaaccca?agccgatgca 1860
gcgctcacaa?actgggccct?caacctcagt?cgagaataca?tctccattcc?ggcggaagtc 1920
tatgaacttg?gcccgtaaga?ccccagaata?tccccagagg?catgtcaagt?gctgaatgat 1980
ttcttagcaa?cgctggatcc?gactacatgt?catacactaa?gctcaactac?cccgctgcct 2040
ttgcatccga?aggcaacccg?ctcgctgggg?gctctttccc?gggtgaaatg?gacccctacg 2100
tacacggcat?caaggatagg?atggacgttg?acgatgaaac?gggcgtcttc?tctatcgaag 2160
taagttgacc?gcactcaacc?tgtccatctt?cttgctaacg?atttgccagc?acatggctcg 2220
gttctccgag?ttggctatcg?catttgttgt?cgagcaggct?gggtgggata?atacatggcg 2280
gtagagtata?tacagggatg?tttccagctt?catagcatat?agagctggta?tatagtcatt 2340
gtgcttacaa?tatataccat?tctattgagt?tcttgacaga?gttattatgt?cagaatggta 2400
atcagtctaa?atcaatgcgc?ccttaaatca?agaagtacac?tagtgcccat?gaccaaaaca 2460
atttccactt?acacatacca?cctatctgcc?tcactacgaa?acccttacca?tacaatgttt 2520
acgttgtgct?cctttcaata?ctccatttcc?atagttcatg?ctatcgtggg?ataaacatgc 2580
acatatcctc 2590
<210>55
<211>3290
<212>DNA
<213〉aspergillus niger
<400>55
gagaggcaga?aggagtcatt?tatcacttgt?attccaatgt?attttccatt?tatagatact 60
gcattcaaat?gcaccgttta?gcatagcatc?ccacattcta?tttcattcca?atctcatgcc 120
attgccatcc?ccggtattaa?tttacttctc?cgccttatct?tgcaatcttg?caatctcttt 180
ctcctcgtta?tcacgcgttc?ctgcaggcgc?acctccgatg?gcactgcagc?cggagtcccc 240
gcggcgccgg?cactactaaa?gactaaagtg?tctagtctag?cctccaatgt?gctcacctcc 300
atcagcatct?catccattta?tcttctgacg?atgtcatctg?caggctccac?cccctccggc 360
cgccccgacg?ctctccgacg?gtgcacaaca?atcaattctg?cagtcacgct?caagattcgt 420
ccctgccgga?ctcctcatgc?cgtgcctggt?ttaatctatg?caatggagta?aggtagtatc 480
gcctagcagg?agcggagttc?ctgctgcgct?cacgccatgg?tgccggcgca?gacataaatc 540
gctcgtttcc?tccggcgctg?gccgttctct?cgagccagtt?tgtctgttgt?ggttgtagga 600
tcctctgttc?ccctcgacag?ctcacaatgc?gttccttctc?cgttgtcgct?gccgcgtcac 660
tggcgctctc?ttgggcgtct?ctggcccagg?ctgctcgccc?ccgtcttgtg?cccaagccta 720
tctctcggcc?agcttcgagt?aagtcggctg?cgactacggg?tgaggcttat?tttgagcagc 780
tgctggacca?tcacaacccg?gagaagggaa?cgttttccca?gcggtactgg?tggagtactg 840
aatactgggg?tggacctggg?tcaccggtgc?gtctctgaca?tttggtctta?tgaccggcca 900
tattgaaact?tagccggtgg?caaggtccgc?aatcatgagg?aacattgctg?attaaactag 960
gtggtcctct?ttaaccctgg?agaggtctct?gccgatggct?atgaggggta?tctcaccaac 1020
gatactctca?ctggtgtcta?tgcgcaggag?atccagggtg?ccgtcattct?cattgaacgt 1080
gagtgtcact?gctaccatgg?aaaaaagaca?ttcgctgatc?gaccccaatc?tagaccgcta 1140
ctggggcgac?tcttcgcctt?atgaggtgct?caatgccgaa?acacttcagt?atctcacact 1200
ggatcagtcc?attctggaca?tgacctactt?cgccgagacg?gtaaagctgc?agttcgataa 1260
tagcagccgc?agcaatgcgc?agaatgctgt?atgttacctt?caccgctcta?tgtttctgat 1320
aggtactgac?aacgtagccc?tgggtcatgg?tcggtggctc?atacagcggt?gccttgacgg 1380
cttggaccga?gtctatcgcg?cctggaacgt?tctgggctta?ccatgccacc?agtgcgcctg 1440
tggaggctat?ctatgacttt?gtaggtgtag?cctgctcttg?ttatctatac?ttgcagctaa 1500
ccaagccagt?ggcaatactt?ctaccccatt?cagcaaggta?tggcacagaa?ctgcagcaag 1560
gatgtgtctc?tggtagccga?gtatgtcgac?aaaattggga?agaatggaac?tgccaaggaa 1620
cagcaggagc?tcaaagaatt?gtttggtctg?ggagctgttg?agcattacga?tgactttgcc 1680
gcgtgagtac?ttcaaagtct?atagacgagc?ttttctgaca?ggaacagtgt?cctgcccaac 1740
ggaccgtacc?tctggcaaga?caacgacttt?gtcacaggat?actcttcctt?cttccagttc 1800
tgtgatgctg?tcgaggtgag?ttaccaccag?attcctcttg?attgaagcaa?tatactaacg 1860
gacacagggt?gtcgaagccg?gcgcggcagt?gacccccggc?cccgagggcg?tcggacttga 1920
aaaggccctg?gccaactacg?caaactggtt?caattcaacc?atactcccta?actgtatttc 1980
accatctctt?gtctcgttcc?tctcccttat?cctcccagac?taacctagtg?acagactgcg 2040
caagctacgg?ctactggacc?gacgaatgga?gcgtcgcctg?tttcgacagc?tataatgcct 2100
cgagccccat?cttcaccgac?acctccgtgg?gtaaccctgt?cgaccgccaa?tgggaatggt 2160
tcctctgcaa?cgagcctttc?ttctggtggc?aggagtgcgt?accccttacc?tcattcatga 2220
taacacacga?acaattccac?taacaaagat?ccagcggtgc?ccccgaggga?acctccacta 2280
ttgtgccccg?gctcgtcagc?gcctcctact?ggcaacgcca?atgcccgctc?tacttccccg 2340
aagttaacgg?ctacacgtac?ggcagcgcga?agggtaaaaa?ctccgctacg?gtgaacagct 2400
ggacgggtgg?atgggatatg?acccgcaaca?cgacgcggtt?gatctggacg?aacgggtagg 2460
tctcccccta?atttccgttg?aatgtgatgt?gaagataaac?tcaatgctaa?taaattgaga 2520
aggcaatatg?acccctggcg?cgactccggt?gtgtcgagca?ctttccggcc?cggtggtccg 2580
ctggttagca?cggcgaacga?acccgtgcag?attattccgg?gcgggttcca?ttgctcggac 2640
ttgtatatgg?aggattacta?tgcgaatgag?ggtgtgagga?aggtggttga?taatgaggtg 2700
aagcagatta?aggagtgggt?ggaggagtat?tatgcttgat?gaagatactg?gtggacatat 2760
ggagtgtaca?taagatgaat?ggtcataaaa?tgatgatggt?agatacggct?atggctgttg 2820
attagatggt?cctttcgcat?ttcctaatta?ctgagcacgt?gctccatggt?atgggaagtg 2880
gagacgttgc?tatatatatt?gactgtcggg?ctattgttca?cggcgtagaa?gctagacgct 2940
ttgtctatgt?ggccttcact?aaagaccgtg?actctgccca?gtcttccccc?cttcgaggac 3000
ctggtattag?ccaaacccac?ccacaaacct?aacaaagatc?atcgtgacat?tgaagtcact 3060
ctaggtactg?ctggcgctga?ttacagtggc?tcaattcgaa?catttcaaca?gcacataagg 3120
gaagggtcgc?ttcacttgct?accttgatac?gaaagcagcc?acgcccaaca?cttatagggg 3180
tgacaaccat?cggcatgctg?ggttatctac?tatatctcct?gattctgtgg?atcctggaga 3240
tcgatctggt?acactaatct?actacaatgc?atgtgaagta?gggataggca 3290
<210>56
<211>2044
<212>DNA
<213〉aspergillus niger
<400>56
ggctttgttg?ggctgagcgc?tacttctttc?tctctcttgg?tctgttcgtt?gctccgccag 60
ttggttcact?cagcctcgta?acatcagtat?accaggctaa?gtcaggactt?tggcccccat 120
actgcttccc?ctttttttat?aaaactcaat?ccttctggaa?aggattctat?ttctcaattc 180
tcagactact?taatacgttc?tttgttttca?aattgttttg?tttctgaaac?ttgccgggcc 240
ctatcccctc?ttttttatag?tccgcctgtc?gacatcatat?ccagagtgag?ccaccatgca 300
gctcctccag?tccctcattg?ttgccgtttg?cttcagctac?ggcgtcctct?ccttacccca 360
tggcccgtca?aaccagcaca?aagcacgttc?cttcaaggtt?gaacgggtcc?gtcgtggaac 420
cggtgctctg?catgggcccg?ctgctctccg?caaagcatac?cggaagtacg?gaatagctcc 480
cagcagtttc?aacatcgatc?tggcagactt?taaacccatt?acgacaaccc?atgctgctgc 540
tgggagcgag?attgcagagc?ctgatcagac?tggcgctgtc?agtgctactt?ccgtcgagaa 600
cgatgccgag?ttcgtttcgc?ctgttcttat?tggcggccag?aagatcgtca?tgacatttga 660
cactggttct?tctgacttgt?aagtcttgga?tgcagctgtt?tactctttgg?tacagtgatt 720
aacgtcgatc?tacagttggg?tgttcgatac?gaatctcaat?gaaaccttga?cgggacacac 780
ggagtacaac?ccttcgaact?cctcgacctt?caagaagatg?gacggataca?ccttcgatgt 840
ctcgtatggt?gacgactcgt?acgcctctgg?ccccgtcgga?acggataccg?tcaacattgg 900
cggcgccatt?gtcaaggagc?aagccttcgg?tgtccccgac?caggtatccc?agtcgttcat 960
cgaggacacg?aactccaacg?gcctggtcgg?gttgggcttt?tcctccatca?acaccatcaa 1020
accggaggcg?caagacacgt?tcttcgccaa?tgtcgcacca?agtctggacg?agcccgtcat 1080
gaccgcctcg?ctcaaggctg?acggagtggg?cgagtacgag?ttcggcacga?tcgacaaaga 1140
caagtaccag?ggcaacattg?ccaacatcag?cgtggactca?tcgaacggat?actggcagtt 1200
ctccactccc?aagtactccg?tggcagacgg?agagctgaag?gacattggaa?gcttgaacac 1260
ctcgatcgcg?gacaccggta?cctcccttat?gctgctggat?gaagacgtgg?ttactgccta 1320
ctatgcgcaa?gttcccaact?cggtctacgt?gagcagtgcc?ggtggttaca?tctacccctg 1380
caacaccact?cttcccagct?tctcgcttgt?cctcggcgag?tcgagcctgg?ccacgatccc 1440
cggtaacctg?atcaatttct?ccaaggttgg?caccaacacc?accaccggac?aggcctgtaa 1500
gttgctcccc?ttcttttgca?tgattgaaca?tgattgactg?attgtgctgg?ttagtgtgct 1560
ttggcggcat?tcaatccaac?ggaaacacct?cgctgcagat?tctgggcgat?attttcctga 1620
aggccttttt?cgttgtcttc?gacatgcgcg?gcccctcgct?tggtgttgcc?tctcccaaga 1680
actagtttcc?ttttcctgta?cttttccccc?gcgtgtaata?atatcgtctg?attttttgga 1740
ctgtctccta?cgtgggcaag?atggatggat?agtttgctca?cgtgcattgc?tttaccttgg 1800
gtctgtgagt?caaggcagga?gtgcgtggct?gtatctacaa?ttcaagttac?agtgccgacc 1860
gttattgcct?tccacatcga?aaaacataga?cactctttct?aaccctaatc?catgatacaa 1920
gtatatactt?cgagtccata?ttatggtggt?gtatcaaggc?gccatgttta?tatctaatga 1980
aaccaacgta?ggtctcatct?tcatacgttg?tttaaaaggt?gccgaagaat?atacgaagat 2040
agat 2044
<210>57
<211>3916
<212>DNA
<213〉aspergillus niger
<400>57
ttcgcagata?ttcgagtcaa?taccttgtat?attaacggaa?aagggtttgg?gaagcgttgc 60
cttcaaggat?gaaattcaaa?acgtagagta?tcttgacctc?aatgacctca?tgatcccctt 120
gaccgtacag?ctagtgatct?cacggtggta?attgctcgat?tcgattccaa?actacagcaa 180
gaagcatgcc?cgacaggaaa?gtcaagttac?aagagatcta?gaacggggct?gctacggctc 240
tgaccaacct?ttgtctgttc?tagatgaggc?tgcagtgacg?taactccggc?ccaagaaaat 300
gggtggtaac?cgaccgttgg?aaatcccatg?gaactggcgg?ggttcaaatt?cccgataact 360
gtaccgaatc?cttgtatccg?gatataggcg?accgatagta?gtagctatag?tcagacgtag 420
cacagcatta?ctgtgtcccc?ctggtcataa?gagtatttgt?tacaataaga?agggaccgtc 480
tagttgtgta?tcacaacaac?tgacacttgc?ggaacaggta?tcagatcctt?gcgctggcat 540
cgactccagc?aatggcttgc?tctgtttcgg?acgaatatca?tcgggctaga?ctgtgacctg 600
aaggatcgat?ccaggagttt?gacggcttgg?gtttctaatc?cgatctggaa?gattattgtt 660
tagtcaagac?cgggaacagc?aagaaccgga?agattatctg?tttaactact ttgccaaaac 720
agttattcaa?tgtcatgctg?agtgcgatgg?ggacccaagc?tcacgagtga?tgctgatcaa 780
agggtccgtt?cggtttggga?aaggaagggc?gccctgtgct?tgccgttgga?atccacggaa 840
cgattccgat?tgactgcacg?ggatttgcaa?actgactccc?agtgggacga?agaaagaaac 900
ccatcttact?ttgcggaggc?aggatggcac?tttgtgtcgg?aagggtggtg?actcctggtg 960
ttgccgagaa?gatggaatgg?tggagaattg?ccttgaaaat?gaggctgtag?gggcactaac 1020
ccagtcgggc?cgagcgtgac?gcctttcccg?atgaggcagg?tcaggtgggt?gtcacgggtc 1080
tatcttatcg?cttatcatct?gaccggttcc?tggcagaagc?tccccttccc?agctcctcgt 1140
atttattcct?ccccaggttg?ttgtttgctc?ttctccctgt?ctcgccttct?ctccagcctc 1200
cattcaacgg?gctccatccc?cttctctccg?gatccctcta?tcccttattc?ttccttagat 1260
atcattattc?atatagtgcc?ttgtttcgct?caccatgcgc?attgactccg?cggcgctaca 1320
tctggtccca?gtcctcctgg?gccaggtcgg?tgctttacaa?ttacccttgg?tccaagactc 1380
caattcacag?tggcagaaac?caaatgcagg?tgataaaccc?ctaattagct?ctccgttgct 1440
tcaagagcag?gtcaaggcgg?agaatctgtt?ggacagggcc?cggcagcttt?acaagattgc 1500
ggagctggga?gaagacgagt?ataaccaccc?cactcgcgtc?attggcagta?aaggtacgat 1560
atattttttc?atcatgtccc?tggaatacga?taattagctg?acaacctttg?ctccccaggt 1620
caccttggca?cgctcgacta?catatactcc?acccttaccg?acctcggtga?ttattatact 1680
gtcgtcaatc?agtccttccc?tgccgtgagc?ggtaatgtct?tcgagtctcg?ccttgtcctt 1740
ggtcacgatg?ttcccaagtc?agctacacca?atgggtctca?ctcccccaac?gaggaataag 1800
gagccggtat?atggctccct?ggttgctgta?tccaacctcg?ggtgtgaggc?ctcggactac 1860
tcgtccaact?tgaaaggcgc?cgttgcattt?atcagtcggg?gaagctgtcc?gttcgggacc 1920
aagtctcaat?tagctggtaa?agcgggagct?gttgctgccg?tcatctacaa?caacgagcgg 1980
ggtgacctaa?gcggaactct?aggaaaccca?acccccgatc?atgttgctac?ctttggtatc 2040
tcagacgagg?atgctgcccc?agtcctggag?aagttgaata?aaggcgagaa?ggtggacgct 2100
atcgcctacg?ttgatgcgat?agtagagacc?atccacacca?ccaatatcat?cgcgcagacc 2160
acggatggtg?acccgaacaa?ttgtgtaatg?ctgggtggcc?acagtgacag?cgtggccgag 2220
ggcccgggta?tcaatgacga?cgggtccggt?actctgaccc?ttttggagct?tgccacattg 2280
ctcacccagt?tccgtgtcaa?caactgcgtg?cgatttgctt?ggtgggccgc?cgaggaggaa 2340
ggccttctcg?gatctgacta?ttacgtgtcc?gttctcacac?cggaagagaa?ccgcaagatc 2400
cgcttgttca?tggactacga?catgctcggc?tcgccgaact?ttgcgtacca?agtttacaat 2460
gccactaatg?ctgtgaaccc?cgagggatct?gaggagcttc?gtgatctgta?caccgacttt 2520
tacgaagatc?atgggttcaa?ctacacgtac?attccgtttg?acggacgcag?cgactatgat 2580
gccttcattc?ggcatggtat?cccgggtggt?ggcattgcca?cgggagcaga?gggtatcaag 2640
actgtcgagg?aagcggacat?gtttggtggg?gttgctggcc?aatggtatga?cccgtgttac 2700
catcagatct?gcgatacggt?ggccaatgtg?aacttgactg?cgtgggagtg?gaacaccaag 2760
gtaggaccgc?atccagcatt?agttactgtt?atgccgatca?ttcttttgct?aactgggatg 2820
atttacctta?gctcgttgcc?cactccattg?cgacttacgc?caagtccttt?gacggattcc 2880
cggaacggtc?cgatgaaccc?atcagccctg?ctgcttttga?ggaaccgaag?taccatggcc 2940
acgcgttgca?attgtaagat?ccgtgtgccc?caaagcttgg?tagtggggca?aatatctgta 3000
gcagagacca?agtcctttct?cgaacctgag?tcccacttgg?tctttccatc?ttttgagttg 3060
aacaagtaga?ccgttactcg?tcatgtagac?gaagacctgg?cagaaccgtt?gtactatgta 3120
gacatttatc?ggggattgtc?tgttatgaat?tcatgtgctt?gtgggatatg?gttaggtatt 3180
tctcgcaaat?gaccacggct?tcctctatca?tttcccgcct?cgcaccctca?taccgatttc 3240
cgttaactta?atatcatctg?tagacttcgc?ggtaatacta?cagggaccca?gagcgtcctg 3300
tggggagccc?aaatccagaa?tggaacagct?gcatcggtgc?ttaatctatt?gtccatacga 3360
cgcagaggca?ctttcagtct?aagctaaaag?caagcattat?tcagagatac?agtgagtgtc 3420
aatatgccgt?tggttcatgc?gcgattcgtg?caaaaacagc?ccaccgccct?atataacaga 3480
gtatattgct?ctctgcctct?ccgggtagag?atcgacattt?ccgggaccgc?catgaaacgt 3540
tggtgggcct?cggagcgtcg?aggattgaca?ctagggccgc?gctagaatcc?cccagggtct 3600
gcaaaatacc?ctatggggtg?acctcgaaca?gggcgtgaaa?cggcaattcc?tccgaaagcg 3660
ttgcgaaagt?gtctacaaag?tggtgatcca?gaccatcacg?cggttccgga?acaattgccc 3720
ttcttatttg?gcactttacg?gcgtggagtg?gagtcatccc?cctttgttga?aacaacacgg 3780
gcatgtttcc?tttgccgtcc?ggttcgttac?ctataaagac?agggtaggtc?tgttcgggaa 3840
aaagacacaa?tcagcgccta?tcccgtccgt?cgaagtctat?tgccataccc?tatcacggat 3900
catcagac?tc?ataaca 3916
<210>58
<211>1443
<212>DNA
<213〉aspergillus niger
<400>58
atgcatctcc?cacagcgtct?cgttacagca?gcgtgtcttt?gcgccagtgc?cacggctttc 60
atcccataca?ccatcaaact?cgatacgtcg?gacgacatct?cagcccgtga?ttcattagct 120
cgtcgtttcc?tgccagtacc?aaaaccaagc?gatgctctag?cagacgattc?cacctcatct 180
gccagcgatg?agtccctgtc?actgaacatc?aaaaggattc?ccgttcgtcg?tgacaatgat 240
ttcaagattg?tggtagcgga?aactccctct?tggtctaaca?ccgccgctct?cgatcaagat 300
ggtagcgaca?tttcatacat?ctctgtcgtc?aacattgggt?ctgatgagaa?atctatgtac 360
atgttgctcg?acacaggcgg?ctctgatacc?tgggttttcg?gttccaactg?cacgtccaca 420
ccctgcacga?tgcacaatac?cttcggttcg?gacgattctt?cgacccttga?aatgacatcg 480
gaagagtgga?gtgtgggcta?tggaactggg?tctgtcagcg?gcttgctagg?aaaagacaag 540
ctcacgattg?caaatgtcac?tgtacgcatg?actttcggac?ttgcttccaa?cgcatcggat 600
aacttcgagt?cgtacccaat?ggacggcatt?ctcggtctcg?gtcgaaccaa?cgatagttcc 660
tacgacaacc?caacattcat?ggatgccgtt?gcagaaagta?acgttttcaa?gtcgaatatc 720
gttggcttcg?ccctttcacg?tagccccgcc?aaggatggca?cggtcagctt?tggcactact 780
gacaaggaca?agtacaccgg?cgatatcacc?tacaccgata?ccgtcggatc?ggacagctat 840
tggcgcattc?ccgtggacga?tgtctatgtt?ggcggcactt?catgcgattt?ctccaacaaa 900
tcagccatca?tcgataccgg?aacttcttat?gctatgctgc?cttcaagcga?ctcgaagacg 960
ctgcacagtc?tcattcccgg?cgccaaatct?tcggggagct?accacattat?tccgtgcaac 1020
acaactacta?agctacaagt?ggcattctct?ggtgtgaatt?acaccatctc?gccgaaggac 1080
tacgtgggag?caacttcagg?ttctggatgc?gtttcgaaca?ttatcagcta?cgacttattt 1140
ggtgatgaca?tctggctcct?gggtgacacg?tttctcaaaa?atgtgtatgc?tgtgtttgac 1200
tacgatgagt?tacgggtcgg?atttgcagag?cgttcctcga?acaccacctc?tgcgtcgaac 1260
tctacgagct?ctggaacaag?cagcacctcg?ggatccacta?caacgggcag?ctcaacgact 1320
acgacgagct?ctgctagctc?tagtagttca?tctgatgctg?aatcaggaag?tagcatgacc 1380
attcccgctc?ctcagtattt?cttctctgct?ctggcgattg?cttccttcat?gctttggctc 1440
tag 1443
<210>59
<211>3300
<212>DNA
<213〉aspergillus niger
<400>59
atgcttcgtg?gtcttcgtga?tgtcgtatta?ttacaatttg?caatcccctt?gttcttgcta 60
ttgcatttta?gattatcgct?acggggtgtg?atcacaggat?ttggttctaa?atcacatttc 120
cagagaccat?tgagcaaaat?gtcatctact?caaaagagcc?atttcaagct?actccagaag 180
ttcaaaccgg?agtactcgcc?tagcgagttt?gctcagtatg?agtcggagag?aacaggcatg 240
agggtagtgg?tcattgacca?aaaaggaccc?aaagtcacag?gttattttgt?tctagccaca 300
gagattctcg?atgattcagg?tgctcctcac?acgttggagc?acttgtgctt?tatgggctcg 360
cggaactata?gatataaggg?cttccttgac?aagctagcaa?cacgtgttta?ttcgagcacc 420
aatgcctgga?cggccacaga?ccacacggcc?tacaccttgg?acacagcagg?ctgggaaggg 480
ttcgctcaaa?tcttgcccgt?gtacctagag?catgttatag?ctccaacact?gacagatgaa 540
gggtgctata?ccgaagtgca?tcatattgat?ggcgctggag?acgacgctgg?agtcgtctac 600
tcggagatgc?agggtgtgca?gaataactct?gcagagttaa?tcgatctaac?cgctcgtcga 660
ttgacttacc?cgcatggtgt?aggttttcgc?tacgagacag?gcggtatgat?ggagcagctc 720
cgcgtcctca?ccgcggaccg?tatccgagcg?ttccatcgtg?agatgtacca?gcccaagaac 780
ttatgcctaa?tcatcacagg?cgaagtagat?caccagaaca?tgctggagac?cttggacaag 840
ttcgaagata?ctattctaga?tgtcattccc?agtcctgatt?cacctttcaa?gaggccgtgg 900
gtagattcca?agcaggcgcc?gccattggag?aagtccattg?tccagactgt?ggaatttccg 960
gaagaagatg?aatctttcgg?ggagatagaa?attagattcc?tcggtccgga?ctgtaccgac 1020
cctgttcaaa?ccggggctgt?caatgttgca?ttgctgtatc?tggccggttc?atctgcttct 1080
ctattggata?acatcctggt?tgagaaggag?cagctcgcca?gtgctgtcta?ttatgctacc 1140
gaagatcatc?ccagcattga?gatccgcttc?acattaacca?gtgtggagac?agagaaactc 1200
gcgaaggtag?agcaacggtt?tttcgaagtg?ctcaaggacg?ctatggagaa?agatttagac 1260
atgaggtata?tcaaggagtg?cattgaccgg?caaagacgga?cctggaagtt?ctctaccgaa 1320
agctccgcct?cttcctttgc?ggagtacgtg?atctcggatt?ttcttttcgg?aaagagagac 1380
ggatcgacta?tgcttgatgt?tgcgaccttg?caagagtacg?acgtgctgga?gaagtggagt 1440
gaagaacagt?ggcgcagttt?tatcaaaaca?tggatttctg?atgccaacca?tgtcactatc 1500
cttggtgttc?cgtccgttaa?gatgtctgac?acattaaaga?aggaggagga?agctagagtc 1560
gcagagcaaa?agaagcgctt?gggtgatgag?gggctgaaga?agttggccga?caagctggaa 1620
aaagctaaag?ctgaaaatga?caaggagatc?cccaaggaga?tgctggagag?gttccaaatc 1680
cctggaatag?agtctatcca?tttcgtggac?actactacag?ccaggtctgg?tgcagccctc 1740
gatgccgggc?gcccatccca?caaggcgcaa?aaactggtgg?atgctgatgg?ctctgatctg 1800
cccttgttca?tccatttcga?gcatatcccc?agtagcttcg?tgcagctctc?cctcctcatc 1860
tcggcacagg?ccgtacctgt?gcagcttcgt?ccactgctgt?ctgtgtatac?tgaggcattc 1920
ttcaacctgc?ctgtcaaccg?gaacggggaa?accatcaact?ttgagcaggt?ggttgtcgag 1980
ttggaaaggg?atactgttgg?ctactccatg?gaaggagcta?gaagcctagg?aaactcggag 2040
atgttgcgga?tctcattcca?ggtggagctt?gagaagtatc?acacggcgat?cgcatggatc 2100
caggaacttt?cctggaactc?gattttcgat?gtcgagcgac?tccgagcgat?taccagtcga 2160
ctgctctccg?atgtgcccga?ttccaagcgt?agtggcgacg?acatgctcgc?ggctgttcat 2220
gtgatggtcc?actatgcagc?agagtctatt?gttcgggctc?ggagcacctt?ggtgaaggcg 2280
cgttatttga?aacggatcaa?gaagcaatta?gcagaagagc?cgaagtctgt?cgttgcgcgg 2340
atggaagaaa?tcagagatgc?gcttttccgt?ttcgagaaca?tgcgagtctt?agttatcgct 2400
gacctggaga?aacttcaaaa?ccctgtgtca?gcatggaaac?catttgctga?gcgtttgggt 2460
gcaggtgccc?ctctacagcc?tatcacgact?agaagaccgt?tgctcagtga?ggcaggccag 2520
aagttgggcg?gtaagtcgta?tgtggttcct?atgccgacga?ttgattcatc?gttcgcatat 2580
gctaccgcac?gtggtttgga?ttcttatgat?gatccaagac?ttcctgcctt?aatggttgca 2640
attgcataca?tgaacgcggt?tgagggtccc?ctctgggttg?cagttcgagg?caagggtttg 2700
gcatatggca?cgaactttgc?ctataacatt?gataccggat?tcgtcaactt?cgacgtttac 2760
cgctccccca?acgcccataa?agccttcgac?tccagcaagc?agattgttga?ggatcacctc 2820
tctggtgcga?tgcccttcga?tcccttgatg?ctggagggtt?ccattagcag?cattgtggta 2880
agctttgcga?atgaacagtc?gacaattggt?agcgcagcct?caggcagttt?catccgacag 2940
gtgattcggc?gcctgcctag?cgactacaag?gagcgggtgc?tcaagcaggt?gcgggctact 3000
agcgttgatg?acgtgaaagg?cgctctgaag?gacatcattc?tgcctttgtt?taacccgtcc 3060
acggccaata?tcgtggttac?ctgcgctaca?gtgcttgagg?agactatcaa?ggaaggtctc 3120
caggcatcgg?gattcacgcc?tgcggtgcag?ccactcaaag?aattcgaaga?tgactatggg 3180
ctgaaggtcg?gcgatgacga?ggacgaggag?tccgacgatg?acgacgatga?gtatgaaacc 3240
ggatctgaag?atgaagatga?cagtgatgaa?gacatggagg?atgacgaaga?tgatgagtga 3300
<210>60
<211>2181
<212>DNA
<213〉aspergillus niger
<400>60
atgggagctc?ttcagtggct?gtccatcacg?gctgctgcgg?cctccgcagt?gtcagccttg 60
accccggagc?agatgatcgg?tgccccacgg?agaaccgaag?ttataccaaa?cccctccggt 120
gacaccggtc?tattctcgac?ctcccaatgg?tcgtttgaca?ctcattctga?gagcacctgg 180
tggagcttga?tcgacctcca?atcgggcaag?accaccactc?tcaccgatga?tagcgatatc 240
gaggagatca?tctggcttgg?ctctgacaat?tctacgctcc?tctacatcaacagcaccaac 300
gcgcaggttc?ccggtggcgt?ggagctgtgg?attgcggact?cttctgactt?tgcaaatgct 360
tacaaggcag?cctctctctc?cgccggtttt?ctcggcatca?aatcaaccgt?gacagattcc 420
ggcgacgtgc?atttcatcct?tcgtggaaag?tcctatccca?acggaacggc?atacaatgat 480
cagctcgccg?agacctatcc?cagtacagcc?cgcatctacg?acagcatctt?tgtgcggcac 540
tgggacactt?acctgaccac?cgcctcccac?gctgtattct?ccggtaccct?gcaaagctcg 600
accagcgacg?acggcaatgt?tcaatatacc?tcttcagggg?gattgaccaa?cctggttaac 660
ccagtcaagg?gtgccgaaag?cccattccct?ccttttggag?gcaacgacga?ctatgacctc 720
tcgcctgacg?gcaaatgggt?taccttcaag?agcaaagcgc?cagagctgcc?tcttgctaac 780
aacacggctg?cctatgtcta?tctcgtccca?cacgacggct?ctgcgactgc?ctttgccgtc 840
aacggccctg?atagtcctgc?aaccccggag?ggagttgaag?gagaatccaa?caatcccgtg 900
ttctcccctg?atagcgacaa?aatagcgtac?ttccaaatgg?ctactaatac?atacgagtcg 960
gaccgcaacg?tgctatacgt?atactccatc?gccgatgaca?ccatcactcc?ccttgcaaag 1020
gactgggacc?gatcgcctag?ctccgtgaca?tgggtcgatg?gagacaacct?cgtcgtggca 1080
agccaagatc?taggacgaac?cagacttttc?gccatcccag?gcgatgcagg?ggacgacttc 1140
aagcccacga?acttcaccga?cggcggctcc?gtgtcggctc?aatacgtcct?atccaactct 1200
accctcctcg?tcacgtccag?cgccttctgg?acaagctgga?gcgtctacac?cgccagccct 1260
gacgagggcg?tgatcaacac?actggcctca?gccaacgaga?tcgaccccga?gcttagcggc 1320
cttagttcct?ccgactttga?agagttctac?tttgacggca?actggactac?cctccaagga 1380
tggatcacct?acccccaaga?cttcgactca?tccaagaaat?accccctcgc?cttcctcatc 1440
cacggcggcc?ccgaagacgc?ctgggcggat?gaatggaacc?tgaaatggca?ctccaaggtc 1500
ttcgccgacc?agggatacgt?cgtcgtccag?ccaaacccca?caggaagcac?cgggttcggc 1560
cagcagctca?cagacgctat?ccaacttaac?tggaccggcg?ccgcctacga?cgacctaacc 1620
aaagcctggc?aatacgtgca?cgatacctac?gacttcatcg?acacggacaa?cggcgtcgcc 1680
gcgggtccca?gcttcggcgc?gttcatgatc?acctggatcc?agggcgatga?ctttggacgc 1740
aagttcaagg?cgctggttag?ccatgatggt?ccgttcattg?gcgatgcgtg?ggtcgagacg 1800
gatgagttat?ggtttgttga?gcatgagttc?aacggcacct?tctggcaagc?gcgcgacgca 1860
ttccacaaca?cggatccatc?cggccccagc?cgcgtcctcg?catacagcac?cccccagctc 1920
gtcatccaca?gtgacaagga?ttatcgcata?cctgtggcaa?atgggattgg?actgtttaat 1980
acgctgcagg?agaggggcgt?gcccagtcgg?tttttgaatt?tcccggatga?ggatcattgg 2040
gtcaccgggc?aagaaaacag?cctcgtctgg?tatcagcagg?tgctgggatg?gattaatcgg 2100
tattctgggg?tgggagggtc?gaatcctgat?gcgattgctt?tggaggatac?ggtgaatccg 2160
gtggtggatt?tgaatccttg?a 2181
<210>61
<211>1695
<212>DNA
<213〉aspergillus niger
<400>61
atgacgaggc?agacttctct?cgttcccagg?ctactaacgc?tagcctcact?agctgcactt 60
tcacaagcag?agctaggcaa?gatccaatgg?aaaggatctt?gcaacttgac?cacttatccg 120
gcattgatct?gtggaacact?agacgtgcca?tacgactaca?cggagtcaaa?ttccagcaag 180
acactgactc?tcgacatcgc?caagtggcca?gcgaccaaga?aaccagtctc?ggagcccatc 240
atatttaact?ttggaggacc?tggtgtcaat?tcgttcgagg?gccttgggct?ttatggagag 300
gaatttcagg?ctattcttgg?aggtcacaat?gatttgatag?cttttaacaa?ccgaggcgtt 360
ggaaacacca?tcccgttctc?ctgctacagc?gatgacgcca?cccgtgaact?cgtcgccctt 420
caagctccta?acgacggcag?agcgtccagc?acggctttgg?gagaaatctg?ggcccagaac 480
gcaaacatcg?cacaggcatg?ctatgctacg?aacaatcaaa?ctggtagtct?tattggaact 540
agctttgctg?caagggacat?catgcaggtc?gctgatgcgc?tcagtggaaa?ggatagtttg 600
gtcaactact?ggggattctc?atacggcact?acaatcggtg?ctgttctcgc?agccatgttc 660
ccggatcgaa?tggggaatgt?cgcgcttgac?ggagtggaca?accccagaga?ggctctttat 720
ggatacaacg?cacaagcggt?tgtggacgtc?gacaaagttt?tcgaaggatt?ctgcacgggc 780
tgcatggccg?caccggacct?ctgccctatc?gccaaggagt?acaccagcgc?cgccaacttg 840
gaagccgcaa?tttacctgat?gctggaaaac?ctcaagtaca?acccgattgc?cattcccgaa 900
accggtggaa?tcgtaacttg?gagcgacgtc?aagtcgacca?tttttgaggc?catgtacctg 960
ccaagctctt?ggcccttgac?ctctgagctt?ctttactacg?tgcaaacccg?caacacaacg 1020
atccttggca?actctgaagt?atacgacacc?atcaaatcct?acggtcaatc?ggcttctttg 1080
acttcggctt?ccgatgaggt?cggcacggcc?attacatgct?ccgacaagca?tcgatctgcc 1140
accattaaag?aggtcctccc?gtacgtcaaa?gccagacagg?ctctgaccaa?gatcggaagt 1200
gatggctcgg?acggcgacat?gagatgcgcg?cagtggaatc?cgaagatgtt?cgccaaggag 1260
cgctactccg?gtgactttga?agtcaagaca?gccaacccgg?tgttgattct?gagcaacact 1320
tacgatccag?cgactcctct?tcccgcagcg?aagaacctga?cagagacctt?tgagggaagt 1380
gtcttgctcg?agcagaacgg?atacggtcat?actaccctgt?ctatgccatc?tctttgcact 1440
gccaaggccg?tccgggctta?cttcaccaat?ggcacattgc?ccgctgacgg?aacgatctgc 1500
caggtggacg?tgcctctgtt?cacgaacttg?acctacaagg?atgtgtggcc?gaagagtttc 1560
caacggagcg?ttgagtcgag?ggatgatgcg?actatcctca?aggctttgat?gtcggtccgt 1620
gataagatgt?cgcgacgcag?gatgtgtatt?tatttgtaca?ccaacagcgc?ttcatggaga 1680
ccggaacttc?cctga 1695
<210>62
<211>1581
<212>DNA
<213〉aspergillus niger
<400>62
atgtactact?ctctctgggt?tgctgccttg?gtggccgcgc?tgcccgtctc?ccgggcccag 60
tttgtggctc?cgcccacgga?tctcattccc?accaagggat?atctcgacat?ccccgtccgc 120
tacaaacagg?tccccaccgg?catttgtgag?actgatccca?gtgtcaagag?cttctccggt 180
tacgtcgatg?tcgctgagca?tgagcacatc?ttcttctggt?tcttcgaggc?gcgcaaccaa 240
gatcccaccg?aggctccctt?gaccgtctgg?atcaatggag?gcatgtctga?ccccggtcct 300
ggttcctcct?ccatgatcgg?cttgttccaa?gagcacggcc?catgcggcat?tgacgccaat 360
ggctccgtct?acaacaaccc?ctactcctgg?aacaacgcca?gcaacatgct?ctacatcgac 420
cagcccgtgc?agaccggctt?ctcctacagc?attccggttc?ccggctatgt?ggattcttcc 480
acagacaatg?gttttatggg?cgcatttcct?cagtactcgc?gcgaaacctt?ccacttcacc 540
acggagagtt?atggcggcca?ctacgggccc?gtcttcaacg?agtacatcga?ggagcagaac 600
gcccatctcc?agccgggagc?caagaagatc?caactgggca?gtgtgatgat?cggcaatggc 660
tggtatgacc?cgattattca?ataccaggcc?tactacaact?ttacggtata?tccgggcaac 720
acatacgact?acctgccatt?caacaagtcc?atcagctcgc?tgatgtacaa?caacctctat 780
ggccccggaa?actgcctcga?ccagctctac?gactgcgccg?cccgaggcat?cgacgagatc 840
tgcagcactg?ccgacgattt?ttgcgccaac?gaggtcgaaa?acgtctacga?catttactcc 900
ggtcgggatg?agtatgactt?tcgtgaactc?actccggacc?cgttccctta?cgagttctac 960
gttgactacc?tgaacaaagc?gtccgtgcag?gccgccatcg?gcgcatacat?caattacacg 1020
gagagcaaca?acgctgttgg?actcgccttt?tcgtccaccg?gtgacgacgg?gcgactcatg 1080
aacaccatcc?aggatgtggg?caagctgctc?aaacagggtg?tcacggtggt?catgtacgcc 1140
ggggatgccg?actataactg?caactggctg?ggtggggaag?ccgtgtcgtt?gcaggtcaag 1200
gccgccaact?tcagtagtgc?gggttacacc?aacattgtca?cctcggatgg?agtgacacac 1260
ggccaggtgc?gccaggcggg?gcaatttgcc?tttgtgcgag?tgtatgagag?tggacatgag 1320
gttcccttct?atcaaccctt?gcttgcgctg?gagatgtttg?agcgcgtcat?tggcggcaag 1380
gatgtggcga?cgggaaagat?tcccatctcg?tcgagtttac?agacggtggg?cacgcccaag 1440
agttactacc?gggagggcaa?cagcacgatt?cagtgggagg?tgttggattc?tctggcgacg 1500
tacaacacaa?ccacgaatgc?tccgaacccg?gtgagccgga?ggctgaagcg?gatgggacca 1560
gctttgcggt?ttcagatgta?g 1581
<210>63
<211>3471
<212>DNA
<213〉aspergillus niger
<400>63
atgtcttgcg?tctggctcca?catccacaaa?aggagcctac?tgtctgtcgc?tacgaacaat 60
tctgttgcga?gggccgctgc?ctctacctcc?gccgcgccgc?cgccgccgtc?atcgccgccg 120
cctggttcta?atacttattc?gcctctttat?cgccccatca?ccaatcccat?cggatttact 180
ttgtcgcctg?cgaggtcact?agtttctcgc?aatcctaaat?ttcctgccta?tcggcgctct 240
agtcgacact?tttctttgtg?cccggccgct?gcaacgcccg?gtgtcaccac?gagcatctgc 300
cctggtcagg?cgcccgtccg?ctctctcagc?tcgctcatta?tacactctac?gagaccccgt 360
gctatacgta?tccgtaccga?ccagatggat?ttgaatggag?acgcaggcgc?caagcgcaag 420
cgcagctcca?tcaccacacc?cgccgaacgg?cccgtaaagc?accttcgccc?cgaatcgagc 480
gcattgacac?ccggggattc?gacgcctgcc?aatgggactg?tatacgatgt?ggaggatgat 540
gaagatgcga?gtcgtctgct?gcctgtaggg?cctgctcagg?ccgactcacc?ggaatggcaa 600
gctaccatag?aggaggttgt?gaaaagcgta?gtgtctatcc?acttctgtca?gacctgctcc 660
ttcgacacgg?agctgtccat?gagtagtcag?gctactgggt?ttgtggtaga?tgcagagaat 720
gggtacatat?tgacaaaccg?acacgtggtt?tgcccgggac?ctttctgggg?atactgcatc 780
tttgataacc?atgaggaatg?cgacgttcgt?cctgtgtatc?gggaccctgt?tcacgacttt 840
ggaattttga?aattcgaccc?gaaggctatt?cgatatatga?aattgaggga?actgaaactg 900
cagccggatg?cagctaaagt?gggatcagaa?attcgcgttg?tgggtaatga?tgcaggagaa 960
aaactgagta?ttctgtctgg?tgtcattagt?cggctggata?gaaacgcgcc?cgaatacggc 1020
gatggctaca?gtgacttcaa?tacgaattac?atccaggccg?ccgcagcagc?tagcggtgga 1080
agttccggca?gtcctgtagt?taacattgat?ggccatgcga?ttgctctgca?ggccggtggt 1140
cgtgcagacg?gtgcagcgac?ggattacttc?ctccctctgg?accgaccgct?acgcgcactg 1200
gaatgcatcc?gtcgcggaga?gcctgtcacg?cgtggaacga?ttcagacgca?gtggatcttg 1260
aagccgttcg?acgagtgtcg?tcggttgggc?ttgacgcctg?agtgggaggc?gaccgtgcgt 1320
aaagcagcgc?ccacggaaac?cagcatgctg?gtggccgaga?tcatcctgcc?tgaaggcccg 1380
gcggacggaa?agctcgagga?aggagacgtg?ctcctgcagg?tcaacggggt?gcttctcacc 1440
caattcatcc?ggttggatga?catcctggat?tcgagtgttg?ggcagacagt?gcgtctgctt 1500
gtccaaagag?gcggtcagaa?tgtggagatt?gagtgccagg?ttggcgacct?gcatgccatc 1560
acgcccgacc?ggttcgtgac?ggtggctgga?ggcacgttcc?ataacctgtc?ttaccagcag 1620
tcgcggctgt?atgccatcgc?tactcgcggt?gtctacgtct?gcgaggctgc?cggctccttc 1680
aaactggaaa?acacactgtc?aggatggatc?atcgactcgg?tggacaagcg?gcccactcgc 1740
aatctggatg?agttcgtgga?ggtgatgcga?acgattcccg?atcgttcgcg?cgtggtcatc 1800
tcgtatcggc?atattcgcga?tctccacacc?cgaggcacca?gcatcgtcta?tatcgatcga 1860
cactggcacc?ccaagatgcg?actggctgtg?cgcaacgacg?acaccggtct?gtgggacttt 1920
tcggacctcg?cggaccctat?cccagctctt?cctccggttc?cgaggaaagc?cgatttcatt 1980
caactcgatg?gtgttagcca?gcctgctgcg?gccgacattg?tgcgcagctt?cgtacgagta 2040
tcctgtacga?tgcccctgaa?gctggacggc?tacccccagg?ccaagaagac?tgggttcgga 2100
ttggtcgtcg?atgcagagaa?gggtttggtg?gttgtgtcgc?gagcgatcgt?gccgtacgac 2160
ctctgcgaca?tcaacgtcac?ggtggccgac?tccatcatcg?tgaacgctaa?agtagttttc 2220
ctgcatccgc?tccaaaacta?cagcatcatc?cagtacgacc?caagcctggt?gcaggcgccg 2280
gttcagagtg?ccaaactcgc?caccgactac?atcaagcagg?gacaggacac?gatctttgtg 2340
ggattcaacc?agaacttccg?gattgtcgtg?gccaagaccg?ccgtaaccga?catcaccact 2400
gtttctattc?cagccaacgc?gtccgcaccg?cgctaccgcg?cgatcaacct?ggacgccatc 2460
actgtggaca?ccggactcag?cgggcagtgt?tctaacggtg?tcctgattgg?cgaggacgga 2520
gtggtgcagg?cattgtggtt?gaactatctt?ggagaacgca?catctaattc?gcataaggat 2580
gtggaatacc?atctaggatt?tgcgactcca?tctcttcttc?ctgtcctgtc?gaaggtgcag 2640
cagggagaga?tgccggaatt?gcggattctg?aacatggaga?gctacgtggt?ccagatgagt 2700
caagctcgta?tcatgggcgt?gtcggaggaa?tggatcgaga?aggtgacgca?agctaaccca 2760
tcgcggcatc?agctcttcat?ggtgcgcaag?gtcgattgcc?caccgcctgg?gttcaactca 2820
gcggccgaca?cgttcgagga?gggtgatatc?atcctgacct?tggacggaca?gctgatcacc 2880
cgcgtctcgg?agttggatat?catgtacgag?aaggatacgc?tggaagccct?gattgttcga 2940
aatggacaag?aaatgcggat?ccaggtgccg?actgttccaa?cagaggacct?agagactgac 3000
cgtgcggtcg?tgttctgtgg?tgctgtgttg?cagaaaccac?accatgcggt?ccgtcagcag 3060
atttctaagc?tacacagcga?agtctacgtc?agcgcaagaa?gtcgcggatc?cccctcctac 3120
caatacggct?tggccccaac?caatttcatc?accgccgtaa?acggcgttcc?aaccccgaac 3180
ctggaccgct?tctccgaaga?agtgagcaaa?atccccgaca?acacatattt?ccgcctacgg 3240
gcggtgacat?tcgacaatgt?gccgtgggta?gtgaccgtga?agaagaacga?tcattacttc 3300
cccatgtccg?agtatatcaa?agaccagtcc?cagccttccg?gttggcggac?cgtgtctcac 3360
gacaaggata?aatataaaga?cggcattgca?ccggatgctg?cgaacttgaa?cccggatgct 3420
atggacgaag?ggtttgatgg?agtcagtgat?attgagccgg?atttggagtg?a 3471
<210>64
<211>1611
<212>DNA
<213〉aspergillus niger
<400>64
atgagagtcc?ttccagctgc?tatgctggtt?ggagcggcca?cggcggccgt?tcctcccttc 60
cagcaggtcc?ttggaggtaa?cggtgccaag?cacggtgccg?accatgcggc?cgaggtccct 120
gcggatcaca?gtgccgacgg?gttctccaag?ccgctgcacg?cattccagga?ggaactgaag 180
tctctctctg?acgaggctcg?taagctttgg?gatgaggtgg?ccagcttctt?cccggagagc 240
atggatcaga?accctctctt?ttccctcccc?aagaagcaca?accgccgtcc?cgactcgcac 300
tgggaccaca?tcgtcgatgg?caagctggaa?gcctatgatc?tcagggtcaa?gaagaccgat 360
cctggctctc?ttggcatcga?ccccggcgtg?aagcagtaca?ccggttatct?cgatgacaac 420
gagaatgata?agcatttgtt?ctactggttc?ttcgagtctc?gcaatgaccc?cgagaatgat 480
cccgttgttc?tgtggctgaa?cggtggccct?gggtgctctt?ccctcaccgg?tctcttcatg 540
gagcttggcc?ctagcagcat?caacaagaag?atccagccgg?tctacaatga?ctacgcttgg 600
aactccaacg?cgtccgtgat?cttccttgac?cagcctgtca?atgtcggtta?ctcctacagt 660
aactctgctg?tcagcgacac?ggtcgctgct?ggcaaggacg?tctatgcctt?gcttaccctc 720
ttcttcaaac?aattccccga?gtatgctaag?caggacttcc?acattgccgg?tgaatcttat 780
gctggtcact?atatccccgt?cttcgcttcg?gagatcctgt?ctcacaagaa?gcgcaacatc 840
aacctgcagt?ccgttctcat?tggcaacggt?ctcaccgacg?gatacaccca?gtacgagtac 900
taccgtccca?tggcctgcgg?tgacggcggt?tacccagctg?tcttggacga?gagctcctgc 960
cagtccatgg?acaacgctct?tcctcgctgc?cagtctatga?ttgagtcttg?ctacagttcc 1020
gagagcgctt?gggtttgtgt?cccggcctcc?atctactgta?acaacgccct?ccttgcccct 1080
taccagcgca?ctgggcagaa?cgtctatgat?gtccgtggta?agtgcgagga?tagctctaac 1140
ctttgctact?cggctatggg?ctacgtcagc?gactacctga?acaagcccga?agtcatcgag 1200
gctgttggcg?ctgaggtcaa?cggctacgac?tcgtgcaact?ttgacatcaa?ccgcaacttc 1260
ctcttccacg?gtgactggat?gaagccctac?caccgcctcg?ttccgggact?cctggagcag 1320
atccctgtct?tgatctatgc?cggtgatgct?gatttcattt?gcaactggct?gggcaacaag 1380
gcctggactg?aagccctgga?gtggcccgga?caggctgaat?atgcctccgc?tgagctggag 1440
gatctggtca?ttgtcgacaa?tgagcacacg?ggcaagaaga?ttggccaggt?taagtcccat 1500
ggcaacttca?ccttcatgcg?tctctatggt?ggtggccaca?tggtcccgat?ggaccagccc 1560
gagtcgagtc?tcgagttctt?caaccgctgg?ttgggaggtg?aatggttcta?a 1611
<210>65
<211>840
<212>DNA
<213〉aspergillus niger
<400>65
atgaagttca?caaattatct?cttgacgact?gcaacgctcg?caagcagtgt?cctagcggct 60
cctgctcccc?gcaccggttt?ggaggacaga?ctccgtgccc?ggtcattgca?gcgtcaatca 120
catcctctgg?cacctattcc?acttgacaca?tccaccaaag?agaattccag?actcctcgaa 180
gccgacgaga?ataccaccca?tgttacatac?agcagtaact?gggcgggcgc?agtgcgcgag 240
caaccacctc?cgcaaggcac?gtattctgcc?gtgtcggcaa?cctttcgtgt?accagaaccc 300
acggcgcaag?gggggagcgg?aacgcaggct?gggtcggcct?gggtcgggat?agatggcgac 360
acatacagca?acgccattct?acagacagga?gtcgacttct?acgtggaaaa?cgggcagacg 420
tacaacgatg?cctggtatga?gtggtaccca?gactatgcat?atgacttcga?cctagatgta 480
agcacagggg?acacgatcgt?cgccaaggtg?gaagccatct?cgccaagtca?aggtgtagcc 540
actattgaga?acatatcgac?ggggaagaag?gccacgcaga?cgatcagagc?cccagctgcg 600
acagctaccc?ttgccggcca?gaatgccgac?tggatcgtgg?aggatttcca?gtctggcgac 660
tcaatggtcg?atctggctgg?ctttggcgag?atcagcttct?ggggcgtgca?agcacaagga 720
ggagggtcta?catggggtgt?agatgatgcg?actattgtcg?aactgaagca?gggcaacgaa 780
gtgttgacag?acgtggaggt?gcaaagtgat?tcggccttta?cggtgaaata?tacgagctga 840
<210>66
<211>1722
<212>DNA
<213〉aspergillus niger
<400>66
atgatatatg?tcaactatat?cctgggactt?ctgtccctct?tacacaccgc?tgtagccaca 60
gctcctgatt?atgtcgtggt?agaccaactg?aacagcatcc?ccgacggatg?gacaaaaggc 120
gcagctcccc?cgccatttac?tccgatgaag?ttctggttgt?cgatgcatca?cgagtacaag 180
gcggacttcg?agcagaaagt?catcgatatc?tcgacacccg?gtcaccggga?ttatggacgg 240
catatgaaac?gcaacgatgt?catggccttt?atgcgcccat?ccgatcaggt?ctcaaagatc 300
atcttctctt?ggcttgagtc?ggagcatgtt?ccaccaaatg?ccatcgaaga?tcgcggggat 360
tgggtcgcct?tcacagtccc?gttggcccaa?gcacaatcaa?tgatgaagac?cgatttttac 420
aacttccacc?acctggaaac?aaacacaacc?caaattagga?ccctcaagta?ctccgttccc 480
gagcaagtcg?atgctcatct?gcaaatgatc?cagccaacga?ctcgcttcgg?ccgacctaag 540
acacaaacca?gcctaccgag?cctcatgcca?gtgtcggtta?acattgatga?aataagcgaa 600
gactgcttga?caggcgtgac?gcccatttgc?cttcgccagc?tctatggttt?acctagcacc 660
aaggcaagcc?ccgactcgag?aaacgtcctc?ggaatttccg?gctatctgga?ccagtacgcg 720
cgctacagtg?acctcgacga?gtttctagcc?gtatactctc?caaacagcgt?agacgccgac 780
ttctccgtag?tatcgatcaa?cggaggccaa?aacccacaaa?actcacaaga?gggaagcaca 840
gaggccagtc?tcgacatcca?atacgccctc?tccatggcat?ttgacgctaa?cgcgactttc 900
tacactaccg?ccggacgtgc?gccatccccg?tatctcgaac?agctccagta?tctggtgggt 960
cttccggacg?aggatcttcc?tgcagtgctt?agcacgtctt?acggcgagga?tgagcaaagt 1020
ctgccggagg?aatacacaga?agccacgtgc?aatttatttg?cccaattagg?tgcacgcggg 1080
gtctcggtga?tcttcagcag?cggagactcg?ggcgtcggag?gatcgtgtgt?atctaacgac 1140
ggaagccaga?ggacccgctt?tcagcctatc?ttcccggcgt?cgtgcccgtt?tgttacatcc 1200
gtgggtggga?ctgagggcgt?cgggccggaa?aaggctgtgg?acttttcgag?tggagggttc 1260
tccgagcgct?ttgctcgccc?gtcgtaccag?aatgcgagtg?tggaagcata?ccttgcccgc 1320
ttaggagata?aatgggatgg?attgtataat?ccagacggac?ggggtattcc?tgatgtgtcg 1380
gcccaggcta?gcaactatgt?aatcagggac?catgggcaat?ggctacaaac?tgcgggaaca 1440
agtgctgccg?cccctgtctt?tgcagcagtc?atctctcgac?tgaacgctgc?acgtctcgag 1500
cagggtaaac?ctacactagg?gtttctgaat?ccttggctgt?actcactcga?ccagcaagga 1560
tttacggata?ttgtagacgg?cggatcagtg?ggttgtgacg?ggtcaaatgg?aggagctctt 1620
gtcccgtatg?ccagttggaa?tgccaccaag?ggatgggatc?cggttactgg?gctggggaca 1680
cctctgtatc?agactctgga?gcagttggcg?cagtctgctt?ag 1722
<210>67
<211>1758
<212>DNA
<213〉aspergillus niger
<400>67
atgcgttctt?ccggtctcta?cacagcactc?ctgtgctccc?tggccgcctc?gaccaacgcg 60
attgtccatg?aaaagctcgc?cgcggtcccc?tccggctggc?atcatgtcga?agatgctggc 120
tccgaccacc?agataagctt?gtcgatcgcg?ctggcacgca?agaacctcga?tcagcttgaa 180
tccaagctga?aagacttgtc?aacacctggc?gaatcgcaat?acggccagtg?gctggaccag 240
gaggatgtcg?acacgctgtt?cccggtggcc?agcgacaagg?ctgtgattaa?ctggctgcgc 300
agcgccaaca?tcacccatat?ttcccgccag?ggcagcttgg?tgaactttgc?gaccacggtc 360
gataaggtga?acaagcttct?caacgccacc?tttgcctact?accaaagcgg?ctcttcccag 420
agattgcgca?caacagagta?ctccatcccg?gatgatctgg?tcgactcaat?cgacctcatc 480
tccccaacga?ccttcttcgg?caaggaaaag?accactgctg?gtctgaacca?gcgggcgcaa 540
aagattgaca?cccatgtggc?caaacgctcc?aacagctcgt?cctgtgccga?tgtcatcacg 600
ctgtcctgcc?tgaaggagat?gtacaatttt?ggcaactaca?ctcccagcgc?ctcgtcgggc 660
agcaagctgg?gcttcggcag?cttcctgaac?gaatccgcct?cgtattctga?ccttgccaag 720
ttcgagaagc?tgtttaacct?gccctcccag?agcttttccg?tggagttggt?caacggcggt 780
gtcaatgatc?agaatcaatc?gacggcttcc?ttgaccgagg?cggacctcga?tgtggaattg 840
ctcgtcggag?ttgctcatcc?cctcccggtg?actgagttca?tcacttctgg?cgaacctgcc 900
gccgacaacg?agaacgagcc?ttacctccag?tactatgagt?accttctctc?caagcccaac 960
tcggctctgc?cccaagtgat?ttccaactcc?tatggtgacg?acgaacagac?cgttccagag 1020
tactacgcca?agcgagtctg?caacctgatc?ggacttgttg?gcctgcgcgg?catcagtgtc 1080
ctcgagtcgt?ccggtgacga?aggtatcgga?tctggctgcc?gaaccaccga?cggcaccaac 1140
cgaacccaat?tcaaccccat?cttcccggcc?acctgtccct?acgtgactgc?cgtgggagga 1200
acaatgtcct?atgcccccga?aatcgcctgg?gaagccagtt?ccggcggatt?cagcaactac 1260
ttcgagcggg?cgtggttcca?gaaggaagct?gtgcagaact?acctggcgca?ccacatcacc 1320
aacgagacca?agcagtacta?ctcgcaattc?gccaacttta?gcggtcgcgg?atttcctgac 1380
gttgctgccc?atagctttga?gccttcatat?gaggttatct?tctacggcgc?ccgctacggc 1440
tccggcggta?cctcagccgc?gtgtcccctt?ttctctgcgc?tagtgggcat?gctgaacgat 1500
gctcgtctgc?gggcgggcaa?gtccacgctg?ggtttcttga?accccctgct?ctatagcaag 1560
gggtacagag?cgttgactga?tgtgacgggg?ggccagtcga?tcggatgcaa?tggcattgat 1620
ccgcagaatg?atgagactgt?tgccggcgcg?ggcattatcc?cgtgggcgca?ctggaatgcc 1680
acggtcggat?gggatccggt?gactggattg?ggacttcctg?actttgagaa?gttgaggcag 1740
ttggtgctgt?cgttgtag 1758
<210>68
<211>798
<212>DNA
<213〉aspergillus niger
<400>68
atgaagacta?ctgctctctt?gaccgccggc?ctgctggcca?ccactgctat?ggccgctcct 60
ctgacggcca?agcgccaggc?tgctcgggcc?aagcgctcca?cgaaccgcca?gagcaaccct 120
cccttcaagc?ctggcaccaa?cgaggtcctc?gcccttaacg?gcaccaagaa?tgtggagtac 180
agctccaact?gggccggtgc?cgtcctcatt?ggcactggtt?acactgccgt?gaccgccgag 240
ttcgtcgtgc?ccaccccctc?cgtgccctcc?ggtggctcga?gccgcgagga?gtactgtgcc 300
tccgcctggg?tgggcattga?cggtgacacc?tgtgacactg?ctatcctcca?gaccggtgtg 360
gacttttgtg?tccagggcag?cgaggtgagc?ttcgatgcct?ggtacgagtg?gtaccccgac 420
tacgcctacg?acttcagcgg?catctccatc?tcggccggtg?ataccatcaa?ggtcaccgtc 480
gatgccagca?gcgacaccac?cggtactgcc?acgattgaga?acgtgagcac?tggtaccacg 540
gtcacccaca?gcttcacggg?cggtgttgat?ggtgatctgt?gtgagtacaa?cgctgagtgg 600
atcgtcgagg?acttcgagga?ggatgactcc?ctcgttccct?ttgccgactt?tggcaccgtg 660
actttcacca?gctgctccgc?taccaaggat?ggttcctctg?ttggccctga?ggatgctacc 720
atcatcgaca?tcgagcagaa?tgaggtgctg?acctccgttt?ccgtctccag?tagcgaggtc 780
gttgtcaagt?acgtctaa 798
<210>69
<211>1743
<212>DNA
<213〉aspergillus niger
<400>69
atggtcgcct?tttcccgcat?ctcggcaggc?ttcgcccttg?ccgcccctgc?cctggccagc 60
gtcgtcctgg?agaccgtcaa?gtctgttccc?agcgactgga?agctcgtgga?ggctgctgat 120
accagctcca?caatttcttt?gtccgttgct?ctggcgcgtc?agaacctgga?ccagttggag 180
gagaagctcc?tggccgtgtc?cacccctggc?aaggacacct?acggccagtt?cttggatctg 240
gacgacatca?atgagcagtt?tcctctcgca?gatgacgctg?ctgttgtggc?ttggctgaag 300
aaggcaggcg?tcacccagat?ccataaggag?ggtggtctgc?tgaactttgc?gaccactgtg 360
ggcacagcca?accagcttct?caacaccacc?ttctcggtgt?acaagagcgg?atctacccag 420
aagctgcgca?caacgcaata?ctctgttccg?gatgagctga?ccgggtccat?tgatctcatc 480
tcgccgactg?ttttctttgg?aaagtccaac?gctgcgcgct?cggcggccgt?gcgtgcttcg 540
cagactacca?aggagaccag?cagaaagaag?agcagtaatg?tgtgcgagta?catcactccg 600
gattgcctca?aagagcagta?tagcattgac?tatacgcccg?aggcatcgtc?gggaagtcgt 660
gttgggtttg?gcagtttctt?gaacgagtcg?gccttgtact?cggatttgga?tctgttcacc 720
cagtactttg?acattcccca?gcagagtttc?actgttgaga?ctatcaacgg?gggaatcaac 780
aaccaggaga?atgatccgga?tggtgaagcc?gatctcgatg?tccagaacat?cgtgggcatc 840
tcgcatccct?tgccggtgac?ggagtacatt?accggaggat?ctcctccatt?cattcccgac 900
gtcgagacta?ctaccgacga?gaacgagcct?tacctgcagt?actacgagta?tctgctggcc 960
aagaccaacg?acgagctgcc?actggttatc?agcaactcgt?acggcgatga?cgaagatacc 1020
gttcccattg?cctacgccac?ccgcgtatgc?aacctcatcg?gcctgatggg?cacacgtggt 1080
atctccatcc?tcgagtcttc?cggcgactct?ggtgtgggcg?gcgcatgcat?gtccaacgac 1140
ggcaccgaca?agaccgaatt?cacccccatg?ttcccaggaa?catgcccgta?catcaccgcg 1200
gtcggcggca?cccaagacgt?gcccgaagtc?gcctgggtgg?acagctccgg?cggcttcagc 1260
aactacttct?cgcagccgtc?gtaccagtcg?gatcaggtgg?agacctacct?ggacaagtac 1320
atctctgcct?cgacgaagaa?gtactacgag?cagtacacca?acttcagcgg?tcgcgcgttc 1380
cctgacgtgt?ctgcgtttgc?aggttctcct?tactacgaaa?cttatattga?tggtcagctc 1440
ggccttgtgg?cgggtacttc?tggcgctagc?cctgtgtttg?cggggatcgt?cgcgctgctg 1500
aacgatgccc?gtctgcgggc?caacaagaca?tccttgggct?tcctgaaccc?ttggctgtac 1560
tcgagcggct?acaagagcct?gaatgacatt?accagtggcg?aggcagtggg?ctgccaaggc 1620
gatgtggagg?gcgctggagt?cattccttgg?gcgagctgga?atgccacgac?gggatgggat 1680
ccggcgacag?ggctgggaac?gcctaatttt?gccaagctga?aggaggcggt?tcttgcgttg 1740
taa 1743
<210>70
<211>1896
<212>DNA
<213〉aspergillus niger
<400>70
atgcatggtc?tgcgcctagt?atgcagcata?gggacattgc?ctttggttat?cctggcatat 60
ccggcggctt?cattgcatac?aacttcagca?gccgtggact?tggactccct?tcgtctgacc 120
tctaactccg?aatacgtcaa?ttctgtccat?gtagacacga?atcgatcagt?cgcagtgtcc 180
gctgaagaac?attataccga?tacagcagct?cgactggttc?agaacattgt?tcctggagcg 240
agctttcgtc?tcatcgatga?ccactttgtc?ggcgacaatg?gagttgcaca?tgtatacttc 300
cgccaaacgc?tccatggtat?tgacattgac?aatgcggatt?tcaatgttaa?tattggaaaa 360
gatggactgg?tcttgtcttt?cggacattcg?ttcttcacag?gcgcgttgcc?gagcagccat 420
ctggacaata?ccaacgtttt?gagtccggag?gctgcactta?gaggagcaag?ggacgctata 480
cagcttccac?tgactattga?caatgtttct?actgaagctg?cagaggggcg?gaacgagtac 540
atattcagag?aggcagtggg?agcggtatct?gaccccaaag?ctaagctagt?ctaccttgtc 600
aagccagaag?ggactctggc?gctcacctgg?aggatagaaa?cagacatgta?tgagcactgg 660
ctactgacat?acattgatgc?agagactacc?actgtccacg?gcgtggttga?ctatgtcgca 720
gacgcgacat?atcaagttta?tccctggggc?acaaacgatc?cagcagaagg?acatcgcacc 780
attgtcaccg?acccctggga?cctatccgca?tccgcataca?cctggataag?cgatggacgg 840
gacaactaca?ccacaaccag?aggcaacaat?gccatcgcac?actggaatcc?gaccggcggt 900
ggctcctatc?tctacaacct?acgtccatcc?gaccccaact?tgaatttcca?atggccatac 960
tccccaaaca?tgtccccacc?ccgatcatac?atcaacgcct?ccatcgtcca?actcttctac 1020
acagcaaacg?cctaccacga?cctcctctat?acactcggct?tcaccgaatc?cgctggcaac 1080
ttccaatgga?ataacagcgc?ccacggcggc?cgagacaaag?actacgtgat?cctcaacgca 1140
caagacggct?ccgggttcag?caacgcaaac?tttgcaaccc?cacccgatgg?tatccccggc 1200
cgtatgcgca?tgtacatctg?gatcgagtct?actccgtcgc?gtgatggaag?ttttgacgcg 1260
ggcattgtaa?ttcacgaata?cactcacggt?gtatccaatc?gtctcaccgg?cggctcccac 1320
aacgccggat?gcctcagcgc?cctcgaatcg?ggtggcatgg?gcgaaggctg?gggcgacttt 1380
atggcgacgg?ccatccgaat?caagcccaac?gatacacgca?caacgtctta?cactatgggt 1440
gcatgggcag?ataatgataa?atgtggtgtc?cgggactatc?cttattctac?ctcctttact 1500
gagaaccctt?tgaactatac?gagcgtgaat?accatgaacg?gcgtgcacgc?catcggaact 1560
gtctgggcaa?ccatgctata?cgaggtcttg?tggaacctca?tcgacaagta?cgggaagaat 1620
gatgggtcga?ggccggtgtt?tagaaacggg?gtgcctacag?atggaaagta?cttgatgatg 1680
aagttggtgg?tggatgggat?ggcactgcaa?ccatgtaatc?cgaacttcgt?gcaagccagg 1740
gacgcgatcc?ttgacgcaga?cattgtgttg?actggcggga?agaatcgctg?tgagatctgg 1800
agggggtttg?cgaagagagg?attggggcaa?ggagcggctc?atagtagttt?aaattggatg 1860
cggaggggga?gtacacttct?tcctacggga?tgttag 1896
<210>71
<211>1185
<212>DNA
<213〉aspergillus niger
<400>71
atggtcgtct?tcagcaaaac?cgctgccctc?gttctgggtc?tgtcctccgc?cgtctctgcg 60
gcgccggctc?ctactcgcaa?gggcttcacc?atcaaccaga?ttgcccggcc?tgccaacaag 120
acccgcacca?tcaacctgcc?aggcatgtac?gcccgttccc?tggccaagtt?tggcggtacg 180
gtgccccaga?gcgtgaagga?ggctgccagc?aagggtagtg?ccgtgaccac?gccccagaac 240
aatgacgagg?agtacctgac?tcccgtcact?gtcggaaagt?ccaccctcca?tctggacttt 300
gacaccggat?ctgcagatct?ctgggtcttc?tcggacgagc?tcccttcctc?ggagcagacc 360
ggtcacgatc?tgtacacgcc?tagctccagc?gcgaccaagc?tgagcggcta?cacttgggac 420
atctcctacg?gtgacggcag?ctcggccggc?ggagacgtgt?accgggatac?tgtcactgtc 480
ggcggtgtca?ccaccaacaa?gcaggctgtt?gaagcagcca?gcaagatcag?ctccgagttc 540
gttcagaaca?cggccaatga?cggccttttg?ggactggcct?ttagctccat?caacactgtc 600
cagcccaagg?cgcagaccac?cttcttcgac?accgtcaagt?cccagctgga?ctctcccctt 660
ttcgccgtgc?agctgaagca?cgacgccccc?ggtgtttacg?actttggcta?catcgatgac 720
tccaagtaca?ccggttctat?cacctacacg?gatgccgata?gctcccaggg?ttactggggc 780
ttcagcaccg?acggctacag?tatcggtgac?ggcagctcca?gctccagcgg?cttcagcgcc 840
attgctgaca?ccggtaccac?cctcatcctc?ctcgatgacg?aaatcgtctc?cgcctactac 900
gagcaggttt?ctggcgctca?ggagagcgag?gaagccggtg?gctacgtttt?ctcttgctcg 960
accaaccccc?ctgacttcac?tgtcgtgatt?ggcgactaca?aggccgttgt?tccgggcaag 1020
tacatcaact?acgctcccat?ctcgactggc?agctccacct?gctttggcgg?tatccagagc 1080
aacagcggtc?tgggactgtc?catcctgggt?gatgttttct?tgaagagcca?gtacgtggtc 1140
ttcaactctg?agggccctaa?gctgggattc?gccgctcagg?cttag 1185
<210>72
<211>1197
<212>DNA
<213〉aspergillus niger
<400>72
atgaagtcag?cctccttgct?cacagcatcc?gtgctgttgg?gctgtgcctc?cgccgaggtt 60
cacaagctca?agcttaacaa?ggtgcctctg?gaagagcagc?tttacacgca?taacatcgac 120
gcccatgtcc?gcgctctggg?ccagaagtac?atgggtatcc?gcccgtccat?ccacaaagag 180
ctggtcgagg?agaaccctat?caatgacatg?agccgtcatg?atgttctggt?ggacaacttc 240
ctgaacgcac?agtacttctc?tgagatcgag?ctgggtactc?ccccccagaa?gttcaaggtt 300
gtcctggaca?ctggcagctc?gaacctttgg?gttccttcga?gcgaatgcag?ctctatcgcc 360
tgctacctcc?acaacaagta?tgattcgtct?gcctccagta?cgtatcacaa?gaatggcagt 420
gaattcgccg?tcaagtacgg?ctctggcagc?cttagcggat?tcatttctca?ggacaccctg 480
aagattggcg?acctgaaggt?caagggacag?gacttcgctg?aggcgaccaa?tgagcctggc 540
cttgcctttg?ccttcggccg?gttcgatggc?attctcggct?tgggttatga?caccatctcc 600
gtgaacaaga?ttgttcctcc?cttctacaac?atgcttgacc?agggactcct?cgacgagccg 660
gtctttgcct?tctaccttgg?agataccaac?aaggagggtg?acgagtccgt?ggcgaccttc 720
ggtggtgtcg?acaaggacca?ctacaccggc?gagctgatca?agattcccct?ccgtcgcaag 780
gcttactggg?aggttgagct?tgacgccatt?gctcttggcg?atgatgttgc?tgagatggag 840
aacaccggtg?tcattctgga?cactggtacc?tccctgattg?ctctgcctgc?tgacctggct 900
gagatgatca?atgctcagat?cggtgctaag?aagggctgga?ccggccagta?caccgttgac 960
tgcgacaagc?gctcgtccct?gcccgatgtt?actttcaccc?ttgccggcca?caacttcacc 1020
atctcctcgt?atgactacac?cttggaggtg?cagggctctt?gcgtcagtgc?cttcatgggc 1080
atggacttcc?ctgagccggt?tggtcccttg?gccattttgg?gcgatgcgtt?cctgcgcaag 1140
tggtacagcg?tgtatgacct?gggcaacagc?gctgttggtc?tggccaaggc?caagtaa 1197
<210>73
<211>1182
<212>DNA
<213〉aspergillus niger
<400>73
atgcgcaagt?accgcttcca?tcccaccaag?cctggtccct?acactctcag?cagctccatc 60
caacagaccg?gtcgtccgta?cactgaaaag?cccatcgggg?gtcgggccca?tatccggcag 120
ctggtgcgga?agaagagcac?caccagcgat?gaggttggcg?aggttccggc?cgaagatgtg 180
cagaacgact?ccatgtatct?ggcgaccgtg?gggatcggaa?ccccggcgca?gaacctgaag 240
ttggactttg?acactggttc?agctgatctt?tgggtctggt?ccaacaaact?cccctcaacc 300
cttctatccg?agaacaagac?ccatgcgatc?ttcgactcgt?ccaaatcgag?caccttcaag 360
accttggaag?gtgaatcctg?gcaaatctcc?tacggagatg?gatcctccgc?atcagggagt 420
gtgggcaccg?acgacgtcaa?cattggcggc?gtagtcgtca?agaaccaagc?cgttgagctg 480
gcagagaaga?tgtccagcac?attcgcccaa?ggcgaagggg?acggattgct?cggtctagca 540
ttcagcaaca?tcaacacggt?acagccaaag?tccgtgaaaa?cgcccgtcga?gaacatgatc 600
ctgcaggatg?acattcccaa?gtcggctgag?ctgttcacgg?ccaagctgga?tacctggcgg 660
gacactgatg?acgagtcgtt?ttacaccttt?ggcttcattg?accaggatct?ggtgaagacg 720
gcaggtgaag?aggtctacta?cacccctgtc?gataacagtc?aaggcttctg?gctattcaac 780
tcgacctccg?cgacggtaaa?tggaaagacc?attaaccggt?cgggtaacac?cgccattgct 840
gataccggta?cgacgctggc?cttggtggac?gatgacacgt?gtgaggccat?ttatagtgca 900
attgacggcg?cctattatga?tcaggaagta?cagggctgga?tctatccgac?cgatacggcg 960
caggataagc?tacccactgt?gtcgtttgcc?gtgggtgaaa?agcagttcgt?ggtgcagaag 1020
gaggacctgg?cgttttcgga?ggcgaagacg?ggctatgtct?atggaggaat?ccaaagtcgt 1080
ggtgatatga?ccatggacat?cttgggagac?acatttttga?agagtattta?tgctgtaagt 1140
gcattgctgt?tggcgttaag?gggtgatatc?gaagctcact?aa 1182
<210>74
<211>849
<212>DNA
<213〉aspergillus niger
<400>74
atgaagttct?ctaccatcct?taccggctcc?ctcttcgcca?ctgccgctct?ggctgctcct 60
ctcactgaga?agcgccgtgc?tcgcaaggag?gcccgcgccg?ctggcaagcg?ccacagcaac 120
cctccctaca?tccctggttc?cgacaaggag?atcctcaagc?tgaacggcac?ctccaacgag 180
gattacagct?ccaactgggc?tggtgccgtc?ctgatcggcg?acggctacac?caaggtcact 240
ggcgagttca?ctgtccccag?tgtctctgct?ggatctagca?gctccagtgg?ctacggcggt 300
ggctacggct?actacaagaa?caagagacaa?tccgaggagt?actgcgcctc?cgcttgggtt 360
ggtatcgacg?gtgacacctg?cgagaccgct?attctccaga?ctggtgtcga?cttctgctac 420
gaggatggcc?agacttccta?cgatgcctgg?tacgagtggt?accccgacta?cgcctacgac 480
ttcaacgaca?tcaccatctc?cgagggtgac?accatcaagg?tcactgtcga?ggccaccagc 540
aagagcagcg?gtagcgccac?cgttgagaac?ctgaccactg?gccagtccgt?cacccacacc 600
ttcagcggca?acgtcgaggg?tgacctttgc?gagaccaacg?ccgagtggat?cgtcgaggac 660
ttcgagtctg?gtgactctct?tgtggctttc?gctgacttcg?gctccgttac?cttcaccaat 720
gctgaggcta?ccagcgacgg?ttccactgtc?ggcccctctg?acgctaccgt?tatggacatt 780
gagcaggatg?gcaccgtcct?caccgagacc?tccgtctctg?gcgacagcgt?cactgtcacc 840
tacgtttaa 849
<210>75
<211>822
<212>DNA
<213〉aspergillus niger
<400>75
atgggagatt?acggccccgg?agtgtcgtca?ctcacggcac?agctacctgg?aaatccgcct 60
gtctctgaaa?cagatcagga?tgagatctca?gtacttgtaa?cgggctttgg?gccattcaag 120
tctaatctag?tgaacgcctc?atatctgata?gcctcgtccc?taccaccctc?tttcacattc 180
tcacctgcat?cttcagacgg?ctctgatgct?gttccccgtc?gagtttcgat?aaatgtccat 240
ccttcaccca?tacccgttgc?atattcatcg?gtgcggacga?ccctccccgt?cattctcgat 300
gactatgcca?agacgcacgg?aggccgacgc?ccagacatcg?tcatacacat?tggcatagca 360
gcaatgagga?actactattc?cgtggagacg?caggctcacc?gtgatgggta?tctgatgtcc 420
gacatcaaag?gcagatccgg?gtacgaggat?ggcgagaagc?tgtggaggga?gctcgacttg 480
ccactggtgc?ttagggctgg?cccttcagag?ggacacgcct?cggagaagaa?acatctcagc 540
ccccgtccac?cggacgaaga?tttcctagca?gcatggaaga?cattttgccc?tccagaaacc 600
gatgcgcgga?tctccactga?tgccggacgt?tatctctgcg?agttcatcct?gtacaccagc 660
ttggcactgg?cataccaggc?gggtgaggat?cgcaatgtca?ccttcttcca?tgttcccgcg 720
tcatgcttgg?atgaggatat?agagacgggc?aaggaggttg?ccgtcgcgct?aatcaaggct 780
cttgtgacta?gctggagtga?gcagcagcac?agcgttccct?ag 822
<210>76
<211>1629
<212>DNA
<213〉aspergillus niger
<400>76
atgggctcaa?ggcagggaaa?ggcccccttt?ggctggggta?ctcagtcact?tgctcacttt 60
ggtatcaacc?cagaccttgg?gttgcacaac?cagcagaacc?tcaactccct?catttcacat 120
tcagcgatgg?ccactgcgtt?ggagacggaa?tatgccacca?tccctattga?ccataacaac 180
gcatcggctg?gcacttatca?aaatcggttc?tgggtcagcg?atgaattcta?tcagcctggc 240
aacccgatat?ttgtgtacga?taccggggag?tcggatggcg?gatcgatagc?ccagtcctac 300
ctaacctcca?ctctctcctt?cttcagagaa?ttcctgatcg?aattcaacgc?catgggaatc 360
gcctgggagc?acagatacta?tggaaactcg?accccggctc?ccgtatccta?tgaaactcca 420
cccgaggcat?ggcaatacct?caccaccaag?caggcgctcg?cggaccttcc?gtactttgct 480
agtaacttta?gccgcgagaa?gtatcctgac?atggacctga?cgccgcaggg?cacgccgtgg 540
atcatggtgg?gcggctcgta?cgcagggatt?cgtgctgcat?taactcgcaa?ggagtaccca 600
gagacgatat?tcgcagcctt?ttcctcatcg?tctccggtgg?aagcacaggt?caatatgagc 660
gcgtattacg?accaagtcta?tcgtggcatg?gttgccagcg?gatggaccaa?ctgctcggca 720
gatatccacg?ctgctctgga?atatattgac?gatcaacttt?cggatgaaga?tacagctacc 780
tcggtcaaac?aacttttctt?cggatctggc?gccgagacca?actccaacgg?tgatttcact 840
gcagcgctaa?ctgccatcta?cggctacttc?caaagttatg?gtatggcggg?aggtattgga 900
ggtctaggcg?cattctgcga?gtatctcgaa?attgatccca?agacgaacgg?gactacagga 960
ccggatggcc?ttgcccctac?gtatggcggc?cagtatgtcg?ccgaacgatg?ggccgcatgg 1020
ccaacctttc?tcgagctggt?caatctgaat?atggggacca?actgcgggcc?tcaggacgcg 1080
tctcagccaa?ttgactgtga?cttttccaag?ccatacggcg?atccctcggc?catcacttgg 1140
acttggcaat?actgcagcga?atgggggttc?ttccaggcga?acaacgatgg?gccgcactcg 1200
ctggcctcgc?gatatcagtc?ggtggaatac?cagcaagaag?tatgtaaccg?gcagttcccc 1260
gatgcagtgg?acaagggact?gctgcctccg?tcgccgcggg?cggatgatgt?caaccaagag 1320
tttgggggat?ggacgatccg?cccgtccaat?gtttacttca?gcggaggaga?attcgatccg 1380
tggcgatcat?tgtccattct?gtcgacagaa?gatttcgcac?ctcaaggggt?ggagtttacg 1440
agcgcgatcc?cagcctgtgg?ggtgcagacc?aatgaggaca?ccgtctttgg?atacgtcatg 1500
cagaactcgg?aacattgctt?tgactttcaa?gcgacgccga?ccgtggggaa?gttatcacgc 1560
ggcatcttca?catccgcctt?gttgcaatgg?ctcgaatgtt?ttggacagaa?ctcaagccaa 1620
tccaggtga 1629
<210>77
<211>1176
<212>DNA
<213〉aspergillus niger
<400>77
atgaagctct?caatagctct?tgcactcggc?gcaacggctt?cgacgggggt?gttggctgct 60
gttgtaccgc?agcaagaacc?gctgataacc?ccccaagatc?ccccaactca?tcatcatcag 120
gagaagttct?tgatcgagtt?ggctccttat?cagacgagat?gggttaccga?ggaagaaaag 180
tgggacttaa?aactggatgg?cgtgaacttc?atcgatatta?ctgaagaacg?aaacactggg 240
ttctacccaa?cgttgcatgc?tggtagctat?gttcactatc?cgccgacgat?gaagcatgcg 300
gagaaggtgg?ttccccttct?gcggggtctc?tccaaggaca?acatggagca?aaacctcaac 360
aaatttacct?catttcacac?tcgctactat?aggtcgtcca?ctggtattga?gtccgcaaag 420
tggctataca?gtagggtttc?ggatgtcatt?gagcagtcgg?gtgcagcaga?gtacggcgcc 480
actgtggagc?agttcgctca?ctcatggggc?caattcagta?tcattgctcg?gatcccaggc 540
cagactaaca?aaactgttgt?cctgggcgca?catcaggaca?gcatcaatct?tttcctcccc 600
tccatcctag?ctgcacctgg?tgccgatgat?gacggaagtg?gaaccgtgac?tatactcgaa 660
gctttgcgtg?gtctgctgca?gtcagacgcc?attgtccggg?gcaacgcttc?caacacaatc 720
gaattccact?ggtactcggc?agaggaaggt?ggtatgcttg?gttcgcaagc?catattctct 780
caatataaga?gagataagcg?agacatcaag?gcgatgcttc?aacaggatat?gactggttat 840
acccagggag?ctctggacgc?cggtcgtcaa?gaagccattg?ggattatggt?tgactacgtt 900
gatgagggac?tgacacaatt?cctcaaagat?gtcactactg?agtattgtgg?tattggctac 960
atcgaaacca?gatgtggcta?cgcctgttcg?gaccacacgt?ccgcaagcaa?atatggctat 1020
cccgcagcta?tggcgacgga?atccgaaatg?gaaaacagca?acaagaggat?ccacacgact 1080
gatgacagca?tccggtatct?aagcttcgat?catatgctgg?agcatgcgag?gttgacactt 1140
ggcttcgctt?acgagctggc?ctttgctcaa?ttctag 1176
<210>78
<211>1329
<212>DNA
<213〉aspergillus niger
<400>78
atgagaacta?ctacgtcttt?tgctaggctt?gcattggcag?tggcctcagt?tggtattgtc 60
tttgctagtc?caacaaaaaa?taacgatggg?aaactggtat?atggctcacc?agaatccgtc 120
ggcatgatat?ccgccccttt?gcaccaaatg?gtccaaaatg?ttagcgcata?tacacatgct 180
gccaactata?gcaagttctc?gtacgacaaa?gtccatccca?tcgagccagg?gtctgttacc 240
ctggtggctc?tcgacggtgt?catcgtcagc?gaatttgcct?tgggcaagag?aaatctctac 300
gccgatgtca?acggcaccaa?tttacctcga?tacctgcagg?aagacaccac?cctggataca 360
gtctacgata?tggcaagcct?cacgaagctg?ttcaccacgg?tagctgcttt?acgggaactt 420
gacgctggtc?gaattgcgct?taatgtaact?gttgcaactt?atataccgga?ctttgcgacg 480
aatgggaagg?agaatattac?tatcttggag?ctgttcacgc?atacaagcgg?tttcgcttct 540
gatccatcgc?caccactttt?ctctgcttat?tatacgacgt?atgatgaacg?cattaaagca 600
attttgacgc?aaaaaattat?caataccccc?ggcagcacat?acctctactt?agatctcaac 660
tttatgtcgc?tgggcctcgt?tatcgagacc?gtaacgggac?gtgccctgga?tgatcttatt 720
tatgacttca?ccagaccgct?tgaaatgaca?tctaccttct?tcaaccgcgg?gaatatcgaa 780
ggctctacac?cccagtcacc?caactacgac?cgcacagccg?tacaagaatt?tcagatcgca 840
gccctcggac?cctcagaacc?acagcgtcca?caaccagtgc?gcggcacagt?tcacgacgag 900
aacgcatggt?ccctagacgg?cgtatcaggt?catgcaggtc?tattctccac?tgtgcgcgat 960
acagcgacat?tctgccagat?gatcctcaac?aacggcacat?atgcaggcca?acggatcctt 1020
tctcgaacag?cggtagacat?gattttcaca?aacttcaatg?ccaggtttcc?gggggatgct 1080
cgtagtttag?ggtttgagtt?ggatcagtat?tctactgcgg?gaccgatggc?gagtttgcaa 1140
actgcgagtc?acactggatt?tactgggact?acgttggtga?tggataggac?gtataacgcc 1200
ttttggttgc?attttagtaa?ccgggtgcat?ccgtctaggg?catggtctag?caatactatt 1260
gtgagagagg?ctattgggta?ttgggttggg?aagagcttgg?ggttggatgt?tgcgtttgct 1320
ctgttgtaa 1329
<210>79
<211>1839
<212>DNA
<213〉aspergillus niger
<400>79
atggcgtcct?ggttgctctc?gacgctcctt?tttctgagcc?cgtccttggt?gtcagccaaa 60
tcggccgcag?actattatgt?tcactccttg?cccggtgccc?ccgaggggcc?cttgctgaag 120
atgcatgccg?gccatattga?ggtggatcca?cagaacaatg?gaaatctttt?cttctggcac 180
taccagaatc?gccatattgc?caaccgccag?cggactgtga?tctggttgaa?cggtggtccc 240
ggatgtagtt?ccatggacgg?cgcgttgatg?gaggtcggtc?cgtatcgcct?gaaggacaat 300
gaaaccttga?cctataatga?gggttcctgg?gacgaattcg?ccaatttgtt?gttcgtcgat 360
cagccagtcg?gaaccgggtt?cagttatgtc?aacacggaca?gctatcttca?tgagctcgat 420
gagatgtcgg?ctcagttcat?tgtctttctg?gaagagtggt?tcagattatt?tccggagtat 480
gaacgcgatg?atatctacat?tgccggcgag?tcttacgccg?gtcagcatat?tccatacatc 540
gccaaagcca?tccaggaacg?gaacaagaac?gttcaaggga?agaccatcgc?ttcgtggaat 600
ctaaaaggcc?tattgattgg?caatggttgg?atttctccta?atgaacagta?catgtcctac 660
ttgccctacg?catatgaaga?aggccttatc?aaggaaggca?gccggaccgc?gaaggaactc 720
gaagttttac?agtcagtctg?taagtccagg?ctggaaactg?gcaagaacaa?ggtccacctc 780
aacgactgcg?agaaggtcat?gaatgctctg?ttggataaga?cggtcgaaga?caacaaatgt 840
ctcaacatgt?atgacatccg?ccttcgtgac?accaccgatg?catgcggtat?gaactggccc 900
accgacctgg?aggacgtgaa?gccctatctg?cagcgggaag?atgtggttaa?agcgcttaac 960
atcaatccgg?agaagaagtc?tggctgggtg?gagtgttcag?gtgcagtgag?cagcgctttc 1020
aatccgcaaa?agtccccgcc?ctcggttcaa?ctacttcccg?gcttgctgga?atcgggactt 1080
caaatcctcc?ttttcagcgg?agacaaggac?ctgatttgca?accatgttgg?aacggaacag 1140
ctcatcaata?acatgaagtg?gaacggaggc?acgggtttcg?agacctcacc?tggcgtctgg 1200
gctcctcgac?acgactggag?tttcgaaggc?gagccggcgg?gtatctatca?atatgccaga 1260
aacctgactt?acgtgctcat?ctacaacgca?agccatatgg?ttccctacga?ccttcctcgt 1320
cagagccggg?acatgctaga?tcgcttcatg?aatgtcgata?tcgcgagcat?cggaggcagc 1380
cccgccgact?cgcgcattga?cggcgagaag?ctgccccaga?cgtcggtggg?cggccatccc 1440
aacagcaccg?cggcggagga?gcaggagaag?gagaggatca?aggagacgga?atggaaagcc 1500
tacgccaagt?caggcgaagc?cgttctcctc?gtcgtcatta?tcggtgtatt?agtttggggc 1560
ttcttcatct?ggcgcagccg?ccggcgtcac?cagggatacc?ggggcgtctg?gcataaggac 1620
atgagcggaa?gctctgttct?cgagcggttc?cacaacaagc?gcacgggagg?cgcagacgtc 1680
gaagcggggg?atttcgacga?ggcggagctc?gatgaccttc?attctccaga?cctcgaaaga 1740
gaacactacg?ccgtgggcga?ggacagcgac?gaggatgata?tttcacgaca?gcattctcaa 1800
caggcctccc?gagccggggg?cagtcataat?ctatcctag 1839
<210>80
<211>1596
<212>DNA
<213〉aspergillus niger
<400>80
atgtttctga?tttcacctgc?agtgacagtt?gcggctgcac?ttctgctgat?caacggcgca 60
ggagcaactc?aatctgaacg?aagtcgggct?gccgctcatt?tttccaaacg?tcatccgacg 120
taccgtgctg?cgaccagagc?ccagtcgagc?aacacttccg?actaccgatt?cttcaataat 180
aggaccaagc?cccacttggt?ggaaagctta?cccgatgtgc?acttcgatgt?tggggagatg 240
tactcggggt?cgatccctat?cgatgacagc?aacaatggat?ctcgatccct?gttttatatc 300
ttccaaccta?agataggcga?accttcagac?gaccttacca?tttacctcaa?tggagggcca 360
ggctgttcct?ccgaacaggg?attctttcag?gaaaatggca?ggttcacatg?gcagcctggt 420
acctatgcac?ccgtcatcaa?cgaatattct?tgggtcaatt?tgacgaacat?gctatgggtt 480
gaccaaccag?tcggaaccgg?attttccgtt?ggaaatgtta?cagccaccaa?cgaagaagag 540
attgccgccg?attttctcga?cttctttgaa?aagtttgaag?atctatacgg?gataaagaac 600
tttcgcattt?tcatgaccgg?tgagagctac?gccggtcgct?atgttcccta?tatctcgtcg 660
gcaatgctag?acaagaacga?caccacgcgt?ttcaatctga?gcggagccct?tctttatgac 720
gcctgcatcg?gccaatggga?ctacatccag?gccgaactcc?ctgcctaccc?cttcgtcaag 780
cagcacgctt?cactattcaa?cttcaatcag?tcctacatga?acgagcttga?aaccacctac 840
gaagaatgcg?gctacaaggc?ctacttcgat?gagtactttg?cctttccacc?aagcggcatc 900
caacccccaa?aatacatgaa?ctactccgag?tgcgacatct?ataacatgat?ctactacgaa 960
gcctataacc?cgaacccatg?cttcaatccc?taccgcgtca?ttgatgagtg?tccacttctc 1020
tgggacgtcc?tgggctggcc?gacagacttg?gcatacgagc?ctgcgcccac?cacatacttc 1080
aaccgtatcg?atgtcaagaa?ggccctgcac?gcccccatgg?atgtggaatg?ggagctctgc 1140
agctacgacc?tcgtcttcgc?tggaggcgac?gctgacccgg?gtccggagca?gcaaggggat 1200
gactcaccca?accccaccga?gggtgtcctc?ccgcgtgtta?ttgaggcgac?caaccgcgtg 1260
ctcattgcca?acggtgactg?ggactacctg?attatcacca?acggcaccct?cctcgccatc 1320
cagaatatga?cctggaacgg?ccagctgggc?ttccagtccg?cacctgccac?accgatcgat 1380
attcagatgc?ccgatctcca?gtgggttgag?atttttgagg?cccaggaggg?atatggaggg 1440
ctggatggcc?ctcagggggt?tatgggtgta?caacattatg?agcgcggttt?gatgtgggcg 1500
gagacatatc?agtcggggca?taagcaggct?caggatcagg?gccgtgtctc?gtatcgccat 1560
ctgcagtggc?tgttggggca?agttgagatt?ctttag 1596
<210>81
<211>1596
<212>DNA
<213〉aspergillus niger
<400>81
atgctgtttc?gcagtctgtt?gtcgacggct?gtcctagccg?tctcgctgtg?cacggataat 60
gcttcagctg?ctaaacatgg?tcgatttggc?caaaaagctc?gcgacgccat?gaacatcgcg 120
aagcgttccg?ctaacgccgt?gaaacactcg?ttgaagatcc?ctgtcgagga?ctatcagttc 180
ttgaacaaca?agactaagcc?ttaccgcgtg?gaaagcctgc?ctgatgttca?cttcgatctg 240
ggcgagatgt?attccggctt?ggtccctatt?gagaagggca?acgtgtcacg?gtcccttttc 300
tttgtcttcc?agcccactat?tggcgagcct?gtggatgaga?tcaccatctg?gctgaatggt 360
ggccctggtt?gcagttccct?tgaggccttt?ctccaggaga?atggtagatt?cgtgtggcag 420
cctggaacct?accagcctgt?tgagaaccca?tactcgtggg?tgaatctcac?caatgttctg 480
tgggttgacc?aacctgtggg?aacgggattc?tctctgggtg?tcccaaccgc?tacgtccgag 540
gaggagattg?ctgaagactt?tgtgaagttc?ttcaagaact?ggcagcagat?ctttgggatc 600
aaaaacttca?agatctatgt?tactggagaa?agttatgcgg?gccgttatgt?tccttacata 660
tccgctgctt?tcctagatca?gaatgataca?gaacacttca?acctaaaagg?tgcactggca 720
tatgatccct?gtattggtca?gtttgactac?gtgcaggagg?aagcacctgt?tgttcccttt 780
gtccagaaga?acaatgccct?cttcaatttc?aatgcaagct?ttttggcgga?actagagagc 840
atccatgagc?aatgtggata?caaggatttc?atcgaccagt?atctagtctt?cccagcatcc 900
ggtgtccagc?cgccaaaggc?tatgaactgg?agcgatccca?cctgtgatgt?ttatgacatc 960
gttaataacg?ccgtcctgga?tcccaacccg?tgcttcaacc?cctacgaaat?caacgagatg 1020
tgccccattc?tctgggacgt?tcttggattc?cccaccgaag?tcgactatct?ccctgcgggc 1080
gccagcatct?actttgaccg?cgctgatgtt?aagcgtgcca?tgcacgctcc?taacatcacc 1140
tggtccgagt?gctcggtgga?gagcgtcttt?gtcgggggcg?acggcggtcc?cgagcaggag 1200
ggcgactact?cggccaaccc?catcgagcat?gtcttgcccc?aggtcatcga?aggcaccaac 1260
cgagttctga?tcggtaacgg?tgattatgac?atggtcatcc?ttaccaacgg?cacccttctc 1320
tcgatccaga?acatgacatg?gaatggaaag?cttggattcg?acacggcccc?cagcaccccc 1380
atcaacatcg?acatccctga?cctgatgtac?aatgaagtgt?tcattgagaa?cggctatgac 1440
ccacaaggtg?gtcagggtgt?catgggcatc?cagcactatg?agcgtggtct?tatgtgggct 1500
gagaccttcc?agagcggaca?catgcagccc?caattccaac?ccagagtgtc?ataccgtcac 1560
cttgagtggc?tgcttggccg?gcgggatacc?ctgtaa 1596
<210>82
<211>1479
<212>DNA
<213〉aspergillus niger
<400>82
atgaaaggtg?cggcgctaat?tcctcttgcg?gcgggcattc?cttttgccca?tggcctgtct 60
ctccataaac?gcgacgggcc?tgccgtcgtt?cgtatgccca?ttgagcgcag?gagcgcccag 120
tccttgcaga?aacgagattc?tacggtcggt?gtgactttgc?agaactggga?tgcgacctat 180
tacgcagtca?acctgacgtt?aggaacacct?gcgcaaaagg?tatcattagc?tttggacact 240
ggcagcagcg?acctctgggt?gaacaccggc?aactcaactt?actgctcaat?cgacaatcta 300
tgcacccctt?atggcttgta?caatgccagc?gaatcgtcta?ctgtaaagac?cgtgggcaca 360
cacctcaacg?atacatatgc?ggacggcaca?aacctttacg?gtccttatgt?gaccgataag 420
ctcacgatcg?gcaacacaac?aatcgataat?atgcagtttg?ggatcgccga?gtcaacgact 480
agtaaacgcg?ggatcgccgg?cgtcggttac?aagatttcga?cctaccaagc?cgagcatgac 540
gacaaagtct?acgccaacct?ccctcaggcc?ctcgtcgaca?gcggtgccat?taagtctgct 600
gcgtacagca?tatggctaga?tagtttggag?gcgtcgactg?gctccctcct?tttcggaggt 660
gtcaatacag?ccaagtacaa?gggcgatctg?cagactcttc?cgatcattcc?tgtgtatggc 720
aaatactact?ccctcgccat?cgcccttacg?gagctcagcg?ttgcgaccga?ctccaactcc 780
agtagcttca?ccgacagtct?ccccctctct?gtgtcactcg?atactggcac?caccatgacg 840
gcactgccca?gcgacctggt?caacaaggtc?tacgatgcgc?tcaacgcaac?ctacgacaag 900
acatacgaca?tggcctacat?cgactgcgac?actagagagg?cggattacaa?tgtaacatac 960
agtttctccg?gggcaacgat?caccgtgagc?atgagtgagc?tgattatccc?cgcaacggag 1020
ccggggtggc?ccgacaacac?gtgtgtcttg?ggcctcgtgc?ctagccagcc?gggcgtgaac 1080
ctgctcggtg?atacattcct?gcgcagtgcg?tacgtcgtgt?atgatctcga?gaacaacgaa 1140
atctctctcg?ccaataccaa?tttcaatcca?ggcgacgatg?atatcctcga?aatcggaacg 1200
ggaacgtctg?ctgtgccagg?agccacaccg?gttccctctg?ctgtctcttc?tgcaactgga 1260
aatggactga?tctcgtctgg?caccgcagtg?cccacgctgt?cgggtgtcac?aataactgct 1320
acagccacag?caaccggctc?aaccggcact?ggctctagcg?gtggttcgtc?ggctgaagcc 1380
acgagtactt?cctcggaggg?cgctgcggcg?caagctacga?gcaacccgat?gaacctgctc 1440
ccaggacttg?cgggtatcgg?cctacttctc?gctctgtaa 1479
<210>83
<211>1836
<212>DNA
<213〉aspergillus niger
<400>83
atgctgtcgt?ctctccttag?ccagggagca?gccgtatccc?tcgcggtgtt?gtcgctgctc 60
ccttcgcctg?tagccgcgga?gatcttcgaa?aagctatccg?gcgtccccaa?tggctggaga 120
tacgccaaca?atcctcaagg?caacgaggtc?attcgcttgc?aaatcgccct?tcagcagcat 180
gatgtcgctg?gtttcgaaca?agccgtgatg?gatatgtcca?cccccggaca?cgccgactat 240
ggaaagcatt?tccgcaccca?cgatgagatg?aagcgcatgt?tgctccccag?cgagactgcc 300
gtcgactcag?tccgcgactg?gctggaatcc?gccggtgtcc?acaatatcca?ggtcgacgcc 360
gactgggtca?agttccatac?caccgtaaac?aaggccaatg?ccctgctgga?tgccgacttc 420
aagtggtatg?tcagcgacgc?caagcatatt?cgtcgtctgc?gcaccctgca?atactccatc 480
cccgacgccc?tggtctcgca?catcaacatg?atccagccca?ccacccgctt?tggccagatc 540
cagcccaacc?gtgccaccat gcgcagcaag?cccaagcacg?ccgatgagac?attcctcacc 600
gcagccaccc?tggcccagaa?cacctcccac?tgcgactcca?tcatcacacc?gcactgtctg 660
aagcagctgt?acaacatcgg?tgactaccag?gccgatccca?agtccggcag?caagatcggc 720
tttgccagct?accttgagga?atacgcccgg?tatgccgatc?tcgagaggtt?cgagcagcac 780
ctggctccca?atgccatcgg?ccagaacttc?agcgtcgtcc?aattcaacgg?cggcctcaac 840
gatcagcttt?catcgagtga?cagcggcgaa?gccaacctcg?acctgcagta?catcctgggc 900
gtcagcgctc?ccgtccccat?caccgagtac?agcaccggcg?gacgcggcga?actagtcccc 960
gacctgagct?cccccgaccc?caacgacaac?agcaacgagc?cctaccttga?cttccttcag 1020
ggaatcctca?agcttaacaa?ctccgacctc?ccacaagtca?tctctacctc?ctacggtgaa 1080
gacgaacaga?ctatccccgt?cccctacgcc?cgcaccgtct?gcaacctcta?cgcccaactc 1140
ggcagccgcg?gcgtctctgt?aatcttctcc?agcggcgact?ccggcgtcgg?cgccgcctgc 1200
ctcaccaacg?acggcaccaa?ccgcacgcac?ttccctcctc?aattccccgc?ctcctgcccc 1260
tgggtaacct?ccgtcggcgc?aacctccaag?acctcccccg?agcaagccgt?ctccttctcc 1320
tccggcggct?tctccgacct?ctggccccgc?ccctcctacc?aacacgccgc?cgtgcaaacc 1380
tacctcacca?agcacctggg?caacaagttc?tcggggcttt?tcaacgcctc?cggccgcgcc 1440
ttccccgacg?tctccgcgca?gggcgtcaac?tacgctgttt?acgacaaggg?catgcttggc 1500
cagttcgacg?ggacgagttg?ctccgcgccg?acgttcagtg?gcgtcatcgc?gttgttgaac 1560
gatgcgagac?tgagggccgg?gttgcctgtg?atggggttct?tgaatccgtt?cctgtatggt 1620
gtcggaagtg?agaagggtgc?gttgaatgat?attgtgaacg?gcgggagtgt?gggttgtgat 1680
gggaggaatc?ggttcggggg?cacgcctaat?ggtagtcctg?ttgtgccgtt?tgctagttgg 1740
aatgccacga?ccgggtggga?tcctgtgtcg?gggttgggaa?cgccggattt?tgcgaagttg 1800
aaaggggtgg?cgttgggtga?ggagggtggt?aattaa 1836
<210>84
<211>1437
<212>DNA
<213〉aspergillus niger
<400>84
atgtggctct?ttctcgtgtg?cagtatcctg?ctgccacttg?gagtagtcaa?cgcacagtct 60
caatacttca?acaacaaaac?caaagaattc?gtcgtcaatg?gctctgctat?tccttttgtc 120
gatttcgaca?ttggcgagtc?ctatgcgggc?tacctaccca?acacgccttc?tggaatctcg 180
agtctatact?tctggttctt?tccatcttct?gatcctgatg?cgtctgatga?gatcaccgtc 240
tggctgaatg?gcggcccagg?atgcagctct?ctggcaggca?tcatgctcga?gaacggcccc 300
tttctatggc?aacctggtac?ctaccgaccc?gtgcgcaacc?cttatgcctg?gaacaacctc 360
acaaatatgg?tgtacattga?tcagcctgct?ggaacgggat?tctcgcttgg?cccgtctacg 420
gtggtctcag?aatttgatgt?agccagacag?tttatggact?tctggaggcg?gttcatgaaa 480
acattcgatc?tgcagaatcg?aaagatatat?ctcactggcg?agagctatgc?gggccagtac 540
atcccataca?tcgcgtcgca?gatgcttgac?caggatgatg?atgagtattt?ccgggttgcc 600
ggcatccaga?tcaatgatcc?ctacatcaat?gagctgccag?ttttgcaaga?tgttgcgacc 660
gtcaatcagc?accgctccct?ctttcccttt?aatgacacct?tcatgagtca?aatcaccaag 720
ctttccgacg?attgtggcta?cacttcgttt?cttgacgatg?cccttacctt?tccaccccgt 780
tctcaattcc?catcagtgcc?ctataatgct?agctgcaaca?tctgggatat?cataaacaac 840
gcttctctag?ctctcaaccc?atgcttcaac?cgctaccata?tccccgacgc?ctgccccacc 900
ccctggaacc?cagtcggcgg?ccccatcgtt?ggacttggtc?cgaccaacta?cttcaaccgc 960
agtgacgtcc?agaaagccat?caacgcgtac?ccaacggact?atttcgtctg?caaggatgga 1020
atcttcccga?cggccaacgg?actggacaca?tcccctccaa?gctccctggg?accgctgccg 1080
cgcgtcatcg?aacagaccaa?caataccatc?attgcgcacg?gcctgatgga?tttcgagctg 1140
ctggcgcagg?gaaccctgat?cagtatccag?aatatgacct?ggaatgggaa?gcaggggttc 1200
gagcgggagc?cggtggagcc?gttgttcgtg?ccgtatggtg?gatcatcggg?aggaggcgtg 1260
ctgggaacgg?cacatacaga?gcgtggattg?acattttcga?cagtatttag?ttcaggacat 1320
gaaatcccgg?aatatgcacc?gggggcggca?tatcgccagc?tggagttttt?gctggggagg 1380
gttgcgaatc?tgtcgacaat?tattgagcag?gtgcagataa?cagagcagaa?tggttga 1437
<210>85
<211>633
<212>DNA
<213〉aspergillus niger
<400>85
atgtccaaac?tctccgctgc?tatctccaag?ctctccctct?ccaccatagc?caccactctg 60
ctcctcctta?cccccccaac?caccgcctac?ttctacaaat?atcccgccct?cttcgtctac 120
aaagacacca?actgcaccga?tatctccttc?tcacttgtct?acccctccct?gggtaactgc 180
aacggcggat?actacgacta?cgcgggctca?ttccagatgt?tcaatatcga?tgctgcgtat 240
acctgtaatg?gcagtgactc?gacactgatg?tttgagatgt?ataatagctc?cggctcggat 300
tgtggagatg?agagtgattt?gttgtttaga?cagccggtga?cggaggagtg?tactgttgcg 360
gatgtggaga?gtccggggcc?gttggagatg?ccggtttggt?ttgagttggg?gtcactattg 420
gggaattgtg?gtgggatggc?tggtactatg?ttgttcggtg?tggggattct?tgagggtggg 480
ttagagacta?aattatactg?gaaatgttat?tcatcaaggc?tgaatacaag?tgtaaccgtg 540
cacagattat?ctttgatact?gtctatgggc?tgtacgagcg?tctctgactc?ctacaatgag 600
ttagcggctg?cacattacta?tgaggacctg?tga 633
<210>86
<211>1827
<212>DNA
<213〉aspergillus niger
<400>86
atgcgtcacc?tcttatcact?gctggtgctt?ctgatcgcat?cggccgccct?ggtctccgcc 60
gtccccgccg?gctccattat?cactccacaa?ccacccgtcg?agcccgttca?ccttctctct 120
tcccagccct?ctgatccccg?aaggccatgg?atccgcctcc?gtgactggat?catcgagtcc 180
atatggggca?tcgaaaaacc?cgcatctcgt?cgattcccac?tcaacgattc?cccgcgcaat 240
cgctctcctc?cctcccggat?tctggcgcgc?tacggtagtg?acgtcgtact?tcgtttcagc 300
ctgcgcaatc?acgatgaggc?cgaggcattg?gcccaggctg?cagacattct?attcctggac 360
gtatgggcgt?ctactccagc?attcgtagat?atccgactgg?ccgaggaagt?caccgcatat 420
actcccctaa?tagacaacct?ggcagagaga?atctatacga?cctatccatc?taaaaagccg 480
ataggacttg?aaggacaatc?tggatttgcg?tcctcgagtc?gacctgcgcc?aaagttcggt 540
gacctttttt?tccacgagta?tcagcctttg?tccgtcatta?tcccctggat?gcggctgctg 600
gcttccatgt?ttccatccca?tgtgcgcatg?attagcgttg?gagtatctta?cgagggtcgc 660
gaaattcccg?ccctccgact?gagcgcaggc?agctccaccg?cggcgtcagg?ccctcgtaaa 720
acaatcatcg?ttacgggtgg?tagccatgcc?cgcgaatgga?ttggcacctc?aaccgtgaac 780
catgtaatgt?acacgctcat?taccaagtat?ggcaaatcca?aggccgttac?ccgccttcta 840
caggacttcg?actggatcat?gatccccacg?atcaatcccg?acggctatgt?ttatacctgg 900
gagacggacc?gactatggcg?caagaatcga?cagcggacca?gcctacgctt?ctgtcccgga 960
atcgatcttg?accgcgcctg?gggcttcgaa?tgggacggcg?gtcggacccg?cgctaaccct 1020
tgttcagaaa?actatgctgg?agacgagccc?ttcgagggaa?tggaagcaca?acaattagca 1080
cagtgggcgc?tcaacgagac?acaaaacaac?aatgccgaca?tcgtgagctt?ccttgacctt 1140
cactcttact?ctcaaacaat?tctctacccc?ttctcctact?cctgctcctc?gatccctcca 1200
acgctcgaga?gcctggaaga?gctaggcctt?ggcctagcca?aggccattcg?gtacgcgact 1260
cacgaaatct?acgatgtcac?ttctgcctgc?gaaggcatcg?tcacggccag?tgcggcagat 1320
aacaaccccg?ggcggttctt?ccccattggt?ggcaactccg?gtggcagtgc?gttggactgg 1380
ttttaccacc?aagtgcacgc?gacttattca?taccagatca?agcttcgtga?tcgcggaagc 1440
tacgggttcc?tccttccgtc?tgaacacatc?atccccaccg?gcaaggagat?ctacaatgtt 1500
gttctgaaat?tgggatcctt?cctcatcgga?ggcgactcat?ttgacgtcga?ttgggaatca 1560
gaactcttcg?atctgtcaaa?ggacgaatcc?gatctggata?gccgctattc?aaaatccaat 1620
gaccgctccc?cggcgtatct?acacaacgcc?aacggccccc?tgcccaacat?tgacgaagac 1680
gaagataagg?aatgggtaat?ggtggaggaa?gaagactaca?cagacgatga?cgacgacgat 1740
gatgatgatg?atgaagaaga?ggaagaggaa?gaggaagata?catattgggc?caccgaacac 1800
acatacgaat?ttcggcgacg?acgctga 1827
<210>87
<211>1251
<212>DNA
<213〉aspergillus niger
<400>87
atggctttcc?tcaaacgcat?tctcccgctg?ctggccctca?tcttacctgc?agttttcagt 60
gccacagaac?aggtccctca?tccgaccatc?cagaccatcc?cggggaagta?cattgttact 120
ttcaagtccg?gcattgacaa?tgcgaagatt?gagtctcatg?ccgcatgggt?aacggagctc 180
cacaggcgca?gcttagaagg?ccgcagtaca?accgaagatg?accttcccgc?cgggatcgaa 240
agaacgtaca?gaattgccaa?ttttgctggg?tacgcggggt?ctttcgatga?gaaaactatc 300
gaggagatcc?gcaaacatga?ccatgtagct?tatgtggaac?aagatcaggt?ctggtatctc 360
gatacgctag?ttaccgaaag?gcgagctcct?tggggactgg?ggagcatttc?tcaccgtggt 420
gggtctagca?ccgactacat?ctatgatgac?agcgctgggg?agggtacata?cgcttatgta 480
gtggacaccg?gcatcttggc?tacgcataat?gagtttggtg?gtcgtgctag?cctggcatat 540
aatgctgcag?ggggtgagca?cgttgatgat?gttggacatg?gtacacatgt?agcagggacc 600
atcgggggca?aaacatacgg?ggtttcgaaa?aacgctcacc?tactgtccgt?gaaggtgttt 660
gtaggtgaat?ccagctcgac?atcggtcatt?ctggatggct?tcaattgggc?cgccaatgat 720
attgtgagca?agaaccggac?cagtaaggcg?gcgataaata?tgagtcttgg?tggaggctac 780
tcctatgcgt?ttaacaatgc?agttgagaat?gcttttgacg?agggtgtgct?ctcttgtgtt 840
gccgctggaa?atgagaatag?agatgcagca?cggactagcc?cggcttctgc?acccgacgcc 900
attactgttg?ccgctatcaa?cagaagcaat?gcccgtgcgt?cattctcaaa?ctacggctct 960
gtggttgaca?tttttgcccc?gggagagcaa?gtactttctg?catggaccgg?ctcgaactcg 1020
gccaccaaca?cgatctccgg?cacgtccatg?gctacacccc?atgtgacagg?tttgatcctc 1080
tatttgatgg?gcttgcggga?ccttgctacc?ccagcggctg?caacgaccga?gctcaagagg 1140
ttggctacgc?ggaatgctgt?caccaatgtg?gcgggtagcc?ccaatcttct?ggcctacaat 1200
ggaaacagcg?gcgtgtcaaa?agggggtagc?gatgatggag?atgaggacta?g 1251
<210>88
<211>1368
<212>DNA
<213〉aspergillus niger
<400>88
atgatcaccc?ttttgtcggc?cctgttcggc?agcgtagtat?atgccgctac?gcagaccgtg 60
ttagggccag?agggggctga?tccctttacg?gtgtttcgca?gcccacactc?accggcattt 120
tcaattcgca?tccaggagca?gaatgactcg?atctgtgatg?ctcgttcacc?ccaattcact 180
ggttggctcg?acattggccc?gaagcatctt?ttcttttggt?attttgaaag?ccagaatgac 240
cccttccatg?atcccctaac?gctatggatg?actgggggcc?caggagactc?gagtatgatt 300
ggacttttcg?aagaagttgg?cccttgccgg?attaatgagt?ttgggaatgg?aacagatcac 360
aacccctggg?cctggaccaa?gaattcatca?cttctttttg?ttgaccagcc?agtcgatgtc 420
gggttttcct?atatcgatga?gggctatgag?ctgcctcatg?actcacgtga?agccgcggtg 480
gacatgcatc?ggttcttgcg?attattcata?tccgagattt?ttcctcacaa?acagttcctt 540
cccgttcacc?tttccggtga?atcttacgca?ggccggtaca?ttccttatct?ggcgacccaa 600
atcttggaac?aaaatgaact?gtataaagat?agccccagga?taccgctgaa?atcgtgcttg 660
gtgggtaacg?gattcatgtc?acccaaggat?gcaacgttcg?ggtattggga?aacactgtgt 720
actactaact?caggagtccc?atctcctatc?ttcaatgaaa?ctaggtgcga?tattatggcg 780
gcgaatatgc?cgcactgtat?ggatctatat?gacatatgca?ttcaacactc?agaccccgcg 840
atatgtcatg?cggcccagtc?cgtctgttac?gatagtgttg?tagggctcat?ggccaaatta 900
ttgctaagga?tgacgacagt?cactgcacct?tgtgagatcg?acgaaatgtg?ctatatcgaa 960
gcggctctaa?ttgagagata?tttgaattcg?ccatctgttt?gggaggccct?gtcgccaccg 1020
caacaggtta?ccgaatacaa?attcgtcgct?acttctgtta?ttgatgcatt?tgctcaatca 1080
gcggacggca?tggtgtcgag?ctcgaagcag?atcgctttct?tactcgcaaa?taatgttgac 1140
ttcttagcgt?atcaaggcaa?ccttgatctc?gcctgtaata?cggctggcaa?cctacgttgg 1200
gcgaactcgc?tttcttggaa?aggccagaca?gaatttaccg?caaagccctt?acttccgtgg 1260
gaaattcagg?tttcggtcgg?tgaagggacg?gacgaaacgt?cacgctttgc?ctttgtgact 1320
gtggacaacg?ctggacacct?gttgcgggac?tcaaagattt?caaactga 1368
<210>89
<211>2376
<212>DNA
<213〉aspergillus niger
<400>89
atgcggtttc?tcacttattc?cctgcccttc?attgcaagtg?ctatctcgct?ctttggggtc 60
aatgtacaag?ctcgatcaca?agctccaagt?gccatccgtc?atgtgtcgac?gcttgaccag 120
cccaccatca?agacaccctc?acagcgggtc?gatcaccttg?accactttga?catcaccttc 180
aatattcatg?acaagcacca?gcggataaag?ctggagctgg?agcccaacca?tgacatcctg 240
gcggaagacg?catccgtaca?gtatctcgac?gcggacggga?acgtgcgacg?gcacgagccc 300
attgctccac?atgagcataa?ggtcttcaag?gggaggagtc?tactcgggcg?aggaaaaggc 360
atgtgggatc?cggtcggatg?ggcgcggatc?tacttgaagc?aggatggctc?agagccacta 420
tttgagggag?tcttcagtat?cgacggcgac?aaccatcacg?ttcagctgaa?atcggcatac 480
atggagaaga?aacgccccgt?ggatgtcgac?cttcccgact?cagcgactga?ctatatgatc 540
ttctaccggg?attcggatat?ggtgcgtcta?catacggaac?tcaagcggtc?gtcgctcgga 600
tcgacctcgt?gtcaagccga?tcagctcggc?ttcaacacta?accccaacca?ccctgtgcta 660
caaccgtatg?gccaggcaga?gaccgatacg?tggggagcaa?tttcattgaa?ctccttgttt 720
ggactcaaca?agcgccaatc?cgatatcgga?agtgtgtctg?gcaatgcggg?cggagtcaat 780
ctggcgtcga?ccattggtga?tacttcgggc?tgtccgagta?cgaagcaagt?agctttgatt 840
ggtgttgcaa?cggactgcgc?ctttaccggc?tcattcaaca?acgagactgc?cgccaaggaa 900
tgggtcatca?gtactgtcaa?cagcgcgtcc?aatgtctacg?aaaagtcctt?caacattacg 960
attgggctgc?ggaatctgac?tatcaccgac?agctcatgcc?ccgacaaccc?gcccgcggcc 1020
acggcatgga?acatgccctg?ctccagcggc?aatctcacct?cccgactgga?tctgttttcc 1080
aagtggcgcg?gtgagcaatc?ggatgacaat?gcttattgga?ccctgatgag?cgattgcgcg 1140
acgggcaacg?aggtcggact?gtcatggctt?ggccaactct?gcaatagcga?tgcttcttcg 1200
gatggctcga?gcacggtcag?tggaactaac?gtcgtcgttc?ggtcttccgg?ctcggattgg 1260
cagatctttg?ctcatgaatc?tggccacacc?tttggcgctg?tccacgactg?tgactcccag 1320
acctgcgcgg?aggatctcga?agcctcgtcc?cagtgctgtc?cgttgacctc?gagcacctgc 1380
aacgccaacg?ggaaatacat?catgaatcct?acaactggaa?cagacatcac?tgcgttctcg 1440
caatgcacta?tcggaaatat?atgcgcagcc?ctgggccgca?acagcgttaa?gtccagttgt 1500
ctctccgcca?accgcgacgt?caccacctac?actggcagcc?agtgcggcaa?cggaattgtc 1560
gagtccggcg?aagactgcga?ttgtggcggg?gaagatggtt?gcggcgacaa?caactgctgc 1620
gacgcgaaga?catgcaagtt?caagtcggga?gctgtgtgtg?atgactccaa?cgacagctgc 1680
tgttcaagct?gccaattctc?ctcagctggg?acggtatgtc?gtgccagtcg?cggcgactgc 1740
gacgtggcag?agacctgcag?cggcaactcc?agtacttgtc?ctaccgactc?gttcaagaag 1800
gacggcacga?gctgcggcag?cagtggctcg?ggacttgcct?gcgctagtgg?ccaatgcacc 1860
agccgcgact?accagtgccg?cagtgtgatg?ggcagtctcc?tccacagcaa?cgacacctac 1920
gcctgttcct?ccttcagttc?ctcctgcgaa?ctggtctgca?cctccccgaa?gatcggcacg 1980
tgctacagcg?tcaaccaaaa?cttcctcgac?ggcactccct?gcggtagtgg?cggctactgc 2040
agcaacggcg?actgcaaggg?ccaaaacgtc?gaatcctgga?tcaagaacca?caaaggtatc 2100
gtcattggtg?tcgcctgcgc?cgtaggcgcc?ctgatccttt?tggccctgat?gacctgcatc 2160
gtaaaccgct?gtcgccgggc?tcgcgcgcca?aaacccgtcc?cgcgtccagt?gccttacggg 2220
ccgtggcccg?gcgctaggcc?tcccccgccg?ccgcccatga?accagtggcc?ggcgcgaggc 2280
tatcaaggct?tagggaatga?gccgccgccc?ccgtatccag?gtgtacctgg?tcagccagta 2340
ccgcaacata?tgcctcccca?ggggcggtac?gcttga 2376
<210>90
<211>1446
<212>DNA
<213〉aspergillus niger
<400>90
atgcgtttcc?taagcagtgc?agccctattc?ggcctggcgt?atgcctccac?ccaggcggtc 60
ctccagccag?aggaaccatc?cgacttccgt?acattccaca?gcccatattc?cccgcaccac 120
tcgatccgca?tccgccagca?gaatgaatca?atctgcgctg?cccattccgc?ccaatacacc 180
ggctggctcg?acatcggccg?taaacatctc?ttcttctggt?actttgagag?ccagaatgac 240
cctgccaatg?atcccctcac?tctctggatg?acaggagggc?caggggggtc?cagcatgatc 300
ggtctgtttg?aagaagtcgg?gccatgtctg?atcaatgagt?acggcaatgg?cacttactac 360
aatccgtggg?gctggtcccg?gaactcctcc?ctactatttg?tcgatcagcc?agtcgatgtg 420
ggattttcgt?acgtcgatga?aggagaggac?ctgccgggcg?attcgcatca?agctgcaatt 480
gacatgcatc?ggttcttgca?gttgtttgtc?tcggaggttt?tcccgcaatt?gcagactctt 540
cccgttcatc?tttctggtga?atcgtatgct?ggtcactatg?tcccttacct?cggcagtcag 600
atcgtccaac?agaacaagct?ctatcccact?gagccccagg?tccttctgca?ctcatgtctc 660
gtaggcaacg?gctactattc?tcctcgcgac?actacctacg?gctactggga?aaccctctgc 720
accactaacc?ctggagtccc?cgagcccgtc?ttcaaccgaa?ccagatgcga?catcatggcg 780
gccaatatgc?cgcgatgcat?ggaagtatcc?gacgtatgtg?ttcggaaccc?cgatccagct 840
atctgccatg?ctgcgtcgga?ggtatgctac?gagggcgtga?tcggatggta?tgatgacgag 900
tctggtgaag?gtggtcggaa?taggtttgat?ataaccgctc?cctgcgccct?tgacggcata 960
tgctacatcg?aggccgctcg?catcgagcag?tacctgaaca?cacccgcagt?ttgggctgct 1020
ctatcaccac?ccaaagaaat?caaagaatac?aaggttactt?ccgacaatgt?gtcgcgcgca 1080
ttcgatctca?cttcagacac?gatgacgcca?gcgtctgagc?aagtcgcgtt?cctgcttgcg 1140
aatcaggtac?atttcctggc?gtatcagggc?aatctcgatc?tggcgtgtaa?tacggcgggt 1200
aatctgcgct?gggcgcattc?tctgccatgg?agaggtcagg?tcgagttcgc?gtcgaaggcg 1260
ctgcggccat?ggagttgggt?agatgtggta?tctggaaaag?gtggagtggc?tggaacgacg 1320
aaggaggagt?cgaggtttgc?gctagttacg?gttgatgggg?cgggacattt?tcttcctcaa 1380
gatagacctg?atatcgcgtt?ggatatgatg?gtgcgctgga?tatccggggc?atcgtttact 1440
gagtga 1446
<210>91
<211>960
<212>DNA
<213〉aspergillus niger
<400>91
atgacattgt?tactcaactt?ccacgcgctc?tttacagtca?ttcttgttgc?caatctttca 60
accagatgca?gcgcactgct?ctctggacgt?gacttttgct?ccacgccagc?gcccggtgag 120
tcactccgag?cggagcatag?gaggctgtat?gatgtacagg?cccaacgtga?cagcaccgcc 180
gaggagagcc?gggaggtggt?gccttggatt?gaaatcgaga?catggtttca?tattgtaagc 240
agcaatgaag?cagcaaacac?agtatcagac?gacatgatca?ccagccagct?ttcctatctt 300
cagaaggcat?atgaaagtgc?gactatcacc?tatcggttgg?agggcataac?tcgtcacata 360
aatgactcgt?gggcgcgaaa?tgatgatgaa?ctggggatga?agaatgccct?acgaaggggc 420
aattatggca?cattaaatgt?ctatttccaa?acagatctcc?aggcgtcatc?cgacgagaat 480
tctcgggact?atccaaatga?cggtaaccga?cgaacagatg?tgtcagatca?atcatcatca 540
actgtcctag?gcttctgtac?gttgcctgac?ccgagtgtga?attccagcag?ccctcgttcc 600
agctacatca?aggatggttg?taacgtgtta?gcggatatca?tgccgggtgg?tagtttagcg 660
cagtacaaca?aaggcggcac?agcggttcat?gaggttggcc?attggaatgg?gctgctgcat 720
acgttcgaag?gtgaatcgtg?ctcccctgat?aatgaaggag?attacattga?tgacaccccg 780
gagcaatctg?agcctacgag?cggatgtccc?gccgagaaag?attcatgccc?cgatcttcct 840
ggccttgatg?ctattcataa?ttttatggac?tattcatctg?atgactgtta?tgagagtttt 900
actccagatc?aagcggagag?aatgaggagt?atgtggtccg?ctatgcggga?agggaagtga 960
<210>92
<211>1920
<212>DNA
<213〉aspergillus niger
<400>92
atgcatgtct?cacttttcct?actcagtgtt?acggcagcgt?ttgccagccc?aacaccccat 60
aactatgttg?ttcatgagcg?gcgcgatgca?ttgcccagtg?tctgggtaga?agaaagccgg 120
ctggacaaag?gtgccctact?gcctatgcgg?atagggctta?ctcagtccaa?cctggatcgt 180
ggccatgatt?tattgatgga?ggtgtctcat?ccacaatcgt?ctcgctacgg?aaagcatctc 240
tccagcgagg?aggtgcacga?cctatttgcc?ccgtcgaatg?aggccgtcga?gaccgtccga 300
acctggattg?aatccgccgg?aattgctcca?agccgcatct?cgcaatcata?caacaagcag 360
tggctacagt?tcgatgccca?tgcaagcgag?gttgagcagc?ttctgcagac?ggaatactac 420
atctacaccc?atgccgacac?gggaagttcc?catgtgacat?gccacgagta?ccatgtgccc 480
gaaaccatcc?aatcgcacat?cgactacata?acaccaggag?taaagatgct?ggaagtgcgc 540
ggcacgccct?ccaaaaagag?agatgcagag?aagcgctctc?ttggcagtct?gcccccaatc 600
ttagcaccac?taccaatcaa?tatcacgaag?attttcgacg?acccgctagc?acactgcgat 660
ctggcggtaa?ccccagactg?cattcgagcc?atgtacaaca?tcaccaaagg?aacaacagcc 720
acaaagggca?acgagctcgg?catcttcgag?gacctaggag?acatctacag?ccaagatgac 780
ctcaaccttt?tcttcgccaa?ctttgccagc?gacatcccac?agggaaccca?tccaaccctc 840
gactccatcg?acggcgccac?cgccccaaca?gacgtcacca?acgccggccc?cgaatccgac 900
ctggacttcc?aaatcgccta?cccaatcatc?tggccccaga?acaccatcct?ctaccaaacc 960
gacgacccca?actacgaaga?caactacaac?ttcaaaggac?tcctcaacaa?cttcctctac 1020
gccatcgacg?gctcctattg?caacgaaacc?tcctctctag?accctcaata?cccagatccc 1080
tccccaggcg?gctactcctc?ccccaagcaa?tgcggcgtct?acacccccac?aaacgtaatc 1140
tccatctcct?acggcagccc?cgaagccgac?ctccccatcg?cctaccaacg?ccgccaatgc 1200
cacgagttca?tgaaactcgg?ccttcagggc?atcagcgtgg?tcgtcgcatc?gggcgactcc 1260
ggcgtcgcct?ccagcacggg?cacctgcttt?ggcgatgcag?acaacgtctt?cgtcccagat 1320
ttcccagcca?catgtcccta?tctcaccgca?gtaggaggca?catacctccc?cctaggcgca 1380
gacgcagcca?aggaccagga?aatagcagtc?acccgcttcc?cctccggcgg?cggcttcagc 1440
aatatctacg?cccgaccatc?ctaccagaac?cactccgtgg?agacctattt?ctccactacc 1500
agcgacgacc?tcacctaccc?ttactactcc?ggagtaaact?acacagactt?ctccaacaca 1560
gatggggtat?acaaccgcat?cggacgagga?taccccgatg?tttcagctat?cgcagacaat 1620
atcatcatct?acaaccaggg?cgaagcgaca?ctggtgggtg?gtacgtctgc?cgcggcgccg 1680
gcgttcgcgg?ccatgttgac?gcgcattaac?gaggagaggc?tggcgaaggg?gaagtccacg 1740
gtggggtttg?tgaacccggt?gctgtatgaa?catcctgagg?cgtttaggga?tgtgactgtt 1800
gggtcgaatc?ccgggtgtgg?gactgatggg?ttcccggttg?ctggggggtg?ggatccggtg 1860
acggggttgg?ggacgccgcg?gtttgaggat?ttgatggata?tatttgtggg?tgatgattga 1920
<210>93
<211>1116
<212>DNA
<213〉aspergillus niger
<400>93
atggcttcca?agaccctcct?actcattccg?gcactggcca?cagccgctct?gggaagtgta 60
ttggacctag?atatcaaggt?agaccttgga?accccaggtg?gcccgtttga?tttgatgtac 120
gacaccggat?catcaacact?ctgggtgctt?gatagcaatt?gtacagatga?ttgtccaaat 180
gttagcgggt?actcccgaca?cggctacaac?ctcacctcta?ctggtgtcaa?cttaggtgtc 240
aacgacagca?ttgcttacag?cggaggcact?gtcagcggct?tcactgccac?ggatattctc 300
acggttcccg?acaccaacgt?ctcatatcgc?cagagctttg?ccgtcattac?cgacagtacc 360
tgggcggcct?tagcagccga?tgggttcatc?ggcctggcat?cgtctaccat?cgcattcaag 420
aatactacga?cagccgtcga?acagatgatg?caggatggac?ttttggatga?acctcgattc 480
gccatatatg?caggttcagg?ggaatcgacc?gtgaccaacc?ctaatccgga?gaataatggc 540
gtgttcacct?ttggtggcag?ccatgaggaa?acctatgcgg?acggggaact?gcaatggatg 600
aagatgctct?ccccctttga?aatatacaaa?acaaatctcc?ttggaattca?gggacacaac 660
aactccgatg?gccaggccct?gtcaagcgac?gtcctgaact?ggtacggcca?gactaatcta 720
ttcaacgtcg?caggtgcttc?atcgataagc?attcccaacg?accagattga?ggcgatgtat 780
gccctaacgc?ctttctcata?cgctgacatc?tcatctggat?accgacctct?gtgctccgat 840
ttcaatgata?catggtcgat?ctcttttaca?atgggcttct?atggcgaggg?tgtcaccttc 900
aatttgaccg?gtgatcagct?ggccgtgcct?ggctatcagg?acgacgacca?ctgcttccct 960
cccttcaatc?catgggacag?ctacaacacg?attattggtc?agcattggtt?gagcaatttc 1020
tatgctgtat?tcgacttcgg?atcattcgac?ccggagacat?acgatatacg?tgttgggctg 1080
gctcctttga?agaaggaata?cctgccgagc?gcttga 1116
<210>94
<211>1245
<212>DNA
<213〉aspergillus niger
<400>94
atgtttccct?gctctcgtat?ttggtctctg?ctcgttgcag?ccgccaccgc?tagtgctgta 60
cccaccagtc?tggccaccac?gcacctgcaa?tcggttgact?tgcttctgac?tcgcagttct 120
tacgggtttc?ttactgacat?agcccttgga?actccgggtc?agagcctgcc?gtatctggtt 180
gactggacct?ggaccggcca?ctatgtggtg?accaccttgt?gctacaacga?tcccaccgcc 240
acctacgatt?gtctcaacgt?cgatcagaaa?attttcaacc?agactttgtc?atccactttt 300
atcaaccaaa?ctgaccagta?tggctatctt?tactgggatc?ccaaccactt?ctactttacg 360
gagcccgcag?cagccgatgt?ggcgacggac?atgctgcgca?tcggtcccac?cgcggtgaac 420
accaccatcc?aagcagccaa?tttcgtcttc?aacgagacta?ttagcgcatt?ccctttctcg 480
ggagtatatg?gactctcacc?tgtttttcag?ggtgacaatc?gatccgtgca?agcgtccttc 540
taccaaggat?ggaggagcgg?cgcctggcac?tctccaattg?tctcttttat?ctactgccac 600
gacaatgcca?ccaaagcggt?atgcagtggt?tacgacggcc?ttcagacact?aggcggatac 660
aacacctctc?acgtccaggg?agatatcacc?tggtacgaca?tcattgtcac?ggaggcgatc 720
aacacgctgg?actttgtcta?tgcgccagcc?gtgattaatt?attgggcgtt?gaacctcacg 780
cgcttctcta?tcggagacga?agagcaagag?ctcaacaaga?ccactactct?ggatggaaag 840
caagccgccg?ttgccgcgtt?cgaccacgct?tcgtatggtc?gcggtgcccc?agtgtctgtg 900
tacggttacc?agcgtctagt?cgagctggtc?ggggcaaaag?ccgtcacgct?ttccgatcct 960
ccaaataacg?gtgagcaggg?attctatcag?ttcgattgcc?ggaactcgag?tttactgcca 1020
ccgctgcggt?atgagtttgc?cgggtcagag?cgggcgtggg?agattgtgcc?cgagaactat 1080
gtggaggtgc?tggcgaacgg?aaccaataag?tgcaccttta?atgtacgcac?cctgggagat 1140
ggagcgatgg?taatgggaaa?ttttggcgag?acatttgcca?ttgataagta?tgtcatgttt 1200
gactttgaga?agttgcaggt?ggggattgca?gacttcgcgt?ggtaa 1245
<210>95
<211>1443
<212>DNA
<213〉aspergillus niger
<400>95
atgcatctcc?cacagcgtct?cgttacagca?gcgtgtcttt?gcgccagtgc?cacggctttc 60
atcccataca?ccatcaaact?cgatacgtcg?gacgacatct?cagcccgtga?ttcattagct 120
cgtcgtttcc?tgccagtacc?aaaaccaagc?gatgctctag?cagacgattc?cacctcatct 180
gccagcgatg?agtccctgtc?actgaacatc?aaaaggattc?ccgttcgtcg?tgacaatgat 240
ttcaagattg?tggtagcgga?aactccctct?tggtctaaca?ccgccgctct?cgatcaagat 300
ggtagcgaca?tttcatacat?ctctgtcgtc?aacattgggt?ctgatgagaa?atctatgtac 360
atgttgctcg?acacaggcgg?ctctgatacc?tgggttttcg?gttccaactg?cacgtccaca 420
ccctgcacga?tgcacaatac?cttcggttcg?gacgattctt?cgacccttga?aatgacatcg 480
gaagagtgga?gtgtgggcta?tggaactggg?tctgtcagcg?gcttgctagg?aaaagacaag 540
ctcacgattg?caaatgtcac?tgtacgcatg?actttcggac?ttgcttccaa?cgcatcggat 600
aacttcgagt?cgtacccaat?ggacggcatt?ctcggtctcg?gtcgaaccaa?cgatagttcc 660
tacgacaacc?caacattcat?ggatgccgtt?gcagaaagta?acgttttcaa?gtcgaatatc 720
gttggcttcg?ccctttcacg?tagccccgcc?aaggatggca?cggtcagctt?tggcactact 780
gacaaggaca?agtacaccgg?cgatatcacc?tacaccgata?ccgtcggatc?ggacagctat 840
tggcgcattc?ccgtggacga?tgtctatgtt?ggcggcactt?catgcgattt?ctccaacaaa 900
tcagccatca?tcgataccgg?aacttcttat?gctatgctgc?cttcaagcga?ctcgaagacg 960
ctgcacagtc?tcattcccgg?cgccaaatct?tcggggagct?accacattat?tccgtgcaac 1020
acaactacta?agctacaagt?ggcattctct?ggtgtgaatt?acaccatctc?gccgaaggac 1080
tacgtgggag?caacttcagg?ttctggatgc?gtttcgaaca?ttatcagcta?cgacttattt 1140
ggtgatgaca?tctggctcct?gggtgacacg?tttctcaaaa?atgtgtatgc?tgtgtttgac 1200
tacgatgagt?tacgggtcgg?atttgcagag?cgttcctcga?acaccacctc?tgcgtcgaac 1260
tctacgagct?ctggaacaag?cagcacctcg?ggatccacta?caacgggcag?ctcaacgact 1320
acgacgagct?ctgctagctc?tagtagttca?tctgatgctg?aatcaggaag?tagcatgacc 1380
attcccgctc?ctcagtattt?cttctctgct?ctggcgattg?cttccttcat?gctttggctc 1440
tag 1443
<210>96
<211>1401
<212>DNA
<213〉aspergillus niger
<400>96
atgacgtctt?ctaccttgcg?ccttgccgtc?gcgttggctt?tgtcaacttg?cagcagtgcc 60
ctatcgagcc?agcgagatga?ttcacttgtg?gttccatttc?cttttggcaa?tcttgaggat 120
gtccatattg?ccaagcggga?tagctccaag?acagtagaag?ctcctctagt?gatatatggc 180
gacagctact?ggatgaacgc?ctcaattgga?acccctgcgc?agtcactaag?tttcctacta 240
gatcttacgc?gctcaagggt?cgagcccgca?tacaccctcg?atgagaatta?cgaatgttct 300
gacgatgaac?tctgctccga?attcggcttc?tacaaaccca?ccgattcatc?cacttatcag 360
catctcacct?acacacagag?acacgatgca?ggtgtcgact?actcctacct?tgataccata 420
actcttggag?atcacgcaac?cgacaatgtc?ccactggaca?tgtatctttt?gtcctacatt 480
tcctacagct?ccctcggtct?ctcctccgtc?aacaccagct?tcccctacat?cctggtcgat 540
cgcggcctca?ccacctcccc?atccttcagc?ctaatcggcg?acaacggaaa?caccaccacc 600
cccagcatca?tctttggagg?catcaacacc?tccaaattca?acgggcccct?gcaagccttc 660
tccttcgcag?accacagcat?caccaacaat?ccattcgtca?ccgtcgaagc?tgactccctc 720
caactaacca?ccaacaccaa?cgataattcc?acctacccta?ttccctcctc?cacccccatg 780
atgctcagaa?ccgaagaact?aatcacctac?ctccccaact?cgaccgtcca?atccctctac 840
accgacctta?acataaccat?ggacggcgtg?atctccactt?caagattcta?cggggtcctt 900
ccctgcgccc?gccaggaaac?cgaatctcac?acaatctctc?tagccatcgg?caacatgacc 960
ttctctgtgt?cctgggatga?gctcttcgtc?ccgtggacgc?gtgacggact?atgcaagttc 1020
ggcattcagg?cccaggattc?agattacaaa?actcgtgcgg?agctgggtgt?tccctttctg 1080
agacggatgt?atgtcgctgt?ggattataat?aatcagtttg?tgggcgttgc?gacgctgaag 1140
gatgatgatg?atcagaatgg?aggtgaagat?gagattgtgg?agattggcac?tgggacggcg 1200
ttgcctagtg?ctgtcgggga?ttggccggct?agtgttacgg?cgtatacgcc?tgctgcttct 1260
acagggacgg?cggctgcgac?gttgacattc?acgacggcga?cgtctagcgg?gggaggtgtg 1320
gtgccgacgg?gtctatcaga?gttgggtagg?gcgtttttgg?tgccgggggt?gctggggatg 1380
gctgttttgc?aggctgttta?g 1401
<210>97
<211>1632
<212>DNA
<213〉aspergillus niger
<400>97
atgatgcgac?cgatacttct?ccccctactg?ggggtatttc?tgcagacctc?ctcggcatcc 60
aatccctatg?taatgagctg?gtcttcccaa?gcctacggtc?cagatggccc?gtggcaggcc 120
gtatccatcg?acgtgggcag?caaccagcag?acggtcgatc?tttaccccgg?agccaactat 180
gctagcacga?tcctgatgag?cactctctgc?acgaacaaaa?ccctgtcatc?cacctgctac 240
gctgccgaag?caggcacgtt?caaccaaaac?acctccacca?ctgcctacac?caccgccagc 300
tcgtgggaaa?caacttactg?ggccgtcgag?ggtggaagcc?aagaggctgt?gctcggcgat 360
gaggtcacct?tagggtcgtt?tgtcgtcccc?aatgtgagct?tcgaagccat?ctaccagacc 420
taccagacct?atcccaatgg?catcgcctat?cctgtctcgg?tcggcagtct?ggccctgggg 480
ggtccgtact?tgtcggatac?cgtctccaat?tcgacggtcc?tgaacatgat?cgcaggatgg 540
ctttactcgt?ccaacgacat?tccgtcctac?tcgtacggca?tgcatatcgg?gtcggtagac 600
cccaaaatcc?caggctccct?gatcttgggg?ggctacgata?agagccgagt?gatcggagac 660
gtgagtgcgc?agggagtagt?gtcttcgagt?ggtcttttgg?aacttgaatt?aaaggatatt 720
gggctgggtg?ttgcggcggg?ttcctctccc?ttcagcttca?acaacgaaag?tggcttgttt 780
ctccaaagca?gtggttcggt?tcaggccaag?accgtccaga?ttgatccaac?caagccctac 840
atgtaccttc?cccaggcgac?atgcgatgcc?atcacctcca?ccatgccgat?ctccttcaat 900
tccagcttgg?ggctatactt?ctgggacacc?acgagcgatg?attatctgaa?tatcacgtct 960
tccgccgcat?acctctcctt?tgtgttcaac?atgaatgggg?tcaacaacaa?gaacattacc 1020
atcaagattc?ccttttccca?gctcaatctt?acgctgcaag?aaccgctggt?cgatcaaaac 1080
gtcacctact?tcccgtgctt?cctcactacc?tccaccccgg?tgctcggtcg?agcctttctc 1140
cagtccgcat?tcgttggggt?gaactggttc?aacgggaaca?actcgggcac?atggtttctg 1200
gcacaggccc?ccggcccggg?ttacgccagt?gaagacatca?cccggatcgc?agtgagtgac 1260
acgtcgcttt?ctgcctctaa?cggtacctgg?gaagagacct?gggctacgta?ctggggcatc 1320
aaaacatccg?acaactcgag?cagctccaag?agtggcctgt?cttccggtgc?caaaattgga 1380
attggcgtcg?gggtgggtgt?cggtggagca?gtgttgatcg?cagcaggtat?agccattgca 1440
ttctgtcttc?gccgtcgccg?cggggcgagt?caagaggcgg?ctggagagca?acggaggtcg 1500
atgtttaggg?gctttgcgga?gctaccggga?ggtgctcaca?gtgaaccggc?gaaggagttg 1560
gatacgaaga?tgcataagcc?gccgcaggaa?atgatggctt?cgcaggaggt?agagcgatac 1620
gagctggggt?ga 1632
<210>98
<211>2535
<212>DNA
<213〉aspergillus niger
<400>98
atgcgtctta?caggtggtgt?cgctgcggct?ctgggcctct?gcgctgctgc?ctccgcttct 60
ctccatcccc?atcgttccta?cgagacccat?gattacttcg?ctctacacct?tgatgaatcc 120
acctcgccgg?ccgacgtcgc?ccaacgacta?ggtgctcgcc?acgaaggccc?cgtcggagaa 180
ttaccctcac?atcatacctt?ctcgataccc?cgtgaaaaca?gtgacgatgt?ccatgcgctg 240
ctggatcaat?tgcgcgatcg?tcggaggtta?cgccgccgct?ccggagatga?cgccgctgtc 300
cttccctcct?tggtcgggcg?agacgaaggt?ctaggtggca?ttctttggtc?cgagaagctg 360
gctccccaga?gaaagctcca?taaaagagtg?ccgccgacag?gatatgctgc?cagatcgccc 420
gtcaacactc?agaatgaccc?ccaagcgctt?gcggcgcaga?aacgcattgc?ctcggaattg 480
ggcatcgcgg?accccatctt?cggcgaacaa?tggcatttgt?ataatactgt?tcagttgggc 540
catgatctta?acgtgacggg?tatctggctg?gagggcgtta?cagggcaggg?tgtcacgacg 600
gctattgtcg?atgacggttt?ggacatgtac?agcaacgatc?ttaggccgaa?ctattttgcg 660
gcgggttctt?atgactataa?cgacaaagta?ccagagccga?ggccgcgctt?gagcgatgac 720
cgccacggta?ctagatgcgc?gggtgaaatc?ggtgcggcga?agaacgacgt?gtgcggggtt 780
ggtgttgcgt?atgatagtcg?catcgctggt?attcggattc?tctccgcacc?cattgatgac 840
actgatgagg?ctgcggctat?taactacgcc?tatcaggaga?acgatatcta?ctcgtgttcc 900
tggggtccct?atgacgatgg?cgccacaatg?gaagccccgg?gcaccctgat?caagcgggcc 960
atggtcaatg?gtatccaaaa?tggtcgtggt?ggaaaaggct?cggtttttgt?gtttgcggct 1020
ggtaacggtg?ccattcatga?cgataactgt?aactttgacg?gttacaccaa?cagtatctac 1080
agcatcacgg?tgggtgccat?tgatcgggag?ggtaaccatc?ctccgtattc?ggaatcctgc 1140
tcggcgcaac?tggtggttgc?ctacagcagc?ggcgccagtg?atgcaattca?taccacggac 1200
gtcggcacag?acaagtgctc?gactacccat?ggtggaactt?cggcggccgg?cccgctcgct 1260
gcgggaaccg?tggcgctggc?cctcagtgtg?cggccggaac?tcacctggcg?tgacgttcag 1320
tatttgatga?ttgaggcggc?agtgcctgtt?catgaagatg?atggaagctg?gcaggacact 1380
aagaacggga?agaagttcag?ccatgactgg?ggatatggta?aggtcgacac?atatacgctg 1440
gtgaaacggg?cagagacctg?ggatctggtg?aagcctcaag?cctggctcca?ttccccctgg 1500
cagcgggttg?agcatgagat?cccacagggc?gagcagggct?tggctagttc?gtacgaggtg 1560
acggaggata?tgttgaaggg?agccaacctg?gaacggctgg?agcatgtcac?ggtcaccatg 1620
aatgttaacc?acacccgccg?aggcgatctc?agcgtggagt?tacggagccc?tgacggtcgg 1680
gtcagtcacc?tcagtacgcc?ccggcggcca?gataatcaag?aggtgggcta?tgttgactgg 1740
accttcatga?gcgttgctca?ctggggcgag?tccgggattg?gcaaatggac?tgtgattgtc 1800
aaggacacca?atgtcaacga?gcatactggg?caattcatcg?attggcgact?caacttgtgg 1860
ggcgaggcga?ttgacggagc?cgagcagcct?ctccacccca?tgcctactga?acacgatgac 1920
gaccacagct?atgaggaagg?aaacgtggct?accacgagca?tcagcgccgt?tcccacgaaa 1980
accgagctgc?ctgacaagcc?cactggtggc?gttgatcgcc?cggtgaacgt?taagcctaca 2040
acatccgcga?tgccgaccgg?tagtcttaca?gagcccatcg?atgatgaaga?actccagaag 2100
acccctagta?cagaggcaag?ctcaacacca?agtccttctc?cgaccaccgc?gtcagatagt 2160
atcctgcctt?ccttcttccc?cacgttcggt?gcgtcgaagc?ggacgcaagt?ttggatctac 2220
gctgcgatcg?gctccatcat?tgtgttctgc?attggcctgg?gcgtctactt?ccatgtgcag 2280
cgccgcaaac?gtattcgcga?cgacagccgg?gatgactacg?atttcgagat?gatcgaggac 2340
gaggatgagc?tacaggcaat?gaacggacgg?tcgaaccgtt?cacgtcgccg?gggtggcgag 2400
ctgtacaatg?cttttgcggg?cgagagcgat?gaggaaccgt?tattcagtga?tgaggatgat 2460
gaaccgtatc?gggatcgggg?gatcagcggc?gaacaagaac?gggagggcgc?agatggagag 2520
cattctcgga?gatga 2535
<210>99
<211>450
<212>DNA
<213〉aspergillus niger
<400>99
atgaagacct?tctctaccgt?cacctctctc?ctcgctctct?tctcctcggc?tctggccgca 60
cccgttgaca?gcgctgaagc?cgccggcacc?accgtctctg?tctcatacga?cactgcctac 120
gatgtctctg?gagcttcctt?gaccaccgtc?tcctgctcgg?acggtgccaa?cggcctgatc 180
aataagggct?actccaactt?cggctccctt?ccgggcttcc?ccaagattgg?aggcgcccct 240
accattgcag?gctggaactc?tcccaactgc?ggcaagtgct?acgccctgac?gtacaacggc 300
cagacagtca?acattctggc?cattgattcc?gcacctggtg?gcttcaacat?cgctctggag 360
gccatgaaca?ccctcaccaa?caaccaggcc?cagcagctgg?gtcgtatcga?agctacctat 420
actgaggtgg?atgtcagtct?ttgcgcataa 450
<210>100
<211>891
<212>DNA
<213〉aspergillus niger
<400>100
atggctcaaa?tattctggct?ttcactcttc?ctgcttgtct?cttgggtcag?agccgagtcc 60
aaccgcaccg?aggtggacct?gattttccca?agaaatgata?cctttgcgcc?aatgcctttg 120
atgccggttg?tattcgccgt?tcaagcccct?tccgtcgccc?ataaagttaa?tacatacatc 180
gagtacggct?attacccagt?aggccgtcca?aatgaaacag?ttattggcca?gaccgaccat 240
gtgtccgact?caacaaacga?aaccacttat?ttcagtgtct?ctggtatcgg?cagaacgttc 300
aataccactg?gcagctggga?gctgttttgg?aggctgagat?ggaccaattg?ttcaatctca 360
gaagactcga?gatactacaa?ccaatcctac?ccctggatat?cctccccata?catcgacggt 420
agcctcaaca?tcgacaaggt?ctatgagggc?tttcactaca?cagcatacaa?tgtcattgtc 480
gacagggtta?ccttcagcac?tcgcgaagat?gctagccaac?ccaacctcac?gaccctcacc 540
aatagcgaga?actgcgataa?agtctcgtct?cttgctctat?tgtcgattgt?ggactcccta 600
aggattccac?cccagttacc?ccaagaagat?attgataccg?tgtcaatgtg?cccacaactc 660
gccgatgcca?ggctaaattc?aacttcaact?tcaagcccct?gcagcgttag?cattagtccc 720
gaggttgagt?ctaatatcct?ggccaagatc?gcagacaatg?aatgcaataa?cgcacttcac 780
cccgctgtga?gttgcaccac?tgaagaaacc?aaggaaggca?gcgcgagcag?ccatgaccac 840
ggccatgctg?tatggcttgt?cattacgcta?gcttttgcct?tccttttcta?a 891
<210>101
<211>933
<212>DNA
<213〉aspergillus niger
<400>101
atgggtggtc?gagatgtcgc?cattctcagc?aggcactttg?ctgtgacatc?ctcacaaagt 60
gttaatggcg?ttgtctctgg?gatgttccaa?cacacagtca?cctcttcacc?cagcttcact 120
accaaccaat?tcttcaagaa?gaagttcact?gctgcaattg?ctactgccat?tttcgcaagc 180
gttgccgtcg?cagctcccca?gcgtggcctc?gaggcccgcc?tcaaggcccg?cggcagcagc 240
aagggatccc?gacccctcca?ggcagttgct?agacctgcat?caaccaagaa?ccagaccaac 300
gttgagtaca?gctccaactg?gtccggtgcc?gtgctggtgg?agcctccctc?tgctgcagcg 360
acctacactg?cggtgaccgg?caccttcact?gtccctgagc?ccaccggcaa?ctctggaggc 420
agtcaggctg?catctgcctg?ggttggtatc?gacggtgata?cctatggaaa?cgccattctt 480
cagaccggtg?ttgacttcac?cgtgaccgac?ggagaggcct?cgttcgatgc?ctggtatgag 540
tggtacccgg?attacgccta?cgacttcagc?ggcatcgaca?tctcggcagg?cgatgagatt 600
gttgccattg?tggagtccta?cacctcgact?accggtattg?ccattattga?gaacaagagc 660
accggccaga?aggtgtccaa?ggagctgtcg?tccagctcca?gcctcggtgg?acagaacgct 720
gagtggattg?tggaagactt?cgaggaaaat?ggttcgctcg?tcaacctggt?ggactttggc 780
accgtcacct?tcactggtgc?tgttgccaag?gcggcgggtg?gtgagagtgt?tggacttacc 840
gatgcgacca?tcatcgagat?tgaggagaat?ggccaggttg?tcactgacgt?taccatcgac 900
agcgactctg?aggtgaccat?cacctacgag?taa 933
<210>102
<211>2046
<212>DNA
<213〉aspergillus niger
<400>102
atgcgctgct?ccctcatctc?ccttctaggc?ctggcggcca?tcccggccct?tggaggctgt 60
cccttcgcac?acactgcgaa?catgggcatt?gataacatgg?tgaaagcaca?cgctcacatg 120
tcccgaccgt?tgattgcctc?caagagcagc?ccctcaactg?ttcctacctc?ctctagcacc 180
ccttctgtcg?ggcagaaagg?cgtgttcatg?atgaaccgca?ttgctcctgg?cacatccgag 240
ctctacattg?ccaacacaga?tggcagtaat?gaacgcccac?tcctctccaa?ccccgtctac 300
gagtaccatg?cctccttctc?cccggatgta?gaatggatca?ccttcaccag?cgagcgcaat 360
ggtgacggta?actctgacat?ctaccgcgta?cggaccaacg?gctccgatct?ccaggaattg 420
gttgccacgc?ctgcagtgga?agactccgtt?gttatctctc?ccaacggccg?cctggcagcc 480
tacgtctcca?ccgccaacaa?catgaaggca?aacatctgga?tccttgatct?tcagaccggc 540
gcgcagtgga?acctcacaaa?tacacccacc?actgccgcca?actcctccct?catggagagc 600
tatctccgtc?ctgcctggtc?tcctgatggc?gaatggatcg?ccttctcttc?ggaccgcaac 660
acccaatggg?acggacacgg?cgtaccgacc?ttcctcggcc?gcacgggctg?ggagacgacg 720
caagaactct?ctctctacgc?catccgtccc?aatggctctg?acttccgtca?gatcatctcc 780
aagccatact?actctcttgg?atctccgaaa?tggtcagcag?acggtaaacg?catcgtctac 840
tacgaaatga?cccgggaaga?cacctacaac?gcccatcgtc?cagaaaccat?taccacagcc 900
aactcgacga?tcatgtccgt?agacttcgag?acaggcaccg?atgtgcgcgt?ggaagtcgcc 960
ggctccggtg?tcaagcaatt?ccctcagtac?ctggacaaga?acggcaccat?cgcctacacc 1020
ctcaaaggcg?gcaccagcga?gggcttctac?acgaccgcgg?gactctacgt?caacacgacc 1080
tcggcgaccc?tcaggtcccc?ggcgtggtct?cccgacggca?agcaagtagt?ctacgaaaag 1140
agcacctgga?gcatccgctc?ggggtacaag?cagctctaca?gctgggacag?tgactgggac 1200
taccgcttca?cggacgtctt?ccctcaggtc?tcgcaccagg?agcgcgtcgc?catcacacag 1260
aagcagctgg?gcaattcgtc?catcgtgacg?ttgaacacaa?ccggaggcga?cttgcaactc 1320
gtctacgacc?ccagcacggc?ggactttgtc?agcgatgacg?aaaccacagg?actgagcgct 1380
taccagccca?gctggtcacc?ctgcggcgag?tggctcgtct?tcggcgtcgg?attctggttc 1440
gagacgagag?aagcctcagg?cggatggatc?gtgcgggcca?ccgccaacgg?gagctactcg 1500
gaggttctcg?tgaacagcag?ctactccatc?accgaggatg?gagccctgaa?cagcgggttc 1560
ccgagtttct?cgccggatgg?caagaaagtg?gtgtatcggg?tttggggagc?cgacactgca 1620
acctacggca?acgccagcga?gatcgggctg?cgggtgctgg?acctcgagac?gcgaaagaca 1680
accgtcctaa?ccacagaatg?ggacaatctg?ccccagttct?ctcccgatgg?agagctcatc 1740
ctattcacac?gcaaaaccag?cacgtacaat?tacgatgtgt?gcacgatccg?gccggatggg 1800
acagatctcc?gcgtgttgac?gagcagcggt?gctaatgatg?cgcatgcggt?ctggtcgcag 1860
gatggacgga?ttatgtggtc?taccggcatg?tatgggttcc?ggtttgagtg?tgcgctgtat 1920
ggtgatacgt?tccagccgta?tgggcaggtt?atgattatgg?atgcggatgg?gggaaataag 1980
aagttgatga?ccaactcgat?gtgggaagat?tcgatgccgt?tgttcttgcc?gagggaggta 2040
ctttag 2046
<210>103
<211>1875
<212>DNA
<213〉aspergillus niger
<400>103
atgcctccgg?atgcaaaatc?gcctggctac?cagcctggta?tggcagtatt?accatctagg 60
ccacatcctg?ccaagggaaa?agccattcga?ttcctccttt?cccttgcatt?ggtcgcgttt 120
gctattgttc?aattatgtgg?taatttccac?aaaaatagga?gcgttgaaca?acagcttcag 180
agtcaaacac?ttgatgatga?gtcctttaaa?tgggaagatg?ttactcctac?caagcaactc 240
gtataccatc?catgctttgg?tgatcacgaa?tgcgctcgct?tgtcgcttcc?aatgaattgg 300
aaccgaactg?atggtgaagg?gtcaaaaatt?gccttggcgg?ttatcaaact?tcctgccaag 360
gtacctgtca?cagatgcgcg?atatggtggt?gccattcttc?tgaatccagg?tggtcctggt 420
ggatccggag?tgagcatggt?ctttagatac?gggaaagcta?tccagaccat?cgtcgactcc 480
ccagaatcac?caagtgcaga?ttcagcgagc?ggaaagtatt?tcgatgttgt?tagctttgat 540
ccaagagggg?tcaacaacac?aacacctaat?ttttcctgct?tccctgaccc?cgcgacgagg 600
aaagcgtggt?tactgcagtc?agaggcagag?ggtctacttg?ggagttctga?aggagtcttc 660
gatactcgat?gggcaaggta?cgaagctttt?gagcggctac?tttcgacagc?tccgaacact 720
ttcccagttg?gaacaaacgt?tgacgccgag?aggataaggc?tgcacaaccg?ttggaaaaaa 780
ggggaggaga?agctgctata?ctggggcttt?tcctatggga?caatcctggg?ttccacgttt 840
gcggctatgc?agcctcatcg?cataaaccgt?gctgtcatag?acggagtctg?caacgctgat 900
gattattacg?ccggcaactg?gcttaccaat?ttacaagatt?cggatgcagc?attcaataaa 960
tttttcgagt?actgctacac?agctggccca?tcagcgtgtc?cgtttgcgct?cggcggagat 1020
cccgaagatc?tcaagtctcg?ttatgagcag?attttgacca?atcttacatc?gagccctatt 1080
gctgtgtctc?cttctggaaa?taggggccca?gagataataa?cctatagtga?tgtgaagtca 1140
ttggtcgtgc?aagctctcta?tgtgcctttg?aaattattcg?atttggtggc?taggctatta 1200
gctgagctcg?agcaaggtaa?cggctcttca?ttcgctgact?tgaagtatga?agccaaacaa 1260
tggccagtac?cgcctccatg?cgattcctcg?tccacacaat?acaaagtacc?tggcgagagt 1320
gatcaggagg?ccgggaggaa?tatcctatgt?acagatggtc?caggcctcga?cggaactgcc 1380
aaggaggatt?tccggagcta?ctggaatatg?ctccggggac?aaagtaaggc?ggttggagat 1440
ttctgggccg?aggttcgcat?gtcgtgtgtc?aaactggaga?cgcgacctga?gtggcgctat 1500
gatggtatgc?gtatccaagg?gcccttcgca?ggcaatacat?cgcacccatt?gctgtttatc 1560
gggaatactt?atgatccagt?aacgccgcta?cggaatgctc?atacgatggc?gcgtggattt 1620
cctgagtcaa?tcgttctaga?gcagaactct?gtcggacatt?gcacactgag?tggcccatcc 1680
ttgtgtacag?cgaaagcgat?acgccagtat?ttccagaccg?gagagttacc?tgaccccgga 1740
actgtttgcc?aggtagagga?gcttcccttt?cgtcttgccg?gatatgagag?aagtcaggtc 1800
atgtcgccag?gtgacacaga?attgatgtcc?gccttgcatt?cgctgagcga?gttccgccat 1860
ctgctaggcg?cgtga 1875
<210>104
<211>1665
<212>DNA
<213〉aspergillus niger
<400>104
atgttgagta?gtctgctgct?tgggggtctt?ctgggtctag?cgaccgctca?atttcctccc 60
gagccggaag?gcatcactgt?gctcaagtcc?aagttgcatg?agaatgtgac?tatttctttc 120
aaagagcctg?gaatttgcga?aactacgccg?ggtgtccgat?cttattcggg?ctatgtacac 180
cttccccccg?cctcaaccag?cttcttttgg?tttttcgaag?cccgcaaaga?tcccagcaat 240
gcgcctctgg?ccatctggct?caatggcggt?ccgggtggct?cgtcgctcat?ggggctcctt 300
gaagaattag?gtccttgttc?cattgcatca?gactccaaga?ccacagtcct?caatccttgg 360
agttggaaca?atgaagtcaa?tcttctattc?cttgaccagc?caactcaagt?cggcttctca 420
tacgatgtcc?caacaaatgg?cactttgaca?gctaatggga?ctgcattcgc?ggctcacgct 480
ctatggcatt?tcgcgcaaac?ctggtttttc?gagttcccac?actacaagcc?aaacgatgat 540
cgtgtcagtc?tctgggctga?aagttacgga?ggccattatg?gtccaggcat?ctttcggttc 600
ttccaacagc?agaatgacaa?aatcgcagag?gggactgcag?aagacggtgc?acagtatttg 660
catctcgaca?cgcttggcat?tgtgaacggc?ttgatggata?tggtgatcca?agaagaggct 720
tacattactt?ggccatacaa?taacgtaagg?ctcgcccctt?cttcattcaa?ctcgcgaggc 780
tttcgcgatc?aggccctcgc?ctgcgaagcg?gctttgaaag?aacgcgattc?cggcttgcct 840
cactcaggga?agaatatctc?tgaaatttgc?ggaggccttg?cactagaatg?gggagatggc 900
cccatcacct?actaccacac?cttcaatcgc?gggtggtacg?acatcgccca?tcctaagaac 960
gacccattcc?ctgccaagca?catgctcgga?tatttgacgc?aggagtccgt?ccttgccgct 1020
cttggggtac?cagtcaattt?cacatcgtct?tcgagtgccg?tggctacaca?gttcataaaa 1080
acctttgata?tcgtccacgg?cggcttcctg?gatgcaattg?gctacctcct?cgacagtggt 1140
gtaaaagtac?acatgatgta?cggagatcgt?gattacgcct?gcaattgggt?cgggggcgaa 1200
aaagccagcc?ttgcagttcc?gtattcccgt?atcaccgaat?ttgccgacac?gggatactcc 1260
ccactcctta?cgcccgacgg?gatcagcggc?atgacccgcc?agctgggcaa?ctacagcttc 1320
actcgcgtct?tccaagccgg?gcatgaggtc?ccctcctacc?agcctgtcgc?ggcgtatgag 1380
atcttcatgc?gggcgacatt?caacaaagat?atccctactg?gcctcttggc?tgttgatgac 1440
gaattccagt?cggttggacc?taaggatacg?tggcatatca?agaatatccc?tcctattatg 1500
ccaaagccgc?agtgctatgt?tctaagtccc?ggcacgtgta?ccccggaggt?ttgggagacc 1560
gttttgaacg?gatccgcgac?ggtaaaggat?tggtatgtcg?tggatgatag?cgcgggtgtt 1620
gaggaccacg?aggggttcag?cattcttgga?ggggatgagt?tgtag 1665
<210>105
<211>1737
<212>DNA
<213〉aspergillus niger
<400>105
atgaccaggt?ttcaattgct?tccccttgtc?gcagggctgc?ttgccccttc?aattgcagcc 60
cttagcatcc?cttccccgca?gcagatcctc?gattctctca?ctttcggaga?gcacaccgac 120
ggcttttgtc?cgctggcacc?caaggttgag?gttcctgacg?atggtttctt?tccagctctc 180
aagttcgtag?aagatgcctc?gttcaagtcg?cgccaagtca?atcgtctctc?cagggcggtt 240
caagttccga?ccgcaatcga?cgactacatg?aaggatccct?acgacgaaaa?gttcgcccca 300
ttcctcgact?tccagaagct?cctgcagacc?ctctttcccc?tcacccactc?ctacgcccgc 360
gtagatcaca?tcaaccgatt?tggtctcgtc?ttcaccctca?atggcacaga?tgactcgctc 420
aagcccctgc?tattcaccgc?gcaccaggac?gtcgtgccca?tcaacgaccc?tgccgactgg 480
acctatcccc?ccttcgatgg?ccactacgac?ggcgaatggc?tctggggccg?cggtgccagc 540
gactgcaaga?acgtcctgat?cggtctcatg?tccgttgttg?aagacctact?ctcccaaaag 600
tgggagccaa?cccgcacagt?cgtcctggcc?ttcggattcg?acgaagaatc?ccacggcttc 660
ctcggcgccg?gatccatcgc?caaattcctt?gagaagaaat?acggaccgga?cagcttcgaa 720
tttatcctcg?acgaaggcgg?catgggcctc?gaagttctag?acgacaacaa?caacggcgtc 780
gtctacgctc?tccccggcgt?tggcgaaaag?ggcagcatcg?acgttgtgct?cactctggcc 840
gtaccaggcg?gccacagctc?cgtgccccct?ccacacacgg?gaatcggcat?catcgccgag 900
atcatctatg?agctagaacg?ccaggacctc?ttcgtccccg?tcctagacac?tcaccacccg 960
acccgcaaga?tgctcgaatg?ccaagtccgc?cactccccct?cgcaagtcga?accgtggctc 1020
gcctccgccc?tccaatcaag?cgactacatc?tccctagcag?agaaactggc?ctcctcgcgc 1080
ggcgacaagt?tccgcttcat?cctccaaacc?tcccaagcag?cggacatcat?caacggcggc 1140
gtcaaatcca?acgctctccc?cgagaaaatc?aacgccctcg?tcaactaccg?catcgctctg 1200
caccaaaccc?cagacgatat?caagaaccgc?gctgtggaga?tcatctctcc?catcgtcaag 1260
aaatataacc?tctccctcac?ggccttcccg?gaaagcgaca?ccgttgaccc?ctccctcaac 1320
aaccacctca?cccttactac?cctcagcggc?gccctcagtc?ccgccccggt?cagcccaacg 1380
gacatcgaca?ccgacgccgt?ctgggcccgt?ttctcgggcg?tcactcgctc?ggtcttcgaa 1440
tctgtcccta?gtctcgaggg?cagaaaggtc?gtcgtgagcg?gcgacatcat?gaccgggaat 1500
acggatacga?gattctactg?ggctttgtcg?aggaatattt?acaggtggag?tccgtcgagg 1560
gcgggtaaag?cgctgaatat?tcatactgtt?gatgagagga?tcgatattga?tattcatctt 1620
gaggcgatga?tgctgtatta?cgatcttatt?cgctctttcg?atggacggac?cgattcatct 1680
gtcatttctg?ctgcgtcggc?agctgctgat?gatgaacttg?ctcacgacgt?gctgtga 1737
<210>106
<211>1371
<212>DNA
<213〉aspergillus niger
<400>106
atgaagagca?ccactcttct?ttccttggcc?tgggctgccc?agtccgccta?ttccctctct 60
atccacgagc?gcgatgaacc?cgctactctt?cagttcaact?ttgaacgtcg?tcagatcgcc 120
gaccggtccc?gtcggaagcg?atcgacggcc?tcggccgacc?tcgttaacct?ggctacgaat 180
cttggctaca?cgatgaacct?cacactcggc?actcccggcc?aggaagtcag?tgtgacgttg 240
gacaccggca?gcagcgatct?ctgggtcaat?ggggccaact?cgtccgtctg?cccctgtacc 300
gattacggct?cttacaactc?aagcgcttct?tccacctaca?ccttcgtgaa?cgatgagttt 360
tatatccagt?atgtcgacgg?cagtgaagcc?acaggcgact?atgtcaacga?tactctaaag 420
ttctccaatg?tgactttgac?gaactttcaa?tttgccgtcg?catatgacgg?cgactccgag 480
gagggggtcc?tcggtatcgg?atacgccagc?aatgaagcca?gccaggccac?cgtcggtggt 540
ggtgaataca?ccaacttccc?cgaagccctc?gtcgatcaag?gcgcgatcaa?ctggccggcc 600
tacagtctat?ggctcgatga?cctcgacgaa?ggaaaaggca?ccattctgtt?cggcggagtc 660
aacaccgcca?agtactacgg?cagcctgcag?accctgccta?tcgtctccat?cgaagacatg 720
tacgtcgagt?tcgcggtcaa?cctgacggcc?gtgcaccttg?agaagaacgg?caactccgtc 780
tcggtcaaca?acagcgccac?gcaattcccc?atccccgccg?tgctggacag?cggcacggcc 840
ctgacctaca?tcccgacctc?cgccgcagcc?agcatctacg?aggccgtcgg?tgcccaatac 900
ctgagcgagt?acgggtacgg?agtgatcgag?tgcgacgtca?aggacgaaga?cttcaccttc 960
ctgttcgact?ttggatcctt?caacatgagc?gttgacatca?gcgagatgat?cctcgaggcc 1020
agttccgaca?tgaccgacat?gaacgtttgt?acgtttggcc?tcgcagtgat?cgaaaatgag 1080
gccctgctgg?gcgatacctt?cctgcgcagc?gcatacgtcg?tctacgatct?cggaaacaac 1140
gagatctccc?tggccaaggc?caacttcaac?cccggcgagg?accacgtcct?ggagatcggc 1200
accggatcgg?atgccgtgcc?caaggcgacg?ggggcgacgg?cgaccggcgc?ggcagccaca 1260
tccacggcct?cgagcgacaa?gtcggacaag?gagagttcgg?ctacagtgcc?gcgcagccag 1320
attgtctcgc?tggtggcggg?agtcttggtc?ggtgttttct?tggttctgta?a 1371
<210>107
<211>1995
<212>DNA
<213〉aspergillus niger
<400>107
atgttggtcc?gtcagcttgc?cctggctctg?gccattgcgg?ccttgtccga?tgccattccg 60
acatccatca?agcatgtcct?gcacgagaaa?cgtcacaagc?ccgcatccga?ctgggtgaag 120
ggtgcgcgcg?ttgagagcga?tgcggtcctg?cctatgcgca?ttggccttgc?ccagaacaac 180
ttggacaagg?gctatgactt?cctgatggaa?gtatcggacc?ccaagtcttc?caaatacggc 240
cagtactggt?cggcagacga?ggtgcacgac?atcttttcgc?catccgagga?ggctgttgag 300
gcagtgagag?aatggcttgt?cgcctctggt?atccatccgt?cgcgggtggt?gcactccgac 360
aacaagggct?ggctcgcgtt?cgacgcctac?gcccatgaag?ccgagaggct?gttcatgacg 420
gaattccacg?agcacgagag?cgaccgaagt?gctaagatca?gggttggatg?cgaccaatac 480
cacgtccccg?aacacatcca?gaagcacatc?gactacatta?cccctggagt?gaagctcacc 540
caggtcgtga?agaggaccaa?caaagtcaag?cgtgcttccc?aactagctca?ctcttccaag 600
gccaagtctg?ctgcccaagg?tccgcagcca?ctccccaaca?aggccaagtt?cctgcctgaa 660
gacctccgcg?gctgcggtta?caacatcacc?ccctcgtgta?tcaaggcctt?gtatcagatc 720
ccagacgcta?agacggcgac?cccgaacaac?agcctgggtc?tgtacgagca?gggtgactac 780
tttgccaagt?ccgacctcga?cctcttctat?aaggagtatg?cgccgtgggt?tccccagggt 840
acctatccca?tcccagccct?gattgatggc?gccaattact?cggttccttc?ctacagctcc 900
ctgaacacgg?gtgaatccga?cattgacatt?gacatggcct?actccctgct?ctaccctcag 960
caggtgaccc?tctaccaggt?tgacgaccag?ctctacgaac?cagtcgaggt?cgacacaacc 1020
aatctgttca?acaccttcct?cgacgctctc?gatggctcct?actgcaccta?cagcgcctac 1080
ggcgagaccg?gcgatgaccc?gtcgatcgac?cccgtatacc?ccgacacccg?ccccggcggc 1140
tacaaaggaa?agctccagtg?cggcgtctat?aagcccacta?acgtaatcag?cgcctcctac 1200
ggccaatccg?aagccgacct?ccccgtcagc?tacaccaagc?gccaatgcaa?tgagttcatg 1260
aagctcggtc?tacagggaca?ctccatcctc?ttcgcgtctg?gcgactacgg?cgtcgcgtct 1320
ttcgccggcg?acggtgacga?gaacggctgt?ctcggcccag?agggcaagat?cttcaacccc 1380
cagtacccct?ccaactgccc?ctacgtcacc?tccgttggag?gtaccatgct?gtgcggctac 1440
cagaccgtca?acgacagcga?gagcgtcatg?cacgttaacc?ttggcggaac?cgcaagtaac 1500
ttcagcactt?ctggtggctt?ctcgaattac?ttcccccaac?cggcatatca?gtttgctgct 1560
gtggagcaat?acttccggtc?tgcgaacctg?tcgtatccgt?attactcgga?gtttgaggtc 1620
gatgttaaca?cgaccaaggg?tctctacaat?aggcttggtc?gtgcttatcc?ggatgtctcg 1680
gcgaatggag?cgcatttccg?cgcttatatg?gatggatacg?attatcattg?gtatggatcg 1740
agtttggcgt?cgcctttgtt?cgcgtcggtt?cttactttgc?tcaacgagga?acgcttcgct 1800
atcggcaagg?gccccgtggg?attcgtgaat?cccgtgcttt?atgcttatcc?gcaagtgctg 1860
aacgatatca?ctaatggtac?taatgctggg?tgtggaactt?atgggtttag?tgctattgag 1920
ggatgggatc?ccgctagtgg?tttgggtacg?cctaactacc?cattgatgaa?ggagctgttc 1980
ctctctttgc?cttag 1995
<210>108
<211>1563
<212>DNA
<213〉aspergillus niger
<400>108
atgcgggtta?ccacggcaat?tgcttcatta?ctactggtcg?gctcggccac?cagtctccaa 60
aatcctcatc?gtcgggctgt?tccgccccct?ctctcgcatc?gcagcgtagc?gtctcgctcc 120
gtgcccgttg?agcgccgaac?caccgacttt?gagtatttga?ctaacaagac?tgcaagattc 180
ctggtcaatg?gcacaagcat?ccccgaagtc?gatttcgacg?tcggcgagtc?ctacgccggc 240
cttctcccca?atacgcccac?tggcaattct?agcctattct?tctggttctt?cccctcgcaa 300
aatccagagg?ccagcgatga?gatcaccatc?tggctcaacg?gcggccccgg?atgtagctcc 360
ctagacggcc?tgcttcaaga?gaacggccca?ttcctctggc?agcctggcac?ttacaagccc 420
gttcctaatc?catactcatg?gaccaacctc?accaatgtgg?tttacatcga?ccaacccgcc 480
ggcacaggct?tctccccggg?cccctcgacc?gtaaataacg?aggaagacgt?ggctgcccag 540
ttcaacagct?ggttcaagca?cttcgtcgac?accttcgacc?tgcacggccg?caaggtctac 600
atcaccggtg?aaagctacgc?gggcatgtac?gtcccctaca?ttgccgatgc?catgctgaac 660
gaggaggata?caacctactt?caacttgaag?ggtatccaga?tcaacgaccc?gtccatcaac 720
agcgactcgg?tcatgatgta?ctcccccgcc?gtccgccatc?tgaaccacta?caacaacatc 780
ttccagctaa?actccacttt?cctctcctac?atcaacgcca?aagccgacaa?gtgcggctac 840
aacgccttcc?tcgacaaagc?catcacctac?ccacccccca?gtcccttccc?caccgcccct 900
gaaatcaccg?aagactgcca?agtctgggac?gaagtcgtca?tggccgccta?cgacatcaac 960
ccctgcttca?attactacca?cctgatcgac?ttctgcccct?acctctggga?cgtgctcggc 1020
ttcccctccc?tcgcctccgg?cccaaacaac?tacttcaacc?gctccgacgt?ccagaagatc 1080
ctgcacgtcc?ctccaacgga?ctactccgtg?tgctcggaga?ccgtcatctt?cgcgaacggc 1140
gacggcagcg?accccagctc?ctggggtccc?ctacccagcg?tcatcgaacg?cactaacaac 1200
actatcatcg?gccacggctg?gctcgattac?ctcctcttct?tgaacggctc?gctcgccaca 1260
atccagaaca?tgacctggaa?cggtaagcaa?gggttccagc?gtcctcccgt?ggaaccgctc 1320
ttcgtccctt?accattatgg?tctggctgag?ctgtactggg?gcgatgagcc?tgacccgtat 1380
aaccttgatg?ctggcgctgg?atacctgggt?acagcgcata?ccgagcgcgg?gttgactttc 1440
agctcggtgt?atttgtctgg?tcatgaaatc?ccgcagtatg?ttcctggtgc?ggcttaccgc 1500
cagttggagt?tcctgctcgg?taggattagt?agtctttcgg?cgaaggggaa?ctatacctct 1560
tga 1563
<210>109
<211>1656
<212>DNA
<213〉aspergillus niger
<400>109
atgcgtggct?ctcggttggt?gctcttgttg?cccctggctg?cacttagttg?tgctatgccc 60
gagaatgaat?ggtcatctac?gataagaagg?cagttaccaa?aagcgtccac?tggcgtcaaa 120
tcgataaaaa?ccccaaacaa?tgtcactatc?aggtataaag?aaccaggaac?cgaaggaatt 180
tgtgagacaa?cacctggggt?caaatcatac?tccggatatg?tcgatctttc?gccagagtcg 240
catactttct?tttggttttt?cgagtcacgc?cgtgaccccg?aaaatgatcc?agtgactctg 300
tggctgaatg?gtggccctgg?aagcgattcc?ttgattgggc?tttttgaaga?gttgggtccg 360
tgtcacatca?caccagagta?cgaatcaatc?atcaatcagt?actcctggaa?cgaggtcacc 420
aatcttcttt?tcttgtctca?gcccctcggt?gtggggttct?cttacagtga?aaccgaggcc 480
gggtccttga?atccatttac?tggagccgtc?gagaacgcct?cctttgctgg?agttcagggt 540
cgatacccag?ttattgatgc?cactatcatc?gacacgaccg?atatcgctgc?acgcgcaacc 600
tgggaggtgc?ttcagggctt?cctcagtggc?ctgtcgcagc?tagattccga?agtcaagtcc 660
aaggagttca?acctgtggac?agagagttac?ggaggacact?atggaccagc?gttcttcaat 720
catttctacg?agcaaaattc?gaagatcgct?agcggggaag?tcaatggcgt?ccaactgaat 780
tttaactccc?tcgggattat?caacggcatc?attgatgccg?cgattcaggc?agactactac 840
gcagactttg?ccgttaataa?tacatatgga?atcaaagctg?tcaatgacac?agtgtacaac 900
tatatgaagt?tcgccaacac?gatgccaaat?ggatgccagg?atcaggttgc?ttcgtgtaaa 960
ttgaccaata?ggacctcgct?ttctgattat?gctatatgta?cagaagcagc?caatatgtgc 1020
agggacaatg?tcgaagggcc?ttactaccag?tttggcggcc?gtggcgtgta?tgatattcgg 1080
cacccctaca?atgacccgac?cccgccgtcc?tactttgttg?actacctcaa?gaaagactca 1140
gtcatggatg?ctatcggcgt?ggacattaac?tacaccgagt?ccagcggcga?agtatattat 1200
gcattccagc?agaccggcga?ctttgtatgg?ccgaatttca?ttgaggacct?cgaagagatc 1260
ctccaactcc?ccgtacgcgt?gtcgttgatc?tacggcgatg?ccgactatat?ctgtaactgg 1320
ttcggcggtc?aggccatctc?actcgcagtt?aactaccccc?atgcagctca?gttccgtgca 1380
gcgggataca?cacccatgac?agtagatggg?gtcgaatacg?gtgagactcg?cgagtatggc 1440
aacttttcgt?tcacccgcgt?atatcaggct?gggcacgagg?ttccatacta?tcaaccgatc 1500
gcagcgttgc?agctgttcaa?ccgtacttta?tttggatggg?atattgcagc?gggtacaact 1560
cagatttggc?ccgaatatag?caccaacggg?acatcgcagg?ctacacacac?ggagtcgttc 1620
gtgccactgt?ccacggcgtc?gagtaccgtc?aattag 1656
<210>110
<211>1872
<212>DNA
<213〉aspergillus niger
<400>110
atgccttttc?ccttttcgtc?cgctcttctc?ggctatatct?taactacgag?cactactctc 60
acctccctag?tcgcaggaca?gtattaccct?ccgacgcctg?aggatctcac?cgttattcat 120
tcggagatat?tccctggtgc?gaggatctcc?tataagcaac?ccctcggcat?ctgcaccacc 180
accccctcca?cccccagcta?ctccggctac?atccacctcc?ccccacacac?ccttaccaat 240
ctctccattc?caggaatcag?catctcgcaa?ccatacccta?tcaatacctt?tttctggtac 300
tttccttccc?gccatcacca?caacaatgat?acatccccac?tcaccatctg?gatgaacggc 360
gggcccggcg?gatcctccat?gattgggcta?tttcaagaga?acgggccatg?tactgtgaat 420
acggactcga?attccacggc?ctataatccc?tggtcgtgga?atgagtacgt?cgatatgttg 480
tatattgagc?agccggtgca?gacgggattt?agttatgatg?tgttgaggaa?tgggacgtta 540
gatttgaatg?agacgttttt?ggtggggacg?ttgccgagtc?aggatgtgca?tgggacggtg 600
aatgggacgg?ttaatggggg?aagggcgctt?tgggttgcgt?tgcaggtttg?gttgggtgaa 660
ttctctgaat?atgtttcttc?tgttgacggg?aatggtggtg?gtgatgacag?ggtgagtata 720
tggacggagt?catatggggg?acggtatgga?ccggcataca?cggcgctctt?tcaggagatg 780
aatgagagga?ttgagagtgg?ggaggtaagc?accgggaaga?agatccattt?ggatacgctg 840
ggcattatca?atgggtgtgt?ggatttactc?gtgcaggtcc?cttcgttccc?tgagcaggcg 900
tataacaata?cgtatgggat?cgagggaatc?aatcgcacgc?tctacgaccg?ggctatggat 960
agttggagca?agcctggcgg?gtgcagggat?atgatcatcg?agtgtcgcga?tgctggcgag 1020
ctcggagatc?ccctcatcat?ctgcgaggag?gcgtcggact?actgttcgcg?ggagatcaag 1080
agcctgtata?cggatacctc?cgggcgagga?tactacgaca?tagcgcattt?cacgccggat 1140
gcagctctcg?tgccttactt?cgtcgggttc?ttgaatcgcc?catgggtgca?aaaggcactt 1200
ggggtcccgg?tgaactatac?catgtcgtca?gaggcagtgg?ggaacagttt?cgcctcgacg 1260
ggcgattatc?cgcgaaatga?tccccgcgga?atgatcgggg?atattggata?cttgcttgac 1320
tccggtgtca?aggtggctat?ggtatatggg?gaccgggact?atgcttgtcc?gtggcgcggc 1380
ggggaagatg?tcagcctgct?ggtggagtac?gaggatgcgg?agaagttccg?tgctgctggg 1440
tatgccgaag?tgcagacgaa?gtcatcctac?gttgggggtc?tagtaaggca?gtatgggaac 1500
ttctcgttca?cgcgtgtctt?tcaggcgggc?catgaggtgc?cattttatca?gcccgaaacg 1560
gcgtatgaga?tttttaatcg?cgctcagttt?aattgggata?ttgcgacggg?aggcatttct 1620
ctggagcaga?atcagagcta?tgggacggag?ggaccgtcgt?caacgtggca?tatcaaaaac 1680
gaagtgccgg?agagccctga?gccgacgtgc?tatttgttgg?cgatggattc?gacttgtacg 1740
gatgagcaga?gggaacgggt?gctgagtggg?gatgcggtgg?tgagggattg?ggttgttgtt 1800
gatgatattg?aggctgaaag?ctcgttcagc?ggtgttggtg?atcagctggc?acaggtccct 1860
ttgggacatt?ga 1872
<210>111
<211>1320
<212>DNA
<213〉aspergillus niger
<400>111
atgagaacat?ctactctttt?gctcctctgg?agcactgcag?gagcagcttt?ggcttctccg 60
tacccgcttc?ccgactcgca?agtagtcttc?gccgcggatc?acgaggtccc?gaatacacag 120
ggcaaacacg?tcgtggacga?ggccatactc?tcggcgctga?acgctcattc?tgacccagtc 180
gctgcaatgg?tgtctctacg?tcccgaaact?gcagcttttc?tagctgaacc?tcgtctcttg 240
cacattcggg?gcgaagagaa?ggcggaatgg?atgaccgaag?gcgacaagct?gcgcctccgc 300
caacgcggaa?agaagttcat?ggacattacc?gagcatcagg?acttctacgc?agagcaggcg 360
atggcttcgt?ttgctgggga?tcctaatctt?cccaagctgt?cccataaagg?tctcgtcaag 420
ccgctgttct?ctcaaatcga?gacggaacga?atgcacgata?tcctgcagca?catgacctcc 480
tactacaatc?gatactacgg?tgattatcac?ggcgagatga?gctccgaatg?gctgcacgac 540
tacattgctg?cgatcatctc?caaatcgcct?ttccgcaccc?acatctctct?cgaatacttc 600
acccatcctt?tccgccaatc?ttcaattatt?gcacgcttcg?agcctaaagt?tcgcagcttc 660
tcccaacctt?tgaccatcat?tggtgcgcac?caagattcgg?ccaattatct?ttttcccctg 720
ctgcccgccc?ctggcgctga?cgatgactgt?tccggcactg?tcagtatcct?cgaggccttc 780
cgcgttctgg?cggagaatgg?ctacacgccc?aaggacgggc?ctgttgaatt?ccattggtat 840
gcggctgaag?aggccgggct?actgggcagc?caagccatcg?cgcggtacaa?gaaggagcag 900
ggcgctaaaa?ttgatgccat?gatggagttt?gatatgacgg?cttttattgc?ccgtaacgcc 960
accgagacca?tcgggtttgt?tgcaacccaa?gccgatgcag?cgctcacaaa?ctgggccctc 1020
aacctcagtc?gagaatacat?ctccattccg?gcggaagtct?atgaacttgg?ccccaacgct 1080
ggatccgact?acatgtcata?cactaagctc?aactaccccg?ctgcctttgc?atccgaaggc 1140
aacccgctcg?ctgggggctc?tttcccgggt?gaaatggacc?cctacgtaca?cggcatcaag 1200
gataggatgg?acgttgacga?tgaaacgggc?gtcttctcta?tcgaacacat?ggctcggttc 1260
tccgagttgg?ctatcgcatt?tgttgtcgag?caggctgggt?gggataatac?atggcggtag 1320
<210>112
<211>1581
<212>DNA
<213〉aspergillus niger
<400>112
atgcgttcct?tctccgttgt?cgctgccgcg?tcactggcgc?tctcttgggc?gtctctggcc 60
caggctgctc?gcccccgtct?tgtgcccaag?cctatctctc?ggccagcttc?gagtaagtcg 120
gctgcgacta?cgggtgaggc?ttattttgag?cagctgctgg?accatcacaa?cccggagaag 180
ggaacgtttt?cccagcggta?ctggtggagt?actgaatact?ggggtggacc?tgggtcaccg 240
gtggtcctct?ttaaccctgg?agaggtctct?gccgatggct?atgaggggta?tctcaccaac 300
gatactctca?ctggtgtcta?tgcgcaggag?atccagggtg?ccgtcattct?cattgaacac 360
cgctactggg?gcgactcttc?gccttatgag?gtgctcaatg?ccgaaacact?tcagtatctc 420
acactggatc?agtccattct?ggacatgacc?tacttcgccg?agacggtaaa?gctgcagttc 480
gataatagca?gccgcagcaa?tgcgcagaat?gctccctggg?tcatggtcgg?tggctcatac 540
agcggtgcct?tgacggcttg?gaccgagtct?atcgcgcctg?gaacgttctg?ggcttaccat 600
gccaccagtg?cgcctgtgga?ggctatctat?gacttttggc?aatacttcta?ccccattcag 660
caaggtatgg?cacagaactg?cagcaaggat?gtgtctctgg?tagccgagta?tgtcgacaaa 720
attgggaaga?atggaactgc?caaggaacag?caggagctca?aagaattgtt?tggtctggga 780
gctgttgagc?attacgatga?ctttgccgct?gtcctgccca?acggaccgta?cctctggcaa 840
gacaacgact?ttgtcacagg?atactcttcc?ttcttccagt?tctgtgatgc?tgtcgagggt 900
gtcgaagccg?gcgcggcagt?gacccccggc?cccgagggcg?tcggacttga?aaaggccctg 960
gccaactacg?caaactggtt?caattcaacc?atactcccta?actactgcgc?aagctacggc 1020
tactggaccg?acgaatggag?cgtcgcctgt?ttcgacagct?ataatgcctc?gagccccatc 1080
ttcaccgaca?cctccgtggg?taaccctgtc?gaccgccaat?gggaatggtt?cctctgcaac 1140
gagcctttct?tctggtggca?ggacggtgcc?cccgagggaa?cctccactat?tgtgccccgg 1200
ctcgtcagcg?cctcctactg?gcaacgccaa?tgcccgctct?acttccccga?agttaacggc 1260
tacacgtacg?gcagcgcgaa?gggtaaaaac?tccgctacgg?tgaacagctg?gacgggtgga 1320
tgggatatga?cccgcaacac?gacgcggttg?atctggacga?acgggcaata?tgacccctgg 1380
cgcgactccg?gtgtgtcgag?cactttccgg?cccggtggtc?cgctggttag?cacggcgaac 1440
gaacccgtgc?agattattcc?gggcgggttc?cattgctcgg?acttgtatat?ggaggattac 1500
tatgcgaatg?agggtgtgag?gaaggtggtt?gataatgagg?tgaagcagat?taaggagtgg 1560
gtggaggagt?attatgcttg?a 1581
<210>113
<211>1275
<212>DNA
<213〉aspergillus niger
<400>113
atgcagctcc?tccagtccct?cattgttgcc?gtttgcttca?gctacggcgt?cctctcctta 60
ccccatggcc?cgtcaaacca?gcacaaagca?cgttccttca?aggttgaacg?ggtccgtcgt 120
ggaaccggtg?ctctgcatgg?gcccgctgct?ctccgcaaag?cataccggaa?gtacggaata 180
gctcccagca?gtttcaacat?cgatctggca?gactttaaac?ccattacgac?aacccatgct 240
gctgctggga?gcgagattgc?agagcctgat?cagactggcg?ctgtcagtgc?tacttccgtc 300
gagaacgatg?ccgagttcgt?ttcgcctgtt?cttattggcg?gccagaagat?cgtcatgaca 360
tttgacactg?gttcttctga?cttttgggtg?ttcgatacga?atctcaatga?aaccttgacg 420
ggacacacgg?agtacaaccc?ttcgaactcc?tcgaccttca?agaagatgga?cggatacacc 480
ttcgatgtct?cgtatggtga?cgactcgtac?gcctctggcc?ccgtcggaac?ggataccgtc 540
aacattggcg?gcgccattgt?caaggagcaa?gccttcggtg?tccccgacca?ggtatcccag 600
tcgttcatcg?aggacacgaa?ctccaacggc?ctggtcgggt?tgggcttttc?ctccatcaac 660
accatcaaac?cggaggcgca?agacacgttc?ttcgccaatg?tcgcaccaag?tctggacgag 720
cccgtcatga?ccgcctcgct?caaggctgac?ggagtgggcg?agtacgagtt?cggcacgatc 780
gacaaagaca?agtaccaggg?caacattgcc?aacatcagcg?tggactcatc?gaacggatac 840
tggcagttct?ccactcccaa?gtactccgtg?gcagacggag?agctgaagga?cattggaagc 900
ttgaacacct?cgatcgcgga?caccggtacc?tcccttatgc?tgctggatga?agacgtggtt 960
actgcctact?atgcgcaagt?tcccaactcg?gtctacgtga?gcagtgccgg?tggttacatc 1020
tacccctgca?acaccactct?tcccagcttc?tcgcttgtcc?tcggcgagtc?gagcctggcc 1080
acgatccccg?gtaacctgat?caatttctcc?aaggttggca?ccaacaccac?caccggacag 1140
gccttgtgct?ttggcggcat?tcaatccaac?ggaaacacct?cgctgcagat?tctgggcgat 1200
attttcctga?aggccttttt?cgttgtcttc?gacatgcgcg?gcccctcgct?tggtgttgcc 1260
tctcccaaga?actag 1275
<210>114
<211>1647
<212>DNA
<213〉aspergillus niger
<400>114
atgcgcattg?actccgcggc?gctacatctg?gtcccagtcc?tcctgggcca?ggtcggtgct 60
ttacaattac?ccttggtcca?agactccaat?tcacagtggc?agaaaccaaa?tgcaggtgat 120
aaacccctaa?ttagctctcc?gttgcttcaa?gagcaggtca?aggcggagaa?tctgttggac 180
agggcccggc?agctttacaa?gattgcggag?ctgggagaag?acgagtataa?ccaccccact 240
cgcgtcattg?gcagtaaagg?tcaccttggc?acgctcgact?acatatactc?cacccttacc 300
gacctcggtg?attattatac?tgtcgtcaat?cagtccttcc?ctgccgtgag?cggtaatgtc 360
ttcgagtctc?gccttgtcct?tggtcacgat?gttcccaagt?cagctacacc?aatgggtctc 420
actcccccaa?cgaggaataa?ggagccggta?tatggctccc?tggttgctgt?atccaacctc 480
gggtgtgagg?cctcggacta?ctcgtccaac?ttgaaaggcg?ccgttgcatt?tatcagtcgg 540
ggaagctgtc?cgttcgggac?caagtctcaa?ttagctggta?aagcgggagc?tgttgctgcc 600
gtcatctaca?acaacgagcg?gggtgaccta?agcggaactc?taggaaaccc?aacccccgat 660
catgttgcta?cctttggtat?ctcagacgag?gatgctgccc?cagtcctgga?gaagttgaat 720
aaaggcgaga?aggtggacgc?tatcgcctac?gttgatgcga?tagtagagac?catccacacc 780
accaatatca?tcgcgcagac?cacggatggt?gacccgaaca?attgtgtaat?gctgggtggc 840
cacagtgaca?gcgtggccga?gggcccgggt?atcaatgacg?acgggtccgg?tactctgacc 900
cttttggagc?ttgccacatt?gctcacccag?ttccgtgtca?acaactgcgt?gcgatttgct 960
tggtgggccg?ccgaggagga?aggccttctc?ggatctgact?attacgtgtc?cgttctcaca 1020
ccggaagaga?accgcaagat?ccgcttgttc?atggactacg?acatgctcgg?ctcgccgaac 1080
tttgcgtacc?aagtttacaa?tgccactaat?gctgtgaacc?ccgagggatc?tgaggagctt 1140
cgtgatctgt?acaccgactt?ttacgaagat?catgggttca?actacacgta?cattccgttt 1200
gacggacgca?gcgactatga?tgccttcatt?cggcatggta?tcccgggtgg?tggcattgcc 1260
acgggagcag?agggtatcaa?gactgtcgag?gaagcggaca?tgtttggtgg?ggttgctggc 1320
caatggtatg?acccgtgtta?ccatcagatc?tgcgatacgg?tggccaatgt?gaacttgact 1380
gcgtgggagt?ggaacaccaa?gctcgttgcc?cactccattg?cgacttacgc?caagtccttt 1440
gacggattcc?cggaacggtc?cgatgaaccc?atcagccctg?ctgcttttga?ggaaccgaag 1500
taccatggcc?acgcgttgca?attacttcgc?ggtaatacta?cagggaccca?gagcgtcctg 1560
tggggagccc?aaatccagaa?tggaacagct?gcatcggtgc?ttaatctatt?gtccatacga 1620
cgcagaggca?ctttcagtct?aagctaa 1647
<210>115
<211>480
<212>PRT
<213〉aspergillus niger
<400>115
Met?His?Leu?Pro?Gln?Arg?Leu?Val?Thr?Ala?Ala?Cys?Leu?Cys?Ala?Ser
1 5 10 15
Ala?Thr?Ala?Phe?Ile?Pro?Tyr?Thr?Ile?Lys?Leu?Asp?Thr?Ser?Asp?Asp
20 25 30
Ile?Ser?Ala?Arg?Asp?Ser?Leu?Ala?Arg?Arg?Phe?Leu?Pro?Val?Pro?Lys
35 40 45
Pro?Ser?Asp?Ala?Leu?Ala?Asp?Asp?Ser?Thr?Ser?Ser?Ala?Ser?Asp?Glu
50 55 60
Ser?Leu?Ser?Leu?Asn?Ile?Lys?Arg?Ile?Pro?Val?Arg?Arg?Asp?Asn?Asp
65 70 75 80
Phe?Lys?Ile?Val?Val?Ala?Glu?Thr?Pro?Ser?Trp?Ser?Asn?Thr?Ala?Ala
85 90 95
Leu?Asp?Gln?Asp?Gly?Ser?Asp?Ile?Ser?Tyr?Ile?Ser?Val?Val?Asn?Ile
100 105 110
Gly?Ser?Asp?Glu?Lys?Ser?Met?Tyr?Met?Leu?Leu?Asp?Thr?Gly?Gly?Ser
115 120 125
Asp?Thr?Trp?Val?Phe?Gly?Ser?Asn?Cys?Thr?Ser?Thr?Pro?Cys?Thr?Met
130 135 140
His?Asn?Thr?Phe?Gly?Ser?Asp?Asp?Ser?Ser?Thr?Leu?Glu?Met?Thr?Ser
145 150 155 160
Glu?Glu?Trp?Ser?Val?Gly?Tyr?Gly?Thr?Gly?Ser?Val?Ser?Gly?Leu?Leu
165 170 175
Gly?Lys?Asp?Lys?Leu?Thr?Ile?Ala?Asn?Val?Thr?Val?Arg?Met?Thr?Phe
180 185 190
Gly?Leu?Ala?Ser?Asn?Ala?Ser?Asp?Asn?Phe?Glu?Ser?Tyr?Pro?Met?Asp
195 200 205
Gly?Ile?Leu?Gly?Leu?Gly?Arg?Thr?Asn?Asp?Ser?Ser?Tyr?Asp?Asn?Pro
210 215 220
Thr?Phe?Met?Asp?Ala?Val?Ala?Glu?Ser?Asn?Val?Phe?Lys?Ser?Asn?Ile
225 230 235 240
Val?Gly?Phe?Ala?Leu?Ser?Arg?Ser?Pro?Ala?Lys?Asp?Gly?Thr?Val?Ser
245 250 255
Phe?Gly?Thr?Thr?Asp?Lys?Asp?Lys?Tyr?Thr?Gly?Asp?Ile?Thr?Tyr?Thr
260 265 270
Asp?Thr?Val?Gly?Ser?Asp?Ser?Tyr?Trp?Arg?Ile?Pro?Val?Asp?Asp?Val
275 280 285
Tyr?Val?Gly?Gly?Thr?Ser?Cys?Asp?Phe?Ser?Asn?Lys?Ser?Ala?Ile?Ile
290 295 300
Asp?Thr?Gly?Thr?Ser?Tyr?Ala?Met?Leu?Pro?Ser?Ser?Asp?Ser?Lys?Thr
305 310 315 320
Leu?His?Ser?Leu?Ile?Pro?Gly?Ala?Lys?Ser?Ser?Gly?Ser?Tyr?His?Ile
325 330 335
Ile?Pro?Cys?Asn?Thr?Thr?Thr?Lys?Leu?Gln?Val?Ala?Phe?Ser?Gly?Val
340 345 350
Asn?Tyr?Thr?Ile?Ser?Pro?Lys?Asp?Tyr?Val?Gly?Ala?Thr?Ser?Gly?Ser
355 360 365
Gly?Cys?Val?Ser?Asn?Ile?Ile?Ser?Tyr?Asp?Leu?Phe?Gly?Asp?Asp?Ile
370 375 380
Trp?Leu?Leu?Gly?Asp?Thr?Phe?Leu?Lys?Asn?Val?Tyr?Ala?Val?Phe?Asp
385 390 395 400
Tyr?Asp?Glu?Leu?Arg?Val?Gly?Phe?Ala?Glu?Arg?Ser?Ser?Asn?Thr?Thr
405 410 415
Ser?Ala?Ser?Asn?Ser?Thr?Ser?Ser?Gly?Thr?Ser?Ser?Thr?Ser?Gly?Ser
420 425 430
Thr?Thr?Thr?Gly?Ser?Ser?Thr?Thr?Thr?Thr?Ser?Ser?Ala?Ser?Ser?Ser
435 440 445
Ser?Ser?Ser?Asp?Ala?Glu?Ser?Gly?Ser?Ser?Met?Thr?Ile?Pro?Ala?Pro
450 455 460
Gln?Tyr?Phe?Phe?Ser?Ala?Leu?Ala?Ile?Ala?Ser?Phe?Met?Leu?Trp?Leu
465 470 475 480
<210>116
<211>1099
<212>PRT
<213〉aspergillus niger
<400>116
Met?Leu?Arg?Gly?Leu?Arg?Asp?Val?Val?Leu?Leu?Gln?Phe?Ala?Ile?Pro
1 5 10 15
Leu?Phe?Leu?Leu?Leu?His?Phe?Arg?Leu?Ser?Leu?Arg?Gly?Val?Ile?Thr
20 25 30
Gly?Phe?Gly?Ser?Lys?Ser?His?Phe?Gln?Arg?Pro?Leu?Ser?Lys?Met?Ser
35 40 45
Ser?Thr?Gln?Lys?Ser?His?Phe?Lys?Leu?Leu?Gln?Lys?Phe?Lys?Pro?Glu
50 55 60
Tyr?Ser?Pro?Ser?Glu?Phe?Ala?Gln?Tyr?Glu?Ser?Glu?Arg?Thr?Gly?Met
65 70 75 80
Arg?Val?Val?Val?Ile?Asp?Gln?Lys?Gly?Pro?Lys?Val?Thr?Gly?Tyr?Phe
85 90 95
Val?Leu?Ala?Thr?Glu?Ile?Leu?Asp?Asp?Ser?Gly?Ala?Pro?His?Thr?Leu
100 105 110
Glu?His?Leu?Cys?Phe?Met?Gly?Ser?Arg?Asn?Tyr?Arg?Tyr?Lys?Gly?Phe
115 120 125
Leu?Asp?Lys?Leu?Ala?Thr?Arg?Val?Tyr?Ser?Ser?Thr?Asn?Ala?Trp?Thr
130 135 140
Ala?Thr?Asp?His?Thr?Ala?Tyr?Thr?Leu?Asp?Thr?Ala?Gly?Trp?Glu?Gly
145 150 155 160
Phe?Ala?Gln?Ile?Leu?Pro?Val?Tyr?Leu?Glu?His?Val?Ile?Ala?Pro?Thr
165 170 175
Leu?Thr?Asp?Glu?Gly?Cys?Tyr?Thr?Glu?Val?His?His?Ile?Asp?Gly?Ala
180 185 190
Gly?Asp?Asp?Ala?Gly?Val?Val?Tyr?Ser?Glu?Met?Gln?Gly?Val?Gln?Asn
195 200 205
Asn?Ser?Ala?Glu?Leu?Ile?Asp?Leu?Thr?Ala?Arg?Arg?Leu?Thr?Tyr?Pro
210 215 220
His?Gly?Val?Gly?Phe?Arg?Tyr?Glu?Thr?Gly?Gly?Met?Met?Glu?Gln?Leu
225 230 235 240
Arg?Val?Leu?Thr?Ala?Asp?Arg?Ile?Arg?Ala?Phe?His?Arg?Glu?Met?Tyr
245 250 255
Gln?Pro?Lys?Asn?Leu?Cys?Leu?Ile?Ile?Thr?Gly?Glu?Val?Asp?His?Gln
260 265 270
Asn?Met?Leu?Glu?Thr?Leu?Asp?Lys?Phe?Glu?Asp?Thr?Ile?Leu?Asp?Val
275 280 285
Ile?Pro?Ser?Pro?Asp?Ser?Pro?Phe?Lys?Arg?Pro?Trp?Val?Asp?Ser?Lys
290 295 300
Gln?Ala?Pro?Pro?Leu?Glu?Lys?Ser?Ile?Val?Gln?Thr?Val?Glu?Phe?Pro
305 310 315 320
Glu?Glu?Asp?Glu?Ser?Phe?Gly?Glu?Ile?Glu?Ile?Arg?Phe?Leu?Gly?Pro
325 330 335
Asp?Cys?Thr?Asp?Pro?Val?Gln?Thr?Gly?Ala?Val?Asn?Val?Ala?Leu?Leu
340 345 350
Tyr?Leu?Ala?Gly?Ser?Ser?Ala?Ser?Leu?Leu?Asp?Asn?Ile?Leu?Val?Glu
355 360 365
Lys?Glu?Gln?Leu?Ala?Ser?Ala?Val?Tyr?Tyr?Ala?Thr?Glu?Asp?His?Pro
370 375 380
Ser?Ile?Glu?Ile?Arg?Phe?Thr?Leu?Thr?Ser?Val?Glu?Thr?Glu?Lys?Leu
385 390 395 400
Ala?Lys?Val?Glu?Gln?Arg?Phe?Phe?Glu?Val?Leu?Lys?Asp?Ala?Met?Glu
405 410 415
Lys?Asp?Leu?Asp?Met?Arg?Tyr?Ile?Lys?Glu?Cys?Ile?Asp?Arg?Gln?Arg
420 425 430
Arg?Thr?Trp?Lys?Phe?Ser?Thr?Glu?Ser?Ser?Ala?Ser?Ser?Phe?Ala?Glu
435 440 445
Tyr?Val?Ile?Ser?Asp?Phe?Leu?Phe?Gly?Lys?Arg?Asp?Gly?Ser?Thr?Met
450 455 460
Leu?Asp?Val?Ala?Thr?Leu?Gln?Glu?Tyr?Asp?Val?Leu?Glu?Lys?Trp?Ser
465 470 475 480
Glu?Glu?Gln?Trp?Arg?Ser?Phe?Ile?Lys?Thr?Trp?Ile?Ser?Asp?Ala?Asn
485 490 495
His?Val?Thr?Ile?Leu?Gly?Val?Pro?Ser?Val?Lys?Met?Ser?Asp?Thr?Leu
500 505 510
Lys?Lys?Glu?Glu?Glu?Ala?Arg?Val?Ala?Glu?Gln?Lys?Lys?Arg?Leu?Gly
515 520 525
Asp?Glu?Gly?Leu?Lys?Lys?Leu?Ala?Asp?Lys?Leu?Glu?Lys?Ala?Lys?Ala
530 535 540
Glu?Asn?Asp?Lys?Glu?Ile?Pro?Lys?Glu?Met?Leu?Glu?Arg?Phe?Gln?Ile
545 550 555 560
Pro?Gly?Ile?Glu?Ser?Ile?His?Phe?Val?Asp?Thr?Thr?Thr?Ala?Arg?Ser
565 570 575
Gly?Ala?Ala?Leu?Asp?Ala?Gly?Arg?Pro?Ser?His?Lys?Ala?Gln?Lys?Leu
580 585 590
Val?Asp?Ala?Asp?Gly?Ser?Asp?Leu?Pro?Leu?Phe?Ile?His?Phe?Glu?His
595 600 605
Ile?Pro?Ser?Ser?Phe?Val?Gln?Leu?Ser?Leu?Leu?Ile?Ser?Ala?Gln?Ala
610 615 620
Val?Pro?Val?Gln?Leu?Arg?Pro?Leu?Leu?Ser?Val?Tyr?Thr?Glu?Ala?Phe
625 630 635 640
Phe?Asn?Leu?Pro?Val?Asn?Arg?Asn?Gly?Glu?Thr?Ile?Asn?Phe?Glu?Gln
645 650 655
Val?Val?Val?Glu?Leu?Glu?Arg?Asp?Thr?Val?Gly?Tyr?Ser?Met?Glu?Gly
660 665 670
Ala?Arg?Ser?Leu?Gly?Asn?Ser?Glu?Met?Leu?Arg?Ile?Ser?Phe?Gln?Val
675 680 685
Glu?Leu?Glu?Lys?Tyr?His?Thr?Ala?Ile?Ala?Trp?Ile?Gln?Glu?Leu?Ser
690 695 700
Trp?Asn?Ser?Ile?Phe?Asp?Val?Glu?Arg?Leu?Arg?Ala?Ile?Thr?Ser?Arg
705 710 715 720
Leu?Leu?Ser?Asp?Val?Pro?Asp?Ser?Lys?Arg?Ser?Gly?Asp?Asp?Met?Leu
725 730 735
Ala?Ala?Val?His?Val?Met?Val?His?Tyr?Ala?Ala?Glu?Ser?Ile?Val?Arg
740 745 750
Ala?Arg?Ser?Thr?Leu?Val?Lys?Ala?Arg?Tyr?Leu?Lys?Arg?Ile?Lys?Lys
755 760 765
Gln?Leu?Ala?Glu?Glu?Pro?Lys?Ser?Val?Val?Ala?Arg?Met?Glu?Glu?Ile
770 775 780
Arg?Asp?Ala?Leu?Phe?Arg?Phe?Glu?Asn?Met?Arg?Val?Leu?Val?Ile?Ala
785 790 795 800
Asp?Leu?Glu?Lys?L Gln?Asn?Pro?Val?Ser?Ala?Trp?Lys?Pro?Phe?Ala
805 810 815
Glu?Arg?Leu?Gly?Ala?Gly?Ala?Pro?Leu?Gln?Pro?Ile?Thr?Thr?Arg?Arg
820 825 830
Pro?Leu?Leu?Ser?Glu?Ala?Gly?Gln?Lys?Leu?Gly?Gly?Lys?Ser?Tyr?Val
835 840 845
Val?Pro?Met?Pro?Thr?Ile?Asp?Ser?Ser?Phe?Ala?Tyr?Ala?Thr?Ala?Arg
850 855 860
Gly?Leu?Asp?Ser?Tyr?Asp?Asp?Pro?Arg?Leu?Pro?Ala?Leu?Met?Val?Ala
865 870 875 880
Ile?Ala?Tyr?Met?Asn?Ala?Val?Glu?Gly?Pro?Leu?Trp?Val?Ala?Val?Arg
885 890 895
Gly?Lys?Gly?Leu?Ala?Tyr?Gly?Thr?Asn?Phe?Ala?Tyr?Asn?Ile?Asp?Thr
900 905 910
Gly?Phe?Val?Asn?Phe?Asp?Val?Tyr?Arg?Ser?Pro?Asn?Ala?His?Lys?Ala
915 920 925
Phe?Asp?Ser?Ser?Lys?Gln?Ile?Val?Glu?Asp?His?Leu?Ser?Gly?Ala?Met
930 935 940
Pro?Phe?Asp?Pro?Leu?Met?Leu?Glu?Gly?Ser?Ile?Ser?Ser?Ile?Val?Val
945 950 955 960
Ser?Phe?Ala?Asn?Glu?Gln?Ser?Thr?Ile?Gly?Ser?Ala?Ala?Ser?Gly?Ser
965 970 975
Phe?Ile?Arg?Gln?Val?Ile?Arg?Arg?Leu?Pro?Ser?Asp?Tyr?Lys?Glu?Arg
980 985 990
Val?Leu?Lys?Gln?Val?Arg?Ala?Thr?Ser?Val?Asp?Asp?Val?Lys?Gly?Ala
995 1000 1005
Leu?Lys Asp?Ile?Ile?Leu?Pro Leu?Phe?Asn?Pro?Ser Thr?Ala?Asn
1010 1015 1020
Ile?Val Val?Thr?Cys?Ala?Thr Val?Leu?Glu?Glu?Thr Ile?Lys?Glu
1025 1030 1035
Gly?Leu Gln?Ala?Ser?Gly?Phe Thr?Pro?Ala?Val?Gln Pro?Leu?Lys
1040 1045 1050
Glu?Phe Glu?Asp?Asp?Tyr?Gly Leu?Lys?Val?Gly?Asp Asp?Glu?Asp
1055 1060 1065
Glu?Glu Ser?Asp?Asp?Asp?Asp Asp?Glu?Tyr?Glu?Thr Gly?Ser?Glu
1070 1075 1080
Asp?Glu Asp?Asp?Ser?Asp?Glu Asp?Met?Glu?Asp?Asp Glu?Asp?Asp
1085 1090 1095
Glu
<210>117
<211>726
<212>PRT
<213〉aspergillus niger
<400>117
Met?Gly?Ala?Leu?Gln?Trp?Leu?Ser?Ile?Thr?Ala?Ala?Ala?Ala?Ser?Ala
1 5 10 15
Val?Ser?Ala?Leu?Thr?Pro?Glu?Gln?Met?Ile?Gly?Ala?Pro?Arg?Arg?Thr
20 25 30
Glu?Val?Ile?Pro?Asn?Pro?Ser?Gly?Asp?Thr?Gly?Leu?Phe?Ser?Thr?Ser
35 40 45
Gln?Trp?Ser?Phe?Asp?Thr?His?Ser?Glu?Ser?Thr?Trp?Trp?Ser?Leu?Ile
50 55 60
Asp?Leu?Gln?Ser?Gly?Lys?Thr?Thr?Thr?Leu?Thr?Asp?Asp?Ser?Asp?Ile
65 70 75 80
Glu?Glu?Ile?Ile?Trp?Leu?Gly?Ser?Asp?Asn?Ser?Thr?Leu?Leu?Tyr?Ile
85 90 95
Asn?Ser?Thr?Asn?Ala?Gln?Val?Pro?Gly?Gly?Val?Glu?Leu?Trp?Ile?Ala
100 105 110
Asp?Ser?Ser?Asp?Phe?Ala?Asn?Ala?Tyr?Lys?Ala?Ala?Ser?Leu?Ser?Ala
115 120 125
Gly?Phe?Leu?Gly?Ile?Lys?Ser?Thr?Val?Thr?Asp?Ser?Gly?Asp?Val?His
130 135 140
Phe?Ile?Leu?Arg?Gly?Lys?Ser?Tyr?Pro?Asn?Gly?Thr?Ala?Tyr?Asn?Asp
145 150 155 160
Gln?Leu?Ala?Glu?Thr?Tyr?Pro?Ser?Thr?Ala?Arg?Ile?Tyr?Asp?Ser?Ile
165 170 175
Phe?Val?Arg?His?Trp?Asp?Thr?Tyr?Leu?Thr?Thr?Ala?Ser?His?Ala?Val
180 185 190
Phe?Ser?Gly?Thr?Leu?Gln?Ser?Ser?Thr?Ser?Asp?Asp?Gly?Asn?Val?Gln
195 200 205
Tyr?Thr?Ser?Ser?Gly?Gly?Leu?Thr?Asn?Leu?Val?Asn?Pro?Val?Lys?Gly
210 215 220
Ala?Glu?Ser?Pro?Phe?Pro?Pro?Phe?Gly?Gly?Asn?Asp?Asp?Tyr?Asp?Leu
225 230 235 240
Ser?Pro?Asp?Gly?Lys?Trp?Val?Thr?Phe?Lys?Ser?Lys?Ala?Pro?Glu?Leu
245 250 255
Pro?Leu?Ala?Asn?Asn?Thr?Ala?Ala?Tyr?Val?Tyr?Leu?Val?Pro?His?Asp
260 265 270
Gly?Ser?Ala?Thr?Ala?Phe?Ala?Val?Asn?Gly?Pro?Asp?Ser?Pro?Ala?Thr
275 280 285
Pro?Glu?Gly?Val?Glu?Gly?Glu?Ser?Asn?Asn?Pro?Val?Phe?Ser?Pro?Asp
290 295 300
Ser?Asp?Lys?Ile?Ala?Tyr?Phe?Gln?Met?Ala?Thr?Asn?Thr?Tyr?Glu?Ser
305 310 315 320
Asp?Arg?Asn?Val?Leu?Tyr?Val?Tyr?Ser?Ile?Ala?Asp?Asp?Thr?Ile?Thr
325 330 335
Pro?Leu?Ala?Lys?Asp?Trp?Asp?Arg?Ser?Pro?Ser?Ser?Val?Thr?Trp?Val
340 345 350
Asp?Gly?Asp?Asn?Leu?Val?Val?Ala?Ser?Gln?Asp?Leu?Gly?Arg?Thr?Arg
355 360 365
Leu?Phe?Ala?Ile?Pro?Gly?Asp?Ala?Gly?Asp?Asp?Phe?Lys?Pro?Thr?Asn
370 375 380
Phe?Thr?Asp?Gly?Gly?Ser?Val?Ser?Ala?Gln?Tyr?Val?Leu?Ser?Asn?Ser
385 390 395 400
Thr?Leu?Leu?Val?Thr?Ser?Ser?Ala?Phe?Trp?Thr?Ser?Trp?Ser?Val?Tyr
405 410 415
Thr?Ala?Ser?Pro?Asp?Glu?Gly?Val?Ile?Asn?Thr?Leu?Ala?Ser?Ala?Asn
420 425 430
Glu?Ile?Asp?Pro?Glu?Leu?Ser?Gly?Leu?Ser?Ser?Ser?Asp?Phe?Glu?Glu
435 440 445
Phe?Tyr?Phe?Asp?Gly?Asn?Trp?Thr?Thr?Leu?Gln?Gly?Trp?Ile?Thr?Tyr
450 455 460
Pro?Gln?Asp?Phe?Asp?Ser?Ser?Lys?Lys?Tyr?Pro?Leu?Ala?Phe?Leu?Ile
465 470 475 480
His?Gly?Gly?Pro?Glu?Asp?Ala?Trp?Ala?Asp?Glu?Trp?Asn?Leu?Lys?Trp
485 490 495
His?Ser?Lys?Val?Phe?Ala?Asp?Gln?Gly?Tyr?Val?Val?Val?Gln?Pro?Asn
500 505 510
Pro?Thr?Gly?Ser?Thr?Gly?Phe?Gly?Gln?Gln?Leu?Thr?Asp?Ala?Ile?Gln
515 520 525
Leu?Asn?Trp?Thr?Gly?Ala?Ala?Tyr?Asp?Asp?Leu?Thr?Lys?Ala?Trp?Gln
530 535 540
Tyr?Val?His?Asp?Thr?Tyr?Asp?Phe?Ile?Asp?Thr?Asp?Asn?Gly?Val?Ala
545 550 555 560
Ala?Gly?Pro?Ser?Phe?Gly?Ala?Phe?Met?Ile?Thr?Trp?Ile?Gln?Gly?Asp
565 570 575
Asp?Phe?Gly?Arg?Lys?Phe?Lys?Ala?Leu?Val?Ser?His?Asp?Gly?Pro?Phe
580 585 590
Ile?Gly?Asp?Ala?Trp?Val?Glu?Thr?Asp?Glu?Leu?Trp?Phe?Val?Glu?His
595 600 605
Glu?Phe?Asn?Gly?Thr?Phe?Trp?Gln?Ala?Arg?Asp?Ala?Phe?His?Asn?Thr
610 615 620
Asp?Pro?Ser?Gly?Pro?Ser?Arg?Val?Leu?Ala?Tyr?Ser?Thr?Pro?Gln?Leu
625 630 635 640
Val?Ile?His?Ser?Asp?Lys?Asp?Tyr?Arg?Ile?Pro?Val?Ala?Asn?Gly?Ile
645 650 655
Gly?Leu?Phe?Asn?Thr?Leu?Gln?Glu?Arg?Gly?Val?Pro?Ser?Arg?Phe?Leu
660 665 670
Asn?Phe?Pro?Asp?Glu?Asp?His?Trp?Val?Thr?Gly?Gln?Glu?Asn?Ser?Leu
675 680 685
Val?Trp?Tyr?Gln?Gln?Val?Leu?Gly?Trp?Ile?Asn?Arg?Tyr?Ser?Gly?Val
690 695 700
Gly?Gly?Ser?Asn?Pro?Asp?Ala?Ile?Ala?Leu?Glu?Asp?Thr?Val?Asn?Pro
705 710 715 720
Val?Val?Asp?Leu?Asn?Pro
725
<210>118
<211>564
<212>PRT
<213〉aspergillus niger
<400>118
Met?Thr?Arg?Gln?Thr?Ser?Leu?Val?Pro?Arg?Leu?Leu?Thr?Leu?Ala?Ser
1 5 10 15
Leu?Ala?Ala?Leu?Ser?Gln?Ala?Glu?Leu?Gly?Lys?Ile?Gln?Trp?Lys?Gly
20 25 30
Ser?Cys?Asn?Leu?Thr?Thr?Tyr?Pro?Ala?Leu?Ile?Cys?Gly?Thr?Leu?Asp
35 40 45
Val?Pro?Tyr?Asp?Tyr?Thr?Glu?Ser?Asn?Ser?Ser?Lys?Thr?Leu?Thr?Leu
50 55 60
Asp?Ile?Ala?Lys?Trp?Pro?Ala?Thr?Lys?Lys?Pro?Val?Ser?Glu?Pro?Ile
65 70 75 80
Ile?Phe?Asn?Phe?Gly?Gly?Pro?Gly?Val?Asn?Ser?Phe?Glu?Gly?Leu?Gly
85 90 95
Leu?Tyr?Gly?Glu?Glu?Phe?Gln?Ala?Ile?Leu?Gly?Gly?His?Asn?Asp?Leu
100 105 110
Ile?Ala?Phe?Asn?Asn?Arg?Gly?Val?Gly?Asn?Thr?Ile?Pro?Phe?Ser?Cys
115 120 125
Tyr?Ser?Asp?Asp?Ala?Thr?Arg?Glu?Leu?Val?Ala?Leu?Gln?Ala?Pro?Asn
130 135 140
Asp?Gly?Arg?Ala?Ser?Ser?Thr?Ala?Leu?Gly?Glu?Ile?Trp?Ala?Gln?Asn
145 150 155 160
Ala?Asn?Ile?Ala?Gln?Ala?Cys?Tyr?Ala?Thr?Asn?Asn?Gln?Thr?Gly?Ser
165 170 175
Leu?Ile?Gly?Thr?Ser?Phe?Ala?Ala?Arg?Asp?Ile?Met?Gln?Val?Ala?Asp
180 185 190
Ala?Leu?Ser?Gly?Lys?Asp?Ser?Leu?Val?Asn?Tyr?Trp?Gly?Phe?Ser?Tyr
195 200 205
Gly?Thr?Thr?Ile?Gly?Ala?Val?Leu?Ala?Ala?Met?Phe?Pro?Asp?Arg?Met
210 215 220
Gly?Asn?Val?Ala?Leu?Asp?Gly?Val?Asp?Asn?Pro?Arg?Glu?Ala?Leu?Tyr
225 230 235 240
Gly?Tyr?Asn?Ala?Gln?Ala?Val?Val?Asp?Val?Asp?Lys?Val?Phe?Glu?Gly
245 250 255
Phe?Cys?Thr?Gly?Cys?Met?Ala?Ala?Pro?Asp?Leu?Cys?Pro?Ile?Ala?Lys
260 265 270
Glu?Tyr?Thr?Ser?Ala?Ala?Asn?Leu?Glu?Ala?Ala?Ile?Tyr?Leu?Met?Leu
275 280 285
Glu?Asn?Leu?Lys?Tyr?Asn?Pro?Ile?Ala?Ile?Pro?Glu?Thr?Gly?Gly?Ile
290 295 300
Val?Thr?Trp?Ser?Asp?Val?Lys?Ser?Thr?Ile?Phe?Glu?Ala?Met?Tyr?Leu
305 310 315 320
Pro?Ser?Ser?Trp?Pro?Leu?Thr?Ser?Glu?Leu?Leu?Tyr?Tyr?Val?Gln?Thr
325 330 335
Arg?Asn?Thr?Thr?Ile?Leu?Gly?Asn?Ser?Glu?Val?Tyr?Asp?Thr?Ile?Lys
340 345 350
Ser?Tyr?Gly?Gln?Ser?Ala?Ser?Leu?Thr?Ser?Ala?Ser?Asp?Glu?Val?Gly
355 360 365
Thr?Ala?Ile?Thr?Cys?Ser?Asp?Lys?His?Arg?Ser?Ala?Thr?Ile?Lys?Glu
370 375 380
Val?Leu?Pro?Tyr?Val?Lys?Ala?Arg?Gln?Ala?Leu?Thr?Lys?Ile?Gly?Ser
385 390 395 400
Asp?Gly?Ser?Asp?Gly?Asp?Met?Arg?Cys?Ala?Gln?Trp?Asn?Pro?Lys?Met
405 410 415
Phe?Ala?Lys?Glu?Arg?Tyr?Ser?Gly?Asp?Phe?Glu?Val?Lys?Thr?Ala?Asn
420 425 430
Pro?Val?Leu?Ile?Leu?Ser?Asn?Thr?Tyr?Asp?Pro?Ala?Thr?Pro?Leu?Pro
435 440 445
Ala?Ala?Lys?Asn?Leu?Thr?Glu?Thr?Phe?Glu?Gly?Ser?Val?Leu?Leu?Glu
450 455 460
Gln?Asn?Gly?Tyr?Gly?His?Thr?Thr?Leu?Ser?Met?Pro?Ser?Leu?Cys?Thr
465 470 475 480
Ala?Lys?Ala?Val?Arg?Ala?Tyr?Phe?Thr?Asn?Gly?Thr?Leu?Pro?Ala?Asp
485 490 495
Gly?Thr?Ile?Cys?Gln?Val?Asp?Val?Pro?Leu?Phe?Thr?Asn?Leu?Thr?Tyr
500 505 510
Lys?Asp?Val?Trp?Pro?Lys?Ser?Phe?Gln?Arg?Ser?Val?Glu?Ser?Arg?Asp
515 520 525
Asp?Ala?Thr?Ile?Leu?Lys?Ala?Leu?Met?Ser?Val?Arg?Asp?Lys?Met?Ser
530 535 540
Arg?Arg?Arg?Met?Cys?Ile?Tyr?Leu?Tyr?Thr?Asn?Ser?Ala?Ser?Trp?Arg
545 550 555 560
Pro?Glu?Leu?Pro
<210>119
<211>526
<212>PRT
<213〉aspergillus niger
<400>119
Met?Tyr?Tyr?Ser?Leu?Trp?Val?Ala?Ala?Leu?Val?Ala?Ala?Leu?Pro?Val
1 5 10 15
Ser?Arg?Ala?Gln?Phe?Val?Ala?Pro?Pro?Thr?Asp?Leu?Ile?Pro?Thr?Lys
20 25 30
Gly?Tyr?Leu?Asp?Ile?Pro?Val?Arg?Tyr?Lys?Gln?Val?Pro?Thr?Gly?Ile
35 40 45
Cys?Glu?Thr?Asp?Pro?Ser?Val?Lys?Ser?Phe?Ser?Gly?Tyr?Val?Asp?Val
50 55 60
Ala?Glu?His?Glu?His?Ile?Phe?Phe?Trp?Phe?Phe?Glu?Ala?Arg?Asn?Gln
65 70 75 80
Asp?Pro?Thr?Glu?Ala?Pro?Leu?Thr?Val?Trp?Ile?Asn?Gly?Gly?Met?Ser
85 90 95
Asp?Pro?Gly?Pro?Gly?Ser?Ser?Ser?Met?Ile?Gly?Leu?Phe?Gln?Glu?His
100 105 110
Gly?Pro?Cys?Gly?Ile?Asp?Ala?Asn?Gly?Ser?Val?Tyr?Asn?Asn?Pro?Tyr
115 120 125
Ser?Trp?Asn?Asn?Ala?Ser?Asn?Met?Leu?Tyr?Ile?Asp?Gln?Pro?Val?Gln
130 135 140
Thr?Gly?Phe?Ser?Tyr?Ser?Ile?Pro?Val?Pro?Gly?Tyr?Val?Asp?Ser?Ser
145 150 155 160
Thr?Asp?Asn?Gly?Phe?Met?Gly?Ala?Phe?Pro?Gln?Tyr?Ser?Arg?Glu?Thr
165 170 175
Phe?His?Phe?Thr?Thr?Glu?Ser?Tyr?Gly?Gly?His?Tyr?Gly?Pro?Val?Phe
180 185 190
Asn?Glu?Tyr?Ile?Glu?Glu?Gln?Asn?Ala?His?Leu?Gln?Pro?Gly?Ala?Lys
195 200 205
Lys?Ile?Gln?Leu?Gly?Ser?Val?Met?Ile?Gly?Asn?Gly?Trp?Tyr?Asp?Pro
210 215 220
Ile?Ile?Gln?Tyr?Gln?Ala?Tyr?Tyr?Asn?Phe?Thr?Val?Tyr?Pro?Gly?Asn
225 230 235 240
Thr?Tyr?Asp?Tyr?Leu?Pro?Phe?Asn?Lys?Ser?Ile?Ser?Ser?Leu?Met?Tyr
245 250 255
Asn?Asn?Leu?Tyr?Gly?Pro?Gly?Asn?Cys?Leu?Asp?Gln?Leu?Tyr?Asp?Cys
260 265 270
Ala?Ala?Arg?Gly?Ile?Asp?Glu?Ile?Cys?Ser?Thr?Ala?Asp?Asp?Phe?Cys
275 280 285
Ala?Asn?Glu?Val?Glu?Asn?Val?Tyr?Asp?Ile?Tyr?Ser?Gly?Arg?Asp?Glu
290 295 300
Tyr?Asp?Phe?Arg?Glu?Leu?Thr?Pro?Asp?Pro?Phe?Pro?Tyr?Glu?Phe?Tyr
305 310 315 320
Val?Asp?Tyr?Leu?Asn?Lys?Ala?Ser?Val?Gln?Ala?Ala?Ile?Gly?Ala?Tyr
325 330 335
Ile?Asn?Tyr?Thr?Glu?Ser?Asn?Asn?Ala?Val?Gly?Leu?Ala?Phe?Ser?Ser
340 345 350
Thr?Gly?Asp?Asp?Gly?Arg?Leu?Met?Asn?Thr?Ile?Gln?Asp?Val?Gly?Lys
355 360 365
Leu?Leu?Lys?Gln?Gly?Val?Thr?Val?Val?Met?Tyr?Ala?Gly?Asp?Ala?Asp
370 375 380
Tyr?Asn?Cys?Asn?Trp?Leu?Gly?Gly?Glu?Ala?Val?Ser?Leu?Gln?Val?Lys
385 390 395 400
Ala?Ala?Asn?Phe?Ser?Ser?Ala?Gly?Tyr?Thr?Asn?Ile?Val?Thr?Ser?Asp
405 410 415
Gly?Val?Thr?His?Gly?Gln?Val?Arg?Gln?Ala?Gly?Gln?Phe?Ala?Phe?Val
420 425 430
Arg?Val?Tyr?Glu?Ser?Gly?His?Glu?Val?Pro?Phe?Tyr?Gln?Pro?Leu?Leu
435 440 445
Ala?Leu?Glu?Met?Phe?Glu?Arg?Val?Ile?Gly?Gly?Lys?Asp?Val?Ala?Thr
450 455 460
Gly?Lys?Ile?Pro?Ile?Ser?Ser?Ser?Leu?Gln?Thr?Val?Gly?Thr?Pro?Lys
465 470 475 480
Ser?Tyr?Tyr?Arg?Glu?Gly?Asn?Ser?Thr?Ile?Gln?Trp?Glu?Val?Leu?Asp
485 490 495
Ser?Leu?Ala?Thr?Tyr?Asn?Thr?Thr?Thr?Asn?Ala?Pro?Asn?Pro?Val?Ser
500 505 510
Arg?Arg?Leu?Lys?Arg?Met?Gly?Pro?Ala?Leu?Arg?Phe?Gln?Met
515 520 525
<210>120
<211>1156
<212>PRT
<213〉aspergillus niger
<400>120
Met?Ser?Cys?Val?Trp?Leu?His?Ile?His?Lys?Arg?Ser?Leu?Leu?Ser?Val
1 5 10 15
Ala?Thr?Asn?Asn?Ser?Val?Ala?Arg?Ala?Ala?Ala?Ser?Thr?Ser?Ala?Ala
20 25 30
Pro?Pro?Pro?Pro?Ser?Ser?Pro?Pro?Pro?Gly?Ser?Asn?Thr?Tyr?Ser?Pro
35 40 45
Leu?Tyr?Arg?Pro?Ile?Thr?Asn?Pro?Ile?Gly?Phe?Thr?Leu?Ser?Pro?Ala
50 55 60
Arg?Ser?Leu?Val?Ser?Arg?Asn?Pro?Lys?Phe?Pro?Ala?Tyr?Arg?Arg?Ser
65 70 75 80
Ser?Arg?His?Phe?Ser?Leu?Cys?Pro?Ala?Ala?Ala?Thr?Pro?Gly?Val?Thr
85 90 95
Thr?Ser?Ile?Cys?Pro?Gly?Gln?Ala?Pro?Val?Arg?Ser?Leu?Ser?Ser?Leu
100 105 110
Ile?Ile?His?Ser?Thr?Arg?Pro?Arg?Ala?Ile?Arg?Ile?Arg?Thr?Asp?Gln
115 120 125
Met?Asp?Leu?Asn?Gly?Asp?Ala?Gly?Ala?Lys?Arg?Lys?Arg?Ser?Ser?Ile
130 135 140
Thr?Thr?Pro?Ala?Glu?Arg?Pro?Val?Lys?His?Leu?Arg?Pro?Glu?Ser?Ser
145 150 155 160
Ala?Leu?Thr?Pro?Gly?Asp?Ser?Thr?Pro?Ala?Asn?Gly?Thr?Val?Tyr?Asp
165 170 175
Val?Glu?Asp?Asp?Glu?Asp?Ala?Ser?Arg?Leu?Leu?Pro?Val?Gly?Pro?Ala
180 185 190
Gln?Ala?Asp?Ser?Pro?Glu?Trp?Gln?Ala?Thr?Ile?Glu?Glu?Val?Val?Lys
195 200 205
Ser?Val?Val?Ser?Ile?His?Phe?Cys?Gln?Thr?Cys?Ser?Phe?Asp?Thr?Glu
210 215 220
Leu?Ser?Met?Ser?Ser?Gln?Ala?Thr?Gly?Phe?Val?Val?Asp?Ala?Glu?Asn
225 230 235 240
Gly?Tyr?Ile?Leu?Thr?Asn?Arg?His?Val?Val?Cys?Pro?Gly?Pro?Phe?Trp
245 250 255
Gly?Tyr?Cys?Ile?Phe?Asp?Asn?His?Glu?Glu?Cys?Asp?Val?Arg?Pro?Val
260 265 270
Tyr?Arg?Asp?Pro?Val?His?Asp?Phe?Gly?Ile?Leu?Lys?Phe?Asp?Pro?Lys
275 280 285
Ala?Ile?Arg?Tyr?Met?Lys?Leu?Arg?Glu?Leu?Lys?Leu?Gln?Pro?Asp?Ala
290 295 300
Ala?Lys?Val?Gly?Ser?Glu?Ile?Arg?Val?Val?Gly?Asn?Asp?Ala?Gly?Glu
305 310 315 320
Lys?Leu?Ser?Ile?Leu?Ser?Gly?Val?Ile?Ser?Arg?Leu?Asp?Arg?Asn?Ala
325 330 335
Pro?Glu?Tyr?Gly?Asp?Gly?Tyr?Ser?Asp?Phe?Asn?Thr?Asn?Tyr?Ile?Gln
340 345 350
Ala?Ala?Ala?Ala?Ala?Ser?Gly?Gly?Ser?Ser?Gly?Ser?Pro?Val?Val?Asn
355 360 365
Ile?Asp?Gly?His?Ala?Ile?Ala?Leu?Gln?Ala?Gly?Gly?Arg?Ala?Asp?Gly
370 375 380
Ala?Ala?Thr?Asp?Tyr?Phe?Leu?Pro?Leu?Asp?Arg?Pro?Leu?Arg?Ala?Leu
385 390 395 400
Glu?Cys?Ile?Arg?Arg?Gly?Glu?Pro?Val?Thr?Arg?Gly?Thr?Ile?Gln?Thr
405 410 415
Gln?Trp?Ile?Leu?Lys?Pro?Phe?Asp?Glu?Cys?Arg?Arg?Leu?Gly?Leu?Thr
420 425 430
Pro?Glu?Trp?Glu?Ala?Thr?Val?Arg?Lys?Ala?Ala?Pro?Thr?Glu?Thr?Ser
435 440 445
Met?Leu?Val?Ala?Glu?Ile?Ile?Leu?Pro?Glu?Gly?Pro?Ala?Asp?Gly?Lys
450 455 460
Leu?Glu?Glu?Gly?Asp?Val?Leu?Leu?Gln?Val?Asn?Gly?Val?Leu?Leu?Thr
465 470 475 480
Gln?Phe?Ile?Arg?Leu?Asp?Asp?Ile?Leu?Asp?Ser?Ser?Val?Gly?Gln?Thr
485 490 495
Val?Arg?Leu?Leu?Val?Gln?Arg?Gly?Gly?Gln?Asn?Val?Glu?Ile?Glu?Cys
500 505 510
Gln?Val?Gly?Asp?Leu?His?Ala?Ile?Thr?Pro?Asp?Arg?Phe?Val?Thr?Val
515 520 525
Ala?Gly?Gly?Thr?Phe?His?Asn?Leu?Ser?Tyr?Gln?Gln?Ser?Arg?Leu?Tyr
530 535 540
Ala?Ile?Ala?Thr?Arg?Gly?Val?Tyr?Val?Cys?Glu?Ala?Ala?Gly?Ser?Phe
545 550 555 560
Lys?Leu?Glu?Asn?Thr?Leu?Ser?Gly?Trp?Ile?Ile?Asp?Ser?Val?Asp?Lys
565 570 575
Arg?Pro?Thr?Arg?Asn?Leu?Asp?Glu?Phe?Val?Glu?Val?Met?Arg?Thr?Ile
580 585 590
Pro?Asp?Arg?Ser?Arg?Val?Val?Ile?Ser?Tyr?Arg?His?Ile?Arg?Asp?Leu
595 600 605
His?Thr?Arg?Gly?Thr?Ser?Ile?Val?Tyr?Ile?Asp?Arg?His?Trp?His?Pro
610 615 620
Lys?Met?Arg?Leu?Ala?Val?Arg?Asn?Asp?Asp?Thr?Gly?Leu?Trp?Asp?Phe
625 630 635 640
Ser?Asp?Leu?Ala?Asp?Pro?Ile?Pro?Ala?Leu?Pro?Pro?Val?Pro?Arg?Lys
645 650 655
Ala?Asp?Phe?Ile?Gln?Leu?Asp?Gly?Val?Ser?Gln?Pro?Ala?Ala?Ala?Asp
660 665 670
Ile?Val?Arg?Ser?Phe?Val?Arg?Val?Ser?Cys?Thr?Met?Pro?Leu?Lys?Leu
675 680 685
Asp?Gly?Tyr?Pro?Gln?Ala?Lys?Lys?Thr?Gly?Phe?Gly?Leu?Val?Val?Asp
690 695 700
Ala?Glu?Lys?Gly?Leu?Val?Val?Val?Ser?Arg?Ala?Ile?Val?Pro?Tyr?Asp
705 710 715 720
Leu?Cys?Asp?Ile?Asn?Val?Thr?Val?Ala?Asp?Ser?Ile?Ile?Val?Asn?Ala
725 730 735
Lys?Val?Val?Phe?Leu?His?Pro?Leu?Gln?Asn?Tyr?Ser?Ile?Ile?Gln?Tyr
740 745 750
Asp?Pro?Ser?Leu?Val?Gln?Ala?Pro?Val?Gln?Ser?Ala?Lys?Leu?Ala?Thr
755 760 765
Asp?Tyr?Ile?Lys?Gln?Gly?Gln?Asp?Thr?Ile?Phe?Val?Gly?Phe?Asn?Gln
770 775 780
Asn?Phe?Arg?Ile?Val?Val?Ala?Lys?Thr?Ala?Val?Thr?Asp?Ile?Thr?Thr
785 790 795 800
Val?Ser?Ile?Pro?Ala?Asn?Ala?Ser?Ala?Pro?Arg?Tyr?Arg?Ala?Ile?Asn
805 810 815
Leu?Asp?Ala?Ile?Thr?Val?Asp?Thr?Gly?Leu?Ser?Gly?Gln?Cys?Ser?Asn
820 825 830
Gly?Val?Leu?Ile?Gly?Glu?Asp?Gly?Val?Val?Gln?Ala?Leu?Trp?Leu?Asn
835 840 845
Tyr?Leu?Gly?Glu?Arg?Thr?Ser?Asn?Ser?His?Lys?Asp?Val?Glu?Tyr?His
850 855 860
Leu?Gly?Phe?Ala?Thr?Pro?Ser?Leu?Leu?Pro?Val?Leu?Ser?Lys?Val?Gln
865 870 875 880
Gln?Gly?Glu?Met?Pro?Glu?Leu?Arg?Ile?Leu?Asn?Met?Glu?Ser?Tyr?Val
885 890 895
Val?Gln?Met?Ser?Gln?Ala?Arg?Ile?Met?Gly?Val?Ser?Glu?Glu?Trp?Ile
900 905 910
Glu?Lys?Val?Thr?Gln?Ala?Asn?Pro?Ser?Arg?His?Gln?Leu?Phe?Met?Val
915 920 925
Arg?Lys?Val?Asp?Cys?Pro?Pro?Pro?Gly?Phe?Asn?Ser?Ala?Ala?Asp?Thr
930 935 940
Phe?Glu?Glu?Gly?Asp?Ile?Ile?Leu?Thr?Leu?Asp?Gly?Gln?Leu?Ile?Thr
945 950 955 960
Arg?Val?Ser?Glu?Leu?Asp?Ile?Met?Tyr?Glu?Lys?Asp?Thr?Leu?Glu?Ala
965 970 975
Leu?Ile?Val?Arg?Asn?Gly?Gln?Glu?Met?Arg?Ile?Gln?Val?Pro?Thr?Val
980 985 990
Pro?Thr?Glu?Asp?Leu?Glu?Thr?Asp?Arg?Ala?Val?Val?Phe?Cys?Gly?Ala
995 1000 1005
Val?Leu?Gln?Lys?Pro?His?His?Ala?Val?Arg?Gln?Gln?Ile?Ser?Lys
1010 1015 1020
Leu?His?Ser?Glu?Val?Tyr?Val?Ser?Ala?Arg?Ser?Arg?Gly?Ser?Pro
1025 1030 1035
Ser?Tyr?Gln?Tyr?Gly?Leu?Ala?Pro?Thr?Asn?Phe?Ile?Thr?Ala?Val
1040 1045 1050
Asn?Gly?Val?Pro?Thr?Pro?Asn?Leu?Asp?Arg?Phe?Ser?Glu?Glu?Val
1055 1060 1065
Ser?Lys?Ile?Pro?Asp?Asn?Thr?Tyr?Phe?Arg?Leu?Arg?Ala?Val?Thr
1070 1075 1080
Phe?Asp?Asn?Val?Pro?Trp?Val?Val?Thr?Val?Lys?Lys?Asn?Asp?His
1085 1090 1095
Tyr?Phe?Pro?Met?Ser?Glu?Tyr?Ile?Lys?Asp?Gln?Ser?Gln?Pro?Ser
1100 1105 1110
Gly?Trp?Arg?Thr?Val?Ser?His?Asp?Lys?Asp?Lys?Tyr?Lys?Asp?Gly
1115 1120 1125
Ile?Ala?Pro?Asp?Ala?Ala?Asn?Leu?Asn?Pro?Asp?Ala?Met?Asp?Glu
1130 1135 1140
Gly?Phe?Asp?Gly?Val?Ser?Asp?Ile?Glu?Pro?Asp?Leu?Glu
1145 1150 1155
<210>121
<211>536
<212>PRT
<213〉aspergillus niger
<400>121
Met?Arg?Val?Leu?Pro?Ala?Ala?Met?Leu?Val?Gly?Ala?Ala?Thr?Ala?Ala
1 5 10 15
Val?Pro?Pro?Phe?Gln?Gln?Val?Leu?Gly?Gly?Asn?Gly?Ala?Lys?His?Gly
20 25 30
Ala?Asp?His?Ala?Ala?Glu?Val?Pro?Ala?Asp?His?Ser?Ala?Asp?Gly?Phe
35 40 45
Ser?Lys?Pro?Leu?His?Ala?Phe?Gln?Glu?Glu?Leu?Lys?Ser?Leu?Ser?Asp
50 55 60
Glu?Ala?Arg?Lys?Leu?Trp?Asp?Glu?Val?Ala?Ser?Phe?Phe?Pro?Glu?Ser
65 70 75 80
Met?Asp?Gln?Asn?Pro?Leu?Phe?Ser?Leu?Pro?Lys?Lys?His?Asn?Arg?Arg
85 90 95
Pro?Asp?Ser?His?Trp?Asp?His?Ile?Val?Asp?Gly?Lys?Leu?Glu?Ala?Tyr
100 105 110
Asp?Leu?Arg?Val?Lys?Lys?Thr?Asp?Pro?Gly?Ser?Leu?Gly?Ile?Asp?Pro
115 120 125
Gly?Val?Lys?Gln?Tyr?Thr?Gly?Tyr?Leu?Asp?Asp?Asn?Glu?Asn?Asp?Lys
130 135 140
His?Leu?Phe?Tyr?Trp?Phe?Phe?Glu?Ser?Arg?Asn?Asp?Pro?Glu?Asn?Asp
145 150 155 160
Pro?Val?Val?Leu?Trp?Leu?Asn?Gly?Gly?Pro?Gly?Cys?Ser?Ser?Leu?Thr
165 170 175
Gly?Leu?Phe?Met?Glu?Leu?Gly?Pro?Ser?Ser?Ile?Asn?Lys?Lys?Ile?Gln
180 185 190
Pro?Val?Tyr?Asn?Asp?Tyr?Ala?Trp?Asn?Ser?Asn?Ala?Ser?Val?Ile?Phe
195 200 205
Leu?Asp?Gln?Pro?Val?Asn?Val?Gly?Tyr?Ser?Tyr?Ser?Asn?Ser?Ala?Val
210 215 220
Ser?Asp?Thr?Val?Ala?Ala?Gly?Lys?Asp?Val?Tyr?Ala?Leu?Leu?Thr?Leu
225 230 235 240
Phe?Phe?Lys?Gln?Phe?Pro?Glu?Tyr?Ala?Lys?Gln?Asp?Phe?His?Ile?Ala
245 250 255
Gly?Glu?Ser?Tyr?Ala?Gly?His?Tyr?Ile?Pro?Val?Phe?Ala?Ser?Glu?Ile
260 265 270
Leu?Ser?His?Lys?Lys?Arg?Asn?Ile?Asn?Leu?Gln?Ser?Val?Leu?Ile?Gly
275 280 285
Asn?Gly?Leu?Thr?Asp?Gly?Tyr?Thr?Gln?Tyr?Glu?Tyr?Tyr?Arg?Pro?Met
290 295 300
Ala?Cys?Gly?Asp?Gly?Gly?Tyr?Pro?Ala?Val?Leu?Asp?Glu?Ser?Ser?Cys
305 310 315 320
Gln?Ser?Met?Asp?Asn?Ala?Leu?Pro?Arg?Cys?Gln?Ser?Met?Ile?Glu?Ser
325 330 335
Cys?Tyr?Ser?Ser?Glu?Ser?Ala?Trp?Val?Cys?Val?Pro?Ala?Ser?Ile?Tyr
340 345 350
Cys?Asn?Asn?Ala?Leu?Leu?Ala?Pro?Tyr?Gln?Arg?Thr?Gly?Gln?Asn?Val
355 360 365
Tyr?Asp?Val?Arg?Gly?Lys?Cys?Glu?Asp?Ser?Ser?Asn?Leu?Cys?Tyr?Ser
370 375 380
Ala?Met?Gly?Tyr?Val?Ser?Asp?Tyr?Leu?Asn?Lys?Pro?Glu?Val?Ile?Glu
385 390 395 400
Ala?Val?Gly?Ala?Glu?Val?Asn?Gly?Tyr?Asp?Ser?Cys?Asn?Phe?Asp?Ile
405 410 415
Asn?Arg?Asn?Phe?Leu?Phe?His?Gly?Asp?Trp?Met?Lys?Pro?Tyr?His?Arg
420 425 430
Leu?Val?Pro?Gly?Leu?Leu?Glu?Gln?Ile?Pro?Val?Leu?Ile?Tyr?Ala?Gly
435 440 445
Asp?Ala?Asp?Phe?Ile?Cys?Asn?Trp?Leu?Gly?Asn?Lys?Ala?Trp?Thr?Glu
450 455 460
Ala?Leu?Glu?Trp?Pro?Gly?Gln?Ala?Glu?Tyr?Ala?Ser?Ala?Glu?Leu?Glu
465 470 475 480
Asp?Leu?Val?Ile?Val?Asp?Asn?Glu?His?Thr?Gly?Lys?Lys?Ile?Gly?Gln
485 490 495
Val?Lys?Ser?His?Gly?Asn?Phe?Thr?Phe?Met?Arg?Leu?Tyr?Gly?Gly?Gly
500 505 510
His?Met?Val?Pro?Met?Asp?Gln?Pro?Glu?Ser?Ser?Leu?Glu?Phe?Phe?Asn
515 520 525
Arg?Trp?Leu?Gly?Gly?Glu?Trp?Phe
530 535
<210>122
<211>279
<212>PRT
<213〉aspergillus niger
<400>122
Met?Lys?Phe?Thr?Asn?Tyr?Leu?Leu?Thr?Thr?Ala?Thr?Leu?Ala?Ser?Ser
1 5 10 15
Val?Leu?Ala?Ala?Pro?Ala?Pro?Arg?Thr?Gly?Leu?Glu?Asp?Arg?Leu?Arg
20 25 30
Ala?Arg?Ser?Leu?Gln?Arg?Gln?Ser?His?Pro?Leu?Ala?Pro?Ile?Pro?Leu
35 40 45
Asp?Thr?Ser?Thr?Lys?Glu?Asn?Ser?Arg?Leu?Leu?Glu?Ala?Asp?Glu?Asn
50 55 60
Thr?Thr?His?Val?Thr?Tyr?Ser?Ser?Asn?Trp?Ala?Gly?Ala?Val?Arg?Glu
65 70 75 80
Gln?Pro?Pro?Pro?Gln?Gly?Thr?Tyr?Ser?Ala?Val?Ser?Ala?Thr?Phe?Arg
85 90 95
Val?Pro?Glu?Pro?Thr?Ala?Gln?Gly?Gly?Ser?Gly?Thr?Gln?Ala?Gly?Ser
100 105 110
Ala?Trp?Val?Gly?Ile?Asp?Gly?Asp?Thr?Tyr?Ser?Asn?Ala?Ile?Leu?Gln
115 120 125
Thr?Gly?Val?Asp?Phe?Tyr?Val?Glu?Asn?Gly?Gln?Thr?Tyr?Asn?Asp?Ala
130 135 140
Trp?Tyr?Glu?Trp?Tyr?Pro?Asp?Tyr?Ala?Tyr?Asp?Phe?Asp?Leu?Asp?Val
145 150 155 160
Ser?Thr?Gly?Asp?Thr?Ile?Val?Ala?Lys?Val?Glu?Ala?Ile?Ser?Pro?Ser
165 170 175
Gln?Gly?Val?Ala?Thr?Ile?Glu?Asn?Ile?Ser?Thr?Gly?Lys?Lys?Ala?Thr
180 185 190
Gln?Thr?Ile?Arg?Ala?Pro?Ala?Ala?Thr?Ala?Thr?Leu?Ala?Gly?Gln?Asn
195 200 205
Ala?Asp?Trp?Ile?Val?Glu?Asp?Phe?Gln?Ser?Gly?Asp?Ser?Met?Val?Asp
210 215 220
Leu?Ala?Gly?Phe?Gly?Glu?Ile?Ser?Phe?Trp?Gly?Val?Gln?Ala?Gln?Gly
225 230 235 240
Gly?Gly?Ser?Thr?Trp?Gly?Val?Asp?Asp?Ala?Thr?Ile?Val?Glu?Leu?Lys
245 250 255
Gln?Gly?Asn?Glu?Val?Leu?Thr?Asp?Val?Glu?Val?Gln?Ser?Asp?Ser?Ala
260 265 270
Phe?Thr?Val?Lys?Tyr?Thr?Ser
275
<210>123
<211>573
<212>PRT
<213〉aspergillus niger
<400>123
Met?Ile?Tyr?Val?Asn?Tyr?Ile?Leu?Gly?Leu?Leu?Ser?Leu?Leu?His?Thr
1 5 10 15
Ala?Val?Ala?Thr?Ala?Pro?Asp?Tyr?Val?Val?Val?Asp?Gln?Leu?Asn?Ser
20 25 30
Ile?Pro?Asp?Gly?Trp?Thr?Lys?Gly?Ala?Ala?Pro?Pro?Pro?Phe?Thr?Pro
35 40 45
Met?Lys?Phe?Trp?Leu?Ser?Met?His?His?Glu?Tyr?Lys?Ala?Asp?Phe?Glu
50 55 60
Gln?Lys?Val?Ile?Asp?Ile?Ser?Thr?Pro?Gly?His?Arg?Asp?Tyr?Gly?Arg
65 70 75 80
His?Met?Lys?Arg?Asn?Asp?Val?Met?Ala?Phe?Met?Arg?Pro?Ser?Asp?Gln
85 90 95
Val?Ser?Lys?Ile?Ile?Phe?Ser?Trp?Leu?Glu?Ser?Glu?His?Val?Pro?Pro
100 105 110
Asn?Ala?Ile?Glu?Asp?Arg?Gly?Asp?Trp?Val?Ala?Phe?Thr?Val?Pro?Leu
115 120 125
Ala?Gln?Ala?Gln?Ser?Met?Met?Lys?Thr?Asp?Phe?Tyr?Asn?Phe?His?His
130 135 140
Leu?Glu?Thr?Asn?Thr?Thr?Gln?Ile?Arg?Thr?Leu?Lys?Tyr?Ser?Val?Pro
145 150 155 160
Glu?Gln?Val?Asp?Ala?His?Leu?Gln?Met?Ile?Gln?Pro?Thr?Thr?Arg?Phe
165 170 175
Gly?Arg?Pro?Lys?Thr?Gln?Thr?Ser?Leu?Pro?Ser?Leu?Met?Pro?Val?Ser
180 185 190
Val?Asn?Ile?Asp?Glu?Ile?Ser?Glu?Asp?Cys?Leu?Thr?Gly?Val?Thr?Pro
195 200 205
Ile?Cys?Leu?Arg?Gln?Leu?Tyr?Gly?Leu?Pro?Ser?Thr?Lys?Ala?Ser?Pro
210 215 220
Asp?Ser?Arg?Asn?Val?Leu?Gly?Ile?Ser?Gly?Tyr?Leu?Asp?Gln?Tyr?Ala
225 230 235 240
Arg?Tyr?Ser?Asp?Leu?Asp?Glu?Phe?Leu?Ala?Val?Tyr?Ser?Pro?Asn?Ser
245 250 255
Val?Asp?Ala?Asp?Phe?Ser?Val?Val?Ser?Ile?Asn?Gly?Gly?Gln?Asn?Pro
260 265 270
Gln?Asn?Ser?Gln?Glu?Gly?Ser?Thr?Glu?Ala?Ser?Leu?Asp?Ile?Gln?Tyr
275 280 285
Ala?Leu?Ser?Met?Ala?Phe?Asp?Ala?Asn?Ala?Thr?Phe?Tyr?Thr?Thr?Ala
290 295 300
Gly?Arg?Ala?Pro?Ser?Pro?Tyr?Leu?Glu?Gln?Leu?Gln?Tyr?Leu?Val?Gly
305 310 315 320
Leu?Pro?Asp?Glu?Asp?Leu?Pro?Ala?Val?Leu?Ser?Thr?Ser?Tyr?Gly?Glu
325 330 335
Asp?Glu?Gln?Ser?Leu?Pro?Glu?Glu?Tyr?Thr?Glu?Ala?Thr?Cys?Asn?Leu
340 345 350
Phe?Ala?Gln?Leu?Gly?Ala?Arg?Gly?Val?Ser?Val?Ile?Phe?Ser?Ser?Gly
355 360 365
Asp?Ser?Gly?Val?Gly?Gly?Ser?Cys?Val?Ser?Asn?Asp?Gly?Ser?Gln?Arg
370 375 380
Thr?Arg?Phe?Gln?Pro?Ile?Phe?Pro?Ala?Ser?Cys?Pro?Phe?Val?Thr?Ser
385 390 395 400
Val?Gly?Gly?Thr?Glu?Gly?Val?Gly?Pro?Glu?Lys?Ala?Val?Asp?Phe?Ser
405 410 415
Ser?Gly?Gly?Phe?Ser?Glu?Arg?Phe?Ala?Arg?Pro?Ser?Tyr?Gln?Asn?Ala
420 425 430
Ser?Val?Glu?Ala?Tyr?Leu?Ala?Arg?Leu?Gly?Asp?Lys?Trp?Asp?Gly?Leu
435 440 445
Tyr?Asn?Pro?Asp?Gly?Arg?Gly?Ile?Pro?Asp?Val?Ser?Ala?Gln?Ala?Ser
450 455 460
Asn?Tyr?Val?Ile?Arg?Asp?His?Gly?Gln?Trp?Leu?Gln?Thr?Ala?Gly?Thr
465 470 475 480
Ser?Ala?Ala?Ala?Pro?Val?Phe?Ala?Ala?Val?Ile?Ser?Arg?Leu?Asn?Ala
485 490 495
Ala?Arg?Leu?Glu?Gln?Gly?Lys?Pro?Thr?Leu?Gly?Phe?Leu?Asn?Pro?Trp
500 505 510
Leu?Tyr?Ser?Leu?Asp?Gln?Gln?Gly?Phe?Thr?Asp?Ile?Val?Asp?Gly?Gly
515 520 525
Ser?Val?Gly?Cys?Asp?Gly?Ser?Asn?Gly?Gly?Ala?Leu?Val?Pro?Tyr?Ala
530 535 540
Ser?Trp?Asn?Ala?Thr?Lys?Gly?Trp?Asp?Pro?Val?Thr?Gly?Leu?Gly?Thr
545 550 555 560
Pro?Leu?Tyr?Gln?Thr?Leu?Glu?Gln?Leu?Ala?Gln?Ser?Ala
565 570
<210>124
<211>585
<212>PRT
<213〉aspergillus niger
<400>124
Met?Arg?Ser?Ser?Gly?Leu?Tyr?Thr?Ala?Leu?Leu?Cys?Ser?Leu?Ala?Ala
1 5 10 15
Ser?Thr?Asn?Ala?Ile?Val?His?Glu?Lys?Leu?Ala?Ala?Val?Pro?Ser?Gly
20 25 30
Trp?His?His?Val?Glu?Asp?Ala?Gly?Ser?Asp?His?Gln?Ile?Ser?Leu?Ser
35 40 45
Ile?Ala?Leu?Ala?Arg?Lys?Asn?Leu?Asp?Gln?Leu?Glu?Ser?Lys?Leu?Lys
50 55 60
Asp?Leu?Ser?Thr?Pro?Gly?Glu?Ser?Gln?Tyr?Gly?Gln?Trp?Leu?Asp?Gln
65 70 75 80
Glu?Asp?Val?Asp?Thr?Leu?Phe?Pro?Val?Ala?Ser?Asp?Lys?Ala?Val?Ile
85 90 95
Asn?Trp?Leu?Arg?Ser?Ala?Asn?Ile?Thr?His?Ile?Ser?Arg?Gln?Gly?Ser
100 105 110
Leu?Val?Asn?Phe?Ala?Thr?Thr?Val?Asp?Lys?Val?Asn?Lys?Leu?Leu?Asn
115 120 125
Ala?Thr?Phe?Ala?Tyr?Tyr?Gln?Ser?Gly?Ser?Ser?Gln?Arg?Leu?Arg?Thr
130 135 140
Thr?Glu?Tyr?Ser?Ile?Pro?Asp?Asp?Leu?Val?Asp?Ser?Ile?Asp?Leu?Ile
145 150 155 160
Ser?Pro?Thr?Thr?Phe?Phe?Gly?Lys?Glu?Lys?Thr?Thr?Ala?Gly?Leu?Asn
165 170 175
Gln?Arg?Ala?Gln?Lys?Ile?Asp?Thr?His?Val?Ala?Lys?Arg?Ser?Asn?Ser
180 185 190
Ser?Ser?Cys?Ala?Asp?Val?Ile?Thr?Leu?Ser?Cys?Leu?Lys?Glu?Met?Tyr
195 200 205
Asn?Phe?Gly?Asn?Tyr?Thr?Pro?Ser?Ala?Ser?Ser?Gly?Ser?Lys?Leu?Gly
210 215 220
Phe?Gly?Ser?Phe?Leu?Asn?Glu?Ser?Ala?Ser?Tyr?Ser?Asp?Leu?Ala?Lys
225 230 235 240
Phe?Glu?Lys?Leu?Phe?Asn?Leu?Pro?Ser?Gln?Ser?Phe?Ser?Val?Glu?Leu
245 250 255
Val?Asn?Gly?Gly?Val?Asn?Asp?Gln?Asn?Gln?Ser?Thr?Ala?Ser?Leu?Thr
260 265 270
Glu?Ala?Asp?Leu?Asp?Val?Glu?Leu?Leu?Val?Gly?Val?Ala?His?Pro?Leu
275 280 285
Pro?Val?Thr?Glu?Phe?Ile?Thr?Ser?Gly?Glu?Pro?Ala?Ala?Asp?Asn?Glu
290 295 300
Asn?Glu?Pro?Tyr?Leu?Gln?Tyr?Tyr?Glu?Tyr?Leu?Leu?Ser?Lys?Pro?Asn
305 310 315 320
Ser?Ala?Leu?Pro?Gln?Val?Ile?Ser?Asn?Ser?Tyr?Gly?Asp?Asp?Glu?Gln
325 330 335
Thr?Val?Pro?Glu?Tyr?Tyr?Ala?Lys?Arg?Val?Cys?Asn?Leu?Ile?Gly?Leu
340 345 350
Val?Gly?Leu?Arg?Gly?Ile?Ser?Val?Leu?Glu?Ser?Ser?Gly?Asp?Glu?Gly
355 360 365
Ile?Gly?Ser?Gly?Cys?Arg?Thr?Thr?Asp?Gly?Thr?Asn?Arg?Thr?Gln?Phe
370 375 380
Asn?Pro?Ile?Phe?Pro?Ala?Thr?Cys?Pro?Tyr?Val?Thr?Ala?Val?Gly?Gly
385 390 395 400
Thr?Met?Ser?Tyr?Ala?Pro?Glu?Ile?Ala?Trp?Glu?Ala?Ser?Ser?Gly?Gly
405 410 415
Phe?Ser?Asn?Tyr?Phe?Glu?Arg?Ala?Trp?Phe?Gln?Lys?Glu?Ala?Val?Gln
420 425 430
Asn?Tyr?Leu?Ala?His?His?Ile?Thr?Asn?Glu?Thr?Lys?Gln?Tyr?Tyr?Ser
435 440 445
Gln?Phe?Ala?Asn?Phe?Ser?Gly?Arg?Gly?Phe?Pro?Asp?Val?Ala?Ala?His
450 455 460
Ser?Phe?Glu?Pro?Ser?Tyr?Glu?ValIle?Phe?Tyr?Gly?Ala?Arg?Tyr?Gly
465 470 475 480
Ser?Gly?Gly?Thr?Ser?Ala?Ala?Cys?Pro?Leu?Phe?Ser?Ala?Leu?Val?Gly
485 490 495
Met?Leu?Asn?Asp?Ala?Arg?Leu?Arg?Ala?Gly?Lys?Ser?Thr?Leu?Gly?Phe
500 505 510
Leu?Asn?Pro?Leu?Leu?Tyr?Ser?Lys?Gly?Tyr?Arg?Ala?Leu?Thr?Asp?Val
515 520 525
Thr?Gly?Gly?Gln?Ser?Ile?Gly?Cys?Asn?Gly?Ile?Asp?Pro?Gln?Asn?Asp
530 535 540
Glu?Thr?Val?Ala?Gly?Ala?Gly?Ile?Ile?Pro?Trp?Ala?His?Trp?Asn?Ala
545 550 555 560
Thr?Val?Gly?Trp?Asp?Pro?Val?Thr?Gly?Leu?Gly?Leu?Pro?Asp?Phe?Glu
565 570 575
Lys?Leu?Arg?Gln?Leu?Val?Leu?Ser?Leu
580 585
<210>125
<211>265
<212>PRT
<213〉aspergillus niger
<400>125
Met?Lys?Thr?Thr?Ala?Leu?Leu?Thr?Ala?Gly?Leu?Leu?Ala?Thr?Thr?Ala
1 5 10 15
Met?Ala?Ala?Pro?Leu?Thr?Ala?Lys?Arg?Gln?Ala?Ala?Arg?Ala?Lys?Arg
20 25 30
Ser?Thr?Asn?Arg?Gln?Ser?Asn?Pro?Pro?Phe?Lys?Pro?Gly?Thr?Asn?Glu
35 40 45
Val?Leu?Ala?Leu?Asn?Gly?Thr?Lys?Asn?Val?Glu?Tyr?Ser?Ser?Asn?Trp
50 55 60
Ala?Gly?Ala?Val?Leu?Ile?Gly?Thr?Gly?Tyr?Thr?Ala?Val?Thr?Ala?Glu
65 70 75 80
Phe?Val?Val?Pro?Thr?Pro?Ser?Val?Pro?Ser?Gly?Gly?Ser?Ser?Arg?Glu
85 90 95
Glu?Tyr?Cys?Ala?Ser?Ala?Trp?Val?Gly?Ile?Asp?Gly?Asp?Thr?Cys?Asp
100 105 110
Thr?Ala?Ile?Leu?Gln?Thr?Gly?Val?Asp?Phe?Cys?Val?Gln?Gly?Ser?Glu
115 120 125
Val?Ser?Phe?Asp?Ala?Trp?Tyr?Glu?Trp?Tyr?Pro?Asp?Tyr?Ala?Tyr?Asp
130 135 140
Phe?Ser?Gly?Ile?Ser?Ile?Ser?Ala?Gly?Asp?Thr?Ile?Lys?Val?Thr?Val
145 150 155 160
Asp?Ala?Ser?Ser?Asp?Thr?Thr?Gly?Thr?Ala?Thr?Ile?Glu?Asn?Val?Ser
165 170 175
Thr?Gly?Thr?Thr?Val?Thr?His?Ser?Phe?Thr?Gly?Gly?Val?Asp?Gly?Asp
180 185 190
Leu?Cys?Glu?Tyr?Asn?Ala?Glu?Trp?Ile?Val?Glu?Asp?Phe?Glu?Glu?Asp
195 200 205
Asp?Ser?Leu?Val?Pro?Phe?Ala?Asp?Phe?Gly?Thr?Val?Thr?Phe?Thr?Ser
210 215 220
Cys?Ser?Ala?Thr?Lys?Asp?Gly?Ser?Ser?Val?Gly?Pro?Glu?Asp?Ala?Thr
225 230 235 240
Ile?Ile?Asp?Ile?Glu?Gln?Asn?Glu?Val?Leu?Thr?Ser?Val?Ser?Val?Ser
245 250 255
Ser?Ser?Glu?Val?Val?Val?Lys?Tyr?Val
260 265
<210>126
<211>580
<212>PRT
<213〉aspergillus niger
<400>126
Met?Val?Ala?Phe?Ser?Arg?Ile?Ser?Ala?Gly?Phe?Ala?Leu?Ala?Ala?Pro
1 5 10 15
Ala?Leu?Ala?Ser?Val?Val?Leu?Glu?Thr?Val?Lys?Ser?Val?Pro?Ser?Asp
20 25 30
Trp?Lys?Leu?Val?Glu?Ala?Ala?Asp?Thr?Ser?Ser?Thr?Ile?Ser?Leu?Ser
35 40 45
Val?Ala?Leu?Ala?Arg?Gln?Asn?Leu?Asp?Gln?Leu?Glu?Glu?Lys?Leu?Leu
50 55 60
Ala?Val?Ser?Thr?Pro?Gly?Lys?Asp?Thr?Tyr?Gly?Gln?Phe?Leu?Asp?Leu
65 70 75 80
Asp?Asp?Ile?Asn?Glu?Gln?Phe?Pro?Leu?Ala?Asp?Asp?Ala?Ala?Val?Val
85 90 95
Ala?Trp?Leu?Lys?Lys?Ala?Gly?Val?Thr?Gln?Ile?His?Lys?Glu?Gly?Gly
100 105 110
Leu?Leu?Asn?Phe?Ala?Thr?Thr?Val?Gly?Thr?Ala?Asn?Gln?Leu?Leu?Asn
115 120 125
Thr?Thr?Phe?Ser?Val?Tyr?Lys?Ser?Gly?Ser?Thr?Gln?Lys?Leu?Arg?Thr
130 135 140
Thr?Gln?Tyr?Ser?Val?Pro?Asp?Glu?Leu?Thr?Gly?Ser?Ile?Asp?Leu?Ile
145 150 155 160
Ser?Pro?Thr?Val?Phe?Phe?Gly?Lys?Ser?Asn?Ala?Ala?Arg?Ser?Ala?Ala
165 170 175
Val?Arg?Ala?Ser?Gln?Thr?Thr?Lys?Glu?Thr?Ser?Arg?Lys?Lys?Ser?Ser
180 185 190
Asn?Val?Cys?Glu?Tyr?Ile?Thr?Pro?Asp?Cys?Leu?Lys?Glu?Gln?Tyr?Ser
195 200 205
Ile?Asp?Tyr?Thr?Pro?Glu?Ala?Ser?Ser?Gly?Ser?Arg?Val?Gly?Phe?Gly
210 215 220
Ser?Phe?Leu?Asn?Glu?Ser?Ala?Leu?Tyr?Ser?Asp?Leu?Asp?Leu?Phe?Thr
225 230 235 240
Gln?Tyr?Phe?Asp?Ile?Pro?Gln?Gln?Ser?Phe?Thr?Val?Glu?Thr?Ile?Asn
245 250 255
Gly?Gly?Ile?Asn?Asn?Gln?Glu?Asn?Asp?Pro?Asp?Gly?Glu?Ala?Asp?Leu
260 265 270
Asp?Val?Gln?Asn?Ile?Val?Gly?Ile?Ser?His?Pro?Leu?Pro?Val?Thr?Glu
275 280 285
Tyr?Ile?Thr?Gly?Gly?Ser?Pro?Pro?Phe?Ile?Pro?Asp?Val?Glu?Thr?Thr
290 295 300
Thr?Asp?Glu?Asn?Glu?Pro?Tyr?Leu?Gln?Tyr?Tyr?Glu?Tyr?Leu?Leu?Ala
305 310 315 320
Lys?Thr?Asn?Asp?Glu?Leu?Pro?Leu?Val?Ile?Ser?Asn?Ser?Tyr?Gly?Asp
325 330 335
Asp?Glu?Asp?Thr?Val?Pro?Ile?Ala?Tyr?Ala?Thr?Arg?Val?Cys?Asn?Leu
340 345 350
Ile?Gly?Leu?Met?Gly?Thr?Arg?Gly?Ile?Ser?Ile?Leu?Glu?Ser?Ser?Gly
355 360 365
Asp?Ser?Gly?Val?Gly?Gly?Ala?Cys?Met?Ser?Asn?Asp?Gly?Thr?Asp?Lys
370 375 380
Thr?Glu?Phe?Thr?Pro?Met?Phe?Pro?Gly?Thr?Cys?Pro?Tyr?Ile?Thr?Ala
385 390 395 400
Val?Gly?Gly?Thr?Gln?Asp?Val?Pro?Glu?Val?Ala?Trp?Val?Asp?Ser?Ser
405 410 415
Gly?Gly?Phe?Ser?Asn?Tyr?Phe?Ser?Gln?Pro?Ser?Tyr?Gln?Ser?Asp?Gln
420 425 430
Val?Glu?Thr?Tyr?Leu?Asp?Lys?Tyr?Ile?Ser?Ala?Ser?Thr?Lys?Lys?Tyr
435 440 445
Tyr?Glu?Gln?Tyr?Thr?Asn?Phe?Ser?Gly?Arg?Ala?Phe?Pro?Asp?Val?Ser
450 455 460
Ala?Phe?Ala?Gly?Ser?Pro?Tyr?Tyr?Glu?Thr?Tyr?Ile?Asp?Gly?Gln?Leu
465 470 475 480
Gly?Leu?Val?Ala?Gly?Thr?Ser?Gly?Ala?Ser?Pro?Val?Phe?Ala?Gly?Ile
485 490 495
Val?Ala?Leu?Leu?Asn?Asp?Ala?Arg?Leu?Arg?Ala?Asn?Lys?Thr?Ser?Leu
500 505 510
Gly?Phe?Leu?Asn?Pro?Trp?Leu?Tyr?Ser?Ser?Gly?Tyr?Lys?Ser?Leu?Asn
515 520 525
Asp?Ile?Thr?Ser?Gly?Glu?Ala?Val?Gly?Cys?Gln?Gly?Asp?Val?Glu?Gly
530 535 540
Ala?Gly?Val?Ile?Pro?Trp?Ala?Ser?Trp?Asn?Ala?Thr?Thr?Gly?Trp?Asp
545 550 555 560
Pro?Ala?Thr?Gly?Leu?Gly?Thr?Pro?Asn?Phe?Ala?Lys?Leu?Lys?Glu?Ala
565 570 575
Val?Leu?Ala?Leu
580
<210>127
<211>631
<212>PRT
<213〉aspergillus niger
<400>127
Met?His?Gly?Leu?Arg?Leu?Val?Cys?Ser?Ile?Gly?Thr?Leu?Pro?Leu?Val
1 5 10 15
Ile?Leu?Ala?Tyr?Pro?Ala?Ala?Ser?Leu?His?Thr?Thr?Ser?Ala?Ala?Val
20 25 30
Asp?Leu?Asp?Ser?Leu?Arg?Leu?Thr?Ser?Asn?Ser?Glu?Tyr?Val?Asn?Ser
35 40 45
Val?His?Val?Asp?Thr?Asn?Arg?Ser?Val?Ala?Val?Ser?Ala?Glu?Glu?His
50 55 60
Tyr?Thr?Asp?Thr?Ala?Ala?Arg?Leu?Val?Gln?Asn?Ile?Val?Pro?Gly?Ala
65 70 75 80
Ser?Phe?Arg?Leu?Ile?Asp?Asp?His?Phe?Val?Gly?Asp?Asn?Gly?Val?Ala
85 90 95
His?Val?Tyr?Phe?Arg?Gln?Thr?Leu?His?Gly?Ile?Asp?Ile?Asp?Asn?Ala
100 105 110
Asp?Phe?Asn?Val?Asn?Ile?Gly?Lys?Asp?Gly?Leu?Val?Leu?Ser?Phe?Gly
115 120 125
His?Ser?Phe?Phe?Thr?Gly?Ala?Leu?Pro?Ser?Ser?His?Leu?Asp?Asn?Thr
130 135 140
Asn?Val?Leu?Ser?Pro?Glu?Ala?Ala?Leu?Arg?Gly?Ala?Arg?Asp?Ala?Ile
145 150 155 160
Gln?Leu?Pro?Leu?Thr?Ile?Asp?Asn?Val?Ser?Thr?Glu?Ala?Ala?Glu?Gly
165 170 175
Arg?Asn?Glu?Tyr?Ile?Phe?Arg?Glu?Ala?Val?Gly?Ala?Val?Ser?Asp?Pro
180 185 190
Lys?Ala?Lys?Leu?Val?Tyr?Leu?Val?Lys?Pro?Glu?Gly?Thr?Leu?Ala?Leu
195 200 205
Thr?Trp?Arg?Ile?Glu?Thr?Asp?Met?Tyr?Glu?His?Trp?Leu?Leu?Thr?Tyr
210 215 220
Ile?Asp?Ala?Glu?Thr?Thr?Thr?Val?His?Gly?Val?Val?Asp?Tyr?Val?Ala
225 230 235 240
Asp?Ala?Thr?Tyr?Gln?Val?Tyr?Pro?Trp?Gly?Thr?Asn?Asp?Pro?Ala?Glu
245 250 255
Gly?His?Arg?Thr?Ile?Val?Thr?Asp?Pro?Trp?Asp?Leu?Ser?Ala?Ser?Ala
260 265 270
Tyr?Thr?Trp?Ile?Ser?Asp?Gly?Arg?Asp?Asn?Tyr?Thr?Thr?Thr?Arg?Gly
275 280 285
Asn?Asn?Ala?Ile?Ala?His?Trp?Asn?Pro?Thr?Gly?Gly?Gly?Ser?Tyr?Leu
290 295 300
Tyr?Asn?Leu?Arg?Pro?Ser?Asp?Pro?Asn?Leu?Asn?Phe?Gln?Trp?Pro?Tyr
305 310 315 320
Ser?Pro?Asn?Met?Ser?Pro?Pro?Arg?Ser?Tyr?Ile?Asn?Ala?Ser?Ile?Val
325 330 335
Gln?Leu?Phe?Tyr?Thr?Ala?Asn?Ala?Tyr?His?Asp?Leu?Leu?Tyr?Thr?Leu
340 345 350
Gly?Phe?Thr?Glu?Ser?Ala?Gly?Asn?Phe?Gln?Trp?Asn?Asn?Ser?Ala?His
355 360 365
Gly?Gly?Arg?Asp?Lys?Asp?Tyr?Val?Ile?Leu?Asn?Ala?Gln?Asp?Gly?Ser
370 375 380
Gly?Phe?Ser?Asn?Ala?Asn?Phe?Ala?Thr?Pro?Pro?Asp?Gly?Ile?Pro?Gly
385 390 395 400
Arg?Met?Arg?Met?Tyr?Ile?Trp?Ile?Glu?Ser?Thr?Pro?Ser?Arg?Asp?Gly
405 410 415
Ser?Phe?Asp?Ala?Gly?Ile?Val?Ile?His?Glu?Tyr?Thr?His?Gly?Val?Ser
420 425 430
Asn?Arg?Leu?Thr?Gly?Gly?Ser?His?Asn?Ala?Gly?Cys?Leu?Ser?Ala?Leu
435 440 445
Glu?Ser?Gly?Gly?Met?Gly?Glu?Gly?Trp?Gly?Asp?Phe?Met?Ala?Thr?Ala
450 455 460
Ile?Arg?Ile?Lys?Pro?Asn?Asp?Thr?Arg?Thr?Thr?Ser?Tyr?Thr?Met?Gly
465 470 475 480
Ala?Trp?Ala?Asp?Asn?Asp?Lys?Cys?Gly?Val?Arg?Asp?Tyr?Pro?Tyr?Ser
485 490 495
Thr?Ser?Phe?Thr?Glu?Asn?Pro?Leu?Asn?Tyr?Thr?Ser?Val?Asn?Thr?Met
500 505 510
Asn?Gly?Val?His?Ala?Ile?Gly?Thr?Val?Trp?Ala?Thr?Met?Leu?Tyr?Glu
515 520 525
Val?Leu?Trp?Asn?Leu?Ile?Asp?Lys?Tyr?Gly?Lys?Asn?Asp?Gly?Ser?Arg
530 535 540
Pro?Val?Phe?Arg?Asn?Gly?Val?Pro?Thr?Asp?Gly?Lys?Tyr?Leu?Met?Met
545 550 555 560
Lys?Leu?Val?Val?Asp?Gly?Met?Ala?Leu?Gln?Pro?Cys?Asn?Pro?Asn?Phe
565 570 575
Val?Gln?Ala?Arg?Asp?Ala?Ile?Leu?Asp?Ala?Asp?Ile?Val?Leu?Thr?Gly
580 585 590
Gly?Lys?Asn?Arg?Cys?Glu?Ile?Trp?Arg?Gly?Phe?Ala?Lys?Arg?Gly?Leu
595 600 605
Gly?Gln?Gly?Ala?Ala?His?Ser?Ser?Leu?Asn?Trp?Met?Arg?Arg?Gly?Ser
610 615 620
Thr?Leu?Leu?Pro?Thr?Gly?Cys
625 630
<210>128
<211>394
<212>PRT
<213〉aspergillus niger
<400>128
Met?Val?Val?Phe?Ser?Lys?Thr?Ala?Ala?Leu?Val?Leu?Gly?Leu?Ser?Ser
1 5 10 15
Ala?Val?Ser?Ala?Ala?Pro?Ala?Pro?Thr?Arg?Lys?Gly?Phe?Thr?Ile?Asn
20 25 30
Gln?Ile?Ala?Arg?Pro?Ala?Asn?Lys?Thr?Arg?Thr?Ile?Asn?Leu?Pro?Gly
35 40 45
Met?Tyr?Ala?Arg?Ser?Leu?Ala?Lys?Phe?Gly?Gly?Thr?Val?Pro?Gln?Ser
50 55 60
Val?Lys?Glu?Ala?Ala?Ser?Lys?Gly?Ser?Ala?Val?Thr?Thr?Pro?Gln?Asn
65 70 75 80
Asn?Asp?Glu?Glu?Tyr?Leu?Thr?Pro?Val?Thr?Val?Gly?Lys?Ser?Thr?Leu
85 90 95
His?Leu?Asp?Phe?Asp?Thr?Gly?Ser?Ala?Asp?Leu?Trp?Val?Phe?Ser?Asp
100 105 110
Glu?Leu?Pro?Ser?Ser?Glu?Gln?Thr?Gly?His?Asp?Leu?Tyr?Thr?Pro?Ser
115 120 125
Ser?Ser?Ala?Thr?Lys?Leu?Ser?Gly?Tyr?Thr?Trp?Asp?Ile?Ser?Tyr?Gly
130 135 140
Asp?Gly?Ser?Ser?Ala?Ser?Gly?Asp?Val?Tyr?Arg?Asp?Thr?Val?Thr?Val
145 150 155 160
Gly?Gly?Val?Thr?Thr?Asn?Lys?Gln?Ala?Val?Glu?Ala?Ala?Ser?Lys?Ile
165 170 175
Ser?Ser?Glu?Phe?Val?Gln?Asn?Thr?Ala?Asn?Asp?Gly?Leu?Leu?Gly?Leu
180 185 190
Ala?Phe?Ser?Ser?Ile?Asn?Thr?Val?Gln?Pro?Lys?Ala?Gln?Thr?Thr?Phe
195 200 205
Phe?Asp?Thr?Val?Lys?Ser?Gln?Leu?Asp?Ser?Pro?Leu?Phe?Ala?Val?Gln
210 215 220
Leu?Lys?His?Asp?Ala?Pro?Gly?Val?Tyr?Asp?Phe?Gly?Tyr?Ile?Asp?Asp
225 230 235 240
Ser?Lys?Tyr?Thr?Gly?Ser?Ile?Thr?Tyr?Thr?Asp?Ala?Asp?Ser?Ser?Gln
245 250 255
Gly?Tyr?Trp?Gly?Phe?Ser?Thr?Asp?Gly?Tyr?Ser?Ile?Gly?Asp?Gly?Ser
260 265 270
Ser?Ser?Ser?Ser?Gly?Phe?Ser?Ala?Ile?Ala?Asp?Thr?Gly?Thr?Thr?Leu
275 280 285
Ile?Leu?Leu?Asp?Asp?Glu?Ile?Val?Ser?Ala?Tyr?Tyr?Glu?Gln?Val?Ser
290 295 300
Gly?Ala?Gln?Glu?Ser?Glu?Glu?Ala?Gly?Gly?Tyr?Val?Phe?Ser?Cys?Ser
305 310 315 320
Thr?Asn?Pro?Pro?Asp?Phe?Thr?Val?Val?Ile?Gly?Asp?Tyr?Lys?Ala?Val
325 330 335
Val?Pro?Gly?Lys?Tyr?Ile?Asn?Tyr?Ala?Pro?Ile?Ser?Thr?Gly?Ser?Ser
340 345 350
Thr?Cys?Phe?Gly?Gly?Ile?Gln?Ser?Asn?Ser?Gly?Leu?Gly?Leu?Ser?Ile
355 360 365
Leu?Gly?Asp?Val?Phe?Leu?Lys?Ser?Gln?Tyr?Val?Val?Phe?Asn?Ser?Glu
370 375 380
Gly?Pro?Lys?Leu?Gly?Phe?Ala?Ala?Gln?Ala
385 390
<210>129
<211>398
<212>PRT
<213〉aspergillus niger
<400>129
Met?Lys?Ser?Ala?Ser?Leu?Leu?Thr?Ala?Ser?Val?Leu?Leu?Gly?Cys?Ala
1 5 10 15
Ser?Ala?Glu?Val?His?Lys?Leu?Lys?Leu?Asn?Lys?Val?Pro?Leu?Glu?Glu
20 25 30
Gln?Leu?Tyr?Thr?His?Asn?Ile?Asp?Ala?His?Val?Arg?Ala?Leu?Gly?Gln
35 40 45
Lys?Tyr?Met?Gly?Ile?Arg?Pro?Ser?Ile?His?Lys?Glu?Leu?Val?Glu?Glu
50 55 60
Asn?Pro?Ile?Asn?Asp?Met?Ser?Arg?His?Asp?Val?Leu?Val?Asp?Asn?Phe
65 70 75 80
Leu?Asn?Ala?Gln?Tyr?Phe?Ser?Glu?Ile?Glu?Leu?Gly?Thr?Pro?Pro?Gln
85 90 95
Lys?Phe?Lys?Val?Val?Leu?Asp?Thr?Gly?Ser?Ser?Asn?Leu?Trp?Val?Pro
100 105 110
Ser?Ser?Glu?Cys?Ser?Ser?Ile?Ala?Cys?Tyr?Leu?His?Asn?Lys?Tyr?Asp
115 120 125
Ser?Ser?Ala?Ser?Ser?Thr?Tyr?His?Lys?Asn?Gly?Ser?Glu?Phe?Ala?Ile
130 135 140
Lys?Tyr?Gly?Ser?Gly?Ser?Leu?Ser?Gly?Phe?Ile?Ser?Gln?Asp?Thr?Leu
145 150 155 160
Lys?Ile?Gly?Asp?Leu?Lys?Val?Lys?Gly?Gln?Asp?Phe?Ala?Glu?Ala?Thr
165 170 175
Asn?Glu?Pro?Gly?Leu?Ala?Phe?Ala?Phe?Gly?Arg?Phe?Asp?Gly?Ile?Leu
180 185 190
Gly?Leu?Gly?Tyr?Asp?Thr?Ile?Ser?Val?Asn?Lys?Ile?Val?Pro?Pro?Phe
195 200 205
Tyr?Asn?Met?Leu?Asp?Gln?Gly?Leu?Leu?Asp?Glu?Pro?Val?Phe?Ala?Phe
210 215 220
Tyr?Leu?Gly?Asp?Thr?Asn?Lys?Glu?Gly?Asp?Glu?Ser?Val?Ala?Thr?Phe
225 230 235 240
Gly?Gly?Val?Asp?Lys?Asp?His?Tyr?Thr?Gly?Glu?Leu?Ile?Lys?Ile?Pro
245 250 255
Leu?Arg?Arg?Lys?Ala?Tyr?Trp?Glu?Val?Glu?Leu?Asp?Ala?Ile?Ala?Leu
260 265 270
Gly?Asp?Asp?Val?Ala?Glu?Met?Glu?Asn?Thr?Gly?Val?Ile?Leu?Asp?Thr
275 280 285
Gly?Thr?Ser?Leu?Ile?Ala?Leu?Pro?Ala?Asp?Leu?Ala?Glu?Met?Ile?Asn
290 295 300
Ala?Gln?Ile?Gly?Ala?Lys?Lys?Gly?Trp?Thr?Gly?Gln?Tyr?Thr?Val?Asp
305 310 315 320
Cys?Asp?Lys?Arg?Ser?Ser?Leu?Pro?Asp?Val?Thr?Phe?Thr?Leu?Ala?Gly
325 330 335
His?Asn?Phe?Thr?Ile?Ser?Ser?Tyr?Asp?Tyr?Thr?Leu?Glu?Val?Gln?Gly
340 345 350
Ser?Cys?Val?Ser?Ala?Phe?Met?Gly?Met?Asp?Phe?Pro?Glu?Pro?Val?Gly
355 360 365
Pro?Leu?Ala?Ile?Leu?Gly?Asp?Ala?Phe?Leu?Arg?Lys?Trp?Tyr?Ser?Val
370 375 380
Tyr?Asp?Leu?Gly?Asn?Ser?Ala?Val?Gly?Leu?Ala?Lys?Ala?Lys
385 390 395
<210>130
<211>393
<212>PRT
<213〉aspergillus niger
<400>130
Met?Arg?Lys?Tyr?Arg?Phe?His?Pro?Thr?Lys?Pro?Gly?Pro?Tyr?Thr?Leu
1 5 10 15
Ser?Ser?Ser?Ile?Gln?Gln?Thr?Gly?Arg?Pro?Tyr?Thr?Glu?Lys?Pro?Ile
20 25 30
Gly?Gly?Arg?Ala?His?Ile?Arg?Gln?Leu?Val?Arg?Lys?Lys?Ser?Thr?Thr
35 40 45
Ser?Asp?Glu?Val?Gly?Glu?Val?Pro?Ala?Glu?Asp?Val?Gln?Asn?Asp?Ser
50 55 60
Met?Tyr?Leu?Ala?Thr?Val?GlyIle?Gly?Thr?Pro?Ala?Gln?Asn?Leu?Lys
65 70 75 80
Leu?Asp?Phe?Asp?Thr?Gly?Ser?Ala?Asp?Leu?Trp?Val?Trp?Ser?Asn?Lys
85 90 95
Leu?Pro?Ser?Thr?Leu?Leu?Ser?Glu?Asn?Lys?Thr?His?Ala?Ile?Phe?Asp
100 105 110
Ser?Ser?Lys?Ser?Ser?Thr?Phe?Lys?Thr?Leu?Glu?Gly?Glu?Ser?Trp?Gln
115 120 125
Ile?Ser?Tyr?Gly?Asp?Gly?Ser?Ser?Ala?Ser?Gly?Ser?Val?Gly?Thr?Asp
130 135 140
Asp?Val?Asn?Ile?Gly?Gly?Val?Val?Val?Lys?Asn?Gln?Ala?Val?Glu?Leu
145 150 155 160
Ala?Glu?Lys?Met?Ser?Ser?Thr?Phe?Ala?Gln?Gly?Glu?Gly?Asp?Gly?Leu
165 170 175
Leu?Gly?Leu?Ala?Phe?Ser?Asn?Ile?Asn?Thr?Val?Gln?Pro?Lys?Ser?Val
180 185 190
Lys?Thr?Pro?Val?Glu?Asn?Met?Ile?Leu?Gln?Asp?Asp?Ile?Pro?Lys?Ser
195 200 205
Ala?Glu?Leu?Phe?Thr?Ala?Lys?Leu?Asp?Thr?Trp?Arg?Asp?Thr?Asp?Asp
210 215 220
Glu?Ser?Phe?Tyr?Thr?Phe?Gly?Phe?Ile?Asp?Gln?Asp?Leu?Val?Lys?Thr
225 230 235 240
Ala?Gly?Glu?Glu?Val?Tyr?Tyr?Thr?Pro?Val?Asp?Asn?Ser?Gln?Gly?Phe
245 250 255
Trp?Leu?Phe?Asn?Ser?Thr?Ser?Ala?Thr?Val?Asn?Gly?Lys?Thr?Ile?Asn
260 265 270
Arg?Ser?Gly?Asn?Thr?Ala?Ile?Ala?Asp?Thr?Gly?Thr?Thr?Leu?Ala?Leu
275 280 285
Val?Asp?Asp?Asp?Thr?Cys?Glu?Ala?Ile?Tyr?Ser?Ala?Ile?Asp?Gly?Ala
290 295 300
Tyr?Tyr?Asp?Gln?Glu?Val?Gln?Gly?Trp?Ile?Tyr?Pro?Thr?Asp?Thr?Ala
305 310 315 320
Gln?Asp?Lys?Leu?Pro?Thr?Val?Ser?Phe?Ala?Val?Gly?Glu?Lys?Gln?Phe
325 330 335
Val?Val?Gln?Lys?Glu?Asp?Leu?Ala?Phe?Ser?Glu?Ala?Lys?Thr?Gly?Tyr
340 345 350
Val?Tyr?Gly?Gly?Ile?Gln?Ser?Arg?Gly?Asp?Met?Thr?Met?Asp?Ile?Leu
355 360 365
Gly?Asp?Thr?Phe?Leu?Lys?Ser?Ile?Tyr?Ala?Val?Ser?Ala?Leu?Leu?Leu
370 375 380
Ala?Leu?Arg?Gly?Asp?Ile?Glu?Ala?His
385 390
<210>131
<211>282
<212>PRT
<213〉aspergillus niger
<400>131
Met?Lys?Phe?Ser?Thr?Ile?Leu?Thr?Gly?Ser?Leu?Phe?Ala?Thr?Ala?Ala
1 5 10 15
Leu?Ala?Ala?Pro?Leu?Thr?Glu?Lys?Arg?Arg?Ala?Arg?Lys?Glu?Ala?Arg
20 25 30
Ala?Ala?Gly?Lys?Arg?His?Ser?Asn?Pro?Pro?Tyr?Ile?Pro?Gly?Ser?Asp
35 40 45
Lys?Glu?Ile?Leu?Lys?Leu?Asn?Gly?Thr?Ser?Asn?Glu?Asp?Tyr?Ser?Ser
50 55 60
Asn?Trp?Ala?Gly?Ala?Val?Leu?Ile?Gly?Asp?Gly?Tyr?Thr?Lys?Val?Thr
65 70 75 80
Gly?Glu?Phe?Thr?Val?Pro?Ser?Val?Ser?Ala?Gly?Ser?Ser?Ser?Ser?Ser
85 90 95
Gly?Tyr?Gly?Gly?Gly?Tyr?Gly?Tyr?Tyr?Lys?Asn?Lys?Arg?Gln?Ser?Glu
100 105 110
Glu?Tyr?Cys?Ala?Ser?Ala?Trp?Val?Gly?Ile?Asp?Gly?Asp?Thr?Cys?Glu
115 120 125
Thr?Ala?Ile?Leu?Gln?Thr?Gly?Val?Asp?Phe?Cys?Tyr?Glu?Asp?Gly?Gln
130 135 140
Thr?Ser?Tyr?Asp?Ala?Trp?Tyr?Glu?Trp?Tyr?Pro?Asp?Tyr?Ala?Tyr?Asp
145 150 155 160
Phe?Asn?Asp?Ile?Thr?Ile?Ser?Glu?Gly?Asp?Thr?Ile?Lys?Val?Thr?Val
165 170 175
Glu?Ala?Thr?Ser?Lys?Ser?Ser?Gly?Ser?Ala?Thr?Val?Glu?Asn?Leu?Thr
180 185 190
Thr?Gly?Gln?Ser?Val?Thr?His?Thr?Phe?Ser?Gly?Asn?Val?Glu?Gly?Asp
195 200 205
Leu?Cys?Glu?Thr?Asn?Ala?Glu?Trp?Ile?Val?Glu?Asp?Phe?Glu?Ser?Gly
210 215 220
Asp?Ser?Leu?Val?Ala?Phe?Ala?Asp?Phe?Gly?Ser?Val?Thr?Phe?Thr?Asn
225 230 235 240
Ala?Glu?Ala?Thr?Ser?Asp?Gly?Ser?Thr?Val?Gly?Pro?Ser?Asp?Ala?Thr
245 250 255
Val?Met?Asp?Ile?Glu?Gln?Asp?Gly?Thr?Val?Leu?Thr?Glu?Thr?Ser?Val
260 265 270
Ser?Gly?Asp?Ser?Val?Thr?Val?Thr?Tyr?Val
275 280
<210>132
<211>273
<212>PRT
<213〉aspergillus niger
<400>132
Met?Gly?Asp?Tyr?Gly?Pro?Gly?Val?Ser?Ser?Leu?Thr?Ala?Gln?Leu?Pro
1 5 10 15
Gly?Asn?Pro?Pro?Val?Ser?Glu?Thr?Asp?Gln?Asp?Glu?Ile?Ser?Val?Leu
20 25 30
Val?Thr?Gly?Phe?Gly?Pro?Phe?Lys?Ser?Asn?Leu?Val?Asn?Ala?Ser?Tyr
35 40 45
Leu?Ile?Ala?Ser?Ser?Leu?Pro?Pro?Ser?Phe?Thr?Phe?Ser?Pro?Ala?Ser
50 55 60
Ser?Asp?Gly?Ser?Asp?Ala?Val?Pro?Arg?Arg?Val?Ser?Ile?Asn?Val?His
65 70 75 80
Pro?Ser?Pro?Ile?Pro?Val?Ala?Tyr?Ser?Ser?Val?Arg?Thr?Thr?Leu?Pro
85 90 95
Val?Ile?Leu?Asp?Asp?Tyr?Ala?Lys?Thr?His?Gly?Gly?Arg?Arg?Pro?Asp
100 105 110
Ile?Val?Ile?His?Ile?Gly?Ile?Ala?Ala?Met?Arg?Asn?Tyr?Tyr?Ser?Val
115 120 125
Glu?Thr?Gln?Ala?His?Arg?Asp?Gly?Tyr?Leu?Met?Ser?Asp?Ile?Lys?Gly
130 135 140
Arg?Ser?Gly?Tyr?Glu?Asp?Gly?Glu?Lys?Leu?Trp?Arg?Glu?Leu?Asp?Leu
145 150 155 160
Pro?Leu?Val?Leu?Arg?Ala?Gly?Pro?Ser?Glu?Gly?His?Ala?Ser?Glu?Lys
165 170 175
Lys?His?Leu?Ser?Pro?Arg?Pro?Pro?Asp?Glu?Asp?Phe?Leu?Ala?Ala?Trp
180 185 190
Lys?Thr?Phe?Cys?Pro?Pro?Glu?Thr?Asp?Ala?Arg?Ile?Ser?Thr?Asp?Ala
195 200 205
Gly?Arg?Tyr?Leu?Cys?Glu?Phe?Ile?Leu?Tyr?Thr?Ser?Leu?Ala?Leu?Ala
210 215 220
Tyr?Gln?Ala?Gly?Glu?Asp?Arg?Asn?Val?Thr?Phe?Phe?His?Val?Pro?Ala
225 230 235 240
Ser?Cys?Leu?Asp?Glu?Asp?Ile?Glu?Thr?Gly?Lys?Glu?Val?Ala?Val?Ala
245 250 255
Leu?Ile?Lys?Ala?Leu?Val?Thr?Ser?Trp?Ser?Glu?Gln?Gln?His?Ser?Val
260 265 270
Pro
<210>133
<211>542
<212>PRT
<213〉aspergillus niger
<400>133
Met?Gly?Ser?Arg?Gln?Gly?Lys?Ala?Pro?Phe?Gly?Trp?Gly?Thr?Gln?Ser
1 5 10 15
Leu?Ala?His?Phe?Gly?Ile?Asn?Pro?Asp?Leu?Gly?Leu?His?Asn?Gln?Gln
20 25 30
Asn?Leu?Asn?Ser?Leu?Ile?Ser?His?Ser?Ala?Met?Ala?Thr?Ala?Leu?Glu
35 40 45
Thr?Glu?Tyr?Ala?Thr?Ile?Pro?Ile?Asp?His?Asn?Asn?Ala?Ser?Ala?Gly
50 55 60
Thr?Tyr?Gln?Asn?Arg?Phe?Trp?Val?Ser?Asp?Glu?Phe?Tyr?Gln?Pro?Gly
65 70 75 80
Asn?Pro?Ile?Phe?Val?Tyr?Asp?Thr?Gly?Glu?Ser?Asp?Gly?Gly?Ser?Ile
85 90 95
Ala?Gln?Ser?Tyr?Leu?Thr?Ser?Thr?Leu?Ser?Phe?Phe?Arg?Glu?Phe?Leu
100 105 110
Ile?Glu?Phe?Asn?Ala?Met?Gly?Ile?Ala?Trp?Glu?His?Arg?Tyr?Tyr?Gly
115 120 125
Asn?Ser?Thr?Pro?Ala?Pro?Val?Ser?Tyr?Glu?Thr?Pro?Pro?Glu?Ala?Trp
130 135 140
Gln?Tyr?Leu?Thr?Thr?Lys?Gln?Ala?Leu?Ala?Asp?Leu?Pro?Tyr?Phe?Ala
145 150 155 160
Ser?Asn?Phe?Ser?Arg?Glu?Lys?Tyr?Pro?Asp?Met?Asp?Leu?Thr?Pro?Gln
165 170 175
Gly?Thr?Pro?Trp?Ile?Met?Val?Gly?Gly?Ser?Tyr?Ala?Gly?Ile?Arg?Ala
180 185 190
Ala?Leu?Thr?Arg?Lys?Glu?Tyr?Pro?Glu?Thr?Ile?Phe?Ala?Ala?Phe?Ser
195 200 205
Ser?Ser?Ser?Pro?Val?Glu?Ala?Gln?Val?Asn?Met?Ser?Ala?Tyr?Tyr?Asp
210 215 220
Gln?Val?Tyr?Arg?Gly?Met?Val?Ala?Ser?Gly?Trp?Thr?Asn?Cys?Ser?Ala
225 230 235 240
Asp?Ile?His?Ala?Ala?Leu?Glu?Tyr?Ile?Asp?Asp?Gln?Leu?Ser?Asp?Glu
245 250 255
Asp?Thr?Ala?Thr?Ser?Val?Lys?Gln?Leu?Phe?Phe?Gly?Ser?Gly?Ala?Glu
260 265 270
Thr?Asn?Ser?Asn?Gly?Asp?Phe?Thr?Ala?Ala?Leu?Thr?Ala?Ile?Tyr?Gly
275 280 285
Tyr?Phe?Gln?Ser?Tyr?Gly?Met?Ala?Gly?Gly?Ile?Gly?Gly?Leu?Gly?Ala
290 295 300
Phe?Cys?Glu?Tyr?Leu?Glu?Ile?Asp?Pro?Lys?Thr?Asn?Gly?Thr?Thr?Gly
305 310 315 320
Pro?Asp?Gly?Leu?Ala?Pro?Thr?Tyr?Gly?Gly?Gln?Tyr?Val?Ala?Glu?Arg
325 330 335
Trp?Ala?Ala?Trp?Pro?Thr?Phe?Leu?Glu?Leu?Val?Asn?Leu?Asn?Met?Gly
340 345 350
Thr?Asn?Cys?Gly?Pro?Gln?Asp?Ala?Ser?Gln?Pro?Ile?Asp?Cys?Asp?Phe
355 360 365
Ser?Lys?Pro?Tyr?Gly?Asp?Pro?Ser?Ala?Ile?Thr?Trp?Thr?Trp?Gln?Tyr
370 375 380
Cys?Ser?Glu?Trp?Gly?Phe?Phe?Gln?Ala?Asn?Asn?Asp?Gly?Pro?His?Ser
385 390 395 400
Leu?Ala?Ser?Arg?Tyr?Gln?Ser?Val?Glu?Tyr?Gln?Gln?Glu?Val?Cys?Asn
405 410 415
Arg?Gln?Phe?Pro?Asp?Ala?Val?Asp?Lys?Gly?Leu?Leu?Pro?Pro?Ser?Pro
420 425 430
Arg?Ala?Asp?Asp?Val?Asn?Gln?Glu?Phe?Gly?Gly?Trp?Thr?Ile?Arg?Pro
435 440 445
Ser?Asn?Val?Tyr?Phe?Ser?Gly?Gly?Glu?Phe?Asp?Pro?Trp?Arg?Ser?Leu
450 455 460
Ser?Ile?Leu?Ser?Thr?Glu?Asp?Phe?Ala?Pro?Gln?Gly?Val?Glu?Phe?Thr
465 470 475 480
Ser?Ala?Ile?Pro?Ala?Cys?Gly?Val?Gln?Thr?Asn?Glu?Asp?Thr?Val?Phe
485 490 495
Gly?Tyr?Val?Met?Gln?Asn?Ser?Glu?His?Cys?Phe?Asp?Phe?Gln?Ala?Thr
500 505 510
Pro?Thr?Val?Gly?Lys?Leu?Ser?Arg?Gly?Ile?Phe?Thr?Ser?Ala?Leu?Leu
515 520 525
Gln?Trp?Leu?Glu?Cys?Phe?Gly?Gln?Asn?Ser?Ser?Gln?Ser?Arg
530 535 540
<210>134
<211>391
<212>PRT
<213〉aspergillus niger
<400>134
Met?Lys?Leu?Ser?Ile?Ala?Leu?Ala?Leu?Gly?Ala?Thr?Ala?Ser?Thr?Gly
1 5 10 15
Val?Leu?Ala?Ala?Val?Val?Pro?Gln?Gln?Glu?Pro?Leu?Ile?Thr?Pro?Gln
20 25 30
Asp?Pro?Pro?Thr?His?His?His?Gln?Glu?Lys?Phe?Leu?Ile?Glu?Leu?Ala
35 40 45
Pro?Tyr?Gln?Thr?Arg?Trp?Val?Thr?Glu?Glu?Glu?Lys?Trp?Asp?Leu?Lys
50 55 60
Leu?Asp?Gly?Val?Asn?Phe?Ile?Asp?Ile?Thr?Glu?Glu?Arg?Asn?Thr?Gly
65 70 75 80
Phe?Tyr?Pro?Thr?Leu?His?Ala?Gly?Ser?Tyr?Val?His?Tyr?Pro?Pro?Thr
85 90 95
Met?Lys?His?Ala?Glu?Lys?Val?Val?Pro?Leu?Leu?Arg?Gly?Leu?Ser?Lys
100 105 110
Asp?Asn?Met?Glu?Gln?Asn?Leu?Asn?Lys?Phe?Thr?Ser?Phe?His?Thr?Arg
115 120 125
Tyr?Tyr?Arg?Ser?Ser?Thr?Gly?Ile?Glu?Ser?Ala?Lys?Trp?Leu?Tyr?Ser
130 135 140
Arg?Val?Ser?Asp?Val?Ile?Glu?Gln?Ser?Gly?Ala?Ala?Glu?Tyr?Gly?Ala
145 150 155 160
Thr?Val?Glu?Gln?Phe?Ala?His?Ser?Trp?Gly?Gln?Phe?Ser?Ile?Ile?Ala
165 170 175
Arg?Ile?Pro?Gly?Gln?Thr?Asn?Lys?Thr?Val?Val?Leu?Gly?Ala?His?Gln
180 185 190
Asp?Ser?Ile?Asn?Leu?Phe?Leu?Pro?Ser?Ile?Leu?Ala?Ala?Pro?Gly?Ala
195 200 205
Asp?Asp?Asp?Gly?Ser?Gly?Thr?Val?Thr?Ile?Leu?Glu?Ala?Leu?Arg?Gly
210 215 220
Leu?Leu?Gln?Ser?Asp?Ala?Ile?Val?Arg?Gly?Asn?Ala?Ser?Asn?Thr?Ile
225 230 235 240
Glu?Phe?His?Trp?Tyr?Ser?Ala?Glu?Glu?Gly?Gly?Met?Leu?Gly?Ser?Gln
245 250 255
Ala?Ile?Phe?Ser?Gln?Tyr?Lys?Arg?Asp?Lys?Arg?Asp?Ile?Lys?Ala?Met
260 265 270
Leu?Gln?Gln?Asp?Met?Thr?Gly?Tyr?Thr?Gln?Gly?Ala?Leu?Asp?Ala?Gly
275 280 285
Arg?Gln?Glu?Ala?Ile?Gly?Ile?Met?Val?Asp?Tyr?Val?Asp?Glu?Gly?Leu
290 295 300
Thr?Gln?Phe?Leu?Lys?Asp?Val?Thr?Thr?Glu?Tyr?Cys?Gly?Ile?Gly?Tyr
305 310 315 320
Ile?Glu?Thr?Arg?Cys?Gly?Tyr?Ala?Cys?Ser?Asp?His?Thr?Ser?Ala?Ser
325 330 335
Lys?Tyr?Gly?Tyr?Pro?Ala?Ala?Met?Ala?Thr?Glu?Ser?Glu?Met?Glu?Asn
340 345 350
Ser?Asn?Lys?Arg?Ile?His?Thr?Thr?Asp?Asp?Ser?Ile?Arg?Tyr?Leu?Ser
355 360 365
Phe?Asp?His?Met?Leu?Glu?His?Ala?Arg?Leu?Thr?Leu?Gly?Phe?Ala?Tyr
370 375 380
Glu?Leu?Ala?Phe?Ala?Gln?Phe
385 390
<210>135
<211>442
<212>PRT
<213〉aspergillus niger
<400>135
Met?Arg?Thr?Thr?Thr?Ser?Phe?Ala?Arg?Leu?Ala?Leu?Ala?Val?Ala?Ser
1 5 10 15
Val?Gly?Ile?Val?Phe?Ala?Ser?Pro?Thr?Lys?Asn?Asn?Asp?Gly?Lys?Leu
20 25 30
Val?Tyr?Gly?Ser?Pro?Glu?Ser?Val?Gly?Met?Ile?Ser?Ala?Pro?Leu?His
35 40 45
Gln?Met?Val?Gln?Asn?Val?Ser?Ala?Tyr?Thr?His?Ala?Ala?Asn?Tyr?Ser
50 55 60
Lys?Phe?Ser?Tyr?Asp?Lys?Val?His?Pro?Ile?Glu?Pro?Gly?Ser?Val?Thr
65 70 75 80
Leu?Val?Ala?Leu?Asp?Gly?Val?Ile?Val?Ser?Glu?Phe?Ala?Leu?Gly?Lys
85 90 95
Arg?Asn?Leu?Tyr?Ala?Asp?Val?Asn?Gly?Thr?Asn?Leu?Pro?Arg?Tyr?Leu
100 105 110
Gln?Glu?Asp?Thr?Thr?Leu?Asp?Thr?Val?Tyr?Asp?Met?Ala?Ser?Leu?Thr
115 120 125
Lys?Leu?Phe?Thr?Thr?Val?Ala?Ala?Leu?Arg?Glu?Leu?Asp?Ala?Gly?Arg
130 135 140
Ile?Ala?Leu?Asn?Val?Thr?Val?Ala?Thr?Tyr?Ile?Pro?Asp?Phe?Ala?Thr
145 150 155 160
Asn?Gly?Lys?Glu?Asn?Ile?Thr?Ile?Leu?Glu?Leu?Phe?Thr?His?Thr?Ser
165 170 175
Gly?Phe?Ala?Ser?Asp?Pro?Ser?Pro?Pro?Leu?Phe?Ser?Ala?Tyr?Tyr?Thr
180 185 190
Thr?Tyr?Asp?Glu?Arg?Ile?Lys?Ala?Ile?Leu?Thr?Gln?Lys?Ile?Ile?Asn
195 200 205
Thr?Pro?Gly?Ser?Thr?Tyr?Leu?Tyr?Leu?Asp?Leu?Asn?Phe?Met?Ser?Leu
210 215 220
Gly?Leu?Val?Ile?Glu?Thr?Val?Thr?Gly?Arg?Ala?Leu?Asp?Asp?Leu?Ile
225 230 235 240
Tyr?Asp?Phe?Thr?Arg?Pro?Leu?Glu?Met?Thr?Ser?Thr?Phe?Phe?Asn?Arg
245 250 255
Gly?Asn?Ile?Glu?Gly?Ser?Thr?Pro?Gln?Ser?Pro?Asn?Tyr?Asp?Arg?Thr
260 265 270
Ala?Val?Gln?Glu?Phe?Gln?Ile?Ala?Ala?Leu?Gly?Pro?Ser?Glu?Pro?Gln
275 280 285
Arg?Pro?Gln?Pro?Val?Arg?Gly?Thr?Val?His?Asp?Glu?Asn?Ala?Trp?Ser
290 295 300
Leu?Asp?Gly?Val?Ser?Gly?His?Ala?Gly?Leu?Phe?Ser?Thr?Val?Arg?Asp
305 310 315 320
Thr?Ala?Thr?Phe?Cys?Gln?Met?Ile?Leu?Asn?Asn?Gly?Thr?Tyr?Ala?Gly
325 330 335
Gln?Arg?Ile?Leu?Ser?Arg?Thr?Ala?Val?Asp?Met?Ile?Phe?Thr?Asn?Phe
340 345 350
Asn?Ala?Arg?Phe?Pro?Gly?Asp?Ala?Arg?Ser?Leu?Gly?Phe?Glu?Leu?Asp
355 360 365
Gln?Tyr?Ser?Thr?Ala?Gly?Pro?Met?Ala?Ser?Leu?Gln?Thr?Ala?Ser?His
370 375 380
Thr?Gly?Phe?Thr?Gly?Thr?Thr?Leu?Val?Met?Asp?Arg?Thr?Tyr?Asn?Ala
385 390 395 400
Phe?Trp?Leu?His?Phe?Ser?Asn?Arg?Val?His?Pro?Ser?Arg?Ala?Trp?Ser
405 410 415
Ser?Asn?Thr?Ile?Val?Arg?Glu?Ala?Ile?Gly?Tyr?Trp?Val?Gly?Lys?Ser
420 425 430
Leu?Gly?Leu?Asp?Val?Ala?Phe?Ala?Leu?Leu
435 440
<210>136
<211>612
<212>PRT
<213〉aspergillus niger
<400>136
Met?Ala?Ser?Trp?Leu?Leu?Ser?Thr?Leu?Leu?Phe?Leu?Ser?Pro?Ser?Leu
1 5 10 15
Val?Ser?Ala?Lys?Ser?Ala?Ala?Asp?Tyr?Tyr?Val?His?Ser?Leu?Pro?Gly
20 25 30
Ala?Pro?Glu?Gly?Pro?Leu?Leu?Lys?Met?His?Ala?Gly?His?Ile?Glu?Val
35 40 45
Asp?Pro?Gln?Asn?Asn?Gly?Asn?Leu?Phe?Phe?Trp?His?Tyr?Gln?Asn?Arg
50 55 60
His?Ile?Ala?Asn?Arg?Gln?Arg?Thr?Val?Ile?Trp?Leu?Asn?Gly?Gly?Pro
65 70 75 80
Gly?Cys?Ser?Ser?Met?Asp?Gly?Ala?Leu?Met?Glu?Val?Gly?Pro?Tyr?Arg
85 90 95
Leu?Lys?Asp?Asn?Glu?Thr?Leu?Thr?Tyr?Asn?Glu?Gly?Ser?Trp?Asp?Glu
100 105 110
Phe?Ala?Asn?Leu?Leu?Phe?Val?Asp?Gln?Pro?Val?Gly?Thr?Gly?Phe?Ser
115 120 125
Tyr?Val?Asn?Thr?Asp?Ser?Tyr?Leu?His?Glu?Leu?Asp?Glu?Met?Ser?Ala
130 135 140
Gln?Phe?Ile?Val?Phe?Leu?Glu?Glu?Trp?Phe?Arg?Leu?Phe?Pro?Glu?Tyr
145 150 155 160
Glu?Arg?Asp?Asp?Ile?Tyr?Ile?Ala?Gly?Glu?Ser?Tyr?Ala?Gly?Gln?His
165 170 175
Ile?Pro?Tyr?Ile?Ala?Lys?Ala?Ile?Gln?Glu?Arg?Asn?Lys?Asn?Val?Gln
180 185 190
Gly?Lys?Thr?Ile?Ala?Ser?Trp?Asn?Leu?Lys?Gly?Leu?Leu?Ile?Gly?Asn
195 200 205
Gly?Trp?Ile?Ser?Pro?Asn?Glu?Gln?Tyr?Met?Ser?Tyr?Leu?Pro?Tyr?Ala
210 215 220
Tyr?Glu?Glu?Gly?Leu?Ile?Lys?Glu?Gly?Ser?Arg?Thr?Ala?Lys?Glu?Leu
225 230 235 240
Glu?Val?Leu?Gln?Ser?Val?Cys?Lys?Ser?Arg?Leu?Glu?Thr?Gly?Lys?Asn
245 250 255
Lys?Val?His?Leu?Asn?Asp?Cys?Glu?Lys?Val?Met?Asn?Ala?Leu?Leu?Asp
260 265 270
Lys?Thr?Val?Glu?Asp?Asn?Lys?Cys?Leu?Asn?Met?Tyr?Asp?Ile?Arg?Leu
275 280 285
Arg?Asp?Thr?Thr?Asp?Ala?Cys?Gly?Met?Asn?Trp?Pro?Thr?Asp?Leu?Glu
290 295 300
Asp?Val?Lys?Pro?Tyr?Leu?Gln?Arg?Glu?Asp?Val?Val?Lys?Ala?Leu?Asn
305 310 315 320
Ile?Asn?Pro?Glu?Lys?Lys?Ser?Gly?Trp?Val?Glu?Cys?Ser?Gly?Ala?Val
325 330 335
Ser?Ser?Ala?Phe?Asn?Pro?Gln?Lys?Ser?Pro?Pro?Ser?Val?Gln?Leu?Leu
340 345 350
Pro?Gly?Leu?Leu?Glu?Ser?Gly?Leu?Gln?Ile?Leu?Leu?Phe?Ser?Gly?Asp
355 360 365
Lys?Asp?Leu?Ile?Cys?Asn?His?Val?Gly?Thr?Glu?Gln?Leu?Ile?Asn?Asn
370 375 380
Met?Lys?Trp?Asn?Gly?Gly?Thr?Gly?Phe?Glu?Thr?Ser?Pro?Gly?Val?Trp
385 390 395 400
Ala?ProArg?His?Asp?Trp?Ser?Phe?Glu?Gly?Glu?Pro?Ala?Gly?Ile?Tyr
405 410 415
Gln?Tyr?Ala?Arg?Asn?Leu?Thr?Tyr?Val?Leu?Ile?Tyr?Asn?Ala?Ser?His
420 425 430
Met?Val?Pro?Tyr?Asp?Leu?Pro?Arg?Gln?Ser?Arg?Asp?Met?Leu?Asp?Arg
435 440 445
Phe?Met?Asn?Val?Asp?Ile?Ala?Ser?Ile?Gly?Gly?Ser?Pro?Ala?Asp?Ser
450 455 460
Arg?Ile?Asp?Gly?Glu?Lys?Leu?Pro?Gln?Thr?Ser?Val?Gly?Gly?His?Pro
465 470 475 480
Asn?Ser?Thr?Ala?Ala?Glu?Glu?Gln?Glu?Lys?Glu?Arg?Ile?Lys?Glu?Thr
485 490 495
Glu?Trp?Lys?Ala?Tyr?Ala?Lys?Ser?Gly?Glu?Ala?Val?Leu?Leu?Val?Val
500 505 510
Ile?Ile?Gly?Val?Leu?Val?Trp?Gly?Phe?Phe?Ile?Trp?Arg?Ser?Arg?Arg
515 520 525
Arg?His?Gln?Gly?Tyr?Arg?Gly?Val?Trp?His?Lys?Asp?Met?Ser?Gly?Ser
530 535 540
Ser?Val?Leu?Glu?Arg?Phe?His?Asn?Lys?Arg?Thr?Gly?Gly?Ala?Asp?Val
545 550 555 560
Glu?Ala?Gly?Asp?Phe?Asp?Glu?Ala?Glu?Leu?Asp?Asp?Leu?His?Ser?Pro
565 570 575
Asp?Leu?Glu?Arg?Glu?His?Tyr?Ala?Val?Gly?Glu?Asp?Ser?Asp?Glu?Asp
580 585 590
Asp?Ile?Ser?Arg?Gln?His?Ser?Gln?Gln?Ala?Ser?Arg?Ala?Gly?Gly?Ser
595 600 605
His?Asn?Leu?Ser
610
<210>137
<211>531
<212>PRT
<213〉aspergillus niger
<400>137
Met?Phe?Leu?Ile?Ser?Pro?Ala?Val?Thr?Val?Ala?Ala?Ala?Leu?Leu?Leu
1 5 10 15
Ile?Asn?Gly?Ala?Gly?Ala?Thr?Gln?Ser?Glu?Arg?Ser?Arg?Ala?Ala?Ala
20 25 30
His?Phe?Ser?Lys?Arg?His?Pro?Thr?Tyr?Arg?Ala?Ala?Thr?Arg?Ala?Gln
35 40 45
Ser?Ser?Asn?Thr?Ser?Asp?Tyr?Arg?Phe?Phe?Asn?Asn?Arg?Thr?Lys?Pro
50 55 60
His?Leu?Val?Glu?Ser?Leu?Pro?Asp?Val?His?Phe?Asp?Val?Gly?GLU?Met
65 70 75 80
Tyr?Ser?Gly?Ser?Ile?Pro?Ile?Asp?Asp?Ser?Asn?Asn?Gly?Ser?Arg?Ser
85 90 95
Leu?Phe?Tyr?Ile?Phe?Gln?Pro?Lys?Ile?Gly?Glu?Pro?Ser?Asp?Asp?Leu
100 105 110
Thr?Ile?Tyr?Leu?Asn?Gly?Gly?Pro?Gly?Cys?Ser?Ser?Glu?Gln?Gly?Phe
115 120 125
Phe?Gln?Glu?Asn?Gly?Arg?Phe?Thr?Trp?Gln?Pro?Gly?Thr?Tyr?Ala?Pro
130 135 140
Val?Ile?Asn?Glu?Tyr?Ser?Trp?Val?Asn?Leu?Thr?Asn?Met?Leu?Trp?Val
145 150 155 160
Asp?Gln?Pro?Val?Gly?Thr?Gly?Phe?Ser?Val?Gly?Asn?Val?Thr?Ala?Thr
165 170 175
Asn?Glu?Glu?Glu?Ile?Ala?Ala?Asp?Phe?Leu?Asp?Phe?Phe?Glu?Lys?Phe
180 185 190
Glu?Asp?Leu?Tyr?Gly?Ile?Lys?Asn?Phe?Arg?Ile?Phe?Met?Thr?Gly?Glu
195 200 205
Ser?Tyr?Ala?Gly?Arg?Tyr?Val?Pro?Tyr?Ile?Ser?Ser?Ala?Met?Leu?Asp
210 215 220
Lys?Asn?Asp?Thr?Thr?Arg?Phe?Asn?Leu?Ser?Gly?Ala?Leu?Leu?TYR?Asp
225 230 235 240
Ala?Cys?Ile?Gly?Gln?Trp?Asp?Tyr?Ile?Gln?Ala?Glu?Leu?Pro?Ala?Tyr
245 250 255
Pro?Phe?Val?Lys?Gln?His?Ala?Ser?Leu?Phe?Asn?Phe?Asn?Gln?Ser?Tyr
260 265 270
Met?Asn?Glu?Leu?Glu?Thr?Thr?Tyr?Glu?Glu?Cys?Gly?Tyr?Lys?Ala?Tyr
275 280 285
Phe?Asp?Glu?Tyr?Phe?Ala?Phe?Pro?Pro?Ser?Gly?Ile?Gln?Pro?Pro?Lys
290 295 300
Tyr?Met?Asn?Tyr?Ser?Glu?Cys?Asp?Ile?Tyr?Asn?Met?Ile?Tyr?Tyr?Glu
305 310 315 320
Ala?Tyr?Asn?Pro?Asn?Pro?Cys?Phe?Asn?Pro?Tyr?Arg?Val?Ile?Asp?Glu
325 330 335
Cys?Pro?Leu?Leu?Trp?Asp?Val?Leu?Gly?Trp?Pro?Thr?Asp?Leu?Ala?Tyr
340 345 350
Glu?Pro?Ala?Pro?Thr?Thr?Tyr?Phe?Asn?Arg?Ile?Asp?Val?Lys?Lys?Ala
355 360 365
Leu?His?Ala?Pro?Met?Asp?Val?Glu?Trp?Glu?Leu?Cys?Ser?Tyr?Asp?Leu
370 375 380
Val?Phe?Ala?Gly?Gly?Asp?Ala?Asp?Pro?Gly?Pro?Glu?Gln?Gln?Gly?Asp
385 390 395 400
Asp?Ser?Pro?Asn?Pro?Thr?Glu?Gly?Val?Leu?Pro?Arg?Val?Ile?Glu?Ala
405 410 415
Thr?Asn?Arg?Val?Leu?Ile?Ala?Asn?Gly?Asp?Trp?Asp?Tyr?Leu?Ile?Ile
420 425 430
Thr?Asn?Gly?Thr?Leu?Leu?Ala?Ile?Gln?Asn?Met?Thr?Trp?Asn?Gly?Gln
435 440 445
Leu?Gly?Phe?Gln?Ser?Ala?Pro?Ala?Thr?Pro?Ile?Asp?Ile?Gln?Met?Pro
450 455 460
Asp?Leu?Gln?Trp?Val?Glu?Ile?Phe?Glu?Ala?Gln?Glu?Gly?Tyr?Gly?Gly
465 470 475 480
Leu?Asp?Gly?Pro?Gln?Gly?Val?Met?Gly?Val?Gln?His?Tyr?Glu?Arg?Gly
485 490 495
Leu?Met?Trp?Ala?Glu?Thr?Tyr?Gln?Ser?Gly?His?Lys?Gln?Ala?Gln?Asp
500 505 510
Gln?Gly?Arg?Val?Ser?Tyr?Arg?His?Leu?Gln?Trp?Leu?Leu?Gly?Gln?Val
515 520 525
Glu?Ile?Leu
530
<210>138
<211>531
<212>PRT
<213〉aspergillus niger
<400>138
Met?Leu?Phe?Arg?Ser?Leu?Leu?Ser?Thr?Ala?Val?Leu?Ala?Val?Ser?Leu
1 5 10 15
Cys?Thr?Asp?Asn?Ala?Ser?Ala?Ala?Lys?His?Gly?Arg?Phe?Gly?Gln?Lys
20 25 30
Ala?Arg?Asp?Ala?Met?Asn?Ile?Ala?Lys?Arg?Ser?Ala?Asn?Ala?Val?Lys
35 40 45
His?Ser?Leu?Lys?Ile?Pro?Val?Glu?Asp?Tyr?Gln?Phe?Leu?Asn?Asn?Lys
50 55 60
Thr?Lys?Pro?Tyr?Arg?Val?Glu?Ser?Leu?Pro?Asp?Val?His?Phe?Asp?Leu
65 70 75 80
Gly?Glu?Met?Tyr?Ser?Gly?Leu?Val?Pro?Ile?Glu?Lys?Gly?Asn?Val?Ser
85 90 95
Arg?Ser?Leu?Phe?Phe?Val?Phe?Gln?Pro?Thr?Ile?Gly?Glu?Pro?Val?Asp
100 105 110
Glu?Ile?Thr?Ile?Trp?Leu?Asn?Gly?Gly?Pro?Gly?Cys?Ser?Ser?Leu?Glu
115 120 125
Ala?Phe?Leu?Gln?Glu?Asn?Gly?Arg?Phe?Val?Trp?Gln?Pro?Gly?Thr?Tyr
130 135 140
Gln?Pro?Val?Glu?Asn?Pro?Tyr?Ser?Trp?Val?Asn?Leu?Thr?Asn?Val?Leu
145 150 155 160
Trp?Val?Asp?Gln?Pro?Val?Gly?Thr?Gly?Phe?Ser?Leu?Gly?Val?Pro?Thr
165 170 175
Ala?Thr?Ser?Glu?Glu?Glu?Ile?Ala?Glu?Asp?Phe?Val?Lys?Phe?Phe?Lys
180 185 190
Asn?Trp?Gln?Gln?Ile?Phe?Gly?Ile?Lys?Asn?Phe?Lys?Ile?Tyr?Val?Thr
195 200 205
Gly?Glu?Ser?Tyr?Ala?Gly?Arg?Tyr?Val?Pro?Tyr?Ile?Ser?Ala?Ala?Phe
210 215 220
Leu?Asp?Gln?Asn?Asp?Thr?Glu?His?Phe?Asn?Leu?Lys?Gly?Ala?Leu?Ala
225 230 235 240
Tyr?Asp?Pro?Cys?Ile?Gly?Gln?Phe?Asp?Tyr?Val?Gln?Glu?Glu?Ala?Pro
245 250 255
Val?Val?Pro?Phe?Val?Gln?Lys?Asn?Asn?Ala?Leu?Phe?Asn?Phe?Asn?Ala
260 265 270
Ser?Phe?Leu?Ala?Glu?Leu?Glu?Ser?Ile?His?Glu?Gln?Cys?Gly?Tyr?Lys
275 280 285
Asp?Phe?Ile?Asp?Gln?Tyr?Leu?Val?Phe?Pro?Ala?Ser?Gly?Val?Gln?Pro
290 295 300
Pro?Lys?Ala?Met?Asn?Trp?Ser?Asp?Pro?Thr?Cys?Asp?Val?Tyr?Asp?Ile
305 310 315 320
Val?Asn?Asn?Ala?Val?Leu?Asp?Pro?Asn?Pro?Cys?Phe?Asn?Pro?Tyr?Glu
325 330 335
Ile?Asn?Glu?Met?Cys?Pro?Ile?Leu?Trp?Asp?Val?Leu?Gly?Phe?Pro?Thr
340 345 350
Glu?Val?Asp?Tyr?Leu?Pro?Ala?Gly?Ala?Ser?Ile?Tyr?Phe?Asp?Arg?Ala
355 360 365
Asp?Val?Lys?Arg?Ala?Met?His?Ala?Pro?Asn?Ile?Thr?Trp?Ser?Glu?Cys
370 375 380
Ser?Val?Glu?Ser?Val?Phe?Val?Gly?Gly?Asp?Gly?Gly?Pro?Glu?Gln?Glu
385 390 395 400
Gly?Asp?Tyr?Ser?Ala?Asn?Pro?Ile?Glu?His?Val?Leu?Pro?Gln?Val?Ile
405 410 415
Glu?Gly?Thr?Asn?Arg?Val?Leu?Ile?Gly?Asn?Gly?Asp?Tyr?Asp?Met?Val
420 425 430
Ile?Leu?Thr?Asn?Gly?Thr?Leu?Leu?Ser?Ile?Gln?Asn?Met?Thr?Trp?Asn
435 440 445
Gly?Lys?Leu?Gly?Phe?Asp?Thr?Ala?Pro?Ser?Thr?Pro?Ile?Asn?Ile?Asp
450 455 460
Ile?Pro?Asp?Leu?Met?Tyr?Asn?Glu?Val?Phe?Ile?Glu?Asn?Gly?Tyr?Asp
465 470 475 480
Pro?Gln?Gly?Gly?Gln?Gly?Val?Met?Gly?Ile?Gln?His?Tyr?Glu?Arg?Gly
485 490 495
Leu?Met?Trp?Ala?Glu?Thr?Phe?Gln?Ser?Gly?His?Met?Gln?Pro?Gln?Phe
500 505 510
Gln?Pro?Arg?Val?Ser?Tyr?Arg?His?Leu?Glu?Trp?Leu?Leu?Gly?Arg?Arg
515 520 525
Asp?Thr?Leu
530
<210>139
<211>492
<212>PRT
<213〉aspergillus niger
<400>139
Met?Lys?Gly?Ala?Ala?Leu?Ile?Pro?Leu?Ala?Ala?Gly?Ile?Pro?Phe?Ala
1 5 10 15
His?Gly?Leu?Ser?Leu?His?Lys?Arg?Asp?Gly?Pro?Ala?Val?Val?Arg?Met
20 25 30
Pro?Ile?Glu?Arg?Arg?Ser?Ala?Gln?Ser?Leu?Gln?Lys?Arg?Asp?Ser?Thr
35 40 45
Val?Gly?Val?Thr?Leu?Gln?Asn?Trp?Asp?Ala?Thr?Tyr?Tyr?Ala?Val?Asn
50 55 60
Leu?Thr?Leu?Gly?Thr?Pro?Ala?Gln?Lys?Val?Ser?Leu?Ala?Leu?Asp?Thr
65 70 75 80
Gly?Ser?Ser?Asp?Leu?Trp?Val?Asn?Thr?Gly?Asn?Ser?Thr?Tyr?Cys?Ser
85 90 95
Ile?Asp?Asn?Leu?Cys?Thr?Pro?Tyr?Gly?Leu?Tyr?Asn?Ala?Ser?Glu?Ser
100 105 110
Ser?Thr?Val?Lys?Thr?Val?Gly?Thr?His?Leu?Asn?Asp?Thr?Tyr?Ala?Asp
115 120 125
Gly?Thr?Asn?Leu?Tyr?Gly?Pro?Tyr?Val?Thr?Asp?Lys?Leu?Thr?Ile?Gly
130 135 140
Asn?Thr?Thr?Ile?Asp?Asn?Met?Gln?Phe?Gly?Ile?Ala?Glu?Ser?Thr?Thr
145 150 155 160
Ser?Lys?Arg?Gly?Ile?Ala?Gly?Val?Gly?Tyr?Lys?Ile?Ser?Thr?Tyr?Gln
165 170 175
Ala?Glu?His?Asp?Asp?Lys?Val?Tyr?Ala?Asn?Leu?Pro?Gln?Ala?Leu?Val
180 185 190
Asp?Ser?Gly?Ala?Ile?Lys?Ser?Ala?Ala?Tyr?Ser?Ile?Trp?Leu?Asp?Ser
195 200 205
Leu?Glu?Ala?Ser?Thr?Gly?Ser?Leu?Leu?Phe?Gly?Gly?Val?Asn?Thr?Ala
210 215 220
Lys?Tyr?Lys?Gly?Asp?Leu?Gln?Thr?Leu?Pro?Ile?Ile?Pro?Val?Tyr?Gly
225 230 235 240
Lys?Tyr?Tyr?Ser?Leu?Ala?Ile?Ala?Leu?Thr?Glu?Leu?Ser?Val?Ala?Thr
245 250 255
Asp?Ser?Asn?Ser?Ser?Ser?Phe?Thr?Asp?Ser?Leu?Pro?Leu?Ser?Val?Ser
260 265 270
Leu?Asp?Thr?Gly?Thr?Thr?Met?Thr?Ala?Leu?Pro?Ser?Asp?Leu?Val?Asn
275 280 285
Lys?Val?Tyr?Asp?Ala?Leu?Asn?Ala?Thr?Tyr?Asp?Lys?Thr?Tyr?Asp?Met
290 295 300
Ala?Tyr?Ile?Asp?Cys?Asp?Thr?Arg?Glu?Ala?Asp?Tyr?Asn?Val?Thr?Tyr
305 310 315 320
Ser?Phe?Ser?Gly?Ala?Thr?Ile?Thr?Val?Ser?Met?Ser?Glu?Leu?Ile?Ile
325 330 335
Pro?Ala?Thr?Glu?Pro?Gly?Trp?Pro?Asp?Asn?Thr?Cys?Val?Leu?Gly?Leu
340 345 350
Val?Pro?Ser?Gln?Pro?Gly?Val?Asn?Leu?Leu?Gly?Asp?Thr?Phe?Leu?Arg
355 360 365
Ser?Ala?Tyr?Val?Val?Tyr?Asp?Leu?Glu?Asn?Asn?Glu?Ile?Ser?Leu?Ala
370 375 380
Asn?Thr?Asn?Phe?Asn?Pro?Gly?Asp?Asp?Asp?Ile?Leu?Glu?Ile?Gly?Thr
385 390 395 400
Gly?Thr?Ser?Ala?Val?Pro?Gly?Ala?Thr?Pro?Val?Pro?Ser?Ala?Val?Ser
405 410 415
Ser?Ala?Thr?Gly?Asn?Gly?Leu?Ile?Ser?Ser?Gly?Thr?Ala?Val?Pro?Thr
420 425 430
Leu?Ser?Gly?Val?Thr?Ile?Thr?Ala?Thr?Ala?Thr?Ala?Thr?Gly?Ser?Thr
435 440 445
Gly?Thr?Gly?Ser?Ser?Gly?Gly?Ser?Ser?Ala?Glu?Ala?Thr?Ser?Thr?Ser
450 455 460
Ser?Glu?Gly?Ala?Ala?Ala?Gln?Ala?Thr?Ser?Asn?Pro?Met?Asn?Leu?Leu
465 470 475 480
Pro?Gly?Leu?Ala?Gly?Ile?Gly?Leu?Leu?Leu?Ala?Leu
485 490
<210>140
<211>611
<212>PRT
<213〉aspergillus niger
<400>140
Met?Leu?Ser?Ser?Leu?Leu?Ser?Gln?Gly?Ala?Ala?Val?Ser?Leu?Ala?Val
1 5 10 15
Leu?Ser?Leu?Leu?Pro?Ser?Pro?Val?Ala?Ala?Glu?Ile?Phe?Glu?Lys?Leu
20 25 30
Ser?Gly?Val?Pro?Asn?Gly?Trp?Arg?Tyr?Ala?Asn?Asn?Pro?Gln?Gly?Asn
35 40 45
Glu?Val?Ile?Arg?Leu?Gln?Ile?Ala?Leu?Gln?Gln?His?Asp?Val?Ala?Gly
50 55 60
Phe?Glu?Gln?Ala?Val?Met?Asp?Met?Ser?Thr?Pro?Gly?His?Ala?Asp?Tyr
65 70 75 80
Gly?Lys?His?Phe?Arg?Thr?His?Asp?Glu?Met?Lys?Arg?Met?Leu?Leu?Pro
85 90 95
Ser?Glu?Thr?Ala?Val?Asp?Ser?Val?Arg?Asp?Trp?Leu?Glu?Ser?Ala?Gly
100 105 110
Val?His?Asn?Ile?Gln?Val?Asp?Ala?Asp?Trp?Val?Lys?Phe?His?Thr?Thr
115 120 125
Val?Asn?Lys?Ala?Asn?Ala?Leu?Leu?Asp?Ala?Asp?Phe?Lys?Trp?Tyr?Val
130 135 140
Ser?Asp?Ala?Lys?His?Ile?Arg?Arg?Leu?Arg?Thr?Leu?Gln?Tyr?Ser?Ile
145 150 155 160
Pro?Asp?Ala?Leu?Val?Ser?His?Ile?Asn?Met?Ile?Gln?Pro?Thr?Thr?Arg
165 170 175
Phe?Gly?Gln?Ile?Gln?Pro?Asn?Arg?Ala?Thr?Met?Arg?Ser?Lys?Pro?Lys
180 185 190
His?Ala?Asp?Glu?Thr?Phe?Leu?Thr?Ala?Ala?Thr?Leu?Ala?Gln?Asn?Thr
195 200 205
Ser?His?Cys?Asp?Ser?Ile?Ile?Thr?Pro?His?Cys?Leu?Lys?Gln?Leu?Tyr
210 215 220
Asn?Ile?Gly?Asp?Tyr?Gln?Ala?Asp?Pro?Lys?Ser?Gly?Ser?Lys?Ile?Gly
225 230 235 240
Phe?Ala?Ser?Tyr?Leu?Glu?Glu?Tyr?Ala?Arg?Tyr?Ala?Asp?Leu?Glu?Arg
245 250 255
Phe?Glu?Gln?His?Leu?Ala?Pro?Asn?Ala?Ile?Gly?Gln?Asn?Phe?Ser?Val
260 265 270
Val?Gln?Phe?Asn?Gly?Gly?Leu?Asn?Asp?Gln?Leu?Ser?Ser?Ser?Asp?Ser
275 280 285
Gly?Glu?Ala?Asn?Leu?Asp?Leu?Gln?Tyr?Ile?Leu?Gly?Val?Ser?Ala?Pro
290 295 300
Val?Pro?Ile?Thr?Glu?Tyr?Ser?Thr?Gly?Gly?Arg?Gly?Glu?Leu?Val?Pro
305 310 315 320
Asp?Leu?Ser?Ser?Pro?Asp?Pro?Asn?Asp?Asn?Ser?Asn?Glu?Pro?Tyr?Leu
325 330 335
Asp?Phe?Leu?Gln?Gly?Ile?Leu?Lys?Leu?Asn?Asn?Ser?Asp?Leu?Pro?Gln
340 345 350
Val?Ile?Ser?Thr?Ser?Tyr?Gly?Glu?Asp?Glu?Gln?Thr?Ile?Pro?Val?Pro
355 360 365
Tyr?Ala?Arg?Thr?Val?Cys?Asn?Leu?Tyr?Ala?Gln?Leu?Gly?Ser?Arg?Gly
370 375 380
Val?Ser?Val?Ile?Phe?Ser?Ser?Gly?Asp?Ser?Gly?Val?Gly?Ala?Ala?Cys
385 390 395 400
Leu?Thr?Asn?Asp?Gly?Thr?Asn?Arg?Thr?His?Phe?Pro?Pro?Gln?Phe?Pro
405 410 415
Ala?Ser?Cys?Pro?Trp?Val?Thr?Ser?Val?Gly?Ala?Thr?Ser?Lys?Thr?Ser
420 425 430
Pro?Glu?Gln?Ala?Val?Ser?Phe?Ser?Ser?Gly?Gly?Phe?Ser?Asp?Leu?Trp
435 440 445
Pro?Arg?Pro?Ser?Tyr?Gln?His?Ala?Ala?Val?Gln?Thr?Tyr?Leu?Thr?Lys
450 455 460
His?Leu?Gly?Asn?Lys?Phe?Ser?Gly?Leu?Phe?Asn?Ala?Ser?Gly?Arg?Ala
465 470 475 480
Phe?Pro?Asp?Val?Ser?Ala?Gln?Gly?Val?Asn?Tyr?Ala?Val?Tyr?Asp?Lys
485 490 495
Gly?Met?Leu?Gly?Gln?Phe?Asp?Gly?Thr?Ser?Cys?Ser?Ala?Pro?Thr?Phe
500 505 510
Ser?Gly?Val?Ile?Ala?Leu?Leu?Asn?Asp?Ala?Arg?Leu?Arg?Ala?Gly?Leu
515 520 525
Pro?Val?Met?Gly?Phe?Leu?Asn?Pro?Phe?Leu?Tyr?Gly?Val?Gly?Ser?Glu
530 535 540
Lys?Gly?Ala?Leu?Asn?Asp?Ile?Val?Asn?Gly?Gly?Ser?Val?Gly?Cys?Asp
545 550 555 560
Gly?Arg?Asn?Arg?Phe?Gly?Gly?Thr?Pro?Asn?Gly?Ser?Pro?Val?Val?Pro
565 570 575
Phe?Ala?Ser?Trp?Asn?Ala?Thr?Thr?Gly?Trp?Asp?Pro?Val?Ser?Gly?Leu
580 585 590
Gly?Thr?Pro?Asp?Phe?Ala?Lys?Leu?Lys?Gly?Val?Ala?Leu?Gly?Glu?Glu
595 600 605
Gly?Gly?Asn
610
<210>141
<211>478
<212>PRT
<213〉aspergillus niger
<400>141
Met?Trp?Leu?Phe?Leu?Val?Cys?Ser?Ile?Leu?Leu?Pro?Leu?Gly?Val?Val
1 5 10 15
Asn?Ala?Gln?Ser?Gln?Tyr?Phe?Asn?Asn?Lys?Thr?Lys?Glu?Phe?Val?Val
20 25 30
Asn?Gly?Ser?Ala?Ile?Pro?Phe?Val?Asp?Phe?Asp?Ile?Gly?Glu?Ser?Tyr
35 40 45
Ala?Gly?Tyr?Leu?Pro?Asn?Thr?Pro?Ser?Gly?Ile?Ser?Ser?Leu?Tyr?Phe
50 55 60
Trp?Phe?Phe?Pro?Ser?Ser?Asp?Pro?Asp?Ala?Ser?Asp?Glu?Ile?Thr?Val
65 70 75 80
Trp?Leu?Asn?Gly?Gly?Pro?Gly?Cys?Ser?Ser?Leu?Ala?Gly?Ile?Met?Leu
85 90 95
Glu?Asn?Gly?Pro?Phe?Leu?Trp?Gln?Pro?Gly?Thr?Tyr?Arg?Pro?Val?Arg
100 105 110
Asn?Pro?Tyr?Ala?Trp?Asn?Asn?Leu?Thr?Asn?Met?Val?Tyr?Ile?Asp?Gln
115 120 125
Pro?Ala?Gly?Thr?Gly?Phe?Ser?Leu?Gly?Pro?Ser?Thr?Val?Val?Ser?Glu
130 135 140
Phe?Asp?Val?Ala?Arg?Gln?Phe?Met?Asp?Phe?Trp?Arg?Arg?Phe?Met?Lys
145 150 155 160
Thr?Phe?Asp?Leu?Gln?Asn?Arg?Lys?Ile?Tyr?Leu?Thr?Gly?Glu?Ser?Tyr
165 170 175
Ala?Gly?Gln?Tyr?Ile?Pro?Tyr?Ile?Ala?Ser?Gln?Met?Leu?Asp?Gln?Asp
180 185 190
Asp?Asp?Glu?Tyr?Phe?Arg?Val?Ala?Gly?Ile?Gln?Ile?Asn?Asp?Pro?Tyr
195 200 205
Ile?Asn?Glu?Leu?Pro?Val?Leu?Gln?Asp?Val?Ala?Thr?Val?Asn?Gln?His
210 215 220
Arg?Ser?Leu?Phe?Pro?Phe?Asn?Asp?Thr?Phe?Met?Ser?Gln?Ile?Thr?Lys
225 230 235 240
Leu?Ser?Asp?Asp?Cys?Gly?Tyr?Thr?Ser?Phe?Leu?Asp?Asp?Ala?Leu?Thr
245 250 255
Phe?Pro?Pro?Arg?Ser?Gln?Phe?Pro?Ser?Val?Pro?Tyr?Asn?Ala?Ser?Cys
260 265 270
Asn?Ile?Trp?Asp?Ile?Ile?Asn?Asn?Ala?Ser?Leu?Ala?Leu?Asn?Pro?Cys
275 280 285
Phe?Asn?Arg?Tyr?His?Ile?Pro?Asp?Ala?Cys?Pro?Thr?Pro?Trp?Asn?Pro
290 295 300
Val?Gly?Gly?Pro?Ile?Val?Gly?Leu?Gly?Pro?Thr?Asn?Tyr?Phe?Asn?Arg
305 310 315 320
Ser?Asp?Val?Gln?Lys?Ala?Ile?Asn?Ala?Tyr?Pro?Thr?Asp?Tyr?Phe?Val
325 330 335
Cys?Lys?Asp?Gly?Ile?Phe?Pro?Thr?Ala?Asn?Gly?Leu?Asp?Thr?Ser?Pro
340 345 350
Pro?Ser?Ser?Leu?Gly?Pro?Leu?Pro?Arg?Val?Ile?Glu?Gln?Thr?Asn?Asn
355 360 365
Thr?Ile?Ile?Ala?His?Gly?Leu?Met?Asp?Phe?Glu?Leu?Leu?Ala?Gln?Gly
370 375 380
Thr?Leu?Ile?Ser?Ile?Gln?Asn?Met?Thr?Trp?Asn?Gly?Lys?Gln?Gly?Phe
385 390 395 400
Glu?Arg?Glu?Pro?Val?Glu?Pro?Leu?Phe?Val?Pro?Tyr?Gly?Gly?Ser?Ser
405 410 415
Gly?Gly?Gly?Val?Leu?Gly?Thr?Ala?His?Thr?Glu?Arg?Gly?Leu?Thr?Phe
420 425 430
Ser?Thr?Val?Phe?Ser?Ser?Gly?His?Glu?Ile?Pro?Glu?Tyr?Ala?Pro?Gly
435 440 445
Ala?Ala?Tyr?Arg?Gln?Leu?Glu?Phe?Leu?Leu?Gly?Arg?Val?Ala?Asn?Leu
450 455 460
Ser?Thr?Ile?Ile?Glu?Gln?Val?Gln?Ile?Thr?Glu?Gln?Asn?Gly
465 470 475
<210>142
<211>210
<212>PRT
<213〉aspergillus niger
<400>142
Met?Ser?Lys?Leu?Ser?Ala?Ala?Ile?Ser?Lys?Leu?Ser?Leu?Ser?Thr?Ile
1 5 10 15
Ala?Thr?Thr?Leu?Leu?Leu?Leu?Thr?Pro?Pro?Thr?Thr?Ala?Tyr?Phe?Tyr
20 25 30
Lys?Tyr?Pro?Ala?Leu?Phe?Val?Tyr?Lys?Asp?Thr?Asn?Cys?Thr?Asp?Ile
35 40 45
Ser?Phe?Ser?Leu?Val?Tyr?Pro?Ser?Leu?Gly?Asn?Cys?Asn?Gly?Gly?Tyr
50 55 60
Tyr?Asp?Tyr?Ala?Gly?Ser?Phe?Gln?Met?Phe?Asn?Ile?Asp?Ala?Ala?Tyr
65 70 75 80
Thr?Cys?Asn?Gly?Ser?Asp?Ser?Thr?Leu?Met?Phe?Glu?Met?Tyr?Asn?Ser
85 90 95
Ser?Gly?Ser?Asp?Cys?Gly?Asp?Glu?Ser?Asp?Leu?Leu?Phe?Arg?Gln?Pro
100 105 110
Val?Thr?Glu?Glu?Cys?Thr?Val?Ala?Asp?Val?Glu?Ser?Pro?Gly?Pro?Leu
115 120 125
Glu?Met?Pro?Val?Trp?Phe?Glu?Leu?Gly?Ser?Leu?Leu?Gly?Asn?Cys?Gly
130 135 140
Gly?Met?Ala?Gly?Thr?Met?Leu?Phe?Gly?Val?Gly?Ile?Leu?Glu?Gly?Gly
145 150 155 160
Leu?Glu?Thr?Lys?Leu?Tyr?Trp?Lys?Cys?Tyr?Ser?Ser?Arg?Leu?Asn?Thr
165 170 175
Ser?Val?Thr?Val?His?Arg?Leu?Ser?Leu?Ile?Leu?Ser?Met?Gly?Cys?Thr
180 185 190
Ser?Val?Ser?Asp?Ser?Tyr?Asn?Glu?Leu?Ala?Ala?Ala?His?Tyr?Tyr?Glu
195 200 205
Asp?Leu
210
<210>143
<211>608
<212>PRT
<213〉aspergillus niger
<400>143
Met?Arg?His?Leu?Leu?Ser?Leu?Leu?Val?Leu?Leu?Ile?Ala?Ser?Ala?Ala
1 5 10 15
Leu?Val?Ser?Ala?Val?Pro?Ala?Gly?Ser?Ile?Ile?Thr?Pro?Gln?Pro?Pro
20 25 30
Val?Glu?Pro?Val?His?Leu?Leu?Ser?Ser?Gln?Pro?Ser?Asp?Pro?Arg?Arg
35 40 45
Pro?Trp?Ile?Arg?Leu?Arg?Asp?Trp?Ile?Ile?Glu?Ser?Ile?Trp?Gly?Ile
50 55 60
Glu?Lys?Pro?Ala?Ser?Arg?Arg?Phe?Pro?Leu?Asn?Asp?Ser?Pro?Arg?Asn
65 70 75 80
Arg?Ser?Pro?Pro?Ser?Arg?Ile?Leu?Ala?Arg?Tyr?Gly?Ser?Asp?Val?Val
85 90 95
Leu?Arg?Phe?Ser?Leu?Arg?Asn?His?Asp?Glu?Ala?Glu?Ala?Leu?Ala?Gln
100 105 110
Ala?Ala?Asp?Ile?Leu?Phe?Leu?Asp?Val?Trp?Ala?Ser?Thr?Pro?Ala?Phe
115 120 125
Val?Asp?Ile?Arg?Leu?Ala?Glu?Glu?Val?Thr?Ala?Tyr?Thr?Pro?Leu?Ile
130 135 140
Asp?Asn?Leu?Ala?Glu?Arg?Ile?Tyr?Thr?Thr?Tyr?Pro?Ser?Lys?Lys?Pro
145 150 155 160
Ile?Gly?Leu?Glu?Gly?Gln?Ser?Gly?Phe?Ala?Ser?Ser?Ser?Arg?Pro?Ala
165 170 175
Pro?Lys?Phe?Gly?Asp?Leu?Phe?Phe?His?Glu?Tyr?Gln?Pro?Leu?Ser?Val
180 185 190
Ile?Ile?Pro?Trp?Met?Arg?Leu?Leu?Ala?Ser?Met?Phe?Pro?Ser?His?Val
195 200 205
Arg?Met?Ile?Ser?Val?Gly?Val?Ser?Tyr?Glu?Gly?Arg?Glu?Ile?Pro?Ala
210 215 220
Leu?Arg?Leu?Ser?Ala?Gly?Ser?Ser?Thr?Ala?Ala?Ser?Gly?Pro?Arg?Lys
225 230 235 240
Thr?Ile?Ile?Val?Thr?Gly?Gly?Ser?His?Ala?Arg?Glu?Trp?Ile?Gly?Thr
245 250 255
Ser?Thr?Val?Asn?His?Val?Met?Tyr?Thr?Leu?Ile?Thr?Lys?Tyr?Gly?Lys
260 265 270
Ser?Lys?Ala?Val?Thr?Arg?Leu?Leu?Gln?Asp?Phe?Asp?Trp?Ile?Met?Ile
275 280 285
Pro?Thr?Ile?Asn?Pro?Asp?Gly?Tyr?Val?Tyr?Thr?Trp?Glu?Thr?Asp?Arg
290 295 300
Leu?Trp?Arg?Lys?Asn?Arg?Gln?Arg?Thr?Ser?Leu?Arg?Phe?Cys?Pro?Gly
305 310 315 320
Ile?Asp?Leu?Asp?Arg?Ala?Trp?Gly?Phe?Glu?Trp?Asp?Gly?Gly?Arg?Thr
325 330 335
Arg?Ala?Asn?Pro?Cys?Ser?Glu?Asn?Tyr?Ala?Gly?Asp?Glu?Pro?Phe?Glu
340 345 350
Gly?Met?Glu?Ala?Gln?Gln?Leu?Ala?Gln?Trp?Ala?Leu?Asn?Glu?Thr?Gln
355 360 365
Asn?Asn?Asn?Ala?Asp?Ile?Val?Ser?Phe?Leu?Asp?Leu?His?Ser?Tyr?Ser
370 375 380
Gln?Thr?Ile?Leu?Tyr?Pro?Phe?Ser?Tyr?Ser?Cys?Ser?Ser?Ile?Pro?Pro
385 390 395 400
Thr?Leu?Glu?Ser?Leu?Glu?Glu?Leu?Gly?Leu?Gly?Leu?Ala?Lys?Ala?Ile
405 410 415
Arg?Tyr?Ala?Thr?His?Glu?Ile?Tyr?Asp?Val?Thr?Ser?Ala?Cys?Glu?Gly
420 425 430
Ile?Val?Thr?Ala?Ser?Ala?Ala?Asp?Asn?Asn?Pro?Gly?Arg?Phe?Phe?Pro
435 440 445
Ile?Gly?Gly?Asn?Ser?Gly?Gly?Ser?Ala?Leu?Asp?Trp?Phe?Tyr?His?Gln
450 455 460
Val?His?Ala?Thr?Tyr?Ser?Tyr?Gln?Ile?Lys?Leu?Arg?Asp?Arg?Gly?Ser
465 470 475 480
Tyr?Gly?Phe?Leu?Leu?Pro?Ser?Glu?His?Ile?Ile?Pro?Thr?Gly?Lys?Glu
485 490 495
Ile?Tyr?Asn?Val?Val?Leu?Lys?Leu?Gly?Ser?Phe?Leu?Ile?Gly?Gly?Asp
500 505 510
Ser?Phe?Asp?Val?Asp?Trp?Glu?Ser?Glu?Leu?Phe?Asp?Leu?Ser?Lys?Asp
515 520 525
Glu?Ser?Asp?Leu?Asp?Ser?Arg?Tyr?Ser?Lys?Ser?Asn?Asp?Arg?Ser?Pro
530 535 540
Ala?Tyr?Leu?His?Asn?Ala?Asn?Gly?Pro?Leu?Pro?Asn?Ile?Asp?Glu?Asp
545 550 555 560
Glu?Asp?Lys?Glu?Trp?Val?Met?Val?Glu?Glu?Glu?Asp?Tyr?Thr?Asp?Asp
565 570 575
Asp?Asp?Asp?Asp?Asp?Asp?Asp?Asp?Glu?Glu?Glu?Glu?Glu?Glu?Glu?Glu
580 585 590
Asp?Thr?Tyr?Trp?Ala?Thr?Glu?His?Thr?Tyr?Glu?Phe?Arg?Arg?Arg?Arg
595 600 605
<210>144
<211>416
<212>PRT
<213〉aspergillus niger
<400>144
Met?Ala?Phe?Leu?Lys?Arg?Ile?Leu?Pro?Leu?Leu?Ala?Leu?Ile?Leu?Pro
1 5 10 15
Ala?Val?Phe?Ser?Ala?Thr?Glu?Gln?Val?Pro?His?Pro?Thr?Ile?Gln?Thr
20 25 30
Ile?Pro?Gly?Lys?Tyr?Ile?Val?Thr?Phe?Lys?Ser?Gly?Ile?Asp?Asn?Ala
35 40 45
Lys?Ile?Glu?Ser?His?Ala?Ala?Trp?Val?Thr?Glu?Leu?His?Arg?Arg?Ser
50 55 60
Leu?Glu?Gly?Arg?Ser?Thr?Thr?Glu?Asp?Asp?Leu?Pro?Ala?Gly?Ile?Glu
65 70 75 80
Arg?Thr?Tyr?Arg?Ile?Ala?Asn?Phe?Ala?Gly?Tyr?Ala?Gly?Ser?Phe?Asp
85 90 95
Glu?Lys?Thr?Ile?Glu?Glu?Ile?Arg?Lys?His?Asp?His?Val?Ala?Tyr?Val
100 105 110
Glu?Gln?Asp?Gln?Val?Trp?Tyr?Leu?Asp?Thr?Leu?Val?Thr?Glu?Arg?Arg
115 120 125
Ala?Pro?Trp?Gly?Leu?Gly?Ser?Ile?Ser?His?Arg?Gly?Gly?Ser?Ser?Thr
130 135 140
Asp?Tyr?Ile?Tyr?Asp?Asp?Ser?Ala?Gly?Glu?Gly?Thr?Tyr?Ala?Tyr?Val
145 150 155 160
Val?Asp?Thr?Gly?Ile?Leu?Ala?Thr?His?Asn?Glu?Phe?Gly?Gly?Arg?Ala
165 170 175
Ser?Leu?Ala?Tyr?Asn?Ala?Ala?Gly?Gly?Glu?His?Val?Asp?Asp?Val?Gly
180 185 190
His?Gly?Thr?His?Val?Ala?Gly?Thr?Ile?Gly?Gly?Lys?Thr?Tyr?Gly?Val
195 200 205
Ser?Lys?Asn?Ala?His?Leu?Leu?Ser?Val?Lys?Val?Phe?Val?Gly?Glu?Ser
210 215 220
Ser?Ser?Thr?Ser?Val?Ile?Leu?Asp?Gly?Phe?Asn?Trp?Ala?Ala?Asn?Asp
225 230 235 240
Ile?Val?Ser?Lys?Asn?Arg?Thr?Ser?Lys?Ala?Ala?Ile?Asn?Met?Ser?Leu
245 250 255
Gly?Gly?Gly?Tyr?Ser?Tyr?Ala?Phe?Asn?Asn?Ala?Val?Glu?Asn?Ala?Phe
260 265 270
Asp?Glu?Gly?Val?Leu?Ser?Cys?Val?Ala?Ala?Gly?Asn?Glu?Asn?Arg?Asp
275 280 285
Ala?Ala?Arg?Thr?Ser?Pro?Ala?Ser?Ala?Pro?Asp?Ala?Ile?Thr?Val?Ala
290 295 300
Ala?Ile?Asn?Arg?Ser?Asn?Ala?Arg?Ala?Ser?Phe?Ser?Asn?Tyr?Gly?Ser
305 310 315 320
Val?Val?Asp?Ile?Phe?Ala?Pro?Gly?Glu?Gln?Val?Leu?Ser?Ala?Trp?Thr
325 330 335
Gly?Ser?Asn?Ser?Ala?Thr?Asn?Thr?Ile?Ser?Gly?Thr?Ser?Met?Ala?Thr
340 345 350
Pro?His?Val?Thr?Gly?Leu?Ile?Leu?Tyr?Leu?Met?Gly?Leu?Arg?Asp?Leu
355 360 365
Ala?Thr?Pro?Ala?Ala?Ala?Thr?Thr?Glu?Leu?Lys?Arg?Leu?Ala?Thr?Arg
370 375 380
Asn?Ala?Val?Thr?Asn?Val?Ala?Gly?Ser?Pro?Asn?Leu?Leu?Ala?Tyr?Asn
385 390 395 400
Gly?Asn?Ser?Gly?Val?Ser?Lys?Gly?Gly?Ser?Asp?Asp?Gly?Asp?Glu?Asp
405 410 415
<210>145
<211>455
<212>PRT
<213〉aspergillus niger
<400>145
Met?Ile?Thr?Leu?Leu?Ser?Ala?Leu?Phe?Gly?Ser?Val?Val?Tyr?Ala?Ala
1 5 10 15
Thr?Gln?Thr?Val?Leu?Gly?Pro?Glu?Gly?Ala?Asp?Pro?Phe?Thr?Val?Phe
20 25 30
Arg?Ser?Pro?His?Ser?Pro?Ala?Phe?Ser?Ile?Arg?Ile?Gln?Glu?Gln?Asn
35 40 45
Asp?Ser?Ile?Cys?Asp?Ala?Arg?Ser?Pro?Gln?Phe?Thr?Gly?Trp?Leu?Asp
50 55 60
Ile?Gly?Pro?Lys?His?Leu?Phe?Phe?Trp?Tyr?Phe?Glu?Ser?Gln?Asn?Asp
65 70 75 80
Pro?Phe?His?Asp?Pro?Leu?Thr?Leu?Trp?Met?Thr?Gly?Gly?Pro?Gly?Asp
85 90 95
Ser?Ser?Met?Ile?Gly?Leu?Phe?Glu?Glu?Val?Gly?Pro?Cys?Arg?Ile?Asn
100 105 110
Glu?Phe?Gly?Asn?Gly?Thr?Asp?His?Asn?Pro?Trp?Ala?Trp?Thr?Lys?Asn
115 120 125
Ser?Ser?Leu?Leu?Phe?Val?Asp?Gln?Pro?Val?Asp?Val?Gly?Phe?Ser?Tyr
130 135 140
Ile?Asp?Glu?Gly?Tyr?Glu?Leu?Pro?His?Asp?Ser?Arg?Glu?Ala?Ala?Val
145 150 155 160
Asp?Met?His?Arg?Phe?Leu?Arg?Leu?Phe?Ile?Ser?Glu?Ile?Phe?Pro?His
165 170 175
Lys?Gln?Phe?Leu?Pro?Val?His?Leu?Ser?Gly?Glu?Ser?Tyr?Ala?Gly?Arg
180 185 190
Tyr?Ile?Pro?Tyr?Leu?Ala?Thr?Gln?Ile?Leu?Glu?Gln?Asn?Glu?Leu?Tyr
195 200 205
Lys?Asp?Ser?Pro?Arg?Ile?Pro?Leu?Lys?Ser?Cys?Leu?Val?Gly?Asn?Gly
210 215 220
Phe?Met?Ser?Pro?Lys?Asp?Ala?Thr?Phe?Gly?Tyr?Trp?Glu?Thr?Leu?Cys
225 230 235 240
Thr?Thr?Asn?Ser?Gly?Val?Pro?Ser?Pro?Ile?Phe?Asn?Glu?Thr?Arg?Cys
245 250 255
Asp?Ile?Met?Ala?Ala?Asn?Met?Pro?His?Cys?Met?Asp?Leu?Tyr?Asp?Ile
260 265 270
Cys?Ile?Gln?His?Ser?Asp?Pro?Ala?Ile?Cys?His?Ala?Ala?Gln?Ser?Val
275 280 285
Cys?Tyr?Asp?Ser?Val?Val?Gly?Leu?Met?Ala?Lys?Leu?Leu?Leu?Arg?Met
290 295 300
Thr?Thr?Val?Thr?Ala?Pro?Cys?Glu?Ile?Asp?Glu?Met?Cys?Tyr?Ile?Glu
305 310 315 320
Ala?Ala?Leu?Ile?Glu?Arg?Tyr?Leu?Asn?Ser?Pro?Ser?Val?Trp?Glu?Ala
325 330 335
Leu?Ser?Pro?Pro?Gln?Gln?Val?Thr?Glu?Tyr?Lys?Phe?Val?Ala?Thr?Ser
340 345 350
Val?Ile?Asp?Ala?Phe?Ala?Gln?Ser?Ala?Asp?Gly?Met?Val?Ser?Ser?Ser
355 360 365
Lys?Gln?Ile?Ala?Phe?Leu?Leu?Ala?Asn?Asn?Val?Asp?Phe?Leu?Ala?Tyr
370 375 380
Gln?Gly?Asn?Leu?Asp?Leu?Ala?Cys?Asn?Thr?Ala?Gly?Asn?Leu?Arg?Trp
385 390 395 400
Ala?Asn?Ser?Leu?Ser?Trp?Lys?Gly?Gln?Thr?Glu?Phe?Thr?Ala?Lys?Pro
405 410 415
Leu?Leu?Pro?Trp?Glu?Ile?Gln?Val?Ser?Val?Gly?Glu?Gly?Thr?Asp?Glu
420 425 430
Thr?Ser?Arg?Phe?Ala?Phe?Val?Thr?Val?Asp?Asn?Ala?Gly?His?Leu?Leu
435 440 445
Arg?Asp?Ser?Lys?Ile?Ser?Asn
450 455
<210>146
<211>791
<212>PRT
<213〉aspergillus niger
<400>146
Met?Arg?Phe?Leu?Thr?Tyr?Ser?Leu?Pro?Phe?Ile?Ala?Ser?Ala?Ile?Ser
1 5 10 15
Leu?Phe?Gly?Val?Asn?Val?Gln?Ala?Arg?Ser?Gln?Ala?Pro?Ser?Ala?Ile
20 25 30
Arg?His?Val?Ser?Thr?Leu?Asp?Gln?Pro?Thr?Ile?Lys?Thr?Pro?Ser?Gln
35 40 45
Arg?Val?Asp?His?Leu?Asp?His?Phe?Asp?Ile?Thr?Phe?Asn?Ile?His?Asp
50 55 60
Lys?His?Gln?Arg?Ile?Lys?Leu?Glu?Leu?Glu?Pro?Asn?His?Asp?Ile?Leu
65 70 75 80
Ala?Glu?Asp?Ala?Ser?Val?Gln?Tyr?Leu?Asp?Ala?Asp?Gly?Asn?Val?Arg
85 90 95
Arg?His?Glu?Pro?Ile?Ala?Pro?His?Glu?His?Lys?Val?Phe?Lys?Gly?Arg
100 105 110
Ser?Leu?Leu?Gly?Arg?Gly?Lys?Gly?Met?Trp?Asp?Pro?Val?Gly?Trp?Ala
115 120 125
Arg?Ile?Tyr?Leu?Lys?Gln?Asp?Gly?Ser?Glu?Pro?Leu?Phe?Glu?Gly?Val
130 135 140
Phe?Ser?Ile?Asp?Gly?Asp?Asn?His?His?Val?Gln?Leu?Lys?Ser?Ala?Tyr
145 150 155 160
Met?Glu?Lys?Lys?Arg?Pro?Val?Asp?Val?Asp?Leu?Pro?Asp?Ser?Ala?Thr
165 170 175
Asp?Tyr?Met?Ile?Phe?Tyr?Arg?Asp?Ser?Asp?Met?Val?Arg?Leu?His?Thr
180 185 190
Glu?Leu?Lys?Arg?Ser?Ser?Leu?Gly?Ser?Thr?Ser?Cys?Gln?Ala?Asp?Gln
195 200 205
Leu?Gly?Phe?Asn?Thr?Asn?Pro?Asn?His?Pro?Val?Leu?Gln?Pro?Tyr?Gly
210 215 220
Gln?Ala?Glu?Thr?Asp?Thr?Trp?Gly?Ala?Ile?Ser?Leu?Asn?Ser?Leu?Phe
225 230 235 240
Gly?Leu?Asn?Lys?Arg?Gln?Ser?Asp?Ile?Gly?Ser?Val?Ser?Gly?Asn?Ala
245 250 255
Gly?Gly?Val?Asn?Leu?Ala?Ser?Thr?Ile?Gly?Asp?Thr?Ser?Gly?Cys?Pro
260 265 270
Ser?Thr?Lys?Gln?Val?Ala?Leu?Ile?Gly?Val?Ala?Thr?Asp?Cys?Ala?Phe
275 280 285
Thr?Gly?Ser?Phe?Asn?Asn?Glu?Thr?Ala?Ala?Lys?Glu?Trp?Val?Ile?Ser
290 295 300
Thr?Val?Asn?Ser?Ala?Ser?Asn?Val?Tyr?Glu?Lys?Ser?Phe?Asn?Ile?Thr
305 310 315 320
Ile?Gly?Leu?Arg?Asn?Leu?Thr?Ile?Thr?Asp?Ser?Ser?Cys?Pro?Asp?Asn
325 330 335
Pro?Pro?Ala?Ala?Thr?Ala?Trp?Asn?Met?Pro?Cys?Ser?Ser?Gly?Asn?Leu
340 345 350
Thr?Ser?Arg?Leu?Asp?Leu?Phe?Ser?Lys?Trp?Arg?Gly?Glu?Gln?Ser?Asp
355 360 365
Asp?Asn?Ala?Tyr?Trp?Thr?Leu?Met?Ser?Asp?Cys?Ala?Thr?Gly?Asn?Glu
370 375 380
Val?Gly?Leu?Ser?Trp?Leu?Gly?Gln?Leu?Cys?Asn?Ser?Asp?Ala?Ser?Ser
385 390 395 400
Asp?Gly?Ser?Ser?Thr?Val?Ser?Gly?Thr?Asn?Val?Val?Val?Arg?Ser?Ser
405 410 415
Gly?Ser?Asp?Trp?Gln?Ile?Phe?Ala?His?Glu?Ser?Gly?His?Thr?Phe?Gly
420 425 430
Ala?Val?His?Asp?Cys?Asp?Ser?Gln?Thr?Cys?Ala?Glu?Asp?Leu?Glu?Ala
435 440 445
Ser?Ser?Gln?Cys?Cys?Pro?Leu?Thr?Ser?Ser?Thr?Cys?Asn?Ala?Asn?Gly
450 455 460
Lys?Tyr?Ile?Met?Asn?Pro?Thr?Thr?Gly?Thr?Asp?Ile?Thr?Ala?Phe?Ser
465 470 475 480
Gln?Cys?Thr?Ile?Gly?Asn?Ile?Cys?Ala?Ala?Leu?Gly?Arg?Asn?Ser?Val
485 490 495
Lys?Ser?Ser?Cys?Leu?Ser?Ala?Asn?Arg?Asp?Val?Thr?Thr?Tyr?Thr?Gly
500 505 510
Ser?Gln?Cys?Gly?Asn?Gly?Ile?Val?Glu?Ser?Gly?Glu?Asp?Cys?Asp?Cys
515 520 525
Gly?Gly?Glu?Asp?Gly?Cys?Gly?Asp?Asn?Asn?Cys?Cys?Asp?Ala?Lys?Thr
530 535 540
Cys?Lys?Phe?Lys?Ser?Gly?Ala?Val?Cys?Asp?Asp?Ser?Asn?Asp?Ser?Cys
545 550 555 560
Cys?Ser?Ser?Cys?Gln?Phe?Ser?Ser?Ala?Gly?Thr?Val?Cys?Arg?Ala?Ser
565 570 575
Arg?Gly?Asp?Cys?Asp?Val?Ala?Glu?Thr?Cys?Ser?Gly?Asn?Ser?Ser?Thr
580 585 590
Cys?Pro?Thr?Asp?Ser?Phe?Lys?Lys?Asp?Gly?Thr?Ser?Cys?Gly?Ser?Ser
595 600 605
Gly?Ser?Gly?Leu?Ala?Cys?Ala?Ser?Gly?Gln?Cys?Thr?Ser?Arg?Asp?Tyr
610 615 620
Gln?Cys?Arg?Ser?Val?Met?Gly?Ser?Leu?Leu?His?Ser?Asn?Asp?Thr?Tyr
625 630 635 640
Ala?Cys?Ser?Ser?Phe?Ser?Ser?Ser?Cys?Glu?Leu?Val?Cys?Thr?Ser?Pro
645 650 655
Lys?Ile?Gly?Thr?Cys?Tyr?Ser?Val?Asn?Gln?Asn?Phe?Leu?Asp?Gly?Thr
660 665 670
Pro?Cys?Gly?Ser?Gly?Gly?Tyr?Cys?Ser?Asn?Gly?Asp?Cys?Lys?Gly?Gln
675 680 685
Asn?Val?Glu?Ser?Trp?Ile?Lys?Asn?His?Lys?Gly?Ile?Val?Ile?Gly?Val
690 695 700
Ala?Cys?Ala?Val?Gly?Ala?Leu?Ile?Leu?Leu?Ala?Leu?Met?Thr?Cys?Ile
705 710 715 720
Val?Asn?Arg?Cys?Arg?Arg?Ala?Arg?Ala?Pro?Lys?Pro?Val?Pro?Arg?Pro
725 730 735
Val?Pro?Tyr?Gly?Pro?Trp?Pro?Gly?Ala?Arg?Pro?Pro?Pro?Pro?Pro?Pro
740 745 750
Met?Asn?Gln?Trp?Pro?Ala?Arg?Gly?Tyr?Gln?Gly?Leu?Gly?Asn?Glu?Pro
755 760 765
Pro?Pro?Pro?Tyr?Pro?Gly?Val?Pro?Gly?Gln?Pro?Val?Pro?Gln?His?Met
770 775 780
Pro?Pro?Gln?Gly?Arg?Tyr?Ala
785 790
<210>147
<211>481
<212>PRT
<213〉aspergillus niger
<400>147
Met?Arg?Phe?Leu?Ser?Ser?Ala?Ala?Leu?Phe?Gly?Leu?Ala?Tyr?Ala?Ser
1 5 10 15
Thr?Gln?Ala?Val?Leu?Gln?Pro?Glu?Glu?Pro?Ser?Asp?Phe?Arg?Thr?Phe
20 25 30
His?Ser?Pro?Tyr?Ser?Pro?His?His?Ser?Ile?Arg?Ile?Arg?Gln?Gln?Asn
35 40 45
Glu?Ser?Ile?Cys?Ala?Ala?His?Ser?Ala?Gln?Tyr?Thr?Gly?Trp?Leu?Asp
50 55 60
Ile?Gly?Arg?Lys?His?Leu?Phe?Phe?Trp?Tyr?Phe?Glu?Ser?Gln?Asn?Asp
65 70 75 80
Pro?Ala?Asn?Asp?Pro?Leu?Thr?Leu?Trp?Met?Thr?Gly?Gly?Pro?Gly?Gly
85 90 95
Ser?Ser?Met?Ile?Gly?Leu?Phe?Glu?Glu?Val?Gly?Pro?Cys?Leu?Ile?Asn
100 105 110
Glu?Tyr?Gly?Asn?Gly?Thr?Tyr?Tyr?Asn?Pro?Trp?Gly?Trp?Ser?Arg?Asn
115 120 125
Ser?Ser?Leu?Leu?Phe?Val?Asp?Gln?Pro?Val?Asp?Val?Gly?Phe?Ser?Tyr
130 135 140
Val?Asp?Glu?Gly?Glu?Asp?Leu?Pro?Gly?Asp?Ser?His?Gln?Ala?Ala?Ile
145 150 155 160
Asp?Met?His?Arg?Phe?Leu?Gln?Leu?Phe?Val?Ser?Glu?Val?Phe?Pro?Gln
165 170 175
Leu?Gln?Thr?Leu?Pro?Val?His?Leu?Ser?Gly?Glu?Ser?Tyr?Ala?Gly?His
180 185 190
Tyr?Val?Pro?Tyr?Leu?Gly?Ser?Gln?Ile?Val?Gln?Gln?Asn?Lys?Leu?Tyr
195 200 205
Pro?Thr?Glu?Pro?Gln?Val?Leu?Leu?His?Ser?Cys?Leu?Val?Gly?Asn?Gly
210 215 220
Tyr?Tyr?Ser?Pro?Arg?Asp?Thr?Thr?Tyr?Gly?Tyr?Trp?Glu?Thr?Leu?Cys
225 230 235 240
Thr?Thr?Asn?Pro?Gly?Val?Pro?Glu?Pro?Val?Phe?Asn?Arg?Thr?Arg?Cys
245 250 255
Asp?Ile?Met?Ala?Ala?Asn?Met?Pro?Arg?Cys?Met?Glu?Val?Ser?Asp?Val
260 265 270
Cys?Val?Arg?Asn?Pro?Asp?Pro?Ala?Ile?Cys?His?Ala?Ala?Ser?Glu?Val
275 280 285
Cys?Tyr?Glu?Gly?Val?Ile?Gly?Trp?Tyr?Asp?Asp?Glu?Ser?Gly?Glu?Gly
290 295 300
Gly?Arg?Asn?Arg?Phe?Asp?Ile?Thr?Ala?Pro?Cys?Ala?Leu?Asp?Gly?Ile
305 310 315 320
Cys?Tyr?Ile?Glu?Ala?Ala?Arg?Ile?Glu?Gln?Tyr?Leu?Asn?Thr?Pro?Ala
325 330 335
Val?Trp?Ala?Ala?Leu?Ser?Pro?Pro?Lys?Glu?Ile?Lys?Glu?Tyr?Lys?Val
340 345 350
Thr?Ser?Asp?Asn?Val?Ser?Arg?Ala?Phe?Asp?Leu?Thr?Ser?Asp?Thr?Met
355 360 365
Thr?Pro?Ala?Ser?Glu?Gln?Val?Ala?Phe?Leu?Leu?Ala?Asn?Gln?Val?His
370 375 380
Phe?Leu?Ala?Tyr?Gln?Gly?Asn?Leu?Asp?Leu?Ala?Cys?Asn?Thr?Ala?Gly
385 390 395 400
Asn?Leu?Arg?Trp?Ala?His?Ser?Leu?Pro?Trp?Arg?Gly?Gln?Val?Glu?Phe
405 410 415
Ala?Ser?Lys?Ala?Leu?Arg?Pro?Trp?Ser?Trp?Val?Asp?Val?Val?Ser?Gly
420 425 430
Lys?Gly?Gly?Val?Ala?Gly?Thr?Thr?Lys?Glu?Glu?Ser?Arg?Phe?Ala?Leu
435 440 445
Val?Thr?Val?Asp?Gly?Ala?Gly?His?Phe?Leu?Pro?Gln?Asp?Arg?Pro?Asp
450 455 460
Ile?Ala?Leu?Asp?Met?Met?Val?Arg?Trp?Ile?Ser?Gly?Ala?Ser?Phe?Thr
465 470 475 480
Glu
<210>148
<211>319
<212>PRT
<213〉aspergillus niger
<400>148
Met?Thr?Leu?Leu?Leu?Asn?Phe?His?Ala?Leu?Phe?Thr?Val?Ile?Leu?Val
1 5 10 15
Ala?Asn?Leu?Ser?Thr?Arg?Cys?Ser?Ala?Leu?Leu?Ser?Gly?Arg?Asp?Phe
20 25 30
Cys?Ser?Thr?Pro?Ala?Pro?Gly?Glu?Ser?Leu?Arg?Ala?Glu?His?Arg?Arg
35 40 45
Leu?Tyr?Asp?Val?Gln?Ala?Gln?Arg?Asp?Ser?Thr?Ala?Glu?Glu?Ser?Arg
50 55 60
Glu?Val?Val?Pro?Trp?Ile?Glu?Ile?Glu?Thr?Trp?Phe?His?Ile?Val?Ser
65 70 75 80
Ser?Asn?Glu?Ala?Ala?Asn?Thr?Val?Ser?Asp?Asp?Met?Ile?Thr?Ser?Gln
85 90 95
Leu?Ser?Tyr?Leu?Gln?Lys?Ala?Tyr?Glu?Ser?Ala?Thr?Ile?Thr?Tyr?Arg
100 105 110
Leu?Glu?Gly?Ile?Thr?Arg?His?Ile?Asn?Asp?Ser?Trp?Ala?Arg?Asn?Asp
115 120 125
Asp?Glu?Leu?Gly?Met?Lys?Asn?Ala?Leu?Arg?Arg?Gly?Asn?Tyr?Gly?Thr
130 135 140
Leu?Asn?Val?Tyr?Phe?Gln?Thr?Asp?Leu?Gln?Ala?Ser?Ser?Asp?Glu?Asn
145 150 155 160
Ser?Arg?Asp?Tyr?Pro?Asn?Asp?Gly?Asn?Arg?Arg?Thr?Asp?Val?Ser?Asp
165 170 175
Gln?Ser?Ser?Ser?Thr?Val?Leu?Gly?Phe?Cys?Thr?Leu?Pro?Asp?Pro?Ser
180 185 190
Val?Asn?Ser?Ser?Ser?Pro?Arg?Ser?Ser?Tyr?Ile?Lys?Asp?Gly?Cys?Asn
195 200 205
Val?Leu?Ala?Asp?Ile?Met?Pro?Gly?Gly?Ser?Leu?Ala?Gln?Tyr?Asn?Lys
210 215 220
Gly?Gly?Thr?Ala?Val?His?Glu?Val?Gly?His?Trp?Asn?Gly?Leu?Leu?His
225 230 235 240
Thr?Phe?Glu?Gly?Glu?Ser?Cys?Ser?Pro?Asp?Asn?Glu?Gly?Asp?Tyr?Ile
245 250 255
Asp?Asp?Thr?Pro?Glu?Gln?Ser?Glu?Pro?Thr?Ser?Gly?Cys?Pro?Ala?Glu
260 265 270
Lys?Asp?Ser?Cys?Pro?Asp?Leu?Pro?Gly?Leu?Asp?Ala?Ile?His?Asn?Phe
275 280 285
Met?Asp?Tyr?Ser?Ser?Asp?Asp?Cys?Tyr?Glu?Ser?Phe?Thr?Pro?Asp?Gln
290 295 300
Ala?Glu?Arg?Met?Arg?Ser?Met?Trp?Ser?Ala?Met?Arg?Glu?Gly?Lys
305 310 315
<210>149
<211>639
<212>PRT
<213〉aspergillus niger
<400>149
Met?His?Val?Ser?Leu?Phe?Leu?Leu?Ser?Val?Thr?Ala?Ala?Phe?Ala?Ser
1 5 10 15
Pro?Thr?Pro?His?Asn?Tyr?Val?Val?His?Glu?Arg?Arg?Asp?Ala?Leu?Pro
20 25 30
Ser?Val?Trp?Val?Glu?Glu?Ser?Arg?Leu?Asp?Lys?Gly?Ala?Leu?Leu?Pro
35 40 45
Met?Arg?Ile?Gly?Leu?Thr?Gln?Ser?Asn?Leu?Asp?Arg?Gly?His?Asp?Leu
50 55 60
Leu?Met?Glu?Val?Ser?His?Pro?Gln?Ser?Ser?Arg?Tyr?Gly?Lys?His?Leu
65 70 75 80
Ser?Ser?Glu?Glu?Val?His?Asp?Leu?Phe?Ala?Pro?Ser?Asn?Glu?Ala?Val
85 90 95
Glu?Thr?Val?Arg?Thr?Trp?Ile?Glu?Ser?Ala?Gly?Ile?Ala?Pro?Ser?Arg
100 105 110
Ile?Ser?Gln?Ser?Tyr?Asn?Lys?Gln?Trp?Leu?Gln?Phe?Asp?Ala?His?Ala
115 120 125
Ser?Glu?Val?Glu?Gln?Leu?Leu?Gln?Thr?Glu?Tyr?Tyr?Ile?Tyr?Thr?His
130 135 140
Ala?Asp?Thr?Gly?Ser?Ser?His?Val?Thr?Cys?His?Glu?Tyr?His?Val?Pro
145 150 155 160
Glu?Thr?Ile?Gln?Ser?His?Ile?Asp?Tyr?Ile?Thr?Pro?Gly?Val?Lys?Met
165 170 175
Leu?Glu?Val?Arg?Gly?Thr?Pro?Ser?Lys?Lys?Arg?Asp?Ala?Glu?Lys?Arg
180 185 190
Ser?Leu?Gly?Ser?Leu?Pro?Pro?Ile?Leu?Ala?Pro?Leu?Pro?Ile?Asn?Ile
195 200 205
Thr?Lys?Ile?Phe?Asp?Asp?Pro?Leu?Ala?His?Cys?Asp?Leu?Ala?Val?Thr
210 215 220
Pro?Asp?Cys?Ile?Arg?Ala?Met?Tyr?Asn?Ile?Thr?Lys?Gly?Thr?Thr?Ala
225 230 235 240
Thr?Lys?Gly?Asn?Glu?Leu?Gly?Ile?Phe?Glu?Asp?Leu?Gly?Asp?Ile?Tyr
245 250 255
Ser?Gln?Asp?Asp?Leu?Asn?Leu?Phe?Phe?Ala?Asn?Phe?Ala?Ser?Asp?Ile
260 265 270
Pro?Gln?Gly?Thr?His?Pro?Thr?Leu?Asp?Ser?Ile?Asp?Gly?Ala?Thr?Ala
275 280 285
Pro?Thr?Asp?Val?Thr?Asn?Ala?Gly?Pro?Glu?Ser?Asp?Leu?Asp?Phe?Gln
290 295 300
Ile?Ala?Tyr?Pro?Ile?Ile?Trp?Pro?Gln?Asn?Thr?Ile?Leu?Tyr?Gln?Thr
305 310 315 320
Asp?Asp?Pro?Asn?Tyr?Glu?Asp?Asn?Tyr?Asn?Phe?Lys?Gly?Leu?Leu?Asn
325 330 335
Asn?Phe?Leu?Tyr?Ala?Ile?Asp?Gly?Ser?Tyr?Cys?Asn?Glu?Thr?Ser?Ser
340 345 350
Leu?Asp?Pro?Gln?Tyr?Pro?Asp?Pro?Ser?Pro?Gly?Gly?Tyr?Ser?Ser?Pro
355 360 365
Lys?Gln?Cys?Gly?Val?Tyr?Thr?Pro?Thr?Asn?Val?Ile?Ser?Ile?Ser?Tyr
370 375 380
Gly?Ser?Pro?Glu?Ala?Asp?Leu?Pro?Ile?Ala?Tyr?Gln?Arg?Arg?Gln?Cys
385 390 395 400
His?Glu?Phe?Met?Lys?Leu?Gly?Leu?Gln?Gly?Ile?Ser?Val?Val?Val?Ala
405 410 415
Ser?Gly?Asp?Ser?GlyVal?Ala?Ser?Ser?Thr?Gly?Thr?Cys?Phe?Gly?Asp
420 425 430
Ala?Asp?Asn?Val?Phe?Val?Pro?Asp?Phe?Pro?Ala?Thr?Cys?Pro?Tyr?Leu
435 440 445
Thr?Ala?Val?Gly?Gly?Thr?Tyr?Leu?Pro?Leu?Gly?Ala?Asp?Ala?Ala?Lys
450 455 460
Asp?Gln?Glu?Ile?Ala?Val?Thr?Arg?Phe?Pro?Ser?Gly?Gly?Gly?Phe?Ser
465 470 475 480
Asn?Ile?Tyr?Ala?Arg?Pro?Ser?Tyr?Gln?Asn?His?Ser?Val?Glu?Thr?Tyr
485 490 495
Phe?Ser?Thr?Thr?Ser?Asp?Asp?Leu?Thr?Tyr?Pro?Tyr?Tyr?Ser?Gly?Val
500 505 510
Asn?Tyr?Thr?Asp?Phe?Ser?Asn?Thr?Asp?Gly?Val?Tyr?Asn?Arg?Ile?Gly
515 520 525
Arg?Gly?Tyr?Pro?Asp?Val?Ser?Ala?Ile?Ala?Asp?Asn?Ile?Ile?Ile?Tyr
530 535 540
Asn?Gln?Gly?Glu?Ala?Thr?Leu?Val?Gly?Gly?Thr?Ser?Ala?Ala?Ala?Pro
545 550 555 560
Ala?Phe?Ala?Ala?Met?Leu?Thr?Arg?Ile?Asn?Glu?Glu?Arg?Leu?Ala?Lys
565 570 575
Gly?Lys?Ser?Thr?Val?Gly?Phe?Val?Asn?Pro?Val?Leu?Tyr?Glu?His?Pro
580 585 590
Glu?Ala?Phe?Arg?Asp?Val?Thr?Val?Gly?Ser?Asn?Pro?Gly?Cys?Gly?Thr
595 600 605
Asp?Gly?Phe?Pro?Val?Ala?Gly?Gly?Trp?Asp?Pro?Val?Thr?Gly?Leu?Gly
610 615 620
Thr?Pro?Arg?Phe?Glu?Asp?Leu?Met?Asp?Ile?Phe?Val?Gly?Asp?Asp
625 630 635
<210>150
<211>371
<212>PRT
<213〉aspergillus niger
<400>150
Met?Ala?Ser?Lys?Thr?Leu?Leu?Leu?Ile?Pro?Ala?Leu?Ala?Thr?Ala?Ala
1 5 10 15
Leu?Gly?Ser?Val?Leu?Asp?Leu?Asp?Ile?Lys?Val?Asp?Leu?Gly?Thr?Pro
20 25 30
Gly?Gly?Pro?Phe?Asp?Leu?Met?Tyr?Asp?Thr?Gly?Ser?Ser?Thr?Leu?Trp
35 40 45
Val?Leu?Asp?Ser?Asn?Cys?Thr?Asp?Asp?Cys?Pro?Asn?Val?Ser?Gly?Tyr
50 55 60
Ser?Arg?His?Gly?Tyr?Asn?Leu?Thr?Ser?Thr?Gly?Val?Asn?Leu?Gly?Val
65 70 75 80
Asn?Asp?Ser?Ile?Ala?Tyr?Ser?Gly?Gly?Thr?Val?Ser?Gly?Phe?Thr?Ala
85 90 95
Thr?Asp?Ile?Leu?Thr?Val?Pro?Asp?Thr?Asn?Val?Ser?Tyr?Arg?Gln?Ser
100 105 110
Phe?Ala?Val?Ile?Thr?Asp?Ser?Thr?Trp?Ala?Ala?Leu?Ala?Ala?Asp?Gly
115 120 125
Phe?Ile?Gly?Leu?Ala?Ser?Ser?Thr?Ile?Ala?Phe?Lys?Asn?Thr?Thr?Thr
130 135 140
Ala?Val?Glu?Gln?Met?Met?Gln?Asp?Gly?Leu?Leu?Asp?Glu?Pro?Arg?Phe
145 150 155 160
Ala?Ile?Tyr?Ala?Gly?Ser?Gly?Glu?Ser?Thr?Val?Thr?Asn?Pro?Asn?Pro
165 170 175
Glu?Asn?Asn?Gly?Val?Phe?Thr?Phe?Gly?Gly?Ser?His?Glu?Glu?Thr?Tyr
180 185 190
Ala?Asp?Gly?Glu?Leu?Gln?Trp?Met?Lys?Met?Leu?Ser?Pro?Phe?Glu?Ile
195 200 205
Tyr?Lys?Thr?Asn?Leu?Leu?Gly?Ile?Gln?Gly?His?Asn?Asn?Ser?Asp?Gly
210 215 220
Gln?Ala?Leu?Ser?Ser?Asp?Val?Leu?Asn?Trp?Tyr?Gly?Gln?Thr?Asn?Leu
225 230 235 240
Phe?Asn?Val?Ala?Gly?Ala?Ser?Ser?Ile?Ser?Ile?Pro?Asn?Asp?Gln?Ile
245 250 255
Glu?Ala?Met?Tyr?Ala?Leu?Thr?Pro?Phe?Ser?Tyr?Ala?Asp?Ile?Ser?Ser
260 265 270
Gly?Tyr?Arg?Pro?Leu?Cys?Ser?Asp?Phe?Asn?Asp?Thr?Trp?Ser?Ile?Ser
275 280 285
Phe?Thr?Met?Gly?Phe?Tyr?Gly?Glu?Gly?Val?Thr?Phe?Asn?Leu?Thr?Gly
290 295 300
Asp?Gln?Leu?Ala?Val?Pro?Gly?Tyr?Gln?Asp?Asp?Asp?His?Cys?Phe?Pro
305 310 315 320
Pro?Phe?Asn?Pro?Trp?Asp?Ser?Tyr?Asn?Thr?Ile?Ile?Gly?Gln?His?Trp
325 330 335
Leu?Ser?Asn?Phe?Tyr?Ala?Val?Phe?Asp?Phe?Gly?Ser?Phe?Asp?Pro?Glu
340 345 350
Thr?Tyr?Asp?Ile?Arg?Val?Gly?Leu?Ala?Pro?Leu?Lys?Lys?Glu?Tyr?Leu
355 360 365
Pro?Ser?Ala
370
<210>151
<211>414
<212>PRT
<213〉aspergillus niger
<400>151
Met?Phe?Pro?Cys?Ser?Arg?Ile?Trp?Ser?Leu?Leu?Val?Ala?Ala?Ala?Thr
1 5 10 15
Ala?Ser?Ala?Val?Pro?Thr?Ser?Leu?Ala?Thr?Thr?His?Leu?Gln?Ser?Val
20 25 30
Asp?Leu?Leu?Leu?Thr?Arg?Ser?Ser?Tyr?Gly?Phe?Leu?Thr?Asp?Ile?Ala
35 40 45
Leu?Gly?Thr?Pro?Gly?Gln?Ser?Leu?Pro?Tyr?Leu?Val?Asp?Trp?Thr?Trp
50 55 60
Thr?Gly?His?Tyr?Val?Val?Thr?Thr?Leu?Cys?Tyr?Asn?Asp?Pro?Thr?Ala
65 70 75 80
Thr?Tyr?Asp?Cys?Leu?Asn?Val?Asp?Gln?Lys?Ile?Phe?Asn?Gln?Thr?Leu
85 90 95
Ser?Ser?Thr?Phe?Ile?Asn?Gln?Thr?Asp?Gln?Tyr?Gly?Tyr?Leu?Tyr?Trp
100 105 110
Asp?Pro?Asn?His?Phe?Tyr?Phe?Thr?Glu?Pro?Ala?Ala?Ala?Asp?Val?Ala
115 120 125
Thr?Asp?Met?Leu?Arg?Ile?Gly?Pro?Thr?Ala?Val?Asn?Thr?Thr?Ile?Gln
130 135 140
Ala?Ala?Asn?Phe?Val?Phe?Asn?Glu?Thr?Ile?Ser?Ala?Phe?Pro?Phe?Ser
145 150 155 160
Gly?Val?Tyr?Gly?Leu?Ser?Pro?Val?Phe?Gln?Gly?Asp?Asn?Arg?Ser?Val
165 170 175
Gln?Ala?Ser?Phe?Tyr?Gln?Gly?Trp?Arg?Ser?Gly?Ala?Trp?His?Ser?Pro
180 185 190
Ile?Val?Ser?Phe?Ile?Tyr?Cys?His?Asp?Asn?Ala?Thr?Lys?Ala?Val?Cys
195 200 205
Ser?Gly?Tyr?Asp?Gly?Leu?Gln?Thr?Leu?Gly?Gly?Tyr?Asn?Thr?Ser?His
210 215 220
Val?Gln?Gly?Asp?Ile?Thr?Trp?Tyr?Asp?Ile?Ile?Val?Thr?Glu?Ala?Ile
225 230 235 240
Asn?Thr?Leu?Asp?Phe?Val?Tyr?Ala?Pro?Ala?Val?Ile?Asn?Tyr?Trp?Ala
245 250 255
Leu?Asn?Leu?Thr?Arg?Phe?Ser?Ile?Gly?Asp?Glu?Glu?Gln?Glu?Leu?Asn
260 265 270
Lys?Thr?Thr?Thr?Leu?Asp?Gly?Lys?Gln?Ala?Ala?Val?Ala?Ala?Phe?Asp
275 280 285
His?Ala?Ser?Tyr?Gly?Arg?Gly?Ala?Pro?Val?Ser?Val?Tyr?Gly?Tyr?Gln
290 295 300
Arg?Leu?Val?Glu?Leu?Val?Gly?Ala?Lys?Ala?Val?Thr?Leu?Ser?Asp?Pro
305 310 315 320
Pro?Asn?Asn?Gly?Glu?Gln?Gly?Phe?Tyr?Gln?Phe?Asp?Cys?Arg?Asn?Ser
325 330 335
Ser?Leu?Leu?Pro?Pro?Leu?Arg?Tyr?Glu?Phe?Ala?Gly?Ser?Glu?Arg?Ala
340 345 350
Trp?Glu?Ile?Val?Pro?Glu?Asn?Tyr?Val?Glu?Val?Leu?Ala?Asn?Gly?Thr
355 360 365
Asn?Lys?Cys?Thr?Phe?Asn?Val?Arg?Thr?Leu?Gly?Asp?Gly?Ala?Met?Val
370 375 380
Met?Gly?Asn?Phe?Gly?Glu?Thr?Phe?Ala?Ile?Asp?Lys?Tyr?Val?Met?Phe
385 390 395 400
Asp?Phe?Glu?Lys?Leu?Gln?Val?Gly?Ile?Ala?Asp?Phe?Ala?Trp
405 410
<210>152
<211>480
<212>PRT
<213〉aspergillus niger
<400>152
Met?His?Leu?Pro?Gln?Arg?Leu?Val?Thr?Ala?Ala?Cys?Leu?Cys?Ala?Ser
1 5 10 15
Ala?Thr?Ala?Phe?Ile?Pro?Tyr?Thr?Ile?Lys?Leu?Asp?Thr?Ser?Asp?Asp
20 25 30
Ile?Ser?Ala?Arg?Asp?Ser?Leu?Ala?Arg?Arg?Phe?Leu?Pro?Val?Pro?Lys
35 40 45
Pro?Ser?Asp?Ala?Leu?Ala?Asp?Asp?Ser?Thr?Ser?Ser?Ala?Ser?Asp?Glu
50 55 60
Ser?Leu?Ser?Leu?Asn?Ile?Lys?Arg?Ile?Pro?Val?Arg?Arg?Asp?Asn?Asp
65 70 75 80
Phe?Lys?Ile?Val?Val?Ala?Glu?Thr?Pro?Ser?Trp?Ser?Asn?Thr?Ala?Ala
85 90 95
Leu?Asp?Gln?Asp?Gly?Ser?Asp?Ile?Ser?Tyr?Ile?Ser?Val?Val?Asn?Ile
100 105 110
Gly?Ser?Asp?Glu?Lys?Ser?Met?Tyr?Met?Leu?Leu?Asp?Thr?Gly?Gly?Ser
115 120 125
Asp?Thr?Trp?Val?Phe?Gly?Ser?Asn?Cys?Thr?Ser?Thr?Pro?Cys?Thr?Met
130 135 140
His?Asn?Thr?Phe?Gly?Ser?Asp?Asp?Ser?Ser?Thr?Leu?Glu?Met?Thr?Ser
145 150 155 160
Glu?Glu?Trp?Ser?Val?Gly?Tyr?Gly?Thr?Gly?Ser?Val?Ser?Gly?Leu?Leu
165 170 175
Gly?Lys?Asp?Lys?Leu?Thr?Ile?Ala?Asn?Val?Thr?Val?Arg?Met?Thr?Phe
180 185 190
Gly?Leu?Ala?Ser?Asn?Ala?Ser?Asp?Asn?Phe?Glu?Ser?Tyr?Pro?Met?Asp
195 200 205
Gly?Ile?Leu?Gly?Leu?Gly?Arg?Thr?Asn?Asp?Ser?Ser?Tyr?Asp?Asn?Pro
210 215 220
Thr?Phe?Met?Asp?Ala?Val?Ala?Glu?Ser?Asn?Val?Phe?Lys?Ser?Asn?Ile
225 230 235 240
Val?Gly?Phe?Ala?Leu?Ser?Arg?Ser?Pro?Ala?Lys?Asp?Gly?Thr?Val?Ser
245 250 255
Phe?Gly?Thr?Thr?Asp?Lys?Asp?Lys?Tyr?Thr?Gly?Asp?Ile?Thr?Tyr?Thr
260 265 270
Asp?Thr?Val?Gly?Ser?Asp?Ser?Tyr?Trp?Arg?Ile?Pro?Val?Asp?Asp?Val
275 280 285
Tyr?Val?Gly?Gly?Thr?Ser?Cys?Asp?Phe?Ser?Asn?Lys?Ser?Ala?Ile?Ile
290 295 300
Asp?Thr?Gly?Thr?Ser?Tyr?Ala?Met?Leu?Pro?Ser?Ser?Asp?Ser?Lys?Thr
305 310 315 320
Leu?His?Ser?Leu?Ile?Pro?Gly?Ala?Lys?Ser?Ser?Gly?Ser?Tyr?His?Ile
325 330 335
Ile?Pro?Cys?Asn?Thr?Thr?Thr?Lys?Leu?Gln?Val?Ala?Phe?Ser?Gly?Val
340 345 350
Asn?Tyr?Thr?Ile?Ser?Pro?Lys?Asp?Tyr?Val?Gly?Ala?Thr?Ser?Gly?Ser
355 360 365
Gly?Cys?Val?Ser?Asn?Ile?Ile?Ser?Tyr?Asp?Leu?Phe?Gly?Asp?Asp?Ile
370 375 380
Trp?Leu?Leu?Gly?Asp?Thr?Phe?Leu?Lys?Asn?Val?Tyr?Ala?Val?Phe?Asp
385 390 395 400
Tyr?Asp?Glu?Leu?Arg?Val?Gly?Phe?Ala?Glu?Arg?Ser?Ser?Asn?Thr?Thr
405 410 415
Ser?Ala?Ser?Asn?Ser?Thr?Ser?Ser?Gly?Thr?Ser?Ser?Thr?Ser?Gly?Ser
420 425 430
Thr?Thr?Thr?Gly?Ser?Ser?Thr?Thr?Thr?Thr?Ser?Ser?Ala?Ser?Ser?Ser
435 440 445
Ser?Ser?Ser?Asp?Ala?Glu?Ser?Gly?Ser?Ser?Met?Thr?Ile?Pro?Ala?Pro
450 455 460
Gln?Tyr?Phe?Phe?Ser?Ala?Leu?Ala?Ile?Ala?Ser?Phe?Met?Leu?Trp?Leu
465 470 475 480
<210>153
<211>466
<212>PRT
<213〉aspergillus niger
<400>153
Met?Thr?Ser?Ser?Thr?Leu?Arg?Leu?Ala?Val?Ala?Leu?Ala?Leu?Ser?Thr
1 5 10 15
Cys?Ser?Ser?Ala?Leu?Ser?Ser?Gln?Arg?Asp?Asp?Ser?Leu?Val?Val?Pro
20 25 30
Phe?Pro?Phe?Gly?Asn?Leu?Glu?Asp?Val?His?Ile?Ala?Lys?Arg?Asp?Ser
35 40 45
Ser?Lys?Thr?Val?Glu?Ala?Pro?Leu?Val?Ile?Tyr?Gly?Asp?Ser?Tyr?Trp
50 55 60
Met?Asn?Ala?Ser?Ile?Gly?Thr?Pro?Ala?Gln?Ser?Leu?Ser?Phe?Leu?Leu
65 70 75 80
Asp?Leu?Thr?Arg?Ser?Arg?Val?Glu?Pro?Ala?Tyr?Thr?Leu?Asp?Glu?Asn
85 90 95
Tyr?Glu?Cys?Ser?Asp?Asp?Glu?Leu?Cys?Ser?Glu?Phe?Gly?Phe?Tyr?Lys
100 105 110
Pro?Thr?Asp?Ser?Ser?Thr?Tyr?Gln?His?Leu?Thr?Tyr?Thr?Gln?Arg?His
115 120 125
Asp?Ala?Gly?Val?Asp?Tyr?Ser?Tyr?Leu?Asp?Thr?Ile?Thr?Leu?Gly?Asp
130 135 140
His?Ala?Thr?Asp?Asn?Val?Pro?Leu?Asp?Met?Tyr?Leu?Leu?Ser?Tyr?Ile
145 150 155 160
Ser?Tyr?Ser?Ser?Leu?Gly?Leu?Ser?Ser?Val?Asn?Thr?Ser?Phe?Pro?Tyr
165 170 175
Ile?Leu?Val?Asp?Arg?Gly?Leu?Thr?Thr?Ser?Pro?Ser?Phe?Ser?Leu?Ile
180 185 190
Gly?Asp?Asn?Gly?Asn?Thr?Thr?Thr?Pro?Ser?Ile?Ile?Phe?Gly?Gly?Ile
195 200 205
Asn?Thr?Ser?Lys?Phe?Asn?Gly?Pro?Leu?Gln?Ala?Phe?Ser?Phe?Ala?Asp
210 215 220
His?Ser?Ile?Thr?Asn?Asn?Pro?Phe?Val?Thr?Val?Glu?Ala?Asp?Ser?Leu
225 230 235 240
Gln?Leu?Thr?Thr?Asn?Thr?Asn?Asp?Asn?Ser?Thr?Tyr?Pro?Ile?Pro?Ser
245 250 255
Ser?Thr?Pro?Met?Met?Leu?Arg?Thr?Glu?Glu?Leu?Ile?Thr?Tyr?Leu?Pro
260 265 270
Asn?Ser?Thr?Val?Gln?Ser?Leu?Tyr?Thr?Asp?Leu?Asn?Ile?Thr?Met?Asp
275 280 285
Gly?Val?Ile?Ser?Thr?Ser?Arg?Phe?Tyr?Gly?Val?Leu?Pro?Cys?Ala?Arg
290 295 300
Gln?Glu?Thr?Glu?Ser?His?Thr?Ile?Ser?Leu?Ala?Ile?Gly?Asn?Met?Thr
305 310 315 320
Phe?Ser?Val?Ser?Trp?Asp?Glu?Leu?Phe?Val?Pro?Trp?Thr?Arg?Asp?Gly
325 330 335
Leu?Cys?Lys?Phe?Gly?Ile?Gln?Ala?Gln?Asp?Ser?Asp?Tyr?Lys?Thr?Arg
340 345 350
Ala?Glu?Leu?Gly?Val?Pro?Phe?Leu?Arg?Arg?Met?Tyr?Val?Ala?Val?Asp
355 360 365
Tyr?Asn?Asn?Gln?Phe?Val?Gly?Val?Ala?Thr?Leu?Lys?Asp?Asp?Asp?Asp
370 375 380
Gln?Asn?Gly?Gly?Glu?Asp?Glu?Ile?Val?Glu?Ile?Gly?Thr?Gly?Thr?Ala
385 390 395 400
Leu?Pro?Ser?Ala?Val?Gly?Asp?Trp?Pro?Ala?Ser?Val?Thr?Ala?Tyr?Thr
405 410 415
Pro?Ala?Ala?Ser?Thr?Gly?Thr?Ala?Ala?Ala?Thr?Leu?Thr?Phe?Thr?Thr
420 425 430
Ala?Thr?Ser?Ser?Gly?Gly?Gly?Val?Val?Pro?Thr?Gly?Leu?Ser?Glu?Leu
435 440 445
Gly?Arg?Ala?Phe?Leu?Val?Pro?Gly?Val?Leu?Gly?Met?Ala?Val?Leu?Gln
450 455 460
Ala?Val
465
<210>154
<211>543
<212>PRT
<213〉aspergillus niger
<400>154
Met?Met?Arg?Pro?Ile?Leu?Leu?Pro?Leu?Leu?Gly?Val?Phe?Leu?Gln?Thr
1 5 10 15
Ser?Ser?Ala?Ser?Asn?Pro?Tyr?Val?Met?Ser?Trp?Ser?Ser?Gln?Ala?Tyr
20 25 30
Gly?Pro?Asp?Gly?Pro?Trp?Gln?Ala?Val?Ser?Ile?Asp?Val?Gly?Ser?Asn
35 40 45
Gln?Gln?Thr?Val?Asp?Leu?Tyr?Pro?Gly?Ala?Asn?Tyr?Ala?Ser?Thr?Ile
50 55 60
Leu?Met?Ser?Thr?Leu?Cys?Thr?Asn?Lys?Thr?Leu?Ser?Ser?Thr?Cys?Tyr
65 70 75 80
Ala?Ala?Glu?Ala?Gly?Thr?Phe?Asn?Gln?Asn?Thr?Ser?Thr?Thr?Ala?Tyr
85 90 95
Thr?Thr?Ala?Ser?Ser?Trp?Glu?Thr?Thr?Tyr?Trp?Ala?Val?Glu?Gly?Gly
100 105 110
Ser?Gln?Glu?Ala?Val?Leu?Gly?Asp?Glu?Val?Thr?Leu?Gly?Ser?Phe?Val
115 120 125
Val?Pro?Asn?Val?Ser?Phe?Glu?Ala?Ile?Tyr?Gln?Thr?Tyr?Gln?Thr?Tyr
130 135 140
Pro?Asn?Gly?Ile?Ala?Tyr?Pro?Val?Ser?Val?Gly?Ser?Leu?Ala?Leu?Gly
145 150 155 160
Gly?Pro?Tyr?Leu?Ser?Asp?Thr?Val?Ser?Asn?Ser?Thr?Val?Leu?Asn?Met
165 170 175
Ile?Ala?Gly?Trp?Leu?Tyr?Ser?Ser?Asn?Asp?Ile?Pro?Ser?Tyr?Ser?Tyr
180 185 190
Gly?Met?His?Ile?Gly?Ser?Val?Asp?Pro?Lys?Ile?Pro?Gly?Ser?Leu?Ile
195 200 205
Leu?Gly?Gly?Tyr?Asp?Lys?Ser?Arg?Val?Ile?Gly?Asp?Val?Ser?Ala?Gln
210 215 220
Gly?Val?Val?Ser?Ser?Ser?Gly?Leu?Leu?Glu?Leu?Glu?Leu?Lys?Asp?Ile
225 230 235 240
Gly?Leu?Gly?Val?Ala?Ala?Gly?Ser?Ser?Pro?Phe?Ser?Phe?Asn?Asn?Glu
245 250 255
Ser?Gly?Leu?Phe?Leu?Gln?Ser?Ser?Gly?Ser?Val?Gln?Ala?Lys?Thr?Val
260 265 270
Gln?Ile?Asp?Pro?Thr?Lys?Pro?Tyr?Met?Tyr?Leu?Pro?Gln?Ala?Thr?Cys
275 280 285
Asp?Ala?Ile?Thr?Ser?Thr?Met?Pro?Ile?Ser?Phe?Asn?Ser?Ser?Leu?Gly
290 295 300
Leu?Tyr?Phe?Trp?Asp?Thr?Thr?Ser?Asp?Asp?Tyr?Leu?Asn?Ile?Thr?Ser
305 310 315 320
Ser?Ala?Ala?Tyr?Leu?Ser?Phe?Val?Phe?Asn?Met?Asn?Gly?Val?Asn?Asn
325 330 335
Lys?Asn?Ile?Thr?Ile?Lys?Ile?Pro?Phe?Ser?Gln?Leu?Asn?Leu?Thr?Leu
340 345 350
Gln?Glu?Pro?Leu?Val?Asp?Gln?Asn?Val?Thr?Tyr?Phe?Pro?Cys?Phe?Leu
355 360 365
Thr?Thr?Ser?Thr?Pro?Val?Leu?Gly?Arg?Ala?Phe?Leu?Gln?Ser?Ala?Phe
370 375 380
Val?Gly?Val?Asn?Trp?Phe?Asn?Gly?Asn?Asn?Ser?Gly?Thr?Trp?Phe?Leu
385 390 395 400
Ala?Gln?Ala?Pro?Gly?Pro?Gly?Tyr?Ala?Ser?Glu?Asp?Ile?Thr?Arg?Ile
405 410 415
Ala?Val?Ser?Asp?Thr?Ser?Leu?Ser?Ala?Ser?Asn?Gly?Thr?Trp?Glu?Glu
420 425 430
Thr?Trp?Ala?Thr?Tyr?Trp?Gly?Ile?Lys?Thr?Ser?Asp?Asn?Ser?Ser?Ser
435 440 445
Ser?Lys?Ser?Gly?Leu?Ser?Ser?Gly?Ala?Lys?Ile?Gly?Ile?Gly?Val?Gly
450 455 460
Val?Gly?Val?Gly?Gly?Ala?Val?Leu?Ile?Ala?Ala?Gly?Ile?Ala?Ile?Ala
465 470 475 480
Phe?Cys?Leu?Arg?Arg?Arg?Arg?Gly?Ala?Ser?Gln?Glu?Ala?Ala?Gly?Glu
485 490 495
Gln?Arg?Arg?Ser?Met?Phe?Arg?Gly?Phe?Ala?Glu?Leu?Pro?Gly?Gly?Ala
500 505 510
His?Ser?Glu?Pro?Ala?Lys?Glu?Leu?Asp?Thr?Lys?Met?His?Lys?Pro?Pro
515 520 525
Gln?Glu?Met?Met?Ala?Ser?Gln?Glu?Val?Glu?Arg?Tyr?Glu?Leu?Gly
530 535 540
<210>155
<211>844
<212>PRT
<213〉aspergillus niger
<400>155
Met?Arg?Leu?Thr?Gly?Gly?Val?Ala?Ala?Ala?Leu?Gly?Leu?Cys?Ala?Ala
1 5 10 15
Ala?Ser?Ala?Ser?Leu?His?Pro?His?Arg?Ser?Tyr?Glu?Thr?His?Asp?Tyr
20 25 30
Phe?Ala?Leu?His?Leu?Asp?Glu?Ser?Thr?Ser?Pro?Ala?Asp?Val?Ala?Gln
35 40 45
Arg?Leu?Gly?Ala?Arg?His?Glu?Gly?Pro?Val?Gly?Glu?Leu?Pro?Ser?His
50 55 60
His?Thr?Phe?Ser?Ile?Pro?Arg?Glu?Asn?Ser?Asp?Asp?Val?His?Ala?Leu
65 70 75 80
Leu?Asp?Gln?Leu?Arg?Asp?Arg?Arg?Arg?Leu?Arg?Arg?Arg?Ser?Gly?Asp
85 90 95
Asp?Ala?Ala?Val?Leu?Pro?Ser?Leu?Val?Gly?Arg?Asp?Glu?Gly?Leu?Gly
100 105 110
Gly?Ile?Leu?Trp?Ser?Glu?Lys?Leu?Ala?Pro?Gln?Arg?Lys?Leu?His?Lys
115 120 125
Arg?Val?Pro?Pro?Thr?Gly?Tyr?Ala?Ala?Arg?Ser?Pro?Val?Asn?Thr?Gln
130 135 140
Asn?Asp?Pro?Gln?Ala?Leu?Ala?Ala?Gln?Lys?Arg?Ile?Ala?Ser?Glu?Leu
145 150 155 160
Gly?Ile?Ala?Asp?Pro?Ile?Phe?Gly?Glu?Gln?Trp?His?Leu?Tyr?Asn?Thr
165 170 175
Val?Gln?Leu?Gly?His?Asp?Leu?Asn?Val?Thr?Gly?Ile?Trp?Leu?Glu?Gly
180 185 190
Val?Thr?Gly?Gln?Gly?Val?Thr?Thr?Ala?Ile?Val?Asp?Asp?Gly?Leu?Asp
195 200 205
Met?Tyr?Ser?Asn?Asp?Leu?Arg?Pro?Asn?Tyr?Phe?Ala?Ala?Gly?Ser?Tyr
210 215 220
Asp?Tyr?Asn?Asp?Lys?Val?Pro?Glu?Pro?Arg?Pro?Arg?Leu?Ser?Asp?Asp
225 230 235 240
Arg?His?Gly?Thr?Arg?Cys?Ala?Gly?Glu?Ile?Gly?Ala?Ala?Lys?Asn?Asp
245 250 255
Val?Cys?Gly?Val?Gly?Val?Ala?Tyr?Asp?Ser?Arg?Ile?Ala?Gly?Ile?Arg
260 265 270
Ile?Leu?Ser?Ala?Pro?Ile?Asp?Asp?Thr?Asp?Glu?Ala?Ala?Ala?Ile?Asn
275 280 285
Tyr?Ala?Tyr?Gln?Glu?Asn?Asp?Ile?Tyr?Ser?Cys?Ser?Trp?Gly?Pro?Tyr
290 295 300
Asp?Asp?Gly?Ala?Thr?Met?Glu?Ala?Pro?Gly?Thr?Leu?Ile?Lys?Arg?Ala
305 310 315 320
Met?Val?Asn?Gly?Ile?Gln?Asn?Gly?Arg?Gly?Gly?Lys?Gly?Ser?Val?Phe
325 330 335
Val?Phe?Ala?Ala?Gly?Asn?Gly?Ala?Ile?His?Asp?Asp?Asn?Cys?Asn?Phe
340 345 350
Asp?Gly?Tyr?Thr?Asn?Ser?Ile?Tyr?Ser?Ile?Thr?Val?Gly?Ala?Ile?Asp
355 360 365
Arg?Glu?Gly?Asn?His?Pro?Pro?Tyr?Ser?Glu?Ser?Cys?Ser?Ala?Gln?Leu
370 375 380
Val?Val?Ala?Tyr?Ser?Ser?Gly?Ala?Ser?Asp?Ala?Ile?His?Thr?Thr?Asp
385 390 395 400
Val?Gly?Thr?Asp?Lys?Cys?Ser?Thr?Thr?His?Gly?Gly?Thr?Ser?Ala?Ala
405 410 415
Gly?Pro?Leu?Ala?Ala?Gly?Thr?Val?Ala?Leu?Ala?Leu?Ser?Val?Arg?Pro
420 425 430
Glu?Leu?Thr?Trp?Arg?Asp?Val?Gln?Tyr?Leu?Met?Ile?Glu?Ala?Ala?Val
435 440 445
Pro?Val?His?Glu?Asp?Asp?Gly?Ser?Trp?Gln?Asp?Thr?Lys?Asn?Gly?Lys
450 455 460
Lys?Phe?Ser?His?Asp?Trp?Gly?Tyr?Gly?Lys?Val?Asp?Thr?Tyr?Thr?Leu
465 470 475 480
Val?Lys?Arg?Ala?Glu?Thr?Trp?Asp?Leu?Val?Lys?Pro?Gln?Ala?Trp?Leu
485 490 495
His?Ser?Pro?Trp?Gln?Arg?Val?Glu?His?Glu?Ile?Pro?Gln?Gly?Glu?Gln
500 505 510
Gly?Leu?Ala?Ser?Ser?Tyr?Glu?Val?Thr?Glu?Asp?Met?Leu?Lys?Gly?Ala
515 520 525
Asn?Leu?Glu?Arg?Leu?Glu?His?Val?Thr?Val?Thr?Met?Asn?Val?Asn?His
530 535 540
Thr?Arg?Arg?Gly?Asp?Leu?Ser?Val?Glu?Leu?Arg?Ser?Pro?Asp?Gly?Arg
545 550 555 560
Val?Ser?His?Leu?Ser?Thr?Pro?Arg?Arg?Pro?Asp?Asn?Gln?Glu?Val?Gly
565 570 575
Tyr?Val?Asp?Trp?Thr?Phe?Met?Ser?Val?Ala?His?Trp?Gly?Glu?Ser?Gly
580 585 590
Ile?Gly?Lys?Trp?Thr?Val?Ile?Val?Lys?Asp?Thr?Asn?Val?Asn?Glu?His
595 600 605
Thr?Gly?Gln?Phe?Ile?Asp?Trp?Arg?Leu?Asn?Leu?Trp?Gly?Glu?Ala?Ile
610 615 620
Asp?Gly?Ala?Glu?Gln?Pro?Leu?His?Pro?Met?Pro?Thr?Glu?His?Asp?Asp
625 630 635 640
Asp?His?Ser?Tyr?Glu?Glu?Gly?Asn?Val?Ala?Thr?Thr?Ser?Ile?Ser?Ala
645 650 655
Val?Pro?Thr?Lys?Thr?Glu?Leu?Pro?Asp?Lys?Pro?Thr?Gly?Gly?Val?Asp
660 665 670
Arg?Pro?Val?Asn?Val?Lys?Pro?Thr?Thr?Ser?Ala?Met?Pro?Thr?Gly?Ser
675 680 685
Leu?Thr?Glu?Pro?Ile?Asp?Asp?Glu?Glu?Leu?Gln?Lys?Thr?Pro?Ser?Thr
690 695 700
Glu?Ala?Ser?Ser?Thr?Pro?Ser?Pro?Ser?Pro?Thr?Thr?Ala?Ser?Asp?Ser
705 710 715 720
Ile?Leu?Pro?Ser?Phe?Phe?Pro?Thr?Phe?Gly?Ala?Ser?Lys?Arg?Thr?Gln
725 730 735
Val?Trp?Ile?Tyr?Ala?Ala?Ile?Gly?Ser?Ile?Ile?Val?Phe?Cys?Ile?Gly
740 745 750
Leu?Gly?Val?Tyr?Phe?His?Val?Gln?Arg?Arg?Lys?Arg?Ile?Arg?Asp?Asp
755 760 765
Ser?Arg?Asp?Asp?Tyr?Asp?Phe?Glu?Met?Ile?Glu?Asp?Glu?Asp?Glu?Leu
770 775 780
Gln?Ala?Met?Asn?Gly?Arg?Ser?Asn?Arg?Ser?Arg?Arg?Arg?Gly?Gly?Glu
785 790 795 800
Leu?Tyr?Asn?Ala?Phe?Ala?Gly?Glu?Ser?Asp?Glu?Glu?Pro?Leu?Phe?Ser
805 810 815
AspGlu?Asp?Asp?Glu?Pro?Tyr?Arg?Asp?Arg?Gly?Ile?Ser?Gly?Glu?Gln
820 825 830
Glu?Arg?Glu?Gly?Ala?Asp?Gly?Glu?His?Ser?Arg?Arg
835 840
<210>156
<211>149
<212>PRT
<213〉aspergillus niger
<400>156
Met?Lys?Thr?Phe?Ser?Thr?Val?Thr?Ser?Leu?Leu?Ala?Leu?Phe?Ser?Ser
1 5 10 15
Ala?Leu?Ala?Ala?Pro?Val?Asp?Ser?Ala?Glu?Ala?Ala?Gly?Thr?Thr?Val
20 25 30
Ser?Val?Ser?Tyr?Asp?Thr?Ala?Tyr?Asp?Val?Ser?Gly?Ala?Ser?Leu?Thr
35 40 45
Thr?Val?Ser?Cys?Ser?Asp?Gly?Ala?Asn?Gly?Leu?Ile?Asn?Lys?Gly?Tyr
50 55 60
Ser?Asn?Phe?Gly?Ser?Leu?Pro?Gly?Phe?Pro?Lys?Ile?Gly?Gly?Ala?Pro
65 70 75 80
Thr?Ile?Ala?Gly?Trp?Asn?Ser?Pro?Asn?Cys?Gly?Lys?Cys?Tyr?Ala?Leu
85 90 95
Thr?Tyr?Asn?Gly?Gln?Thr?Val?Asn?Ile?Leu?Ala?Ile?Asp?Ser?Ala?Pro
100 105 110
Gly?Gly?Phe?Asn?Ile?Ala?Leu?Glu?Ala?Met?Asn?Thr?Leu?Thr?Asn?Asn
115 120 125
Gln?Ala?Gln?Gln?Leu?Gly?Arg?Ile?Glu?Ala?Thr?Tyr?Thr?Glu?Val?Asp
130 135 140
Val?Ser?Leu?Cys?Ala
145
<210>157
<211>296
<212>PRT
<213〉aspergillus niger
<400>157
Met?Ala?Gln?Ile?Phe?Trp?Leu?Ser?Leu?Phe?Leu?Leu?Val?Ser?Trp?Val
1 5 10 15
Arg?Ala?Glu?Ser?Asn?Arg?Thr?Glu?Val?Asp?Leu?Ile?Phe?Pro?Arg?Asn
20 25 30
Asp?Thr?Phe?Ala?Pro?Met?Pro?Leu?Met?Pro?Val?Val?Phe?Ala?Val?Gln
35 40 45
Ala?Pro?Ser?Val?Ala?His?Lys?Val?Asn?Thr?Tyr?Ile?Glu?Tyr?Gly?Tyr
50 55 60
Tyr?Pro?Val?Gly?Arg?Pro?Asn?Glu?Thr?Val?Ile?Gly?Gln?Thr?Asp?His
65 70 75 80
Val?Ser?Asp?Ser?Thr?Asn?Glu?Thr?Thr?Tyr?Phe?Ser?Val?Ser?Gly?Ile
85 90 95
Gly?Arg?Thr?Phe?Asn?Thr?Thr?Gly?Ser?Trp?Glu?Leu?Phe?Trp?Arg?Leu
100 105 110
Arg?Trp?Thr?Asn?Cys?Ser?Ile?Ser?Glu?Asp?Ser?Arg?Tyr?Tyr?Asn?Gln
115 120 125
Ser?Tyr?Pro?Trp?Ile?Ser?Ser?Pro?Tyr?Ile?Asp?Gly?Ser?Leu?Asn?Ile
130 135 140
Asp?Lys?Val?Tyr?Glu?Gly?Phe?His?Tyr?Thr?Ala?Tyr?Asn?Val?Ile?Val
145 150 155 160
Asp?Arg?Val?Thr?Phe?Ser?Thr?Arg?Glu?Asp?Ala?Ser?Gln?Pro?Asn?Leu
165 170 175
Thr?Thr?Leu?Thr?Asn?Ser?Glu?Asn?Cys?Asp?Lys?Val?Ser?Ser?Leu?Ala
180 185 190
Leu?Leu?Ser?Ile?Val?Asp?Ser?Leu?Arg?Ile?Pro?Pro?Gln?Leu?Pro?Gln
195 200 205
Glu?Asp?Ile?Asp?Thr?Val?Ser?Met?Cys?Pro?Gln?Leu?Ala?Asp?Ala?Arg
210 215 220
Leu?Asn?Ser?Thr?Ser?Thr?Ser?Ser?Pro?Cys?Ser?Val?Ser?Ile?Ser?Pro
225 230 235 240
Glu?Val?Glu?Ser?Asn?Ile?Leu?Ala?Lys?Ile?Ala?Asp?Asn?Glu?Cys?Asn
245 250 255
Asn?Ala?Leu?His?Pro?Ala?Val?Ser?Cys?Thr?Thr?Glu?Glu?Thr?Lys?Glu
260 265 270
Gly?Ser?Ala?Ser?Ser?His?Asp?His?Gly?His?Ala?Val?Trp?Leu?Val?Ile
275 280 285
Thr?Leu?Ala?Phe?Ala?Phe?Leu?Phe
290 295
<210>158
<211>310
<212>PRT
<213〉aspergillus niger
<400>158
Met?Gly?Gly?Arg?Asp?Val?Ala?Ile?Leu?Ser?Arg?His?Phe?Ala?Val?Thr
1 5 10 15
Ser?Ser?Gln?Ser?Val?Asn?Gly?Val?Val?Ser?Gly?Met?Phe?Gln?His?Thr
20 25 30
Val?Thr?Ser?Ser?Pro?Ser?Phe?Thr?Thr?Asn?Gln?Phe?Phe?Lys?Lys?Lys
35 40 45
Phe?Thr?Ala?Ala?Ile?Ala?Thr?Ala?Ile?Phe?Ala?Ser?Val?Ala?Val?Ala
50 55 60
Ala?Pro?Gln?Arg?Gly?Leu?Glu?Ala?Arg?Leu?Lys?Ala?Arg?Gly?Ser?Ser
65 70 75 80
Lys?Gly?Ser?Arg?Pro?Leu?Gln?Ala?Val?Ala?Arg?Pro?Ala?Ser?Thr?Lys
85 90 95
Asn?Gln?Thr?Asn?Val?Glu?Tyr?Ser?Ser?Asn?Trp?Ser?Gly?Ala?Val?Leu
100 105 110
Val?Glu?Pro?Pro?Ser?Ala?Ala?Ala?Thr?Tyr?Thr?Ala?Val?Thr?Gly?Thr
115 120 125
Phe?Thr?Val?Pro?Glu?Pro?Thr?Gly?Asn?Ser?Gly?Gly?Ser?Gln?Ala?Ala
130 135 140
Ser?Ala?Trp?Val?Gly?Ile?Asp?Gly?Asp?Thr?Tyr?Gly?Asn?Ala?Ile?Leu
145 150 155 160
Gln?Thr?Gly?Val?Asp?Phe?Thr?Val?Thr?Asp?Gly?Glu?Ala?Ser?Phe?Asp
165 170 175
Ala?Trp?Tyr?Glu?Trp?Tyr?Pro?Asp?Tyr?Ala?Tyr?Asp?Phe?Ser?Gly?Ile
180 185 190
Asp?Ile?Ser?Ala?Gly?Asp?Glu?Ile?Val?Ala?Ile?Val?Glu?Ser?Tyr?Thr
195 200 205
Ser?Thr?Thr?Gly?Ile?Ala?Ile?Ile?Glu?Asn?Lys?Ser?Thr?Gly?Gln?Lys
210 215 220
Val?Ser?Lys?Glu?Leu?Ser?Ser?Ser?Ser?Ser?Leu?Gly?Gly?Gln?Asn?Ala
225 230 235 240
Glu?Trp?Ile?Val?Glu?Asp?Phe?Glu?Glu?Asn?Gly?Ser?Leu?Val?Asn?Leu
245 250 255
Val?Asp?Phe?Gly?Thr?Val?Thr?Phe?Thr?Gly?Ala?Val?Ala?Lys?Ala?Ala
260 265 270
Gly?Gly?Glu?Ser?Val?Gly?Leu?Thr?Asp?Ala?Thr?Ile?Ile?Glu?Ile?Glu
275 280 285
Glu?Asn?Gly?Gln?Val?Val?Thr?Asp?Val?Thr?Ile?Asp?Ser?Asp?Ser?Glu
290 295 300
Val?Thr?Ile?Thr?Tyr?Glu
305 310
<210>159
<211>681
<212>PRT
<213〉aspergillus niger
<400>159
Met?Arg?Cys?Ser?Leu?Ile?Ser?Leu?Leu?Gly?Leu?Ala?Ala?Ile?Pro?Ala
1 5 10 15
Leu?Gly?Gly?Cys?Pro?Phe?Ala?His?Thr?Ala?Asn?Met?Gly?Ile?Asp?Asn
20 25 30
Met?Val?Lys?Ala?His?Ala?His?Met?Ser?Arg?Pro?Leu?Ile?Ala?Ser?Lys
35 40 45
Ser?Ser?Pro?Ser?Thr?Val?Pro?Thr?Ser?Ser?Ser?Thr?Pro?Ser?Val?Gly
50 55 60
Gln?Lys?Gly?Val?Phe?Met?Met?Asn?Arg?Ile?Ala?Pro?Gly?Thr?Ser?Glu
65 70 75 80
Leu?TyrIle?Ala?Asn?Thr?Asp?Gly?Ser?Asn?Glu?Arg?Pro?Leu?Leu?Ser
85 90 95
Asn?Pro?Val?Tyr?Glu?Tyr?His?Ala?Ser?Phe?Ser?Pro?Asp?Val?Glu?Trp
100 105 110
Ile?Thr?Phe?Thr?Ser?Glu?Arg?Asn?Gly?Asp?Gly?Asn?Ser?Asp?Ile?Tyr
115 120 125
Arg?Val?Arg?Thr?Asn?Gly?Ser?Asp?Leu?Gln?Glu?Leu?Val?Ala?Thr?Pro
130 135 140
Ala?Val?Glu?Asp?Ser?Val?Val?Ile?Ser?Pro?Asn?Gly?Arg?Leu?Ala?Ala
145 150 155 160
Tyr?Val?Ser?Thr?Ala?Asn?Asn?Met?Lys?Ala?Asn?Ile?Trp?Ile?Leu?Asp
165 170 175
Leu?Gln?Thr?Gly?Ala?Gln?Trp?Asn?Leu?Thr?Asn?Thr?Pro?Thr?Thr?Ala
180 185 190
Ala?Asn?Ser?Ser?Leu?Met?Glu?Ser?Tyr?Leu?Arg?Pro?Ala?Trp?Ser?Pro
195 200 205
Asp?Gly?Glu?Trp?Ile?Ala?Phe?Ser?Ser?Asp?Arg?Asn?Thr?Gln?Trp?Asp
210 215 220
Gly?His?Gly?Val?Pro?Thr?Phe?Leu?Gly?Arg?Thr?Gly?Trp?Glu?Thr?Thr
225 230 235 240
Gln?Glu?Leu?Ser?Leu?Tyr?Ala?Ile?Arg?Pro?Asn?Gly?Ser?Asp?Phe?Arg
245 250 255
Gln?Ile?Ile?Ser?Lys?Pro?Tyr?Tyr?Ser?Leu?Gly?Ser?Pro?Lys?Trp?Ser
260 265 270
Ala?Asp?Gly?Lys?Arg?Ile?Val?Tyr?Tyr?Glu?Met?Thr?Arg?Glu?Asp?Thr
275 280 285
Tyr?Asn?Ala?His?Arg?Pro?Glu?Thr?Ile?Thr?Thr?Ala?Asn?Ser?Thr?Ile
290 295 300
Met?Ser?Val?Asp?Phe?Glu?Thr?Gly?Thr?Asp?Val?Arg?Val?Glu?Val?Ala
305 310 315 320
Gly?Ser?Gly?Val?Lys?Gln?Phe?Pro?Gln?Tyr?Leu?Asp?Lys?Asn?Gly?Thr
325 330 335
Ile?Ala?Tyr?Thr?Leu?Lys?Gly?Gly?Thr?Ser?Glu?Gly?Phe?Tyr?Thr?Thr
340 345 350
Ala?Gly?Leu?Tyr?Val?Asn?Thr?Thr?Ser?Ala?Thr?Leu?Arg?Ser?Pro?Ala
355 360 365
Trp?Ser?Pro?Asp?Gly?Lys?Gln?Val?Val?Tyr?Glu?Lys?Ser?Thr?Trp?Ser
370 375 380
Ile?Arg?Ser?Gly?Tyr?Lys?Gln?Leu?Tyr?Ser?Trp?Asp?Ser?Asp?Trp?Asp
385 390 395 400
Tyr?Arg?Phe?Thr?Asp?Val?Phe?Pro?Gln?Val?Ser?His?Gln?Glu?Arg?Val
405 410 415
Ala?Ile?Thr?Gln?Lys?Gln?Leu?Gly?Asn?Ser?Ser?Ile?Val?Thr?Leu?Asn
420 425 430
Thr?Thr?Gly?Gly?Asp?Leu?Gln?Leu?Val?Tyr?Asp?Pro?Ser?Thr?Ala?Asp
435 440 445
Phe?Val?Ser?Asp?Asp?Glu?Thr?Thr?Gly?Leu?Ser?Ala?Tyr?Gln?Pro?Ser
450 455 460
Trp?Ser?Pro?Cys?Gly?Glu?Trp?Leu?Val?Phe?Gly?Val?Gly?Phe?Trp?Phe
465 470 475 480
Glu?Thr?Arg?Glu?Ala?Ser?Gly?Gly?Trp?Ile?Val?Arg?Ala?Thr?Ala?Asn
485 490 495
Gly?Ser?Tyr?Ser?Glu?Val?Leu?Val?Asn?Ser?Ser?Tyr?Ser?Ile?Thr?Glu
500 505 510
Asp?Gly?Ala?Leu?Asn?Ser?Gly?Phe?Pro?Ser?Phe?Ser?Pro?Asp?Gly?Lys
515 520 525
Lys?Val?Val?Tyr?Arg?Val?Trp?Gly?Ala?Asp?Thr?Ala?Thr?Tyr?Gly?Asn
530 535 540
Ala?Ser?Glu?Ile?Gly?Leu?Arg?Val?Leu?Asp?Leu?Glu?Thr?Arg?Lys?Thr
545 550 555 560
Thr?Val?Leu?Thr?Thr?Glu?Trp?Asp?Asn?Leu?Pro?Gln?Phe?Ser?Pro?Asp
565 570 575
Gly?Glu?Leu?Ile?Leu?Phe?Thr?Arg?Lys?Thr?Ser?Thr?Tyr?Asn?Tyr?Asp
580 585 590
Val?Cys?Thr?Ile?Arg?Pro?Asp?Gly?Thr?Asp?Leu?Arg?Val?Leu?Thr?Ser
595 600 605
Ser?Gly?Ala?Asn?Asp?Ala?His?Ala?Val?Trp?Ser?Gln?Asp?Gly?Arg?Ile
610 615 620
Met?Trp?Ser?Thr?Gly?Met?Tyr?Gly?Phe?Arg?Phe?Glu?Cys?Ala?Leu?Tyr
625 630 635 640
Gly?Asp?Thr?Phe?Gln?Pro?Tyr?Gly?Gln?Val?Met?Ile?Met?Asp?Ala?Asp
645 650 655
Gly?Gly?Asn?Lys?Lys?Leu?Met?Thr?Asn?Ser?Met?Trp?Glu?Asp?Ser?Met
660 665 670
Pro?Leu?Phe?Leu?Pro?Arg?Glu?Val?Leu
675 680
<210>160
<211>624
<212>PRT
<213〉aspergillus niger
<400>160
Met?Pro?Pro?Asp?Ala?Lys?Ser?Pro?Gly?Tyr?Gln?Pro?Gly?Met?Ala?Val
1 5 10 15
Leu?Pro?Ser?Arg?Pro?His?Pro?Ala?Lys?Gly?Lys?Ala?Ile?Arg?Phe?Leu
20 25 30
Leu?Ser?Leu?Ala?Leu?Val?Ala?Phe?Ala?Ile?Val?Gln?Leu?Cys?Gly?Asn
35 40 45
Phe?His?Lys?Asn?Arg?Ser?Val?Glu?Gln?Gln?Leu?Gln?Ser?Gln?Thr?Leu
50 55 60
Asp?Asp?Glu?Ser?Phe?Lys?Trp?Glu?Asp?Val?Thr?Pro?Thr?Lys?Gln?Leu
65 70 75 80
Val?Tyr?His?Pro?Cys?Phe?Gly?Asp?His?Glu?Cys?Ala?Arg?Leu?Ser?Leu
85 90 95
Pro?Met?Asn?Trp?Asn?Arg?Thr?Asp?Gly?Glu?Gly?Ser?Lys?Ile?Ala?Leu
100 105 110
Ala?Val?Ile?Lys?Leu?Pro?Ala?Lys?Val?Pro?Val?Thr?Asp?Ala?Arg?Tyr
115 120 125
Gly?Gly?Ala?Ile?Leu?Leu?Asn?Pro?Gly?Gly?Pro?Gly?Gly?Ser?Gly?Val
130 135 140
Ser?Met?Val?Phe?Arg?Tyr?Gly?Lys?Ala?Ile?Gln?Thr?Ile?Val?Asp?Ser
145 150 155 160
Pro?Glu?Ser?Pro?Ser?Ala?Asp?Ser?Ala?Ser?Gly?Lys?Tyr?Phe?Asp?Val
165 170 175
Val?Ser?Phe?Asp?Pro?Arg?Gly?Val?Asn?Asn?Thr?Thr?Pro?Asn?Phe?Ser
180 185 190
Cys?Phe?Pro?Asp?Pro?Ala?Thr?Arg?Lys?Ala?Trp?Leu?Leu?Gln?Ser?Glu
195 200 205
Ala?Glu?Gly?Leu?Leu?Gly?Ser?Ser?Glu?Gly?Val?Phe?Asp?Thr?Arg?Trp
210 215 220
Ala?Arg?Tyr?Glu?Ala?Phe?Glu?Arg?Leu?Leu?Ser?Thr?Ala?Pro?Asn?Thr
225 230 235 240
Phe?Pro?Val?Gly?Thr?Asn?Val?Asp?Ala?Glu?Arg?Ile?Arg?Leu?His?Asn
245 250 255
Arg?Trp?Lys?Lys?Gly?Glu?Glu?Lys?Leu?Leu?Tyr?Trp?Gly?Phe?Ser?Tyr
260 265 270
Gly?Thr?Ile?Leu?Gly?Ser?Thr?Phe?Ala?Ala?Met?Gln?Pro?His?Arg?Ile
275 280 285
Asn?Arg?Ala?Val?Ile?Asp?Gly?Val?Cys?Asn?Ala?Asp?Asp?Tyr?Tyr?Ala
290 295 300
Gly?Asn?Trp?Leu?Thr?Asn?Leu?Gln?Asp?Ser?Asp?Ala?Ala?Phe?Asn?Lys
305 310 315 320
Phe?Phe?Glu?Tyr?Cys?Tyr?Thr?Ala?Gly?Pro?Ser?Ala?Cys?Pro?Phe?Ala
325 330 335
Leu?Gly?Gly?Asp?Pro?Glu?Asp?Leu?Lys?Ser?Arg?Tyr?Glu?Gln?Ile?Leu
340 345 350
Thr?Asn?Leu?Thr?Ser?Ser?Pro?Ile?Ala?Val?Ser?Pro?Ser?Gly?Asn?Arg
355 360 365
Gly?Pro?Glu?Ile?Ile?Thr?Tyr?Ser?Asp?Val?Lys?Ser?Leu?Val?Val?Gln
370 375 380
Ala?Leu?Tyr?Val?Pro?Leu?Lys?Leu?Phe?Asp?Leu?Val?Ala?Arg?Leu?Leu
385 390 395 400
Ala?Glu?Leu?Glu?Gln?Gly?Asn?Gly?Ser?Ser?Phe?Ala?Asp?Leu?Lys?Tyr
405 4l0 415
Glu?Ala?Lys?Gln?Trp?Pro?Val?Pro?Pro?Pro?Cys?Asp?Ser?Ser?Ser?Thr
420 425 430
Gln?Tyr?Lys?Val?Pro?Gly?Glu?Ser?Asp?Gln?Glu?Ala?Gly?Arg?Asn?Ile
435 440 445
Leu?Cys?Thr?Asp?Gly?Pro?Gly?Leu?Asp?Gly?Thr?Ala?Lys?Glu?Asp?Phe
450 455 460
Arg?Ser?Tyr?Trp?Asn?Met?Leu?Arg?Gly?Gln?Ser?Lys?Ala?Val?Gly?Asp
465 470 475 480
Phe?Trp?Ala?Glu?Val?Arg?Met?Ser?Cys?Val?Lys?Leu?Glu?Thr?Arg?Pro
485 490 495
Glu?Trp?Arg?Tyr?Asp?Gly?Met?Arg?Ile?Gln?Gly?Pro?Phe?Ala?Gly?Asn
500 505 510
Thr?Ser?His?Pro?Leu?Leu?Phe?Ile?Gly?Asn?Thr?Tyr?Asp?Pro?Val?Thr
515 520 525
Pro?Leu?Arg?Asn?Ala?His?Thr?Met?Ala?Arg?Gly?Phe?Pro?Glu?Ser?Ile
530 535 540
Val?Leu?Glu?Gln?Asn?Ser?Val?Gly?His?Cys?Thr?Leu?Ser?Gly?Pro?Ser
545 550 555 560
Leu?Cys?Thr?Ala?Lys?Ala?Ile?Arg?Gln?Tyr?Phe?Gln?Thr?Gly?Glu?Leu
565 570 575
Pro?Asp?Pro?Gly?Thr?Val?Cys?Gln?Val?Glu?Glu?Leu?Pro?Phe?Arg?Leu
580 585 590
Ala?Gly?Tyr?Glu?Arg?Ser?Gln?Val?Met?Ser?Pro?Gly?Asp?Thr?Glu?Leu
595 600 605
Met?Ser?Ala?Leu?His?Ser?Leu?Ser?Glu?Phe?Arg?His?Leu?Leu?Gly?Ala
610 615 620
<210>161
<211>554
<212>PRT
<213〉aspergillus niger
<400>161
Met?Leu?Ser?Ser?Leu?Leu?Leu?Gly?Gly?Leu?Leu?Gly?Leu?Ala?Thr?Ala
1 5 10 15
Gln?Phe?Pro?Pro?Glu?Pro?Glu?Gly?Ile?Thr?Val?Leu?Lys?Ser?Lys?Leu
20 25 30
His?Glu?Asn?Val?Thr?Ile?Ser?Phe?Lys?Glu?Pro?Gly?Ile?Cys?Glu?Thr
35 40 45
Thr?Pro?Gly?Val?Arg?Ser?Tyr?Ser?Gly?Tyr?Val?His?Leu?Pro?Pro?Ala
50 55 60
Ser?Thr?Ser?Phe?Phe?Trp?Phe?Phe?Glu?Ala?Arg?Lys?Asp?Pro?Ser?Asn
65 70 75 80
Ala?Pro?Leu?Ala?Ile?Trp?Leu?Asn?Gly?Gly?Pro?Gly?Gly?Ser?Ser?Leu
85 90 95
Met?Gly?Leu?Leu?Glu?Glu?Leu?Gly?Pro?Cys?Ser?Ile?Ala?Ser?Asp?Ser
100 105 110
Lys?Thr?Thr?Val?Leu?Asn?Pro?Trp?Ser?Trp?Asn?Asn?Glu?Val?Asn?Leu
115 120 125
Leu?Phe?Leu?Asp?Gln?Pro?Thr?Gln?Val?Gly?Phe?Ser?Tyr?Asp?Val?Pro
130 135 140
Thr?Asn?Gly?Thr?Leu?Thr?Ala?Asn?Gly?Thr?Ala?Phe?Ala?Ala?His?Ala
145 150 155 160
Leu?Trp?His?Phe?Ala?Gln?Thr?Trp?Phe?Phe?Glu?Phe?Pro?His?Tyr?Lys
165 170 175
Pro?Asn?Asp?Asp?Arg?Val?Ser?Leu?Trp?Ala?Glu?Ser?Tyr?Gly?Gly?His
180 185 190
Tyr?Gly?Pro?Gly?Ile?Phe?Arg?Phe?Phe?Gln?Gln?Gln?Asn?Asp?Lys?Ile
195 200 205
Ala?Glu?Gly?Thr?Ala?Glu?Asp?Gly?Ala?Gln?Tyr?Leu?His?Leu?Asp?Thr
210 215 220
Leu?Gly?Ile?Val?Asn?Gly?Leu?Met?Asp?Met?Val?Ile?Gln?Glu?Glu?Ala
225 230 235 240
Tyr?Ile?Thr?Trp?Pro?Tyr?Asn?Asn?Val?Arg?Leu?Ala?Pro?Ser?Ser?Phe
245 250 255
Asn?Ser?Arg?Gly?Phe?Arg?Asp?Gln?Ala?Leu?Ala?Cys?Glu?Ala?Ala?Leu
260 265 270
Lys?Glu?Arg?Asp?Ser?Gly?Leu?Pro?His?Ser?Gly?Lys?Asn?Ile?Ser?Glu
275 280 285
Ile?Cys?Gly?Gly?Leu?Ala?Leu?Glu?Trp?Gly?Asp?Gly?Pro?Ile?Thr?Tyr
290 295 300
Tyr?His?Thr?Phe?Asn?Arg?Gly?Trp?Tyr?Asp?Ile?Ala?His?Pro?Lys?Asn
305 310 315 320
Asp?Pro?Phe?Pro?Ala?Lys?His?Met?Leu?Gly?Tyr?Leu?Thr?Gln?Glu?Ser
325 330 335
Val?Leu?Ala?Ala?Leu?Gly?Val?Pro?Val?Asn?Phe?Thr?Ser?Ser?Ser?Ser
340 345 350
Ala?Val?Ala?Thr?Gln?Phe?Ile?Lys?Thr?Phe?Asp?Ile?Val?His?Gly?Gly
355 360 365
Phe?Leu?Asp?Ala?Ile?Gly?Tyr?Leu?Leu?Asp?Ser?Gly?Val?Lys?Val?His
370 375 380
Met?Met?Tyr?Gly?Asp?Arg?Asp?Tyr?Ala?Cys?Asn?Trp?Val?Gly?Gly?Glu
385 390 395 400
Lys?Ala?Ser?Leu?Ala?Val?Pro?Tyr?Ser?Arg?Ile?Thr?Glu?Phe?Ala?Asp
405 410 415
Thr?Gly?Tyr?Ser?Pro?Leu?Leu?Thr?Pro?Asp?Gly?Ile?Ser?Gly?Met?Thr
420 425 430
Arg?Gln?Leu?Gly?Asn?Tyr?Ser?Phe?Thr?Arg?Val?Phe?Gln?Ala?Gly?His
435 440 445
Glu?Val?Pro?Ser?Tyr?Gln?Pro?Val?Ala?Ala?Tyr?Glu?Ile?Phe?Met?Arg
450 455 460
Ala?Thr?Phe?Asn?Lys?Asp?Ile?Pro?Thr?Gly?Leu?Leu?Ala?Val?Asp?Asp
465 470 475 480
Glu?Phe?Gln?Ser?Val?Gly?Pro?Lys?Asp?Thr?Trp?His?Ile?Lys?Asn?Ile
485 490 495
Pro?Pro?Ile?Met?Pro?Lys?Pro?Gln?Cys?Tyr?Val?Leu?Ser?Pro?Gly?Thr
500 505 510
Cys?Thr?Pro?Glu?Val?Trp?Glu?Thr?Val?Leu?Asn?Gly?Ser?Ala?Thr?Val
515 520 525
Lys?Asp?Trp?Tyr?Val?Val?Asp?Asp?Ser?Ala?Gly?Val?Glu?Asp?His?Glu
530 535 540
Gly?Phe?Ser?Ile?Leu?Gly?Gly?Asp?Glu?Leu
545 550
<210>162
<211>578
<212>PRT
<213〉aspergillus niger
<400>162
Met?Thr?Arg?Phe?Gln?Leu?Leu?Pro?Leu?Val?Ala?Gly?Leu?Leu?Ala?Pro
1 5 10 15
Ser?Ile?Ala?Ala?Leu?Ser?Ile?Pro?Ser?Pro?Gln?Gln?Ile?Leu?Asp?Ser
20 25 30
Leu?Thr?Phe?Gly?Glu?His?Thr?Asp?Gly?Phe?Cys?Pro?Leu?Ala?Pro?Lys
35 40 45
Val?Glu?Val?Pro?Asp?Asp?Gly?Phe?Phe?Pro?Ala?Leu?Lys?Phe?Val?Glu
50 55 60
Asp?Ala?Ser?Phe?Lys?Ser?Arg?Gln?Val?Asn?Arg?Leu?Ser?Arg?Ala?Val
65 70 75 80
Gln?Val?Pro?Thr?Ala?Ile?Asp?Asp?Tyr?Met?Lys?Asp?Pro?Tyr?Asp?Glu
85 90 95
Lys?Phe?Ala?Pro?Phe?Leu?Asp?Phe?Gln?Lys?Leu?Leu?Gln?Thr?Leu?Phe
100 105 110
Pro?Leu?Thr?His?Ser?Tyr?Ala?Arg?Val?Asp?His?Ile?Asn?Arg?Phe?Gly
115 120 125
Leu?Val?Phe?Thr?Leu?Asn?Gly?Thr?Asp?Asp?Ser?Leu?Lys?Pro?Leu?Leu
130 135 140
Phe?Thr?Ala?His?Gln?Asp?Val?Val?Pro?Ile?Asn?Asp?Pro?Ala?Asp?Trp
145 150 155 160
Thr?Tyr?Pro?Pro?Phe?Asp?Gly?His?Tyr?Asp?Gly?Glu?Trp?Leu?Trp?Gly
165 170 175
Arg?Gly?Ala?Ser?Asp?Cys?Lys?Asn?Val?Leu?Ile?Gly?Leu?Met?Ser?Val
180 185 190
Val?Glu?Asp?Leu?Leu?Ser?Gln?Lys?Trp?Glu?Pro?Thr?Arg?Thr?Val?Val
195 200 205
Leu?Ala?Phe?Gly?Phe?Asp?Glu?Glu?Ser?His?Gly?Phe?Leu?Gly?Ala?Gly
210 215 220
Ser?Ile?Ala?Lys?Phe?Leu?Glu?Lys?Lys?Tyr?Gly?Pro?Asp?Ser?Phe?Glu
225 230 235 240
Phe?Ile?Leu?Asp?Glu?Gly?Gly?Met?Gly?Leu?Glu?Val?Leu?Asp?Asp?Asn
245 250 255
Asn?Asn?Gly?Val?Val?Tyr?Ala?Leu?Pro?Gly?Val?Gly?Glu?Lys?Gly?Ser
260 265 270
Ile?Asp?Val?Val?Leu?Thr?Leu?Ala?Val?Pro?Gly?Gly?His?Ser?Ser?Val
275 280 285
Pro?Pro?Pro?His?Thr?Gly?Ile?Gly?Ile?Ile?Ala?Glu?Ile?Ile?Tyr?Glu
290 295 300
Leu?Glu?Arg?Gln?Asp?Leu?Phe?Val?Pro?Val?Leu?Asp?Thr?His?His?Pro
305 310 315 320
Thr?Arg?Lys?Met?Leu?Glu?Cys?Gln?Val?Arg?His?Ser?Pro?Ser?Gln?Val
325 330 335
Glu?Pro?Trp?Leu?Ala?Ser?Ala?Leu?Gln?Ser?Ser?Asp?Tyr?Ile?Ser?Leu
340 345 350
Ala?Glu?Lys?Leu?Ala?Ser?Ser?Arg?Gly?Asp?Lys?Phe?Arg?Phe?Ile?Leu
355 360 365
Gln?Thr?Ser?Gln?Ala?Ala?Asp?Ile?Ile?Asn?Gly?Gly?Val?Lys?Ser?Asn
370 375 380
Ala?Leu?Pro?Glu?Lys?Ile?Asn?Ala?Leu?Val?Asn?Tyr?Arg?Ile?Ala?Leu
385 390 395 400
His?Gln?Thr?Pro?Asp?Asp?Ile?Lys?Asn?Arg?Ala?Val?Glu?Ile?Ile?Ser
405 410 415
Pro?Ile?Val?Lys?Lys?Tyr?Asn?Leu?Ser?Leu?Thr?Ala?Phe?Pro?Glu?Ser
420 425 430
Asp?Thr?Val?Asp?Pro?Ser?Leu?Asn?Asn?His?Leu?Thr?Leu?Thr?Thr?Leu
435 440 445
Ser?Gly?Ala?Leu?Ser?Pro?Ala?Pro?Val?Ser?Pro?Thr?Asp?Ile?Asp?Thr
450 455 460
Asp?Ala?Val?Trp?Ala?Arg?Phe?Ser?Gly?Val?Thr?Arg?Ser?Val?Phe?Glu
465 470 475 480
Ser?Val?Pro?Ser?Leu?Glu?Gly?Arg?Lys?Val?Val?Val?Ser?Gly?Asp?Ile
485 490 495
Met?Thr?Gly?Asn?Thr?Asp?Thr?Arg?Phe?Tyr?Trp?Ala?Leu?Ser?Arg?Asn
500 505 510
Ile?Tyr?Arg?Trp?Ser?Pro?Ser?Arg?Ala?Gly?Lys?Ala?Leu?Asn?Ile?His
515 520 525
Thr?Val?Asp?Glu?Arg?Ile?Asp?Ile?Asp?Ile?His?Leu?Glu?Ala?Met?Met
530 535 540
Leu?Tyr?Tyr?Asp?Leu?Ile?Arg?Ser?Phe?Asp?Gly?Arg?Thr?Asp?Ser?Ser
545 550 555 560
Val?Ile?Ser?Ala?Ala?Ser?Ala?Ala?Ala?Asp?Asp?Glu?Leu?Ala?His?Asp
565 570 575
Val?Leu
<210>163
<211>456
<212>PRT
<213〉aspergillus niger
<400>163
Met?Lys?Ser?Thr?Thr?Leu?Leu?Ser?Leu?Ala?Trp?Ala?Ala?Gln?Ser?Ala
1 5 10 15
Tyr?Ser?Leu?Ser?Ile?His?Glu?Arg?Asp?Glu?Pro?Ala?Thr?Leu?Gln?Phe
20 25 30
Asn?Phe?Glu?Arg?Arg?Gln?Ile?Ala?Asp?Arg?Ser?Arg?Arg?Lys?Arg?Ser
35 40 45
Thr?Ala?Ser?Ala?Asp?Leu?Val?Asn?Leu?Ala?Thr?Asn?Leu?Gly?Tyr?Thr
50 55 60
Met?Asn?Leu?Thr?Leu?Gly?Thr?Pro?Gly?Gln?Glu?Val?Ser?Val?Thr?Leu
65 70 75 80
Asp?Thr?Gly?Ser?Ser?Asp?Leu?Trp?Val?Asn?Gly?Ala?Asn?Ser?Ser?Val
85 90 95
Cys?Pro?Cys?Thr?Asp?Tyr?Gly?Ser?Tyr?Asn?Ser?Ser?Ala?Ser?Ser?Thr
100 105 110
Tyr?Thr?Phe?Val?Asn?Asp?Glu?Phe?Tyr?Ile?Gln?Tyr?Val?Asp?Gly?Ser
115 120 125
Glu?Ala?Thr?Gly?Asp?Tyr?Val?Asn?Asp?Thr?Leu?Lys?Phe?Ser?Asn?Val
130 135 140
Thr?Leu?Thr?Asn?Phe?Gln?Phe?Ala?Val?Ala?Tyr?Asp?Gly?Asp?Ser?Glu
145 150 155 160
Glu?Gly?Val?Leu?Gly?Ile?Gly?Tyr?Ala?Ser?Asn?Glu?Ala?Ser?Gln?Ala
165 170 175
Thr?Val?Gly?Gly?Gly?Glu?Tyr?Thr?Asn?Phe?Pro?Glu?Ala?Leu?Val?Asp
180 185 190
Gln?Gly?Ala?Ile?Asn?Trp?Pro?Ala?Tyr?Ser?Leu?Trp?Leu?Asp?Asp?Leu
195 200 205
Asp?Glu?Gly?Lys?Gly?Thr?Ile?Leu?Phe?Gly?Gly?Val?Asn?Thr?Ala?Lys
210 215 220
Tyr?Tyr?Gly?Ser?Leu?Gln?Thr?Leu?Pro?Ile?Val?Ser?Ile?Glu?Asp?Met
225 230 235 240
Tyr?Val?Glu?Phe?Ala?Val?Asn?Leu?Thr?Ala?Val?His?Leu?Glu?Lys?Asn
245 250 255
Gly?Asn?Ser?Val?Ser?Val?Asn?Asn?Ser?Ala?Thr?Gln?Phe?Pro?Ile?Pro
260 265 270
Ala?Val?Leu?Asp?Ser?Gly?Thr?Ala?Leu?Thr?Tyr?Ile?Pro?Thr?Ser?Ala
275 280 285
Ala?Ala?Ser?Ile?Tyr?Glu?Ala?Val?Gly?Ala?Gln?Tyr?Leu?Ser?Glu?Tyr
290 295 300
Gly?Tyr?Gly?Val?Ile?Glu?Cys?Asp?Val?Lys?Asp?Glu?Asp?Phe?Thr?Phe
305 310 315 320
Leu?Phe?Asp?Phe?Gly?Ser?Phe?Asn?Met?Ser?Val?Asp?Ile?Ser?Glu?Met
325 330 335
Ile?Leu?Glu?Ala?Ser?Ser?Asp?Met?Thr?Asp?Met?Asn?Val?Cys?Thr?Phe
340 345 350
Gly?Leu?Ala?Val?Ile?Glu?Asn?Glu?Ala?Leu?Leu?Gly?Asp?Thr?Phe?Leu
355 360 365
Arg?Ser?Ala?Tyr?Val?Val?Tyr?Asp?Leu?Gly?Asn?Asn?Glu?Ile?Ser?Leu
370 375 380
Ala?Lys?Ala?Asn?Phe?Asn?Pro?Gly?Glu?Asp?His?Val?Leu?Glu?Ile?Gly
385 390 395 400
Thr?Gly?Ser?Asp?Ala?Val?Pro?Lys?Ala?Thr?Gly?Ala?Thr?Ala?Thr?Gly
405 410 415
Ala?Ala?Ala?Thr?Ser?Thr?Ala?Ser?Ser?Asp?Lys?Ser?Asp?Lys?Glu?Ser
420 425 430
Ser?Ala?Thr?Val?Pro?Arg?Ser?Gln?Ile?Val?Ser?Leu?Val?Ala?Gly?Val
435 440 445
Leu?Val?Gly?Val?Phe?Leu?Val?Leu
450 455
<210>164
<211>664
<212>PRT
<213〉aspergillus niger
<400>164
Met?Leu?Val?Arg?Gln?Leu?Ala?Leu?Ala?Leu?Ala?Ile?Ala?Ala?Leu?Ser
1 5 10 15
Asp?Ala?Ile?Pro?Thr?Ser?Ile?Lys?His?Val?Leu?His?Glu?Lys?Arg?His
20 25 30
Lys?Pro?Ala?Ser?Asp?Trp?Val?Lys?Gly?Ala?Arg?Val?Glu?Ser?Asp?Ala
35 40 45
Val?Leu?Pro?Met?Arg?Ile?Gly?Leu?Ala?Gln?Asn?Asn?Leu?Asp?Lys?Gly
50 55 60
Tyr?Asp?Phe?Leu?Met?Glu?Val?Ser?Asp?Pro?Lys?Ser?Ser?Lys?Tyr?Gly
65 70 75 80
Gln?Tyr?Trp?Ser?Ala?Asp?Glu?Val?His?Asp?Ile?Phe?Ser?Pro?Ser?Glu
85 90 95
Glu?Ala?Val?Glu?Ala?Val?Arg?Glu?Trp?Leu?Val?Ala?Ser?Gly?Ile?His
100 105 110
Pro?Ser?Arg?Val?Val?His?Ser?Asp?Asn?Lys?Gly?Trp?Leu?Ala?Phe?Asp
115 120 125
Ala?Tyr?Ala?His?Glu?Ala?Glu?Arg?Leu?Phe?Met?Thr?Glu?Phe?His?Glu
130 135 140
His?Glu?Ser?Asp?Arg?Ser?Ala?Lys?Ile?Arg?Val?Gly?Cys?Asp?Gln?Tyr
145 150 155 160
His?Val?Pro?Glu?His?Ile?Gln?Lys?His?Ile?Asp?Tyr?Ile?Thr?Pro?Gly
165 170 175
Val?Lys?Leu?Thr?Gln?Val?Val?Lys?Arg?Thr?Asn?Lys?Val?Lys?Arg?Ala
180 185 190
Ser?Gln?Leu?Ala?His?Ser?Ser?Lys?Ala?Lys?Ser?Ala?Ala?Gln?Gly?Pro
195 200 205
Gln?Pro?Leu?Pro?Asn?Lys?Ala?Lys?Phe?Leu?Pro?Glu?Asp?Leu?Arg?Gly
210 215 220
Cys?Gly?Tyr?Asn?Ile?Thr?Pro?Ser?Cys?Ile?Lys?Ala?Leu?Tyr?Gln?Ile
225 230 235 240
Pro?Asp?Ala?Lys?Thr?Ala?Thr?Pro?Asn?Asn?Ser?Leu?Gly?Leu?Tyr?Glu
245 250 255
Gln?Gly?Asp?Tyr?Phe?Ala?Lys?Ser?Asp?Leu?Asp?Leu?Phe?Tyr?Lys?Glu
260 265 270
Tyr?Ala?Pro?Trp?Val?Pro?Gln?Gly?Thr?Tyr?Pro?Ile?Pro?Ala?Leu?Ile
275 280 285
Asp?Gly?Ala?Asn?Tyr?Ser?Val?Pro?Ser?Tyr?Ser?Ser?Leu?Asn?Thr?Gly
290 295 300
Glu?Ser?Asp?Ile?Asp?Ile?Asp?Met?Ala?Tyr?Ser?Leu?Leu?Tyr?Pro?Gln
305 310 315 320
Gln?Val?Thr?Leu?Tyr?Gln?Val?Asp?Asp?Gln?Leu?Tyr?Glu?Pro?Val?Glu
325 330 335
Val?Asp?Thr?Thr?Asn?Leu?Phe?Asn?Thr?Phe?Leu?Asp?Ala?Leu?Asp?Gly
340 345 350
Ser?Tyr?Cys?Thr?Tyr?Ser?Ala?Tyr?Gly?Glu?Thr?Gly?Asp?Asp?Pro?Ser
355 360 365
Ile?Asp?Pro?Val?Tyr?Pro?Asp?Thr?Arg?Pro?Gly?Gly?Tyr?Lys?Gly?Lys
370 375 380
Leu?Gln?Cys?Gly?Val?Tyr?Lys?Pro?Thr?Asn?Val?Ile?Ser?Ala?Ser?Tyr
385 390 395 400
Gly?Gln?Ser?Glu?Ala?Asp?Leu?Pro?Val?Ser?Tyr?Thr?Lys?Arg?Gln?Cys
405 410 415
Asn?Glu?Phe?Met?Lys?Leu?Gly?Leu?Gln?Gly?His?Ser?Ile?Leu?Phe?Ala
420 425 430
Ser?Gly?Asp?Tyr?Gly?Val?Ala?Ser?Phe?Ala?Gly?Asp?Gly?Asp?Glu?Asn
435 440 445
Gly?Cys?Leu?Gly?Pro?Glu?Gly?Lys?Ile?Phe?Asn?Pro?Gln?Tyr?Pro?Ser
450 455 460
Asn?Cys?Pro?Tyr?Val?Thr?Ser?Val?Gly?Gly?Thr?Met?Leu?Tyr?Gly?Tyr
465 470 475 480
Gln?Thr?Val?Asn?Asp?Ser?Glu?Ser?Val?Met?His?Val?Asn?Leu?Gly?Gly
485 490 495
Thr?Ala?Ser?Asn?Phe?Ser?Thr?Ser?Gly?Gly?Phe?Ser?Asn?Tyr?Phe?Pro
500 505 510
Gln?Pro?Ala?Tyr?Gln?Phe?Ala?Ala?Val?Glu?Gln?Tyr?Phe?Gln?Ser?Ala
515 520 525
Asn?Leu?Ser?Tyr?Pro?Tyr?Tyr?Ser?Glu?Phe?Glu?Val?Asp?Val?Asn?Thr
530 535 540
Thr?Lys?Gly?Leu?Tyr?Asn?Arg?Leu?Gly?Arg?Ala?Tyr?Pro?Asp?Val?Ser
545 550 555 560
Ala?Asn?Gly?Ala?His?Phe?Arg?Ala?Tyr?Met?Asp?Gly?Tyr?Asp?Tyr?His
565 570 575
Trp?Tyr?Gly?Ser?Ser?Leu?Ala?Ser?Pro?Leu?Phe?Ala?Ser?Val?Leu?Thr
580 585 590
Leu?Leu?Asn?Glu?Glu?Arg?Phe?Ala?Ile?Gly?Lys?Gly?Pro?Val?Gly?Phe
595 600 605
Val?Asn?Pro?Val?Leu?Tyr?Ala?Tyr?Pro?Gln?Val?Leu?Asn?Asp?Ile?Thr
610 615 620
Asn?Gly?Thr?Asn?Ala?Gly?Cys?Gly?Thr?Tyr?Gly?Phe?Ser?Ala?Ile?Glu
625 630 635 640
Gly?Trp?Asp?Pro?Ala?Ser?Gly?Leu?Gly?Thr?Pro?Asn?Tyr?Pro?Leu?Met
645 650 655
Lys?Glu?Leu?Phe?Leu?Ser?Leu?Pro
660
<210>165
<211>520
<212>PRT
<213〉aspergillus niger
<400>165
Met?Arg?Val?Thr?Thr?Ala?Ile?Ala?Ser?Leu?Leu?Leu?Val?Gly?Ser?Ala
1 5 10 15
Thr?Ser?Leu?Gln?Asn?Pro?His?Arg?Arg?Ala?Val?Pro?Pro?Pro?Leu?Ser
20 25 30
His?Arg?Ser?Val?Ala?Ser?Arg?Ser?Val?Pro?Val?Glu?Arg?Arg?Thr?Thr
35 40 45
Asp?Phe?Glu?Tyr?Leu?Thr?Asn?Lys?Thr?Ala?Arg?Phe?Leu?Val?Asn?Gly
50 55 60
Thr?Ser?Ile?Pro?Glu?Val?Asp?Phe?Asp?Val?Gly?Glu?Ser?Tyr?Ala?Gly
65 70 75 80
Leu?Leu?Pro?Asn?Thr?Pro?Thr?Gly?Asn?Ser?Ser?Leu?Phe?Phe?Trp?Phe
85 90 95
Phe?Pro?Ser?Gln?Asn?Pro?Glu?Ala?Ser?Asp?Glu?Ile?Thr?Ile?Trp?Leu
100 105 110
Asn?Gly?Gly?Pro?Gly?Cys?Ser?Ser?Leu?Asp?Gly?Leu?Leu?Gln?Glu?Asn
115 120 125
Gly?Pro?Phe?Leu?Trp?Gln?Pro?Gly?Thr?Tyr?Lys?Pro?Val?Pro?Asn?Pro
130 135 140
Tyr?Ser?Trp?Thr?Asn?Leu?Thr?Asn?Val?Val?Tyr?Ile?Asp?Gln?Pro?Ala
145 150 155 160
Gly?Thr?Gly?Phe?Ser?Pro?Gly?Pro?Ser?Thr?Val?Asn?Asn?Glu?Glu?Asp
165 170 175
Val?Ala?Ala?Gln?Phe?Asn?Ser?Trp?Phe?Lys?His?Phe?Val?Asp?Thr?Phe
180 185 190
Asp?Leu?His?Gly?Arg?Lys?Val?Tyr?Ile?Thr?Gly?Glu?Ser?Tyr?Ala?Gly
195 200 205
Met?Tyr?Val?Pro?Tyr?Ile?Ala?Asp?Ala?Met?Leu?Asn?Glu?Glu?Asp?Thr
210 215 220
Thr?Tyr?Phe?Asn?Leu?Lys?Gly?Ile?Gln?Ile?Asn?Asp?Pro?Ser?Ile?Asn
225 230 235 240
Ser?Asp?Ser?Val?Met?Met?Tyr?Ser?Pro?Ala?Val?Arg?His?Leu?Asn?His
245 250 255
Tyr?Asn?Asn?Ile?Phe?Gln?Leu?Asn?Ser?Thr?Phe?Leu?Ser?Tyr?Ile?Asn
260 265 270
Ala?Lys?Ala?Asp?Lys?Cys?Gly?Tyr?Asn?Ala?Phe?Leu?Asp?Lys?Ala?Ile
275 280 285
Thr?Tyr?Pro?Pro?Pro?Ser?Pro?Phe?Pro?Thr?Ala?Pro?Glu?Ile?Thr?Glu
290 295 300
Asp?Cys?Gln?Val?Trp?Asp?Glu?Val?Val?Met?Ala?Ala?Tyr?Asp?Ile?Asn
305 310 315 320
Pro?Cys?Phe?Asn?Tyr?Tyr?His?Leu?Ile?Asp?Phe?Cys?Pro?Tyr?Leu?Trp
325 330 335
Asp?Val?Leu?Gly?Phe?Pro?Ser?Leu?Ala?Ser?Gly?Pro?Asn?Asn?Tyr?Phe
340 345 350
Asn?Arg?Ser?Asp?Val?Gln?Lys?Ile?Leu?His?Val?Pro?Pro?Thr?Asp?Tyr
355 360 365
Ser?Val?Cys?Ser?Glu?Thr?Val?Ile?Phe?Ala?Asn?Gly?Asp?Gly?Ser?Asp
370 375 380
Pro?Ser?Ser?Trp?Gly?Pro?Leu?Pro?Ser?Val?Ile?Glu?Arg?Thr?Asn?Asn
385 390 395 400
Thr?Ile?Ile?Gly?His?Gly?Trp?Leu?Asp?Tyr?Leu?Leu?Phe?Leu?Asn?Gly
405 410 415
Ser?Leu?Ala?Thr?Ile?Gln?Asn?Met?Thr?Trp?Asn?Gly?Lys?Gln?Gly?Phe
420 425 430
Gln?Arg?Pro?Pro?Val?Glu?Pro?Leu?Phe?Val?Pro?Tyr?His?Tyr?Gly?Leu
435 440 445
Ala?Glu?Leu?Tyr?Trp?Gly?Asp?Glu?Pro?Asp?Pro?Tyr?Asn?Leu?Asp?Ala
450 455 460
Gly?Ala?Gly?Tyr?Leu?Gly?Thr?Ala?His?Thr?Glu?Arg?Gly?Leu?Thr?Phe
465 470 475 480
Ser?Ser?Val?Tyr?Leu?Ser?Gly?His?Glu?Ile?Pro?Gln?Tyr?Val?Pro?Gly
485 490 495
Ala?Ala?Tyr?Arg?Gln?Leu?Glu?Phe?Leu?Leu?Gly?Arg?Ile?Ser?Ser?Leu
500 505 510
Ser?Ala?Lys?Gly?Asn?Tyr?Thr?Ser
515 520
<210>166
<211>551
<212>PRT
<213〉aspergillus niger
<400>166
Met?Arg?Gly?Ser?Arg?Leu?Val?Leu?Leu?Leu?Pro?Leu?Ala?Ala?Leu?Ser
1 5 10 15
Cys?Ala?Met?Pro?Glu?Asn?Glu?Trp?Ser?Ser?Thr?Ile?Arg?Arg?Gln?Leu
20 25 30
Pro?Lys?Ala?Ser?Thr?Gly?Val?Lys?Ser?Ile?Lys?Thr?Pro?Asn?Asn?Val
35 40 45
Thr?Ile?Arg?Tyr?Lys?Glu?Pro?Gly?Thr?Glu?Gly?Ile?Cys?Glu?Thr?Thr
50 55 60
Pro?Gly?Val?Lys?Ser?Tyr?Ser?Gly?Tyr?Val?Asp?Leu?Ser?Pro?Glu?Ser
65 70 75 80
His?Thr?Phe?Phe?Trp?Phe?Phe?Glu?Ser?Arg?Arg?Asp?Pro?Glu?Asn?Asp
85 90 95
Pro?Val?Thr?Leu?Trp?Leu?Asn?Gly?Gly?Pro?Gly?Ser?Asp?Ser?Leu?Ile
100 105 110
Gly?Leu?Phe?Glu?Glu?Leu?Gly?Pro?Cys?His?Ile?Thr?Pro?Glu?Tyr?Glu
115 120 125
Ser?Ile?Ile?Asn?Gln?Tyr?Ser?Trp?Asn?Glu?Val?Thr?Asn?Leu?Leu?Phe
130 135 140
Leu?Ser?Gln?Pro?Leu?Gly?Val?Gly?Phe?Ser?Tyr?Ser?Glu?Thr?Glu?Ala
145 150 155 160
Gly?Ser?Leu?Asn?Pro?Phe?Thr?Gly?Ala?Val?Glu?Asn?Ala?Ser?Phe?Ala
165 170 175
Gly?Val?Gln?Gly?Arg?Tyr?Pro?Val?Ile?Asp?Ala?Thr?Ile?Ile?Asp?Thr
180 185 190
Thr?Asp?Ile?Ala?Ala?Arg?Ala?Thr?Trp?Glu?Val?Leu?Gln?Gly?Phe?Leu
195 200 205
Ser?Gly?Leu?Ser?Gln?Leu?Asp?Ser?Glu?Val?Lys?Ser?Lys?Glu?Phe?Asn
210 215 220
Leu?Trp?Thr?Glu?Ser?Tyr?Gly?Gly?His?Tyr?Gly?Pro?Ala?Phe?Phe?Asn
225 230 235 240
His?Phe?Tyr?Glu?Gln?Asn?Ser?Lys?Ile?Ala?Ser?Gly?Glu?Val?Asn?Gly
245 250 255
Val?Gln?Leu?Asn?Phe?Asn?Ser?Leu?Gly?Ile?Ile?Asn?Gly?Ile?Ile?Asp
260 265 270
Ala?Ala?Ile?Gln?Ala?Asp?Tyr?Tyr?Ala?Asp?Phe?Ala?Val?Asn?Asn?Thr
275 280 285
Tyr?Gly?Ile?Lys?Ala?Val?Asn?Asp?Thr?Val?Tyr?Asn?Tyr?Met?Lys?Phe
290 295 300
Ala?Asn?Thr?Met?Pro?Asn?Gly?Cys?Gln?Asp?Gln?Val?Ala?Ser?Cys?Lys
305 310 315 320
Leu?Thr?Asn?Arg?Thr?Ser?Leu?Ser?Asp?Tyr?Ala?Ile?Cys?Thr?Glu?Ala
325 330 335
Ala?Asn?Met?Cys?Arg?Asp?Asn?Val?Glu?Gly?Pro?Tyr?Tyr?Gln?Phe?Gly
340 345 350
Gly?Arg?Gly?Val?Tyr?Asp?Ile?Arg?His?Pro?Tyr?Asn?Asp?Pro?Thr?Pro
355 360 365
Pro?Ser?Tyr?Phe?Val?Asp?Tyr?Leu?Lys?Lys?Asp?Ser?Val?Met?Asp?Ala
370 375 380
Ile?Gly?Val?Asp?Ile?Asn?Tyr?Thr?Glu?Ser?Ser?Gly?Glu?Val?Tyr?Tyr
385 390 395 400
Ala?Phe?Gln?Gln?Thr?Gly?Asp?Phe?Val?Trp?Pro?Asn?Phe?Ile?Glu?Asp
405 410 415
Leu?Glu?Glu?Ile?Leu?Gln?Leu?Pro?Val?Arg?Val?Ser?Leu?Ile?Tyr?Gly
420 425 430
Asp?Ala?Asp?Tyr?Ile?Cys?Asn?Trp?Phe?Gly?Gly?Gln?Ala?Ile?Ser?Leu
435 440 445
Ala?Val?Asn?Tyr?Pro?His?Ala?Ala?Gln?Phe?Arg?Ala?Ala?Gly?Tyr?Thr
450 455 460
Pro?Met?Thr?Val?Asp?Gly?Val?Glu?Tyr?Gly?Glu?Thr?Arg?Glu?Tyr?Gly
465 470 475 480
Asn?Phe?Ser?Phe?Thr?Arg?Val?Tyr?Gln?Ala?Gly?His?Glu?Val?Pro?Tyr
485 490 495
Tyr?Gln?Pro?Ile?Ala?Ala?Leu?Gln?Leu?Phe?Asn?Arg?Thr?Leu?Phe?Gly
500 505 510
Trp?Asp?Ile?Ala?Ala?Gly?Thr?Thr?Gln?Ile?Trp?Pro?Glu?Tyr?Ser?Thr
515 520 525
Asn?Gly?Thr?Ser?Gln?Ala?Thr?His?Thr?Glu?Ser?Phe?Val?Pro?Leu?Ser
530 535 540
Thr?Ala?Ser?Ser?Thr?Val?Asn
545 550
<210>167
<211>623
<212>PRT
<213〉aspergillus niger
<400>167
Met?Pro?Phe?Pro?Phe?Ser?Ser?Ala?Leu?Leu?Gly?Tyr?Ile?Leu?Thr?Thr
1 5 10 15
Ser?Thr?Thr?Leu?Thr?Ser?Leu?Val?Ala?Gly?Gln?Tyr?Tyr?Pro?Pro?Thr
20 25 30
Pro?Glu?Asp?Leu?Thr?Val?Ile?His?Ser?Glu?Ile?Phe?Pro?Gly?Ala?Arg
35 40 45
Ile?Ser?Tyr?Lys?Gln?Pro?Leu?Gly?Ile?Cys?Thr?Thr?Thr?Pro?Ser?Thr
50 55 60
Pro?Ser?Tyr?Ser?Gly?Tyr?Ile?His?Leu?Pro?Pro?His?Thr?Leu?Thr?Asn
65 70 75 80
Leu?Ser?Ile?Pro?Gly?Ile?Ser?Ile?Ser?Gln?Pro?Tyr?Pro?Ile?Asn?Thr
85 90 95
Phe?Phe?Trp?Tyr?Phe?Pro?Ser?Arg?His?His?His?Asn?Asn?Asp?Thr?Ser
100 105 110
Pro?Leu?Thr?Ile?Trp?Met?Asn?Gly?Gly?Pro?Gly?Gly?Ser?Ser?Met?Ile
115 120 125
Gly?Leu?Phe?Gln?Glu?Asn?Gly?Pro?Cys?Thr?Val?Asn?Thr?Asp?Ser?Asn
130 135 140
Ser?Thr?Ala?Tyr?Asn?Pro?Trp?Ser?Trp?Asn?Glu?Tyr?Val?Asp?Met?Leu
145 150 155 160
Tyr?Ile?Glu?Gln?Pro?Val?Gln?Thr?Gly?Phe?Ser?Tyr?Asp?Val?Leu?Arg
165 170 175
Asn?Gly?Thr?Leu?Asp?Leu?Asn?Glu?Thr?Phe?Leu?Val?Gly?Thr?Leu?Pro
180 185 190
Ser?Gln?Asp?Val?His?Gly?Thr?Val?Asn?Gly?Thr?Val?Asn?Gly?Gly?Arg
195 200 205
Ala?Leu?Trp?Val?Ala?Leu?Gln?Val?Trp?Leu?Gly?Glu?Phe?Ser?Glu?Tyr
210 215 220
Val?Ser?Ser?Val?Asp?Gly?Asn?Gly?Gly?Gly?Asp?Asp?Arg?Val?Ser?Ile
225 230 235 240
Trp?Thr?Glu?Ser?Tyr?Gly?Gly?Arg?Tyr?Gly?Pro?Ala?Tyr?Thr?Ala?Leu
245 250 255
Phe?Gln?Glu?Met?Asn?Glu?Arg?Ile?Glu?Ser?Gly?Glu?Val?Ser?Thr?Gly
260 265 270
Lys?Lys?Ile?His?Leu?Asp?Thr?Leu?Gly?Ile?Ile?Asn?Gly?Cys?Val?Asp
275 280 285
Leu?Leu?Val?Gln?Val?Pro?Ser?Phe?Pro?Glu?Gln?Ala?Tyr?Asn?Asn?Thr
290 295 300
Tyr?Gly?Ile?Glu?Gly?Ile?Asn?Arg?Thr?Leu?Tyr?Asp?Arg?Ala?Met?Asp
305 310 315 320
Ser?Trp?Ser?Lys?Pro?Gly?Gly?Cys?Arg?Asp?Met?Ile?Ile?Glu?Cys?Arg
325 330 335
Asp?Ala?Gly?Glu?Leu?Gly?Asp?Pro?Leu?Ile?Ile?Cys?Glu?Glu?Ala?Ser
340 345 350
Asp?Tyr?Cys?Ser?Arg?Glu?Ile?Lys?Ser?Leu?Tyr?Thr?Asn?Thr?Ser?Gly
355 360 365
Arg?Gly?Tyr?Tyr?Asp?Ile?Ala?His?Phe?Thr?Pro?Asp?Ala?Ala?Leu?Val
370 375 380
Pro?Tyr?Phe?Val?Gly?Phe?Leu?Asn?Arg?Pro?Trp?Val?Gln?Lys?Ala?Leu
385 390 395 400
Gly?Val?Pro?Val?Asn?Tyr?Thr?Met?Ser?Ser?Glu?Ala?Val?Gly?Asn?Ser
405 410 415
Phe?Ala?Ser?Thr?Gly?Asp?Tyr?Pro?Arg?Asn?Asp?Pro?Arg?Gly?Met?Ile
420 425 430
Gly?Asp?Ile?Gly?Tyr?Leu?Leu?Asp?Ser?Gly?Val?Lys?Val?Ala?Met?Val
435 440 445
Tyr?Gly?Asp?Arg?Asp?Tyr?Ala?Cys?Pro?Trp?Arg?Gly?Gly?Glu?Asp?Val
450 455 460
Ser?Leu?Leu?Val?Glu?Tyr?Glu?Asp?Ala?Glu?Lys?Phe?Arg?Ala?Ala?Gly
465 470 475 480
Tyr?Ala?Glu?Val?Gln?Thr?Lys?Ser?Ser?Tyr?Val?Gly?Gly?Leu?Val?Arg
485 490 495
Gln?Tyr?Gly?Asn?Phe?Ser?Phe?Thr?Arg?Val?Phe?Gln?Ala?Gly?His?Glu
500 505 510
Val?Pro?Phe?Tyr?Gln?Pro?Glu?Thr?Ala?Tyr?Glu?Ile?Phe?Asn?Arg?Ala
515 520 525
Gln?Phe?Asn?Trp?Asp?Ile?Ala?Thr?Gly?Gly?Ile?Ser?Leu?Glu?Gln?Asn
530 535 540
Gln?Ser?Tyr?Gly?Thr?Glu?Gly?Pro?Ser?Ser?Thr?Trp?His?Ile?Lys?Asn
545 550 555 560
Glu?Val?Pro?Glu?Ser?Pro?Glu?Pro?Thr?Cys?Tyr?Leu?Leu?Ala?Met?Asp
565 570 575
Ser?Thr?Cys?Thr?Asp?Glu?Gln?Arg?Glu?Arg?Val?Leu?Ser?Gly?Asp?Ala
580 585 590
Val?Val?Arg?Asp?Trp?Val?Val?Val?Asp?Asp?Ile?Glu?Ala?Glu?Ser?Ser
595 600 605
Phe?Ser?Gly?Val?Gly?Asp?Gln?Leu?Ala?Gln?Val?Pro?Leu?Gly?His
610 615 620
<210>168
<211>439
<212>PRT
<213〉aspergillus niger
<400>168
Met?Arg?Thr?Ser?Thr?Leu?Leu?Leu?Leu?Trp?Ser?Thr?Ala?Gly?Ala?Ala
1 5 10 15
Leu?Ala?Ser?Pro?Tyr?Pro?Leu?Pro?Asp?Ser?Gln?Val?Val?Phe?Ala?Ala
20 25 30
Asp?His?Glu?Val?Pro?Asn?Thr?Gln?Gly?Lys?His?Val?Val?Asp?Glu?Ala
35 40 45
Ile?Leu?Ser?Ala?Leu?Asn?Ala?His?Ser?Asp?Pro?Val?Ala?Ala?Met?Val
50 55 60
Ser?Leu?Arg?Pro?Glu?Thr?Ala?Ala?Phe?Leu?Ala?Glu?Pro?Arg?Leu?Leu
65 70 75 80
His?Ile?Arg?Gly?Glu?Glu?Lys?Ala?Glu?Trp?Met?Thr?Glu?Gly?Asp?Lys
85 90 95
Leu?Arg?Leu?Arg?Gln?Arg?Gly?Lys?Lys?Phe?Met?Asp?Ile?Thr?Glu?His
100 105 110
Gln?Asp?Phe?Tyr?Ala?Glu?Gln?Ala?Met?Ala?Ser?Phe?Ala?Gly?Asp?Pro
115 120 125
Asn?Leu?Pro?Lys?Leu?Ser?His?Lys?Gly?Leu?Val?Lys?Pro?Leu?Phe?Ser
130 135 140
Gln?Ile?Glu?Thr?Glu?Arg?Met?His?Asp?Ile?Leu?Gln?His?Met?Thr?Ser
145 150 155 160
Tyr?Tyr?Asn?Arg?Tyr?Tyr?Gly?Asp?Tyr?His?Gly?Glu?Met?Ser?Ser?Glu
165 170 175
Trp?Leu?His?Asp?Tyr?Ile?Ala?Ala?Ile?Ile?Ser?Lys?Ser?Pro?Phe?Arg
180 185 190
Thr?His?Ile?Ser?Leu?Glu?Tyr?Phe?Thr?His?Pro?Phe?Arg?Gln?Ser?Ser
195 200 205
Ile?Ile?Ala?Arg?Phe?Glu?Pro?Lys?Val?Arg?Ser?Phe?Ser?Gln?Pro?Leu
210 215 220
Thr?Ile?Ile?Gly?Ala?His?Gln?Asp?Ser?Ala?Asn?Tyr?Leu?Phe?Pro?Leu
225 230 235 240
Leu?Pro?Ala?Pro?Gly?Ala?Asp?Asp?Asp?Cys?Ser?Gly?Thr?Val?Ser?Ile
245 250 255
Leu?Glu?Ala?Phe?Arg?Val?Leu?Ala?Glu?Asn?Gly?Tyr?Thr?Pro?Lys?Asp
260 265 270
Gly?Pro?Val?Glu?Phe?His?Trp?Tyr?Ala?Ala?Glu?Glu?Ala?Gly?Leu?Leu
275 280 285
Gly?Ser?Gln?Ala?Ile?Ala?Arg?Tyr?Lys?Lys?Glu?Gln?Gly?Ala?Lys?Ile
290 295 300
Asp?Ala?Met?Met?Glu?Phe?Asp?Met?Thr?Ala?Phe?Ile?Ala?Arg?Asn?Ala
305 310 315 320
Thr?Glu?Thr?Ile?Gly?Phe?Val?Ala?Thr?Gln?Ala?Asp?Ala?Ala?Leu?Thr
325 330 335
Asn?Trp?Ala?Leu?Asn?Leu?Ser?Arg?Glu?Tyr?Ile?Ser?Ile?Pro?Ala?Glu
340 345 350
Val?Tyr?Glu?Leu?Gly?Pro?Asn?Ala?Gly?Ser?Asp?Tyr?Met?Ser?Tyr?Thr
355 360 365
Lys?Leu?Asn?Tyr?Pro?Ala?Ala?Phe?Ala?Ser?Glu?Gly?Asn?Pro?Leu?Ala
370 375 380
Gly?Gly?Ser?Phe?Pro?Gly?Glu?Met?Asp?Pro?Tyr?Val?His?Gly?Ile?Lys
385 390 395 400
Asp?Arg?Met?Asp?Val?Asp?Asp?Glu?Thr?Gly?Val?Phe?Ser?Ile?Glu?His
405 410 415
Met?Ala?Arg?Phe?Ser?Glu?Leu?Ala?Ile?Ala?Phe?Val?Val?Glu?Gln?Ala
420 425 430
Gly?Trp?Asp?Asn?Thr?Trp?Arg
435
<210>169
<211>526
<212>PRT
<213〉aspergillus niger
<400>169
Met?Arg?Ser?Phe?Ser?Val?Val?Ala?Ala?Ala?Ser?Leu?Ala?Leu?Ser?Trp
1 5 10 15
Ala?Ser?Leu?Ala?Gln?Ala?Ala?Arg?Pro?Arg?Leu?Val?Pro?Lys?Pro?Ile
20 25 30
Ser?Arg?Pro?Ala?Ser?Ser?Lys?Ser?Ala?Ala?Thr?Thr?Gly?Glu?Ala?Tyr
35 40 45
Phe?Glu?Gln?Leu?Leu?Asp?His?His?Asn?Pro?Glu?Lys?Gly?Thr?Phe?Ser
50 55 60
Gln?Arg?Tyr?Trp?Trp?Ser?Thr?Glu?Tyr?Trp?Gly?Gly?Pro?Gly?Ser?Pro
65 70 75 80
Val?Val?Leu?Phe?Asn?Pro?Gly?Glu?Val?Ser?Ala?Asp?Gly?Tyr?Glu?Gly
85 90 95
Tyr?Leu?Thr?Asn?Asp?Thr?Leu?Thr?Gly?Val?Tyr?Ala?Gln?Glu?Ile?Gln
100 105 110
Gly?Ala?Val?Ile?Leu?Ile?Glu?His?Arg?Tyr?Trp?Gly?Asp?Ser?Ser?Pro
115 120 125
Tyr?Glu?Val?Leu?Asn?Ala?Glu?Thr?Leu?Gln?Tyr?Leu?Thr?Leu?Asp?Gln
130 135 140
Ser?Ile?Leu?Asp?Met?Thr?Tyr?Phe?Ala?Glu?Thr?Val?Lys?Leu?Gln?Phe
145 150 155 160
Asp?Asn?Ser?Ser?Arg?Ser?Asn?Ala?Gln?Asn?Ala?Pro?Trp?Val?Met?Val
165 170 175
Gly?Gly?Ser?Tyr?Ser?Gly?Ala?Leu?Thr?Ala?Trp?Thr?Glu?Ser?Ile?Ala
180 185 190
Pro?Gly?Thr?Phe?Trp?Ala?Tyr?His?Ala?Thr?Ser?Ala?Pro?Val?Glu?Ala
195 200 205
Ile?Tyr?Asp?Phe?Trp?Gln?Tyr?Phe?Tyr?Pro?Ile?Gln?Gln?Gly?Met?Ala
210 215 220
Gln?Asn?Cys?Ser?Lys?Asp?Val?Ser?Leu?Val?Ala?Glu?Tyr?Val?Asp?Lys
225 230 235 240
Ile?Gly?Lys?Asn?Gly?Thr?Ala?Lys?Glu?Gln?Gln?Glu?Leu?Lys?Glu?Leu
245 250 255
Phe?Gly?Leu?Gly?Ala?Val?Glu?His?Tyr?Asp?Asp?Phe?Ala?Ala?Val?Leu
260 265 270
Pro?Asn?Gly?Pro?Tyr?Leu?Trp?Gln?Asp?Asn?Asp?Phe?Val?Thr?Gly?Tyr
275 280 285
Ser?Ser?Phe?Phe?Gln?Phe?Cys?Asp?Ala?Val?Glu?Gly?Val?Glu?Ala?Gly
290 295 300
Ala?Ala?Val?Thr?Pro?Gly?Pro?Glu?Gly?Val?Gly?Leu?Glu?Lys?Ala?Leu
305 310 315 320
Ala?Asn?Tyr?Ala?Asn?Trp?Phe?Asn?Ser?Thr?Ile?Leu?Pro?Asn?Tyr?Cys
325 330 335
Ala?Ser?Tyr?Gly?Tyr?Trp?Thr?Asp?Glu?Trp?Ser?Val?Ala?Cys?Phe?Asp
340 345 350
Ser?Tyr?Asn?Ala?Ser?Ser?Pro?Ile?Phe?Thr?Asp?Thr?Ser?Val?Gly?Asn
355 360 365
Pro?Val?Asp?Arg?Gln?Trp?Glu?Trp?Phe?Leu?Cys?Asn?Glu?Pro?Phe?Phe
370 375 380
Trp?Trp?Gln?Asp?Gly?Ala?Pro?Glu?Gly?Thr?Ser?Thr?Ile?Val?Pro?Arg
385 390 395 400
Leu?Val?Ser?Ala?Ser?Tyr?Trp?Gln?Arg?Gln?Cys?Pro?Leu?Tyr?Phe?Pro
405 410 415
Glu?Val?Asn?Gly?Tyr?Thr?Tyr?Gly?Ser?Ala?Lys?Gly?Lys?Asn?Ser?Ala
420 425 430
Thr?Val?Asn?Ser?Trp?Thr?Gly?Gly?Trp?Asp?Met?Thr?Arg?Asn?Thr?Thr
435 440 445
Arg?Leu?Ile?Trp?Thr?Asn?Gly?Gln?Tyr?Asp?Pro?Trp?Arg?Asp?Ser?Gly
450 455 460
Val?Ser?Ser?Thr?Phe?Arg?Pro?Gly?Gly?Pro?Leu?Val?Ser?Thr?Ala?Asn
465 470 475 480
Glu?Pro?Val?Gln?Ile?Ile?Pro?Gly?Gly?Phe?His?Cys?Ser?Asp?Leu?Tyr
485 490 495
Met?Glu?Asp?Tyr?Tyr?Ala?Asn?Glu?Gly?Val?Arg?Lys?Val?Val?Asp?Asn
500 505 510
Glu?Val?Lys?Gln?Ile?Lys?Glu?Trp?Val?Glu?Glu?Tyr?Tyr?Ala
515 520 525
<210>170
<211>424
<212>PRT
<213〉aspergillus niger
<400>170
Met?Gln?Leu?Leu?Gln?Ser?Leu?Ile?Val?Ala?Val?Cys?Phe?Ser?Tyr?Gly
1 5 10 15
Val?Leu?Ser?Leu?Pro?His?Gly?Pro?Ser?Asn?Gln?His?Lys?Ala?Arg?Ser
20 25 30
Phe?Lys?Val?Glu?Arg?Val?Arg?Arg?Gly?Thr?Gly?Ala?Leu?His?Gly?Pro
35 40 45
Ala?Ala?Leu?Arg?Lys?Ala?Tyr?Arg?Lys?Tyr?Gly?Ile?Ala?Pro?Ser?Ser
50 55 60
Phe?Asn?Ile?Asp?Leu?Ala?Asp?Phe?Lys?Pro?Ile?Thr?Thr?Thr?His?Ala
65 70 75 80
Ala?Ala?Gly?Ser?Glu?Ile?Ala?Glu?Pro?Asp?Gln?Thr?Gly?Ala?Val?Ser
85 90 95
Ala?Thr?Ser?Val?Glu?Asn?Asp?Ala?Glu?Phe?Val?Ser?Pro?Val?Leu?Ile
100 105 110
Gly?Gly?Gln?Lys?Ile?Val?Met?Thr?Phe?Asp?Thr?Gly?Ser?Ser?Asp?Phe
115 120 125
Trp?Val?Phe?Asp?Thr?Asn?Leu?Asn?Glu?Thr?Leu?Thr?Gly?His?Thr?Glu
130 135 140
Tyr?Asn?Pro?Ser?Asn?Ser?Ser?Thr?Phe?Lys?Lys?Met?Asp?Gly?Tyr?Thr
145 150 155 160
Phe?Asp?Val?Ser?Tyr?Gly?Asp?Asp?Ser?Tyr?Ala?Ser?Gly?Pro?Val?Gly
165 170 175
Thr?Asp?Thr?Val?Asn?Ile?Gly?Gly?Ala?Ile?Val?Lys?Glu?Gln?Ala?Phe
180 185 190
Gly?Val?Pro?Asp?Gln?Val?Ser?Gln?Ser?Phe?Ile?Glu?Asp?Thr?Asn?Ser
195 200 205
Asn?Gly?Leu?Val?Gly?Leu?Gly?Phe?Ser?Ser?Ile?Asn?Thr?Ile?Lys?Pro
210 215 220
Glu?Ala?Gln?Asp?Thr?Phe?Phe?Ala?Asn?Val?Ala?Pro?Ser?Leu?Asp?Glu
225 230 235 240
Pro?Val?Met?Thr?Ala?Ser?Leu?Lys?Ala?Asp?Gly?Val?Gly?Glu?Tyr?Glu
245 250 255
Phe?Gly?Thr?Ile?Asp?Lys?Asp?Lys?Tyr?Gln?Gly?Asn?Ile?Ala?Asn?Ile
260 265 270
Ser?Val?Asp?Ser?Ser?Asn?Gly?Tyr?Trp?Gln?Phe?Ser?Thr?Pro?Lys?Tyr
275 280 285
Ser?Val?Ala?Asp?Gly?Glu?Leu?Lys?Asp?Ile?Gly?Ser?Leu?Asn?Thr?Ser
290 295 300
Ile?Ala?Asp?Thr?Gly?Thr?Ser?Leu?Met?Leu?Leu?Asp?Glu?Asp?Val?Val
305 310 315 320
Thr?Ala?Tyr?Tyr?Ala?Gln?Val?Pro?Asn?Ser?Val?Tyr?Val?Ser?Ser?Ala
325 330 335
Gly?Gly?Tyr?Ile?Tyr?Pro?Cys?Asn?Thr?Thr?Leu?Pro?Ser?Phe?Ser?Leu
340 345 350
Val?Leu?Gly?Glu?Ser?Ser?Leu?Ala?Thr?Ile?Pro?Gly?Asn?Leu?Ile?Asn
355 360 365
Phe?Ser?Lys?Val?Gly?Thr?Asn?Thr?Thr?Thr?Gly?Gln?Ala?Leu?Cys?Phe
370 375 380
Gly?Gly?Ile?Gln?Ser?Asn?Gly?Asn?Thr?Ser?Leu?Gln?Ile?Leu?Gly?Asp
385 390 395 400
Ile?Phe?Leu?Lys?Ala?Phe?Phe?Val?Val?Phe?Asp?Met?Arg?Gly?Pro?Ser
405 410 415
Leu?Gly?Val?Ala?Ser?Pro?Lys?Asn
420
<210>171
<211>548
<212>PRT
<213〉aspergillus niger
<400>171
Met?Arg?Ile?Asp?Ser?Ala?Ala?Leu?His?Leu?Val?Pro?Val?Leu?Leu?Gly
1 5 10 15
Gln?Val?Gly?Ala?Leu?Gln?Leu?Pro?Leu?Val?Gln?Asp?Ser?Asn?Ser?Gln
20 25 30
Trp?Gln?Lys?Pro?Asn?Ala?Gly?Asp?Lys?Pro?Leu?Ile?Ser?Ser?Pro?Leu
35 40 45
Leu?Gln?Glu?Gln?Val?Lys?Ala?Glu?Asn?Leu?Leu?Asp?Arg?Ala?Arg?Gln
50 55 60
Leu?Tyr?Lys?Ile?Ala?Glu?Leu?Gly?Glu?Asp?Glu?Tyr?Asn?His?Pro?Thr
65 70 75 80
Arg?Val?Ile?Gly?Ser?Lys?Gly?His?Leu?Gly?Thr?Leu?Asp?Tyr?Ile?Tyr
85 90 95
Ser?Thr?Leu?Thr?Asp?Leu?Gly?Asp?Tyr?Tyr?Thr?Val?Val?Asn?Gln?Ser
100 105 110
Phe?Pro?Ala?Val?Ser?Gly?Asn?Val?Phe?Glu?Ser?Arg?Leu?Val?Leu?Gly
115 120 125
His?Asp?Val?Pro?Lys?Ser?Ala?Thr?Pro?Met?Gly?Leu?Thr?Pro?Pro?Thr
130 135 140
Arg?Asn?Lys?Glu?Pro?Val?Tyr?Gly?Ser?Leu?Val?Ala?Val?Ser?Asn?Leu
145 150 155 160
Gly?Cys?Glu?Ala?Ser?Asp?Tyr?Ser?Ser?Asn?Leu?Lys?Gly?Ala?Val?Ala
165 170 175
Phe?Ile?Ser?Arg?Gly?Ser?Cys?Pro?Phe?Gly?Thr?Lys?Ser?Gln?Leu?Ala
180 185 190
Gly?Lys?Ala?Gly?Ala?Val?Ala?Ala?Val?Ile?Tyr?Asn?Asn?Glu?Arg?Gly
195 200 205
Asp?Leu?Ser?Gly?Thr?Leu?Gly?Asn?Pro?Thr?Pro?Asp?His?Val?Ala?Thr
210 215 220
Phe?Gly?Ile?Ser?Asp?Glu?Asp?Ala?Ala?Pro?Val?Leu?Glu?Lys?Leu?Asn
225 230 235 240
Lys?Gly?Glu?Lys?Val?Asp?Ala?Ile?Ala?Tyr?Val?Asp?Ala?Ile?Val?Glu
245 250 255
Thr?Ile?His?Thr?Thr?Asn?Ile?Ile?Ala?Gln?Thr?Thr?Asp?Gly?Asp?Pro
260 265 270
Asn?Asn?Cys?Val?Met?Leu?Gly?Gly?His?Ser?Asp?Ser?Val?Ala?Glu?Gly
275 280 285
Pro?Gly?Ile?Asn?Asp?Asp?Gly?Ser?Gly?Thr?Leu?Thr?Leu?Leu?Glu?Leu
290 295 300
Ala?Thr?Leu?Leu?Thr?Gln?Phe?Arg?Val?Asn?Asn?Cys?Val?Arg?Phe?Ala
305 310 315 320
Trp?Trp?Ala?Ala?Glu?Glu?Glu?Gly?Leu?Leu?Gly?Ser?Asp?Tyr?Tyr?Val
325 330 335
Ser?Val?Leu?Thr?Pro?Glu?Glu?Asn?Arg?Lys?Ile?Arg?Leu?Phe?Met?Asp
340 345 350
Tyr?Asp?Met?Leu?Gly?Ser?Pro?Asn?Phe?Ala?Tyr?Gln?Val?Tyr?Asn?Ala
355 360 365
Thr?Asn?Ala?Val?Asn?Pro?Glu?Gly?Ser?Glu?Glu?Leu?Arg?Asp?Leu?Tyr
370 375 380
Thr?Asp?Phe?Tyr?Glu?Asp?His?Gly?Phe?Asn?Tyr?Thr?Tyr?Ile?Pro?Phe
385 390 395 400
Asp?Gly?Arg?Ser?Asp?Tyr?Asp?Ala?Phe?Ile?Arg?His?Gly?Ile?Pro?Gly
405 410 415
Gly?Gly?Ile?Ala?Thr?Gly?Ala?Glu?Gly?Ile?Lys?Thr?Val?Glu?Glu?Ala
420 425 430
Asp?Met?Phe?Gly?Gly?Val?Ala?Gly?Gln?Trp?Tyr?Asp?Pro?Cys?Tyr?His
435 440 445
Gln?Ile?Cys?Asp?Thr?Val?Ala?Asn?Val?Asn?Leu?Thr?Ala?Trp?Glu?Trp
450 455 460
Asn?Thr?Lys?Leu?Val?Ala?His?Ser?Ile?Ala?Thr?Tyr?Ala?Lys?Ser?Phe
465 470 475 480
Asp?Gly?Phe?Pro?Glu?Arg?Ser?Asp?Glu?Pro?Ile?Ser?Pro?Ala?Ala?Phe
485 490 495
Glu?Glu?Pro?Lys?Tyr?His?Gly?His?Ala?Leu?Gln?Leu?Leu?Arg?Gly?Asn
500 505 510
Thr?Thr?Gly?Thr?Gln?Ser?Val?Leu?Trp?Gly?Ala?Gln?Ile?Gln?Asn?Gly
515 520 525
Thr?Ala?Ala?Ser?Val?Leu?Asn?Leu?Leu?Ser?Ile?Arg?Arg?Arg?Gly?Thr
530 535 540
Phe?Ser?Leu?Ser
545
Claims (28)
1. isolating polynucleotide, these polynucleotide can with hybridize according to the polynucleotide sequence that be selected from the sequence of SEQ ID NO:1~SEQ ID NO:57 or be selected from the sequence of SEQ ID NO:58~SEQ ID NO:114.
2. according to the isolating polynucleotide of claim 1, these polynucleotide under height stringency condition can with hybridize according to the polynucleotide that be selected from the sequence of SEQ ID NO:1~SEQ ID NO:57 or be selected from the sequence of SEQ ID NO:58~SEQ ID NO:114.
3. according to the isolating polynucleotide of claim 1 or 2, it can obtain from filamentous fungus.
4. according to the isolating polynucleotide of claim 3, it can obtain from aspergillus niger.
5. isolating polynucleotide, this polynucleotide encoding comprise according to the aminoacid sequence of the sequence that is selected from SEQ IDNO:115~SEQ ID NO:171 or the polypeptide of its function equivalent.
6. isolating polynucleotide, this polynucleotide encoding is according to being selected from SEQ IDNO:115~polypeptide of sequence of SEQ ID NO:171 or at least one functional domain of its function equivalent.
7. isolating polynucleotide, these polynucleotide comprise nucleotide sequence or its function equivalent that basis is selected from the sequence of SEQ ID NO:1~SEQ ID NO:57 or is selected from the sequence of SEQ ID NO:58~SEQ ID NO:114.
8. according to the sequence that is selected from SEQ ID NO:1~SEQ ID NO:57 or be selected from the isolating polynucleotide of the sequence of SEQID NO:58~SEQ ID NO:114.
9. comprise carrier according to the polynucleotide sequence of claim 1~8.
10. according to the carrier of claim 9, wherein should operationally be connected with the adjusting sequence according to the polynucleotide sequence of claim 1~8, this adjusting sequence is suitable for this polynucleotide sequence and expresses in appropriate host cell.
11. according to the carrier of claim 10, wherein said appropriate host cell is a filamentous fungus.
12. preparation is according to the polynucleotide of claim 1~8 or according to the method for the carrier of claim 9~11, this method comprises cultivates with these polynucleotide or this carrier transformed host cells and the step of separating these polynucleotide or this carrier in this host cell.
13. according to the polypeptide of sequence or its function equivalent that are selected from SEQ ID NO:115~SEQ ID NO:171.
14. according to the polypeptide of claim 13, it can obtain from aspergillus niger.
15. isolated polypeptide, this polypeptide can obtain by expressing in appropriate host cell such as aspergillus niger according to the polynucleotide of claim 1~8 or according to the carrier of claim 9~11.
16. comprise the recombinant protein enzyme of the functional domain of protease polypeptide.
17. preparation is according to the method for the polypeptide of claim 13~16, the method includes the steps of, promptly transform appropriate host cell with the isolating polynucleotide of claim 1~8 or according to the carrier of claim 9~11, make cultivate under the condition that these polynucleotide can be expressed this cell and optional from this cell or culture medium the purifying encoded polypeptide.
18. comprise according to the polynucleotide of claim 1~8 or according to the recombinant host cell of the carrier of claim 9~11.
19. express recombinant host cell according to the polypeptide of claim 13~16.
20. comprise the recombinant host cell of polynucleotide of the protease polypeptide of encoding function inactivation.
21. recombinant host cell, the wherein polynucleotide of proteins encoded enzyme polypeptide excalation at least.
22. according to the recombinant host cell of claim 18~21, wherein this host cell is from the Aspergillus species, as aspergillus niger.
23. have the recombinant host cell of protease function defective, this cell can obtain by the method that comprises this step:
A. external sudden change is according to the polynucleotide of claim 1~11,
B. the host cell that comprises native gene is transformed, this native gene comprises the polynucleotide sequence that can hybridize with the polynucleotide of the sudden change that obtains in step a),
C. select and separate recombinant host cell, wherein the polynucleotide of the sudden change that obtained in step a) of this native gene are replaced.
24. the antibody purified that can react with polypeptide according to claim 13~16.
25. comprise fused protein according to the peptide sequence of claim 13~16.
26. whether the diagnosis organism has infected the method for aspergillosis, this method comprises this step:
A. separating bio product that imitate from this doubtful biology that infects aspergillosis,
B. isolating nucleic acid from this sample,
C. determine this isolating nucleic acid whether comprise can with the polynucleotide according to the multi-nucleotide hybrid of claim 1~8.
27. according to the method for claim 26, wherein step c) comprises this isolating nucleic acid of amplification in addition, preferably passes through polymerase chain reaction.
28. diagnose certain organism whether to infect the method for aspergillosis, the method includes the steps of:
A. separating bio product that imitate from this doubtful biology that infects aspergillosis,
B. make this biological sample and react according to the antibody of claim 24,
C. determine whether to have formed immunocomplex.
Applications Claiming Priority (66)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP01200660 | 2001-02-23 | ||
EP01200657.3 | 2001-02-23 | ||
EP01200658.1 | 2001-02-23 | ||
EP01200660.7 | 2001-02-23 | ||
EP01200657 | 2001-02-23 | ||
EP01200658 | 2001-02-23 | ||
EP01200719 | 2001-02-26 | ||
EP01200706.8 | 2001-02-26 | ||
EP01200707 | 2001-02-26 | ||
EP01200708 | 2001-02-26 | ||
EP01200719.1 | 2001-02-26 | ||
EP01200708.4 | 2001-02-26 | ||
EP01200706 | 2001-02-26 | ||
EP01200707.6 | 2001-02-26 | ||
EP01000085 | 2001-03-28 | ||
EP01000087 | 2001-03-28 | ||
EP01000088 | 2001-03-28 | ||
EP01000087.5 | 2001-03-28 | ||
EP01000084.2 | 2001-03-28 | ||
EP01000080.0 | 2001-03-28 | ||
EP01000085.9 | 2001-03-28 | ||
EP01000075.0 | 2001-03-28 | ||
EP01000088.3 | 2001-03-28 | ||
EP01000078.4 | 2001-03-28 | ||
EP01000156.8 | 2001-05-21 | ||
EP01000166.7 | 2001-05-21 | ||
EP01000162.6 | 2001-05-21 | ||
EP01000168.3 | 2001-05-21 | ||
EP01000165.9 | 2001-05-21 | ||
EP01000160.0 | 2001-05-21 | ||
EP01000159.2 | 2001-05-21 | ||
EP01000225.1 | 2001-06-20 | ||
EP01000229.3 | 2001-06-20 | ||
EP01000240.0 | 2001-06-21 | ||
EP01000242.6 | 2001-06-21 | ||
EP01000238.4 | 2001-06-21 | ||
EP01000237.6 | 2001-06-21 | ||
EP01000244.2 | 2001-06-21 | ||
EP01000246.7 | 2001-06-21 | ||
EP01000234.3 | 2001-06-21 | ||
EP01000286.3 | 2001-07-12 | ||
EP01000280.6 | 2001-07-12 | ||
EP01000285.5 | 2001-07-12 | ||
EP01000287.1 | 2001-07-12 | ||
EP01000322.6 | 2001-07-30 | ||
EP01000323.4 | 2001-07-30 | ||
EP01000320.0 | 2001-07-30 | ||
EP01000327.5 | 2001-07-30 | ||
EP01000321.8 | 2001-07-30 | ||
EP01000344.0 | 2001-08-02 | ||
EP01000343.2 | 2001-08-02 | ||
EP01000342.4 | 2001-08-02 | ||
EP01000341.6 | 2001-08-02 | ||
EP01000357.2 | 2001-08-09 | ||
EP01000374.7 | 2001-08-16 | ||
EP01000377.0 | 2001-08-16 | ||
EP01000478.6 | 2001-09-20 | ||
EP01000483.6 | 2001-09-20 | ||
EP01000556.9 | 2001-10-22 | ||
EP01000552.8 | 2001-10-22 | ||
EP01000558.5 | 2001-10-22 | ||
EP01000557.7 | 2001-10-22 | ||
EP01000554.4 | 2001-10-22 | ||
EP01000553.6 | 2001-10-22 | ||
EP01204464.0 | 2001-11-15 | ||
EP01205117.3 | 2001-12-21 |
Related Parent Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN02805464A Division CN100582226C (en) | 2001-02-23 | 2002-02-22 | Genes encoding proteolytic enzymes from aspargilli |
Publications (1)
Publication Number | Publication Date |
---|---|
CN101914555A true CN101914555A (en) | 2010-12-15 |
Family
ID=43322195
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN2009102513862A Pending CN101914555A (en) | 2001-02-23 | 2002-02-22 | Novel genes encoding novel proteolytic enzymes |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN101914555A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN109153997A (en) * | 2016-05-24 | 2019-01-04 | 玫帝托克斯股份有限公司 | The recombination of polynucleotide for encoding the polypeptide of the molecule containing report, substrate and stabilization removal part, containing its host cell and application thereof |
CN110234751A (en) * | 2017-02-02 | 2019-09-13 | 拉勒曼德匈牙利流动性管理有限责任公司 | For improving the heterologous protein expression of enzymes of alcoholic fermentation |
CN115074361A (en) * | 2021-03-12 | 2022-09-20 | 中国科学院天津工业生物技术研究所 | Strong promoter from fungus and application thereof |
CN116144687A (en) * | 2023-01-13 | 2023-05-23 | 中山大学 | Acidic protease AGP and preparation method and application thereof |
-
2002
- 2002-02-22 CN CN2009102513862A patent/CN101914555A/en active Pending
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN109153997A (en) * | 2016-05-24 | 2019-01-04 | 玫帝托克斯股份有限公司 | The recombination of polynucleotide for encoding the polypeptide of the molecule containing report, substrate and stabilization removal part, containing its host cell and application thereof |
CN110234751A (en) * | 2017-02-02 | 2019-09-13 | 拉勒曼德匈牙利流动性管理有限责任公司 | For improving the heterologous protein expression of enzymes of alcoholic fermentation |
CN115074361A (en) * | 2021-03-12 | 2022-09-20 | 中国科学院天津工业生物技术研究所 | Strong promoter from fungus and application thereof |
CN115074361B (en) * | 2021-03-12 | 2025-01-28 | 中国科学院天津工业生物技术研究所 | Strong promoter derived from fungi and its application |
CN116144687A (en) * | 2023-01-13 | 2023-05-23 | 中山大学 | Acidic protease AGP and preparation method and application thereof |
CN116144687B (en) * | 2023-01-13 | 2023-09-01 | 中山大学 | Acid protease AGP and its preparation method and application |
WO2024149219A1 (en) * | 2023-01-13 | 2024-07-18 | 中山大学 | Acid protease agp, preparation method therefor, and use thereof |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN100582226C (en) | Genes encoding proteolytic enzymes from aspargilli | |
KR100905849B1 (en) | Protein hydrolysates enriched in peptides having a carboxy terminal proline residue | |
Boulland et al. | Human IL4I1 is a secreted L-phenylalanine oxidase expressed by mature dendritic cells that inhibits T-lymphocyte proliferation | |
Ito et al. | Anthranilate synthetase, an enzyme specified by the tryptophan operon of Escherichia coli: purification and characterization of component I | |
EP2283129B1 (en) | Proline-specific protease from penicillium chrysogenum | |
BR0115998B1 (en) | Method for the prevention or reduction of turbidity in a beverage, as well as beverages obtainable from said method. | |
KR20140007501A (en) | Modified proteases that inhibit complement activation | |
US20090275079A1 (en) | Novel genes encoding novel proteolytic enzymes | |
Engelhardt et al. | Adequacy of enzymic deconjugation in quantification of folate in foods | |
CN101914555A (en) | Novel genes encoding novel proteolytic enzymes | |
EP2126060B1 (en) | Novel lysyl oxidases | |
KR100880087B1 (en) | New genes encoding new proteases | |
AU2006202723B2 (en) | Novel genes encoding novel proteolytic enzymes | |
AU2008202554A1 (en) | Novel genes encoding novel proteolytic enzymes | |
KR100709300B1 (en) | Blood-Viscosity Reducing Agent | |
CN114369635B (en) | Enzymatic method for preparing muscovy duck plasma source ACE inhibitory peptide | |
RU2423525C2 (en) | New genes coding new proteolytic enzymes | |
JP5577006B2 (en) | Rapid screening method and microorganism obtained by the method | |
ZA200305182B (en) | Protein hydrolysates enriched in peptides having a carboxy terminal proline residue. | |
TW202128980A (en) | Composition for inhibiting ace or suppressing blood pressure elevation, method for producing same, enzyme preparation, polynucleotide and transformant | |
CN114015664A (en) | Luciferase mutant and application thereof | |
AU2002216089B2 (en) | Prolyl endoprotease from aspergillus niger | |
Crowe et al. | Protein translocation in yeast | |
FR2504552A1 (en) | Improving sensitivity cf bio-luminescent assay of microbial cells - by first incubating to increase population or adenosine tri:phosphate content | |
NZ560367A (en) | Novel genes encoding novel proteolytic enzymes |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
C02 | Deemed withdrawal of patent application after publication (patent law 2001) | ||
WD01 | Invention patent application deemed withdrawn after publication |
Application publication date: 20101215 |