CN1062374A - The liquid detergent composition that contains lipase and proteolytic enzyme - Google Patents
The liquid detergent composition that contains lipase and proteolytic enzyme Download PDFInfo
- Publication number
- CN1062374A CN1062374A CN 91111550 CN91111550A CN1062374A CN 1062374 A CN1062374 A CN 1062374A CN 91111550 CN91111550 CN 91111550 CN 91111550 A CN91111550 A CN 91111550A CN 1062374 A CN1062374 A CN 1062374A
- Authority
- CN
- China
- Prior art keywords
- detergent composition
- composition according
- lipase
- acid
- protease
- 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
- 239000000203 mixture Substances 0.000 title claims abstract description 95
- 108091005804 Peptidases Proteins 0.000 title claims abstract description 46
- 239000003599 detergent Substances 0.000 title claims abstract description 44
- 102000004882 Lipase Human genes 0.000 title claims abstract description 38
- 108090001060 Lipase Proteins 0.000 title claims abstract description 38
- 239000004367 Lipase Substances 0.000 title claims abstract description 38
- 102000035195 Peptidases Human genes 0.000 title claims abstract description 38
- 235000019421 lipase Nutrition 0.000 title claims abstract description 38
- 239000007788 liquid Substances 0.000 title claims abstract description 17
- 102000004190 Enzymes Human genes 0.000 claims abstract description 29
- 108090000790 Enzymes Proteins 0.000 claims abstract description 29
- 230000001580 bacterial effect Effects 0.000 claims abstract description 17
- 239000004365 Protease Substances 0.000 claims abstract description 11
- 108010022999 Serine Proteases Proteins 0.000 claims abstract description 4
- 102000012479 Serine Proteases Human genes 0.000 claims abstract description 4
- 239000004615 ingredient Substances 0.000 claims abstract description 4
- MTCFGRXMJLQNBG-UHFFFAOYSA-N Serine Natural products OCC(N)C(O)=O MTCFGRXMJLQNBG-UHFFFAOYSA-N 0.000 claims description 25
- 229930182817 methionine Natural products 0.000 claims description 13
- FFEARJCKVFRZRR-BYPYZUCNSA-N L-methionine Chemical compound CSCC[C@H](N)C(O)=O FFEARJCKVFRZRR-BYPYZUCNSA-N 0.000 claims description 12
- 150000001413 amino acids Chemical class 0.000 claims description 10
- 238000005406 washing Methods 0.000 claims description 10
- DNIAPMSPPWPWGF-UHFFFAOYSA-N monopropylene glycol Natural products CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 9
- 239000004382 Amylase Substances 0.000 claims description 8
- 108010065511 Amylases Proteins 0.000 claims description 8
- 102000013142 Amylases Human genes 0.000 claims description 8
- 102100037486 Reverse transcriptase/ribonuclease H Human genes 0.000 claims description 8
- 235000019418 amylase Nutrition 0.000 claims description 8
- 239000004327 boric acid Substances 0.000 claims description 2
- 230000006641 stabilisation Effects 0.000 claims 2
- 238000011105 stabilization Methods 0.000 claims 2
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 claims 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 claims 1
- 150000001735 carboxylic acids Chemical class 0.000 claims 1
- 230000002366 lipolytic effect Effects 0.000 claims 1
- 235000013772 propylene glycol Nutrition 0.000 claims 1
- 230000000087 stabilizing effect Effects 0.000 claims 1
- 150000002632 lipids Chemical class 0.000 abstract description 5
- MTCFGRXMJLQNBG-REOHCLBHSA-N (2S)-2-Amino-3-hydroxypropansäure Chemical compound OC[C@H](N)C(O)=O MTCFGRXMJLQNBG-REOHCLBHSA-N 0.000 description 24
- 229940088598 enzyme Drugs 0.000 description 24
- 239000002253 acid Substances 0.000 description 23
- -1 Alkylbenzene sulfonate Chemical class 0.000 description 21
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 21
- 238000012986 modification Methods 0.000 description 17
- 230000004048 modification Effects 0.000 description 17
- 125000000217 alkyl group Chemical group 0.000 description 12
- 125000001360 methionine group Chemical group N[C@@H](CCSC)C(=O)* 0.000 description 12
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 11
- 238000007046 ethoxylation reaction Methods 0.000 description 11
- 238000000034 method Methods 0.000 description 11
- 125000004432 carbon atom Chemical group C* 0.000 description 10
- 229910052708 sodium Inorganic materials 0.000 description 10
- 239000011734 sodium Substances 0.000 description 10
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- 235000001014 amino acid Nutrition 0.000 description 8
- 239000000047 product Substances 0.000 description 8
- 150000003839 salts Chemical class 0.000 description 8
- 229960004106 citric acid Drugs 0.000 description 7
- 150000002191 fatty alcohols Chemical class 0.000 description 7
- 239000000654 additive Substances 0.000 description 6
- 125000001931 aliphatic group Chemical group 0.000 description 6
- 239000004094 surface-active agent Substances 0.000 description 6
- 241000894006 Bacteria Species 0.000 description 5
- 125000003342 alkenyl group Chemical group 0.000 description 5
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 5
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 4
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 4
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 4
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 4
- 244000063299 Bacillus subtilis Species 0.000 description 4
- 108010083608 Durazym Proteins 0.000 description 4
- 239000005642 Oleic acid Substances 0.000 description 4
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 4
- 230000000996 additive effect Effects 0.000 description 4
- 239000003945 anionic surfactant Substances 0.000 description 4
- 239000007859 condensation product Substances 0.000 description 4
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 4
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 4
- 230000003019 stabilising effect Effects 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 3
- RKWGIWYCVPQPMF-UHFFFAOYSA-N Chloropropamide Chemical compound CCCNC(=O)NS(=O)(=O)C1=CC=C(Cl)C=C1 RKWGIWYCVPQPMF-UHFFFAOYSA-N 0.000 description 3
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 3
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 3
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 3
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 3
- 108090000787 Subtilisin Proteins 0.000 description 3
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 3
- 239000013543 active substance Substances 0.000 description 3
- 239000001110 calcium chloride Substances 0.000 description 3
- 235000011148 calcium chloride Nutrition 0.000 description 3
- 229910001628 calcium chloride Inorganic materials 0.000 description 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 3
- 238000009833 condensation Methods 0.000 description 3
- 230000005494 condensation Effects 0.000 description 3
- 201000011243 gastrointestinal stromal tumor Diseases 0.000 description 3
- 150000002500 ions Chemical class 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- 229910052700 potassium Inorganic materials 0.000 description 3
- 239000011591 potassium Substances 0.000 description 3
- 239000002994 raw material Substances 0.000 description 3
- HLBBKKJFGFRGMU-UHFFFAOYSA-M sodium formate Chemical compound [Na+].[O-]C=O HLBBKKJFGFRGMU-UHFFFAOYSA-M 0.000 description 3
- NVIFVTYDZMXWGX-UHFFFAOYSA-N sodium metaborate Chemical compound [Na+].[O-]B=O NVIFVTYDZMXWGX-UHFFFAOYSA-N 0.000 description 3
- 229960004418 trolamine Drugs 0.000 description 3
- 108010059892 Cellulase Proteins 0.000 description 2
- 244000060011 Cocos nucifera Species 0.000 description 2
- 235000013162 Cocos nucifera Nutrition 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 239000004435 Oxo alcohol Substances 0.000 description 2
- 150000001336 alkenes Chemical class 0.000 description 2
- 150000004996 alkyl benzenes Chemical class 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 150000003863 ammonium salts Chemical class 0.000 description 2
- 125000000129 anionic group Chemical group 0.000 description 2
- 230000015556 catabolic process Effects 0.000 description 2
- 229940106157 cellulase Drugs 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000004140 cleaning Methods 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000006731 degradation reaction Methods 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 210000000540 fraction c Anatomy 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- 230000007062 hydrolysis Effects 0.000 description 2
- 238000006460 hydrolysis reaction Methods 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 2
- 239000002563 ionic surfactant Substances 0.000 description 2
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 2
- 108090000623 proteins and genes Proteins 0.000 description 2
- 235000019832 sodium triphosphate Nutrition 0.000 description 2
- 239000003760 tallow Substances 0.000 description 2
- JSPLKZUTYZBBKA-UHFFFAOYSA-N trioxidane Chemical compound OOO JSPLKZUTYZBBKA-UHFFFAOYSA-N 0.000 description 2
- OBDUMNZXAIUUTH-HWKANZROSA-N (e)-tetradec-2-ene Chemical compound CCCCCCCCCCC\C=C\C OBDUMNZXAIUUTH-HWKANZROSA-N 0.000 description 1
- LDVVTQMJQSCDMK-UHFFFAOYSA-N 1,3-dihydroxypropan-2-yl formate Chemical compound OCC(CO)OC=O LDVVTQMJQSCDMK-UHFFFAOYSA-N 0.000 description 1
- OWEGMIWEEQEYGQ-UHFFFAOYSA-N 100676-05-9 Natural products OC1C(O)C(O)C(CO)OC1OCC1C(O)C(O)C(O)C(OC2C(OC(O)C(O)C2O)CO)O1 OWEGMIWEEQEYGQ-UHFFFAOYSA-N 0.000 description 1
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 1
- SFHBJXIEBWOOFA-UHFFFAOYSA-N 5-methyl-3,6-dioxabicyclo[6.2.2]dodeca-1(10),8,11-triene-2,7-dione Chemical compound O=C1OC(C)COC(=O)C2=CC=C1C=C2 SFHBJXIEBWOOFA-UHFFFAOYSA-N 0.000 description 1
- 235000014469 Bacillus subtilis Nutrition 0.000 description 1
- PVHBJLXFQGWIFL-UHFFFAOYSA-N C(C(O)CO)OCC(O)CO.[Na] Chemical compound C(C(O)CO)OCC(O)CO.[Na] PVHBJLXFQGWIFL-UHFFFAOYSA-N 0.000 description 1
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 241000282326 Felis catus Species 0.000 description 1
- 229930091371 Fructose Natural products 0.000 description 1
- 239000005715 Fructose Substances 0.000 description 1
- RFSUNEUAIZKAJO-ARQDHWQXSA-N Fructose Chemical compound OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@@H]1O RFSUNEUAIZKAJO-ARQDHWQXSA-N 0.000 description 1
- 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 1
- CKLJMWTZIZZHCS-REOHCLBHSA-N L-aspartic acid Chemical compound OC(=O)[C@@H](N)CC(O)=O CKLJMWTZIZZHCS-REOHCLBHSA-N 0.000 description 1
- LEVWYRKDKASIDU-IMJSIDKUSA-N L-cystine Chemical compound [O-]C(=O)[C@@H]([NH3+])CSSC[C@H]([NH3+])C([O-])=O LEVWYRKDKASIDU-IMJSIDKUSA-N 0.000 description 1
- HNDVDQJCIGZPNO-YFKPBYRVSA-N L-histidine Chemical compound OC(=O)[C@@H](N)CC1=CN=CN1 HNDVDQJCIGZPNO-YFKPBYRVSA-N 0.000 description 1
- GUBGYTABKSRVRQ-PICCSMPSSA-N Maltose Natural products O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1O[C@@H]1[C@@H](CO)OC(O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-PICCSMPSSA-N 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- 101710194948 Protein phosphatase PhpP Proteins 0.000 description 1
- 239000004902 Softening Agent Substances 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 241000223258 Thermomyces lanuginosus Species 0.000 description 1
- 229910021536 Zeolite Inorganic materials 0.000 description 1
- YDONNITUKPKTIG-UHFFFAOYSA-N [Nitrilotris(methylene)]trisphosphonic acid Chemical compound OP(O)(=O)CN(CP(O)(O)=O)CP(O)(O)=O YDONNITUKPKTIG-UHFFFAOYSA-N 0.000 description 1
- 150000008065 acid anhydrides Chemical class 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 125000005466 alkylenyl group Chemical group 0.000 description 1
- 125000003368 amide group Chemical group 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
- 150000008064 anhydrides Chemical class 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 235000003704 aspartic acid Nutrition 0.000 description 1
- JXLHNMVSKXFWAO-UHFFFAOYSA-N azane;7-fluoro-2,1,3-benzoxadiazole-4-sulfonic acid Chemical compound N.OS(=O)(=O)C1=CC=C(F)C2=NON=C12 JXLHNMVSKXFWAO-UHFFFAOYSA-N 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 229940077388 benzenesulfonate Drugs 0.000 description 1
- 229940092714 benzenesulfonic acid Drugs 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
- 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 1
- GUBGYTABKSRVRQ-QUYVBRFLSA-N beta-maltose Chemical compound OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O)[C@H](O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O GUBGYTABKSRVRQ-QUYVBRFLSA-N 0.000 description 1
- 125000005619 boric acid group Chemical group 0.000 description 1
- HXDRSFFFXJISME-UHFFFAOYSA-N butanedioic acid;2,3-dihydroxybutanedioic acid Chemical compound OC(=O)CCC(O)=O.OC(=O)C(O)C(O)C(O)=O HXDRSFFFXJISME-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 150000007942 carboxylates Chemical class 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000006555 catalytic reaction Methods 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 229960002303 citric acid monohydrate Drugs 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 239000002320 enamel (paints) Substances 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- HNDVDQJCIGZPNO-UHFFFAOYSA-N histidine Natural products OC(=O)C(N)CC1=CN=CN1 HNDVDQJCIGZPNO-UHFFFAOYSA-N 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 125000001183 hydrocarbyl group Chemical group 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 150000002596 lactones Chemical class 0.000 description 1
- 150000002741 methionine derivatives Chemical class 0.000 description 1
- 108010020132 microbial serine proteinases Proteins 0.000 description 1
- 102000035118 modified proteins Human genes 0.000 description 1
- 108091005573 modified proteins Proteins 0.000 description 1
- 125000001421 myristyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 239000003346 palm kernel oil Substances 0.000 description 1
- 235000019865 palm kernel oil Nutrition 0.000 description 1
- SECPZKHBENQXJG-FPLPWBNLSA-N palmitoleic acid Chemical compound CCCCCC\C=C/CCCCCCCC(O)=O SECPZKHBENQXJG-FPLPWBNLSA-N 0.000 description 1
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- HWGNBUXHKFFFIH-UHFFFAOYSA-I pentasodium;[oxido(phosphonatooxy)phosphoryl] phosphate Chemical compound [Na+].[Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O HWGNBUXHKFFFIH-UHFFFAOYSA-I 0.000 description 1
- XYFCBTPGUUZFHI-UHFFFAOYSA-O phosphonium Chemical compound [PH4+] XYFCBTPGUUZFHI-UHFFFAOYSA-O 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 235000018102 proteins Nutrition 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 150000003856 quaternary ammonium compounds Chemical class 0.000 description 1
- 125000001453 quaternary ammonium group Chemical group 0.000 description 1
- 238000006268 reductive amination reaction Methods 0.000 description 1
- 230000002829 reductive effect Effects 0.000 description 1
- 238000002741 site-directed mutagenesis Methods 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 150000003384 small molecules Chemical class 0.000 description 1
- MWNQXXOSWHCCOZ-UHFFFAOYSA-L sodium;oxido carbonate Chemical compound [Na+].[O-]OC([O-])=O MWNQXXOSWHCCOZ-UHFFFAOYSA-L 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 235000013599 spices Nutrition 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- OBDUMNZXAIUUTH-UHFFFAOYSA-N trans-2-tetradecene Natural products CCCCCCCCCCCC=CC OBDUMNZXAIUUTH-UHFFFAOYSA-N 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-O triethanolammonium Chemical compound OCC[NH+](CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-O 0.000 description 1
- UNXRWKVEANCORM-UHFFFAOYSA-I triphosphate(5-) Chemical compound [O-]P([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O UNXRWKVEANCORM-UHFFFAOYSA-I 0.000 description 1
- 230000002087 whitening effect Effects 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/38—Products with no well-defined composition, e.g. natural products
- C11D3/386—Preparations containing enzymes, e.g. protease or amylase
- C11D3/38663—Stabilised liquid enzyme compositions
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/83—Mixtures of non-ionic with anionic compounds
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/38—Products with no well-defined composition, e.g. natural products
- C11D3/386—Preparations containing enzymes, e.g. protease or amylase
- C11D3/38618—Protease or amylase in liquid compositions only
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/38—Products with no well-defined composition, e.g. natural products
- C11D3/386—Preparations containing enzymes, e.g. protease or amylase
- C11D3/38627—Preparations containing enzymes, e.g. protease or amylase containing lipase
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/14—Sulfonic acids or sulfuric acid esters; Salts thereof derived from aliphatic hydrocarbons or mono-alcohols
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/38—Cationic compounds
- C11D1/52—Carboxylic amides, alkylolamides or imides or their condensation products with alkylene oxides
- C11D1/525—Carboxylic amides (R1-CO-NR2R3), where R1, R2 or R3 contain two or more hydroxy groups per alkyl group, e.g. R3 being a reducing sugar rest
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/72—Ethers of polyoxyalkylene glycols
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Detergent Compositions (AREA)
Abstract
本发明公开了液体洗涤剂组合物,该洗涤剂组合 物含有常用的洗涤成分和酶体系,其中酶体系含有脂 肪酶或其混合物,和改性的细菌丝氨酸蛋白酶或所说 的蛋白酶的混合物。The invention discloses a liquid detergent composition, the detergent combination The detergent contains commonly used detergent ingredients and an enzyme system, wherein the enzyme system contains lipid Lipase or mixtures thereof, and modified bacterial serine proteases or said mixture of proteases.
Description
The present invention relates to contain the liquid detergent composition of enzyme system.This enzyme system is the proteolytic enzyme of modification and the mixture of lipase.
As everyone knows, in the art, detergent composition can contain enzyme system expediently.This class enzyme system comprises cellulase, proteolytic enzyme, lipase and amylase.Purpose of the present invention particularly is to provide liquid detergent composition, and the enzyme system in this liquid detergent composition contains the mixture of proteolytic enzyme and lipase.
Prepare this class granular detergent composition and can not cause special problem, because these two kinds of enzymes can separate physically.Otherwise, prepare the special technique problem that this class I liquid I detergent mixture causes and be that proteolytic enzyme is counted as a kind of any proteinic Substrate that is present in this detergent composition probably.
Particularly, as can be seen, also may reside in the Degradation that lipase in the detergent composition is easier to take place this proteinoid hydrolysis.The result, the residual activity of the lipase in detergent composition will the very fast minimizing along with the storage time of this detergent composition, so that till now, the liquid detergent composition that preparation contains lipase and proteolytic enzyme simultaneously is impossible, and utilize for commodity, above-mentioned detergent composition but is enough stablizing.
Therefore, the purpose of this invention is to provide a kind of liquid detergent composition that contains the enzyme system that comprises lipase and proteolytic enzyme, wherein said enzyme system is stable.The stable meaning is meant the proteoclastic Degradation that has reduced this lipase basically.
Find now, it is by using the mixture of any lipase or its mixture and bacterial serine proteolytic enzyme or this proteinoid enzyme that this purpose can be implemented, in this proteolytic enzyme, the methionine(Met) adjacent with the Serine of reactive site replaced by other amino acid.In fact, have been found that this special composition will provide the enzyme system that contains proteolytic enzyme and lipase, and lipase will be stable in liquid detergent composition.
The advantage that this solution has is simple, because it only needs commercially available composition.Really, the various lipase that not only are suitable for using in detergent composition are commercially available, and the bacterial serine proteolytic enzyme that is suitable for the various modifications of purpose of the present invention also is commercially available.In addition, detergent composition of the present invention does not need to add special lipase stablizer, and therefore, with regard to the price of product with to the adaptability of environment, detergent composition of the present invention is attractive especially.
The bacterial serine proteolytic enzyme that comprises the modification of the proteolytic enzyme that not only is used for detergent composition but also is suitable for using in composition of the present invention for example is disclosed among the EP-A-0328229.The bacterial serine proteolytic enzyme of modification has especially been described in this patent application, and this kind proteolytic enzyme is commercially available (from GISTBROCADES), and its trade mark is called MAXAPEM15
R
At in March, 1988 the 6th page of disclosed Biotechnology Newswatch() and EP-A-0258 268 a kind of lipase has been described, this lipase is commercially available (from NOVO NORDISKA/S), its trade mark is called LIPOLASE
RThis european patent application has been mentioned LIPOLASE
RCan combine with proteolytic enzyme to form particle enzyme detergent additives.
EP-A-0 381262 has described and has contained proteolytic enzyme and lipase (is preferably LIPOLASE
R) have the detergent composition of stabilising system simultaneously.Disclosed proteolytic enzyme comprises bacteria protease in this reference.
Therefore, the present invention is the liquid detergent composition that contains enzyme system, it is characterized in that this enzyme system contains bacterial serine proteolytic enzyme or its mixture of modification, and lipase or its mixture.The modification of this bacterial serine proteolytic enzyme is to be replaced by other amino acid adjacent to the methionine(Met) of the Serine of avtive spot.
Enzyme system of the present invention contains lipase and proteolytic enzyme.As described in EP0381262 or EP271152, any lipase that is suitable for using in detergent composition can both use in composition of the present invention.As described in the EP-A-0258068 that authorizes NOVO INDUSTRIA/S, the preferred lipase that uses in the present composition is the lipase that is obtained by Humicolalanuginosa.This patent application describes how to obtain said special lipase, but said special lipase also is that commercially available (from NOVO NORDISKA/S, trade(brand)name is LIPOLASE
R).Be applicable to that other commercially available lipase of the present invention are Amono-P Lipase
R, Amono-B Lipase
R, Amono CES Lipase
R, Amono AKG Lipase
R, these lipase are all from Amono pharma-ceuticals(Japan); Toyo Jozo Co(Japan) and US biochemical Corp.(USA) and Diosynth Co.(NL) also become the lipase commodity that are fit to that are used for the present composition.
The general every gram finished product of composition of the present invention contains 0.1 to 10000 steatolysis unit, and preferably every gram finished product contains 10 to 2500 steatolysis units.Steatolysis unit is defined for example at EP0258268(page 5 38 row) in.
Proteolytic enzyme used in the present invention is the bacterial serine proteolytic enzyme of modification.All natural bacteria serine proteases are characterised in that its avtive spot always contains three seed amino acids, and this three seed amino acid is Serine, Histidine and aspartic acid.These amino acid are with the natural form of enzyme and with a kind of like this method location, so that the interior peptide bond of their catalysis split proteins.Another common ground between these bacterial serine proteolytic enzyme is always to have the methionine(Met) adjacent to the Serine of avtive spot that exists with natural order.Be applicable to that those bacterial serine proteolytic enzyme of the present invention are wherein to be replaced by other amino acid adjacent to the methionine(Met) of the Serine of avtive spot.The Serine of avtive spot also can be defined as such Serine, and promptly it is the Serine on 221 that come from together in the amino-acid sequence of the bacterium subtilisin that is produced by Bacillus subtilus (Bacillus Subtilis).Said order is listed among hereinafter Fig. 1.
In the order of this bacterium subtilisin that is produced by Bacillus subtilus, methionine(Met) is right after after the Serine on 221, thus it be need be by other amino acid the methionine(Met) on displaced 222.Possible is, in other the order of bacterial serine proteolytic enzyme, this methionine(Met) always is not right after the back at the Serine of avtive spot.Under these circumstances, it is the methionine(Met) on 222 that come from together in the order of this bacterium subtilisin that is produced by Bacillus subtilus, and this kind methionine(Met) need be replaced by other amino acid.
Certainly, the present invention does not lie in the proteolytic enzyme, opposite of these modifications itself, should be the proteolytic enzyme of these modifications is applied to also contain in the liquid detergent composition of lipase especially.Therefore.Describing in detail and how accessing these modified protein enzymes is not purpose of the present invention.This modification is can be by site-directed mutagenesis or by finishing at for this purpose known any other gene engineering in the art.For example, EP-A-0328229(authorizes GIST-BROCADES N.V.) described how to obtain this proteinoid enzyme.The method of Shi Heing is described among the EP130756 in addition, and the document has also been described the bacterial serine proteolytic enzyme of the modification that is applicable in the composition of the present invention.
In addition, be applicable to that the bacterial serine proteolytic enzyme of some modification in the present composition is commercially available, for example DURAZYM
R(from NOVO), it is SAVINASE
RThe methionine(Met) of modified form.The examples of proteases of another kind of available modification is that MAXAPEM15(is from GIST-BROCADES), it is MAXACAL
RModified form, wherein the methionine(Met) on 216 is replaced.The OPTICLEAN of modification
RAnd OPTIMASE
RThe test sample of (from the SOLVAY enzyme) also is available, and both modifications are that the methionine(Met) on 222 is replaced by Gelucystine.The bacterial serine proteolytic enzyme of the preferred modification of the present invention is MAXAPEM15
R(from GIST BROCADES) and DURAZYM
R(from NOVO).
The general every gram finished product of composition of the present invention contains 0.005 to 10mg active protease, and preferably every gram finished product contains 0.01 to 5.0mg active protease.The mixture of the bacterial serine proteolytic enzyme of the modification that this paper is above-mentioned also is applicable to the present composition.
The remainder of liquid detergent composition of the present invention is by cleaning ingredients commonly used, promptly water, tensio-active agent, help washing and other materials to form.Following narration for these compositions is to have integrity in order to make to narrate, and can not think composition of the present invention is restricted on described those compositions commonly used.
Liquid detergent composition of the present invention contains 5% to 60% of liquid detergent composition gross weight, the organic surface active agent of preferred 10% to 40% weight, this organic surface active agent are selected from non-ionic, anionic, cationic and zwitterionic tensio-active agent and its mixture.
The anion surface activity salt that is fit to is selected from sulfonate and vitriol.Similarly anion surfactant is known in the washing composition technical field, and has been found and is widely used in the commercially available detergent.Preferred anionic surfactants water-soluble sulfonate or vitriol have in their molecular structure and contain about 8 alkyl to about 22 carbon atoms.
The example of this class preferred anionic surfactants surfactant salt is by Sulfated C
6-C
16The reaction product that fatty alcohol (from for example tallow oil, plam oil, palm-kernel oil and Oleum Cocois) obtains; Alkylbenzene sulfonate (alkyl wherein contain have an appointment 9) to about 15 carbon atoms; The alkyl glycerylether sodium sulfonate; The ether sulfate of the fatty alcohol that obtains by tallow oil and Oleum Cocois; Coconut fatty acid monoglyceride vitriol and sulfonate; With in alkyl chain, have about 8 water-soluble salts to the sulfonated alkane of about 22 carbon atoms.Just as U.S.3, in 332,880 the patent specification more fully as described in, sulfonated olefin sheet surface-active agent also is spendable.For example sodium, potassium or alkanol ammonium provide to be used for positively charged ion commonly used that the neutralizing cation of negatively charged ion synthetic sulfonate and/or vitriol can be by being widely used in the washing composition technology.
The negatively charged ion synthetic surfactant composition that is fit among the present invention is that the water-soluble salt preferred alkyl benzene sulfonic acid sodium salt by alkyl benzene sulphonate (ABS) provides, and preferably has the sodium alkyl benzene sulfonate of about 10 to 13 carbon atoms in alkyl.Another kind of preferred anionic surfactants surfactant component is the sodium alkyl sulfate that has about 10 to 15 carbon atoms in alkyl among the present invention.
Be applicable to that ionic surfactant pack of the present invention draws together, by in the presence of acidity or basic catalyst, oxyethane with have an active hydrogen atom, for example the hydrocarbon of hydroxyl, carboxyl or amido carries out condensation and those materials of producing, and comprises that having general formula is RA(CH
2CH
2O)
nThe compound of H, in this general formula, R represents hydrophobic part, the A representative has the group of active hydrogen atom, n represents the mean number of ethylene oxide moiety, and R contains 8 to 22 carbon atoms of having an appointment usually, and they also can be by 1,2-propylene oxide and low-molecular weight compound carry out condensation and form, n usually about 2 to about 24 variations.
The condensation product of the fatty alcohol that the nonionic ethoxylate of preferred class can be by having 12 to 15 carbon atoms and about 4 to 10 moles oxyethane (every mole of fatty alcohol) provides.The ethoxylate that this class is fit to comprises C
12-C
15The condensation of pure and mild 3 to the 9 moles oxyethane (every mol of alcohol) of oxo process produce; Narrow fraction C
14-C
15The condensation product of pure and mild 3 to the 9 moles oxyethane (every mole of aliphatics (oxo process) alcohol) of oxo process; Narrow fraction C
12-C
13The condensation product of pure and mild 6.5 moles of ethylene oxide of aliphatics (oxo process) (every mole of fatty alcohol); C with the ethoxylation degree (moles of ethylene oxide/mole Fatty Alcohol(C12-C14 and C12-C18)) in 4 to 8 scopes
10-C
14The condensation product of coconut Fatty Alcohol(C12-C14 and C12-C18).Although the aliphatics oxo alcohol is mainly straight chain, branching to a certain degree, particularly short chain such as methyl-branched are also arranged, this depends on processing condition and raw material olefin.The degree of branching common in the commodity oxo alcohol is at 15% to 50%(weight %) scope in.
The cats product that is fit to comprises formula R
1R
2R
3R
4N
+Quaternary ammonium compound, in the formula, R
1, R
2And R
3Be methyl, R
4Be C
12-15Alkyl, or R
1Be ethyl or hydroxyethyl, R
2And R
3Be methyl, R
4Be C
12-15Alkyl.
Zwitterionics comprises the quaternary ammonium, Phosphonium of aliphatic series and the derivative of blunderbuss compound, in this derivative, aliphatic series part can be straight chain or side chain, one of them aliphatic substituting group contains has an appointment 8 to about 24 carbon atoms, another substituting group contains the anionic water-soluble group at least.Ammonium sulphonate that particularly preferred zwitter-ion material is ethoxylation and ammonium sulfate [be disclosed in U, S patent 3,925, people such as 262(Laughlin, on December 9th, 1975 published) and 3,929, people such as 678(Laughlin, on December 30th, 1975 published) in].
Semi-polar ionic surfactant pack is drawn together water-soluble amine oxides, and this water-soluble amine oxides contains an alkyl or hydroxyalkyl (contain and have an appointment 8 to about 28 carbon atoms) part and is selected from two portions (can be connected to ring texture arbitrarily) of alkyl and hydroxyalkyl (containing 1 to about 3 carbon atoms).
Has formula
The tensio-active agent of polyhydroxy fatty acid amide also be fit to, in following formula, R
1Be H, C
1-4Alkyl, 2-hydroxyethyl, 2-hydroxypropyl or its mixture, R
2Be C
5-31Alkyl, Z are to have linear hydrocarbyl chain and have at least 3 hydroxyls directly to be connected in polyhydroxy alkyl or its alkoxy derivative on this chain.Preferred R
1Be methyl, R
2Be the C of straight chain
11-15Alkyl chain or alkenyl chain, or its mixture, and Z be in reductive amination process by reducing sugar, deriving as glucose, fructose, maltose, lactones obtains.
Composition of the present invention can further contain builder system.Any builder system commonly used all is fit to, but the mixture of the succsinic acid of citric acid and replacement preferably.
Employed citric acid washing assistant will be present in the finished product with the form of any water-soluble salt of citric acid in enforcement of the present invention.This class salt comprises, for example sodium, potassium, ammonium or alkanol ammonium salts.In fact, using citric acid monohydrate compound slurry is very easily as starting raw material, and it will be neutralized on the spot, so that form above-mentioned salt.
It is R-CH(COOH that the succsinic acid washing assistant of replacement of the present invention has general formula) CH
2(COOH), i.e. the derivative of succsinic acid, in following formula, R is C
10-C
16Alkyl or alkenyl, preferably C
12-C
14Alkenyl.
The succsinic acid washing assistant of these replacements preferably comprises that with their water-soluble salt the form of sodium, potassium, ammonium and alkanol ammonium salts (for example, two or triethanol ammonium) is present in the finished product.
As raw material, preferably use their derivative with the form of two acid or anhydrides of these succsinic acids.Diacid can be neutralized on the spot, and acid anhydride then passes through hydrolysis/N-process.
The specific examples of the succsinic acid washing assistant that replaces comprises lauryl succsinic acid, myristyl succsinic acid, palmityl succsinic acid, 2-dodecenyl succinic succsinic acid (preferably), 2-tetradecene base succsinic acid, or the like.
Preferred builder system includes 4 to 12% citric acid of the succsinic acid washing assistant of 4 to 12% above-mentioned replacement of composition total weight and composition total weight.As another kind of washing assistant, composition of the present invention also can contain lipid acid, preferably oleic acid and Zoomeric acid.
The personnel that are skilled in technique in the art are known to be the performance that the pH value of composition can greatly influence enzyme system.Therefore, composition of the present invention preferably has the pH value that is adjusted in 6 to 10 scopes, is preferably 7.5 to 8.0.
Composition of the present invention also can comprise the enzyme stabilising system.In fact, the invention provides a wherein system of the not obvious destruction native lipase of proteolytic enzyme, but because the existence of other cleaning ingredients, problem of unstable still may take place in this enzyme system or its component easily.Therefore, stablizer may need, these stablizers be use always and be that the present technique field is known.Preferred enzyme stabilising system is selected from boric acid, 1,2-propylene glycol, carboxylic acid and its mixture.The general amount that exists of these enzyme stabilising systems is 0.01% to 5% of a composition total weight.
Composition of the present invention also can contain other enzymes, for example cellulase or amylase.Particularly, under the situation that proteolytic enzyme exists, amylase is seemingly stable, and therefore, composition of the present invention preferably contains amylase.
Composition of the present invention can contain a series of other selectable compositions.The example of the additive of this class comprises: foaming regulator, opalizer, for improving additive for the machine consistency on enamel coating surface, sterilant, dyestuff, spices, the SYNTHETIC OPTICAL WHITNER that comprises perborate and percarbonate, whitening agent, soil release agent, softening agent etc.
The amount that liquid composition of the present invention can contain other additive is generally 0.05 to 5%.These additives comprise the polyamino carboxylate, for example the amino tetraacethyl of ethylene, diethylidene triamino pentaacetic acid, the amino disuccinic acid of ethylene or its water-soluble alkali metal salts.Other additive comprises organic phospho acid, particularly preferably is the amino tetramethylene phosphonic acid of ethylene, hexa-methylene diamino tetramethylene phosphonic acid, diethylidene triamino pentamethylene phosphonic acids and Amino Trimethylene Phosphonic Acid.
Embodiment
Following composition of the present invention be in the table in ratio with the composition of listing mixed.
1 2 3 4 5
Linear alkylbenzene sulfonate 12 7678
C
12-15Sodium alkyl sulfate 22332
C
14-15The vitriol 00220 of alkyl 2.5 ethoxylations
C
12Grape glucamide 00660
The C of 7 ethoxylations
12-15Alcohol 80000
5 ethoxylations
12-15Alcohol 08008
Oleic acid 20000
Citric acid 399 13 15
C
12-14The succsinic acid 10 5576 that alkenyl replaces
Ethanol 44345
1,2-propylene glycol 23312
NaOH 6 8 8 11 11
Diethylenetriamine five (methylene phosphonic acid) 0.5 0.7 0.7 11
Amylase (143KNU/g) 0.1 0.1 0.05 0.2 0.1
Lipolase
R(100KLU/g commercial solution) 0.4 0.2 0.3 0.3 0.3
The PEM15R(50mg/g commercial solution) 0.3 000 0.4
Durazym
R(39mg/g commercial solution) 0 0.2 000
Opticlean M222C
R(test sample) 0 0.1 0 0.4 0
Optimase M222C
R(test sample) 00 0.3 00
CaCl2 0.01 0 0.01 0.01 0.02
Sodium metaborate 2.2 2243
Trolamine 00000
Sodium formiate 00000
Lipid acid 00000
Water and subsidiary-balance are to 100%-
Embodiment
Following composition of the present invention be in the table in ratio with the composition of listing mixed.
6 7 8 9 10
The alkylbenzene sulfonate 5798 10 of straight chain
C
12-15Sodium alkyl sulfate 52 1.75 03
C
14-15The vitriol 20200 of alkyl 2.5 ethoxylations
C
12Grape glucamide 60700
The C of 7 ethoxylations
12-15Alcohol 00 0.5 0 11.6
The C of 5 ethoxylations
12-15Alcohol 0808
Oleic acid 000 3.5 2.5
Citric acid 10 9 9.5 41
C
12-14The succsinic acid 11 0 11.5 00 that alkenyl replaces
Tripoly phosphate sodium STPP 0 20 000
Zeolite 000 26 0
Ethanol 64436
1,2-propylene glycol 3222 1.5
NaOH 9 9 9.8 9 3.5
Diethylenetriamine five (methylene phosphonic acid) 1.0 1.0 1.0 0.5 0.8
Amylase (143KNU/g) 0.2 0.1 0.2 0.05 1
Lipolase
R(100KLU/g commercial solution) 0.5 0.5 0.3 0.2 0.3
The PEM15R(50mg/g commercial solution) 0.4 000 0.2
The DurazymR(39mg/g commercial solution) 00 0.5 0 0.2
Opticlean M222C
R(test sample) 000 0.3 0
Optimase M222C
R(test sample) 0 0.5 000
CaCl2 0.01 0.01 0.02 0.02 0.01
Sodium metaborate 42430
Trolamine 00006
Sodium formiate 00001
Lipid acid 0000 12
Water and subsidiary-balance are to 100%-
Embodiment
Following composition of the present invention be in the table in ratio with the composition of listing mixed.
11 12 13 14 15
The alkylbenzene sulfonate 5798 10 of straight chain
C
12-15Sodium alkyl sulfate 52 1.75 03
C
14-15The vitriol 20200 of alkyl 2.5 ethoxylations
C
12Grape glucamide 60700
The C of 7 ethoxylations
12-15Alcohol 00 0.5 0 11.6
The C of 5 ethoxylations
12-15Alcohol 0808
Oleic acid 000 3.5 2.5
Citric acid 10 9 9.5 41
C
12-14The succsinic acid 11 0 11.5 00 that alkenyl replaces
Tartrate monosuccinic acid salt 0 15 0 17 20
Diethoxyization is gathered (propylene terephthalate) 1.0 0.5 0.7 0 0.5
Ethanol 64436
1,2-propylene glycol 3222 1.5
NaOH 9 9 9.8 9 3.5
Diethylenetriamine five (methylene phosphonic acid) 1.0 1.0 1.0 0.5 0.8
Amylase (143KNU/g) 0.2 0.1 0.2 0.05 1
Lipolase
R(100KLU/g commercial solution) 0.5 0.5 0.3 0.2 0.3
PEM15
R(50mg/g commercial solution) 0.4 000 0.2
Durazym
R(39mg/g commercial solution) 00 0.5 0 0.2
Opticlean M222C
R(test sample) 000 0.3 0
Optimase M222C
R(test sample) 0 0.5 000
CaCl2 0.01 0.01 0.02 0.02 0.01
Sodium metaborate 42430
Trolamine 00006
Sodium formiate 00001
Lipid acid 0000 12
Water and subsidiary-balance are to 100%-
Claims (11)
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP90870212.9 | 1990-11-14 | ||
EP90870212 | 1990-11-14 | ||
EP19910200149 EP0486073B1 (en) | 1990-11-14 | 1991-01-25 | Liquid detergent composition containing lipase and protease |
EP91200149.2 | 1991-01-25 |
Publications (1)
Publication Number | Publication Date |
---|---|
CN1062374A true CN1062374A (en) | 1992-07-01 |
Family
ID=26128002
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN 91111550 Pending CN1062374A (en) | 1990-11-14 | 1991-11-14 | The liquid detergent composition that contains lipase and proteolytic enzyme |
Country Status (14)
Country | Link |
---|---|
EP (1) | EP0486073B1 (en) |
JP (1) | JPH06504555A (en) |
CN (1) | CN1062374A (en) |
AU (1) | AU9041691A (en) |
CA (1) | CA2096256C (en) |
DE (1) | DE69121059T2 (en) |
DK (1) | DK0486073T3 (en) |
ES (1) | ES2091280T3 (en) |
IE (1) | IE913951A1 (en) |
MX (1) | MX9102022A (en) |
NZ (1) | NZ240571A (en) |
TR (1) | TR27423A (en) |
TW (1) | TW215108B (en) |
WO (1) | WO1992008779A1 (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1072718C (en) * | 1993-08-30 | 2001-10-10 | 诺沃·诺迪斯克A/S | Lipase and microorganism thereof, production method and use of the lipase |
CN102444018A (en) * | 2011-10-26 | 2012-05-09 | 芜湖南翔羽绒有限公司 | Biochemical combined fine washing process for down feather |
CN102604754A (en) * | 2012-02-03 | 2012-07-25 | 深圳市绿微康生物工程有限公司 | Biological enzyme cleaning agent and method for preparing same |
CN101925669B (en) * | 2008-01-28 | 2013-08-14 | 埃科莱布有限公司 | Multiple enzyme cleaner for surgical instruments and endoscopes |
CN107810260A (en) * | 2015-06-26 | 2018-03-16 | 荷兰联合利华有限公司 | Laundry detergent composition |
CN107922935A (en) * | 2015-08-28 | 2018-04-17 | 荷兰联合利华有限公司 | Liquid detergent compositions comprising lipase and protease |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE69206795T2 (en) * | 1991-04-30 | 1996-09-05 | Procter & Gamble | LIQUID DETERGENT CONTAINING ARYLBORONIC ACID |
HUT66846A (en) * | 1991-10-16 | 1995-01-30 | Unilever Nv | Aqueous enzymatic detergent compositions |
US5442100A (en) * | 1992-08-14 | 1995-08-15 | The Procter & Gamble Company | β-aminoalkyl and β-N-peptidylaminoalkyl boronic acids |
EP2199386A1 (en) | 1993-10-08 | 2010-06-23 | Novozymes A/S | Amylase variants |
DE4344154A1 (en) * | 1993-12-23 | 1995-06-29 | Henkel Kgaa | Liquid detergent containing enzymes |
JP4733861B2 (en) * | 2001-06-20 | 2011-07-27 | 花王株式会社 | Enzyme particles |
EP2516610A1 (en) * | 2009-12-21 | 2012-10-31 | Danisco US Inc. | Detergent compositions containing thermobifida fusca lipase and methods of use thereof |
DE102013224250A1 (en) | 2013-11-27 | 2015-05-28 | Henkel Ag & Co. Kgaa | Lipase stabilization in dishwashing detergents |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4760025A (en) * | 1984-05-29 | 1988-07-26 | Genencor, Inc. | Modified enzymes and methods for making same |
US4980288A (en) * | 1986-02-12 | 1990-12-25 | Genex Corporation | Subtilisin with increased thermal stability |
ES2058119T3 (en) * | 1986-08-29 | 1994-11-01 | Novo Nordisk As | ENZYMATIC DETERGENT ADDITIVE. |
DK571587D0 (en) * | 1987-11-02 | 1987-11-02 | Novo Industri As | ENZYMATIC DETERGENT COMPOSITION |
CN1056187C (en) * | 1988-02-11 | 2000-09-06 | 金克克国际有限公司 | Proteolytic enzymes and their use in detergents |
CA2006527A1 (en) * | 1988-12-30 | 1990-06-30 | Martin S. Cardinali | Enzymatic liquid detergent compositions |
US4959179A (en) * | 1989-01-30 | 1990-09-25 | Lever Brothers Company | Stabilized enzymes liquid detergent composition containing lipase and protease |
US5030378A (en) * | 1990-01-02 | 1991-07-09 | The Procter & Gamble Company | Liquid detergents containing anionic surfactant, builder and proteolytic enzyme |
-
1991
- 1991-01-25 DK DK91200149T patent/DK0486073T3/en active
- 1991-01-25 DE DE1991621059 patent/DE69121059T2/en not_active Expired - Lifetime
- 1991-01-25 EP EP19910200149 patent/EP0486073B1/en not_active Expired - Lifetime
- 1991-01-25 ES ES91200149T patent/ES2091280T3/en not_active Expired - Lifetime
- 1991-11-04 WO PCT/US1991/008041 patent/WO1992008779A1/en active Application Filing
- 1991-11-04 JP JP4500878A patent/JPH06504555A/en active Pending
- 1991-11-04 CA CA002096256A patent/CA2096256C/en not_active Expired - Fee Related
- 1991-11-04 AU AU90416/91A patent/AU9041691A/en not_active Abandoned
- 1991-11-12 MX MX9102022A patent/MX9102022A/en not_active IP Right Cessation
- 1991-11-13 IE IE395191A patent/IE913951A1/en unknown
- 1991-11-13 NZ NZ24057191A patent/NZ240571A/en unknown
- 1991-11-14 CN CN 91111550 patent/CN1062374A/en active Pending
- 1991-12-04 TR TR106991A patent/TR27423A/en unknown
-
1992
- 1992-01-25 TW TW81100525A patent/TW215108B/zh active
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1072718C (en) * | 1993-08-30 | 2001-10-10 | 诺沃·诺迪斯克A/S | Lipase and microorganism thereof, production method and use of the lipase |
CN101925669B (en) * | 2008-01-28 | 2013-08-14 | 埃科莱布有限公司 | Multiple enzyme cleaner for surgical instruments and endoscopes |
CN102444018A (en) * | 2011-10-26 | 2012-05-09 | 芜湖南翔羽绒有限公司 | Biochemical combined fine washing process for down feather |
CN102604754A (en) * | 2012-02-03 | 2012-07-25 | 深圳市绿微康生物工程有限公司 | Biological enzyme cleaning agent and method for preparing same |
CN102604754B (en) * | 2012-02-03 | 2013-07-03 | 深圳市绿微康生物工程有限公司 | Biological enzyme cleaning agent and method for preparing same |
CN107810260A (en) * | 2015-06-26 | 2018-03-16 | 荷兰联合利华有限公司 | Laundry detergent composition |
CN107810260B (en) * | 2015-06-26 | 2020-07-17 | 荷兰联合利华有限公司 | Laundry detergent compositions |
CN107922935A (en) * | 2015-08-28 | 2018-04-17 | 荷兰联合利华有限公司 | Liquid detergent compositions comprising lipase and protease |
Also Published As
Publication number | Publication date |
---|---|
EP0486073A2 (en) | 1992-05-20 |
NZ240571A (en) | 1994-11-25 |
TW215108B (en) | 1993-10-21 |
AU9041691A (en) | 1992-06-11 |
CA2096256A1 (en) | 1992-05-15 |
MX9102022A (en) | 1992-07-08 |
IE913951A1 (en) | 1992-05-20 |
EP0486073B1 (en) | 1996-07-24 |
EP0486073A3 (en) | 1993-06-23 |
TR27423A (en) | 1995-04-21 |
DE69121059T2 (en) | 1997-03-06 |
JPH06504555A (en) | 1994-05-26 |
DE69121059D1 (en) | 1996-08-29 |
CA2096256C (en) | 1999-05-11 |
ES2091280T3 (en) | 1996-11-01 |
DK0486073T3 (en) | 1996-12-09 |
WO1992008779A1 (en) | 1992-05-29 |
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