CN111424005B - 一株产酪氨酸解氨酶的菌株及应用 - Google Patents
一株产酪氨酸解氨酶的菌株及应用 Download PDFInfo
- Publication number
- CN111424005B CN111424005B CN202010540640.7A CN202010540640A CN111424005B CN 111424005 B CN111424005 B CN 111424005B CN 202010540640 A CN202010540640 A CN 202010540640A CN 111424005 B CN111424005 B CN 111424005B
- Authority
- CN
- China
- Prior art keywords
- strain
- tyrosine
- ammonia lyase
- medium
- tyrosine ammonia
- 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.)
- Active
Links
- 108010052982 Tyrosine 2,3-aminomutase Proteins 0.000 title claims abstract description 26
- NGSWKAQJJWESNS-UHFFFAOYSA-N 4-coumaric acid Chemical compound OC(=O)C=CC1=CC=C(O)C=C1 NGSWKAQJJWESNS-UHFFFAOYSA-N 0.000 claims abstract description 44
- 241000122229 Acinetobacter johnsonii Species 0.000 claims abstract description 17
- OUYCCCASQSFEME-QMMMGPOBSA-N L-tyrosine Chemical compound OC(=O)[C@@H](N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-QMMMGPOBSA-N 0.000 claims description 37
- 239000007788 liquid Substances 0.000 claims description 28
- 238000000855 fermentation Methods 0.000 claims description 24
- 230000004151 fermentation Effects 0.000 claims description 24
- 239000002609 medium Substances 0.000 claims description 22
- 229960004441 tyrosine Drugs 0.000 claims description 20
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 18
- 238000002360 preparation method Methods 0.000 claims description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 13
- 230000001580 bacterial effect Effects 0.000 claims description 10
- 238000004321 preservation Methods 0.000 claims description 9
- COLNVLDHVKWLRT-QMMMGPOBSA-N L-phenylalanine Chemical compound OC(=O)[C@@H](N)CC1=CC=CC=C1 COLNVLDHVKWLRT-QMMMGPOBSA-N 0.000 claims description 8
- 239000001888 Peptone Substances 0.000 claims description 8
- 108010080698 Peptones Proteins 0.000 claims description 8
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 claims description 8
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims description 8
- 238000006243 chemical reaction Methods 0.000 claims description 8
- 235000019319 peptone Nutrition 0.000 claims description 8
- 239000000843 powder Substances 0.000 claims description 8
- 239000001632 sodium acetate Substances 0.000 claims description 8
- 235000017281 sodium acetate Nutrition 0.000 claims description 8
- 239000007787 solid Substances 0.000 claims description 8
- WBYWAXJHAXSJNI-VOTSOKGWSA-M .beta-Phenylacrylic acid Natural products [O-]C(=O)\C=C\C1=CC=CC=C1 WBYWAXJHAXSJNI-VOTSOKGWSA-M 0.000 claims description 7
- WBYWAXJHAXSJNI-SREVYHEPSA-N Cinnamic acid Chemical compound OC(=O)\C=C/C1=CC=CC=C1 WBYWAXJHAXSJNI-SREVYHEPSA-N 0.000 claims description 7
- 229940041514 candida albicans extract Drugs 0.000 claims description 7
- 235000013985 cinnamic acid Nutrition 0.000 claims description 7
- 229930016911 cinnamic acid Natural products 0.000 claims description 7
- 238000000034 method Methods 0.000 claims description 7
- WBYWAXJHAXSJNI-UHFFFAOYSA-N methyl p-hydroxycinnamate Natural products OC(=O)C=CC1=CC=CC=C1 WBYWAXJHAXSJNI-UHFFFAOYSA-N 0.000 claims description 7
- 239000012138 yeast extract Substances 0.000 claims description 7
- 230000004913 activation Effects 0.000 claims description 6
- 229960005190 phenylalanine Drugs 0.000 claims description 6
- 238000003756 stirring Methods 0.000 claims description 6
- 229920001817 Agar Polymers 0.000 claims description 4
- WTDRDQBEARUVNC-LURJTMIESA-N L-DOPA Chemical compound OC(=O)[C@@H](N)CC1=CC=C(O)C(O)=C1 WTDRDQBEARUVNC-LURJTMIESA-N 0.000 claims description 4
- WTDRDQBEARUVNC-UHFFFAOYSA-N L-Dopa Natural products OC(=O)C(N)CC1=CC=C(O)C(O)=C1 WTDRDQBEARUVNC-UHFFFAOYSA-N 0.000 claims description 4
- 235000019764 Soybean Meal Nutrition 0.000 claims description 4
- 240000008042 Zea mays Species 0.000 claims description 4
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 claims description 4
- 235000002017 Zea mays subsp mays Nutrition 0.000 claims description 4
- 239000008272 agar Substances 0.000 claims description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 4
- 238000005119 centrifugation Methods 0.000 claims description 4
- QAIPRVGONGVQAS-UHFFFAOYSA-N cis-caffeic acid Natural products OC(=O)C=CC1=CC=C(O)C(O)=C1 QAIPRVGONGVQAS-UHFFFAOYSA-N 0.000 claims description 4
- 235000005822 corn Nutrition 0.000 claims description 4
- 239000002054 inoculum Substances 0.000 claims description 4
- 239000000203 mixture Substances 0.000 claims description 4
- 229910052760 oxygen Inorganic materials 0.000 claims description 4
- 239000001301 oxygen Substances 0.000 claims description 4
- 239000011780 sodium chloride Substances 0.000 claims description 4
- 239000001509 sodium citrate Substances 0.000 claims description 4
- 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 claims description 4
- 239000011684 sodium molybdate Substances 0.000 claims description 4
- 235000015393 sodium molybdate Nutrition 0.000 claims description 4
- TVXXNOYZHKPKGW-UHFFFAOYSA-N sodium molybdate (anhydrous) Chemical compound [Na+].[Na+].[O-][Mo]([O-])(=O)=O TVXXNOYZHKPKGW-UHFFFAOYSA-N 0.000 claims description 4
- 239000004455 soybean meal Substances 0.000 claims description 4
- 230000001954 sterilising effect Effects 0.000 claims description 4
- 238000004659 sterilization and disinfection Methods 0.000 claims description 4
- MCGBIXXDQFWVDW-UHFFFAOYSA-N 4,5-dihydro-1h-pyrazole Chemical compound C1CC=NN1 MCGBIXXDQFWVDW-UHFFFAOYSA-N 0.000 claims description 3
- 238000005273 aeration Methods 0.000 claims description 3
- 238000006555 catalytic reaction Methods 0.000 claims description 3
- 244000005700 microbiome Species 0.000 claims description 3
- 235000015278 beef Nutrition 0.000 claims description 2
- 239000000284 extract Substances 0.000 claims description 2
- 239000001963 growth medium Substances 0.000 claims description 2
- 238000003860 storage Methods 0.000 claims description 2
- 239000000758 substrate Substances 0.000 abstract description 8
- 238000003786 synthesis reaction Methods 0.000 abstract description 6
- 230000015572 biosynthetic process Effects 0.000 abstract description 4
- 238000000605 extraction Methods 0.000 abstract description 4
- 230000002068 genetic effect Effects 0.000 abstract description 4
- 230000009286 beneficial effect Effects 0.000 abstract description 3
- 230000000694 effects Effects 0.000 abstract description 3
- 238000001228 spectrum Methods 0.000 abstract description 3
- 239000003795 chemical substances by application Substances 0.000 abstract description 2
- 239000012535 impurity Substances 0.000 abstract description 2
- 239000012528 membrane Substances 0.000 abstract description 2
- 230000000813 microbial effect Effects 0.000 abstract description 2
- 239000003960 organic solvent Substances 0.000 abstract description 2
- 238000000926 separation method Methods 0.000 abstract description 2
- 239000004094 surface-active agent Substances 0.000 abstract description 2
- 210000004027 cell Anatomy 0.000 description 9
- 238000004519 manufacturing process Methods 0.000 description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
- 241000196324 Embryophyta Species 0.000 description 4
- 102000004190 Enzymes Human genes 0.000 description 4
- 108090000790 Enzymes Proteins 0.000 description 4
- 230000003197 catalytic effect Effects 0.000 description 4
- 238000004128 high performance liquid chromatography Methods 0.000 description 4
- 238000004811 liquid chromatography Methods 0.000 description 4
- 108020004465 16S ribosomal RNA Proteins 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 239000012533 medium component Substances 0.000 description 3
- 230000009466 transformation Effects 0.000 description 3
- OUYCCCASQSFEME-UHFFFAOYSA-N tyrosine Natural products OC(=O)C(N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-UHFFFAOYSA-N 0.000 description 3
- NGSWKAQJJWESNS-ZZXKWVIFSA-M 4-Hydroxycinnamate Natural products OC1=CC=C(\C=C\C([O-])=O)C=C1 NGSWKAQJJWESNS-ZZXKWVIFSA-M 0.000 description 2
- DFYRUELUNQRZTB-UHFFFAOYSA-N Acetovanillone Natural products COC1=CC(C(C)=O)=CC=C1O DFYRUELUNQRZTB-UHFFFAOYSA-N 0.000 description 2
- 241000894006 Bacteria Species 0.000 description 2
- 240000001659 Oldenlandia diffusa Species 0.000 description 2
- 241000191025 Rhodobacter Species 0.000 description 2
- 229910021529 ammonia Inorganic materials 0.000 description 2
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Natural products OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 2
- 239000000306 component Substances 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 235000013305 food Nutrition 0.000 description 2
- 230000007062 hydrolysis Effects 0.000 description 2
- 238000006460 hydrolysis reaction Methods 0.000 description 2
- 235000005985 organic acids Nutrition 0.000 description 2
- 239000002689 soil Substances 0.000 description 2
- QAIPRVGONGVQAS-DUXPYHPUSA-N trans-caffeic acid Chemical compound OC(=O)\C=C\C1=CC=C(O)C(O)=C1 QAIPRVGONGVQAS-DUXPYHPUSA-N 0.000 description 2
- ACEAELOMUCBPJP-UHFFFAOYSA-N (E)-3,4,5-trihydroxycinnamic acid Natural products OC(=O)C=CC1=CC(O)=C(O)C(O)=C1 ACEAELOMUCBPJP-UHFFFAOYSA-N 0.000 description 1
- VIIAUOZUUGXERI-ZETCQYMHSA-N 3-fluoro-L-tyrosine Chemical compound OC(=O)[C@@H](N)CC1=CC=C(O)C(F)=C1 VIIAUOZUUGXERI-ZETCQYMHSA-N 0.000 description 1
- 208000035143 Bacterial infection Diseases 0.000 description 1
- YSXDQZSDAWXDEQ-UHFFFAOYSA-N Betuloside Natural products CCC(C)OC1OC(CO)C(O)C(O)C1Oc2ccc(O)cc2 YSXDQZSDAWXDEQ-UHFFFAOYSA-N 0.000 description 1
- 102100035882 Catalase Human genes 0.000 description 1
- 108010053835 Catalase Proteins 0.000 description 1
- 241000223233 Cutaneotrichosporon cutaneum Species 0.000 description 1
- WTDRDQBEARUVNC-ZCFIWIBFSA-N D-DOPA Chemical compound OC(=O)[C@H](N)CC1=CC=C(O)C(O)=C1 WTDRDQBEARUVNC-ZCFIWIBFSA-N 0.000 description 1
- COLNVLDHVKWLRT-MRVPVSSYSA-N D-phenylalanine Chemical compound OC(=O)[C@H](N)CC1=CC=CC=C1 COLNVLDHVKWLRT-MRVPVSSYSA-N 0.000 description 1
- 229930182832 D-phenylalanine Natural products 0.000 description 1
- OUYCCCASQSFEME-MRVPVSSYSA-N D-tyrosine Chemical compound OC(=O)[C@H](N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-MRVPVSSYSA-N 0.000 description 1
- 229930195709 D-tyrosine Natural products 0.000 description 1
- 238000007400 DNA extraction Methods 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- MMOPREBWKCZVPO-ZIKNSQGESA-N OC(=O)C=CC1=CC=C(O)C=C1.OC(=O)\C=C\C1=CC=C(O)C=C1 Chemical compound OC(=O)C=CC1=CC=C(O)C=C1.OC(=O)\C=C\C1=CC=C(O)C=C1 MMOPREBWKCZVPO-ZIKNSQGESA-N 0.000 description 1
- 102000004316 Oxidoreductases Human genes 0.000 description 1
- 108090000854 Oxidoreductases Proteins 0.000 description 1
- 238000012408 PCR amplification Methods 0.000 description 1
- 241000222393 Phanerochaete chrysosporium Species 0.000 description 1
- 241000191023 Rhodobacter capsulatus Species 0.000 description 1
- KLLYDTMVSVIJEH-YYMOATHLSA-N Rhododendrin Chemical compound C([C@@H](C)O[C@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O)CC1=CC=C(O)C=C1 KLLYDTMVSVIJEH-YYMOATHLSA-N 0.000 description 1
- 240000004808 Saccharomyces cerevisiae Species 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 108010046334 Urease Proteins 0.000 description 1
- 241000700605 Viruses Species 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 239000003242 anti bacterial agent Substances 0.000 description 1
- 229940088710 antibiotic agent Drugs 0.000 description 1
- -1 aromatic organic acids Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 235000004883 caffeic acid Nutrition 0.000 description 1
- 229940074360 caffeic acid Drugs 0.000 description 1
- 238000007036 catalytic synthesis reaction Methods 0.000 description 1
- 210000000170 cell membrane Anatomy 0.000 description 1
- 150000001851 cinnamic acid derivatives Chemical class 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 238000005265 energy consumption Methods 0.000 description 1
- 238000003912 environmental pollution Methods 0.000 description 1
- AQNDDEOPVVGCPG-UHFFFAOYSA-N esmolol Chemical compound COC(=O)CCC1=CC=C(OCC(O)CNC(C)C)C=C1 AQNDDEOPVVGCPG-UHFFFAOYSA-N 0.000 description 1
- 229960003745 esmolol Drugs 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 244000237330 gutta percha tree Species 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 244000144972 livestock Species 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 238000007833 oxidative deamination reaction Methods 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 244000144977 poultry Species 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- WMOAPGQHTURTAQ-UHFFFAOYSA-N rhododendrin Natural products CC(C)(CCc1ccc(O)cc1)OC2OC(CO)C(O)C(O)C2O WMOAPGQHTURTAQ-UHFFFAOYSA-N 0.000 description 1
- 230000028327 secretion Effects 0.000 description 1
- 238000012163 sequencing technique Methods 0.000 description 1
- 235000013599 spices Nutrition 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N1/00—Microorganisms, e.g. protozoa; Compositions thereof; Processes of propagating, maintaining or preserving microorganisms or compositions thereof; Processes of preparing or isolating a composition containing a microorganism; Culture media therefor
- C12N1/20—Bacteria; Culture media therefor
- C12N1/205—Bacterial isolates
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12R—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES C12C - C12Q, RELATING TO MICROORGANISMS
- C12R2001/00—Microorganisms ; Processes using microorganisms
- C12R2001/01—Bacteria or Actinomycetales ; using bacteria or Actinomycetales
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N1/00—Microorganisms, e.g. protozoa; Compositions thereof; Processes of propagating, maintaining or preserving microorganisms or compositions thereof; Processes of preparing or isolating a composition containing a microorganism; Culture media therefor
- C12N1/20—Bacteria; Culture media therefor
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P7/00—Preparation of oxygen-containing organic compounds
- C12P7/40—Preparation of oxygen-containing organic compounds containing a carboxyl group including Peroxycarboxylic acids
- C12P7/42—Hydroxy-carboxylic acids
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Health & Medical Sciences (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Genetics & Genomics (AREA)
- Biotechnology (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- General Engineering & Computer Science (AREA)
- Microbiology (AREA)
- Medicinal Chemistry (AREA)
- Tropical Medicine & Parasitology (AREA)
- Virology (AREA)
- Biomedical Technology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Enzymes And Modification Thereof (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
Abstract
本发明涉及一株产酪氨酸解氨酶的菌株及应用,属于生物技术领域,所述菌株分类命名为约氏不动杆菌Acinetobacter johnsonii,已于2020年5月15日保存于中国微生物菌种保藏管理委员会普通微生物中心,保藏编号:CGMCC No.19831。本发明提供的菌株遗传稳定性好,培养成本低,产生的酪氨酸解氨酶酶活力高,适用底物谱较宽,可直接利用该菌株直接转化合成对羟基肉桂酸及衍生物,催化合成时无需加入表面活性剂、有机溶剂等透膜剂,避免引入外源杂质,有利于提取分离操作,工业应用具有优势。
Description
技术领域
本发明属于生物技术领域,特别涉及一株生产酪氨酸解氨酶的菌株,以及利用该菌株生产的酪氨酸解氨酶催化制备对羟基肉桂酸及衍生物的方法。
背景技术
4-羟基肉桂酸(p-coumaric acid),又名对香豆酸,广泛存在于自然界植物当中,为白花蛇舌草、海金沙草、杜仲叶的有效成分之一,作为香料或酸化剂在食品行业广泛使用,农业上可以替代抗生素治疗畜禽病毒或细菌性疾病;同时也是合成可心定、杜鹃素、艾司洛尔等重要医药活性物质的中间体,在医药领域的应用前景也非常广阔。另外4-羟基肉桂酸的结构类似物肉桂酸、咖啡酸作为重要的芳香族有机酸,在食品、农业及医药领域广泛应用。现阶段获得对香豆酸的途径主要以化学合成和植物提取为主。化学合成面临反应时间长,高能耗、有毒副产品及环境污染的难题。植物提取则面临成本高、生产力低,生态资源环境等问题。微生物转化法将是生产4-羟基肉桂酸最具前景的替代生产方法。
酪氨酸解氨酶催化L-酪氨酸非氧化脱氨生产对羟基肉桂酸,在植物细胞中普遍存在,目前在一些微生物体内也陆续发现了酪氨酸解氨酶,如荚膜红细菌(Rhodobactercapsulatus)、球形红细菌(Rhodobacters sphaeroides)、丝孢酵母(Trichosporon cutaneum)、黄孢原毛平革菌(Phanerochaete chrysosporium)等。国内外研究者利用上述菌株做了很多研究工作,Todd Vannelli等克隆到酵母菌(Trichosporoncutaneum)的TA L 基因, 在大肠杆菌中表达并纯化,纯化后的酶以比活仅为0.33U/mL。刘沛然等克隆粘红酵母酪氨酸解氨酶在大肠杆菌中的异源表达,比活1.78 U/mg,用于生产4-羟基肉桂酸,产量为196.3 mg/L。一直困扰人们的难题是酪氨酸解氨酶酶的稳定性差,对催化产物耐受性差、易失活,导致催化形成的产物浓度低,距离工业化应用尚有较大的距离。通过筛选高活性及高稳定性的新型酪氨酸解氨酶是解决以上问题的关键所在。
发明内容
本发明的目的是提供从土壤中分离得到的一株高效生产酪氨酸解氨酶的菌株,并应用该菌株产生的酪氨酸解氨酶酶法制备对羟基肉桂酸及衍生物的方法。
本发明是通过如下技术方案来实现的:
一株产酪氨酸解氨酶的菌株Ytld-76,分类命名为约氏不动杆菌Acinetobacterjohnsonii,于2020年5月15日保藏于中国微生物菌种保藏管理委员会普通微生物中心,保藏地址为北京市朝阳区北辰西路1号院3号,保藏编号为:CGMCC No19831。
所述菌株是从烟台地区山坡土壤中分离得到,这是一株酪氨酸解氨酶分泌能力极高的菌株,培养方法简单,生长速度快,不易变异,可以直接用于酶法制备对羟基肉桂酸。
本发明还提供利用所述菌株产生的酪氨酸解氨酶催化制备对羟基肉桂酸及衍生物的方法如下:
1、培养基配制
(1)固体保藏培养基成份及其终浓度:酵母浸粉5 g/L,蛋白胨10 g/L,牛肉膏5 g/L,NaCl 5 g/L,琼脂 20 g/L,pH 7.0,121℃高压蒸汽灭菌20min;
(2)液体种子培养基成份及其终浓度:醋酸钠5-10 g/L,(NH4)2SO4 1-5g/L, KH2PO41- 3g/L,MgSO4 0.1-1g/L,蛋白胨5-10 g/L,酵母浸粉 1-3 g/L, pH 7.0-7.2,121℃高压蒸汽灭菌20min;
(3)发酵培养基成份及其终浓度:醋酸钠5-10 g/L,柠檬酸钠 1-3g/L,(NH4)2SO4 1-5g/L, KH2PO4 1- 3g/L,MgSO4 0.1-1g/L,FeSO4 1-5mg/L,CoCl2 0.1-1mg/L,钼酸钠 0.1-1mg/L,豆粕水解液5-10 g/L,玉米浆 1-5 g/L,L-酪氨酸 1-5 g/L,pH 7.0-7.2,121℃高压蒸汽灭菌20min。
2、菌株活化:挑取菌种划线接种至固体保藏培养基,于恒温培养箱30℃培养24~48h;
3、液体种子制备:挑取活化菌株接种于装有液体种子培养基的三角瓶中,纱布封口,于20-35℃,150~200r/min摇床振荡培养24~48h,得液体种子;
4、液体发酵:按5~10%接种量向发酵培养基接入液体种子,转速200~700r/min,溶氧控制20~50%,pH7.0~7.5,温度26~37℃,通气培养24~48h,得到酪氨酸解氨酶的发酵液,8000r/min离心20min收集菌体细胞;
5、全细胞催化L-酪氨酸(或衍生物)制备对羟基肉桂酸(或衍生物):将10-30g的L-酪氨酸(或衍生物)加入500mL水中,氢氧化钠调pH至8.5~10.0,搅拌均匀,加入离心1L发酵液收集的菌体,并加水定容1L,温度30~50℃,维持转速在50~100 r/min,反应4~20h。
本发明还提供所述约氏不动杆菌Ytld-76在催化L-酪氨酸生产对羟基肉桂酸中的应用。
本发明还提供所述约氏不动杆菌Ytld-76在催化L-苯丙氨酸生产肉桂酸中的应用。
本发明还提供所述约氏不动杆菌Ytld-76在催化L-多巴生产3,4-二羟基肉桂酸中的应用。
本发明与现有技术相比的有益效果:
1、本发明提供的约氏不动杆菌Ytld-76,不同于以往的酪氨酸解氨酶产生菌种,尚未有该菌株产酪氨酸解氨酶的报道,拓宽了产酪氨酸解氨酶的菌种渠道;
2、本发明所提供的约氏不动杆菌Ytld-76遗传稳定性好,培养基成分简单原料成本低,产生的酪氨酸解氨酶稳定性好,能够耐受高浓度产物,对羟基肉桂酸浓度可达26.5g/L,且可作用的底物谱较宽,可直接利用该菌株发酵液直接转化生产对羟基肉桂酸及衍生物,工业应用具有优势。
3、约氏不动杆菌Ytld-76具有良好的细胞膜通透性,有利于底物透过,催化合成肉桂酸衍生物无需加入表面活性剂、有机溶剂等透膜剂,避免引入外源杂质,有利于提取分离操作。
附图说明
图1为约氏不动杆菌Ytld-76基于16S rRNA序列的系统发育树。
具体实施方式
为阐明对本项发明特征的理解,下面结合一些非限定性的实施实例对本发明做进一步阐述。
实施例1:约氏不动杆菌菌株分类
1)菌种特性
在保藏培养基上菌落呈乳白色,近圆形、表面光滑湿润、有光泽、边缘整齐;通过显微镜观察,菌体呈杆状,不能运动,革兰氏阴性;生理生化指标如表1所示。
表1 菌株Ytld-76生理生化特征
项目 | Ytld-76 | 项目 | Ytld-76 |
氧化酶 | - | VP 试验 | - |
淀粉 | - | 触酶试验 | + |
硝酸盐还原 | - | 柠檬酸利用 | + |
脲酶 | - | 明胶水解 | - |
2)菌株鉴定
经DNA提取、PCR扩增和测序获得的16S rRNA 基因序列长度为1446 bp,在GenBank上进行BLAST比对并绘制系统进化树(图1),得出该菌株与Acinetobacter johnsoniiATCC17909(HE651920)碱基相似性达98.2%,结合生理生化指标,将Ytld-76菌株鉴定为约氏不动杆菌(Acinetobacter johnsonii)。16S rRNA序列信息如下:
gggcgtggcggcagctacacatgcagtcgagcggggaagtagtagcttgctacactgacctagcggcggacgggtgagtaatgcttaggaatctgcctattagtgggggacaacattccgaaaggaatgctaataccgcatacgccctacgggggaaagcaggggatcttcggaccttgcgctaatagatgagcctaagtcagattagctagttggtggggtaaaggcctaccaaggcgacgatctgtagcgggtctgagaggatgatccgccacactgggactgagacacggcccagactcctacgggaggcagcagtggggaatattggacaatgggcgaaagcctgatccagccatgccgcgtgtgtgaagaaggccttttggttgtaaagcactttaagcgaggaggaggctaccgagattaataccctgggatagtggacgttactcgcagaataagcaccgggctaactctgtgccagcagccgcggtaatacagagggtgcgagcgttaatcggatttactgggcgtaaagcgtgcgtaggcggctttttaagtcggatgtgaaatccctgagcttaacttaggaattgcattcgatactgggaagctagagtatgggagaggatggtagaattccaggtgtagcggtgaaatgcgtagagatctggaggaataccgatggcgaaggcagccatctggcctaatactgacgctgaggtacgaaagcatggggagcaaacaggattagataccctggtagtccatgccgtaaacgatgtctactagccgttggggcctttgaggctttagtggcgcagctaacgcgataagtagaccgcctggggagtacggtcgcaagactaaaactcaaatgaattgacgggggcccgcacaagcggtggagcatgtggtttaattcgatgcaacgcgaagaaccttacctggtcttgacatagtaagaactttccagagatggattggtgcctttcgggaacttacatacaggtgctgcatggctgtcgtcagctcgtgtcgtgagatgttgggttaagtcccgcaacgagcgcaacccttttccttatttgccagcgggttaagccgggaactttaaggatactgccagtgacaaactggaggaaggcggggacgacgtcaagtcatcatggcccttacgaccagggctacacacgtgctacaatggtcggtacaaagggttgctacctagcgataggatgctaatctcaaaaagccgatcgtagtccggattggagtctgcaactcgactccatgaagtcggaatcgctagtaatcgcggatcagaatgccgcggtgaatacgttcccgggccttgtacacaccgcccgtcacaccatgggaatttgttgcaccagaagtaggtagtctaaccgcaaggaggacgctaccacggtgcccatgggc
3)约氏不动杆菌Ytld-76酪氨酸解氨酶底物特异性
考察了约氏不动杆菌Ytld-76酪氨酸解氨酶的底物特异性。由表2中可见,酪氨酸解氨酶能够较好地催化L-酪氨酸及结构类似物为芳香族不饱和有机酸,具有较宽的底物谱,对D-酪氨酸及结构类似物不能催化。
表2 底物特异性
底物 | 相对酶活(%) |
L-酪氨酸 | 100 |
L-苯丙氨酸 | 28.2 |
L-多巴 | 13.5 |
D-酪氨酸 | 0 |
3-氟-L-酪氨酸 | 5.7 |
D-苯丙氨酸 | 0 |
D-多巴 | 0 |
4)遗传稳定性
采用划线法将约氏不动杆菌Ytld-76在固体培养基上连续传代50次,测定菌体形态、生长速度及转化L-酪氨酸的速度和转化率,与原代菌株无明显差异,遗传稳定性良好。
实施例2 菌株培养与对羟基肉桂酸合成
1)菌株活化:挑取菌种至固体保藏培养基:酵母浸粉5 g/L,蛋白胨10 g/L,NaCl 5g/L,琼脂 20 g/L,pH 7.0,划线接种于恒温培养箱30℃培养48h;
2)液体种子制备:挑取1环活化菌株接种于装有50mL液体种子培养基的500mL三角瓶中,八层纱布封口,于30℃, 200r/min摇床振荡培养24 h,得液体种子;所述的液体种子培养基组分及其终浓度:醋酸钠5 g/L,(NH4)2SO4 1g/L, KH2PO4 1g/L,MgSO4 0.1g/L,蛋白胨5 g/L,酵母浸粉 1 g/L, pH 7.0;
3)液体发酵:按5%接种量在发酵培养基中接入液体种子,所述发酵培养基的成分及终浓度为醋酸钠10 g/L,柠檬酸钠 1g/L,(NH4)2SO4 2 g/L, KH2PO4 1g/L,MgSO4 0.2g/L,FeSO4 1mg/L,CoCl2 0.1mg/L,钼酸钠 0.1mg/L,豆粕水解液10 g/L,玉米浆 5 g/L和L-酪氨酸 2 g/L,转速200~700r/min,溶氧控制20%左右,pH7.0,温度30℃,通气培养36h,得到酪氨酸解氨酶的发酵液,酶活达到298U/L,8000r/min离心20min收集菌体;
4)催化制备对羟基肉桂酸:将10g的L-酪氨酸加入约500mL水中,氢氧化钠调pH至9.0,搅拌均匀,加入离心1L发酵液收集的菌体,并加水定容1L,温度30℃,维持转速在50 r/min,反应4h。HPLC测定对羟基肉桂酸含量为8.9g/L,对酪氨酸摩尔转化率为98.2%。液相色谱条件为:C18 反相柱(5 μm, 250 mm×4.6mm),柱温25℃;检测波长:277nm;流动相:甲醇:水(含0.2% 乙酸)=(50:50, V/V)流速:1mL/min。
实施例3催化L-酪氨酸生产对羟基肉桂酸
1)菌株活化:挑取菌种至固体保藏培养基,划线接种于恒温培养箱30℃培养48h;所述固体保藏培养基的成分及终浓度:酵母浸粉5 g/L,蛋白胨10 g/L,NaCl 5 g/L,琼脂20 g/L,pH 7.0;
2)液体种子制备:挑取1环活化菌株接种于装有50mL液体种子培养基的500mL三角瓶中,八层纱布封口,于30℃, 200r/min摇床振荡培养24 h,得液体种子;所述液体种子培养基组分:醋酸钠 8 g/L,(NH4)2SO4 3g/L, KH2PO4 2g/L,MgSO4 0.5g/L,蛋白胨5 g/L,酵母浸粉 2 g/L, pH 7.0,
3)液体发酵:按5%接种量向组成成分为醋酸钠10 g/L,柠檬酸钠 3g/L,(NH4)2SO4 5g/L, KH2PO4 3g/L,MgSO4 1g/L,FeSO4 3mg/L,CoCl2 0.3mg/L,钼酸钠 0.3 mg/L,豆粕水解液5 g/L,玉米浆 5 g/L,L-酪氨酸 5 g/L的发酵培养基接入液体种子,转速200~700r/min,溶氧控制30%左右,pH7.0,温度30℃,通气培养42h,得到酪氨酸解氨酶的发酵液,8000r/min离心20min收集菌体;
4)催化制备对羟基肉桂酸:将30g的L-酪氨酸加入约500mL水中,氢氧化钠调pH至10.0,搅拌均匀,加入离心1L发酵液收集的菌体,并加水定容1L,温度40℃,维持转速在50r/min,反应16h。HPLC测定对羟基肉桂酸含量为26.5g/L,对酪氨酸摩尔转化率为97.4%。液相色谱条件同实施例2。
实施例4 催化制备肉桂酸
菌种活化、液体种子制备及酪氨酸解氨酶液体发酵同实施例3。将10g的L-苯丙氨酸加入约500mL水中,氢氧化钠调pH至9.5,搅拌均匀,加入离心1L发酵液收集的菌体,并加水定容1L,温度40℃,维持转速在50 r/min,反应6h。HPLC测定肉桂酸含量为8.8g/L,对苯丙氨酸摩尔转化率为98.1%。液相色谱条件同实施例2。
实施例5 催化制备3,4-二羟基肉桂酸
菌种活化、液体种子制备及酪氨酸解氨酶液体发酵同实施例3。将10g的L-多巴加入约500mL水中,氢氧化钠调pH至8.5,搅拌均匀,加入离心1L发酵液收集的菌体,并加水定容1L,温度40℃,维持转速在50 r/min,反应10h。HPLC测定肉桂酸含量为9.0g/L,对苯丙氨酸摩尔转化率为98.5%。液相色谱条件同实施例2。
序列表
<110> 鲁东大学
<120> 一株产酪氨酸解氨酶的菌株及应用
<160> 1
<170> SIPOSequenceListing 1.0
<210> 1
<211> 1446
<212> DNA
<213> 约氏不动杆菌Ytld-76(Acinetobacter johnsonii)
<400> 1
gggcgtggcg gcagctacac atgcagtcga gcggggaagt agtagcttgc tacactgacc 60
tagcggcgga cgggtgagta atgcttagga atctgcctat tagtggggga caacattccg 120
aaaggaatgc taataccgca tacgccctac gggggaaagc aggggatctt cggaccttgc 180
gctaatagat gagcctaagt cagattagct agttggtggg gtaaaggcct accaaggcga 240
cgatctgtag cgggtctgag aggatgatcc gccacactgg gactgagaca cggcccagac 300
tcctacggga ggcagcagtg gggaatattg gacaatgggc gaaagcctga tccagccatg 360
ccgcgtgtgt gaagaaggcc ttttggttgt aaagcacttt aagcgaggag gaggctaccg 420
agattaatac cctgggatag tggacgttac tcgcagaata agcaccgggc taactctgtg 480
ccagcagccg cggtaataca gagggtgcga gcgttaatcg gatttactgg gcgtaaagcg 540
tgcgtaggcg gctttttaag tcggatgtga aatccctgag cttaacttag gaattgcatt 600
cgatactggg aagctagagt atgggagagg atggtagaat tccaggtgta gcggtgaaat 660
gcgtagagat ctggaggaat accgatggcg aaggcagcca tctggcctaa tactgacgct 720
gaggtacgaa agcatgggga gcaaacagga ttagataccc tggtagtcca tgccgtaaac 780
gatgtctact agccgttggg gcctttgagg ctttagtggc gcagctaacg cgataagtag 840
accgcctggg gagtacggtc gcaagactaa aactcaaatg aattgacggg ggcccgcaca 900
agcggtggag catgtggttt aattcgatgc aacgcgaaga accttacctg gtcttgacat 960
agtaagaact ttccagagat ggattggtgc ctttcgggaa cttacataca ggtgctgcat 1020
ggctgtcgtc agctcgtgtc gtgagatgtt gggttaagtc ccgcaacgag cgcaaccctt 1080
ttccttattt gccagcgggt taagccggga actttaagga tactgccagt gacaaactgg 1140
aggaaggcgg ggacgacgtc aagtcatcat ggcccttacg accagggcta cacacgtgct 1200
acaatggtcg gtacaaaggg ttgctaccta gcgataggat gctaatctca aaaagccgat 1260
cgtagtccgg attggagtct gcaactcgac tccatgaagt cggaatcgct agtaatcgcg 1320
gatcagaatg ccgcggtgaa tacgttcccg ggccttgtac acaccgcccg tcacaccatg 1380
ggaatttgtt gcaccagaag taggtagtct aaccgcaagg aggacgctac cacggtgccc 1440
atgggc 1446
Claims (5)
1.一株产酪氨酸解氨酶的菌株,分类命名为约氏不动杆菌Acinetobacter johnsonii,保藏于中国微生物菌种保藏管理委员会普通微生物中心,保藏日期为2020年5月15日,保藏编号为:CGMCC No. 19831。
2.利用权利要求1所述菌株制备对羟基肉桂酸及衍生物的方法,其特征所述方法在于如下:
1)培养基配制
(1)固体保藏培养基成分及其终浓度:酵母浸粉5 g/L,蛋白胨10 g/L,牛肉膏5 g/L,NaCl 5 g/L,琼脂 20 g/L,pH 7.0,121℃高压蒸汽灭菌20min;
(2)液体种子培养基成分及其终浓度:醋酸钠5-10 g/L,(NH4)2SO4 1-5g/L, KH2PO4 1-3g/L,MgSO4 0.1-1g/L,蛋白胨5-10 g/L,酵母浸粉 1-3 g/L, pH 7.0-7.2,121℃高压蒸汽灭菌20min;
(3)发酵培养基成分及其终浓度:醋酸钠5-10 g/L,柠檬酸钠 1-3g/L,(NH4)2SO4 1-5g/L, KH2PO4 1- 3g/L,MgSO4 0.1-1g/L,FeSO4 1-5mg/L,CoCl2 0.1-1mg/L,钼酸钠 0.1-1mg/L,豆粕水解液5-10 g/L,玉米浆 1-5 g/L,L-酪氨酸 1-5 g/L,pH 7.0-7.2,121℃高压蒸汽灭菌20min;
2)菌株活化:挑取菌种划线接种至固体保藏培养基,于恒温培养箱30℃培养24~48h;
3)液体种子制备:挑取活化菌株接种于装有液体种子培养基的三角瓶中,纱布封口,于20-35℃,150~200r/min摇床振荡培养24~48h,得液体种子;
4)液体发酵:按5~10%接种量向发酵培养基接入液体种子,转速200~700r/min,溶氧控制20~50%,pH7.0~7.5,温度26~37℃,通气培养24~48h,得到酪氨酸解氨酶的发酵液,8000r/min离心20min收集菌体细胞;
5)全细胞催化L-酪氨酸或衍生物制备对羟基肉桂酸或衍生物:将10-30g的L-酪氨酸或衍生物加入500mL水中,氢氧化钠调pH至8.5~10.0,搅拌均匀,加入离心1L发酵液收集的菌体,并加水定容1L,温度30~50℃,维持转速在50~100 r/min,反应4~20h。
3.权利要求1所述菌株在催化L-酪氨酸生产对羟基肉桂酸中的应用。
4.权利要求1所述菌株在催化L-苯丙氨酸生产肉桂酸中的应用。
5.权利要求1所述菌株在催化L-多巴生产3,4-二羟基肉桂酸中的应用。
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202010540640.7A CN111424005B (zh) | 2020-06-15 | 2020-06-15 | 一株产酪氨酸解氨酶的菌株及应用 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202010540640.7A CN111424005B (zh) | 2020-06-15 | 2020-06-15 | 一株产酪氨酸解氨酶的菌株及应用 |
Publications (2)
Publication Number | Publication Date |
---|---|
CN111424005A CN111424005A (zh) | 2020-07-17 |
CN111424005B true CN111424005B (zh) | 2020-08-21 |
Family
ID=71551401
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN202010540640.7A Active CN111424005B (zh) | 2020-06-15 | 2020-06-15 | 一株产酪氨酸解氨酶的菌株及应用 |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN111424005B (zh) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2022082362A1 (zh) * | 2020-10-19 | 2022-04-28 | 陈振暐 | 代谢酪氨酸的非病原性细菌基因表现系统及转化株、其用于制备降低尿毒素的组合物的用途以及利用其代谢酪氨酸的方法 |
CN118497253B (zh) * | 2024-07-15 | 2024-10-15 | 广州酒家集团利口福食品有限公司 | 一种增强巴斯德毕赤酵母对对羟基肉桂酸耐受能力的方法 |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7067302B2 (en) * | 2002-07-23 | 2006-06-27 | E. I. Du Pont De Nemours And Company | DNA and amino acid sequence of a tyrosine ammonia lyase enzyme from the bacterium Rhodobacter sphaeroides |
WO2016189121A1 (en) * | 2015-05-28 | 2016-12-01 | Evolva Sa | Biosynthesis of phenylpropanoids and phenylpropanoid derivatives |
CN110938579A (zh) * | 2019-12-13 | 2020-03-31 | 杭州唯铂莱生物科技有限公司 | 酪氨酸解氨酶重组菌、酪氨酸解氨酶及其制备方法和应用 |
-
2020
- 2020-06-15 CN CN202010540640.7A patent/CN111424005B/zh active Active
Also Published As
Publication number | Publication date |
---|---|
CN111424005A (zh) | 2020-07-17 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN102174449B (zh) | 一种高产γ-氨基丁酸的生产方法及应用 | |
CN102321563B (zh) | 一株拟无枝酸菌及利用其全细胞转化制备香草醛的方法 | |
CN101792727B (zh) | 一株凝结芽孢杆菌及其在l-乳酸钠制备中的应用 | |
CA1168999A (en) | Method for preparing 2,5-diketo-d-gluconic acid | |
CN104805050A (zh) | 一种负离子粉促进微生物发酵的方法 | |
CN1940078B (zh) | 一种生物防腐剂苯乳酸的制备方法 | |
CN111424005B (zh) | 一株产酪氨酸解氨酶的菌株及应用 | |
CN113637607B (zh) | 一株拟无枝酸菌及其应用 | |
CN109652348A (zh) | 一株耐受性强、高产酸和乙偶姻的巴氏醋杆菌及在山西老陈醋生产中的应用 | |
CN103911295A (zh) | 毛栓菌菌株及其在利用市政脱水污泥生产漆酶中的应用 | |
CN101314782B (zh) | 发酵生产辅酶q10的方法 | |
CN113174344B (zh) | 一种产膜海鞘素b的菌种及其应用 | |
CN1516737A (zh) | 一种通过共培养制备五倍子酸的方法 | |
CN101205523A (zh) | 一种酿酒酵母及其在制备β-羟基苯丙酸乙酯中的应用 | |
CN100370032C (zh) | 微生物法生产二羟基丙酮 | |
CN1421523A (zh) | 一种黑曲霉菌及用其生产香草酸和香草醛的微生物转化方法 | |
WO2021056683A1 (zh) | 一株产脂肪酶菌株及其应用 | |
CN105969811B (zh) | 利用植物乳杆菌发酵没食子酸制备焦性没食子酸的方法 | |
US3994781A (en) | Process for the production of protein | |
CN108018246B (zh) | 一株联产壳聚糖酶和γ-聚谷氨酸的菌株及其应用 | |
CN112094762A (zh) | 一株葡萄牙棒孢酵母菌株及其应用 | |
CN115975826B (zh) | 一种酿酒酵母mStr003及其在生产β-熊果苷中的应用 | |
CN119913086B (zh) | 一株产乳清酸的不动杆菌菌株和应用以及产乳清酸的方法 | |
CN100396773C (zh) | 一种用于生产冠菌素的基因工程菌及其构建方法 | |
CN114437963B (zh) | 橄榄链霉菌及其在生物合成香兰素中的应用 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | Publication | ||
PB01 | Publication | ||
SE01 | Entry into force of request for substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
GR01 | Patent grant | ||
GR01 | Patent grant | ||
TR01 | Transfer of patent right | ||
TR01 | Transfer of patent right |
Effective date of registration: 20210202 Address after: No.1666, East Ring Road, juancheng County, Heze City, Shandong Province 274600 Patentee after: SHANDONG YANGCHENG BIOTECH Co.,Ltd. Address before: 264025 No. 184 Hongqi Middle Road, Zhifu District, Shandong, Yantai Patentee before: LUDONG University |