RU2013140115A - METHOD FOR PRODUCING L-AMINO ACIDS USING THE BACTERIA OF THE Enterobacteriaceae FAMILY IN WHICH THE EXPRESSION OF THE znuACB GENERAL CLUSTER IS DISORDERED - Google Patents
METHOD FOR PRODUCING L-AMINO ACIDS USING THE BACTERIA OF THE Enterobacteriaceae FAMILY IN WHICH THE EXPRESSION OF THE znuACB GENERAL CLUSTER IS DISORDERED Download PDFInfo
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- RU2013140115A RU2013140115A RU2013140115/10A RU2013140115A RU2013140115A RU 2013140115 A RU2013140115 A RU 2013140115A RU 2013140115/10 A RU2013140115/10 A RU 2013140115/10A RU 2013140115 A RU2013140115 A RU 2013140115A RU 2013140115 A RU2013140115 A RU 2013140115A
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- 241000894006 Bacteria Species 0.000 title claims abstract 40
- 150000008575 L-amino acids Chemical class 0.000 title claims abstract 11
- 241000588921 Enterobacteriaceae Species 0.000 title claims abstract 3
- 238000004519 manufacturing process Methods 0.000 title 1
- 108091008053 gene clusters Proteins 0.000 claims abstract 16
- 108090000623 proteins and genes Proteins 0.000 claims abstract 14
- AHLPHDHHMVZTML-BYPYZUCNSA-N L-Ornithine Chemical compound NCCC[C@H](N)C(O)=O AHLPHDHHMVZTML-BYPYZUCNSA-N 0.000 claims abstract 10
- RHGKLRLOHDJJDR-BYPYZUCNSA-N L-citrulline Chemical compound NC(=O)NCCC[C@H]([NH3+])C([O-])=O RHGKLRLOHDJJDR-BYPYZUCNSA-N 0.000 claims abstract 10
- WHUUTDBJXJRKMK-VKHMYHEASA-N L-glutamic acid Chemical compound OC(=O)[C@@H](N)CCC(O)=O WHUUTDBJXJRKMK-VKHMYHEASA-N 0.000 claims abstract 8
- MTCFGRXMJLQNBG-REOHCLBHSA-N (2S)-2-Amino-3-hydroxypropansäure Chemical compound OC[C@H](N)C(O)=O MTCFGRXMJLQNBG-REOHCLBHSA-N 0.000 claims abstract 6
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 claims abstract 6
- DCXYFEDJOCDNAF-REOHCLBHSA-N L-asparagine Chemical compound OC(=O)[C@@H](N)CC(N)=O DCXYFEDJOCDNAF-REOHCLBHSA-N 0.000 claims abstract 6
- HNDVDQJCIGZPNO-YFKPBYRVSA-N L-histidine Chemical compound OC(=O)[C@@H](N)CC1=CN=CN1 HNDVDQJCIGZPNO-YFKPBYRVSA-N 0.000 claims abstract 6
- ROHFNLRQFUQHCH-YFKPBYRVSA-N L-leucine Chemical compound CC(C)C[C@H](N)C(O)=O ROHFNLRQFUQHCH-YFKPBYRVSA-N 0.000 claims abstract 6
- AYFVYJQAPQTCCC-GBXIJSLDSA-N L-threonine Chemical compound C[C@@H](O)[C@H](N)C(O)=O AYFVYJQAPQTCCC-GBXIJSLDSA-N 0.000 claims abstract 6
- OUYCCCASQSFEME-QMMMGPOBSA-N L-tyrosine Chemical compound OC(=O)[C@@H](N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-QMMMGPOBSA-N 0.000 claims abstract 6
- KZSNJWFQEVHDMF-BYPYZUCNSA-N L-valine Chemical compound CC(C)[C@H](N)C(O)=O KZSNJWFQEVHDMF-BYPYZUCNSA-N 0.000 claims abstract 6
- ONIBWKKTOPOVIA-BYPYZUCNSA-N L-Proline Chemical compound OC(=O)[C@@H]1CCCN1 ONIBWKKTOPOVIA-BYPYZUCNSA-N 0.000 claims abstract 5
- ODKSFYDXXFIFQN-BYPYZUCNSA-N L-arginine Chemical compound OC(=O)[C@@H](N)CCCN=C(N)N ODKSFYDXXFIFQN-BYPYZUCNSA-N 0.000 claims abstract 5
- 229930064664 L-arginine Natural products 0.000 claims abstract 5
- 235000014852 L-arginine Nutrition 0.000 claims abstract 5
- ZDXPYRJPNDTMRX-VKHMYHEASA-N L-glutamine Chemical compound OC(=O)[C@@H](N)CCC(N)=O ZDXPYRJPNDTMRX-VKHMYHEASA-N 0.000 claims abstract 5
- 229930182816 L-glutamine Natural products 0.000 claims abstract 5
- AHLPHDHHMVZTML-UHFFFAOYSA-N Orn-delta-NH2 Natural products NCCCC(N)C(O)=O AHLPHDHHMVZTML-UHFFFAOYSA-N 0.000 claims abstract 5
- 229960002173 citrulline Drugs 0.000 claims abstract 5
- 229960002743 glutamine Drugs 0.000 claims abstract 5
- 229960003104 ornithine Drugs 0.000 claims abstract 5
- 230000001771 impaired effect Effects 0.000 claims abstract 4
- QDGAVODICPCDMU-UHFFFAOYSA-N 2-amino-3-[3-[bis(2-chloroethyl)amino]phenyl]propanoic acid Chemical compound OC(=O)C(N)CC1=CC=CC(N(CCCl)CCCl)=C1 QDGAVODICPCDMU-UHFFFAOYSA-N 0.000 claims abstract 3
- CKLJMWTZIZZHCS-UHFFFAOYSA-N D-OH-Asp Natural products OC(=O)C(N)CC(O)=O CKLJMWTZIZZHCS-UHFFFAOYSA-N 0.000 claims abstract 3
- QNAYBMKLOCPYGJ-UHFFFAOYSA-N D-alpha-Ala Natural products CC([NH3+])C([O-])=O QNAYBMKLOCPYGJ-UHFFFAOYSA-N 0.000 claims abstract 3
- 239000004471 Glycine Substances 0.000 claims abstract 3
- QNAYBMKLOCPYGJ-UWTATZPHSA-N L-Alanine Natural products C[C@@H](N)C(O)=O QNAYBMKLOCPYGJ-UWTATZPHSA-N 0.000 claims abstract 3
- CKLJMWTZIZZHCS-UWTATZPHSA-N L-Aspartic acid Natural products OC(=O)[C@H](N)CC(O)=O CKLJMWTZIZZHCS-UWTATZPHSA-N 0.000 claims abstract 3
- FFEARJCKVFRZRR-UHFFFAOYSA-N L-Methionine Natural products CSCCC(N)C(O)=O FFEARJCKVFRZRR-UHFFFAOYSA-N 0.000 claims abstract 3
- QNAYBMKLOCPYGJ-REOHCLBHSA-N L-alanine Chemical compound C[C@H](N)C(O)=O QNAYBMKLOCPYGJ-REOHCLBHSA-N 0.000 claims abstract 3
- CKLJMWTZIZZHCS-REOHCLBHSA-N L-aspartic acid Chemical compound OC(=O)[C@@H](N)CC(O)=O CKLJMWTZIZZHCS-REOHCLBHSA-N 0.000 claims abstract 3
- AGPKZVBTJJNPAG-WHFBIAKZSA-N L-isoleucine Chemical compound CC[C@H](C)[C@H](N)C(O)=O AGPKZVBTJJNPAG-WHFBIAKZSA-N 0.000 claims abstract 3
- 229930182844 L-isoleucine Natural products 0.000 claims abstract 3
- 239000004395 L-leucine Substances 0.000 claims abstract 3
- 235000019454 L-leucine Nutrition 0.000 claims abstract 3
- FFEARJCKVFRZRR-BYPYZUCNSA-N L-methionine Chemical compound CSCC[C@H](N)C(O)=O FFEARJCKVFRZRR-BYPYZUCNSA-N 0.000 claims abstract 3
- 229930195722 L-methionine Natural products 0.000 claims abstract 3
- 229930182821 L-proline Natural products 0.000 claims abstract 3
- 239000004473 Threonine Substances 0.000 claims abstract 3
- 229960003767 alanine Drugs 0.000 claims abstract 3
- 229960001230 asparagine Drugs 0.000 claims abstract 3
- 229960005261 aspartic acid Drugs 0.000 claims abstract 3
- 229960002989 glutamic acid Drugs 0.000 claims abstract 3
- 229960002449 glycine Drugs 0.000 claims abstract 3
- 229960002885 histidine Drugs 0.000 claims abstract 3
- 229960000310 isoleucine Drugs 0.000 claims abstract 3
- 229960003136 leucine Drugs 0.000 claims abstract 3
- 229960004452 methionine Drugs 0.000 claims abstract 3
- 229960002429 proline Drugs 0.000 claims abstract 3
- 229960001153 serine Drugs 0.000 claims abstract 3
- IFGCUJZIWBUILZ-UHFFFAOYSA-N sodium 2-[[2-[[hydroxy-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyphosphoryl]amino]-4-methylpentanoyl]amino]-3-(1H-indol-3-yl)propanoic acid Chemical compound [Na+].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 IFGCUJZIWBUILZ-UHFFFAOYSA-N 0.000 claims abstract 3
- WPLOVIFNBMNBPD-ATHMIXSHSA-N subtilin Chemical compound CC1SCC(NC2=O)C(=O)NC(CC(N)=O)C(=O)NC(C(=O)NC(CCCCN)C(=O)NC(C(C)CC)C(=O)NC(=C)C(=O)NC(CCCCN)C(O)=O)CSC(C)C2NC(=O)C(CC(C)C)NC(=O)C1NC(=O)C(CCC(N)=O)NC(=O)C(CC(C)C)NC(=O)C(NC(=O)C1NC(=O)C(=C/C)/NC(=O)C(CCC(N)=O)NC(=O)C(CC(C)C)NC(=O)C(C)NC(=O)CNC(=O)C(NC(=O)C(NC(=O)C2NC(=O)CNC(=O)C3CCCN3C(=O)C(NC(=O)C3NC(=O)C(CC(C)C)NC(=O)C(=C)NC(=O)C(CCC(O)=O)NC(=O)C(NC(=O)C(CCCCN)NC(=O)C(N)CC=4C5=CC=CC=C5NC=4)CSC3)C(C)SC2)C(C)C)C(C)SC1)CC1=CC=CC=C1 WPLOVIFNBMNBPD-ATHMIXSHSA-N 0.000 claims abstract 3
- 229960002898 threonine Drugs 0.000 claims abstract 3
- 229960004441 tyrosine Drugs 0.000 claims abstract 3
- 229960004295 valine Drugs 0.000 claims abstract 3
- 241000588722 Escherichia Species 0.000 claims abstract 2
- 241000588724 Escherichia coli Species 0.000 claims abstract 2
- 241000520272 Pantoea Species 0.000 claims abstract 2
- 241000588696 Pantoea ananatis Species 0.000 claims abstract 2
- 230000002779 inactivation Effects 0.000 claims abstract 2
- 230000003313 weakening effect Effects 0.000 claims abstract 2
- 101150091587 znuA gene Proteins 0.000 claims abstract 2
- 101150036585 znuB gene Proteins 0.000 claims abstract 2
- 101150097224 znuC gene Proteins 0.000 claims abstract 2
- 239000012531 culture fluid Substances 0.000 claims 4
- 238000000034 method Methods 0.000 claims 3
- 150000003839 salts Chemical class 0.000 claims 3
- -1 L-cysteine, L-glutamic acids Chemical class 0.000 claims 2
- 229940049906 glutamate Drugs 0.000 claims 2
- 229930195712 glutamate Natural products 0.000 claims 2
- 238000009825 accumulation Methods 0.000 claims 1
- 235000015097 nutrients Nutrition 0.000 claims 1
- PWKSKIMOESPYIA-UHFFFAOYSA-N 2-acetamido-3-sulfanylpropanoic acid Chemical compound CC(=O)NC(CS)C(O)=O PWKSKIMOESPYIA-UHFFFAOYSA-N 0.000 abstract 1
Classifications
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- 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
- C12P13/00—Preparation of nitrogen-containing organic compounds
- C12P13/04—Alpha- or beta- amino acids
-
- 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
- C12P13/00—Preparation of nitrogen-containing organic compounds
- C12P13/04—Alpha- or beta- amino acids
- C12P13/10—Citrulline; Arginine; Ornithine
-
- 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
- C12P13/00—Preparation of nitrogen-containing organic compounds
- C12P13/04—Alpha- or beta- amino acids
- C12P13/14—Glutamic acid; Glutamine
-
- 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
- C12P13/00—Preparation of nitrogen-containing organic compounds
- C12P13/04—Alpha- or beta- amino acids
- C12P13/24—Proline; Hydroxyproline; Histidine
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- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Zoology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Microbiology (AREA)
- General Chemical & Material Sciences (AREA)
- Biotechnology (AREA)
- Health & Medical Sciences (AREA)
- Biochemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
Abstract
1. Бактерия-продуцент L-аминокислоты семейства Enterobacteriaceae, отличающаяся тем, что указанная бактерия модифицирована таким образом, что экспрессия, по меньшей мере, одного из генов кластера генов znuACB нарушена.2. Бактерия по п.1, отличающаяся тем, что указанная бактерия принадлежит к роду Escherichia.3. Бактерия по п.2, отличающаяся тем, что указанная бактерия есть Escherichia coli.4. Бактерия по п.1, отличающаяся тем, что указанная бактерия принадлежит к роду Pantoea.5. Бактерия по п.4, отличающаяся тем, что указанная бактерия есть Pantoea ananatis.6. Бактерия по п.1, отличающаяся тем, что указанная экспрессия, по меньшей мере, одного из генов кластера генов znuACB нарушена за счет инактивации, по меньшей мере, одного из генов кластера генов znuACB.7. Бактерия по п.6, отличающаяся тем, что указанный, по меньшей мере, один из генов кластера генов znuACB делегирован.8. Бактерия по п.1, отличающаяся тем, что указанная экспрессия, по меньшей мере, одного из генов кластера генов znuACB нарушена за счет ослабления экспрессии, по меньшей мере, одного из генов кластера генов znuACB.9. Бактерия по п.1, отличающаяся тем, что указанный кластер генов znuACB делегирован.10. Бактерия по п.1 или пп.6-9, отличающаяся тем, что указанные гены кластера генов znuACB выбраны из группы, состоящей из генов znuA, znuB и znuC.11. Бактерия по п.1, отличающаяся тем, что указанная L-аминокислота выбрана из группы, состоящей из L-аланина, L-аргинина, L-аспарагина, L-аспарагиновой кислоты, L-цитруллина, L-цистеина, L-глутаминовой кислоты, L-глутамина, глицина, L-гистидина, L-изолейцина, L-лейцина, L-лизина, L-метионина, L-орнитина, L-фенилаланина, L-пролина, L-серина, L-треонина, L-триптофана, L-тирозина и L-валина.12. Бактерия по п.11, отличающаяся те1. A bacterium producing L-amino acids of the Enterobacteriaceae family, characterized in that said bacterium is modified in such a way that expression of at least one of the genes of the znuACB gene cluster is impaired. The bacterium according to claim 1, characterized in that said bacterium belongs to the genus Escherichia. The bacterium according to claim 2, characterized in that said bacterium is Escherichia coli. 4. The bacterium according to claim 1, characterized in that said bacterium belongs to the genus Pantoea. The bacterium according to claim 4, characterized in that said bacterium is Pantoea ananatis. 6. The bacterium according to claim 1, characterized in that said expression of at least one of the genes of the znuACB gene cluster is violated by inactivation of at least one of the genes of the znuACB gene cluster. The bacterium according to claim 6, characterized in that said at least one of the genes of the znuACB gene cluster is delegated. The bacterium according to claim 1, characterized in that said expression of at least one of the genes of the znuACB gene cluster is impaired by weakening the expression of at least one of the genes of the znuACB gene cluster. The bacterium according to claim 1, characterized in that said znuACB gene cluster is delegated. The bacterium according to claim 1 or claims 6 to 9, characterized in that said genes of the znuACB gene cluster are selected from the group consisting of znuA, znuB and znuC genes. The bacterium according to claim 1, characterized in that said L-amino acid is selected from the group consisting of L-alanine, L-arginine, L-asparagine, L-aspartic acid, L-citrulline, L-cysteine, L-glutamic acid, L-glutamine, glycine, L-histidine, L-isoleucine, L-leucine, L-lysine, L-methionine, L-ornithine, L-phenylalanine, L-proline, L-serine, L-threonine, L-tryptophan, L-tyrosine and L-valine. 12. The bacterium according to claim 11, characterized in
Claims (15)
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| RU2013140115/10A RU2013140115A (en) | 2013-08-30 | 2013-08-30 | METHOD FOR PRODUCING L-AMINO ACIDS USING THE BACTERIA OF THE Enterobacteriaceae FAMILY IN WHICH THE EXPRESSION OF THE znuACB GENERAL CLUSTER IS DISORDERED |
| PCT/JP2014/072346 WO2015030019A1 (en) | 2013-08-30 | 2014-08-20 | A METHOD FOR PRODUCING AN L-AMINO ACID USING A BACTERIUM OF THE FAMILY ENTEROBACTERIACEAE HAVING ATTENUATED EXPRESSION OF THE znuACB GENE CLUSTER |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| RU2013140115/10A RU2013140115A (en) | 2013-08-30 | 2013-08-30 | METHOD FOR PRODUCING L-AMINO ACIDS USING THE BACTERIA OF THE Enterobacteriaceae FAMILY IN WHICH THE EXPRESSION OF THE znuACB GENERAL CLUSTER IS DISORDERED |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| RU2013140115A true RU2013140115A (en) | 2015-03-10 |
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| RU2013140115/10A RU2013140115A (en) | 2013-08-30 | 2013-08-30 | METHOD FOR PRODUCING L-AMINO ACIDS USING THE BACTERIA OF THE Enterobacteriaceae FAMILY IN WHICH THE EXPRESSION OF THE znuACB GENERAL CLUSTER IS DISORDERED |
Country Status (2)
| Country | Link |
|---|---|
| RU (1) | RU2013140115A (en) |
| WO (1) | WO2015030019A1 (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP7491312B2 (en) | 2018-12-27 | 2024-05-28 | 味の素株式会社 | Method for producing basic L-amino acids or their salts by fermentation of bacteria belonging to the Enterobacteriaceae family |
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| SU875663A1 (en) | 1978-06-30 | 1982-09-15 | Всесоюзный научно-исследовательский институт генетики и селекции промышленных микроорганизмов | Strains e. coli vniigenetika voltage 334 ru no.6 and vniigenetika voltage 334 no.7 producersof l-treonite and method for preparing them |
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| JPS565099A (en) | 1979-06-25 | 1981-01-20 | Ajinomoto Co Inc | Production of l-histidine through fermentation process and microorganism used therefor |
| JPS5618596A (en) | 1979-07-23 | 1981-02-21 | Ajinomoto Co Inc | Production of l-lysine through fermentation process |
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-
2013
- 2013-08-30 RU RU2013140115/10A patent/RU2013140115A/en not_active Application Discontinuation
-
2014
- 2014-08-20 WO PCT/JP2014/072346 patent/WO2015030019A1/en not_active Ceased
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| WO2015030019A1 (en) | 2015-03-05 |
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