RU2010105710A - Mutant adenylate cyclase, the DNA encoding it, the bacterium of the family Enterobacteriaceae containing the indicated DNA, and the method of obtaining L-amino acids - Google Patents
Mutant adenylate cyclase, the DNA encoding it, the bacterium of the family Enterobacteriaceae containing the indicated DNA, and the method of obtaining L-amino acids Download PDFInfo
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- RU2010105710A RU2010105710A RU2010105710/10A RU2010105710A RU2010105710A RU 2010105710 A RU2010105710 A RU 2010105710A RU 2010105710/10 A RU2010105710/10 A RU 2010105710/10A RU 2010105710 A RU2010105710 A RU 2010105710A RU 2010105710 A RU2010105710 A RU 2010105710A
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- adenylate cyclase
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- 241000894006 Bacteria Species 0.000 title claims abstract 17
- 150000008575 L-amino acids Chemical class 0.000 title claims abstract 9
- 102000030621 adenylate cyclase Human genes 0.000 title claims abstract 9
- 108060000200 adenylate cyclase Proteins 0.000 title claims abstract 9
- 238000000034 method Methods 0.000 title claims abstract 7
- 241000588921 Enterobacteriaceae Species 0.000 title claims abstract 3
- KDXKERNSBIXSRK-YFKPBYRVSA-N L-lysine Chemical compound NCCCC[C@H](N)C(O)=O KDXKERNSBIXSRK-YFKPBYRVSA-N 0.000 claims abstract 8
- -1 aromatic L-amino acid Chemical class 0.000 claims abstract 8
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims abstract 6
- MTCFGRXMJLQNBG-REOHCLBHSA-N (2S)-2-Amino-3-hydroxypropansäure Chemical compound OC[C@H](N)C(O)=O MTCFGRXMJLQNBG-REOHCLBHSA-N 0.000 claims abstract 4
- FWMNVWWHGCHHJJ-SKKKGAJSSA-N 4-amino-1-[(2r)-6-amino-2-[[(2r)-2-[[(2r)-2-[[(2r)-2-amino-3-phenylpropanoyl]amino]-3-phenylpropanoyl]amino]-4-methylpentanoyl]amino]hexanoyl]piperidine-4-carboxylic acid Chemical group C([C@H](C(=O)N[C@H](CC(C)C)C(=O)N[C@H](CCCCN)C(=O)N1CCC(N)(CC1)C(O)=O)NC(=O)[C@H](N)CC=1C=CC=CC=1)C1=CC=CC=C1 FWMNVWWHGCHHJJ-SKKKGAJSSA-N 0.000 claims abstract 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract 4
- 235000019766 L-Lysine Nutrition 0.000 claims abstract 4
- DCXYFEDJOCDNAF-REOHCLBHSA-N L-asparagine Chemical compound OC(=O)[C@@H](N)CC(N)=O DCXYFEDJOCDNAF-REOHCLBHSA-N 0.000 claims abstract 4
- WHUUTDBJXJRKMK-VKHMYHEASA-N L-glutamic acid Chemical compound OC(=O)[C@@H](N)CCC(O)=O WHUUTDBJXJRKMK-VKHMYHEASA-N 0.000 claims abstract 4
- 229930182816 L-glutamine Natural products 0.000 claims abstract 4
- HNDVDQJCIGZPNO-YFKPBYRVSA-N L-histidine Chemical compound OC(=O)[C@@H](N)CC1=CN=CN1 HNDVDQJCIGZPNO-YFKPBYRVSA-N 0.000 claims abstract 4
- ROHFNLRQFUQHCH-YFKPBYRVSA-N L-leucine Chemical compound CC(C)C[C@H](N)C(O)=O ROHFNLRQFUQHCH-YFKPBYRVSA-N 0.000 claims abstract 4
- AYFVYJQAPQTCCC-GBXIJSLDSA-N L-threonine Chemical compound C[C@@H](O)[C@H](N)C(O)=O AYFVYJQAPQTCCC-GBXIJSLDSA-N 0.000 claims abstract 4
- QIVBCDIJIAJPQS-VIFPVBQESA-N L-tryptophane Chemical compound C1=CC=C2C(C[C@H](N)C(O)=O)=CNC2=C1 QIVBCDIJIAJPQS-VIFPVBQESA-N 0.000 claims abstract 4
- 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 4
- KZSNJWFQEVHDMF-BYPYZUCNSA-N L-valine Chemical compound CC(C)[C@H](N)C(O)=O KZSNJWFQEVHDMF-BYPYZUCNSA-N 0.000 claims abstract 4
- 239000004472 Lysine Substances 0.000 claims abstract 4
- 235000018102 proteins Nutrition 0.000 claims abstract 4
- 108090000623 proteins and genes Proteins 0.000 claims abstract 4
- 102000004169 proteins and genes Human genes 0.000 claims abstract 4
- PWKSKIMOESPYIA-UHFFFAOYSA-N 2-acetamido-3-sulfanylpropanoic acid Chemical compound CC(=O)NC(CS)C(O)=O PWKSKIMOESPYIA-UHFFFAOYSA-N 0.000 claims abstract 2
- 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 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract 2
- QNAYBMKLOCPYGJ-UHFFFAOYSA-N D-alpha-Ala Natural products CC([NH3+])C([O-])=O QNAYBMKLOCPYGJ-UHFFFAOYSA-N 0.000 claims abstract 2
- 241000588722 Escherichia Species 0.000 claims abstract 2
- 241000588724 Escherichia coli Species 0.000 claims abstract 2
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 claims abstract 2
- QNAYBMKLOCPYGJ-UWTATZPHSA-N L-Alanine Natural products C[C@@H](N)C(O)=O QNAYBMKLOCPYGJ-UWTATZPHSA-N 0.000 claims abstract 2
- FFEARJCKVFRZRR-UHFFFAOYSA-N L-Methionine Natural products CSCCC(N)C(O)=O FFEARJCKVFRZRR-UHFFFAOYSA-N 0.000 claims abstract 2
- ONIBWKKTOPOVIA-BYPYZUCNSA-N L-Proline Chemical compound OC(=O)[C@@H]1CCCN1 ONIBWKKTOPOVIA-BYPYZUCNSA-N 0.000 claims abstract 2
- QNAYBMKLOCPYGJ-REOHCLBHSA-N L-alanine Chemical compound C[C@H](N)C(O)=O QNAYBMKLOCPYGJ-REOHCLBHSA-N 0.000 claims abstract 2
- ODKSFYDXXFIFQN-BYPYZUCNSA-N L-arginine Chemical compound OC(=O)[C@@H](N)CCCN=C(N)N ODKSFYDXXFIFQN-BYPYZUCNSA-N 0.000 claims abstract 2
- 229930064664 L-arginine Natural products 0.000 claims abstract 2
- 235000014852 L-arginine Nutrition 0.000 claims abstract 2
- CKLJMWTZIZZHCS-REOHCLBHSA-N L-aspartic acid Chemical compound OC(=O)[C@@H](N)CC(O)=O CKLJMWTZIZZHCS-REOHCLBHSA-N 0.000 claims abstract 2
- ZDXPYRJPNDTMRX-VKHMYHEASA-N L-glutamine Chemical compound OC(=O)[C@@H](N)CCC(N)=O ZDXPYRJPNDTMRX-VKHMYHEASA-N 0.000 claims abstract 2
- 125000003338 L-glutaminyl group Chemical group O=C([*])[C@](N([H])[H])([H])C([H])([H])C([H])([H])C(=O)N([H])[H] 0.000 claims abstract 2
- AGPKZVBTJJNPAG-WHFBIAKZSA-N L-isoleucine Chemical compound CC[C@H](C)[C@H](N)C(O)=O AGPKZVBTJJNPAG-WHFBIAKZSA-N 0.000 claims abstract 2
- 229930182844 L-isoleucine Natural products 0.000 claims abstract 2
- 239000004395 L-leucine Substances 0.000 claims abstract 2
- 235000019454 L-leucine Nutrition 0.000 claims abstract 2
- FFEARJCKVFRZRR-BYPYZUCNSA-N L-methionine Chemical compound CSCC[C@H](N)C(O)=O FFEARJCKVFRZRR-BYPYZUCNSA-N 0.000 claims abstract 2
- 229930195722 L-methionine Natural products 0.000 claims abstract 2
- 229930182821 L-proline Natural products 0.000 claims abstract 2
- 239000004473 Threonine Substances 0.000 claims abstract 2
- 229960003767 alanine Drugs 0.000 claims abstract 2
- 125000000539 amino acid group Chemical group 0.000 claims abstract 2
- 229960001230 asparagine Drugs 0.000 claims abstract 2
- 229910052799 carbon Inorganic materials 0.000 claims abstract 2
- 239000012531 culture fluid Substances 0.000 claims abstract 2
- 229960002989 glutamic acid Drugs 0.000 claims abstract 2
- 229960002743 glutamine Drugs 0.000 claims abstract 2
- 229960002885 histidine Drugs 0.000 claims abstract 2
- 229960000310 isoleucine Drugs 0.000 claims abstract 2
- 229960003136 leucine Drugs 0.000 claims abstract 2
- 238000004519 manufacturing process Methods 0.000 claims abstract 2
- 229960004452 methionine Drugs 0.000 claims abstract 2
- 235000015097 nutrients Nutrition 0.000 claims abstract 2
- 229960002429 proline Drugs 0.000 claims abstract 2
- 229960001153 serine Drugs 0.000 claims abstract 2
- 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 2
- 229960002898 threonine Drugs 0.000 claims abstract 2
- 229960004799 tryptophan Drugs 0.000 claims abstract 2
- 229960004441 tyrosine Drugs 0.000 claims abstract 2
- 229960004295 valine Drugs 0.000 claims abstract 2
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
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
- C12N9/88—Lyases (4.)
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Y—ENZYMES
- C12Y406/00—Phosphorus-oxygen lyases (4.6)
- C12Y406/01—Phosphorus-oxygen lyases (4.6.1)
- C12Y406/01001—Aodenylate cyclase (4.6.1.1)
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- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Zoology (AREA)
- Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Genetics & Genomics (AREA)
- General Health & Medical Sciences (AREA)
- General Engineering & Computer Science (AREA)
- Biochemistry (AREA)
- Biotechnology (AREA)
- Microbiology (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Molecular Biology (AREA)
- Biomedical Technology (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
Abstract
1. Мутантная аденилатциклаза, выбранная из группы, состоящей из: ! (A) белка, в котором L-лизин в положении, соответствующем положению 432 в SEQ ID NO: 2, замещен другим аминокислотным остатком; и ! (B) варианта белка (А), обладающего аденилатциклазной активностью. ! 2. Мутантная аденилатциклаза по п.1, отличающаяся тем, что L-лизин в положении, соответствующем положению 432 в SEQ ID NO: 2, замещен L-глутамином. ! 3. ДНК, кодирующая аденилатциклазу по любому из пп.1 и 2. ! 4. Бактерия семейства Enterobacteriaceae, содержащая ДНК по п.3. ! 5. Бактерия по п.4, отличающаяся тем, что указанная бактерия способна к продукции L-аминокислот. ! 6. Бактерия по п.4, отличающаяся тем, что указанная бактерия принадлежит к роду Escherichia. ! 7. Бактерия по п.6, отличающаяся тем, что указанной бактерией является бактерия Escherichia coli. ! 8. Способ получения L-аминокислоты, включающий выращивание бактерии по любому из пп.5-7 в питательной среде, содержащей в качестве единственного источника углерода этанол или глицерин, и выделение указанной L-аминокислоты из культуральной жидкости. ! 9. Способ по п.8, отличающийся тем, что указанная L-аминокислота выбрана из группы, состоящей из ароматической L-аминокислоты и неароматической L-аминокислоты. ! 10. Способ по п.9, отличающийся тем, что указанная ароматическая L-аминокислота выбрана из группы, состоящей из L-фенилаланина, L-тирозина и L-триптофана. ! 11. Способ по п.9, отличающийся тем, что указанная неароматическая L-аминокислота выбрана из группы, состоящей из L-треонина, L-лизина, L-цистеина, L-метионина, L-лейцина, L-изолейцина, L-валина, L-гистидина, L-глицина, L-серина, L-аланина, L-аспарагина, L-аспартата, L-глутамина, L-глутаминовой кислоты, L-пролина и L-аргини 1. Mutant adenylate cyclase selected from the group consisting of:! (A) a protein in which L-lysine at the position corresponding to position 432 in SEQ ID NO: 2 is substituted with another amino acid residue; and! (B) a variant of the protein (A) having adenylate cyclase activity. ! 2. The mutant adenylate cyclase according to claim 1, characterized in that L-lysine at the position corresponding to position 432 in SEQ ID NO: 2 is substituted with L-glutamine. ! 3. DNA encoding adenylate cyclase according to any one of claims 1 and 2.! 4. A bacterium of the Enterobacteriaceae family containing DNA according to claim 3. ! 5. The bacterium according to claim 4, characterized in that said bacterium is capable of producing L-amino acids. ! 6. The bacterium according to claim 4, characterized in that said bacterium belongs to the genus Escherichia. ! 7. The bacterium according to claim 6, characterized in that said bacterium is Escherichia coli. ! 8. A method for producing an L-amino acid, comprising growing the bacterium according to any one of claims 5 to 7 in a nutrient medium containing ethanol or glycerol as the sole carbon source, and isolating said L-amino acid from the culture fluid. ! 9. The method of claim 8, wherein said L-amino acid is selected from the group consisting of an aromatic L-amino acid and a non-aromatic L-amino acid. ! 10. The method according to claim 9, characterized in that said aromatic L-amino acid is selected from the group consisting of L-phenylalanine, L-tyrosine and L-tryptophan. ! 11. The method according to claim 9, characterized in that said non-aromatic L-amino acid is selected from the group consisting of L-threonine, L-lysine, L-cysteine, L-methionine, L-leucine, L-isoleucine, L-valine , L-histidine, L-glycine, L-serine, L-alanine, L-asparagine, L-aspartate, L-glutamine, L-glutamic acid, L-proline and L-arginine
Claims (11)
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| RU2010105710/10A RU2471868C2 (en) | 2010-02-18 | 2010-02-18 | Mutant adenylate cyclase, dna coding it, bacteria of enterobacteriaceae family containing said dan and method for preparing l-amino acids |
| PCT/JP2011/052967 WO2011102305A2 (en) | 2010-02-18 | 2011-02-04 | A METHOD FOR PRODUCING AN L-AMINO ACID USING A BACTERIUM OF THE Enterobacteriaceae FAMILY HAVING A MUTANT ADENYLATE CYCLASE |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| RU2010105710/10A RU2471868C2 (en) | 2010-02-18 | 2010-02-18 | Mutant adenylate cyclase, dna coding it, bacteria of enterobacteriaceae family containing said dan and method for preparing l-amino acids |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| RU2010105710A true RU2010105710A (en) | 2011-08-27 |
| RU2471868C2 RU2471868C2 (en) | 2013-01-10 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| RU2010105710/10A RU2471868C2 (en) | 2010-02-18 | 2010-02-18 | Mutant adenylate cyclase, dna coding it, bacteria of enterobacteriaceae family containing said dan and method for preparing l-amino acids |
Country Status (2)
| Country | Link |
|---|---|
| RU (1) | RU2471868C2 (en) |
| WO (1) | WO2011102305A2 (en) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR101996767B1 (en) * | 2018-11-29 | 2019-07-04 | 씨제이제일제당 (주) | cAMP receptor protein variant and method for producing L-amino acid using the same |
| KR101991206B1 (en) * | 2018-11-29 | 2019-06-19 | 씨제이제일제당 (주) | cAMP receptor protein variant and method for producing L-amino acid using the same |
| JP7793519B2 (en) | 2019-12-19 | 2026-01-05 | ビーエーエスエフ ソシエタス・ヨーロピア | Increased space-time yield, carbon conversion efficiency, and carbon substrate adaptability in producing fine chemicals |
| EP4370653A2 (en) | 2021-07-16 | 2024-05-22 | Biosyntia ApS | Microbial cell factories producing vitamin b compounds |
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-
2010
- 2010-02-18 RU RU2010105710/10A patent/RU2471868C2/en active
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2011
- 2011-02-04 WO PCT/JP2011/052967 patent/WO2011102305A2/en not_active Ceased
Also Published As
| Publication number | Publication date |
|---|---|
| WO2011102305A2 (en) | 2011-08-25 |
| WO2011102305A3 (en) | 2015-07-09 |
| RU2471868C2 (en) | 2013-01-10 |
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