FR2217296A1 - Organic cpds. prepn. by co-enzymatic reduction - with continuous regeneration of the oxidised coenzyme with a reducing agent - Google Patents
Organic cpds. prepn. by co-enzymatic reduction - with continuous regeneration of the oxidised coenzyme with a reducing agentInfo
- Publication number
- FR2217296A1 FR2217296A1 FR7235901A FR7235901A FR2217296A1 FR 2217296 A1 FR2217296 A1 FR 2217296A1 FR 7235901 A FR7235901 A FR 7235901A FR 7235901 A FR7235901 A FR 7235901A FR 2217296 A1 FR2217296 A1 FR 2217296A1
- Authority
- FR
- France
- Prior art keywords
- acid
- prepn
- imine
- reducing agent
- aldehyde
- 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.)
- Granted
Links
Classifications
-
- 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
- C12P1/00—Preparation of compounds or compositions, not provided for in groups C12P3/00 - C12P39/00, by using microorganisms or enzymes
-
- 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
- C12P13/06—Alanine; Leucine; Isoleucine; Serine; Homoserine
-
- 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
- C12P7/00—Preparation of oxygen-containing organic compounds
- C12P7/40—Preparation of oxygen-containing organic compounds containing a carboxyl group including Peroxycarboxylic acids
- C12P7/56—Lactic acid
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Zoology (AREA)
- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Biotechnology (AREA)
- Microbiology (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Biochemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Mycology (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
Abstract
The matls. reduced contain aldehyde, ketone, acid, imine, quinone, quinone-imine, hydroxy acid, hydroxy aldehyde gps., and are reduced by an enzyme and a coreactor (I) (coenzyme) which is regenerated by redn. with cpd. (II) contg. alcohol, aldehyde, acid, imine, thiol functions. (I) is nicotinamide adenin dinucleotide (phosphate) or flavin adenin dinucleotide. (II) is an alcohol (ethanol) in presence of ethanol dehydrogenase. pH of reaction mixt. is 8.0-9.0, reaction temp. is room temp. -40 degrees C. The process is used for reductive amination of alpha-ketoglutaric acid or pyruvic acid, or reductive carboxylation of amino acetone.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR7235901A FR2217296A1 (en) | 1972-10-10 | 1972-10-10 | Organic cpds. prepn. by co-enzymatic reduction - with continuous regeneration of the oxidised coenzyme with a reducing agent |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR7235901A FR2217296A1 (en) | 1972-10-10 | 1972-10-10 | Organic cpds. prepn. by co-enzymatic reduction - with continuous regeneration of the oxidised coenzyme with a reducing agent |
Publications (2)
Publication Number | Publication Date |
---|---|
FR2217296A1 true FR2217296A1 (en) | 1974-09-06 |
FR2217296B1 FR2217296B1 (en) | 1975-03-28 |
Family
ID=9105450
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
FR7235901A Granted FR2217296A1 (en) | 1972-10-10 | 1972-10-10 | Organic cpds. prepn. by co-enzymatic reduction - with continuous regeneration of the oxidised coenzyme with a reducing agent |
Country Status (1)
Country | Link |
---|---|
FR (1) | FR2217296A1 (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0023346A2 (en) * | 1979-07-25 | 1981-02-04 | Degussa Aktiengesellschaft | Process for the continuous enzymatic transformation of water-soluble alpha-keto carbonic acids into the corresponding amino acids |
EP0024547A2 (en) * | 1979-07-25 | 1981-03-11 | Degussa Aktiengesellschaft | Process for the continuous enzymatic transformation of water-soluble alpha-keto carbonic acids into the corresponding alpha-hydroxy carbonic acids |
EP0034213A1 (en) * | 1980-02-13 | 1981-08-26 | Ivan Endre Modrovich | A stabilized aqueous coenzyme solution for use in a clinical assay, a method of stabilizing a labile coenzyme in an aqueous clinical assay solution and a kit for use in said clinical assay |
EP0118750A2 (en) * | 1983-02-09 | 1984-09-19 | Phillips Petroleum Company | Regeneration of NAD(P) cofactor |
FR2583432A1 (en) * | 1985-06-13 | 1986-12-19 | Inst Francais Du Petrole | PROCESS FOR THE ENZYMATIC PRODUCTION OF L-A-AMINO ACIDS FROM A-KETOACIDES |
EP0215414A2 (en) * | 1985-09-09 | 1987-03-25 | Kuraray Co., Ltd. | Process for producing L-phenylalanine |
-
1972
- 1972-10-10 FR FR7235901A patent/FR2217296A1/en active Granted
Non-Patent Citations (1)
Title |
---|
NEANT * |
Cited By (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0023346A2 (en) * | 1979-07-25 | 1981-02-04 | Degussa Aktiengesellschaft | Process for the continuous enzymatic transformation of water-soluble alpha-keto carbonic acids into the corresponding amino acids |
EP0024547A2 (en) * | 1979-07-25 | 1981-03-11 | Degussa Aktiengesellschaft | Process for the continuous enzymatic transformation of water-soluble alpha-keto carbonic acids into the corresponding alpha-hydroxy carbonic acids |
EP0024547A3 (en) * | 1979-07-25 | 1981-05-06 | Degussa Aktiengesellschaft | Process for the continuous enzymatic transformation of water-soluble alpha-keto carbonic acids into the corresponding alpha-hydroxy carbonic acids |
EP0023346A3 (en) * | 1979-07-25 | 1981-05-13 | Degussa Aktiengesellschaft | Process for the continuous enzymatic transformation of water-soluble alpha-keto carbonic acids into the corresponding amino acids |
EP0034213A1 (en) * | 1980-02-13 | 1981-08-26 | Ivan Endre Modrovich | A stabilized aqueous coenzyme solution for use in a clinical assay, a method of stabilizing a labile coenzyme in an aqueous clinical assay solution and a kit for use in said clinical assay |
EP0118750A3 (en) * | 1983-02-09 | 1986-02-05 | Phillips Petroleum Company | Regeneration of nad(p) cofactor |
EP0118750A2 (en) * | 1983-02-09 | 1984-09-19 | Phillips Petroleum Company | Regeneration of NAD(P) cofactor |
FR2583432A1 (en) * | 1985-06-13 | 1986-12-19 | Inst Francais Du Petrole | PROCESS FOR THE ENZYMATIC PRODUCTION OF L-A-AMINO ACIDS FROM A-KETOACIDES |
EP0206904A2 (en) * | 1985-06-13 | 1986-12-30 | Institut Français du Pétrole | Process for the enzymatic production of L-alpha amino acids from alpha keto acids |
EP0206904A3 (en) * | 1985-06-13 | 1989-03-08 | Institut Francais Du Petrole | Process for the enzymatic production of l-alpha amino acids from alpha keto acids |
EP0215414A2 (en) * | 1985-09-09 | 1987-03-25 | Kuraray Co., Ltd. | Process for producing L-phenylalanine |
EP0215414A3 (en) * | 1985-09-09 | 1988-05-04 | Kuraray Co., Ltd. | Process for producing l-phenylalanine |
US5420023A (en) * | 1985-09-09 | 1995-05-30 | Kuraray Co., Ltd. | Process for producing L-phenylalanine |
Also Published As
Publication number | Publication date |
---|---|
FR2217296B1 (en) | 1975-03-28 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
ST | Notification of lapse |