AU2002347652A8 - Process for the preparation of an enantiomerically enriched a-amino acid - Google Patents
Process for the preparation of an enantiomerically enriched a-amino acidInfo
- Publication number
- AU2002347652A8 AU2002347652A8 AU2002347652A AU2002347652A AU2002347652A8 AU 2002347652 A8 AU2002347652 A8 AU 2002347652A8 AU 2002347652 A AU2002347652 A AU 2002347652A AU 2002347652 A AU2002347652 A AU 2002347652A AU 2002347652 A8 AU2002347652 A8 AU 2002347652A8
- Authority
- AU
- Australia
- Prior art keywords
- preparation
- amino acid
- enantiomerically enriched
- enantiomerically
- enriched
- 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.)
- Abandoned
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
- C12P13/08—Lysine; Diaminopimelic acid; Threonine; Valine
-
- 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
- C12P13/06—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
- C12P13/12—Methionine; Cysteine; Cystine
-
- 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
- C12P13/22—Tryptophan; Tyrosine; Phenylalanine; 3,4-Dihydroxyphenylalanine
- C12P13/222—Phenylalanine
-
- 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
- C12P41/00—Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture
- C12P41/006—Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture by reactions involving C-N bonds, e.g. nitriles, amides, hydantoins, carbamates, lactames, transamination reactions, or keto group formation from racemic mixtures
- C12P41/009—Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture by reactions involving C-N bonds, e.g. nitriles, amides, hydantoins, carbamates, lactames, transamination reactions, or keto group formation from racemic mixtures by reactions involving hydantoins or carbamoylamino compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (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)
- Analytical Chemistry (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Enzymes And Modification Thereof (AREA)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
NL1019416 | 2001-11-23 | ||
NL1019416A NL1019416C2 (en) | 2001-11-23 | 2001-11-23 | Process for preparing an enantiomerically enriched α-amino acid. |
PCT/NL2002/000758 WO2003044206A2 (en) | 2001-11-23 | 2002-11-22 | Process for the preparation of an enantiomerically enriched a-amino acid |
Publications (2)
Publication Number | Publication Date |
---|---|
AU2002347652A1 AU2002347652A1 (en) | 2003-06-10 |
AU2002347652A8 true AU2002347652A8 (en) | 2003-06-10 |
Family
ID=19774336
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AU2002347652A Abandoned AU2002347652A1 (en) | 2001-11-23 | 2002-11-22 | Process for the preparation of an enantiomerically enriched a-amino acid |
Country Status (6)
Country | Link |
---|---|
EP (1) | EP1446492A2 (en) |
JP (1) | JP2005509439A (en) |
CN (1) | CN1592789A (en) |
AU (1) | AU2002347652A1 (en) |
NL (1) | NL1019416C2 (en) |
WO (1) | WO2003044206A2 (en) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1928103B (en) * | 2006-08-30 | 2010-09-01 | 石家庄中天生物技术有限责任公司 | Method of producing D-p-hydroxy-phenyl glycine by heterogeneous enzyme catalysis method |
CN106676157A (en) * | 2017-02-20 | 2017-05-17 | 南华大学 | Application of legionella thalli in preparing amino acid profile transformation agent |
CN110714035A (en) * | 2019-11-15 | 2020-01-21 | 江南大学 | Method for preparing D-aliphatic amino acid by cascade reaction |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
IT1209495B (en) * | 1984-02-02 | 1989-08-30 | A San Donato Milanese Milano | PROCEDURE FOR THE PREPARATION OF L-ALPHA-AMINO ACIDS. |
DE4316928C2 (en) * | 1993-05-19 | 1995-03-16 | Degussa | New microorganisms, their use and process for the production of L-alpha-amino acids |
DE19519717C1 (en) * | 1995-05-30 | 1996-08-22 | Degussa | New microorganism DSM 9771 for prepn of L-alpha-amino acids |
IT1276163B1 (en) * | 1995-11-23 | 1997-10-27 | Eniricerche Spa | IMPROVED PROCEDURE FOR THE PREPARATION OF D-ALPHA-AMINO ACIDS |
NL1017250C1 (en) * | 2001-01-31 | 2002-08-01 | Dsm Nv | Process for the preparation of enantiomerically enriched amino acids. |
-
2001
- 2001-11-23 NL NL1019416A patent/NL1019416C2/en not_active IP Right Cessation
-
2002
- 2002-11-22 CN CN 02823310 patent/CN1592789A/en active Pending
- 2002-11-22 EP EP02783830A patent/EP1446492A2/en not_active Withdrawn
- 2002-11-22 AU AU2002347652A patent/AU2002347652A1/en not_active Abandoned
- 2002-11-22 JP JP2003545827A patent/JP2005509439A/en active Pending
- 2002-11-22 WO PCT/NL2002/000758 patent/WO2003044206A2/en active Application Filing
Also Published As
Publication number | Publication date |
---|---|
NL1019416C2 (en) | 2003-06-02 |
WO2003044206A2 (en) | 2003-05-30 |
CN1592789A (en) | 2005-03-09 |
JP2005509439A (en) | 2005-04-14 |
WO2003044206A3 (en) | 2003-12-18 |
AU2002347652A1 (en) | 2003-06-10 |
EP1446492A2 (en) | 2004-08-18 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
MK6 | Application lapsed section 142(2)(f)/reg. 8.3(3) - pct applic. not entering national phase |