AU9341298A - Method for producing cyclic alpha-amino acids free from enantiomers or their n-protected derivatives by means of d-specific aminoacylase - Google Patents

Method for producing cyclic alpha-amino acids free from enantiomers or their n-protected derivatives by means of d-specific aminoacylase

Info

Publication number
AU9341298A
AU9341298A AU93412/98A AU9341298A AU9341298A AU 9341298 A AU9341298 A AU 9341298A AU 93412/98 A AU93412/98 A AU 93412/98A AU 9341298 A AU9341298 A AU 9341298A AU 9341298 A AU9341298 A AU 9341298A
Authority
AU
Australia
Prior art keywords
enantiomers
amino acids
protected derivatives
producing cyclic
cyclic alpha
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
Application number
AU93412/98A
Inventor
Martin Sauter
Oleg Werbitzky
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Lonza AG
Original Assignee
Lonza AG
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Lonza AG filed Critical Lonza AG
Publication of AU9341298A publication Critical patent/AU9341298A/en
Abandoned legal-status Critical Current

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
    • 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
    • C12P13/00—Preparation of nitrogen-containing organic compounds
    • C12P13/04—Alpha- or beta- amino acids
    • C12P13/24—Proline; Hydroxyproline; Histidine
    • 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
    • C12P17/00—Preparation of heterocyclic carbon compounds with only O, N, S, Se or Te as ring hetero atoms
    • C12P17/10—Nitrogen as only ring hetero atom
    • 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
    • C12P17/00—Preparation of heterocyclic carbon compounds with only O, N, S, Se or Te as ring hetero atoms
    • C12P17/10—Nitrogen as only ring hetero atom
    • C12P17/12—Nitrogen as only ring hetero atom containing a six-membered hetero ring
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Zoology (AREA)
  • Wood Science & Technology (AREA)
  • Health & Medical Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Biotechnology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Health & Medical Sciences (AREA)
  • Microbiology (AREA)
  • Biochemistry (AREA)
  • General Engineering & Computer Science (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Analytical Chemistry (AREA)
  • Medicinal Chemistry (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • Virology (AREA)
  • Biomedical Technology (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
AU93412/98A 1997-08-11 1998-08-11 Method for producing cyclic alpha-amino acids free from enantiomers or their n-protected derivatives by means of d-specific aminoacylase Abandoned AU9341298A (en)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
CH188897 1997-08-11
CH1888/97 1997-08-11
CH286897 1997-12-12
CH2868/97 1997-12-12
PCT/EP1998/005087 WO1999007873A1 (en) 1997-08-11 1998-08-11 METHOD FOR PRODUCING CYCLIC α-AMINO ACIDS FREE FROM ENANTIOMERS OR THEIR N-PROTECTED DERIVATIVES BY MEANS OF A D-SPECIFIC AMINOACYLASE

Publications (1)

Publication Number Publication Date
AU9341298A true AU9341298A (en) 1999-03-01

Family

ID=25688929

Family Applications (1)

Application Number Title Priority Date Filing Date
AU93412/98A Abandoned AU9341298A (en) 1997-08-11 1998-08-11 Method for producing cyclic alpha-amino acids free from enantiomers or their n-protected derivatives by means of d-specific aminoacylase

Country Status (5)

Country Link
EP (1) EP1005563A1 (en)
JP (1) JP2002509441A (en)
AU (1) AU9341298A (en)
CA (1) CA2299324A1 (en)
WO (1) WO1999007873A1 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2825717B1 (en) * 2001-06-08 2005-02-18 Rhodia Chimie Sa STEREOSELECTIVE PREPARATION OF CYCLIC AMINO ACIDS

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3929570A1 (en) * 1989-09-06 1991-03-07 Degussa MICROBIOLOGICALLY MANUFACTURED N-ACYL-L-PROLIN-ACYLASE, METHOD FOR THEIR OBTAINMENT AND ITS USE
GB9321325D0 (en) * 1993-10-15 1993-12-08 Chiros Ltd Microorganism and its use
CA2150526C (en) * 1994-06-09 2005-11-15 Andreas Kiener Biotechnological process for the preparation of cyclic s-.alpha.-amino carboxylic acids and r-.alpha.-amino carboxamides
CN1213400A (en) * 1996-03-13 1999-04-07 隆萨股份公司 Process for producing N-protected D-proline derivatives

Also Published As

Publication number Publication date
WO1999007873A1 (en) 1999-02-18
JP2002509441A (en) 2002-03-26
CA2299324A1 (en) 1999-02-18
EP1005563A1 (en) 2000-06-07

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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