SK282099B6 - Mikroorganizmy a bezbunkové enzýmy zúžitkujúce n-chránený derivát prolínu a spôsob jeho výroby - Google Patents

Mikroorganizmy a bezbunkové enzýmy zúžitkujúce n-chránený derivát prolínu a spôsob jeho výroby Download PDF

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Publication number
SK282099B6
SK282099B6 SK1171-98A SK117198A SK282099B6 SK 282099 B6 SK282099 B6 SK 282099B6 SK 117198 A SK117198 A SK 117198A SK 282099 B6 SK282099 B6 SK 282099B6
Authority
SK
Slovakia
Prior art keywords
amino acid
proline
acid derivative
protected
formula
Prior art date
Application number
SK1171-98A
Other languages
English (en)
Slovak (sk)
Other versions
SK117198A3 (en
Inventor
Martin Sauter
Daniel Venetz
Fabienne Henzen
Diego Schmidhalter
Gabriela Pfaffen
Oleg Werbitzky
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 SK117198A3 publication Critical patent/SK117198A3/sk
Publication of SK282099B6 publication Critical patent/SK282099B6/sk

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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
    • 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
    • C12P41/007—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 acyl derivatives of racemic amines
    • 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
    • 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
    • C12N9/14—Hydrolases (3)
    • C12N9/78—Hydrolases (3) acting on carbon to nitrogen bonds other than peptide bonds (3.5)
    • C12N9/80—Hydrolases (3) acting on carbon to nitrogen bonds other than peptide bonds (3.5) acting on amide bonds in linear amides (3.5.1)
    • 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
    • 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)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Health & Medical Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Biotechnology (AREA)
  • General Health & Medical Sciences (AREA)
  • General Engineering & Computer Science (AREA)
  • Microbiology (AREA)
  • Biochemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Biomedical Technology (AREA)
  • Analytical Chemistry (AREA)
  • Molecular Biology (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • Virology (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Enzymes And Modification Thereof (AREA)
  • Micro-Organisms Or Cultivation Processes Thereof (AREA)
  • Pyrrole Compounds (AREA)
SK1171-98A 1996-03-13 1997-03-12 Mikroorganizmy a bezbunkové enzýmy zúžitkujúce n-chránený derivát prolínu a spôsob jeho výroby SK282099B6 (sk)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CH65696 1996-03-13
PCT/EP1997/001262 WO1997033987A1 (de) 1996-03-13 1997-03-12 Verfahren zur herstellung von n-geschützten d-prolinderivaten

Publications (2)

Publication Number Publication Date
SK117198A3 SK117198A3 (en) 1999-03-12
SK282099B6 true SK282099B6 (sk) 2001-11-06

Family

ID=4192092

Family Applications (1)

Application Number Title Priority Date Filing Date
SK1171-98A SK282099B6 (sk) 1996-03-13 1997-03-12 Mikroorganizmy a bezbunkové enzýmy zúžitkujúce n-chránený derivát prolínu a spôsob jeho výroby

Country Status (12)

Country Link
US (1) US20020037559A1 (ko)
EP (1) EP0896617A1 (ko)
JP (1) JP2000506728A (ko)
KR (1) KR19990087341A (ko)
CN (1) CN1213400A (ko)
AU (1) AU2155797A (ko)
CA (1) CA2245543A1 (ko)
CZ (1) CZ281198A3 (ko)
NO (1) NO984206D0 (ko)
PL (1) PL328795A1 (ko)
SK (1) SK282099B6 (ko)
WO (1) WO1997033987A1 (ko)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2001506500A (ja) * 1996-12-16 2001-05-22 ロンザ アーゲー Ｄ−プロリン誘導体を調製する方法
JP2002509441A (ja) * 1997-08-11 2002-03-26 ロンザ アーゲー Ｄ−特異的アミノアシラーゼを使用するエナンチオマー的に純粋な環状α−アミノ酸およびそのＮ−保護誘導体の製造方法
DE10050123A1 (de) * 2000-10-11 2002-04-25 Degussa Verfahren zur Herstellung von Aminosäuren
AU2004295187A1 (en) * 2003-12-04 2005-06-16 Pfizer Inc. Methods for the preparation of stereoisomerically enriched amines
CN104244919B (zh) 2012-03-30 2016-06-29 味之素株式会社 化妆品组合物
CN104592083A (zh) * 2015-01-06 2015-05-06 宁波海硕生物科技有限公司 一种制备n-乙酰-dl-硫代脯氨酸的方法

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4401820A (en) * 1981-01-23 1983-08-30 Tanabe Seiyaku Co., Ltd. Process for racemizing optically active α-amino acids or a salt thereof
DE3929570A1 (de) * 1989-09-06 1991-03-07 Degussa Mikrobiologisch hergestellte n-acyl-l-prolin-acylase, verfahren zu ihrer gewinnung und ihre verwendung
US5219741A (en) * 1989-09-06 1993-06-15 Degussa Ag Method of making L-proline using an N-acyl-L-protine acylase
DE4116980A1 (de) * 1991-05-24 1992-11-26 Degussa Verfahren zur herstellung enantiomerenreiner offenkettiger n-alkyl-l oder d-aminosaeuren

Also Published As

Publication number Publication date
SK117198A3 (en) 1999-03-12
CN1213400A (zh) 1999-04-07
AU2155797A (en) 1997-10-01
NO984206L (no) 1998-09-11
PL328795A1 (en) 1999-02-15
CZ281198A3 (cs) 1998-12-16
US20020037559A1 (en) 2002-03-28
WO1997033987A1 (de) 1997-09-18
KR19990087341A (ko) 1999-12-27
NO984206D0 (no) 1998-09-11
JP2000506728A (ja) 2000-06-06
CA2245543A1 (en) 1997-09-18
EP0896617A1 (de) 1999-02-17

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