ES2051903T3 - Procedimiento para la preparacion biotecnologica continua de isomero optico s(+) de acido 2-(6-metoxi-2-naftil) propionico. - Google Patents

Procedimiento para la preparacion biotecnologica continua de isomero optico s(+) de acido 2-(6-metoxi-2-naftil) propionico.

Info

Publication number
ES2051903T3
ES2051903T3 ES89103246T ES89103246T ES2051903T3 ES 2051903 T3 ES2051903 T3 ES 2051903T3 ES 89103246 T ES89103246 T ES 89103246T ES 89103246 T ES89103246 T ES 89103246T ES 2051903 T3 ES2051903 T3 ES 2051903T3
Authority
ES
Spain
Prior art keywords
metoxi
optical isomer
naftil
continuous
procedure
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.)
Expired - Lifetime
Application number
ES89103246T
Other languages
English (en)
Inventor
Daniele Bianchi
Pietro Cesti
Carlo Pina
Ezio Battistel
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.)
Enichem SpA
Original Assignee
Enichem SpA
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
Priority claimed from IT19532/88A external-priority patent/IT1217341B/it
Priority claimed from IT8821558A external-priority patent/IT1226553B/it
Application filed by Enichem SpA filed Critical Enichem SpA
Application granted granted Critical
Publication of ES2051903T3 publication Critical patent/ES2051903T3/es
Anticipated expiration legal-status Critical
Expired - Lifetime 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
    • C12P7/00—Preparation of oxygen-containing organic compounds
    • C12P7/40—Preparation of oxygen-containing organic compounds containing a carboxyl group including Peroxycarboxylic 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
    • C12N11/00—Carrier-bound or immobilised enzymes; Carrier-bound or immobilised microbial cells; Preparation thereof
    • C12N11/02—Enzymes or microbial cells immobilised on or in an organic carrier
    • C12N11/08—Enzymes or microbial cells immobilised on or in an organic carrier the carrier being a synthetic polymer
    • C12N11/082—Enzymes or microbial cells immobilised on or in an organic carrier the carrier being a synthetic polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C12N11/087—Acrylic polymers
    • 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
    • C12P41/003—Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture by ester formation, lactone formation or the inverse reactions
    • C12P41/005—Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture by ester formation, lactone formation or the inverse reactions by esterification of carboxylic acid groups in the enantiomers or the inverse reaction
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S435/00—Chemistry: molecular biology and microbiology
    • Y10S435/8215—Microorganisms
    • Y10S435/911—Microorganisms using fungi
    • Y10S435/921—Candida

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Zoology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Wood Science & Technology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Health & Medical Sciences (AREA)
  • Genetics & Genomics (AREA)
  • General Engineering & Computer Science (AREA)
  • Microbiology (AREA)
  • Biochemistry (AREA)
  • Biotechnology (AREA)
  • General Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Biomedical Technology (AREA)
  • Analytical Chemistry (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)

Abstract

PREPARACION BIOTECNOLOGICA CONTINUA DE UN ISOMERO OPTICO S(T) DEL ACIDO 2 - (6 METOXI - 2 - NAFTILO) PROPIONICO QUE CONSISTE EN LA REACCION DE UN ESTER RACEMICO (R,S) DE ACIDO 2 - (6 METOXI - 2 NAFTILO) PROPIONICO QUE TIENE PUNTO DE EBULLICION MENOR A 50 (GRADOS) C DE LA FORMULA(I), DONDE R1 ES UN RADICAL ALQUILO C2 - C10, CICLOALQUILO C4 C6, FENILO, TETRAHIDRO PIRANILO, TETRAHIDROFURANILO, Y UN GRUPO (CH2CH2O)N - R2 DONDE N ES DE 2 A 15, Y R2 ES UN GRUPO ALQUILO C1 C4, CON LA LIPASA OBTENIDA DE CANDIDA CYLINDRACEA A TEMPERATURA QUE VA DE 20 A 60 (GRADOS) C Y UN PH DE 5 A 8, POR ALIMENTACION DE DICHO ESTER DE MANERA CONTINUA EN UN BIREACTOR QUE CONTIENE DICHA LIPASA INMOVILIZADA EN UN TRANSPORTADOR POROSO SELECTIVO DESDE UNA RESINA ABSORBENTE DEL TIPO POLIESTER QUE TIENE UNA POROSIDAD DE 50 A 1000 AMSTRONGS Y UNA GRANULOMETRIA DE 1 A 0.01 MM.
ES89103246T 1988-02-25 1989-02-24 Procedimiento para la preparacion biotecnologica continua de isomero optico s(+) de acido 2-(6-metoxi-2-naftil) propionico. Expired - Lifetime ES2051903T3 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
IT19532/88A IT1217341B (it) 1988-02-25 1988-02-25 Processo per la preparazione biotecnologica in continuo dell'isomero ottico s (+) dell'acido 2-(6-metossi-2-naftil) propionico
IT8821558A IT1226553B (it) 1988-07-29 1988-07-29 Processo per la preparazione biotecnologica in continuo dell'isomero ottico s (+) dell'acido 2 -(6-metossi-2-naftil) propionico.

Publications (1)

Publication Number Publication Date
ES2051903T3 true ES2051903T3 (es) 1994-07-01

Family

ID=26327198

Family Applications (1)

Application Number Title Priority Date Filing Date
ES89103246T Expired - Lifetime ES2051903T3 (es) 1988-02-25 1989-02-24 Procedimiento para la preparacion biotecnologica continua de isomero optico s(+) de acido 2-(6-metoxi-2-naftil) propionico.

Country Status (8)

Country Link
US (1) US5229280A (es)
EP (1) EP0330217B1 (es)
JP (1) JPH01304897A (es)
AU (1) AU619249B2 (es)
DE (1) DE68914703T2 (es)
ES (1) ES2051903T3 (es)
HU (1) HU204576B (es)
IL (1) IL89379A (es)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2626288B1 (es) * 1988-01-27 1990-05-18 Rhone Poulenc Sante
IT1247533B (it) * 1991-04-26 1994-12-17 Mini Ricerca Scient Tecnolog Processo per la separazione degli isomeri ottici di acidi carbossilici alfa-sostitutivi
WO1993023547A1 (en) * 1992-05-15 1993-11-25 Syntex Pharmaceuticals International Limited ENZYMATIC PROCESS FOR PRODUCTION OF S-6-METHOXY-α-METHYL-2-NAPHTHALENEACETIC ACID
US5457051A (en) * 1993-03-09 1995-10-10 Sepracor, Inc. Enantioselective hydrolysis of ketoprofen esters by beauveria bassiana and enzymes derived therefrom
WO1997019048A1 (en) * 1995-11-17 1997-05-29 Aeci Limited Synthesis of propionic acid derivatives
WO1999037754A2 (en) * 1998-01-26 1999-07-29 Pharm-Eco Laboratories, Inc. Enzyme activated supports for enantiomeric separations
US6844574B1 (en) 1999-03-12 2005-01-18 Sumitomo Chemical Company, Limited III-V compound semiconductor
JP4192331B2 (ja) * 1999-04-16 2008-12-10 住友化学株式会社 光学活性２−オキソビシクロ［３．１．０］ヘキサン−６−カルボン酸誘導体の製造方法
WO2007092314A2 (en) 2006-02-02 2007-08-16 Verenium Corporation Esterases and related nucleic acids and methods

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3663467A (en) * 1968-08-30 1972-05-16 Rohm & Haas Porous polymers based on trimethylolpropane trimethacrylate and related materials
US3891412A (en) * 1974-05-06 1975-06-24 Johns Manville Trimethylolpropane use of macroreticular polymers of trimethacrylate for making chromatographic separations
GB1536822A (en) * 1976-05-31 1978-12-20 Sumitomo Chemical Co Immobilized non-specific proteases
DK402583D0 (da) * 1983-09-05 1983-09-05 Novo Industri As Fremgangsmade til fremstilling af et immobiliseret lipasepraeparat og anvendelse deraf
DE3345660A1 (de) * 1983-12-16 1985-06-27 Boehringer Mannheim Gmbh, 6800 Mannheim Verfahren zur gewinnung von d(+)naproxen
IT1201408B (it) * 1985-03-22 1989-02-02 Montedison Spa Processo per la preparazione biotecnologica di acidi alfa-arilalcanoici otticamente attivi
EP0197474B1 (en) * 1985-04-01 1991-07-10 Kanegafuchi Kagaku Kogyo Kabushiki Kaisha Process for preparing optically active indoline-2-carboxylic acid
DE3532026A1 (de) * 1985-09-09 1987-03-19 Hoechst Ag Verfahren zur herstellung optisch aktiver (alpha)-phenoxypropionsaeure und deren derivate
JP2509200B2 (ja) * 1985-12-20 1996-06-19 ウイスコンシン・アルムナイ・リサ−チ・フアウンデイシヨン （Ｓ）−α−メチルアリ−ル酢酸の製造方法
GB8600245D0 (en) * 1986-01-07 1986-02-12 Shell Int Research Preparation of 2-arylpropionic acids
EP0382767B1 (en) * 1987-09-28 1993-12-15 Novo Nordisk A/S Method for immobilizing lipase
US4897352A (en) * 1988-01-15 1990-01-30 The Dow Chemical Company Acrylate based adsorbent resin for the immobilization of enzymes

Also Published As

Publication number Publication date
IL89379A0 (en) 1989-09-10
HUT52822A (en) 1990-08-28
JPH01304897A (ja) 1989-12-08
IL89379A (en) 1992-12-01
AU3014789A (en) 1989-08-31
DE68914703D1 (de) 1994-05-26
US5229280A (en) 1993-07-20
EP0330217A3 (en) 1991-01-16
AU619249B2 (en) 1992-01-23
DE68914703T2 (de) 1994-09-08
EP0330217B1 (en) 1994-04-20
EP0330217A2 (en) 1989-08-30
HU204576B (en) 1992-01-28

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