ZA961015B - Process for the enzymatic synthesis of beta-lactam antibiotics in the presence of an ezyme inhibitor - Google Patents

Process for the enzymatic synthesis of beta-lactam antibiotics in the presence of an ezyme inhibitor

Info

Publication number
ZA961015B
ZA961015B ZA961015A ZA961015A ZA961015B ZA 961015 B ZA961015 B ZA 961015B ZA 961015 A ZA961015 A ZA 961015A ZA 961015 A ZA961015 A ZA 961015A ZA 961015 B ZA961015 B ZA 961015B
Authority
ZA
South Africa
Prior art keywords
ezyme
beta
inhibitor
lactam antibiotics
enzymatic synthesis
Prior art date
Application number
ZA961015A
Other languages
English (en)
Inventor
Maurizio Zenoni
Auro Roberto Tagliani
Emiliano Cannas
Angelo Venturelli
Original Assignee
Acs Dobfar 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
Application filed by Acs Dobfar Spa filed Critical Acs Dobfar Spa
Publication of ZA961015B publication Critical patent/ZA961015B/xx

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
    • C12P37/00—Preparation of compounds having a 4-thia-1-azabicyclo [3.2.0] heptane ring system, e.g. penicillin
    • C12P37/04—Preparation of compounds having a 4-thia-1-azabicyclo [3.2.0] heptane ring system, e.g. penicillin by acylation of the substituent in the 6 position
    • 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
    • C12P35/00—Preparation of compounds having a 5-thia-1-azabicyclo [4.2.0] octane ring system, e.g. cephalosporin
    • C12P35/06—Cephalosporin C; Derivatives thereof
    • 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
    • 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)
    • C12N9/84—Penicillin amidase (3.5.1.11)
    • 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
    • C12P35/00—Preparation of compounds having a 5-thia-1-azabicyclo [4.2.0] octane ring system, e.g. cephalosporin
    • C12P35/04—Preparation of compounds having a 5-thia-1-azabicyclo [4.2.0] octane ring system, e.g. cephalosporin by acylation of the substituent in the 7 position
    • 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
    • C12P37/00—Preparation of compounds having a 4-thia-1-azabicyclo [3.2.0] heptane ring system, e.g. penicillin
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12Y—ENZYMES
    • C12Y305/00—Hydrolases acting on carbon-nitrogen bonds, other than peptide bonds (3.5)
    • C12Y305/01—Hydrolases acting on carbon-nitrogen bonds, other than peptide bonds (3.5) in linear amides (3.5.1)
    • C12Y305/01011—Penicillin amidase (3.5.1.11), i.e. penicillin-amidohydrolase

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Zoology (AREA)
  • Engineering & Computer Science (AREA)
  • Wood Science & Technology (AREA)
  • Health & Medical Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Genetics & Genomics (AREA)
  • General Engineering & Computer Science (AREA)
  • Microbiology (AREA)
  • Biochemistry (AREA)
  • Biotechnology (AREA)
  • General Health & Medical Sciences (AREA)
  • Biomedical Technology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Mycology (AREA)
  • Molecular Biology (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Cephalosporin Compounds (AREA)
  • Immobilizing And Processing Of Enzymes And Microorganisms (AREA)
  • Enzymes And Modification Thereof (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
ZA961015A 1995-02-28 1996-02-08 Process for the enzymatic synthesis of beta-lactam antibiotics in the presence of an ezyme inhibitor ZA961015B (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
ITMI950383A IT1274658B (it) 1995-02-28 1995-02-28 Procedimento enzimatico migliorato per la produzione di penicilline e cefalosporine

Publications (1)

Publication Number Publication Date
ZA961015B true ZA961015B (en) 1996-08-20

Family

ID=11370726

Family Applications (2)

Application Number Title Priority Date Filing Date
ZA961014A ZA961014B (en) 1995-02-28 1996-02-08 Enzymatic process for producing penicillins and cephalosporins
ZA961015A ZA961015B (en) 1995-02-28 1996-02-08 Process for the enzymatic synthesis of beta-lactam antibiotics in the presence of an ezyme inhibitor

Family Applications Before (1)

Application Number Title Priority Date Filing Date
ZA961014A ZA961014B (en) 1995-02-28 1996-02-08 Enzymatic process for producing penicillins and cephalosporins

Country Status (9)

Country Link
EP (1) EP0730035A1 (zh)
JP (1) JPH08242884A (zh)
KR (1) KR960031621A (zh)
CN (1) CN1144274A (zh)
AU (1) AU4579896A (zh)
BR (1) BR9600830A (zh)
CA (1) CA2167118A1 (zh)
IT (1) IT1274658B (zh)
ZA (2) ZA961014B (zh)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2163997B2 (es) * 1999-10-22 2004-07-01 Universidad Complutense De Madrid Procedimiento para la inmovilizacion de una nueva penicilina v acilasa de "streptomyces lavendulae" para la obtencion de acido 6-aminopenicilanico.
ITMI20030042A1 (it) * 2003-01-14 2004-07-15 Univ Degli Studi Trieste Processo di sintesi enzimatica di antibiotici b lattamici.
MX2007007937A (es) 2004-12-27 2007-08-21 Dsm Ip Assets Bv Procedimiento para la sintesis de cefaclor.
US20170101660A1 (en) * 2015-10-07 2017-04-13 Gwangju Institute Of Science And Technology Enzyme-immobilized porous membrane and preparation method of antibiotics using the same

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2150380B1 (zh) * 1971-08-20 1974-10-04 Toyo Jozo Kk
IT1045797B (it) * 1973-12-20 1980-06-10 Snam Progetti Procedimento per la sintesi enzimatica di penicilline e cefalosporine semisintetiche mediante una acilasi insolubile
EP0537255B1 (en) * 1990-07-04 2006-02-15 DSM IP Assets B.V. Process for preparation of beta-lactams
IT1243800B (it) * 1990-08-28 1994-06-28 Sclavo Spa Procedimento migliorato per la preparazione di cefalosporine
SK63894A3 (en) * 1991-12-19 1995-03-08 Novo Nordisk As Method of preparation of beta-lactam antibiotic
DE59306762D1 (de) * 1992-04-16 1997-07-24 Merck Patent Gmbh Aktivierte Trägermaterialien, ihre Herstellung und Verwendung
DE4333213A1 (de) * 1993-09-29 1995-03-30 Merck Patent Gmbh Immobilisierte Proteinase K

Also Published As

Publication number Publication date
AU4579896A (en) 1996-09-05
IT1274658B (it) 1997-07-18
ITMI950383A0 (it) 1995-02-28
ITMI950383A1 (it) 1996-08-28
CA2167118A1 (en) 1996-08-29
BR9600830A (pt) 1997-12-30
JPH08242884A (ja) 1996-09-24
CN1144274A (zh) 1997-03-05
ZA961014B (en) 1996-08-29
EP0730035A1 (en) 1996-09-04
KR960031621A (ko) 1996-09-17

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