发明名称 METHOD FOR PREPARING SEMI-SYNTHETIC AMINOPENICILLINS, AMINOCEPHALOSPORINS OR THEIR N-SUBSTITUTED DERIVATIVES
摘要 FIELD: biotechnology, antibiotics. SUBSTANCE: invention relates to preparing semi-synthetic beta-lactam antibiotics aminopenicillins and aminocephalosporins and their N-substituted derivatives also. Method involves enzymatic transformation of the parent beta-lactam compound in the presence of enzyme system. For realizing method biosynthetic beta-lactam compounds and their chemical analogues are used as parent beta-lactam compounds and biocatalysts of the 2-d generation based on immobilized cells comprising hydrolase for biosynthetic beta-lactams in combination with enzyme amino-beta-lactam synthase specific to derivatives of aminophenylacetic acid are used as enzymes. Amino acid esters are used as acylating agent that are added to reaction mass and flowing molar excess of acylating agent with respect to amino acid is maintained to be 3-4-fold and its total content is 1.9-2.1 M/M of the parent beta-lactam, not above. End products are isolated by direct precipitation as amino-beta- lactams by pH value change, medium dielectric permeability value or by addition of specific precipitating agent, preferably alpha- naphthol, or as N-substituted derivative by pH value change. Invention provides elevating effectiveness of method with its simultaneous simplification. EFFECT: enhanced yield, improved quality of product. 4 cl, 9 ex
申请公布号 RU2221046(C2) 申请公布日期 2004.01.10
申请号 RU20000101270 申请日期 2000.01.21
申请人 发明人 NYS P.S.;KUROCHKINA V.B.;SKLJARENKO A.V.;EGOROV A.M.
分类号 C12P35/04;C12N9/14;C12N11/02;C12P37/04;C12R1/19;C12R1/38;C12R1/64 主分类号 C12P35/04
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