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首页> 外文期刊>Bulletin of the Korean Chemical Society >Enzymatic Synthesis of Cephaloglycin
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Enzymatic Synthesis of Cephaloglycin

机译:酶催化合成头孢霉素

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Cephaloglycin was synthesized directly from D-メ -phenylglycine methyl ester and 7-aminocephalosporanic acid using whole cell enzyme of Xanthomonas citri (IFO 3835). Some optimal conditions for cephaloglycin synthesis were investigated, and yield improvements for its production by several methods were attempted. Using the whole cell enzyme system, the reaction kinetic model for cephaloglycin synthesis is proposed, and the kinetic constants for D-メ -phenylglycine methyl ester hydrolysis, cephaloglycin synthesis, and cephaloglycin hydrolysis were determined. The Km values of D-メ -phenylglycine methyl ester, 7-aminocephalosporanic acid, and cephaloglycin were 11 mM, 24 mM, and 167 mM, and Ki value of D-メ-phenylglycine was 15 mM, respectively. The pattern of product inhibition was found to be competitive one.
机译:头孢霉素是使用柠檬黄单胞菌的全细胞酶(IFO 3835)由D-β-苯基甘氨酸甲酯和7-氨基头孢烷酸直接合成的。研究了一些合成头孢菌素的最佳条件,并尝试通过几种方法提高其产量。利用全细胞酶系统,建立了头孢菌素合成的反应动力学模型,并确定了D-β-苯基甘氨酸甲酯水解,头孢菌素合成和头孢菌素水解的动力学常数。 D-β-苯基甘氨酸甲酯的Km值为11mM,24-mM和167mM,D-β-苯基甘氨酸的Km值为15mM。发现产物抑制的模式是竞争性的。

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