CIESC Journal

• 化工学报 •    下一篇

反胶束体系中酶法合成头孢力新的动力学

石屹峰,虞星炬,袁权   

  1. 中国科学院大连化学物理研究所,中国科学院大连化学物理研究所,中国科学院大连化学物理研究所 大连116012,大连116012,大连116012
  • 出版日期:1997-04-25 发布日期:1997-04-25

KINETICS OF ENZYMATIC SYNTHESIS OF CEPHALEXIN IN REVERSE MICELLES

Shi Yifeng, Yu Xingju and Yuan Quan(Dalian Institute of Chemical Physics , Chinese Academy of Sciences , Dalian 116012)   

  • Online:1997-04-25 Published:1997-04-25

摘要: 利用来自Xanthomonas citri的酰化酶由D-α-苯甘氨酸甲酯和7-ADCA合成头孢力新是典型的动力学控制合成过程,其中既有产物的合成又有产物和底物(D-α-苯甘氨酸甲酯)的水解。动力学分析表明,反应置于反胶束体系将不仅提高酶的催化速度而且提高转移酶活力对水解酶活力的选择性。利用AOT/异辛烷反胶束体系酶法合成头孢力新使水解副反应被抑制,合成途径被强化。水成为反胶束酶反应体系中重要的调节手段,它对反应速度呈“铃形”关系。

Abstract: The acylase from Xanthomanas citri was used to synthesize cephalexin (CEX) from 7 - amino- 3 - deacetoxy - cephalosporanic acid (7 - ADCA) and D - α - phenylglycine methyl ester (PGM) as a kinetic controlled condensed reaction. However, X. citri enzyme catalyzes not only CEX synthesis but also PGM hydrolysis and CEX hydrolysis. The results on a rational analysis of the reaction mechanisms showed that higher activity and higher ratio of transferase to hy-drolase activity are favorable for use in reverse micelles system. The enhancement effect of CEX synthesis parallel with avoiding hydrolysis of PGM and CEX was found when X. citri enzyme was solubilized in AOT/isooctane reverse micelles. The enzyme activity in reverse micelles is governed by the hydration ratio as bell- shaped dependence.

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