A two-step, one-pot enzymatic synthesis of ampicillin from penicillin G potassium salt

被引:12
作者
Du, Li-Li [1 ]
Wu, Qi [1 ]
Chen, Chun-Xiu [1 ]
Liu, Bo-Kai [1 ]
Lin, Xian-Fu [1 ]
机构
[1] Zhejiang Univ, Dept Chem, Hangzhou 310027, Peoples R China
关键词
Penicillin acylase; Ampicillin; Enzymatic synthesis; One-pot; Penicillin G potassium; KINETICALLY CONTROLLED SYNTHESIS; BETA-LACTAM ANTIBIOTICS; ACYLASE-CATALYZED SYNTHESIS; HIGH SUBSTRATE CONCENTRATIONS; EQUILIBRIUM-CONTROLLED SYNTHESIS; FULLY AQUEOUS-MEDIUM; ETHYLENE-GLYCOL; ORGANIC MEDIA; CEPHALEXIN; OPTIMIZATION;
D O I
10.1016/j.molcatb.2008.12.020
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A two-step, one-pot synthesis of ampicillin from penicillin G potassium salt (PGK) in aqueous buffer/organic co-solvent has been achieved. Ethylene glycol (EG) was chosen as the organic co-solvent. Factors including co-solvent content, enzyme loading, reaction temperature and Substrate concentration were investigated. The optimum conditions were as follow: pH 8.0 phosphate buffer solution, 50% EG (v/v), 25 degrees C. 100 mM PGK and 300 mM D-phenylglycine methyl ester (D-PGM). 43.2 IU/ml IPA-750. The maximum yield was 57.3% after a reaction time of 17 h. It is the first report about the synthesis of ampicillin from penicillin G potassium salt in one-pot combining the enzymatic hydrolysis and the subsequent enzymatic condensation, and the novel methodology will have important application in the P-lactam antibiotics industry. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:208 / 211
页数:4
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