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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.
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页码:208 / 211
页数:4
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