CAS Key Laboratory of Green Process and Engineering, Institute of Process Engineering, Chinese Academy of Sciences, Beijing, People's Republic of China.
School of Chemical Engineering, University of Chinese Academy of Sciences, Beijing, People's Republic of China.
Biotechnol Appl Biochem. 2021 Feb;68(1):136-147. doi: 10.1002/bab.1903. Epub 2020 Mar 2.
An efficient method for the enzymatic synthesis of cephalexin (CEX) from 7-amino-3-deacetoxycephalosporanic acid (7-ADCA) and d-phenylglycine methyl ester (PGME) using immobilized penicillin G acylase (IPGA) as catalyst in a suspension aqueous solution system was developed, where the reactant 7-ADCA and product CEX are mainly present as solid particles. The effects of key factors on the enzymatic synthesis were investigated. Results showed that continuous feeding of PGME was more efficient for the synthesis of CEX than the batch mode. Under the optimized conditions, the maximum 7-ADCA conversion ratio of 99.3% and productivity of 200 mmol/L/H were achieved, both of which are much superior to the homogeneous aqueous solution system. Besides, IPGA still retained 95.4% of its initial activity after 10 cycles of enzymatic synthesis, indicating the excellent stability of this approach. The developed approach shows great potential for the industrial production of CEX via an enzyme-based route.
采用固定化青霉素 G 酰化酶(IPGA)作为催化剂,在悬浮水溶液体系中,从 7-氨基-3-去乙酰氧基头孢烷酸(7-ADCA)和 D-苯甘氨酸甲酯(PGME)酶促合成头孢氨苄(CEX)。在该体系中,反应物 7-ADCA 和产物 CEX 主要以固体颗粒形式存在。研究了关键因素对酶促合成的影响。结果表明,与分批模式相比,连续进料 PGME 更有利于 CEX 的合成。在优化条件下,7-ADCA 的最高转化率达到 99.3%,产率达到 200mmol/L/h,均优于均相水溶液体系。此外,IPGA 在 10 次酶合成循环后仍保留其初始活性的 95.4%,表明该方法具有优异的稳定性。该方法为通过酶法途径工业化生产 CEX 提供了巨大潜力。