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[1]赵 艳 张大龙 李键煚 冯进辉 鲍锦库** 吴洽庆** 朱敦明.青霉素G酰化酶突变体酶催化合成顺式头孢丙烯工艺优化[J].应用与环境生物学报,2016,22(03):363-370.[doi:10.3724/SP.J.1145.2015.10033]
 ZHAO Yan,ZHANG Dalong,LI Jianjiong,et al.Process optimization for enzymatic synthesis of cis-cefprozil by a mutant penicillin G acylase*[J].Chinese Journal of Applied & Environmental Biology,2016,22(03):363-370.[doi:10.3724/SP.J.1145.2015.10033]
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青霉素G酰化酶突变体酶催化合成顺式头孢丙烯工艺优化()
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《应用与环境生物学报》[ISSN:1006-687X/CN:51-1482/Q]

卷:
22卷
期数:
2016年03期
页码:
363-370
栏目:
研究论文
出版日期:
2016-06-25

文章信息/Info

Title:
Process optimization for enzymatic synthesis of cis-cefprozil by a mutant penicillin G acylase*
作者:
赵 艳12 张大龙2 李键煚2 冯进辉2 鲍锦库1** 吴洽庆2** 朱敦明2
1四川大学生命科学学院 成都 610064 2中国科学院天津工业生物技术研究所,工业酶国家工程实验室,天津市生物催化技术工程中心 天津 300308
Author(s):
ZHAO Yan12 ZHANG Dalong2 LI Jianjiong2 FENG Jinhui2 BAO Jinku1** WU Qiaqing2** & ZHU Dunming2
1College of Life Sciences, Sichuan University, Chengdu 610064, China 2Institute of Industrial Biotechnology, Chinese Academy of Sciences, Tianjin 300308, China
关键词:
青霉素G酰化酶突变体顺式头孢丙烯固定化
Keywords:
penicillin G acylase mutants cis-cefprozil immobilization
分类号:
TQ464 : Q939.9
DOI:
10.3724/SP.J.1145.2015.10033
摘要:
头孢丙烯作为第二代头孢菌素类抗生素,广泛应用于治疗敏感菌所致的上、下呼吸道感染,皮肤和皮肤软组织感染. 酶法合成头孢丙烯与化学法相比更加绿色环保. 本研究利用来源于大肠杆菌的青霉素G酰化酶(EC 3.5.1.11)野生型WT、突变体βF24A和αF146Y/βF24A合成顺式头孢丙烯(cis-cefprozil). 通过比较不同突变体催化顺式头孢丙烯的合成效率,发现突变体βF24A具有较高合成活性及低水解活性. 以顺式7-氨基-3-丙烯基-4-头孢烷酸(cis-7-APRA)和对羟基苯甘氨酸甲酯(d-HPGME)为底物合成顺式头孢丙烯. 基于水相体系中合成条件优化,最适温度为25 ℃,最适pH为6.0,底物配比Md-HPGME:Mcis-7-APRA = 3:1,酶用量2.6 U/mL,在此最佳条件下转化率可高达99%. 突变体βF24A的固定化酶合成顺式头孢丙烯的转化率为99%,固定化酶连续使用60批次后,活性仍保持52%. 本研究对突变体的筛选和酶催化条件的优化,为酶法合成顺式头孢丙烯奠定了基础. (图7 表3 参40)
Abstract:
Cefprozil is a second generation cephalosporin antibiotics widely used in the treatment of upper and lower respiratory tract infections as well as skin and soft tissue infections caused by sensitive bacteria. Because of the great advantages of biocatalysis over the conventional chemical synthesis by avoiding toxic reagents, solvents and harsh reaction conditions, it is desirable to develop a feasible enzymatic synthesis of cefprozil. In this work, we chose the key sites βF24、αF146 of pecicillin G acylase from Escherichia coli for site-directed mutagenesis. By comparing the synthesis efficiency of WT, βF24A and αF146Y/βF24A, the obtained mutant βF24A which has high synthesis/hydrolysis ratio was used in the enzymatic synthesis of cis-cefprozil from cis-7-APRA and d-HPGME. Based on the aqueous-phase synthesis system, the yield was dependent on the multiple factors. The most suitable temperature and pH was 25 °C and 6.0, respectively, the optimum molar ratio of d-HPGME/cis-7-APRA 3:1 and the enzyme loading 2.6 U/mL. At the optimized conditions, 99% yield was attained with 100 mmol/L of cis-7-APRA. The maximum yield was 99% with immobilized βF24A at the optimized conditions with 100 mmol/L cis-7-APRA. Yields remained 52% after 60 consecutive batch reactions. This paper studies on the selection of mutants and optimization for enzyme catalysis conditions, which provides useful information for enzymatic synthesis of cis-cefprozil.

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更新日期/Last Update: 2016-06-25