酒石酸盐
水解酶
化学
催化作用
生物转化
基质(水族馆)
酒石酸
活动站点
酶
限制
生物化学
立体化学
组合化学
生物
工程类
机械工程
生态学
柠檬酸
作者
Yu Han,Yuelin Luo,Bao-Di Ma,Jie Li,Jian‐He Xu,Xu‐Dong Kong
出处
期刊:Biochemistry
[American Chemical Society]
日期:2024-05-28
卷期号:63 (12): 1578-1587
标识
DOI:10.1021/acs.biochem.4c00141
摘要
l-(+)-Tartaric acid plays important roles in various industries, including pharmaceuticals, foods, and chemicals. cis-Epoxysuccinate hydrolases (CESHs) are crucial for converting cis-epoxysuccinate to l-(+)-tartrate in the industrial production process. There is, however, a lack of detailed structural and mechanistic information on CESHs, limiting the discovery and engineering of these industrially relevant enzymes. In this study, we report the crystal structures of RoCESH and KoCESH-l-(+)-tartrate complex. These structures reveal the key amino acids of the active pocket and the catalytic triad residues and elucidate a dynamic catalytic process involving conformational changes of the active site. Leveraging the structural insights, we identified a robust BmCESH (550 ± 20 U·mg–1) with sustained catalytic activity even at a 3 M substrate concentration. After six batches of transformation, immobilized cells with overexpressed BmCESH maintained 69% of their initial activity, affording an overall productivity of 200 g/L/h. These results provide valuable insights into the development of high-efficiency CESHs and the optimization of biotransformation processes for industrial uses.
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