醛缩酶A
非对映体
位阻效应
基质(水族馆)
苏氨酸
化学
组合化学
酶
生物化学
立体化学
生物
丝氨酸
生态学
作者
Wenlong Zheng,Zhongji Pu,Lanxin Xiao,Gang Xu,Lirong Yang,Haoran Yu,Jianping Wu
摘要
The L-threonine aldolase from Leishmania major was engineered to improve its diastereoselectivity by a CAST/ISM strategy, providing insights into the relationship between the physico-chemical properties of the substrate access path and diastereoselectivity. The steric hindrance, hydrophobic interaction and π-π interaction cooperated to improve the diastereoselectivity of the enzyme, with a diastereomeric excess (de) value reaching 96.3%syn from 26.8%syn.
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