合理设计
基质(水族馆)
醛缩酶A
转氨酶
催化作用
化学
级联
组合化学
定向进化
氨基酸
催化效率
蛋白质工程
底物特异性
酶
甲醛
理论(学习稳定性)
级联反应
有机化学
转氨作用
生物催化
突变
生化工程
立体化学
合成生物学
酶催化
广谱
对映选择合成
作者
Yu Hong,Yanling Xie,X Y Li,Peilong Yang,Wei Luo
标识
DOI:10.1021/acs.jafc.6c02682
摘要
Transaminases (TAs) play a crucial role in asymmetric synthesis, among which ω-TA exhibits a broad substrate spectrum and high enantioselectivity, albeit with limitations such as poor stability and low enzymatic activity. This study aimed to improve the catalytic efficiency of the rate-limiting transaminase in the cascade reaction for 2-amino-4-hydroxybutyric acid, using strategies such as semirational design and DLKcat large model prediction. After single-point and combinatorial mutations, ultimately, a combinatorial mutant, S62T/T68D/Y221Q (VfTA-M3), with a relative specific activity of 379.42% compared to the wild-type (VfTA-WT), was obtained, which also exhibited improved stability relative to the wild-type enzyme. Using this mutant in conjunction with aldolase RtALD, a cascade catalytic system was established for the synthesis of 2-amino-4-hydroxybutyric acid from inexpensive formaldehyde and pyruvate. After 20 h of reaction, the substrate conversion rate reached 80%, laying a solid foundation for the production of other chiral amino acids and chiral amines.
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