磷脂酰胆碱
基质(水族馆)
灵活性(工程)
催化作用
化学
磷脂酶
底物特异性
链霉菌
磷脂酶A2
生物化学
立体化学
磷脂
酶
生物
细菌
数学
生态学
统计
膜
遗传学
作者
Rongkang Hu,Jiale Cao,Chenghao Rong,Siyi Wu,Linxiu Wu
标识
DOI:10.1016/j.ijbiomac.2024.135824
摘要
The catalytic efficiency of Streptomyces klenkii phospholipase D (SkPLD) in soybean phosphatidylcholine (soy-PC) processing is constrained by its acyl chain specificity. To address this limitation, we engineered the substrate-binding pocket of SkPLD to increase its flexibility. The mutant P343A/Y383L exhibited a 7.14-fold increase in catalytic efficiency toward soy-PC compared to the wild type. This enhancement was attributed to improved substrate-binding pocket flexibility, as evidenced by the significantly higher specific activity of the mutant toward PCs with various acyl chains (58.20-327.76 U/mg vs. 13.56-76.67 U/mg). Monomolecular film experiments demonstrated that the P343A/Y383L mutant reduced the energy barrier for PC binding, facilitating favorable interactions with the soy-PC monolayer. Molecular dynamics simulations revealed that the mutant's increased flexibility allowed for easier diffusion and penetration into the soy-PC monolayer, while the non-polar amino acids in the substrate-binding pocket promoted rapid interactions with the acyl chains of PC, ultimately leading to enhanced catalytic activity.
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