化学
磷脂酰丝氨酸
合理设计
催化作用
生物化学
蛋白质工程
酶
立体化学
磷脂酶A
组合化学
磷脂酶
磷脂酶A2
磷脂酶D
磷脂
协同催化
酯交换
表面工程
磷脂酶C
作者
Xinyu Zhao,Xiufeng Wang,Yijie Sheng,Shuizhi Lin,Shuping Xu,Z. Hu,Xueping Ling,Chaoqi Chen,Mingfeng Cao,Haiyang Cui,Ying Lü
标识
DOI:10.1021/acs.jafc.5c17951
摘要
Phosphatidylserine (PS), a major brain phospholipid, supports the central nervous system's health and may alleviate cognitive decline, including in Alzheimer's disease. A key challenge in green enzymatic PS synthesis is the suppression of hydrolysis while enhancing PLD-catalyzed transphosphatidylation. Here, we developed a mechanism-guided engineering strategy for Streptomyces antibioticus phospholipase D (SaPLD). The substitution of W187I increased the PS yield to 58.3%, while V380W improved thermostability. Combining beneficial mutations generated SaPLD-R7 (W187I/V380W/G381A), which overcame the activity-stability trade-off and achieved up to 95.8% PS yield using the enzyme produced by 5 L scale fermentation. Molecular dynamics simulations showed that SaPLD-R7 enhanced substrate binding and catalysis by shortening the key active site distances and reducing local flexibility. Solvent contact and energy analyses further indicated improved stability. This work establishes a structure-mechanism-function framework for enhancing PLD transphosphatidylation and provides a robust enzymatic route for high-efficiency PS production as a valuable functional food ingredient.
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