化学
水解
催化作用
残留物(化学)
活动站点
蛋白质工程
生物物理学
基质(水族馆)
分子动力学
质子
玉米赤霉烯酮
组合化学
蛋白质结构
水解酶
立体化学
疏水效应
酶
生物化学
动力学
反应机理
底物特异性
生物有机化学
作者
Binbin Ouyang,Zhaolin Huang,Chenshuo Song,Dejing Yin,Dawei Ni,Wenli Zhang,Yijian Rao,Wei Xu,Wanmeng Mu
标识
DOI:10.1021/acs.jafc.6c09645
摘要
Zearalenone (ZEN) lactonases are promising biocatalysts for ZEN detoxification, yet the catalytic mechanism underlying ZEN hydrolysis remains poorly understood. Here, we combined structural analysis, quantum-mechanical (QM) calculations, and molecular dynamics (MD) simulations to elucidate the catalytic mechanism and guide enzyme engineering. QM and MD analyses identified a near-attack conformation of the catalytic His245 as essential for proton transfer. Crystal structure analysis revealed that mutations within the active pocket enhanced the local hydrophobic microenvironment, thereby optimizing the reactive conformation through an improved substrate positioning and catalytic residue alignment. Engineering the hydrophobic microenvironment significantly enhanced the activity of ZENM toward multiple substrates. Transfer of the engineered region to another ZEN lactonase, ZHD101, also significantly improved the hydrolytic activity, supporting the potential general applicability of this strategy. Hydrophobic microenvironment engineering might represent a promising strategy for modulating proton transfer and provide a potential framework for improving the activity of ZEN lactonases for food and feed detoxification.
科研通智能强力驱动
Strongly Powered by AbleSci AI