糖基化
化学
产量(工程)
糖基转移酶
催化作用
生物化学
酶
N-连接糖基化
催化效率
组合化学
机制(生物学)
蛋白质工程
反应条件
极性(国际关系)
热稳定性
转移酶
活动站点
立体化学
蛋白质稳定性
糖苷水解酶
作者
Zhiyuan Wang,S. Wang,Wei Tian,Yu Wu,Xiao Guan,Jin Ye,S. X. Wang
标识
DOI:10.1021/acs.jafc.5c17749
摘要
HvUGT13248 and OsUGT79 are homologous glycosyltransferases for deoxynivalenol (DON) glycosylation with limited efficiency. Their distinct features and the underlying catalytic mechanism remain poorly understood. Here, comparative analysis demonstrated that HvUGT13248 exhibited higher catalytic efficiency toward DON and its analogs but was constrained by relatively lower yield and poor stability in practical application. In contrast, OsUGT79 achieved complete conversion under excess donor due to its enhanced resistance to feedback inhibition of UDP and robust thermal stability. Three key active-site residues were identified, and their functional roles were evaluated comparatively. Among these, His38/27 was essential for glycosylation by both HvUGT13248 and OsUGT79. Interaction between His132/His122 and the C4, C7, and C15 positions of DON provided a structural rationale for their differential activities toward C4-substituted trichothecenes. Furthermore, Asp393 played a more critical role in stabilizing the enzyme-substrate complex in HvUGT13248. These findings advance the engineering of both enzymes for improved DON glycosylation.
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