化学
纤维二糖
糖苷水解酶
另一个
糖苷键
糖基
亲核细胞
催化循环
反作用坐标
立体化学
糖基化
过渡状态
水解
低潮区
催化作用
酶
计算化学
里氏木霉
有机化学
纤维素酶
生物化学
作者
Brandon C. Knott,Majid Haddad Momeni,Michael F. Crowley,Lloyd Mackenzie,Andreas W. Götz,Mats Sandgren,Stephen G. Withers,Jerry Ståhlberg,Gregg T. Beckham
摘要
Glycoside hydrolases (GHs) cleave glycosidic linkages in carbohydrates, typically via inverting or retaining mechanisms, the latter of which proceeds via a two-step mechanism that includes formation of a glycosyl-enzyme intermediate. We present two new structures of the catalytic domain of Hypocrea jecorina GH Family 7 cellobiohydrolase Cel7A, namely a Michaelis complex with a full cellononaose ligand and a glycosyl-enzyme intermediate, that reveal details of the 'static' reaction coordinate. We also employ transition path sampling to determine the 'dynamic' reaction coordinate for the catalytic cycle. The glycosylation reaction coordinate contains components of forming and breaking bonds and a conformational change in the nucleophile. Deglycosylation proceeds via a product-assisted mechanism wherein the glycosylation product, cellobiose, positions a water molecule for nucleophilic attack on the anomeric carbon of the glycosyl-enzyme intermediate. In concert with previous structures, the present results reveal the complete hydrolytic reaction coordinate for this naturally and industrially important enzyme family.
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