Department of Molecular Biology and Genetics, Cornell University, Ithaca, NY 14850, USA.
Biotechnol Bioeng. 2010 Oct 1;107(2):195-205. doi: 10.1002/bit.22838.
Recent studies have shown that a number of glycoside hydrolase families do not follow the classical catalytic mechanisms, as they lack a typical catalytic base/nucleophile. A variety of mechanisms are used to replace this function, including substrate-assisted catalysis, a network of several residues, and the use of non-carboxylate residues or exogenous nucleophiles. Removal of the catalytic base/nucleophile by mutation can have a profound impact on substrate specificity, producing enzymes with completely new functions.
最近的研究表明,许多糖苷水解酶家族并不遵循经典的催化机制,因为它们缺乏典型的催化碱/亲核试剂。有多种机制可用于替代此功能,包括底物辅助催化、多个残基网络以及使用非羧酸根残基或外源性亲核试剂。通过突变去除催化碱/亲核试剂会对底物特异性产生深远影响,产生具有全新功能的酶。