定向进化
糖基转移酶
蛋白质工程
突变体
合理设计
生物化学
化学
定向分子进化
酶
计算生物学
底物特异性
基质(水族馆)
组合化学
生物
纳米技术
材料科学
基因
生态学
作者
John B. McArthur,Xi Chen
出处
期刊:Biochemical Society Transactions
[Portland Press]
日期:2016-02-09
卷期号:44 (1): 129-142
被引量:57
摘要
Glycosyltransferases (GTs) are powerful tools for the synthesis of complex and biologically-important carbohydrates. Wild-type GTs may not have all the properties and functions that are desired for large-scale production of carbohydrates that exist in nature and those with non-natural modifications. With the increasing availability of crystal structures of GTs, especially those in the presence of donor and acceptor analogues, crystal structure-guided rational design has been quite successful in obtaining mutants with desired functionalities. With current limited understanding of the structure–activity relationship of GTs, directed evolution continues to be a useful approach for generating additional mutants with functionality that can be screened for in a high-throughput format. Mutating the amino acid residues constituting or close to the substrate-binding sites of GTs by structure-guided directed evolution (SGDE) further explores the biotechnological potential of GTs that can only be realized through enzyme engineering. This mini-review discusses the progress made towards GT engineering and the lessons learned for future engineering efforts and assay development.
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