合理设计
蛋白质工程
生物催化
背景(考古学)
定向进化
高分子
催化效率
生化工程
计算生物学
纳米技术
催化作用
化学
计算机科学
生物分子
组合化学
高分子科学
天然聚合物
材料科学
有机化学
酶
工程类
生物化学
生物
反应机理
古生物学
基因
突变体
作者
Muhammad Bilal,Hafiz M.N. Iqbal,Shuqi Guo,Hongbo Hu,Wei Wang,Xuehong Zhang
标识
DOI:10.1016/j.ijbiomac.2017.10.182
摘要
Over the past years, technological and scientific advances have proven biocatalysis as a sustainable alternative than traditional chemical catalysis including organo- or metallocatalysis. In this context, immobilization based approaches represent simple but effective routes for engineering enzyme catalysts with higher activities than wild-type derivatives. Many enzymes including oxidoreductases have been engineered by rational and directed evolution, to realize the catalytic activity, enantioselectivity, and stability attributes which are essential for their biotechnological exploitation. Induce yet stable activity in enzyme catalysis offer new insights and motivation to engineer efficient catalysts for practical and commercial purposes. It has now become possible to envisage substrate accessibility to the catalytic site of the enzyme by current computational capabilities that reduce the experimental work related to the enzyme selection, screening, and engineering. Herein, state-of-the-art protein engineering approaches for improving enzymatic activities including chemical modification, directed evolution, and rational design or their combination methods are discussed. The emphasis is also given to the applications of the resulting tailored catalysts ranging from fine chemicals to novel pharmaceutical compounds that use biocatalysts as a vital step.
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