定向进化
蛋白质工程
合成生物学
计算生物学
结构生物学
天然产物
代谢工程
化学
基因组工程
蛋白质设计
生物化学
生化工程
化学生物学
组合化学
生物合成
生物
合理设计
酶
基因组
基因组编辑
工程类
基因
遗传学
突变体
作者
Miles A Calzini,Alexandra A Malico,Melissa M Mitchler,Gavin J. Williams
出处
期刊:Protein Engineering Design & Selection
[Oxford University Press]
日期:2021-01-01
卷期号:34
被引量:5
标识
DOI:10.1093/protein/gzab015
摘要
As protein engineering grows more salient, many strategies have emerged to alter protein structure and function, with the goal of redesigning and optimizing natural product biosynthesis. Computational tools, including machine learning and molecular dynamics simulations, have enabled the rational mutagenesis of key catalytic residues for enhanced or altered biocatalysis. Semi-rational, directed evolution and microenvironment engineering strategies have optimized catalysis for native substrates and increased enzyme promiscuity beyond the scope of traditional rational approaches. These advances are made possible using novel high-throughput screens, including designer protein-based biosensors with engineered ligand specificity. Herein, we detail the most recent of these advances, focusing on polyketides, non-ribosomal peptides and isoprenoids, including their native biosynthetic logic to provide clarity for future applications of these technologies for natural product synthetic biology.
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