Expanding the metabolic engineering toolbox with directed evolution

被引:46
作者
Abatemarco, Joseph [1 ]
Hill, Andrew [1 ]
Alper, Hal S. [1 ,2 ]
机构
[1] Univ Texas Austin, Dept Chem Engn, Austin, TX 78712 USA
[2] Univ Texas Austin, Inst Cellular & Mol Biol, Austin, TX 78712 USA
基金
美国国家科学基金会;
关键词
Directed evolution; Metabolic engineering; Pathway engineering; Synthetic biology; ESCHERICHIA-COLI; LABORATORY EVOLUTION; TRANSCRIPTION FACTOR; ADAPTIVE EVOLUTION; SACCHAROMYCES-CEREVISIAE; XYLOSE CATABOLISM; GALACTOSE-OXIDASE; ACID PRODUCTION; EXPRESSION; PROMOTER;
D O I
10.1002/biot.201300021
中图分类号
Q5 [生物化学];
学科分类号
070307 [化学生物学];
摘要
Cellular systems can be engineered into factories that produce high-value chemicals from renewable feedstock. Such an approach requires an expanded toolbox for metabolic engineering. Recently, protein engineering and directed evolution strategies have started to play a growing and critical role within metabolic engineering. This review focuses on the various ways in which directed evolution can be applied in conjunction with metabolic engineering to improve product yields. Specifically, we discuss the application of directed evolution on both catalytic and non-catalytic traits of enzymes, on regulatory elements, and on whole genomes in a metabolic engineering context. We demonstrate how the goals of metabolic pathway engineering can be achieved in part through evolving cellular parts as opposed to traditional approaches that rely on gene overexpression and deletion. Finally, we discuss the current limitations in screening technology that hinder the full implementation of a metabolic pathway-directed evolution approach.
引用
收藏
页码:1397 / 1410
页数:14
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