Expanding the Scope of Site-Specific Recombinases for Genetic and Metabolic Engineering

被引:52
|
作者
Gaj, Thomas
Sirk, Shannon J.
Barbas, Carlos F., III [1 ]
机构
[1] Scripps Res Inst, Skaggs Inst Chem Biol, La Jolla, CA 92037 USA
基金
美国国家卫生研究院;
关键词
protein engineering; recombinase; genome engineering; GAMMA-DELTA RESOLVASE; ZINC-FINGER DOMAINS; DIRECTED EVOLUTION; CRE RECOMBINASE; IN-VITRO; FLP RECOMBINASE; DNA-BINDING; PHI-C31; INTEGRASE; CRYSTAL-STRUCTURE; GENOMIC INTEGRATION;
D O I
10.1002/bit.25096
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Site-specific recombinases are tremendously valuable tools for basic research and genetic engineering. By promoting high-fidelity DNA modifications, site-specific recombination systems have empowered researchers with unprecedented control over diverse biological functions, enabling countless insights into cellular structure and function. The rigid target specificities of many sites-specific recombinases, however, have limited their adoption in fields that require highly flexible recognition abilities. As a result, intense effort has been directed toward altering the properties of site-specific recombination systems by protein engineering. Here, we review key developments in the rational design and directed molecular evolution of site-specific recombinases, highlighting the numerous applications of these enzymes across diverse fields of study. Biotechnol. Bioeng. 2014;111: 1-15. (c) 2013 Wiley Periodicals, Inc.
引用
收藏
页码:1 / 15
页数:15
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