Current and future prospects for CRISPR-based tools in bacteria

被引:92
|
作者
Luo, Michelle L. [1 ]
Leenay, Ryan T. [1 ]
Beisel, Chase L. [1 ]
机构
[1] N Carolina State Univ, Dept Chem & Biomol Engn, Raleigh, NC 27695 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
antimicrobials; Cas9; genetic control; genetic circuits; genome engineering; undomesticated microbes; RNA-GUIDED ENDONUCLEASE; SEQUENCE-SPECIFIC ANTIMICROBIALS; CAS SYSTEMS; ESCHERICHIA-COLI; HUMAN-CELLS; GENE-EXPRESSION; IMMUNE-SYSTEM; ADAPTIVE IMMUNITY; CRYSTAL-STRUCTURE; STREPTOCOCCUS-THERMOPHILUS;
D O I
10.1002/bit.25851
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
CRISPR-Cas systems have rapidly transitioned from intriguing prokaryotic defense systems to powerful and versatile biomolecular tools. This article reviews how these systems have been translated into technologies to manipulate bacterial genetics, physiology, and communities. Recent applications in bacteria have centered on multiplexed genome editing, programmable gene regulation, and sequence-specific antimicrobials, while future applications can build on advances in eukaryotes, the rich natural diversity of CRISPR-Cas systems, and the untapped potential of CRISPR-based DNA acquisition. Overall, these systems have formed the basis of an ever-expanding genetic toolbox and hold tremendous potential for our future understanding and engineering of the bacterial world. Biotechnol. Bioeng. 2016;113: 930-943. (c) 2015 Wiley Periodicals, Inc.
引用
收藏
页码:930 / 943
页数:14
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