Cpf1 Is A Versatile Tool for CRISPR Genome Editing Across Diverse Species of Cyanobacteria

被引:214
作者
Ungerer, Justin [1 ]
Pakrasi, Himadri B. [1 ]
机构
[1] Washington Univ, Dept Biol, Campus Box 1137, St Louis, MO 63130 USA
来源
SCIENTIFIC REPORTS | 2016年 / 6卷
基金
美国国家科学基金会;
关键词
ESCHERICHIA-COLI; ENDONUCLEASE; RESISTANCE; EFFICIENCY; VECTORS; PLASMID; RSF1010;
D O I
10.1038/srep39681
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Cyanobacteria are the ideal organisms for the production of a wide range of bioproducts as they can convert CO2 directly into the desired end product using solar energy. Unfortunately, the engineering of cyanobacteria to create efficient cell factories has been impaired by the cumbersome genetic tools that are currently available for these organisms; especially when trying to accumulate multiple modifications. We sought to construct an efficient and precise tool for generating numerous markerless modifications in cyanobacteria using CRISPR technology and the alternative nuclease, Cpf1. In this study we demonstrate rapid engineering of markerless knock-ins, knock-outs and point mutations in each of three model cyanobacteria; Synechococcus, Synechocystis and Anabaena. The markerless nature of cpf1 genome editing will allow for complex genome modification that was not possible with previously existing technology while facilitating the development of cyanobacteria as highly modified biofactories.
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页数:9
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