Burby Peter E, Simmons Lyle A
Department of Molecular, Cellular, and Developmental Biology, University of Michigan, Ann Arbor, MI, USA.
Bio Protoc. 2017 Apr 20;7(8). doi: 10.21769/BioProtoc.2272.
A fundamental procedure for most modern biologists is the genetic manipulation of the organism under study. Although many different methods for editing bacterial genomes have been used in laboratories for decades, the adaptation of CRISPR/Cas9 technology to bacterial genetics has allowed researchers to manipulate bacterial genomes with unparalleled facility. CRISPR/Cas9 has allowed for genome edits to be more precise, while also increasing the efficiency of transferring mutations into a variety of genetic backgrounds. As a result, the advantages are realized in tractable organisms and organisms that have been refractory to genetic manipulation. Here, we describe our method for editing the genome of the bacterium . Our method is highly efficient, resulting in precise, markerless mutations. Further, after generating the editing plasmid, the mutation can be quickly introduced into several genetic backgrounds, greatly increasing the speed with which genetic analyses may be performed.
对于大多数现代生物学家来说,一个基本的操作流程是对所研究的生物体进行基因操作。尽管几十年来实验室中已经使用了许多不同的编辑细菌基因组的方法,但CRISPR/Cas9技术应用于细菌遗传学,使得研究人员能够以前所未有的便捷方式来操纵细菌基因组。CRISPR/Cas9使基因组编辑更加精确,同时也提高了将突变转移到各种遗传背景中的效率。因此,在易于操作的生物体以及以前难以进行基因操作的生物体中都能体现出这些优势。在这里,我们描述了编辑细菌基因组的方法。我们的方法效率很高,能产生精确的无标记突变。此外,在构建编辑质粒后,突变可以快速引入多种遗传背景中,大大提高了进行遗传分析的速度。