Department of Microbiology and Immunology, University of California, San Francisco, San Francisco, CA 94158, USA.
European Molecular Biology Laboratory, Genome Biology Unit, Meyerhofstrasse 1, 69117 Heidelberg, Germany.
Cell Syst. 2017 Mar 22;4(3):291-305.e7. doi: 10.1016/j.cels.2016.12.013. Epub 2017 Feb 8.
A systems-level understanding of Gram-positive bacteria is important from both an environmental and health perspective and is most easily obtained when high-quality, validated genomic resources are available. To this end, we constructed two ordered, barcoded, erythromycin-resistance- and kanamycin-resistance-marked single-gene deletion libraries of the Gram-positive model organism, Bacillus subtilis. The libraries comprise 3,968 and 3,970 genes, respectively, and overlap in all but four genes. Using these libraries, we update the set of essential genes known for this organism, provide a comprehensive compendium of B. subtilis auxotrophic genes, and identify genes required for utilizing specific carbon and nitrogen sources, as well as those required for growth at low temperature. We report the identification of enzymes catalyzing several missing steps in amino acid biosynthesis. Finally, we describe a suite of high-throughput phenotyping methodologies and apply them to provide a genome-wide analysis of competence and sporulation. Altogether, we provide versatile resources for studying gene function and pathway and network architecture in Gram-positive bacteria.
从环境和健康的角度来看,对革兰氏阳性菌进行系统水平的理解非常重要,而当高质量、经过验证的基因组资源可用时,这一点最容易实现。为此,我们构建了革兰氏阳性模式生物枯草芽孢杆菌的两个有序、编码、红霉素抗性和卡那霉素抗性标记的单基因缺失文库。这两个文库分别包含 3968 个和 3970 个基因,除了四个基因之外,其余基因均有重叠。利用这些文库,我们更新了该生物已知的必需基因集,提供了枯草芽孢杆菌营养缺陷型基因的综合纲要,并鉴定了利用特定碳源和氮源以及在低温下生长所需的基因。我们报告了鉴定催化氨基酸生物合成中几个缺失步骤的酶。最后,我们描述了一套高通量表型分析方法,并将其应用于对感受态和孢子形成进行全基因组分析。总之,我们提供了用于研究革兰氏阳性菌中基因功能和途径以及网络结构的多功能资源。