大肠杆菌
突变体
基因组
生物
基因
遗传学
计算生物学
全基因组测序
基因组学
基因敲除
作者
Tomoya Baba,Hsuan-Cheng Huan,Kirill A. Datsenko,Barry L. Wanner,Hirotada Mori
出处
期刊:Methods in molecular biology
日期:2008-01-01
卷期号:: 183-194
被引量:47
标识
DOI:10.1007/978-1-59745-321-9_12
摘要
The increasing genome sequence data of microorganisms has provided the basis for comprehensive understanding of organisms at the molecular level. Besides sequence data, a large number of experimental and computational resources are required for genome-scale analyses. Escherichia coli K-12 has been one of the best characterized organisms in molecular biology. Recently, the whole-genome sequences of two closely related E. coli K-12 strains, MG1655 (1) and W3110 (2), were compared and confirmed by resequencing selected regions from both strains (2). The availability of highly accurate E. coli K-12 genomes provided an impetus for the cooperative reannotation of both MG1655 and W3110 (3). A set of precisely defined, single-gene knockout mutants of all nonessential genes in E. coli K-12 was constructed based on the recent accurate genome sequence data ([4] and Chapter 11 ). These mutants were designed to create in-frame (nonpolar) deletions upon elimination of the resistance cassette. These mutants have provided new key information on E. coli biology. First, the vast majority of the 3985 genes that were independently disrupted at least twice are probably nonessential, at least under the conditions of selection. Second, the 303 genes that we repeatedly failed to disrupt are candidates for E. coli essential genes. Lastly, phenotypic effects of all these mutations in the uniform genetic background of E. coli BW25113 were assessed by profiling mutants' growth yields on rich and minimal media (4). These mutants should provide not only a basic resource for systematic functional genomics but also an experimental data source for systems biology applications.
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