Construction of Escherichia coli K-12 in-frame, single-gene knockout mutants:: the Keio collection

被引:5341
作者
Baba, Tomoya
Ara, Takeshi
Hasegawa, Miki
Takai, Yuki
Okumura, Yoshiko
Baba, Miki
Datsenko, Kirill A.
Tomita, Masaru
Wanner, Barry L. [1 ]
Mori, Hirotada
机构
[1] Purdue Univ, Dept Biol Sci, W Lafayette, IN 47907 USA
[2] Nara Inst Sci & Technol, Grad Sch Biol Sci, Ikoma, Nara 6300101, Japan
[3] Keio Univ, Inst Adv Biosci, Tsuruoka, Yamagata, Japan
[4] Japan Sci & Technol, CREST, Kawaguchi, Saitama, Japan
关键词
bacterial functional genomics; E; coli/gene; essential gene; knockout mutants; resources; systems biology;
D O I
10.1038/msb4100050
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We have systematically made a set of precisely defined, single-gene deletions of all nonessential genes in Escherichia coli K-12. Open-reading frame coding regions were replaced with a kanamycin cassette flanked by FLP recognition target sites by using a one-step method for inactivation of chromosomal genes and primers designed to create in-frame deletions upon excision of the resistance cassette. Of 4288 genes targeted, mutants were obtained for 3985. To alleviate problems encountered in high-throughput studies, two independent mutants were saved for every deleted gene. These mutants-the 'Keio collection'-provide a new resource not only for systematic analyses of unknown gene functions and gene regulatory networks but also for genome-wide testing of mutational effects in a common strain background, E. coli K-12 BW25113. We were unable to disrupt 303 genes, including 37 of unknown function, which are candidates for essential genes. Distribution is being handled via GenoBase (http://ecoli.aist-nara.ac.jp/).
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页数:11
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