Construction of Escherichia coli gene expression level perturbation collection

被引:28
作者
Kashiwagi, Akiko [1 ]
Sakurai, Takahiro [1 ]
Tsuru, Saburo [1 ]
Ying, Bei-Wen [1 ]
Mori, Kotaro [2 ]
Yomo, Tetsuya [1 ,2 ,3 ]
机构
[1] Osaka Univ, Dept Bioinformat Engn, Grad Sch Informat Sci & Technol, Suita, Osaka 5650871, Japan
[2] Osaka Univ, Grad Sch Frontier Biosci, Suita, Osaka 5650871, Japan
[3] JST, ERATO, Complex Syst Biol Project, Suita, Osaka 5650871, Japan
关键词
Escherichia coli; Strain engineering; Expression level control; PROTEIN; METABOLOME; PHENOTYPES; PROMOTER; SEQUENCE; STRAIN; OMICS;
D O I
10.1016/j.ymben.2008.08.002
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
We generated 61 strains of Escherichia coli in which the expression level of a specific single gene can be changed continuously over a physiologically significant range. In each strain, one auxotrophic gene was deleted from its original position and reinserted at a specific position on the chromosome under the control of the tetA promoter. Therefore, the level of expression of the target gene can be controlled easily by altering the concentrations of inducers, e. g., anhydrotetracycline and doxycycline, in the medium. Protein and mRNA levels and changes in proliferation rate were examined in some of the strains in our collection to determine the ability to control the level of target gene expression over a physiologically significant range. These strains will be useful for extracting omics data sets and for the construction of genome-scale mathematical models, because causality between perturbations in gene expression level and their consequences can be clearly determined. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:56 / 63
页数:8
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