| RRC ID |
4967
|
| Author |
Kashiwagi A, Sakurai T, Tsuru S, Ying BW, Mori K, Yomo T.
|
| Title |
Construction of Escherichia coli gene expression level perturbation collection.
|
| Journal |
Metab Eng
|
| Abstract |
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.
|
| Volume |
11(1)
|
| Pages |
56-63
|
| Published |
2009-1-1
|
| DOI |
10.1016/j.ymben.2008.08.002
|
| PII |
S1096-7176(08)00058-X
|
| PMID |
18790072
|
| MeSH |
Cloning, Molecular
Escherichia coli / genetics
Escherichia coli / metabolism*
Gene Expression Regulation, Bacterial
Genes, Bacterial / physiology*
Molecular Sequence Data
Mutation
Promoter Regions, Genetic
|
| IF |
7.263
|
| Times Cited |
26
|
|
WOS Category
|
BIOTECHNOLOGY & APPLIED MICROBIOLOGY
|
| Resource |
| Prokaryotes E. coli |
ME8569(DH1) |
