Literature DB >> 15184550

Specific growth rate and not cell density controls the general stress response in Escherichia coli.

Julian Ihssen1, Thomas Egli.   

Abstract

In batch cultures of Escherichia coli, the intracellular concentration of the general stress response sigma factor RpoS typically increases during the transition from the exponential to the stationary growth phase. However, because this transition is accompanied by complex physico-chemical and biological changes, which signals predominantly elicit this induction is still the subject of debate. Careful design of the growth environment in chemostat and batch cultures allowed the separate study of individual factors affecting RpoS. Specific growth rate, and not cell density or the nature of the growth-limiting nutrient, controlled RpoS expression and RpoS-dependent hydroperoxidase activity. Furthermore, it was demonstrated that the standard E. coli minimal medium A (MMA) is not suitable for high-cell-density cultivation because it lacks trace elements. Previously reported cell-density effects in chemostat cultures of E. coli can be explained by a hidden, secondary nutrient limitation, which points to the importance of medium design and appropriate experimental set-up for studying cell-density effects.

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Year:  2004        PMID: 15184550     DOI: 10.1099/mic.0.26849-0

Source DB:  PubMed          Journal:  Microbiology        ISSN: 1350-0872            Impact factor:   2.777


  45 in total

1.  Genome-wide expression analysis indicates that FNR of Escherichia coli K-12 regulates a large number of genes of unknown function.

Authors:  Yisheng Kang; K Derek Weber; Yu Qiu; Patricia J Kiley; Frederick R Blattner
Journal:  J Bacteriol       Date:  2005-02       Impact factor: 3.490

2.  Autoinduction of RpoS biosynthesis in the biocontrol strain Pseudomonas sp. M18.

Authors:  Yi-He Ge; Dong-Li Pei; Pei-Yong Feng; Xian-Qing Huang; Yu-Quan Xu
Journal:  Curr Microbiol       Date:  2007-01-02       Impact factor: 2.188

3.  Medium plays a role in determining expression of acrB, marA, and soxS in Escherichia coli.

Authors:  Andrew M Bailey; Mark A Webber; Laura J V Piddock
Journal:  Antimicrob Agents Chemother       Date:  2006-03       Impact factor: 5.191

4.  Genotype-by-environment interactions influencing the emergence of rpoS mutations in Escherichia coli populations.

Authors:  Thea King; Shona Seeto; Thomas Ferenci
Journal:  Genetics       Date:  2006-02-19       Impact factor: 4.562

5.  Protein production by Escherichia coli wild-type and DeltaptsG mutant strains with IPTG induction at the onset.

Authors:  A Picon; M J Teixeira de Mattos; P W Postma
Journal:  J Ind Microbiol Biotechnol       Date:  2008-01-08       Impact factor: 3.346

Review 6.  Survival of Escherichia coli in the environment: fundamental and public health aspects.

Authors:  Jan Dirk van Elsas; Alexander V Semenov; Rodrigo Costa; Jack T Trevors
Journal:  ISME J       Date:  2010-06-24       Impact factor: 10.302

7.  Gene expression analysis of E. coli strains provides insights into the role of gene regulation in diversification.

Authors:  Marius Vital; Benli Chai; Bjørn Østman; James Cole; Konstantinos T Konstantinidis; James M Tiedje
Journal:  ISME J       Date:  2014-10-24       Impact factor: 10.302

Review 8.  Starvation, detoxification, and multidrug resistance in cancer therapy.

Authors:  Changhan Lee; Lizzia Raffaghello; Valter D Longo
Journal:  Drug Resist Updat       Date:  2012-03-04       Impact factor: 18.500

Review 9.  The functional basis of adaptive evolution in chemostats.

Authors:  David Gresham; Jungeui Hong
Journal:  FEMS Microbiol Rev       Date:  2014-12-04       Impact factor: 16.408

10.  Production of glycoprotein vaccines in Escherichia coli.

Authors:  Julian Ihssen; Michael Kowarik; Sandro Dilettoso; Cyril Tanner; Michael Wacker; Linda Thöny-Meyer
Journal:  Microb Cell Fact       Date:  2010-08-11       Impact factor: 5.328

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