Literature DB >> 11244055

Global analysis of Escherichia coli gene expression during the acetate-induced acid tolerance response.

C N Arnold1, J McElhanon, A Lee, R Leonhart, D A Siegele.   

Abstract

The ability of Escherichia coli to survive at low pH is strongly affected by environmental factors, such as composition of the growth medium and growth phase. Exposure to short-chain fatty acids, such as acetate, proprionate, and butyrate, at neutral or nearly neutral pH has also been shown to increase acid survival of E. coli and Salmonella enterica serovar Typhimurium. To investigate the basis for acetate-induced acid tolerance in E. coli O157:H7, genes whose expression was altered by exposure to acetate were identified using gene arrays. The expression of 60 genes was reduced by at least twofold; of these, 48 encode components of the transcription-translation machinery. Expression of 26 genes increased twofold or greater following treatment with acetate. This included six genes whose products are known to be important for survival at low pH. Five of these genes, as well as six other acetate-induced genes, are members of the E. coli RpoS regulon. RpoS, the stress sigma factor, is known to be required for acid tolerance induced by growth at nonlethal low pH or by entry into stationary phase. Disruption of the rpoS gene by a transposon insertion mutation also prevented acetate-induced acid tolerance. However, induction of RpoS expression did not appear to be sufficient to activate the acid tolerance response. Treatment with either NaCl or sodium acetate (pH 7.0) increased expression of an rpoS::lacZ fusion protein, but only treatment with acetate increased acid survival.

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Year:  2001        PMID: 11244055      PMCID: PMC95122          DOI: 10.1128/JB.183.7.2178-2186.2001

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  53 in total

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2.  Global gene expression profiling in Escherichia coli K12. The effects of integration host factor.

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Authors:  M Almirón; A J Link; D Furlong; R Kolter
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Journal:  J Mol Biol       Date:  1997-05-23       Impact factor: 5.469

5.  HDEA, a periplasmic protein that supports acid resistance in pathogenic enteric bacteria.

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6.  Exploring drug-induced alterations in gene expression in Mycobacterium tuberculosis by microarray hybridization.

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7.  The effect of food preservatives on pH homeostasis in Escherichia coli.

Authors:  C V Salmond; R G Kroll; I R Booth
Journal:  J Gen Microbiol       Date:  1984-11

8.  In vitro synthesis of bacteriophage lysozyme.

Authors:  W Salser; R F Gesteland; A Bolle
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9.  Grx5 glutaredoxin plays a central role in protection against protein oxidative damage in Saccharomyces cerevisiae.

Authors:  M T Rodríguez-Manzaneque; J Ros; E Cabiscol; A Sorribas; E Herrero
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10.  Short chain fatty acids in human large intestine, portal, hepatic and venous blood.

Authors:  J H Cummings; E W Pomare; W J Branch; C P Naylor; G T Macfarlane
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  70 in total

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2.  Interfering with different steps of protein synthesis explored by transcriptional profiling of Escherichia coli K-12.

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6.  Validation of reference genes for real-time quantitative PCR studies in gene expression levels of Lactobacillus casei Zhang.

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7.  pH regulates genes for flagellar motility, catabolism, and oxidative stress in Escherichia coli K-12.

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Review 8.  Alternative sigma factors and their roles in bacterial virulence.

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9.  Genes of the GadX-GadW regulon in Escherichia coli.

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10.  Parallel changes in gene expression after 20,000 generations of evolution in Escherichiacoli.

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