Literature DB >> 15805528

Comprehensive characterization of the contribution of individual SigB-dependent general stress genes to stress resistance of Bacillus subtilis.

Dirk Höper1, Uwe Völker, Michael Hecker.   

Abstract

The sigma(B)-dependent general stress regulon of Bacillus subtilis comprises more than 150 members. Induction of this regulon by imposition of environmental or metabolic stress confers multiple, nonspecific, and preemptive stress resistance to nongrowing, nonsporulated cells of B. subtilis. In this study we performed a regulon-wide phenotypic screening analysis to determine the stress sensitivity profiles of 94 mutants defective in candidate members of the general stress regulon that were previously identified in our transcriptional profiling study of the general stress response of B. subtilis. The phenotypic screening analysis included analysis of adaptation to a growth-inhibiting concentration of ethanol (10%, vol/vol) or NaCl (10%, wt/vol), severe heat shock (54 degrees C), and low temperature (survival at 4 degrees C and growth at 12.5 degrees C). Surprisingly, 85% of the mutants tested displayed increased sensitivity at an alpha confidence level of < or =0.01 to at least one of the four stresses tested, and 62% still exhibited increased sensitivity at an alpha of < or =0.001. In essence, we were able to assign 63 genes (28 genes with an alpha of < or =0.001) to survival after ethanol shock, 37 genes (28 genes with an alpha of < or =0.001) to protection from NaCl shock, 34 genes (24 genes with an alpha of < or =0.001) to survival at 4 degrees C, and 10 genes (3 genes with an alpha of < or =0.001) to management of severe heat shock. Interestingly, there was a substantial overlap between the genes necessary for survival during ethanol shock and the genes necessary for survival at 4 degrees C, and there was also an overlap between genes required for survival during ethanol shock and genes required for survival during NaCl shock. Our data provide evidence for the importance of the sigma(B) regulon at low temperatures, not only for growth but also for survival. Moreover, the data imply that a secondary oxidative stress seems to be a common component of the severe stresses tested.

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Year:  2005        PMID: 15805528      PMCID: PMC1070366          DOI: 10.1128/JB.187.8.2810-2826.2005

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


  57 in total

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3.  REQUIREMENTS FOR TRANSFORMATION IN BACILLUS SUBTILIS.

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Journal:  J Bacteriol       Date:  1961-05       Impact factor: 3.490

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Authors:  T A Gaidenko; C W Price
Journal:  J Bacteriol       Date:  1998-07       Impact factor: 3.490

Review 5.  General stress response of Bacillus subtilis and other bacteria.

Authors:  M Hecker; U Völker
Journal:  Adv Microb Physiol       Date:  2001       Impact factor: 3.517

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Authors:  M Igo; M Lampe; C Ray; W Schafer; C P Moran; R Losick
Journal:  J Bacteriol       Date:  1987-08       Impact factor: 3.490

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8.  Identification of the Clostridium perfringens genes involved in the adaptive response to oxidative stress.

Authors:  V Briolat; G Reysset
Journal:  J Bacteriol       Date:  2002-05       Impact factor: 3.490

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Journal:  J Bacteriol       Date:  1977-01       Impact factor: 3.490

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Journal:  J Bacteriol       Date:  2004-03       Impact factor: 3.490

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  46 in total

1.  Phenotypic and transcriptomic analyses of mildly and severely salt-stressed Bacillus cereus ATCC 14579 cells.

Authors:  Heidy M W den Besten; Maarten Mols; Roy Moezelaar; Marcel H Zwietering; Tjakko Abee
Journal:  Appl Environ Microbiol       Date:  2009-04-24       Impact factor: 4.792

2.  The cell wall regulator {sigma}I specifically suppresses the lethal phenotype of mbl mutants in Bacillus subtilis.

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Journal:  J Bacteriol       Date:  2008-12-29       Impact factor: 3.490

3.  Contributions of individual σB-dependent general stress genes to oxidative stress resistance of Bacillus subtilis.

Authors:  Alexander Reder; Dirk Höper; Ulf Gerth; Michael Hecker
Journal:  J Bacteriol       Date:  2012-05-11       Impact factor: 3.490

4.  Red light activates the sigmaB-mediated general stress response of Bacillus subtilis via the energy branch of the upstream signaling cascade.

Authors:  Marcela Avila-Pérez; Jeroen B van der Steen; Remco Kort; Klaas J Hellingwerf
Journal:  J Bacteriol       Date:  2009-11-30       Impact factor: 3.490

5.  Identification of components of the sigma B regulon in Listeria monocytogenes that contribute to acid and salt tolerance.

Authors:  F Abram; E Starr; K A G Karatzas; K Matlawska-Wasowska; A Boyd; M Wiedmann; K J Boor; D Connally; C P O'Byrne
Journal:  Appl Environ Microbiol       Date:  2008-09-19       Impact factor: 4.792

6.  Insights into resistome and stress responses genes in Bubalus bubalis rumen through metagenomic analysis.

Authors:  Bhaskar Reddy; Krishna M Singh; Amrutlal K Patel; Ancy Antony; Harshad J Panchasara; Chaitanya G Joshi
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7.  Aag Hypoxanthine-DNA Glycosylase Is Synthesized in the Forespore Compartment and Involved in Counteracting the Genotoxic and Mutagenic Effects of Hypoxanthine and Alkylated Bases in DNA during Bacillus subtilis Sporulation.

Authors:  Víctor M Ayala-García; Luz I Valenzuela-García; Peter Setlow; Mario Pedraza-Reyes
Journal:  J Bacteriol       Date:  2016-11-18       Impact factor: 3.490

8.  Activity of the osmotically regulated yqiHIK promoter from Bacillus subtilis is controlled at a distance.

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Journal:  J Bacteriol       Date:  2012-07-27       Impact factor: 3.490

9.  Catalase activity as a biomarker for mild-stress-induced robustness in Bacillus weihenstephanensis.

Authors:  Heidy M W den Besten; Styliani Effraimidou; Tjakko Abee
Journal:  Appl Environ Microbiol       Date:  2012-10-12       Impact factor: 4.792

10.  A community-curated consensual annotation that is continuously updated: the Bacillus subtilis centred wiki SubtiWiki.

Authors:  Lope A Flórez; Sebastian F Roppel; Arne G Schmeisky; Christoph R Lammers; Jörg Stülke
Journal:  Database (Oxford)       Date:  2009-09-17       Impact factor: 3.451

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