Literature DB >> 15576792

Terminal oxidases are essential to bypass the requirement for ResD for full Pho induction in Bacillus subtilis.

Matthew Schau1, Amr Eldakak, F Marion Hulett.   

Abstract

The Bacillus subtilis Pho signal transduction network, which regulates the cellular response to phosphate starvation, integrates the activity of three signal transduction systems to regulate the level of the Pho response. This signal transduction network includes a positive feedback loop between the PhoP/PhoR and ResD/ResE two-component systems. Within this network, ResD is responsible for 80% of the Pho response. To date, the role of ResD in the generation of the Pho response has not been understood. Expression of two terminal oxidases requires ResD function, and expression of at least one terminal oxidase is needed for the wild-type Pho response. Previously, our investigators have shown that strains bearing mutations in resD are impaired for growth and acquire secondary mutations which compensate for the loss of the a-type terminal oxidases by allowing production of cytochrome bd. We report here that the expression of cytochrome bd in a DeltaresDE background is sufficient to compensate for the loss of ResD for full Pho induction. A ctaA mutant strain, deficient in the production of heme A, has the same Pho induction phenotype as a DeltaresDE strain. This demonstrates that the production of a-type terminal oxidases is the basis for the role of ResD in Pho induction. Terminal oxidases affect the redox state of the quinone pool. Reduced quinones inhibit PhoR autophosphorylation in vitro, consistent with a requirement for terminal oxidases for full Pho induction in vivo.

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Year:  2004        PMID: 15576792      PMCID: PMC532433          DOI: 10.1128/JB.186.24.8424-8432.2004

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


  52 in total

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Journal:  Science       Date:  2001-06-22       Impact factor: 47.728

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Authors:  Z Prágai; C Eschevins; S Bron; C R Harwood
Journal:  J Bacteriol       Date:  2001-04       Impact factor: 3.490

3.  The unorthodox histidine kinases BvgS and EvgS are responsive to the oxidation status of a quinone electron carrier.

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Journal:  Eur J Biochem       Date:  2002-07

4.  Autoinduction of Bacillus subtilis phoPR operon transcription results from enhanced transcription from EsigmaA- and EsigmaE-responsive promoters by phosphorylated PhoP.

Authors:  Salbi Paul; Stephanie Birkey; Wei Liu; F Marion Hulett
Journal:  J Bacteriol       Date:  2004-07       Impact factor: 3.490

5.  Bacillus subtilis YdiH is a direct negative regulator of the cydABCD operon.

Authors:  Matthew Schau; Yinghua Chen; F Marion Hulett
Journal:  J Bacteriol       Date:  2004-07       Impact factor: 3.490

6.  Identification of a quinone-sensitive redox switch in the ArcB sensor kinase.

Authors:  Roxana Malpica; Bernardo Franco; Claudia Rodriguez; Ohsuk Kwon; Dimitris Georgellis
Journal:  Proc Natl Acad Sci U S A       Date:  2004-08-23       Impact factor: 11.205

7.  Inducible expression of regulatory genes in Bacillus subtilis.

Authors:  D J Henner
Journal:  Methods Enzymol       Date:  1990       Impact factor: 1.600

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9.  Reconstitution of reduced nicotinamide adenine dinucleotide oxidase activity with menadione in membrane vesicles from the menaquinone-deficient Bacillus subtilis aro D. Relation between electron transfer and active transport.

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10.  Molecular cloning, sequencing, and physiological characterization of the qox operon from Bacillus subtilis encoding the aa3-600 quinol oxidase.

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Journal:  J Biol Chem       Date:  1992-05-25       Impact factor: 5.157

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  12 in total

1.  Direct regulation of Bacillus subtilis phoPR transcription by transition state regulator ScoC.

Authors:  Bindiya Kaushal; Salbi Paul; F Marion Hulett
Journal:  J Bacteriol       Date:  2010-04-09       Impact factor: 3.490

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Journal:  J Bacteriol       Date:  2005-07       Impact factor: 3.490

3.  Regulon of the N-acetylglucosamine utilization regulator NagR in Bacillus subtilis.

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Journal:  J Bacteriol       Date:  2011-05-20       Impact factor: 3.490

4.  CcpA causes repression of the phoPR promoter through a novel transcription start site, P(A6).

Authors:  Ankita Puri-Taneja; Salbi Paul; Yinghua Chen; F Marion Hulett
Journal:  J Bacteriol       Date:  2006-02       Impact factor: 3.490

5.  YycH and YycI interact to regulate the essential YycFG two-component system in Bacillus subtilis.

Authors:  Hendrik Szurmant; Michael A Mohan; P Michael Imus; James A Hoch
Journal:  J Bacteriol       Date:  2007-02-16       Impact factor: 3.490

6.  Cys303 in the histidine kinase PhoR is crucial for the phosphotransfer reaction in the PhoPR two-component system in Bacillus subtilis.

Authors:  Amr Eldakak; F Marion Hulett
Journal:  J Bacteriol       Date:  2006-11-03       Impact factor: 3.490

7.  Distinct Interaction Mechanism of RNA Polymerase and ResD at Proximal and Distal Subsites for Transcription Activation of Nitrite Reductase in Bacillus subtilis.

Authors:  Hannah Jacob; Hao Geng; Dasvit Shetty; Nathan Halow; Linda J Kenney; Michiko M Nakano
Journal:  J Bacteriol       Date:  2021-12-13       Impact factor: 3.476

8.  Virulence gene expression is independent of ResDE-regulated respiration control in Bacillus anthracis.

Authors:  Adam C Wilson; James A Hoch; Marta Perego
Journal:  J Bacteriol       Date:  2008-06-06       Impact factor: 3.490

9.  Genomic analysis reveals the major driving forces of bacterial life in the rhizosphere.

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10.  An integrated network approach identifies the isobutanol response network of Escherichia coli.

Authors:  Mark P Brynildsen; James C Liao
Journal:  Mol Syst Biol       Date:  2009-06-16       Impact factor: 11.429

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