Proteomic evidences for rex regulation of metabolism in toxin-producing Bacillus cereus ATCC 14579.

The facultative anaerobe, Bacillus cereus, causes diarrheal diseases in humans. Its ability to deal with oxygen availability is recognized to be critical for pathogenesis. The B. cereus genome comprises a gene encoding a protein with high similarities to the redox regulator, Rex, which is a central...

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Autores principales: Sabrina Laouami, Géremy Clair, Jean Armengaud, Catherine Duport
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Publicado: Public Library of Science (PLoS) 2014
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spelling oai:doaj.org-article:0ed46592bcb244b889b17942e20b29222021-11-25T06:00:53ZProteomic evidences for rex regulation of metabolism in toxin-producing Bacillus cereus ATCC 14579.1932-620310.1371/journal.pone.0107354https://doaj.org/article/0ed46592bcb244b889b17942e20b29222014-01-01T00:00:00Zhttps://doi.org/10.1371/journal.pone.0107354https://doaj.org/toc/1932-6203The facultative anaerobe, Bacillus cereus, causes diarrheal diseases in humans. Its ability to deal with oxygen availability is recognized to be critical for pathogenesis. The B. cereus genome comprises a gene encoding a protein with high similarities to the redox regulator, Rex, which is a central regulator of anaerobic metabolism in Bacillus subtilis and other Gram-positive bacteria. Here, we showed that B. cereus rex is monocistronic and down-regulated in the absence of oxygen. The protein encoded by rex is an authentic Rex transcriptional factor since its DNA binding activity depends on the NADH/NAD+ ratio. Rex deletion compromised the ability of B. cereus to cope with external oxidative stress under anaerobiosis while increasing B. cereus resistance against such stress under aerobiosis. The deletion of rex affects anaerobic fermentative and aerobic respiratory metabolism of B. cereus by decreasing and increasing, respectively, the carbon flux through the NADH-recycling lactate pathway. We compared both the cellular proteome and exoproteome of the wild-type and Δrex cells using a high throughput shotgun label-free quantitation approach and identified proteins that are under control of Rex-mediated regulation. Proteomics data have been deposited to the ProteomeXchange with identifier PXD000886. The data suggest that Rex regulates both the cross-talk between metabolic pathways that produce NADH and NADPH and toxinogenesis, especially in oxic conditions.Sabrina LaouamiGéremy ClairJean ArmengaudCatherine DuportPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 9, Iss 9, p e107354 (2014)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Sabrina Laouami
Géremy Clair
Jean Armengaud
Catherine Duport
Proteomic evidences for rex regulation of metabolism in toxin-producing Bacillus cereus ATCC 14579.
description The facultative anaerobe, Bacillus cereus, causes diarrheal diseases in humans. Its ability to deal with oxygen availability is recognized to be critical for pathogenesis. The B. cereus genome comprises a gene encoding a protein with high similarities to the redox regulator, Rex, which is a central regulator of anaerobic metabolism in Bacillus subtilis and other Gram-positive bacteria. Here, we showed that B. cereus rex is monocistronic and down-regulated in the absence of oxygen. The protein encoded by rex is an authentic Rex transcriptional factor since its DNA binding activity depends on the NADH/NAD+ ratio. Rex deletion compromised the ability of B. cereus to cope with external oxidative stress under anaerobiosis while increasing B. cereus resistance against such stress under aerobiosis. The deletion of rex affects anaerobic fermentative and aerobic respiratory metabolism of B. cereus by decreasing and increasing, respectively, the carbon flux through the NADH-recycling lactate pathway. We compared both the cellular proteome and exoproteome of the wild-type and Δrex cells using a high throughput shotgun label-free quantitation approach and identified proteins that are under control of Rex-mediated regulation. Proteomics data have been deposited to the ProteomeXchange with identifier PXD000886. The data suggest that Rex regulates both the cross-talk between metabolic pathways that produce NADH and NADPH and toxinogenesis, especially in oxic conditions.
format article
author Sabrina Laouami
Géremy Clair
Jean Armengaud
Catherine Duport
author_facet Sabrina Laouami
Géremy Clair
Jean Armengaud
Catherine Duport
author_sort Sabrina Laouami
title Proteomic evidences for rex regulation of metabolism in toxin-producing Bacillus cereus ATCC 14579.
title_short Proteomic evidences for rex regulation of metabolism in toxin-producing Bacillus cereus ATCC 14579.
title_full Proteomic evidences for rex regulation of metabolism in toxin-producing Bacillus cereus ATCC 14579.
title_fullStr Proteomic evidences for rex regulation of metabolism in toxin-producing Bacillus cereus ATCC 14579.
title_full_unstemmed Proteomic evidences for rex regulation of metabolism in toxin-producing Bacillus cereus ATCC 14579.
title_sort proteomic evidences for rex regulation of metabolism in toxin-producing bacillus cereus atcc 14579.
publisher Public Library of Science (PLoS)
publishDate 2014
url https://doaj.org/article/0ed46592bcb244b889b17942e20b2922
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AT jeanarmengaud proteomicevidencesforrexregulationofmetabolismintoxinproducingbacilluscereusatcc14579
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