Cargando…
Cytoplasmic Acidification and the Benzoate Transcriptome in Bacillus subtilis
BACKGROUND: Bacillus subtilis encounters a wide range of environmental pH. The bacteria maintain cytoplasmic pH within a narrow range. Response to acid stress is a poorly understood function of external pH and of permeant acids that conduct protons into the cytoplasm. METHODS AND PRINCIPAL FINDINGS:...
Autores principales: | , , , , , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2009
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2788229/ https://www.ncbi.nlm.nih.gov/pubmed/20011599 http://dx.doi.org/10.1371/journal.pone.0008255 |
_version_ | 1782174949976309760 |
---|---|
author | Kitko, Ryan D. Cleeton, Rebecca L. Armentrout, Erin I. Lee, Grace E. Noguchi, Ken Berkmen, Melanie B. Jones, Brian D. Slonczewski, Joan L. |
author_facet | Kitko, Ryan D. Cleeton, Rebecca L. Armentrout, Erin I. Lee, Grace E. Noguchi, Ken Berkmen, Melanie B. Jones, Brian D. Slonczewski, Joan L. |
author_sort | Kitko, Ryan D. |
collection | PubMed |
description | BACKGROUND: Bacillus subtilis encounters a wide range of environmental pH. The bacteria maintain cytoplasmic pH within a narrow range. Response to acid stress is a poorly understood function of external pH and of permeant acids that conduct protons into the cytoplasm. METHODS AND PRINCIPAL FINDINGS: Cytoplasmic acidification and the benzoate transcriptome were observed in Bacillus subtilis. Cytoplasmic pH was measured with 4-s time resolution using GFPmut3b fluorimetry. Rapid external acidification (pH 7.5 to 6.0) acidified the B. subtilis cytoplasm, followed by partial recovery. Benzoate addition up to 60 mM at external pH 7 depressed cytoplasmic pH but left a transmembrane ΔpH permitting growth; this robust adaptation to benzoate exceeds that seen in E. coli. Cytoplasmic pH was depressed by 0.3 units during growth with 30 mM benzoate. The transcriptome of benzoate-adapted cells was determined by comparing 4,095 gene expression indices following growth at pH 7, +/− 30 mM benzoate. 164 ORFs showed ≥2-fold up-regulation by benzoate (30 mM benzoate/0 mM), and 102 ORFs showed ≥2-fold down-regulation. 42% of benzoate-dependent genes are regulated up or down, respectively, at pH 6 versus pH 7; they are candidates for cytoplasmic pH response. Acid-stress genes up-regulated by benzoate included drug resistance genes (yhbI, yhcA, yuxJ, ywoGH); an oligopeptide transporter (opp); glycine catabolism (gcvPA-PB); acetate degradation (acsA); dehydrogenases (ald, fdhD, serA, yrhEFG, yjgCD); the TCA cycle (citZ, icd, mdh, sucD); and oxidative stress (OYE-family yqjM, ohrB). Base-stress genes down-regulated by benzoate included malate metabolism (maeN), sporulation control (spo0M, spo0E), and the SigW alkali shock regulon. Cytoplasmic pH could mediate alkali-shock induction of SigW. CONCLUSIONS: B. subtilis maintains partial pH homeostasis during growth, and withstands high concentrations of permeant acid stress, higher than for gram-negative neutralophile E. coli. The benzoate adaptation transcriptome substantially overlaps that of external acid, contributing to a cytoplasmic pH transcriptome. |
format | Text |
id | pubmed-2788229 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-27882292009-12-14 Cytoplasmic Acidification and the Benzoate Transcriptome in Bacillus subtilis Kitko, Ryan D. Cleeton, Rebecca L. Armentrout, Erin I. Lee, Grace E. Noguchi, Ken Berkmen, Melanie B. Jones, Brian D. Slonczewski, Joan L. PLoS One Research Article BACKGROUND: Bacillus subtilis encounters a wide range of environmental pH. The bacteria maintain cytoplasmic pH within a narrow range. Response to acid stress is a poorly understood function of external pH and of permeant acids that conduct protons into the cytoplasm. METHODS AND PRINCIPAL FINDINGS: Cytoplasmic acidification and the benzoate transcriptome were observed in Bacillus subtilis. Cytoplasmic pH was measured with 4-s time resolution using GFPmut3b fluorimetry. Rapid external acidification (pH 7.5 to 6.0) acidified the B. subtilis cytoplasm, followed by partial recovery. Benzoate addition up to 60 mM at external pH 7 depressed cytoplasmic pH but left a transmembrane ΔpH permitting growth; this robust adaptation to benzoate exceeds that seen in E. coli. Cytoplasmic pH was depressed by 0.3 units during growth with 30 mM benzoate. The transcriptome of benzoate-adapted cells was determined by comparing 4,095 gene expression indices following growth at pH 7, +/− 30 mM benzoate. 164 ORFs showed ≥2-fold up-regulation by benzoate (30 mM benzoate/0 mM), and 102 ORFs showed ≥2-fold down-regulation. 42% of benzoate-dependent genes are regulated up or down, respectively, at pH 6 versus pH 7; they are candidates for cytoplasmic pH response. Acid-stress genes up-regulated by benzoate included drug resistance genes (yhbI, yhcA, yuxJ, ywoGH); an oligopeptide transporter (opp); glycine catabolism (gcvPA-PB); acetate degradation (acsA); dehydrogenases (ald, fdhD, serA, yrhEFG, yjgCD); the TCA cycle (citZ, icd, mdh, sucD); and oxidative stress (OYE-family yqjM, ohrB). Base-stress genes down-regulated by benzoate included malate metabolism (maeN), sporulation control (spo0M, spo0E), and the SigW alkali shock regulon. Cytoplasmic pH could mediate alkali-shock induction of SigW. CONCLUSIONS: B. subtilis maintains partial pH homeostasis during growth, and withstands high concentrations of permeant acid stress, higher than for gram-negative neutralophile E. coli. The benzoate adaptation transcriptome substantially overlaps that of external acid, contributing to a cytoplasmic pH transcriptome. Public Library of Science 2009-12-14 /pmc/articles/PMC2788229/ /pubmed/20011599 http://dx.doi.org/10.1371/journal.pone.0008255 Text en Kitko et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Kitko, Ryan D. Cleeton, Rebecca L. Armentrout, Erin I. Lee, Grace E. Noguchi, Ken Berkmen, Melanie B. Jones, Brian D. Slonczewski, Joan L. Cytoplasmic Acidification and the Benzoate Transcriptome in Bacillus subtilis |
title | Cytoplasmic Acidification and the Benzoate Transcriptome in Bacillus subtilis
|
title_full | Cytoplasmic Acidification and the Benzoate Transcriptome in Bacillus subtilis
|
title_fullStr | Cytoplasmic Acidification and the Benzoate Transcriptome in Bacillus subtilis
|
title_full_unstemmed | Cytoplasmic Acidification and the Benzoate Transcriptome in Bacillus subtilis
|
title_short | Cytoplasmic Acidification and the Benzoate Transcriptome in Bacillus subtilis
|
title_sort | cytoplasmic acidification and the benzoate transcriptome in bacillus subtilis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2788229/ https://www.ncbi.nlm.nih.gov/pubmed/20011599 http://dx.doi.org/10.1371/journal.pone.0008255 |
work_keys_str_mv | AT kitkoryand cytoplasmicacidificationandthebenzoatetranscriptomeinbacillussubtilis AT cleetonrebeccal cytoplasmicacidificationandthebenzoatetranscriptomeinbacillussubtilis AT armentrouterini cytoplasmicacidificationandthebenzoatetranscriptomeinbacillussubtilis AT leegracee cytoplasmicacidificationandthebenzoatetranscriptomeinbacillussubtilis AT noguchiken cytoplasmicacidificationandthebenzoatetranscriptomeinbacillussubtilis AT berkmenmelanieb cytoplasmicacidificationandthebenzoatetranscriptomeinbacillussubtilis AT jonesbriand cytoplasmicacidificationandthebenzoatetranscriptomeinbacillussubtilis AT slonczewskijoanl cytoplasmicacidificationandthebenzoatetranscriptomeinbacillussubtilis |