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Characterization of mutations in the PAS domain of the EvgS sensor kinase selected by laboratory evolution for acid resistance in Escherichia coli
Laboratory-based evolution and whole-genome sequencing can link genotype and phenotype. We used evolution of acid resistance in exponential phase Escherichia coli to study resistance to a lethal stress. Iterative selection at pH 2.5 generated five populations that were resistant to low pH in early e...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BlackWell Publishing Ltd
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4283999/ https://www.ncbi.nlm.nih.gov/pubmed/24995530 http://dx.doi.org/10.1111/mmi.12704 |
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author | Johnson, Matthew D Bell, James Clarke, Kim Chandler, Rachel Pathak, Prachi Xia, Yandong Marshall, Robert L Weinstock, George M Loman, Nicholas J Winn, Peter J Lund, Peter A |
author_facet | Johnson, Matthew D Bell, James Clarke, Kim Chandler, Rachel Pathak, Prachi Xia, Yandong Marshall, Robert L Weinstock, George M Loman, Nicholas J Winn, Peter J Lund, Peter A |
author_sort | Johnson, Matthew D |
collection | PubMed |
description | Laboratory-based evolution and whole-genome sequencing can link genotype and phenotype. We used evolution of acid resistance in exponential phase Escherichia coli to study resistance to a lethal stress. Iterative selection at pH 2.5 generated five populations that were resistant to low pH in early exponential phase. Genome sequencing revealed multiple mutations, but the only gene mutated in all strains was evgS, part of a two-component system that has already been implicated in acid resistance. All these mutations were in the cytoplasmic PAS domain of EvgS, and were shown to be solely responsible for the resistant phenotype, causing strong upregulation at neutral pH of genes normally induced by low pH. Resistance to pH 2.5 in these strains did not require the transporter GadC, or the sigma factor RpoS. We found that EvgS-dependent constitutive acid resistance to pH 2.5 was retained in the absence of the regulators GadE or YdeO, but was lost if the oxidoreductase YdeP was also absent. A deletion in the periplasmic domain of EvgS abolished the response to low pH, but not the activity of the constitutive mutants. On the basis of these results we propose a model for how EvgS may become activated by low pH. |
format | Online Article Text |
id | pubmed-4283999 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BlackWell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-42839992015-01-14 Characterization of mutations in the PAS domain of the EvgS sensor kinase selected by laboratory evolution for acid resistance in Escherichia coli Johnson, Matthew D Bell, James Clarke, Kim Chandler, Rachel Pathak, Prachi Xia, Yandong Marshall, Robert L Weinstock, George M Loman, Nicholas J Winn, Peter J Lund, Peter A Mol Microbiol Research Articles Laboratory-based evolution and whole-genome sequencing can link genotype and phenotype. We used evolution of acid resistance in exponential phase Escherichia coli to study resistance to a lethal stress. Iterative selection at pH 2.5 generated five populations that were resistant to low pH in early exponential phase. Genome sequencing revealed multiple mutations, but the only gene mutated in all strains was evgS, part of a two-component system that has already been implicated in acid resistance. All these mutations were in the cytoplasmic PAS domain of EvgS, and were shown to be solely responsible for the resistant phenotype, causing strong upregulation at neutral pH of genes normally induced by low pH. Resistance to pH 2.5 in these strains did not require the transporter GadC, or the sigma factor RpoS. We found that EvgS-dependent constitutive acid resistance to pH 2.5 was retained in the absence of the regulators GadE or YdeO, but was lost if the oxidoreductase YdeP was also absent. A deletion in the periplasmic domain of EvgS abolished the response to low pH, but not the activity of the constitutive mutants. On the basis of these results we propose a model for how EvgS may become activated by low pH. BlackWell Publishing Ltd 2014-09 2014-07-24 /pmc/articles/PMC4283999/ /pubmed/24995530 http://dx.doi.org/10.1111/mmi.12704 Text en © 2014 The Authors. Molecular Microbiology published by John Wiley & Sons Ltd. http://creativecommons.org/licenses/by/3.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Johnson, Matthew D Bell, James Clarke, Kim Chandler, Rachel Pathak, Prachi Xia, Yandong Marshall, Robert L Weinstock, George M Loman, Nicholas J Winn, Peter J Lund, Peter A Characterization of mutations in the PAS domain of the EvgS sensor kinase selected by laboratory evolution for acid resistance in Escherichia coli |
title | Characterization of mutations in the PAS domain of the EvgS sensor kinase selected by laboratory evolution for acid resistance in Escherichia coli |
title_full | Characterization of mutations in the PAS domain of the EvgS sensor kinase selected by laboratory evolution for acid resistance in Escherichia coli |
title_fullStr | Characterization of mutations in the PAS domain of the EvgS sensor kinase selected by laboratory evolution for acid resistance in Escherichia coli |
title_full_unstemmed | Characterization of mutations in the PAS domain of the EvgS sensor kinase selected by laboratory evolution for acid resistance in Escherichia coli |
title_short | Characterization of mutations in the PAS domain of the EvgS sensor kinase selected by laboratory evolution for acid resistance in Escherichia coli |
title_sort | characterization of mutations in the pas domain of the evgs sensor kinase selected by laboratory evolution for acid resistance in escherichia coli |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4283999/ https://www.ncbi.nlm.nih.gov/pubmed/24995530 http://dx.doi.org/10.1111/mmi.12704 |
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