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Adaptation to sustained nitrogen starvation by Escherichia coli requires the eukaryote-like serine/threonine kinase YeaG
The Escherichia coli eukaryote-like serine/threonine kinase, encoded by yeaG, is expressed in response to diverse stresses, including nitrogen (N) starvation. A role for yeaG in bacterial stress response is unknown. Here we reveal for the first time that wild-type E. coli displays metabolic heteroge...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4664914/ https://www.ncbi.nlm.nih.gov/pubmed/26621053 http://dx.doi.org/10.1038/srep17524 |
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author | Figueira, Rita Brown, Daniel R. Ferreira, Delfim Eldridge, Matthew J. G. Burchell, Lynn Pan, Zhensheng Helaine, Sophie Wigneshweraraj, Sivaramesh |
author_facet | Figueira, Rita Brown, Daniel R. Ferreira, Delfim Eldridge, Matthew J. G. Burchell, Lynn Pan, Zhensheng Helaine, Sophie Wigneshweraraj, Sivaramesh |
author_sort | Figueira, Rita |
collection | PubMed |
description | The Escherichia coli eukaryote-like serine/threonine kinase, encoded by yeaG, is expressed in response to diverse stresses, including nitrogen (N) starvation. A role for yeaG in bacterial stress response is unknown. Here we reveal for the first time that wild-type E. coli displays metabolic heterogeneity following sustained periods of N starvation, with the metabolically active population displaying compromised viability. In contrast, such heterogeneity in metabolic activity is not observed in an E. coli ∆yeaG mutant, which continues to exist as a single and metabolically active population and thus displays an overall compromised ability to survive sustained periods of N starvation. The mechanism by which yeaG acts, involves the transcriptional repression of two toxin/antitoxin modules, mqsR/mqsA and dinJ/yafQ. This, consequently, has a positive effect on the expression of rpoS, the master regulator of the general bacterial stress response. Overall, results indicate that yeaG is required to fully execute the rpoS-dependent gene expression program to allow E. coli to adapt to sustained N starvation and unravels a novel facet to the regulatory basis that underpins adaptive response to N stress. |
format | Online Article Text |
id | pubmed-4664914 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-46649142015-12-03 Adaptation to sustained nitrogen starvation by Escherichia coli requires the eukaryote-like serine/threonine kinase YeaG Figueira, Rita Brown, Daniel R. Ferreira, Delfim Eldridge, Matthew J. G. Burchell, Lynn Pan, Zhensheng Helaine, Sophie Wigneshweraraj, Sivaramesh Sci Rep Article The Escherichia coli eukaryote-like serine/threonine kinase, encoded by yeaG, is expressed in response to diverse stresses, including nitrogen (N) starvation. A role for yeaG in bacterial stress response is unknown. Here we reveal for the first time that wild-type E. coli displays metabolic heterogeneity following sustained periods of N starvation, with the metabolically active population displaying compromised viability. In contrast, such heterogeneity in metabolic activity is not observed in an E. coli ∆yeaG mutant, which continues to exist as a single and metabolically active population and thus displays an overall compromised ability to survive sustained periods of N starvation. The mechanism by which yeaG acts, involves the transcriptional repression of two toxin/antitoxin modules, mqsR/mqsA and dinJ/yafQ. This, consequently, has a positive effect on the expression of rpoS, the master regulator of the general bacterial stress response. Overall, results indicate that yeaG is required to fully execute the rpoS-dependent gene expression program to allow E. coli to adapt to sustained N starvation and unravels a novel facet to the regulatory basis that underpins adaptive response to N stress. Nature Publishing Group 2015-12-01 /pmc/articles/PMC4664914/ /pubmed/26621053 http://dx.doi.org/10.1038/srep17524 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Figueira, Rita Brown, Daniel R. Ferreira, Delfim Eldridge, Matthew J. G. Burchell, Lynn Pan, Zhensheng Helaine, Sophie Wigneshweraraj, Sivaramesh Adaptation to sustained nitrogen starvation by Escherichia coli requires the eukaryote-like serine/threonine kinase YeaG |
title | Adaptation to sustained nitrogen starvation by Escherichia coli requires the eukaryote-like serine/threonine kinase YeaG |
title_full | Adaptation to sustained nitrogen starvation by Escherichia coli requires the eukaryote-like serine/threonine kinase YeaG |
title_fullStr | Adaptation to sustained nitrogen starvation by Escherichia coli requires the eukaryote-like serine/threonine kinase YeaG |
title_full_unstemmed | Adaptation to sustained nitrogen starvation by Escherichia coli requires the eukaryote-like serine/threonine kinase YeaG |
title_short | Adaptation to sustained nitrogen starvation by Escherichia coli requires the eukaryote-like serine/threonine kinase YeaG |
title_sort | adaptation to sustained nitrogen starvation by escherichia coli requires the eukaryote-like serine/threonine kinase yeag |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4664914/ https://www.ncbi.nlm.nih.gov/pubmed/26621053 http://dx.doi.org/10.1038/srep17524 |
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