Cargando…

The regulatory function of LexA is temperature-dependent in the deep-sea bacterium Shewanella piezotolerans WP3

The SOS response addresses DNA lesions and is conserved in the bacterial domain. The response is governed by the DNA binding protein LexA, which has been characterized in model microorganisms such as Escherichia coli. However, our understanding of its roles in deep-sea bacteria is limited. Here, the...

Descripción completa

Detalles Bibliográficos
Autores principales: Jian, Huahua, Xiong, Lei, He, Ying, Xiao, Xiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4471891/
https://www.ncbi.nlm.nih.gov/pubmed/26150814
http://dx.doi.org/10.3389/fmicb.2015.00627
_version_ 1782376977583308800
author Jian, Huahua
Xiong, Lei
He, Ying
Xiao, Xiang
author_facet Jian, Huahua
Xiong, Lei
He, Ying
Xiao, Xiang
author_sort Jian, Huahua
collection PubMed
description The SOS response addresses DNA lesions and is conserved in the bacterial domain. The response is governed by the DNA binding protein LexA, which has been characterized in model microorganisms such as Escherichia coli. However, our understanding of its roles in deep-sea bacteria is limited. Here, the influence of LexA on the phenotype and gene transcription of Shewanella piezotolerans WP3 (WP3) was investigated by constructing a lexA deletion strain (WP3ΔlexA), which was compared with the wild-type strain. No growth defect was observed for WP3ΔlexA. A total of 481 and 108 genes were differentially expressed at 20 and 4°C, respectively, as demonstrated by comparative whole genome microarray analysis. Furthermore, the swarming motility and dimethylsulfoxide reduction assay demonstrated that the function of LexA was related to temperature. The transcription of the lexA gene was up-regulated during cold acclimatization and after cold shock, indicating that the higher expression level of LexA at low temperatures may be responsible for its temperature-dependent functions. The deep-sea microorganism S. piezotolerans WP3 is the only bacterial species whose SOS regulator has been demonstrated to be significantly influenced by environmental temperatures to date. Our data support the hypothesis that SOS is a formidable strategy used by bacteria against various environmental stresses.
format Online
Article
Text
id pubmed-4471891
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-44718912015-07-06 The regulatory function of LexA is temperature-dependent in the deep-sea bacterium Shewanella piezotolerans WP3 Jian, Huahua Xiong, Lei He, Ying Xiao, Xiang Front Microbiol Microbiology The SOS response addresses DNA lesions and is conserved in the bacterial domain. The response is governed by the DNA binding protein LexA, which has been characterized in model microorganisms such as Escherichia coli. However, our understanding of its roles in deep-sea bacteria is limited. Here, the influence of LexA on the phenotype and gene transcription of Shewanella piezotolerans WP3 (WP3) was investigated by constructing a lexA deletion strain (WP3ΔlexA), which was compared with the wild-type strain. No growth defect was observed for WP3ΔlexA. A total of 481 and 108 genes were differentially expressed at 20 and 4°C, respectively, as demonstrated by comparative whole genome microarray analysis. Furthermore, the swarming motility and dimethylsulfoxide reduction assay demonstrated that the function of LexA was related to temperature. The transcription of the lexA gene was up-regulated during cold acclimatization and after cold shock, indicating that the higher expression level of LexA at low temperatures may be responsible for its temperature-dependent functions. The deep-sea microorganism S. piezotolerans WP3 is the only bacterial species whose SOS regulator has been demonstrated to be significantly influenced by environmental temperatures to date. Our data support the hypothesis that SOS is a formidable strategy used by bacteria against various environmental stresses. Frontiers Media S.A. 2015-06-18 /pmc/articles/PMC4471891/ /pubmed/26150814 http://dx.doi.org/10.3389/fmicb.2015.00627 Text en Copyright © 2015 Jian, Xiong, He and Xiao. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Jian, Huahua
Xiong, Lei
He, Ying
Xiao, Xiang
The regulatory function of LexA is temperature-dependent in the deep-sea bacterium Shewanella piezotolerans WP3
title The regulatory function of LexA is temperature-dependent in the deep-sea bacterium Shewanella piezotolerans WP3
title_full The regulatory function of LexA is temperature-dependent in the deep-sea bacterium Shewanella piezotolerans WP3
title_fullStr The regulatory function of LexA is temperature-dependent in the deep-sea bacterium Shewanella piezotolerans WP3
title_full_unstemmed The regulatory function of LexA is temperature-dependent in the deep-sea bacterium Shewanella piezotolerans WP3
title_short The regulatory function of LexA is temperature-dependent in the deep-sea bacterium Shewanella piezotolerans WP3
title_sort regulatory function of lexa is temperature-dependent in the deep-sea bacterium shewanella piezotolerans wp3
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4471891/
https://www.ncbi.nlm.nih.gov/pubmed/26150814
http://dx.doi.org/10.3389/fmicb.2015.00627
work_keys_str_mv AT jianhuahua theregulatoryfunctionoflexaistemperaturedependentinthedeepseabacteriumshewanellapiezotoleranswp3
AT xionglei theregulatoryfunctionoflexaistemperaturedependentinthedeepseabacteriumshewanellapiezotoleranswp3
AT heying theregulatoryfunctionoflexaistemperaturedependentinthedeepseabacteriumshewanellapiezotoleranswp3
AT xiaoxiang theregulatoryfunctionoflexaistemperaturedependentinthedeepseabacteriumshewanellapiezotoleranswp3
AT jianhuahua regulatoryfunctionoflexaistemperaturedependentinthedeepseabacteriumshewanellapiezotoleranswp3
AT xionglei regulatoryfunctionoflexaistemperaturedependentinthedeepseabacteriumshewanellapiezotoleranswp3
AT heying regulatoryfunctionoflexaistemperaturedependentinthedeepseabacteriumshewanellapiezotoleranswp3
AT xiaoxiang regulatoryfunctionoflexaistemperaturedependentinthedeepseabacteriumshewanellapiezotoleranswp3