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DNA Backbone Sulfur-Modification Expands Microbial Growth Range under Multiple Stresses by its anti-oxidation function

DNA phosphorothioate (PT) modification is a sulfur modification on the backbone of DNA introduced by the proteins DndA-E. It has been detected within many bacteria isolates and metagenomic datasets, including human pathogens, and is considered to be widely distributed in nature. However, little is k...

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Autores principales: Yang, Yan, Xu, Guanpeng, Liang, Jingdan, He, Ying, Xiong, Lei, Li, Hui, Bartlett, Douglas, Deng, Zixin, Wang, Zhijun, Xiao, Xiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5471199/
https://www.ncbi.nlm.nih.gov/pubmed/28615635
http://dx.doi.org/10.1038/s41598-017-02445-1
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author Yang, Yan
Xu, Guanpeng
Liang, Jingdan
He, Ying
Xiong, Lei
Li, Hui
Bartlett, Douglas
Deng, Zixin
Wang, Zhijun
Xiao, Xiang
author_facet Yang, Yan
Xu, Guanpeng
Liang, Jingdan
He, Ying
Xiong, Lei
Li, Hui
Bartlett, Douglas
Deng, Zixin
Wang, Zhijun
Xiao, Xiang
author_sort Yang, Yan
collection PubMed
description DNA phosphorothioate (PT) modification is a sulfur modification on the backbone of DNA introduced by the proteins DndA-E. It has been detected within many bacteria isolates and metagenomic datasets, including human pathogens, and is considered to be widely distributed in nature. However, little is known about the physiological function of this modification, and thus its evolutionary significance and application potential remains largely a mystery. In this study, we focused on the advantages of DNA PT modification to bacterial cells coping with environmental stresses. We show that the mesophile Escherichia coli and the extremophile Shewanella piezotolerans both expanded their growth ranges following exposure to extreme temperature, salinity, pH, pressure, UV, X-ray and heavy metals as a result of DNA phophorothioation. The phophorothioated DNA reacted to both H(2)O(2) and hydroxyl radicals in vivo, and protected genomic DNA as well as sensitive enzymes from intracellular oxidative damage. We further demonstrate that this process has evolved separate from its associated role in DNA restriction and modification. These findings provide a physiological role for a covalent modification widespread in nature and suggest possible applications in biotechnology and biomedicine.
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spelling pubmed-54711992017-06-19 DNA Backbone Sulfur-Modification Expands Microbial Growth Range under Multiple Stresses by its anti-oxidation function Yang, Yan Xu, Guanpeng Liang, Jingdan He, Ying Xiong, Lei Li, Hui Bartlett, Douglas Deng, Zixin Wang, Zhijun Xiao, Xiang Sci Rep Article DNA phosphorothioate (PT) modification is a sulfur modification on the backbone of DNA introduced by the proteins DndA-E. It has been detected within many bacteria isolates and metagenomic datasets, including human pathogens, and is considered to be widely distributed in nature. However, little is known about the physiological function of this modification, and thus its evolutionary significance and application potential remains largely a mystery. In this study, we focused on the advantages of DNA PT modification to bacterial cells coping with environmental stresses. We show that the mesophile Escherichia coli and the extremophile Shewanella piezotolerans both expanded their growth ranges following exposure to extreme temperature, salinity, pH, pressure, UV, X-ray and heavy metals as a result of DNA phophorothioation. The phophorothioated DNA reacted to both H(2)O(2) and hydroxyl radicals in vivo, and protected genomic DNA as well as sensitive enzymes from intracellular oxidative damage. We further demonstrate that this process has evolved separate from its associated role in DNA restriction and modification. These findings provide a physiological role for a covalent modification widespread in nature and suggest possible applications in biotechnology and biomedicine. Nature Publishing Group UK 2017-06-14 /pmc/articles/PMC5471199/ /pubmed/28615635 http://dx.doi.org/10.1038/s41598-017-02445-1 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Yang, Yan
Xu, Guanpeng
Liang, Jingdan
He, Ying
Xiong, Lei
Li, Hui
Bartlett, Douglas
Deng, Zixin
Wang, Zhijun
Xiao, Xiang
DNA Backbone Sulfur-Modification Expands Microbial Growth Range under Multiple Stresses by its anti-oxidation function
title DNA Backbone Sulfur-Modification Expands Microbial Growth Range under Multiple Stresses by its anti-oxidation function
title_full DNA Backbone Sulfur-Modification Expands Microbial Growth Range under Multiple Stresses by its anti-oxidation function
title_fullStr DNA Backbone Sulfur-Modification Expands Microbial Growth Range under Multiple Stresses by its anti-oxidation function
title_full_unstemmed DNA Backbone Sulfur-Modification Expands Microbial Growth Range under Multiple Stresses by its anti-oxidation function
title_short DNA Backbone Sulfur-Modification Expands Microbial Growth Range under Multiple Stresses by its anti-oxidation function
title_sort dna backbone sulfur-modification expands microbial growth range under multiple stresses by its anti-oxidation function
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5471199/
https://www.ncbi.nlm.nih.gov/pubmed/28615635
http://dx.doi.org/10.1038/s41598-017-02445-1
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