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A regulatory network involving Rpo, Gac and Rsm for nitrogen-fixing biofilm formation by Pseudomonas stutzeri

Biofilm and nitrogen fixation are two competitive strategies used by many plant-associated bacteria; however, the mechanisms underlying the formation of nitrogen-fixing biofilms remain largely unknown. Here, we examined the roles of multiple signalling systems in the regulation of biofilm formation...

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Autores principales: Shang, Liguo, Yan, Yongliang, Zhan, Yuhua, Ke, Xiubin, Shao, Yahui, Liu, Yaqun, Yang, Hua, Wang, Shanshan, Dai, Shuling, Lu, Jiasi, Yan, Ning, Yang, Zhimin, Lu, Wei, Liu, Zhu, Chen, Shanchun, Elmerich, Claudine, Lin, Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8249394/
https://www.ncbi.nlm.nih.gov/pubmed/34210981
http://dx.doi.org/10.1038/s41522-021-00230-7
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author Shang, Liguo
Yan, Yongliang
Zhan, Yuhua
Ke, Xiubin
Shao, Yahui
Liu, Yaqun
Yang, Hua
Wang, Shanshan
Dai, Shuling
Lu, Jiasi
Yan, Ning
Yang, Zhimin
Lu, Wei
Liu, Zhu
Chen, Shanchun
Elmerich, Claudine
Lin, Min
author_facet Shang, Liguo
Yan, Yongliang
Zhan, Yuhua
Ke, Xiubin
Shao, Yahui
Liu, Yaqun
Yang, Hua
Wang, Shanshan
Dai, Shuling
Lu, Jiasi
Yan, Ning
Yang, Zhimin
Lu, Wei
Liu, Zhu
Chen, Shanchun
Elmerich, Claudine
Lin, Min
author_sort Shang, Liguo
collection PubMed
description Biofilm and nitrogen fixation are two competitive strategies used by many plant-associated bacteria; however, the mechanisms underlying the formation of nitrogen-fixing biofilms remain largely unknown. Here, we examined the roles of multiple signalling systems in the regulation of biofilm formation by root-associated diazotrophic P. stutzeri A1501. Physiological analysis, construction of mutant strains and microscale thermophoresis experiments showed that RpoN is a regulatory hub coupling nitrogen fixation and biofilm formation by directly activating the transcription of pslA, a major gene involved in the synthesis of the Psl exopolysaccharide component of the biofilm matrix and nifA, the transcriptional activator of nif gene expression. Genetic complementation studies and determination of the copy number of transcripts by droplet digital PCR confirmed that the regulatory ncRNA RsmZ serves as a signal amplifier to trigger biofilm formation by sequestering the translational repressor protein RsmA away from pslA and sadC mRNAs, the latter of which encodes a diguanylate cyclase that synthesises c-di-GMP. Moreover, RpoS exerts a braking effect on biofilm formation by transcriptionally downregulating RsmZ expression, while RpoS expression is repressed posttranscriptionally by RsmA. These findings provide mechanistic insights into how the Rpo/Gac/Rsm regulatory networks fine-tune nitrogen-fixing biofilm formation in response to the availability of nutrients.
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spelling pubmed-82493942021-07-20 A regulatory network involving Rpo, Gac and Rsm for nitrogen-fixing biofilm formation by Pseudomonas stutzeri Shang, Liguo Yan, Yongliang Zhan, Yuhua Ke, Xiubin Shao, Yahui Liu, Yaqun Yang, Hua Wang, Shanshan Dai, Shuling Lu, Jiasi Yan, Ning Yang, Zhimin Lu, Wei Liu, Zhu Chen, Shanchun Elmerich, Claudine Lin, Min NPJ Biofilms Microbiomes Article Biofilm and nitrogen fixation are two competitive strategies used by many plant-associated bacteria; however, the mechanisms underlying the formation of nitrogen-fixing biofilms remain largely unknown. Here, we examined the roles of multiple signalling systems in the regulation of biofilm formation by root-associated diazotrophic P. stutzeri A1501. Physiological analysis, construction of mutant strains and microscale thermophoresis experiments showed that RpoN is a regulatory hub coupling nitrogen fixation and biofilm formation by directly activating the transcription of pslA, a major gene involved in the synthesis of the Psl exopolysaccharide component of the biofilm matrix and nifA, the transcriptional activator of nif gene expression. Genetic complementation studies and determination of the copy number of transcripts by droplet digital PCR confirmed that the regulatory ncRNA RsmZ serves as a signal amplifier to trigger biofilm formation by sequestering the translational repressor protein RsmA away from pslA and sadC mRNAs, the latter of which encodes a diguanylate cyclase that synthesises c-di-GMP. Moreover, RpoS exerts a braking effect on biofilm formation by transcriptionally downregulating RsmZ expression, while RpoS expression is repressed posttranscriptionally by RsmA. These findings provide mechanistic insights into how the Rpo/Gac/Rsm regulatory networks fine-tune nitrogen-fixing biofilm formation in response to the availability of nutrients. Nature Publishing Group UK 2021-07-01 /pmc/articles/PMC8249394/ /pubmed/34210981 http://dx.doi.org/10.1038/s41522-021-00230-7 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Shang, Liguo
Yan, Yongliang
Zhan, Yuhua
Ke, Xiubin
Shao, Yahui
Liu, Yaqun
Yang, Hua
Wang, Shanshan
Dai, Shuling
Lu, Jiasi
Yan, Ning
Yang, Zhimin
Lu, Wei
Liu, Zhu
Chen, Shanchun
Elmerich, Claudine
Lin, Min
A regulatory network involving Rpo, Gac and Rsm for nitrogen-fixing biofilm formation by Pseudomonas stutzeri
title A regulatory network involving Rpo, Gac and Rsm for nitrogen-fixing biofilm formation by Pseudomonas stutzeri
title_full A regulatory network involving Rpo, Gac and Rsm for nitrogen-fixing biofilm formation by Pseudomonas stutzeri
title_fullStr A regulatory network involving Rpo, Gac and Rsm for nitrogen-fixing biofilm formation by Pseudomonas stutzeri
title_full_unstemmed A regulatory network involving Rpo, Gac and Rsm for nitrogen-fixing biofilm formation by Pseudomonas stutzeri
title_short A regulatory network involving Rpo, Gac and Rsm for nitrogen-fixing biofilm formation by Pseudomonas stutzeri
title_sort regulatory network involving rpo, gac and rsm for nitrogen-fixing biofilm formation by pseudomonas stutzeri
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8249394/
https://www.ncbi.nlm.nih.gov/pubmed/34210981
http://dx.doi.org/10.1038/s41522-021-00230-7
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