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Master regulator NtrC controls the utilization of alternative nitrogen sources in Pseudomonas stutzeri A1501

Pseudomonas stutzeri A1501 is a model strain used to study associative nitrogen fixation, and it possesses the nitrogen regulatory NtrC protein in the core genome. Nitrogen sources represent one of the important factors affecting the efficiency of biological nitrogen fixation in the natural environm...

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Autores principales: Yang, Zhimin, Li, Qin, Yan, Yongliang, Ke, Xiubin, Han, Yueyue, Wu, Shaoyu, Lv, Fanyang, Shao, Yahui, Jiang, Shanshan, Lin, Min, Zhang, Yunhua, Zhan, Yuhua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8443478/
https://www.ncbi.nlm.nih.gov/pubmed/34524580
http://dx.doi.org/10.1007/s11274-021-03144-w
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author Yang, Zhimin
Li, Qin
Yan, Yongliang
Ke, Xiubin
Han, Yueyue
Wu, Shaoyu
Lv, Fanyang
Shao, Yahui
Jiang, Shanshan
Lin, Min
Zhang, Yunhua
Zhan, Yuhua
author_facet Yang, Zhimin
Li, Qin
Yan, Yongliang
Ke, Xiubin
Han, Yueyue
Wu, Shaoyu
Lv, Fanyang
Shao, Yahui
Jiang, Shanshan
Lin, Min
Zhang, Yunhua
Zhan, Yuhua
author_sort Yang, Zhimin
collection PubMed
description Pseudomonas stutzeri A1501 is a model strain used to study associative nitrogen fixation, and it possesses the nitrogen regulatory NtrC protein in the core genome. Nitrogen sources represent one of the important factors affecting the efficiency of biological nitrogen fixation in the natural environment. However, the regulation of NtrC during nitrogen metabolism in P. stutzeri A1501 has not been clarified. In this work, a phenotypic analysis of the ntrC mutant characterized the roles of NtrC in nitrogen metabolism and the oxidative stress response of P. stutzeri A1501. To systematically identify NtrC-controlled gene expression, RNA-seq was performed to further analyse the gene expression differences between the wild-type strain and the ∆ntrC mutant under nitrogen fixation conditions. A total of 1431 genes were found to be significantly altered by ntrC deletion, among which 147 associative genes had NtrC-binding sites, and the pathways for nitrogen fixation regulation, nitrogenous compound acquisition and catabolism and nitrate assimilation were discussed. Furthermore, the oxidative stress-related gene (katB), which was upregulated by ntrC deletion, was suggested to be a potential target gene of NtrC, thus highlighting the importance of NtrC in nitrogenase protection against oxygen damage. Based on these findings, we propose that NtrC is a high-ranking element in the regulatory network of P. stutzeri A1501 that controls a variety of nitrogen metabolic and oxidative stress responsive traits required for adaptation to complex rhizosphere environments. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s11274-021-03144-w.
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spelling pubmed-84434782021-10-08 Master regulator NtrC controls the utilization of alternative nitrogen sources in Pseudomonas stutzeri A1501 Yang, Zhimin Li, Qin Yan, Yongliang Ke, Xiubin Han, Yueyue Wu, Shaoyu Lv, Fanyang Shao, Yahui Jiang, Shanshan Lin, Min Zhang, Yunhua Zhan, Yuhua World J Microbiol Biotechnol Original Paper Pseudomonas stutzeri A1501 is a model strain used to study associative nitrogen fixation, and it possesses the nitrogen regulatory NtrC protein in the core genome. Nitrogen sources represent one of the important factors affecting the efficiency of biological nitrogen fixation in the natural environment. However, the regulation of NtrC during nitrogen metabolism in P. stutzeri A1501 has not been clarified. In this work, a phenotypic analysis of the ntrC mutant characterized the roles of NtrC in nitrogen metabolism and the oxidative stress response of P. stutzeri A1501. To systematically identify NtrC-controlled gene expression, RNA-seq was performed to further analyse the gene expression differences between the wild-type strain and the ∆ntrC mutant under nitrogen fixation conditions. A total of 1431 genes were found to be significantly altered by ntrC deletion, among which 147 associative genes had NtrC-binding sites, and the pathways for nitrogen fixation regulation, nitrogenous compound acquisition and catabolism and nitrate assimilation were discussed. Furthermore, the oxidative stress-related gene (katB), which was upregulated by ntrC deletion, was suggested to be a potential target gene of NtrC, thus highlighting the importance of NtrC in nitrogenase protection against oxygen damage. Based on these findings, we propose that NtrC is a high-ranking element in the regulatory network of P. stutzeri A1501 that controls a variety of nitrogen metabolic and oxidative stress responsive traits required for adaptation to complex rhizosphere environments. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s11274-021-03144-w. Springer Netherlands 2021-09-15 2021 /pmc/articles/PMC8443478/ /pubmed/34524580 http://dx.doi.org/10.1007/s11274-021-03144-w Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Paper
Yang, Zhimin
Li, Qin
Yan, Yongliang
Ke, Xiubin
Han, Yueyue
Wu, Shaoyu
Lv, Fanyang
Shao, Yahui
Jiang, Shanshan
Lin, Min
Zhang, Yunhua
Zhan, Yuhua
Master regulator NtrC controls the utilization of alternative nitrogen sources in Pseudomonas stutzeri A1501
title Master regulator NtrC controls the utilization of alternative nitrogen sources in Pseudomonas stutzeri A1501
title_full Master regulator NtrC controls the utilization of alternative nitrogen sources in Pseudomonas stutzeri A1501
title_fullStr Master regulator NtrC controls the utilization of alternative nitrogen sources in Pseudomonas stutzeri A1501
title_full_unstemmed Master regulator NtrC controls the utilization of alternative nitrogen sources in Pseudomonas stutzeri A1501
title_short Master regulator NtrC controls the utilization of alternative nitrogen sources in Pseudomonas stutzeri A1501
title_sort master regulator ntrc controls the utilization of alternative nitrogen sources in pseudomonas stutzeri a1501
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8443478/
https://www.ncbi.nlm.nih.gov/pubmed/34524580
http://dx.doi.org/10.1007/s11274-021-03144-w
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