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Colonization efficiency of Pseudomonas putida is influenced by Fis-controlled transcription of nuoA-N operon
Root colonization of plant growth-promoting bacteria is a complex multistep process that is influenced by several factors. For example, during adherence to plant roots, bacteria have to endure reactive oxygen species (ROS) produced by plants. In this study, we report that the global transcriptional...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6072106/ https://www.ncbi.nlm.nih.gov/pubmed/30071101 http://dx.doi.org/10.1371/journal.pone.0201841 |
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author | Teppo, Annika Lahesaare, Andrio Ainelo, Hanna Samuel, Kadri Kivisaar, Maia Teras, Riho |
author_facet | Teppo, Annika Lahesaare, Andrio Ainelo, Hanna Samuel, Kadri Kivisaar, Maia Teras, Riho |
author_sort | Teppo, Annika |
collection | PubMed |
description | Root colonization of plant growth-promoting bacteria is a complex multistep process that is influenced by several factors. For example, during adherence to plant roots, bacteria have to endure reactive oxygen species (ROS) produced by plants. In this study, we report that the global transcriptional regulator Fis is involved in the regulation of ROS-tolerance of Pseudomonas putida and thereby affects barley root colonization. Fis overexpression reduced both ROS-tolerance and adherence to barley roots and activated the transcription of the nuoA-N operon encoding NADH dehydrogenase I, the first enzyme of a membrane-bound electron-transport chain. The nuoA-N knockout mutation in the fis-overexpression background increased the ROS-tolerance and adherence to barley roots. We show that nuoA has two transcriptional start sites located 104 and 377 nucleotides upstream of the coding sequence, indicating the presence of two promoters. The DNase I footprint analysis revealed four Fis binding sites: Fis-nuo1 to Fis-nuo4, situated between these two promoters. Site-directed mutagenesis in a promoter-lacZ reporter and β-galactosidase assay further confirmed direct binding of Fis to Fis-nuo2 and probably to Fis-nuo4 but not to Fis-nuo1 and Fis-nuo3. Additionally, the results implied that Fis binding to Fis-nuo4 could affect transcription of the nuoA-N operon by modification of upstream DNA topology. Moreover, our transposon mutagenesis results indicated that Fis might be involved in the regulation of several alternative ROS detoxification processes utilizing NADH. |
format | Online Article Text |
id | pubmed-6072106 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-60721062018-08-16 Colonization efficiency of Pseudomonas putida is influenced by Fis-controlled transcription of nuoA-N operon Teppo, Annika Lahesaare, Andrio Ainelo, Hanna Samuel, Kadri Kivisaar, Maia Teras, Riho PLoS One Research Article Root colonization of plant growth-promoting bacteria is a complex multistep process that is influenced by several factors. For example, during adherence to plant roots, bacteria have to endure reactive oxygen species (ROS) produced by plants. In this study, we report that the global transcriptional regulator Fis is involved in the regulation of ROS-tolerance of Pseudomonas putida and thereby affects barley root colonization. Fis overexpression reduced both ROS-tolerance and adherence to barley roots and activated the transcription of the nuoA-N operon encoding NADH dehydrogenase I, the first enzyme of a membrane-bound electron-transport chain. The nuoA-N knockout mutation in the fis-overexpression background increased the ROS-tolerance and adherence to barley roots. We show that nuoA has two transcriptional start sites located 104 and 377 nucleotides upstream of the coding sequence, indicating the presence of two promoters. The DNase I footprint analysis revealed four Fis binding sites: Fis-nuo1 to Fis-nuo4, situated between these two promoters. Site-directed mutagenesis in a promoter-lacZ reporter and β-galactosidase assay further confirmed direct binding of Fis to Fis-nuo2 and probably to Fis-nuo4 but not to Fis-nuo1 and Fis-nuo3. Additionally, the results implied that Fis binding to Fis-nuo4 could affect transcription of the nuoA-N operon by modification of upstream DNA topology. Moreover, our transposon mutagenesis results indicated that Fis might be involved in the regulation of several alternative ROS detoxification processes utilizing NADH. Public Library of Science 2018-08-02 /pmc/articles/PMC6072106/ /pubmed/30071101 http://dx.doi.org/10.1371/journal.pone.0201841 Text en © 2018 Teppo et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Teppo, Annika Lahesaare, Andrio Ainelo, Hanna Samuel, Kadri Kivisaar, Maia Teras, Riho Colonization efficiency of Pseudomonas putida is influenced by Fis-controlled transcription of nuoA-N operon |
title | Colonization efficiency of Pseudomonas putida is influenced by Fis-controlled transcription of nuoA-N operon |
title_full | Colonization efficiency of Pseudomonas putida is influenced by Fis-controlled transcription of nuoA-N operon |
title_fullStr | Colonization efficiency of Pseudomonas putida is influenced by Fis-controlled transcription of nuoA-N operon |
title_full_unstemmed | Colonization efficiency of Pseudomonas putida is influenced by Fis-controlled transcription of nuoA-N operon |
title_short | Colonization efficiency of Pseudomonas putida is influenced by Fis-controlled transcription of nuoA-N operon |
title_sort | colonization efficiency of pseudomonas putida is influenced by fis-controlled transcription of nuoa-n operon |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6072106/ https://www.ncbi.nlm.nih.gov/pubmed/30071101 http://dx.doi.org/10.1371/journal.pone.0201841 |
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