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...

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Main Authors: Annika Teppo, Andrio Lahesaare, Hanna Ainelo, Kadri Samuel, Maia Kivisaar, Riho Teras
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2018-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC6072106?pdf=render
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spelling doaj-f2d97c1ac5cb4b558af8e8eee5cab0802020-11-25T02:02:56ZengPublic Library of Science (PLoS)PLoS ONE1932-62032018-01-01138e020184110.1371/journal.pone.0201841Colonization efficiency of Pseudomonas putida is influenced by Fis-controlled transcription of nuoA-N operon.Annika TeppoAndrio LahesaareHanna AineloKadri SamuelMaia KivisaarRiho TerasRoot 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.http://europepmc.org/articles/PMC6072106?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Annika Teppo
Andrio Lahesaare
Hanna Ainelo
Kadri Samuel
Maia Kivisaar
Riho Teras
spellingShingle Annika Teppo
Andrio Lahesaare
Hanna Ainelo
Kadri Samuel
Maia Kivisaar
Riho Teras
Colonization efficiency of Pseudomonas putida is influenced by Fis-controlled transcription of nuoA-N operon.
PLoS ONE
author_facet Annika Teppo
Andrio Lahesaare
Hanna Ainelo
Kadri Samuel
Maia Kivisaar
Riho Teras
author_sort Annika Teppo
title 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_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_sort colonization efficiency of pseudomonas putida is influenced by fis-controlled transcription of nuoa-n operon.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2018-01-01
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.
url http://europepmc.org/articles/PMC6072106?pdf=render
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