A Complex Interplay between Nitric Oxide, Quorum Sensing, and the Unique Secondary Metabolite Tundrenone Constitutes the Hypoxia Response in Methylobacter

Here, we describe a novel and complex hypoxia response system in a methanotrophic bacterium that involves modules of central carbon metabolism, denitrification, quorum sensing, and a secondary metabolite, tundrenone. This intricate stress response system, so far unique to Methylobacter species, may...

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Main Authors: Zheng Yu, Mitchell Pesesky, Lei Zhang, Jing Huang, Mari Winkler, Ludmila Chistoserdova
Format: Article
Language:English
Published: American Society for Microbiology 2020-01-01
Series:mSystems
Subjects:
Online Access:https://doi.org/10.1128/mSystems.00770-19
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spelling doaj-6c4e0021737541939de5e69a7da434bf2020-11-25T02:03:06ZengAmerican Society for MicrobiologymSystems2379-50772020-01-0151e00770-1910.1128/mSystems.00770-19A Complex Interplay between Nitric Oxide, Quorum Sensing, and the Unique Secondary Metabolite Tundrenone Constitutes the Hypoxia Response in MethylobacterZheng YuMitchell PeseskyLei ZhangJing HuangMari WinklerLudmila ChistoserdovaHere, we describe a novel and complex hypoxia response system in a methanotrophic bacterium that involves modules of central carbon metabolism, denitrification, quorum sensing, and a secondary metabolite, tundrenone. This intricate stress response system, so far unique to Methylobacter species, may be responsible for the persistence and activity of these species across gradients of dioxygen tensions and for the cosmopolitan distribution of these organisms in freshwater and soil environments in the Northern Hemisphere, including the fast-melting permafrosts.Methylobacter species, members of the Methylococcales, have recently emerged as some of the globally widespread, cosmopolitan species that play a key role in the environmental consumption of methane across gradients of dioxygen tensions. In this work, we approached the question of how Methylobacter copes with hypoxia, via laboratory manipulation. Through comparative transcriptomics of cultures grown under high dioxygen partial pressure versus cultures exposed to hypoxia, we identified a gene cluster encoding a hybrid cluster protein along with sensing and regulatory functions. Through mutant analysis, we demonstrated that this gene cluster is involved in the hypoxia stress response. Through additional transcriptomic analyses, we uncovered a complex interconnection between the NO-mediated stress response, quorum sensing, the secondary metabolite tundrenone, and methanol dehydrogenase functions. This novel and complex hypoxia stress response system is so far unique to Methylobacter species, and it may play a role in the environmental fitness of these organisms and in their cosmopolitan environmental distribution.https://doi.org/10.1128/mSystems.00770-19hypoxiamethylobacter tundripaludumnitric oxidehybrid cluster proteinquorum sensingtundrenone
collection DOAJ
language English
format Article
sources DOAJ
author Zheng Yu
Mitchell Pesesky
Lei Zhang
Jing Huang
Mari Winkler
Ludmila Chistoserdova
spellingShingle Zheng Yu
Mitchell Pesesky
Lei Zhang
Jing Huang
Mari Winkler
Ludmila Chistoserdova
A Complex Interplay between Nitric Oxide, Quorum Sensing, and the Unique Secondary Metabolite Tundrenone Constitutes the Hypoxia Response in Methylobacter
mSystems
hypoxia
methylobacter tundripaludum
nitric oxide
hybrid cluster protein
quorum sensing
tundrenone
author_facet Zheng Yu
Mitchell Pesesky
Lei Zhang
Jing Huang
Mari Winkler
Ludmila Chistoserdova
author_sort Zheng Yu
title A Complex Interplay between Nitric Oxide, Quorum Sensing, and the Unique Secondary Metabolite Tundrenone Constitutes the Hypoxia Response in Methylobacter
title_short A Complex Interplay between Nitric Oxide, Quorum Sensing, and the Unique Secondary Metabolite Tundrenone Constitutes the Hypoxia Response in Methylobacter
title_full A Complex Interplay between Nitric Oxide, Quorum Sensing, and the Unique Secondary Metabolite Tundrenone Constitutes the Hypoxia Response in Methylobacter
title_fullStr A Complex Interplay between Nitric Oxide, Quorum Sensing, and the Unique Secondary Metabolite Tundrenone Constitutes the Hypoxia Response in Methylobacter
title_full_unstemmed A Complex Interplay between Nitric Oxide, Quorum Sensing, and the Unique Secondary Metabolite Tundrenone Constitutes the Hypoxia Response in Methylobacter
title_sort complex interplay between nitric oxide, quorum sensing, and the unique secondary metabolite tundrenone constitutes the hypoxia response in methylobacter
publisher American Society for Microbiology
series mSystems
issn 2379-5077
publishDate 2020-01-01
description Here, we describe a novel and complex hypoxia response system in a methanotrophic bacterium that involves modules of central carbon metabolism, denitrification, quorum sensing, and a secondary metabolite, tundrenone. This intricate stress response system, so far unique to Methylobacter species, may be responsible for the persistence and activity of these species across gradients of dioxygen tensions and for the cosmopolitan distribution of these organisms in freshwater and soil environments in the Northern Hemisphere, including the fast-melting permafrosts.Methylobacter species, members of the Methylococcales, have recently emerged as some of the globally widespread, cosmopolitan species that play a key role in the environmental consumption of methane across gradients of dioxygen tensions. In this work, we approached the question of how Methylobacter copes with hypoxia, via laboratory manipulation. Through comparative transcriptomics of cultures grown under high dioxygen partial pressure versus cultures exposed to hypoxia, we identified a gene cluster encoding a hybrid cluster protein along with sensing and regulatory functions. Through mutant analysis, we demonstrated that this gene cluster is involved in the hypoxia stress response. Through additional transcriptomic analyses, we uncovered a complex interconnection between the NO-mediated stress response, quorum sensing, the secondary metabolite tundrenone, and methanol dehydrogenase functions. This novel and complex hypoxia stress response system is so far unique to Methylobacter species, and it may play a role in the environmental fitness of these organisms and in their cosmopolitan environmental distribution.
topic hypoxia
methylobacter tundripaludum
nitric oxide
hybrid cluster protein
quorum sensing
tundrenone
url https://doi.org/10.1128/mSystems.00770-19
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