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Biogeochemical Implications of N(2)O-Reducing Thermophilic Campylobacteria in Deep-Sea Vent Fields, and the Description of Nitratiruptor labii sp. nov.

Nitrous oxide (N(2)O) is a potent greenhouse gas and has significantly increased in the atmosphere. Deep-sea hydrothermal fields are representative environments dominated by mesophilic to thermophilic members of the class Campylobacteria that possess clade II nosZ encoding nitrous oxide reductase. H...

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Autores principales: Fukushi, Muneyuki, Mino, Sayaka, Tanaka, Hirohisa, Nakagawa, Satoshi, Takai, Ken, Sawabe, Tomoo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7476070/
https://www.ncbi.nlm.nih.gov/pubmed/32866828
http://dx.doi.org/10.1016/j.isci.2020.101462
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author Fukushi, Muneyuki
Mino, Sayaka
Tanaka, Hirohisa
Nakagawa, Satoshi
Takai, Ken
Sawabe, Tomoo
author_facet Fukushi, Muneyuki
Mino, Sayaka
Tanaka, Hirohisa
Nakagawa, Satoshi
Takai, Ken
Sawabe, Tomoo
author_sort Fukushi, Muneyuki
collection PubMed
description Nitrous oxide (N(2)O) is a potent greenhouse gas and has significantly increased in the atmosphere. Deep-sea hydrothermal fields are representative environments dominated by mesophilic to thermophilic members of the class Campylobacteria that possess clade II nosZ encoding nitrous oxide reductase. Here, we report a strain HRV44(T) representing the first thermophilic campylobacterium capable of growth by H(2) oxidation coupled to N(2)O reduction. On the basis of physiological and genomic properties, it is proposed that strain HRV44(T) (=JCM 34002 = DSM 111345) represents a novel species of the genus Nitratiruptor, Nitratiruptor labii sp. nov. The comparison of the N(2)O consumption ability of strain HRV44(T) with those of additional Nitratiruptor and other campylobacterial strains revealed the highest level in strain HRV44(T) and suggests the N(2)O-respiring metabolism might be the common physiological trait for the genus Nitratiruptor. Our findings provide insights into contributions of thermophilic Campylobacteria to the N(2)O sink in deep-sea hydrothermal environments.
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spelling pubmed-74760702020-09-11 Biogeochemical Implications of N(2)O-Reducing Thermophilic Campylobacteria in Deep-Sea Vent Fields, and the Description of Nitratiruptor labii sp. nov. Fukushi, Muneyuki Mino, Sayaka Tanaka, Hirohisa Nakagawa, Satoshi Takai, Ken Sawabe, Tomoo iScience Article Nitrous oxide (N(2)O) is a potent greenhouse gas and has significantly increased in the atmosphere. Deep-sea hydrothermal fields are representative environments dominated by mesophilic to thermophilic members of the class Campylobacteria that possess clade II nosZ encoding nitrous oxide reductase. Here, we report a strain HRV44(T) representing the first thermophilic campylobacterium capable of growth by H(2) oxidation coupled to N(2)O reduction. On the basis of physiological and genomic properties, it is proposed that strain HRV44(T) (=JCM 34002 = DSM 111345) represents a novel species of the genus Nitratiruptor, Nitratiruptor labii sp. nov. The comparison of the N(2)O consumption ability of strain HRV44(T) with those of additional Nitratiruptor and other campylobacterial strains revealed the highest level in strain HRV44(T) and suggests the N(2)O-respiring metabolism might be the common physiological trait for the genus Nitratiruptor. Our findings provide insights into contributions of thermophilic Campylobacteria to the N(2)O sink in deep-sea hydrothermal environments. Elsevier 2020-08-15 /pmc/articles/PMC7476070/ /pubmed/32866828 http://dx.doi.org/10.1016/j.isci.2020.101462 Text en © 2020 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Fukushi, Muneyuki
Mino, Sayaka
Tanaka, Hirohisa
Nakagawa, Satoshi
Takai, Ken
Sawabe, Tomoo
Biogeochemical Implications of N(2)O-Reducing Thermophilic Campylobacteria in Deep-Sea Vent Fields, and the Description of Nitratiruptor labii sp. nov.
title Biogeochemical Implications of N(2)O-Reducing Thermophilic Campylobacteria in Deep-Sea Vent Fields, and the Description of Nitratiruptor labii sp. nov.
title_full Biogeochemical Implications of N(2)O-Reducing Thermophilic Campylobacteria in Deep-Sea Vent Fields, and the Description of Nitratiruptor labii sp. nov.
title_fullStr Biogeochemical Implications of N(2)O-Reducing Thermophilic Campylobacteria in Deep-Sea Vent Fields, and the Description of Nitratiruptor labii sp. nov.
title_full_unstemmed Biogeochemical Implications of N(2)O-Reducing Thermophilic Campylobacteria in Deep-Sea Vent Fields, and the Description of Nitratiruptor labii sp. nov.
title_short Biogeochemical Implications of N(2)O-Reducing Thermophilic Campylobacteria in Deep-Sea Vent Fields, and the Description of Nitratiruptor labii sp. nov.
title_sort biogeochemical implications of n(2)o-reducing thermophilic campylobacteria in deep-sea vent fields, and the description of nitratiruptor labii sp. nov.
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7476070/
https://www.ncbi.nlm.nih.gov/pubmed/32866828
http://dx.doi.org/10.1016/j.isci.2020.101462
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