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Methylacidiphilum fumariolicum SolV, a thermoacidophilic ‘Knallgas' methanotroph with both an oxygen-sensitive and -insensitive hydrogenase

Methanotrophs play a key role in balancing the atmospheric methane concentration. Recently, the microbial methanotrophic diversity was extended by the discovery of thermoacidophilic methanotrophs belonging to the Verrucomicrobia phylum in geothermal areas. Here we show that a representative of this...

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Autores principales: Mohammadi, Sepehr, Pol, Arjan, van Alen, Theo A, Jetten, Mike SM, Op den Camp, Huub JM
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5364354/
https://www.ncbi.nlm.nih.gov/pubmed/27935590
http://dx.doi.org/10.1038/ismej.2016.171
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author Mohammadi, Sepehr
Pol, Arjan
van Alen, Theo A
Jetten, Mike SM
Op den Camp, Huub JM
author_facet Mohammadi, Sepehr
Pol, Arjan
van Alen, Theo A
Jetten, Mike SM
Op den Camp, Huub JM
author_sort Mohammadi, Sepehr
collection PubMed
description Methanotrophs play a key role in balancing the atmospheric methane concentration. Recently, the microbial methanotrophic diversity was extended by the discovery of thermoacidophilic methanotrophs belonging to the Verrucomicrobia phylum in geothermal areas. Here we show that a representative of this new group, Methylacidiphilum fumariolicum SolV, is able to grow as a real ‘Knallgas' bacterium on hydrogen/carbon dioxide, without addition of methane. The full genome of strain SolV revealed the presence of two hydrogen uptake hydrogenases genes, encoding an oxygen-sensitive (hup-type) and an oxygen-insensitive enzyme (hhy-type). The hhy-type hydrogenase was constitutively expressed and active and supported growth on hydrogen alone up to a growth rate of 0.03 h(−1), at O(2) concentrations below 1.5%. The oxygen-sensitive hup-type hydrogenase was expressed when oxygen was reduced to below 0.2%. This resulted in an increase of the growth rate to a maximum of 0.047 h(−1), that is 60% of the rate on methane. The results indicate that under natural conditions where both hydrogen and methane might be limiting strain SolV may operate primarily as a methanotrophic ‘Knallgas' bacterium. These findings argue for a revision of the role of hydrogen in methanotrophic ecosystems, especially in soil and related to consumption of atmospheric methane.
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spelling pubmed-53643542017-05-15 Methylacidiphilum fumariolicum SolV, a thermoacidophilic ‘Knallgas' methanotroph with both an oxygen-sensitive and -insensitive hydrogenase Mohammadi, Sepehr Pol, Arjan van Alen, Theo A Jetten, Mike SM Op den Camp, Huub JM ISME J Original Article Methanotrophs play a key role in balancing the atmospheric methane concentration. Recently, the microbial methanotrophic diversity was extended by the discovery of thermoacidophilic methanotrophs belonging to the Verrucomicrobia phylum in geothermal areas. Here we show that a representative of this new group, Methylacidiphilum fumariolicum SolV, is able to grow as a real ‘Knallgas' bacterium on hydrogen/carbon dioxide, without addition of methane. The full genome of strain SolV revealed the presence of two hydrogen uptake hydrogenases genes, encoding an oxygen-sensitive (hup-type) and an oxygen-insensitive enzyme (hhy-type). The hhy-type hydrogenase was constitutively expressed and active and supported growth on hydrogen alone up to a growth rate of 0.03 h(−1), at O(2) concentrations below 1.5%. The oxygen-sensitive hup-type hydrogenase was expressed when oxygen was reduced to below 0.2%. This resulted in an increase of the growth rate to a maximum of 0.047 h(−1), that is 60% of the rate on methane. The results indicate that under natural conditions where both hydrogen and methane might be limiting strain SolV may operate primarily as a methanotrophic ‘Knallgas' bacterium. These findings argue for a revision of the role of hydrogen in methanotrophic ecosystems, especially in soil and related to consumption of atmospheric methane. Nature Publishing Group 2017-04 2016-12-09 /pmc/articles/PMC5364354/ /pubmed/27935590 http://dx.doi.org/10.1038/ismej.2016.171 Text en Copyright © 2017 International Society for Microbial Ecology http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Original Article
Mohammadi, Sepehr
Pol, Arjan
van Alen, Theo A
Jetten, Mike SM
Op den Camp, Huub JM
Methylacidiphilum fumariolicum SolV, a thermoacidophilic ‘Knallgas' methanotroph with both an oxygen-sensitive and -insensitive hydrogenase
title Methylacidiphilum fumariolicum SolV, a thermoacidophilic ‘Knallgas' methanotroph with both an oxygen-sensitive and -insensitive hydrogenase
title_full Methylacidiphilum fumariolicum SolV, a thermoacidophilic ‘Knallgas' methanotroph with both an oxygen-sensitive and -insensitive hydrogenase
title_fullStr Methylacidiphilum fumariolicum SolV, a thermoacidophilic ‘Knallgas' methanotroph with both an oxygen-sensitive and -insensitive hydrogenase
title_full_unstemmed Methylacidiphilum fumariolicum SolV, a thermoacidophilic ‘Knallgas' methanotroph with both an oxygen-sensitive and -insensitive hydrogenase
title_short Methylacidiphilum fumariolicum SolV, a thermoacidophilic ‘Knallgas' methanotroph with both an oxygen-sensitive and -insensitive hydrogenase
title_sort methylacidiphilum fumariolicum solv, a thermoacidophilic ‘knallgas' methanotroph with both an oxygen-sensitive and -insensitive hydrogenase
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5364354/
https://www.ncbi.nlm.nih.gov/pubmed/27935590
http://dx.doi.org/10.1038/ismej.2016.171
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