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Discovery of anaerobic lithoheterotrophic haloarchaea, ubiquitous in hypersaline habitats

Hypersaline anoxic habitats harbour numerous novel uncultured archaea whose metabolic and ecological roles remain to be elucidated. Until recently, it was believed that energy generation via dissimilatory reduction of sulfur compounds is not functional at salt saturation conditions. Recent discovery...

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Autores principales: Sorokin, Dimitry Y, Messina, Enzo, Smedile, Francesco, Roman, Pawel, Damsté, Jaap S Sinninghe, Ciordia, Sergio, Mena, Maria Carmen, Ferrer, Manuel, Golyshin, Peter N, Kublanov, Ilya V, Samarov, Nazar I, Toshchakov, Stepan V, La Cono, Violetta, Yakimov, Michail M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5437934/
https://www.ncbi.nlm.nih.gov/pubmed/28106880
http://dx.doi.org/10.1038/ismej.2016.203
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author Sorokin, Dimitry Y
Messina, Enzo
Smedile, Francesco
Roman, Pawel
Damsté, Jaap S Sinninghe
Ciordia, Sergio
Mena, Maria Carmen
Ferrer, Manuel
Golyshin, Peter N
Kublanov, Ilya V
Samarov, Nazar I
Toshchakov, Stepan V
La Cono, Violetta
Yakimov, Michail M
author_facet Sorokin, Dimitry Y
Messina, Enzo
Smedile, Francesco
Roman, Pawel
Damsté, Jaap S Sinninghe
Ciordia, Sergio
Mena, Maria Carmen
Ferrer, Manuel
Golyshin, Peter N
Kublanov, Ilya V
Samarov, Nazar I
Toshchakov, Stepan V
La Cono, Violetta
Yakimov, Michail M
author_sort Sorokin, Dimitry Y
collection PubMed
description Hypersaline anoxic habitats harbour numerous novel uncultured archaea whose metabolic and ecological roles remain to be elucidated. Until recently, it was believed that energy generation via dissimilatory reduction of sulfur compounds is not functional at salt saturation conditions. Recent discovery of the strictly anaerobic acetotrophic Halanaeroarchaeum compels to change both this assumption and the traditional view on haloarchaea as aerobic heterotrophs. Here we report on isolation and characterization of a novel group of strictly anaerobic lithoheterotrophic haloarchaea, which we propose to classify as a new genus Halodesulfurarchaeum. Members of this previously unknown physiological group are capable of utilising formate or hydrogen as electron donors and elemental sulfur, thiosulfate or dimethylsulfoxide as electron acceptors. Using genome-wide proteomic analysis we have detected the full set of enzymes required for anaerobic respiration and analysed their substrate-specific expression. Such advanced metabolic plasticity and type of respiration, never seen before in haloarchaea, empower the wide distribution of Halodesulfurarchaeum in hypersaline inland lakes, solar salterns, lagoons and deep submarine anoxic brines. The discovery of this novel functional group of sulfur-respiring haloarchaea strengthens the evidence of their possible role in biogeochemical sulfur cycling linked to the terminal anaerobic carbon mineralisation in so far overlooked hypersaline anoxic habitats.
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spelling pubmed-54379342017-05-31 Discovery of anaerobic lithoheterotrophic haloarchaea, ubiquitous in hypersaline habitats Sorokin, Dimitry Y Messina, Enzo Smedile, Francesco Roman, Pawel Damsté, Jaap S Sinninghe Ciordia, Sergio Mena, Maria Carmen Ferrer, Manuel Golyshin, Peter N Kublanov, Ilya V Samarov, Nazar I Toshchakov, Stepan V La Cono, Violetta Yakimov, Michail M ISME J Original Article Hypersaline anoxic habitats harbour numerous novel uncultured archaea whose metabolic and ecological roles remain to be elucidated. Until recently, it was believed that energy generation via dissimilatory reduction of sulfur compounds is not functional at salt saturation conditions. Recent discovery of the strictly anaerobic acetotrophic Halanaeroarchaeum compels to change both this assumption and the traditional view on haloarchaea as aerobic heterotrophs. Here we report on isolation and characterization of a novel group of strictly anaerobic lithoheterotrophic haloarchaea, which we propose to classify as a new genus Halodesulfurarchaeum. Members of this previously unknown physiological group are capable of utilising formate or hydrogen as electron donors and elemental sulfur, thiosulfate or dimethylsulfoxide as electron acceptors. Using genome-wide proteomic analysis we have detected the full set of enzymes required for anaerobic respiration and analysed their substrate-specific expression. Such advanced metabolic plasticity and type of respiration, never seen before in haloarchaea, empower the wide distribution of Halodesulfurarchaeum in hypersaline inland lakes, solar salterns, lagoons and deep submarine anoxic brines. The discovery of this novel functional group of sulfur-respiring haloarchaea strengthens the evidence of their possible role in biogeochemical sulfur cycling linked to the terminal anaerobic carbon mineralisation in so far overlooked hypersaline anoxic habitats. Nature Publishing Group 2017-05 2017-01-20 /pmc/articles/PMC5437934/ /pubmed/28106880 http://dx.doi.org/10.1038/ismej.2016.203 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
Sorokin, Dimitry Y
Messina, Enzo
Smedile, Francesco
Roman, Pawel
Damsté, Jaap S Sinninghe
Ciordia, Sergio
Mena, Maria Carmen
Ferrer, Manuel
Golyshin, Peter N
Kublanov, Ilya V
Samarov, Nazar I
Toshchakov, Stepan V
La Cono, Violetta
Yakimov, Michail M
Discovery of anaerobic lithoheterotrophic haloarchaea, ubiquitous in hypersaline habitats
title Discovery of anaerobic lithoheterotrophic haloarchaea, ubiquitous in hypersaline habitats
title_full Discovery of anaerobic lithoheterotrophic haloarchaea, ubiquitous in hypersaline habitats
title_fullStr Discovery of anaerobic lithoheterotrophic haloarchaea, ubiquitous in hypersaline habitats
title_full_unstemmed Discovery of anaerobic lithoheterotrophic haloarchaea, ubiquitous in hypersaline habitats
title_short Discovery of anaerobic lithoheterotrophic haloarchaea, ubiquitous in hypersaline habitats
title_sort discovery of anaerobic lithoheterotrophic haloarchaea, ubiquitous in hypersaline habitats
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5437934/
https://www.ncbi.nlm.nih.gov/pubmed/28106880
http://dx.doi.org/10.1038/ismej.2016.203
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