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Anaerobic Methanotrophic Archaea of the ANME-2d Cluster Are Active in a Low-sulfate, Iron-rich Freshwater Sediment

ANaerobic MEthanotrophic (ANME) archaea remove the greenhouse gas methane from anoxic environments and diminish its flux to the atmosphere. High methane removal efficiencies are well documented in marine environments, whereas anaerobic oxidation of methane (AOM) was only recently indicated as an imp...

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Autores principales: Weber, Hannah S., Habicht, Kirsten S., Thamdrup, Bo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5389135/
https://www.ncbi.nlm.nih.gov/pubmed/28446901
http://dx.doi.org/10.3389/fmicb.2017.00619
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author Weber, Hannah S.
Habicht, Kirsten S.
Thamdrup, Bo
author_facet Weber, Hannah S.
Habicht, Kirsten S.
Thamdrup, Bo
author_sort Weber, Hannah S.
collection PubMed
description ANaerobic MEthanotrophic (ANME) archaea remove the greenhouse gas methane from anoxic environments and diminish its flux to the atmosphere. High methane removal efficiencies are well documented in marine environments, whereas anaerobic oxidation of methane (AOM) was only recently indicated as an important methane sink in freshwater systems. Freshwater AOM-mediating microorganisms lack taxonomic identification and only little is known about metabolic adaptions to prevailing biogeochemical conditions. One of the first study sites providing information about AOM activity in freshwater sediment is Lake Ørn, a low-sulfate, iron-rich Danish lake. With the aim to identify freshwater AOM-mediating archaea, we incubated AOM-active anoxic, nitrate-free freshwater sediment from Lake Ørn with (13)C-labeled methane ((13)C(CH4)) and (13)C-labeled bicarbonate ((13)C(DIC)) and followed the assimilation of (13)C into RNA by stable isotope probing. While AOM was active, (13)C(CH4) and probably also (13)C(DIC) were incorporated into uncultured archaea of the Methanosarcinales-related cluster ANME-2d, whereas other known ANME lineages were not detected. This finding strongly suggests that ANME-2d archaea perform AOM coupled to sulfate and/or iron reduction and may have the capability of mixed assimilation of CH(4) and DIC. ANME-2d archaea may thus play an important role in controlling methane emissions from nitrate-depleted and low-sulfate freshwater systems.
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spelling pubmed-53891352017-04-26 Anaerobic Methanotrophic Archaea of the ANME-2d Cluster Are Active in a Low-sulfate, Iron-rich Freshwater Sediment Weber, Hannah S. Habicht, Kirsten S. Thamdrup, Bo Front Microbiol Microbiology ANaerobic MEthanotrophic (ANME) archaea remove the greenhouse gas methane from anoxic environments and diminish its flux to the atmosphere. High methane removal efficiencies are well documented in marine environments, whereas anaerobic oxidation of methane (AOM) was only recently indicated as an important methane sink in freshwater systems. Freshwater AOM-mediating microorganisms lack taxonomic identification and only little is known about metabolic adaptions to prevailing biogeochemical conditions. One of the first study sites providing information about AOM activity in freshwater sediment is Lake Ørn, a low-sulfate, iron-rich Danish lake. With the aim to identify freshwater AOM-mediating archaea, we incubated AOM-active anoxic, nitrate-free freshwater sediment from Lake Ørn with (13)C-labeled methane ((13)C(CH4)) and (13)C-labeled bicarbonate ((13)C(DIC)) and followed the assimilation of (13)C into RNA by stable isotope probing. While AOM was active, (13)C(CH4) and probably also (13)C(DIC) were incorporated into uncultured archaea of the Methanosarcinales-related cluster ANME-2d, whereas other known ANME lineages were not detected. This finding strongly suggests that ANME-2d archaea perform AOM coupled to sulfate and/or iron reduction and may have the capability of mixed assimilation of CH(4) and DIC. ANME-2d archaea may thus play an important role in controlling methane emissions from nitrate-depleted and low-sulfate freshwater systems. Frontiers Media S.A. 2017-04-12 /pmc/articles/PMC5389135/ /pubmed/28446901 http://dx.doi.org/10.3389/fmicb.2017.00619 Text en Copyright © 2017 Weber, Habicht and Thamdrup. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Weber, Hannah S.
Habicht, Kirsten S.
Thamdrup, Bo
Anaerobic Methanotrophic Archaea of the ANME-2d Cluster Are Active in a Low-sulfate, Iron-rich Freshwater Sediment
title Anaerobic Methanotrophic Archaea of the ANME-2d Cluster Are Active in a Low-sulfate, Iron-rich Freshwater Sediment
title_full Anaerobic Methanotrophic Archaea of the ANME-2d Cluster Are Active in a Low-sulfate, Iron-rich Freshwater Sediment
title_fullStr Anaerobic Methanotrophic Archaea of the ANME-2d Cluster Are Active in a Low-sulfate, Iron-rich Freshwater Sediment
title_full_unstemmed Anaerobic Methanotrophic Archaea of the ANME-2d Cluster Are Active in a Low-sulfate, Iron-rich Freshwater Sediment
title_short Anaerobic Methanotrophic Archaea of the ANME-2d Cluster Are Active in a Low-sulfate, Iron-rich Freshwater Sediment
title_sort anaerobic methanotrophic archaea of the anme-2d cluster are active in a low-sulfate, iron-rich freshwater sediment
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5389135/
https://www.ncbi.nlm.nih.gov/pubmed/28446901
http://dx.doi.org/10.3389/fmicb.2017.00619
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