Osmoregulation in freshwater anaerobic methane oxidizing archaea under salt stress.

ANME Compatible solutes metabolomics methanotroph salinity adaptation “Ca. Methanoperedens”

Journal

The ISME journal
ISSN: 1751-7370
Titre abrégé: ISME J
Pays: England
ID NLM: 101301086

Informations de publication

Date de publication:
20 Jul 2024
Historique:
received: 11 03 2024
revised: 11 06 2024
accepted: 18 07 2024
medline: 20 7 2024
pubmed: 20 7 2024
entrez: 20 7 2024
Statut: aheadofprint

Résumé

Climate change-driven sea level rise threatens freshwater ecosystems and elicits salinity stress in microbiomes. Methane emissions in these systems are largely mitigated by methane-oxidizing microorganisms. Here, we characterized the physiological and metabolic response of freshwater methanotrophic archaea to salt stress. In our microcosm experiments, inhibition of methanotrophic archaea started at 1%. However, during gradual increase of salt up to 3% in a reactor over 12 weeks, the culture continued to oxidize methane. Using gene expression profiles and metabolomics, we identified a pathway for salt-stress response that produces the osmolyte of anaerobic methanotrophic archaea: N(ε)-acetyl-β-L-lysine. An extensive phylogenomic analysis on N(ε)-acetyl-β-L-lysine-producing enzymes revealed that they are widespread across both bacteria and archaea, indicating a potential horizontal gene transfer and a link to BORG extrachromosomal elements. Physicochemical analysis of bioreactor biomass further indicated the presence of sialic acids and the consumption of intracellular polyhydroxyalkanoates in anaerobic methanotrophs during salt stress.

Identifiants

pubmed: 39030685
pii: 7717430
doi: 10.1093/ismejo/wrae137
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© The Author(s) [2024]. Published by Oxford University Press on behalf of the International Society for Microbial Ecology.

Auteurs

Maider J Echeveste Medrano (MJ)

Department of Microbiology, RIBES, Radboud University, Heyendaalseweg 135, 6525AJ Nijmegen, The Netherlands.

Andy O Leu (AO)

Centre for Microbiome Research (CMR), School of Biomedical Sciences, Queensland University of Technology (QUT), Translational Research Institute (TRI), 37 Kent Street, Woolloongabba QLD 4102, Australia.

Martin Pabst (M)

Department of Environmental Biotechnology, TU-Delft University, Van der Maasweg 9, 2629HZ Delft, The Netherlands.

Yuemei Lin (Y)

Department of Environmental Biotechnology, TU-Delft University, Van der Maasweg 9, 2629HZ Delft, The Netherlands.

Simon J Mcllroy (SJ)

Centre for Microbiome Research (CMR), School of Biomedical Sciences, Queensland University of Technology (QUT), Translational Research Institute (TRI), 37 Kent Street, Woolloongabba QLD 4102, Australia.

Gene W Tyson (GW)

Centre for Microbiome Research (CMR), School of Biomedical Sciences, Queensland University of Technology (QUT), Translational Research Institute (TRI), 37 Kent Street, Woolloongabba QLD 4102, Australia.

Jitske van Ede (J)

Department of Environmental Biotechnology, TU-Delft University, Van der Maasweg 9, 2629HZ Delft, The Netherlands.

Irene Sánchez-Andrea (I)

Department of Environmental Sciences for Sustainability, IE University, C. Cardenal Zúñiga 12, 40003 Segovia, Spain.
Laboratory of Microbiology, Wageningen University, Stippeneng 4, 6708WE Wageningen, The Netherlands.

Mike S M Jetten (MSM)

Department of Microbiology, RIBES, Radboud University, Heyendaalseweg 135, 6525AJ Nijmegen, The Netherlands.

Robert Jansen (R)

Department of Microbiology, RIBES, Radboud University, Heyendaalseweg 135, 6525AJ Nijmegen, The Netherlands.

Cornelia U Welte (CU)

Department of Microbiology, RIBES, Radboud University, Heyendaalseweg 135, 6525AJ Nijmegen, The Netherlands.

Classifications MeSH