Methylotrophic methanogenesis in the Archaeoglobi revealed by cultivation ofCa.Methanoglobus hypatiae from a Yellowstone hot spring

Author:

Lynes Mackenzie M.ORCID,Jay Zackary J.ORCID,Kohtz Anthony J.ORCID,Hatzenpichler RolandORCID

Abstract

AbstractOver the past decade, environmental metagenomics and PCR-based marker gene surveys have revealed that several lineages beyond just a few well-established groups within the Euryarchaeota superphylum harbor the genetic potential for methanogenesis. One of these groups are the Archaeoglobi, a class of thermophilic euryarchaeotes that have long been considered to live non-methanogenic lifestyles. Here, we enrichedCandidatusMethanoglobus hypatiae, a methanogen affiliated with the family Archaeoglobaceae, from a hot spring in Yellowstone National Park. The enrichment is sediment-free, grows at 64-70 °C and a pH of 7.8, and produces methane from mono-, di-, and tri-methylamine.Ca.M. hypatiae is represented by a 1.62 Mb metagenome-assembled genome with an estimated completeness of 100% and accounts for up to 67% of cells in the culture according to fluorescencein situhybridization. Via genome-resolved metatranscriptomics and stable isotope tracing, we demonstrate thatCa.M. hypatiae expresses methylotrophic methanogenesis and energy-conserving pathways for reducing monomethylamine to methane. The detection of Archaeoglobi populations related toCa.M. hypatiae in 36 geochemically diverse geothermal sites within Yellowstone National Park, as revealed through the examination of previously published gene amplicon datasets, implies a previously underestimated contribution to anaerobic carbon cycling in extreme ecosystems.

Publisher

Cold Spring Harbor Laboratory

Reference113 articles.

1. Horizontal gene transfer constrains the timing of methanogen evolution;Nature Ecology & Evolution,2018

2. Discovery of extremely halophilic, methyl-reducing euryarchaea provides insights into the evolutionary origin of methanogenesis;Nature Microbiology,2017

3. Early Microbial Evolution: The Age of Anaerobes

4. Co-evolution of primitive methane-cycling ecosystems and early Earth’s atmosphere and climate;Nature Communications,2020

5. Evidence from fluid inclusions for microbial methanogenesis in the early Archaean era

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