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<scp>ANME</scp> ‐1 archaea may drive methane accumulation and removal in estuarine sediments

R.T. Kevorkian, Sean M. Callahan, Rachel Winstead, Karen G. Lloyd

2021Environmental Microbiology Reports53 citationsDOI

Abstract

ANME-1 archaea subsist on the very low energy of anaerobic oxidation of methane (AOM). Most marine sediments shift from net AOM in the sulfate methane transition zone (SMTZ) to methanogenesis in the methane zone (MZ) below it. In White Oak River estuarine sediments, ANME-1 comprised 99.5% of 16S rRNA genes from amplicons and 100% of 16S rRNA genes from metagenomes of the Methanomicrobia in the SMTZ and 99.9% and 98.3%, respectively, in the MZ. Each of the 16 ANME-1 OTUs (97% similarity) had peaks in the SMTZ that coincided with peaks of putative sulfate-reducing bacteria Desulfatiglans sp. and SEEP-SRB1. In the MZ, ANME-1, but none of the putative sulfate-reducing bacteria or cultured methanogens, increased with depth. Our meta-analysis of public data showed only ANME-1 expressed methanogenic genes during both net AOM and net methanogenesis in an enrichment culture. We conclude that ANME-1 perform AOM in the SMTZ and methanogenesis in the MZ of White Oak River sediments. This metabolic flexibility may expand habitable zones in extraterrestrial environments, since it enables greater energy yields in a fluctuating energetic landscape.

Topics & Concepts

MethanogenesisArchaeaAnaerobic oxidation of methaneMethaneEnvironmental chemistryEnrichment cultureSulfate-reducing bacteriaBacteriaSulfate16S ribosomal RNABiologyEcologyChemistryPaleontologyOrganic chemistryMethane Hydrates and Related PhenomenaMicrobial Community Ecology and PhysiologyHydrocarbon exploration and reservoir analysis
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