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Genomic evidence that microbial carbon degradation is dominated by iron redox metabolism in thawing permafrost

Earth Sciences

Genomic evidence that microbial carbon degradation is dominated by iron redox metabolism in thawing permafrost

K. J. Romanowicz, B. C. Crump, et al.

Discover how microorganisms shape carbon cycling in thawed permafrost! In a groundbreaking study by Karl J. Romanowicz, Byron C. Crump, and George W. Kling, researchers reveal that iron-cycling Gammaproteobacteria thrive during extended thaw, driving carbon degradation processes and altering our understanding of methane suppression in Alaskan wetlands.... show more
Abstract
Microorganisms drive many aspects of organic carbon cycling in thawing permafrost soils, but the compositional trajectory of the post-thaw microbiome and its metabolic activity remain uncertain, which limits our ability to predict permafrost-climate feedbacks in a warming world. Using quantitative metabarcoding and metagenomic sequencing, we determined relative and absolute changes in microbiome composition and functional gene abundance during thaw incubations of wet sedge tundra collected from northern Alaska, USA. Organic soils from the tundra active-layer (0–50 cm), transition-zone (50–70 cm), and permafrost (70+ cm) depths were incubated under reducing conditions at 4 °C for 30 days to mimic an extended thaw duration. Following extended thaw, we found that iron (Fe)-cycling Gammaproteobacteria, specifically the heterotrophic Fe(III)-reducing Rhodoferax sp. and chemoautotrophic Fe(II)-oxidizing Gallionella sp., increased by 3–5 orders of magnitude in absolute abundance within the transition-zone and permafrost microbiomes, accounting for 65% of community abundance. We also found that the abundance of genes for Fe(III) reduction (e.g., MtrE) and Fe(II) oxidation (e.g., Cyc1) increased concurrently with genes for benzoate degradation and pyruvate metabolism, in which pyruvate is used to generate acetate that can be oxidized, along with benzoate, to CO₂ when coupled with Fe(III) reduction. Gene abundance for CH₄ metabolism decreased following extended thaw, suggesting dissimilatory Fe(III) reduction suppresses acetoclastic methanogenesis under reducing conditions. Our genomic evidence indicates that microbial carbon degradation is dominated by iron redox metabolism via an increase in gene abundance associated with Fe(III) reduction and Fe(II) oxidation during initial permafrost thaw, likely increasing microbial respiration while suppressing methanogenesis in wet sedge tundra.
Publisher
ISME Communications
Published On
Nov 23, 2023
Authors
Karl J. Romanowicz, Byron C. Crump, George W. Kling
Tags
permafrost
microbiome
carbon cycling
thaw
Gammaproteobacteria
metabolism
methanogenesis
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