Evidence map›Paper›PMID 39206688›Full record

ArticleThe ISME journal2024

Evolutionary history and origins of Dsr-mediated sulfur oxidation.

Katherine M Klier, Cody Martin, Marguerite V Langwig, Karthik Anantharaman

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Article in The ISME journal, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

8 citing papers in PubMed.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

4 authors.

Katherine M KlierDepartment of Bacteriology, University of Wisconsin-Madison, Madison, WI 53706, United States.
Cody MartinDepartment of Bacteriology, University of Wisconsin-Madison, Madison, WI 53706, United States.
Marguerite V LangwigDepartment of Bacteriology, University of Wisconsin-Madison, Madison, WI 53706, United States.
Karthik AnantharamanDepartment of Bacteriology, University of Wisconsin-Madison, Madison, WI 53706, United States.

Funding

National Science FoundationNational Science Foundation Graduate Research Fellowship OCE2049478UW-Madison Science and Medicine Graduate Research Fellowship (SciMed GRS)
6 · The paper itself

Abstract

Microorganisms play vital roles in sulfur cycling through the oxidation of elemental sulfur and reduction of sulfite. These metabolisms are catalyzed by dissimilatory sulfite reductases (Dsr) functioning in either the reductive or reverse, oxidative direction. Dsr-mediated sulfite reduction is an ancient metabolism proposed to have fueled energy metabolism in some of Earth's earliest microorganisms, whereas sulfur oxidation is believed to have evolved later in association with the widespread availability of oxygen on Earth. Organisms are generally believed to carry out either the reductive or oxidative pathway, yet organisms from diverse phyla have been discovered with gene combinations that implicate them in both pathways. A comprehensive investigation into the metabolisms of these phyla regarding Dsr is currently lacking. Here, we selected one of these phyla, the metabolically versatile candidate phylum SAR324, to study the ecology and evolution of Dsr-mediated metabolism. We confirmed that diverse SAR324 encode genes associated with reductive Dsr, oxidative Dsr, or both. Comparative analyses with other Dsr-encoding bacterial and archaeal phyla revealed that organisms encoding both reductive and oxidative Dsr proteins are constrained to a few phyla. Further, DsrAB sequences from genomes belonging to these phyla are phylogenetically positioned at the interface between well-defined oxidative and reductive bacterial clades. The phylogenetic context and dsr gene content in these organisms points to an evolutionary transition event that ultimately gave way to oxidative Dsr-mediated metabolism. Together, this research suggests that SAR324 and other phyla with mixed dsr gene content are associated with the evolution and origins of Dsr-mediated sulfur oxidation.

Indexed as

ArchaeaBacteriaOxidation-ReductionPhylogenySulfurEvolution, MolecularHydrogensulfite ReductaseHydrogensulfite ReductaseSulfurdissimilatory sulfite reductasemetagenomicsSAR324sulfur oxidation

Identifiers

PMID39206688
PMCPMC11406059

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.