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The evolution and spread of sulfur cycling enzymes reflect the redox state of the early Earth
The biogeochemical sulfur cycle plays a central role in fueling microbial metabolisms, regulating the Earth’s redox state, and affecting climate. However, geochemical reconstructions of the ancient sulfur cycle are confounded by ambiguous isotopic signals. We use phylogenetic reconciliation to ascer...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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American Association for the Advancement of Science
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10328410/ https://www.ncbi.nlm.nih.gov/pubmed/37418533 http://dx.doi.org/10.1126/sciadv.ade4847 |
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author | Mateos, Katherine Chappell, Garrett Klos, Aya Le, Bryan Boden, Joanne Stüeken, Eva Anderson, Rika |
author_facet | Mateos, Katherine Chappell, Garrett Klos, Aya Le, Bryan Boden, Joanne Stüeken, Eva Anderson, Rika |
author_sort | Mateos, Katherine |
collection | PubMed |
description | The biogeochemical sulfur cycle plays a central role in fueling microbial metabolisms, regulating the Earth’s redox state, and affecting climate. However, geochemical reconstructions of the ancient sulfur cycle are confounded by ambiguous isotopic signals. We use phylogenetic reconciliation to ascertain the timing of ancient sulfur cycling gene events across the tree of life. Our results suggest that metabolisms using sulfide oxidation emerged in the Archean, but those involving thiosulfate emerged only after the Great Oxidation Event. Our data reveal that observed geochemical signatures resulted not from the expansion of a single type of organism but were instead associated with genomic innovation across the biosphere. Moreover, our results provide the first indication of organic sulfur cycling from the Mid-Proterozoic onwards, with implications for climate regulation and atmospheric biosignatures. Overall, our results provide insights into how the biological sulfur cycle evolved in tandem with the redox state of the early Earth. |
format | Online Article Text |
id | pubmed-10328410 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-103284102023-07-08 The evolution and spread of sulfur cycling enzymes reflect the redox state of the early Earth Mateos, Katherine Chappell, Garrett Klos, Aya Le, Bryan Boden, Joanne Stüeken, Eva Anderson, Rika Sci Adv Earth, Environmental, Ecological, and Space Sciences The biogeochemical sulfur cycle plays a central role in fueling microbial metabolisms, regulating the Earth’s redox state, and affecting climate. However, geochemical reconstructions of the ancient sulfur cycle are confounded by ambiguous isotopic signals. We use phylogenetic reconciliation to ascertain the timing of ancient sulfur cycling gene events across the tree of life. Our results suggest that metabolisms using sulfide oxidation emerged in the Archean, but those involving thiosulfate emerged only after the Great Oxidation Event. Our data reveal that observed geochemical signatures resulted not from the expansion of a single type of organism but were instead associated with genomic innovation across the biosphere. Moreover, our results provide the first indication of organic sulfur cycling from the Mid-Proterozoic onwards, with implications for climate regulation and atmospheric biosignatures. Overall, our results provide insights into how the biological sulfur cycle evolved in tandem with the redox state of the early Earth. American Association for the Advancement of Science 2023-07-07 /pmc/articles/PMC10328410/ /pubmed/37418533 http://dx.doi.org/10.1126/sciadv.ade4847 Text en Copyright © 2023 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution License 4.0 (CC BY). https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution license (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Earth, Environmental, Ecological, and Space Sciences Mateos, Katherine Chappell, Garrett Klos, Aya Le, Bryan Boden, Joanne Stüeken, Eva Anderson, Rika The evolution and spread of sulfur cycling enzymes reflect the redox state of the early Earth |
title | The evolution and spread of sulfur cycling enzymes reflect the redox state of the early Earth |
title_full | The evolution and spread of sulfur cycling enzymes reflect the redox state of the early Earth |
title_fullStr | The evolution and spread of sulfur cycling enzymes reflect the redox state of the early Earth |
title_full_unstemmed | The evolution and spread of sulfur cycling enzymes reflect the redox state of the early Earth |
title_short | The evolution and spread of sulfur cycling enzymes reflect the redox state of the early Earth |
title_sort | evolution and spread of sulfur cycling enzymes reflect the redox state of the early earth |
topic | Earth, Environmental, Ecological, and Space Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10328410/ https://www.ncbi.nlm.nih.gov/pubmed/37418533 http://dx.doi.org/10.1126/sciadv.ade4847 |
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