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Kinetics of the ancestral carbon metabolism pathways in deep-branching bacteria and archaea

The origin of life is believed to be chemoautotrophic, deriving all biomass components from carbon dioxide, and all energy from inorganic redox couples in the environment. The reductive tricarboxylic acid cycle (rTCA) and the Wood–Ljungdahl pathway (WL) have been recognized as the most ancient carbo...

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Autores principales: Sumi, Tomonari, Harada, Kouji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9814661/
https://www.ncbi.nlm.nih.gov/pubmed/36697601
http://dx.doi.org/10.1038/s42004-021-00585-0
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author Sumi, Tomonari
Harada, Kouji
author_facet Sumi, Tomonari
Harada, Kouji
author_sort Sumi, Tomonari
collection PubMed
description The origin of life is believed to be chemoautotrophic, deriving all biomass components from carbon dioxide, and all energy from inorganic redox couples in the environment. The reductive tricarboxylic acid cycle (rTCA) and the Wood–Ljungdahl pathway (WL) have been recognized as the most ancient carbon fixation pathways. The rTCA of the chemolithotrophic Thermosulfidibacter takaii, which was recently demonstrated to take place via an unexpected reverse reaction of citrate synthase, was reproduced using a kinetic network model, and a competition between reductive and oxidative fluxes on rTCA due to an acetyl coenzyme A (ACOA) influx upon acetate uptake was revealed. Avoiding ACOA direct influx into rTCA from WL is, therefore, raised as a kinetically necessary condition to maintain a complete rTCA. This hypothesis was confirmed for deep-branching bacteria and archaea, and explains the kinetic factors governing elementary processes in carbon metabolism evolution from the last universal common ancestor.
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spelling pubmed-98146612023-01-10 Kinetics of the ancestral carbon metabolism pathways in deep-branching bacteria and archaea Sumi, Tomonari Harada, Kouji Commun Chem Article The origin of life is believed to be chemoautotrophic, deriving all biomass components from carbon dioxide, and all energy from inorganic redox couples in the environment. The reductive tricarboxylic acid cycle (rTCA) and the Wood–Ljungdahl pathway (WL) have been recognized as the most ancient carbon fixation pathways. The rTCA of the chemolithotrophic Thermosulfidibacter takaii, which was recently demonstrated to take place via an unexpected reverse reaction of citrate synthase, was reproduced using a kinetic network model, and a competition between reductive and oxidative fluxes on rTCA due to an acetyl coenzyme A (ACOA) influx upon acetate uptake was revealed. Avoiding ACOA direct influx into rTCA from WL is, therefore, raised as a kinetically necessary condition to maintain a complete rTCA. This hypothesis was confirmed for deep-branching bacteria and archaea, and explains the kinetic factors governing elementary processes in carbon metabolism evolution from the last universal common ancestor. Nature Publishing Group UK 2021-10-22 /pmc/articles/PMC9814661/ /pubmed/36697601 http://dx.doi.org/10.1038/s42004-021-00585-0 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Sumi, Tomonari
Harada, Kouji
Kinetics of the ancestral carbon metabolism pathways in deep-branching bacteria and archaea
title Kinetics of the ancestral carbon metabolism pathways in deep-branching bacteria and archaea
title_full Kinetics of the ancestral carbon metabolism pathways in deep-branching bacteria and archaea
title_fullStr Kinetics of the ancestral carbon metabolism pathways in deep-branching bacteria and archaea
title_full_unstemmed Kinetics of the ancestral carbon metabolism pathways in deep-branching bacteria and archaea
title_short Kinetics of the ancestral carbon metabolism pathways in deep-branching bacteria and archaea
title_sort kinetics of the ancestral carbon metabolism pathways in deep-branching bacteria and archaea
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9814661/
https://www.ncbi.nlm.nih.gov/pubmed/36697601
http://dx.doi.org/10.1038/s42004-021-00585-0
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