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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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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. |
format | Online Article Text |
id | pubmed-9814661 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT sumitomonari kineticsoftheancestralcarbonmetabolismpathwaysindeepbranchingbacteriaandarchaea AT haradakouji kineticsoftheancestralcarbonmetabolismpathwaysindeepbranchingbacteriaandarchaea |