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Older Than Genes: The Acetyl CoA Pathway and Origins

For decades, microbiologists have viewed the acetyl CoA pathway and organisms that use it for H(2)-dependent carbon and energy metabolism, acetogens and methanogens, as ancient. Classical evidence and newer evidence indicating the antiquity of the acetyl CoA pathway are summarized here. The acetyl C...

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Autor principal: Martin, William F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7325901/
https://www.ncbi.nlm.nih.gov/pubmed/32655499
http://dx.doi.org/10.3389/fmicb.2020.00817
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author Martin, William F.
author_facet Martin, William F.
author_sort Martin, William F.
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description For decades, microbiologists have viewed the acetyl CoA pathway and organisms that use it for H(2)-dependent carbon and energy metabolism, acetogens and methanogens, as ancient. Classical evidence and newer evidence indicating the antiquity of the acetyl CoA pathway are summarized here. The acetyl CoA pathway requires approximately 10 enzymes, roughly as many organic cofactors, and more than 500 kDa of combined subunit molecular mass to catalyze the conversion of H(2) and CO(2) to formate, acetate, and pyruvate in acetogens and methanogens. However, a single hydrothermal vent alloy, awaruite (Ni(3)Fe), can convert H(2) and CO(2) to formate, acetate, and pyruvate under mild hydrothermal conditions on its own. The chemical reactions of H(2) and CO(2) to pyruvate thus have a natural tendency to occur without enzymes, given suitable inorganic catalysts. This suggests that the evolution of the enzymatic acetyl CoA pathway was preceded by—and patterned along—a route of naturally occurring exergonic reactions catalyzed by transition metal minerals that could activate H(2) and CO(2) by chemisorption. The principle of forward (autotrophic) pathway evolution from preexisting non-enzymatic reactions is generalized to the concept of patterned evolution of pathways. In acetogens, exergonic reduction of CO(2) by H(2) generates acyl phosphates by highly reactive carbonyl groups undergoing attack by inert inorganic phosphate. In that ancient reaction of biochemical energy conservation, the energy behind formation of the acyl phosphate bond resides in the carbonyl, not in phosphate. The antiquity of the acetyl CoA pathway is usually seen in light of CO(2) fixation; its role in primordial energy coupling via acyl phosphates and substrate-level phosphorylation is emphasized here.
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spelling pubmed-73259012020-07-09 Older Than Genes: The Acetyl CoA Pathway and Origins Martin, William F. Front Microbiol Microbiology For decades, microbiologists have viewed the acetyl CoA pathway and organisms that use it for H(2)-dependent carbon and energy metabolism, acetogens and methanogens, as ancient. Classical evidence and newer evidence indicating the antiquity of the acetyl CoA pathway are summarized here. The acetyl CoA pathway requires approximately 10 enzymes, roughly as many organic cofactors, and more than 500 kDa of combined subunit molecular mass to catalyze the conversion of H(2) and CO(2) to formate, acetate, and pyruvate in acetogens and methanogens. However, a single hydrothermal vent alloy, awaruite (Ni(3)Fe), can convert H(2) and CO(2) to formate, acetate, and pyruvate under mild hydrothermal conditions on its own. The chemical reactions of H(2) and CO(2) to pyruvate thus have a natural tendency to occur without enzymes, given suitable inorganic catalysts. This suggests that the evolution of the enzymatic acetyl CoA pathway was preceded by—and patterned along—a route of naturally occurring exergonic reactions catalyzed by transition metal minerals that could activate H(2) and CO(2) by chemisorption. The principle of forward (autotrophic) pathway evolution from preexisting non-enzymatic reactions is generalized to the concept of patterned evolution of pathways. In acetogens, exergonic reduction of CO(2) by H(2) generates acyl phosphates by highly reactive carbonyl groups undergoing attack by inert inorganic phosphate. In that ancient reaction of biochemical energy conservation, the energy behind formation of the acyl phosphate bond resides in the carbonyl, not in phosphate. The antiquity of the acetyl CoA pathway is usually seen in light of CO(2) fixation; its role in primordial energy coupling via acyl phosphates and substrate-level phosphorylation is emphasized here. Frontiers Media S.A. 2020-06-04 /pmc/articles/PMC7325901/ /pubmed/32655499 http://dx.doi.org/10.3389/fmicb.2020.00817 Text en Copyright © 2020 Martin. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Martin, William F.
Older Than Genes: The Acetyl CoA Pathway and Origins
title Older Than Genes: The Acetyl CoA Pathway and Origins
title_full Older Than Genes: The Acetyl CoA Pathway and Origins
title_fullStr Older Than Genes: The Acetyl CoA Pathway and Origins
title_full_unstemmed Older Than Genes: The Acetyl CoA Pathway and Origins
title_short Older Than Genes: The Acetyl CoA Pathway and Origins
title_sort older than genes: the acetyl coa pathway and origins
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7325901/
https://www.ncbi.nlm.nih.gov/pubmed/32655499
http://dx.doi.org/10.3389/fmicb.2020.00817
work_keys_str_mv AT martinwilliamf olderthangenestheacetylcoapathwayandorigins