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A cyanosulfidic origin of the Krebs cycle
The centrality of the Krebs cycle in metabolism has long been interpreted as evidence of its antiquity, and consequently, questions regarding its provenance, and whether it initially functioned as a cycle or not, have received much attention. The present report shows that prebiotic oxidation of α-hy...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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American Association for the Advancement of Science
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8363140/ https://www.ncbi.nlm.nih.gov/pubmed/34389542 http://dx.doi.org/10.1126/sciadv.abh3981 |
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author | Ritson, Dougal J. |
author_facet | Ritson, Dougal J. |
author_sort | Ritson, Dougal J. |
collection | PubMed |
description | The centrality of the Krebs cycle in metabolism has long been interpreted as evidence of its antiquity, and consequently, questions regarding its provenance, and whether it initially functioned as a cycle or not, have received much attention. The present report shows that prebiotic oxidation of α-hydroxy carboxylates can be achieved by UV photolysis of a simple geochemical species (HS(−)), which leads to α-oxo carboxylates that feature in the Krebs cycle and glyoxylate shunt. Further reaction of these products leads to almost all intermediates of the Krebs cycle proper, succinate semialdehyde bypass, and glyoxylate shunt. Fumarate, the missing Krebs cycle component, and the required α-hydroxy carboxylates can be provided by a highly related hydrogen cyanide chemistry, which also provides precursors for amino acids, nucleotides, and phospholipids. |
format | Online Article Text |
id | pubmed-8363140 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-83631402021-08-20 A cyanosulfidic origin of the Krebs cycle Ritson, Dougal J. Sci Adv Research Articles The centrality of the Krebs cycle in metabolism has long been interpreted as evidence of its antiquity, and consequently, questions regarding its provenance, and whether it initially functioned as a cycle or not, have received much attention. The present report shows that prebiotic oxidation of α-hydroxy carboxylates can be achieved by UV photolysis of a simple geochemical species (HS(−)), which leads to α-oxo carboxylates that feature in the Krebs cycle and glyoxylate shunt. Further reaction of these products leads to almost all intermediates of the Krebs cycle proper, succinate semialdehyde bypass, and glyoxylate shunt. Fumarate, the missing Krebs cycle component, and the required α-hydroxy carboxylates can be provided by a highly related hydrogen cyanide chemistry, which also provides precursors for amino acids, nucleotides, and phospholipids. American Association for the Advancement of Science 2021-08-13 /pmc/articles/PMC8363140/ /pubmed/34389542 http://dx.doi.org/10.1126/sciadv.abh3981 Text en Copyright © 2021 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 | Research Articles Ritson, Dougal J. A cyanosulfidic origin of the Krebs cycle |
title | A cyanosulfidic origin of the Krebs cycle |
title_full | A cyanosulfidic origin of the Krebs cycle |
title_fullStr | A cyanosulfidic origin of the Krebs cycle |
title_full_unstemmed | A cyanosulfidic origin of the Krebs cycle |
title_short | A cyanosulfidic origin of the Krebs cycle |
title_sort | cyanosulfidic origin of the krebs cycle |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8363140/ https://www.ncbi.nlm.nih.gov/pubmed/34389542 http://dx.doi.org/10.1126/sciadv.abh3981 |
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