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A Plausible Metal-Free Ancestral Analogue of the Krebs Cycle Composed Entirely of α-Ketoacids.

Efforts to decipher the prebiotic roots of metabolic pathways have focused on recapitulating modern biological transformations, with metals typically serving in place of cofactors and enzymes. Here, we show that the reaction of glyoxylate with pyruvate under mild aqueous conditions produces a series...

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Detalles Bibliográficos
Autores principales: Stubbs, R. Trent, Yadav, Mahipal, Krishnamurthy, Ramanarayanan, Springsteen, Greg
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8570912/
https://www.ncbi.nlm.nih.gov/pubmed/33046840
http://dx.doi.org/10.1038/s41557-020-00560-7
Descripción
Sumario:Efforts to decipher the prebiotic roots of metabolic pathways have focused on recapitulating modern biological transformations, with metals typically serving in place of cofactors and enzymes. Here, we show that the reaction of glyoxylate with pyruvate under mild aqueous conditions produces a series of α-ketoacid analogs of the reductive citric acid cycle, without the need for metals or enzyme catalysts. The transformations proceed in the same sequence as the reverse Krebs cycle, resembling a proto-metabolic pathway, with glyoxylate acting as both the carbon source and reducing agent. Additionally, the α-ketoacid analogs provide a natural route for the synthesis of amino acids by transamination with glycine, paralleling the extant metabolic mechanisms, and obviating the need for metal-catalyzed abiotic reductive aminations. This emerging sequence of prebiotic reactions could have set the stage for the advent of increasingly sophisticated pathways operating under catalytic control.