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July 15, 2015Angewandte Chemie International Edition333 citationsOpen Access

Ester‐Mediated Amide Bond Formation Driven by Wet–Dry Cycles: A Possible Path to Polypeptides on the Prebiotic Earth

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JFJay G. ForsytheSYShengsheng YuIMIrena Mamajanov

Key Points

  • To explore the mechanism of peptide bond formation using α-hydroxy and α-amino acids under prebiotic conditions.
  • Demonstration of prebiotic reactions involving α-hydroxy acids and α-amino acids
  • Use of wet-cool/dry-hot cycles to facilitate reactions
  • Formation of depsipeptide oligomers through ester and amide linkages.
  • Ester-amide bond exchange leads to an enrichment of amino acids in depsipeptides over time
  • Peptides likely originated from ester-based precursors
  • Prebiotic reactions support the hypothesis of polypeptide formation mechanisms.

Abstract

Although it is generally accepted that amino acids were present on the prebiotic Earth, the mechanism by which α-amino acids were condensed into polypeptides before the emergence of enzymes remains unsolved. Here, we demonstrate a prebiotically plausible mechanism for peptide (amide) bond formation that is enabled by α-hydroxy acids, which were likely present along with amino acids on the early Earth. Together, α-hydroxy acids and α-amino acids form depsipeptides-oligomers with a combination of ester and amide linkages-in model prebiotic reactions that are driven by wet-cool/dry-hot cycles. Through a combination of ester-amide bond exchange and ester bond hydrolysis, depsipeptides are enriched with amino acids over time. These results support a long-standing hypothesis that peptides might have arisen from ester-based precursors.

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Cite This Study

Forsythe et al. (2015) studied this question.

synapsesocial.com/papers/6a08e8f227ceb0c2a2d61902https://doi.org/10.1002/anie.201503792
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