Summary
We report here on the kinetics of formation of the N-blocked dipeptide, N-acetylglycylglycine (Acgly-gly), from N-acetylglycyl adenylate anhydride (Acgly-AMP) and glycine in aqueous solution at 25°C, and at various pH's. The reaction is of interest in that over a physiologically relevant pH range (6–8), peptide synthesis proceeds more rapidly than hydrolysis, even at those pH's at which this compound becomes increasingly susceptible to base-catalyzed hydrolysis. Under similar conditions, the corresponding unblocked aminoacyl adenylate anhydrides are considerably more unstable, and undergo appreciable hydrolysis in the presence of free amino acid. Because N-blocked aminoacyl adenylate anhydrides serve as model compounds of peptidyl adenylate anhydrides, these results suggest that primitive amino acid polymerization systems may have operated by cyclic reactivation of the peptidyl carboxyl group, rather than that of the incoming amino acid.
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Mullins, D.W., Lacey, J.C. Highly efficient peptide formation from N-acetylaminoacyl-AMP anhydride and free amino acid. J Mol Evol 19, 176–178 (1983). https://doi.org/10.1007/BF02300755
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DOI: https://doi.org/10.1007/BF02300755