| Literature DB >> 19071124 |
Maçha Gorlero1, Rafal Wieczorek, Katarzyna Adamala, Alessandra Giorgi, Maria Eugenia Schininà, Pasquale Stano, Pier Luigi Luisi.
Abstract
The dipeptide seryl-histidine (Ser-His) catalyses the condensation of esters of amino acids, peptide fragments, and peptide nucleic acid (PNA) building blocks, bringing to the formation of peptide bonds. Di-, tri- or tetra-peptides can be formed with yields that vary from 0.5% to 60% depending on the nature of the substrate and on the conditions. Other simpler peptides as Gly-Gly, or Gly-Gly-Gly are also effective, although less efficiently. We discuss the results from the viewpoint of primitive chemistry and the origin of long macromolecules by stepwise fragment condensations.Entities:
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Year: 2008 PMID: 19071124 DOI: 10.1016/j.febslet.2008.11.052
Source DB: PubMed Journal: FEBS Lett ISSN: 0014-5793 Impact factor: 4.124