1. Academic Validation
  2. Total synthesis of albicidin: a lead structure from Xanthomonas albilineans for potent antibacterial gyrase inhibitors

Total synthesis of albicidin: a lead structure from Xanthomonas albilineans for potent antibacterial gyrase inhibitors

  • Angew Chem Int Ed Engl. 2015 Feb 2;54(6):1969-73. doi: 10.1002/anie.201409584.
Julian Kretz 1 Dennis Kerwat Vivien Schubert Stefan Grätz Alexander Pesic Siamak Semsary Stéphane Cociancich Monique Royer Roderich D Süssmuth
Affiliations

Affiliation

  • 1 Institut für Organische Chemie, Technische Universität Berlin, Straße des 17 Juni 124, 10623 Berlin (Germany) http://www.biochemie.tu-berlin.de.
Abstract

The peptide Antibiotic albicidin, which is synthesized by the plant pathogenic bacterium Xanthomonas albilineans, displays remarkable Antibacterial activity against various Gram-positive and Gram-negative Microorganisms. The low amounts of albicidin obtainable from the producing organism or through heterologous expression are limiting factors in providing sufficient material for bioactivity profiling and structure-activity studies. Therefore, we developed a convergent total synthesis route toward albicidin. The unexpectedly difficult formation of amide bonds between the aromatic Amino acids was achieved through a triphosgene-mediated coupling strategy. The herein presented synthesis of albicidin confirms the previously determined chemical structure and underlines the extraordinary Antibacterial activity of this compound. The synthetic protocol will provide multigram amounts of albicidin for further profiling of its drug properties.

Keywords

albicidin; gyrase; para-aminobenzoic acid; peptides; total synthesis.

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