Plasticity of the malleobactin pathway and its impact on siderophore action in human pathogenic bacteria

  • Chemistry. 2015 May 26;21(22):8010-4. doi: 10.1002/chem.201500757.
Jakob Franke  1 Keishi Ishida  1 Christian Hertweck  2  3
Affiliations
  • 1. Department of Biomolecular Chemistry, Leibniz Institute for Natural Product Research and Infection Biology (HKI), Beutenbergstr. 11a, 07745 Jena (Germany).
  • 2. Department of Biomolecular Chemistry, Leibniz Institute for Natural Product Research and Infection Biology (HKI), Beutenbergstr. 11a, 07745 Jena (Germany). [email protected].
  • 3. Chair of Natural Product Chemistry, Friedrich Schiller University, Jena (Germany). [email protected].
Abstract

The human pathogenic bacteria Burkholderia mallei, Burkholderia pseudomallei, and Burkholderia thailandensis harbor a highly conserved gene cluster coding for the biosynthesis of the long sought-after malleobactins. Four new, unexpected congeners of the malleobactin family that were isolated and fully characterized in this study feature unusual deviations from the parent, ornibactin-like architecture. Thus, the malleobactin non-ribosomal peptide synthetase (NRPS) has a rare flexibility that yields diverse peptide backbones, of which one candidate confers pronounced siderophore activity (EC50: 8.4 μM, CAS assay). These findings not only unveil a highly diverse assembly line but also are an important addition to the knowledgebase of the pathogens' metabolomes.

Keywords
Burkholderia; chelators; iron; non-ribosomal peptides; siderophores.
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