Structure Elucidation and Activity of KolossinA, the D-/L-Pentadecapeptide Product of a Giant Nonribosomal Peptide Synthetase

The largest continuous bacterial nonribosomal peptide synthetase discovered so far is described. It consists of 15consecutive modules arising from an uninterrupted, fully functional gene in the entomopathogenic bacterium Photorhabdus luminescens. The identification of its cryptic biosynthesis produc...

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Veröffentlicht in:Angewandte Chemie International Edition 2015-08, Vol.54 (35), p.10352-10355
Hauptverfasser: Bode, Helge B, Brachmann, Alexander O, Jadhav, Kirtikumar B, Seyfarth, Lydia, Dauth, Christina, Fuchs, Sebastian W, Kaiser, Marcel, Waterfield, Nick R, Sack, Holger, Heinemann, Stefan H, Arndt, Hans-Dieter
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Sprache:eng
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Zusammenfassung:The largest continuous bacterial nonribosomal peptide synthetase discovered so far is described. It consists of 15consecutive modules arising from an uninterrupted, fully functional gene in the entomopathogenic bacterium Photorhabdus luminescens. The identification of its cryptic biosynthesis product was achieved by using a combination of genome analysis, promoter exchange, isotopic labeling experiments, and total synthesis of a focused collection of peptide candidates. Although it belongs to the growing class of D-/L-peptide natural products, the encoded metabolite kolossinA was found to be largely devoid of antibiotic activity and is likely involved in interspecies communication. A stereoisomer of this peculiar natural product displayed high activity against Trypanosoma brucei rhodesiense, a recalcitrant parasite that causes the deadly disease African sleeping sickness.
ISSN:1433-7851
1521-3773
DOI:10.1002/anie.201502835