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Biosynthesis of the Enterotoxic Pyrrolobenzodiazepine Natural Product Tilivalline

Authors :
Dornisch, Elisabeth
Pletz, Jakob
Glabonjat, Ronald A.
Martin, Florian
Lembacher‐Fadum, Christian
Neger, Margit
Högenauer, Christoph
Francesconi, Kevin
Kroutil, Wolfgang
Zangger, Klaus
Breinbauer, Rolf
Zechner, Ellen L.
Source :
Angewandte Chemie (International Ed. in English)
Publication Year :
2017
Publisher :
John Wiley and Sons Inc., 2017.

Abstract

The nonribosomal enterotoxin tilivalline was the first naturally occurring pyrrolobenzodiazepine to be linked to disease in the human intestine. Since the producing organism Klebsiella oxytoca is part of the intestinal microbiota and the pyrrolobenzodiazepine causes the pathogenesis of colitis it is important to understand the biosynthesis and regulation of tilivalline activity. Here we report the biosynthesis of tilivalline and show that this nonribosomal peptide assembly pathway initially generates tilimycin, a simple pyrrolobenzodiazepine with cytotoxic properties. Tilivalline results from the non‐enzymatic spontaneous reaction of tilimycin with biogenetically generated indole. Through a chemical total synthesis of tilimycin we could corroborate the predictions made about the biosynthesis. Production of two cytotoxic pyrrolobenzodiazepines with distinct functionalities by human gut resident Klebsiella oxytoca has important implications for intestinal disease.

Details

Language :
English
ISSN :
15213773 and 14337851
Volume :
56
Issue :
46
Database :
OpenAIRE
Journal :
Angewandte Chemie (International Ed. in English)
Accession number :
edsair.pmid..........85e4d713946bb640778458701896cf6f