Institute of Molecular Biosciences, University of Graz, Humboldtstrasse 50/I, 8010, Graz, Austria.
Institute of Organic Chemistry, Graz University of Technology, Stremayrgasse 9, 8010, Graz, Austria.
Angew Chem Int Ed Engl. 2017 Nov 13;56(46):14753-14757. doi: 10.1002/anie.201707737. Epub 2017 Oct 18.
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.
非核糖体肠毒素替利万汀是第一个与人类肠道疾病相关的天然吡咯并苯并二氮杂䓬。由于产毒菌氧化酮肠杆菌是肠道微生物群的一部分,并且吡咯并苯并二氮杂䓬导致结肠炎的发病机制,因此了解替利万汀的生物合成和调节非常重要。在这里,我们报告了替利万汀的生物合成,并表明这种非核糖体肽组装途径最初生成具有细胞毒性的替利霉素,这是一种简单的吡咯并苯并二氮杂䓬。替利万汀是由替利霉素与生物生成的吲哚自发非酶反应产生的。通过替利霉素的化学全合成,我们可以证实关于生物合成的预测。人类肠道常驻菌氧化酮肠杆菌产生两种具有不同功能的细胞毒性吡咯并苯并二氮杂䓬,这对肠道疾病有重要影响。