| Literature DB >> 26514647 |
Silke C Wenzel1, Holger Hoffmann2,3, Jidong Zhang2,3, Laurent Debussche2,3, Sabine Haag-Richter2,3, Michael Kurz2,3, Frederico Nardi2,3, Peer Lukat1, Irene Kochems1, Heiko Tietgen2,3, Dietmar Schummer4, Jean-Paul Nicolas2,3, Loreley Calvet2,3, Valerie Czepczor2,3, Patricia Vrignaud2,3, Agnes Mühlenweg5, Stefan Pelzer6, Rolf Müller7, Mark Brönstrup8.
Abstract
The bengamides, sponge-derived natural products that have been characterized as inhibitors of methionine aminopeptidases (MetAPs), have been intensively investigated as anticancer compounds. We embarked on a multidisciplinary project to supply bengamides by fermentation of the terrestrial myxobacterium M. virescens, decipher their biosynthesis, and optimize their properties as drug leads. The characterization of the biosynthetic pathway revealed that bacterial resistance to bengamides is conferred by Leu 154 of the myxobacterial MetAP protein, and enabled transfer of the entire gene cluster into the more suitable production host M. xanthus DK1622. A combination of semisynthesis of microbially derived bengamides and total synthesis resulted in an optimized derivative that combined high cellular potency in the nanomolar range with high metabolic stability, which translated to an improved half-life in mice and antitumor efficacy in a melanoma mouse model.Entities:
Keywords: bengamides; biosynthesis; drug discovery; natural products; resistance
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Year: 2015 PMID: 26514647 DOI: 10.1002/anie.201508277
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336