| Literature DB >> 27404448 |
Heinrich Steinmetz1, Jun Li2,3,4, Chengzhang Fu5, Nestor Zaburannyi5, Birgitte Kunze1, Kirsten Harmrolfs5, Viktoria Schmitt5, Jennifer Herrmann5, Hans Reichenbach4, Gerhard Höfle4, Markus Kalesse6,7,8, Rolf Müller9.
Abstract
Myxobacteria are well-established sources for novel natural products exhibiting intriguing bioactivities. We here report on haprolid (1) isolated from Byssovorax cruenta Har1. The compound exhibits an unprecedented macrolactone comprising four modified amino acids and a polyketide fragment. As configurational assignment proved difficult, a bioinformatic analysis of the biosynthetic gene cluster was chosen to predict the configuration of each stereocenter. In-depth analysis of the corresponding biosynthetic proteins established a hybrid polyketide synthase/nonribosomal peptide synthetase origin of haprolid and allowed for stereochemical assignments. A subsequent total synthesis yielded haprolid and corroborated all predictions made. Intriguingly, haprolid showed cytotoxicity against several cell lines in the nanomolar range whereas other cells were almost unaffected by treatment with the compound.Entities:
Keywords: cell-line-selective cytotoxin; haprolid; polyketide (bio)synthesis; retrosynthesis; structure elucidation
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Year: 2016 PMID: 27404448 DOI: 10.1002/anie.201603288
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336