| Literature DB >> 34219345 |
Minghe Luo1, Houchao Xu2, Yulu Dong1, Kun Shen1, Junlei Lu1, Zhiyong Yin2, Miaomiao Qi1, Guo Sun1, Lingjie Tang1, Jin Xiang1, Zixin Deng1, Jeroen S Dickschat2, Yuhui Sun1.
Abstract
A bioassay-guided fractionation led to the isolation of hangtaimycin (HTM) from Streptomyces spectabilis CCTCC M2017417 and the discovery of its hepatoprotective properties. Structure elucidation by NMR suggested the need for a structural revision. A putative HTM degradation product was also isolated and its structure was confirmed by total synthesis. The biosynthetic gene cluster was identified and resembles a hybrid trans-AT PKS/NRPS biosynthetic machinery whose first PKS enzyme contains an internal dehydrating bimodule, which is usually found split in other trans-AT PKSs. The mechanisms of such dehydrating bimodules have often been proposed, but have never been deeply investigated. Here we present in vivo mutations and in vitro enzymatic experiments that give first and detailed mechanistic insights into catalysis by dehydrating bimodules.Entities:
Keywords: biosynthesis; dehydrating bimodules; natural products; polyketide synthases; trans-acyltransferase
Year: 2021 PMID: 34219345 DOI: 10.1002/anie.202106250
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336