| Literature DB >> 23913990 |
Ezra G Baraban1, Jesse B Morin, Gillian M Phillips, Andrew J Phillips, Scott A Strobel, Jo Handelsman.
Abstract
Endophytes isolated from tropical plants represent a largely untapped reservoir of bioactive secondary metabolites. We screened a library of fungal endophyte extracts for inhibition of the plant pathogen, Pythium ultimum, and purified an active compound using bioassay-guided fractionation. A new nonenolide, (4S,7S,8S,9R)-4-O-succinyl-7,8-dihydroxy-9-heptyl-nonen-9-olide, was isolated and named xyolide. The structure was elucidated by a combination of 1D and 2D NMR methods and the absolute configuration was determined by exciton-coupled circular dichroism. The MIC of xyolide against P. ultimum was 425 µM.Entities:
Keywords: Fungal endophyte; Natural product; Nonenolide; Pythium ultimum
Year: 2013 PMID: 23913990 PMCID: PMC3729479 DOI: 10.1016/j.tetlet.2013.05.093
Source DB: PubMed Journal: Tetrahedron Lett ISSN: 0040-4039 Impact factor: 2.415