| Literature DB >> 24529574 |
Sandra Halecker1, Frank Surup1, Eric Kuhnert1, Kathrin I Mohr2, Nelson L Brock3, Jeroen S Dickschat3, Corina Junker4, Barbara Schulz4, Marc Stadler5.
Abstract
A 3-decalinoyltetramic acid, for which the trivial name hymenosetin is proposed, was isolated from crude extracts of a virulent strain of the ash dieback pathogen, Hymenoscyphus pseudoalbidus (="Chalara fraxinea"). This compound was produced only under certain culture conditions in submerged cultures of the fungus. Its planar structure was determined by NMR spectroscopy and by mass spectrometry. The absolute stereochemistry was assigned by CD spectroscopy and HETLOC data. Hymenosetin exhibited broad spectrum antibacterial and antifungal activities (including strong inhibition of MRSA), as well as moderate cytotoxic effects. So far, the metabolite proved inactive in assays for evaluation of phytotoxicity, whereas viridiol, another secondary metabolite known from H. pseudoalbidus, was regarded as phytotoxic principle of the pathogen against its host, Fraxinus excelsior. Further studies will show whether hymenosetin constitutes a defence metabolite that is produced by the pathogenic fungus to combat other microbes and fungi in the natural environment.Entities:
Keywords: Ash dieback; Hymenoscyphus pseudoalbidus; MRSA; Natural products; Secondary metabolite; Structure elucidation; Tetramic acid
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Year: 2014 PMID: 24529574 DOI: 10.1016/j.phytochem.2014.01.018
Source DB: PubMed Journal: Phytochemistry ISSN: 0031-9422 Impact factor: 4.072