Journal of Natural Products · 2018 · 27 citations · 43 references
Life SciencesBiochemistryMedicinal ChemistryMetabolismMycologyNatural Product BiosynthesisBiotransformation PathwaysFungal MetabolismFungal Natural Product BiosynthesisFungal Secondary MetabolitesMicrobial BiotransformationSecondary Metabolite BiosynthesisBioactive Fungal MetabolitesBiotransformationEndophytic Fungal MetabolitesEpoxidationFungal Bioactive CompoundsFungal Metabolite BiosynthesisStructure Elucidation Of Fungal MetabolitesTransformations
Biotransformation of neoruscogenin (NR, 1, spirosta-5,25(27)-diene-1β,3β-diol), the major bioactive sapogenin of Ruscus preparations, was carried out with the endophytic fungus Alternaria eureka. Fourteen new biotransformation products (2-15) were isolated, and their structures were elucidated by NMR and HRESIMS data analyses. A. eureka affected mainly oxygenation, oxidation, and epoxidation reactions on the B and C rings of the sapogenin to afford compounds 8-15. In addition to these, cleavage of the spiroketal system as in compounds 2-7 and subsequent transformations provided unusual metabolites. This is the first study reporting conversion of the spirostanol skeleton to cholestane-type metabolites 2-5. Additionally, the cleavage of the C-22/C-26 oxygen bridge yielding a furostanol-type steroidal framework and subsequent formation of the epoxy bridge between C-18 and C-22 in 7 was encountered for the first time in steroid chemistry.
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Endophyte: The Evolution of a Term, and Clarification of Its Use and Definition
Dennis Wilson · Oikos · 1995 · 1.1K citations