ACS Omega · 2023 · 17 citations · 19 references
Life SciencesBotanyMicrobiologyBioorganic ChemistryMycologyStructure-activity RelationshipsEnzyme InhibitionFungal BiochemistryFungal Natural Product BiosynthesisFungal Secondary MetabolitesAbsolute Configuration AssignmentAbsolute Configuration DeterminationBacillus SubtilisBioactive Compounds From Marine FungiFungal Bioactive CompoundsMarine Fungal EndophytesMarine Fungal Natural ProductsStructure Elucidation Of Fungal Metabolites
High Resolution Image Download MS PowerPoint Slide Two new octaketides, cytosporones W ( 1 ) and X ( 2 ), along with eight known cytosporone derivatives [(±)- 3–9 ], were isolated from mangrove endophytic fungus Diaporthe sp. ZJHJYZ-1. Compounds 1 and 2 were a pair of epimers, whose configuration of C-1 could mutually convert, causing racemization of the lactone ring. The planar structures of compounds were elucidated through detailed 1D, 2D NMR, and HR-ESI-MS analysis. ECD spectra comparison and modified Mosher ester method were applied to determine the absolute configuration of 1 and 2 . In bioassays, (±)- 3 exhibited promising inhibitory activities against Bacillus subtilis, Pseudomonas aeruginosa, and Penicillium italicum with MIC, respectively, for 12.5, 12.5, and 3.13 μM.
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Christopher G. Pierce, Priya Uppuluri, Floyd L. Wormley et al. · Nature Protocols · 2008 · 775 citations · Full text
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