Publication | Open Access
Pseudoxylallemycins A–F, Cyclic Tetrapeptides with Rare Allenyl Modifications Isolated from <i>Pseudoxylaria</i> sp. X802: A Competitor of Fungus-Growing Termite Cultivars
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Citations
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References
2016
Year
Bioorganic ChemistryFungus-growing Termite CultivarsSecondary MetaboliteOrganic ChemistryCyclic TetrapeptidesMedicinal ChemistryBiosynthesisSynthetic ModificationsNatural Product BiosynthesisBiochemistryNew Cyclic TetrapeptidesAntimicrobial CompoundPharmacologyNatural Product SynthesisAntifungal AgentPseudoxylallemycins A–fNatural SciencesFungus-fungus Pairing AssaysMicrobiologyMedicineDrug Discovery
Based on fungus-fungus pairing assays and HRMS-based dereplication strategy, six new cyclic tetrapeptides, pseudoxylallemycins A-F (1-6), were isolated from the termite-associated fungus Pseudoxylaria sp. X802. Structures were characterized using NMR spectroscopy, HRMS, and Marfey's reaction. Pseudoxylallemycins B-D (2-4) possess a rare and chemically accessible allene moiety amenable for synthetic modifications, and derivatives A-D showed antimicrobial activity against Gram-negative human-pathogenic Pseudomonas aeruginosa and antiproliferative activity against human umbilical vein endothelial cells and K-562 cell lines.
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