Journal of Natural Products · 2007 · 36 citations · 3 references
Life SciencesBiochemistryMicrobiologyAntimicrobial PharmacologyBioorganic ChemistryMycologyAntifungal AgentsAntimicrobial PeptidesFungal BiochemistryFungal Natural Product BiosynthesisFungal Secondary MetabolitesAmino AcidsAntifungal PeptidesBioassay-guided FractionationFungal Bioactive CompoundsStructure Elucidation Of Fungal Metabolites
Two new peptaibols, septocylindrin A (1) and septocylindrin B (2), related to the well-studied membrane-channel-forming peptaibol alamethicin, were obtained from a terrestrial isolate of the fungus Septocylindrium sp. Both 1 and 2 are linear 19-amino acid peptides with a modified phenylalanine C-terminus. Analysis of the HRMS data indicated that they differ only in the 18th residue, where 1 contains Glu and 2 contains Gln. The structures of these two peptaibols were determined by extensive NMR and HRMS analysis. The absolute configurations of amino acids present in 1 were determined using Marfey's methodology. Both compounds were isolated through bioassay-guided fractionation and exhibited significant antibacterial and antifungal activity.
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Chemical nature and sequence of alamethicin
Donald R. Martin, Richard J. Williams · Biochemical Journal · 1976 · 87 citations · Full text