Journal of the American Chemical Society · 2013 · 189 citations · 33 references
Life SciencesMicrobiologyMolecular BiologyEnzymologyMicrobial GeneticsNatural Product BiosynthesisFungal BiochemistryFungal GenomicsFungal Natural Product BiosynthesisFungal Secondary MetabolitesPolyketide BiosynthesisTerpenoid BiosynthesisFungal Metabolite BiosynthesisFungal Polyketide BiosynthesisFungal Polyketide SynthasesFungal Terpenoid BiosynthesisPolyketide Synthase Gene DiscoveryPolyketide Synthase PathwaysTerpene Synthase ActivityTerpene Synthases
Fumagillin 1 is a meroterpenoid from Aspergillus fumigatus that is known for its anti-angiogenic activity by binding to human methionine aminopeptidase 2. The genetic and molecular basis for biosynthesis of 1 had been an enigma despite the availability of the A. fumigatus genome sequence. Here, we report the identification and verification of the fma gene cluster, followed by characterization of the polyketide synthase and acyltransferase involved in biosynthesis of the dioic acid portion of 1. More significantly, we uncovered the elusive β-trans-bergamotene synthase in A. fumigatus as a membrane-bound terpene cyclase.
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Genomic sequence of the pathogenic and allergenic filamentous fungus Aspergillus fumigatus
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Complete Reconstitution of a Highly Reducing Iterative Polyketide Synthase
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