Journal of Natural Products · 2005 · 19 citations · 6 references
PharmacyBiotechnologyMicrobiologyDrug DiscoveryEnzymologyNatural Product BiosynthesisAntibiotic ProductionMicrobial Natural Product BiosynthesisPolyketide BiosynthesisMethyl Group ReplacementMicrobial Production Of PolyketidesPolyketide AntibioticsPolyketide Synthase ComplexesPolyketide Synthase EngineeringPolyketide Synthase Pathways
Two new geldanamycin derivatives produced by genetic engineering of Streptomyces hygroscopicus strain K309-27-1 were isolated and characterized. Removal of the 8-methyl group of geldanamycin was achieved by replacing the AT4 domain of the polyketide synthase with a malonyl AT domain. The resulting strain produced 8-demethyl geldanamycin (2) and 4,5-epoxy-8-demethylgeldanamycin (3). The structures of both molecules were elucidated through interpretation of 1D and 2D NMR data as well as comparison with authentic geldanamycin derivatives. Compounds 2 and 3 displayed moderate cytotoxicity against the human breast cancer cell line SK-BR-3.
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GELDANAMYCIN, A NEW ANTIBIOTIC
C. DeBoer, P. A. MEULMAN, Richard J. Wnuk et al. · The Journal of Antibiotics · 1970 · 467 citations · Full text
Engineered Biosynthesis of Geldanamycin Analogs for Hsp90 Inhibition
Kedar G. Patel, Misty Piagentini, Andreas Rascher et al. · Chemistry & Biology · 2004 · 131 citations · Full text