The Journal of Antibiotics · 2002 · 19 citations · 13 references
Life SciencesBiochemistryMicrobiologyMetabolismMicrobial MetabolismNatural Product BiosynthesisAmino Acid MetabolismAmino Acid ProductionFungal Natural Product BiosynthesisMarine Natural Product BiosynthesisMicrobial Natural Product BiosynthesisSecondary Metabolite BiosynthesisActinomyces PathogenicityActinomycete Secondary Metabolism
Cetoniacytone A (1) and some related minor components (2, 6, 7) were produced by Actinomyces sp. (strain Lu 9419), which was isolated from the intestines of a rose chafer (Cetonia aureata). The structures of the novel metabolites were established by detailed spectroscopic analysis. The absolute configuration of 1 was determined by X-ray analysis and derivatisation with chiral acids. 1 exhibits a significant cytotoxicity against selected tumor cell lines. The biosynthesis of 1 was studied by feeding 13C labelled precursors. The results suggest that the characteristic p-C7N skeleton of the aminocarba sugar is formed via the pentose phosphate pathway by cyclisation of a heptulose phosphate intermediate.
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STUDIES ON VALIDAMYCINS, NEW ANTIBIOTICS. II
Takashi Iwasa, Eiji Higashide, Hiroichi Yamamoto et al. · The Journal of Antibiotics · 1971 · 135 citations · Full text
URSULA DEGWERT, ROSEMARIE VAN HÜLST, Hermann Pape et al. · The Journal of Antibiotics · 1987 · 68 citations · Full text