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Biosynthesis of cladospirone bisepoxide, a member of the spirobisnaphthalene family

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JOURNAL OF ANTIBIOTICS
卷 53, 期 2, 页码 153-157

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JAPAN ANTIBIOT RES ASSN
DOI: 10.7164/antibiotics.53.153

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The biosynthesis of cladospirone bisepoxide (1) was investigated by feeding C-13-labeled acetate to growing cultures of the fungus Sphaeropsidales sp. (strain F-24'707). C-13 NMR spectral analysis demonstrated the polyketide origin of both naphthalene units. The origin of two epoxide oxygens was confirmed as from air by cultivation of the strain in an O-18(2)-enriched atmosphere. The [O-18]incorporation pattern into palmarumycin C-12 (11), the putative precursor of 1 led to the hypothesis that the carbonyl oxygen of 1 is derived from water by exchange of an oxygen atom. inhibition of the biosynthesis of 1 with tricyclazole, an inhibitor of the 1,8-dihydroxynaphthalene (DHN) melanin biosynthesis, confirmed the connection of both biosynthetic pathways.

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