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  • 1
    ISSN: 0947-3440
    Keywords: Aspinolides ; Aspinonene ; Aspyrone co-metabolites ; Aspergillus ; Pentaketides ; Lactones ; Metabolism ; Natural products ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: New 10-membered lactones, named aspinolide A-C (3, 4, 5), and the aspinonene/aspyrone co-metabolites, named trienediol (6), isoaspinonene (7), dihydroaspyrone (8), and dienetriol 9 were discovered by chemical screening methods in the cultures of Aspergillus ochraceus (DSM-7428) under altered fermentation conditions. The structures were established by detailed spectroscopic analysis. The polyketide origin of the skeleton and the biogenesis of the oxygen atoms were verified by feeding sodium [1,2-13C2]acetate and [18O2] gas, respectively, to growing cultures of the fungus. A comprehensive discussion of the supposed biosynthetic pathways draws the conclusion that two polyketide synthases (PKSα, PKSβ) exist, forming two different series of pentaketides in parallel. One pathway leads to branched-chain metabolites by a Favorski-like rearrangement of an epoxide intermediate, while the other involves detachment of the pentaketides from the PKSβ by lactonisation without any rearrangement of the carbon skeleton. The former pathway is affected by an inhibitor of cytochrome P450 dependent monooxygenases.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0947-3440
    Keywords: Ulupyrinone ; Ulufuranol ; Metabolism ; Chemical screening ; Streptomyces ; Structure elucidation ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Chemical Screening with extracts of Actinomycetes strains resulted in the detection, isolation, and structural elucidation of two new heteroaromatic secondary metabolites, named ulupyrinone (1) and ulufuranol (2), from Streptomyces spina (strain FH-S 2144). The absolute configuration of ulufuranol (2) was determined by analysis of the CD spectra of its dibenzoate, 3, using the dibenzoate chirality rule.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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