Abstract
An unusual polyketide with a new carbon skeleton, lindgomycin (1), and the recently described ascosetin (2) were extracted from mycelia and culture broth of different Lindgomycetaceae strains, which were isolated from a sponge of the Kiel Fjord in the Baltic Sea (Germany) and from the Antarctic. Their structures were established by spectroscopic means. In the new polyketide, two distinct domains, a bicyclic hydrocarbon and a tetramic acid, are connected by a bridging carbonyl. The tetramic acid substructure of compound 1 was proved to possess a unique 5-benzylpyrrolidine-2,4-dione unit. The combination of 5-benzylpyrrolidine-2,4-dione of compound 1 in its tetramic acid half and 3-methylbut-3- enoic acid pendant in its decalin half allow the assignment of a new carbon skeleton. The new compound 1 and ascosetin showed antibiotic activities with IC50 value of 5.1 (±0.2) ìM and 3.2 (±0.4) μM, respectively, against methicillin-resistant Staphylococcus aureus.
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Wu, B., Wiese, J., Labes, A., Kramer, A., Schmaljohann, R., & Imhoff, J. F. (2015). Lindgomycin, an unusual antibiotic polyketide from a marine fungus of the lindgomycetaceae. Marine Drugs, 13(8), 4617–4632. https://doi.org/10.3390/md13084617
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