Abstract
Glutarimide-containing polyketides usually exhibit anti-fungi activity, which was well exampled by cycloheximide. In our work, three new polyketide structures, 12-amidestreptimidone (1), 12-carboxylstreptimidone (2) and 3-(5S,8R)-(2-amino-2-oxoethyl-2’-methoxy-2’-oxoethyl)-8,10-dimethyl-7-oxododeca-5-hydroxy-9E,11-diolefin (3) were isolated from Streptomyces sp. JCM 4793. 3 without the glutarimide moiety is not active against fungi as expected, while 1 bearing the amide moiety is much more active than its carboxylic form 2. Here we report the isolation, structural elucidation, antifungal activity, and proposed biosynthesis pathway of 1–3.
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Acknowledgements
This research was supported financially by grants from the National Science Foundation of China (22177050), the Xingdian Talent Support Program of Yunnan Province (XDYC-QNRC-2022-0774), Yunnan Provincial Science and Technology Department (202301AT070323), and Youth Innovation Promotion Association CAS to (2022395).
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Tang, LF., Jihuo, WL., Shi, PD. et al. Cytotoxic glutarimide-containing polyketides isolated from Streptomyces sp. JCM 4793. J Antibiot 77, 627–633 (2024). https://doi.org/10.1038/s41429-024-00743-1
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DOI: https://doi.org/10.1038/s41429-024-00743-1