Abstract
The novel macrolide cruentaren A was produced at levels up to 3.2 mg/liter by cultures of the myxobacterium Byssovorax cruenta. The new compound strongly inhibited the growth of yeasts and filamentous fungi and showed high cytotoxicity against L929 mouse fibroblast cells. A minor co-metabolite of cruentaren A, named cruentaren B, and identified as a six-membered lactone isomer of cruentaren A, showed only marginal cytotoxicity and no antifungal activity. Cruentaren A inhibited F0F1 mitochondrial ATP-hydrolysis in submitochondrial particles of yeasts and beef heart. © Japan Antibiotics Research Association.
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Kunze, B., Steinmetz, H., Höfle, G., Huss, M., Wieczorek, H., & Reichenbach, H. (2006). Cruentaren, a new antifungal salicylate-type macrolide from Byssovorax cruenta (Myxobacteria) with inhibitory effect on mitochondrial ATPase activity: Fermentation and biological properties. Journal of Antibiotics, 59(10), 664–668. https://doi.org/10.1038/ja.2006.89
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