Microbial transformations of natural antitumor agents: oxidation of lapachol by Penicillium notatum.

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Abstract

The naphthoquinone lapachol (1) is readily metabolized by several fungi and streptomycetes. Preparative-scale fermentations with Penicillium notatum (UI 1602) provided a major polar metabolite (4), which was isolated and identified as an intermediate of the Hooker oxidation. The metabolite was synthesized by reacting lapachol with hydrogen peroxide under alkaline conditions.

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Otten, S., & Rosazza, J. P. (1978). Microbial transformations of natural antitumor agents: oxidation of lapachol by Penicillium notatum. Applied and Environmental Microbiology, 35(3), 554–557. https://doi.org/10.1128/aem.35.3.554-557.1978

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