Predominant allylic hydroxylation at carbons 6 and 7 of 4 and 5-ene functionalized steroids by the thermophilic fungus Rhizomucor tauricus IMI23312

A. Christy Hunter, Paul W. Mills, Cinzia Dedi, Howard T. Dodd

    Research output: Contribution to journalArticlepeer-review

    Abstract

    This paper demonstrates for the first time transformation of a series of steroids (progesterone, androst-4-en-3,17-dione, testosterone, pregnenolone and dehydroepiandrosterone) by the thermophilic fungus Rhizomucor tauricus. All transformations were found to be oxidative (monohydroxylation and dihydroxylation) with allylic hydroxylation the predominant route of attack functionalizing the steroidal skeleta. Timed experiments demonstrated that dihydroxylation of progesterone, androst-4-en-3,17-dione and pregnenolone all initiated with hydroxylation on ring-B followed by attack on ring-C. Similar patterns of steroidal transformation to those observed with R. tauricus have been observed with some species of thermophilic Bacilli and mesophilic fungi. All metabolites were isolated by column chromatography and were identified by 1H, 13C NMR, DEPT analysis and other spectroscopic data. The application of thermophilic fungi to steroid transformation may represent a potentially rich source for the generation of new steroidal compounds as well as for uncovering inter and intraspecies similarities and differences in steroid metabolism. © 2007 Elsevier Ltd. All rights reserved.
    Original languageEnglish
    Pages (from-to)155-163
    Number of pages8
    JournalJournal of Steroid Biochemistry and Molecular Biology
    Volume108
    Issue number1-2
    DOIs
    Publication statusPublished - Jan 2008

    Keywords

    • Allylic oxidation
    • Hydroxylation
    • Rhizomucor tauricus
    • Steroid transformation
    • Thermophilic fungus

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