Novel transformations of progesterone by a Mucor sp.

Author:

Madyastha K. Madhava,Srivatsan Jayanthi

Abstract

A Mucor sp. isolated from soil and identified as Mucor piriformis was used to study the mode of transformation of progesterone. Major metabolites isolated and identified were 14α-hydroxyprogesterone, 7β, 14α-dihydroxyprogesterone, 7α, 14α-dihydroxyprogesterone, and 6β, 14α-dihydroxyprogesterone. Among the minor metabolities, 5β, 14α-dihydroxy-pregnane-3, 20-dione has been characterized. Time-course studies of the formation of transformation products showed that hydroxylation at the 14α-position is the first step in the formation of dihydroxyprogesterones. The formation of 7β, 14α-dihydroxyprogesterone and 5β, 14α-dihydroxypregnane-3, 20-dione represents novel transformations by Mucor species.

Publisher

Canadian Science Publishing

Subject

Genetics,Molecular Biology,Applied Microbiology and Biotechnology,General Medicine,Immunology,Microbiology

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1. Non-terpenoid biotransformations by Mucor species;Phytochemistry Reviews;2014-08-01

2. Biotransformation of Some Steroids by Mucor Hiemalis MRC 70325;Journal of Chemical Research;2013-09

3. Transformation of 3β-hydroxy-5-en-steroids by Mucor racemosus;Journal of Molecular Catalysis B: Enzymatic;2008-09

4. Hydroxylation and Dihydroxylation;Biotechnology;2008-03-20

5. Formation of hydroxysteroid derivatives from androst-4-en-3,17-dione by the filamentous fungus Mucor racemosus;Journal of Molecular Catalysis B: Enzymatic;2008-01

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