| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 70871 | Journal of Molecular Catalysis B: Enzymatic | 2010 | 6 Pages |
Biotransformation of androst-4-ene-3,17-dione (1), 3β-hydroxypregnan-5-en-20-one (pregnenolone, 2), 3β-hydroxyandrost-5-en-17-one (DHEA, 3) and estradiol (4) was investigated with fungus of Gelasinospora retispora. Biotransformation of 1 gave 11α-hydroxyandrost-4-ene-3,17-dione (5) in good yield. In the case of compound 2, three compounds, DHEA (3), 3β,17β-dihydroxyandrost-5-ene (6) and 3β,15β-dihydroxyandrost-5-en-17-one (7) were obtained. Moreover, DHEA (3) was converted to 3β,7α-dihydroxyandrost-5-en-17-one (8) and 3β,11α-dihydroxyandrost-5-ene-7,17-dione (9). And it was found that biotransformation of 4 affords 6β-hydroxyestradiol (10).
Graphical abstractFigure optionsDownload full-size imageDownload as PowerPoint slideResearch highlights▶ Biotransformation of androst-4-ene-3,17-dione using Gelasinospora retispora gave 11α-hydroxyandrost-4-ene-3,17-dione with good yield. ▶ Transformation of pregnenolone afforded three products: DHEA, 3β,17α-dihydroxyandrost-5-ene and 3β,15β-dihydroxyandrost-5-en-17-one. ▶ The side-chain of pregnenolone was cleaved and then hydroxylated at C-15β using G. retispora.
