Identification of 16‐dehydropregnenolone as an intermediate in 16‐androstene biosynthesis in neonatal porcine testicular microsomes
Open Access
- 20 August 1984
- journal article
- Published by Wiley in FEBS Letters
- Vol. 174 (1) , 173-178
- https://doi.org/10.1016/0014-5793(84)81099-6
Abstract
The biosynthesis of 16‐androstenes has been studied in neonatal porcine testicular microsomes using 17‐hydroxypregnenolone and 16‐dehydropregnenolone, separately, as substrates. The metabolites formed after microsomal incubation with these substrates were purified, derivatized as O‐methyloxime‐trimethylsilyl ethers and analysed by capillary gas chromatography‐mass spectrometry. In the incubation of 17‐hydroxy‐pregnenolone with microsomes, 16‐dehydropregnenolone was identified as an intermediate in the biosynthesis of 16‐androstenes. Further microsomal incubation of 16‐dehydropregnenolone has established the intermediary role of this steroid in the production of 16‐androstenes.Keywords
This publication has 8 references indexed in Scilit:
- Intermediates in 16‐androstene biosynthesis in neonatal porcine testisFEBS Letters, 1984
- A Novel Pathway of Androst-16-ene Biosynthesis in Immature Pig Testis Microsomal FractionsBiochemical Society Transactions, 1979
- Formation of [17-2H]androsta-5,16-dien-3β-ol from [17,21,21,21]pregnenolone by the microsomal fraction of boar testisBiochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism, 1976
- Simultaneous estimation of urinary steroids by semiautomated gas chromatography. investigation of neo-natal infants and children with abnormal steroid synthesisClinica Chimica Acta; International Journal of Clinical Chemistry, 1976
- CHANGES WITH AGE IN THE OCCURRENCE OF C19 STEROIDS IN THE TESTIS AND SUBMAXILLARY GLAND OF THE BOARReproduction, 1975
- Gas Phase Analytical Methods for the Study of Steroid Hormones and their MetabolitesPublished by Springer Nature ,1968
- A new approach to Δ16-androstenesTetrahedron Letters, 1962
- PROTEIN MEASUREMENT WITH THE FOLIN PHENOL REAGENTJournal of Biological Chemistry, 1951