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3 beta, 17 beta-hydroxysteroid dehydrogenase of Pseudomonas testosteroni. Kinetic evidence for the bifunctional activity at a common catalytic site.

Authors :
Minard P
Legoy MD
Thomas D
Source :
FEBS letters [FEBS Lett] 1985 Aug 19; Vol. 188 (1), pp. 85-90.
Publication Year :
1985

Abstract

3 beta, 17 beta-Hydroxysteroid dehydrogenase (3 beta 17 beta HSDH) is an NAD-dependent dehydrogenase which has a double specificity for the 3- and 17-positions on the steroid skeleton. When dehydroepiandrosterone (DHEA) is used as steroid substrate, and the assay coupled with ketosteroid-isomerase, the two reactions occur alternately and each reaction on the 3-position produces a chromophoric molecule. These two reactions can follow one another without dissociation of the coenzyme from the enzyme binding site. This is confirmed by competition experiments with another dehydrogenase.

Details

Language :
English
ISSN :
0014-5793
Volume :
188
Issue :
1
Database :
MEDLINE
Journal :
FEBS letters
Publication Type :
Academic Journal
Accession number :
2991019
Full Text :
https://doi.org/10.1016/0014-5793(85)80880-2