The catalytic mechanism of the 3-ketosteroid isomerase of Digitalis lanata involves an intramolecular proton transfer and the activity is not associated with the 3β-hydroxysteroid dehydrogenase activity. Issue 14 (6th April 2016)
- Record Type:
- Journal Article
- Title:
- The catalytic mechanism of the 3-ketosteroid isomerase of Digitalis lanata involves an intramolecular proton transfer and the activity is not associated with the 3β-hydroxysteroid dehydrogenase activity. Issue 14 (6th April 2016)
- Main Title:
- The catalytic mechanism of the 3-ketosteroid isomerase of Digitalis lanata involves an intramolecular proton transfer and the activity is not associated with the 3β-hydroxysteroid dehydrogenase activity
- Authors:
- Meitinger, Nadine
Munkert, Jennifer
Maia de Pádua, Rodrigo
de Souza Filho, José Dias
Maid, Harald
Bauer, Walter
Braga, Fernão Castro
Kreis, Wolfgang - Abstract:
- Graphical abstract: Highlights: Reaction mechanism of Digitalis lanata 3KSI is investigated. Isoprogesterone isomerization proceeds via an intramolecular proton transfer. The mechanism is consistent with the mechanism of the bacterial 3KSIs. r Dl 3βHSD does not possess 3-ketosteroid isomerase activity. Abstract: The isomerization of the Δ 5 -3-ketosteroid isoprogesterone into the Δ 4 -3-ketosteroid progesterone has been examined with recombinant 3β-hydroxysteroid dehydrogenase from Digitalis lanata (r Dl 3βHSD), partially purified 3-ketosteroid isomerase from Digitalis lanata ( Dl 3KSI) and under non-enzymatic conditions in deuterium oxide (D2 O). Studies indicate that the isomerization catalyzed by the Dl 3KSI proceeds without significant isotope exchange between the medium and the steroid and thus involves an intramolecular proton transfer consistent with the mechanism of the bacterial 3-ketosteroid isomerase of Pseudomonas testosteroni . For the r Dl 3βHSD as well as under non-enzymatic conditions deuterium was incorporated from the incubation buffer during isomerization. Together with a comparison of the rate of isomerization under the different conditions, it was demonstrated that r Dl 3βHSD does not possess 3-ketosteroid isomerase activity.
- Is Part Of:
- Tetrahedron letters. Volume 57:Issue 14(2016)
- Journal:
- Tetrahedron letters
- Issue:
- Volume 57:Issue 14(2016)
- Issue Display:
- Volume 57, Issue 14 (2016)
- Year:
- 2016
- Volume:
- 57
- Issue:
- 14
- Issue Sort Value:
- 2016-0057-0014-0000
- Page Start:
- 1567
- Page End:
- 1571
- Publication Date:
- 2016-04-06
- Subjects:
- 3KSI Δ5-3-ketosteroid isomerase -- 3βHSD Δ5-3β-hydroxysteroid dehydrogenase
Cardenolide biosynthesis -- Digitalis lanata -- 3β-Hydroxysteroid dehydrogenase -- 3-Ketosteroid isomerase -- Isoprogesterone -- Progesterone
Chemistry, Organic -- Periodicals
547.005 - Journal URLs:
- http://www.elsevier.com/journals ↗
- DOI:
- 10.1016/j.tetlet.2016.02.099 ↗
- Languages:
- English
- ISSNs:
- 0040-4039
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 8796.860000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 1677.xml