Journal of Lipid Research (Sep 1983)
Biotransformation of chenodeoxycholic acid by Pseudomonas species NCIB 10590 under anaerobic conditions.
Abstract
The metabolism of chenodeoxycholic acid by Pseudomonas sp. NCIB 10590 under strict anaerobic conditions was studied. A range of unsaturated acidic and neutral metabolites were isolated and identified. The major acidic product was chola-4,6-dien-3-one-24-oic acid whilst the major neutral product was androsta-4,6-dien-3,17-dione. The major acidic products were 7 alpha-hydroxy-5 beta-cholan-3-oxo-24-oic acid, 3-oxo-4,6-pregnadien-20-carboxylic acid, 7 alpha-hydroxy-3-oxo-1,4-pregnadien-20-carboxylic acid, and 7 alpha-hydroxy-3-oxo-4-pregnen-20-carboxylic acid. The minor neutral products were androsta-1,4,6-trien-3,17-dione, 17 beta-hydroxyandrosta-4,6-dien-3,17-dione, 17 beta-hydroxyandrosta-1,4,6-trien-3-one, 7 alpha-hydroxyandrosta-1,4-dien-3,17-dione, and 7 alpha-hydroxyandrost-4-en-3,17-dione. In contrast to aerobic catabolism of chenodeoxycholic acid by Pseudomonas sp. NCIB 10590 in which 1,4-dienone steroids predominate, the major products described in this study are 4,6-dienone steroids. This is because of the induction of a 7 alpha-dehydroxylase enzyme under anaerobic conditions.