Owen R W, Wait R, Bilton R F
Department of Chemistry and Biochemistry, Liverpool Polytechnic, England.
J Lipid Res. 1988 Apr;29(4):459-68.
The metabolism of ursodeoxycholic acid by Pseudomonas sp NCIB 10590 has been studied in phosphate-buffered mineral salts. The organism completely metabolized ursodeoxycholic acid in 24 hr, and time-course experiments revealed that maximum product formation occurred at 14 hr. The major products detected and identified at 14 hr were 7 beta-hydroxychol-4-en-3-one-24-oic acid, 7 beta-hydroxy-3-oxo-pregna-1,4-diene-20-carboxylic acid, and 7 beta-hydroxyandrosta-1,4-diene-3,17-dione. Several minor intermediates were isolated and evidence is given for the following structures: 7 beta-hydroxy-5 beta-cholan-3-oxo-24-oic acid, 7 beta-hydroxyandrost-4-en-3,17-dione, 7 beta,17 beta-dihydroxyandrosta-1,4-diene-3-one, 3-hydroxy-1,3,5(10)-9,10-seco-androstatriene-3,17-dione-7 beta-ol, and 22 alpha-hydroxymethylpregna-1,4-diene-3-one-7 beta-ol.
在磷酸盐缓冲的矿物盐中,对假单胞菌属NCIB 10590对熊去氧胆酸的代谢进行了研究。该微生物在24小时内完全代谢了熊去氧胆酸,时间进程实验表明,最大产物形成发生在14小时。在14小时检测和鉴定出的主要产物为7β-羟基胆-4-烯-3-酮-24-酸、7β-羟基-3-氧代-孕-1,4-二烯-20-羧酸和7β-羟基雄甾-1,4-二烯-3,17-二酮。分离出了几种次要中间体,并给出了以下结构的证据:7β-羟基-5β-胆烷-3-氧代-24-酸、7β-羟基雄甾-4-烯-3,17-二酮、7β,17β-二羟基雄甾-1,4-二烯-3-酮、3-羟基-1,3,5(10)-9,10-开环-雄甾三烯-3,17-二酮-7β-醇和22α-羟甲基孕-1,4-二烯-3-酮-7β-醇。