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Side chain conjugation prevents bacterial 7-dehydroxylation of bile acids.
- Source :
-
The Journal of biological chemistry [J Biol Chem] 1990 Jul 05; Vol. 265 (19), pp. 10925-8. - Publication Year :
- 1990
-
Abstract
- The effect of side chain conjugation on 7-dehydroxylation of bile acids has been investigated. C24-bile acids and their glycine and taurine conjugates and keto bile acids were incubated with pure strains of Eubacterium sp. VPI 12708. Bile acids of the 5 alpha- or 5 beta-series with a free terminal carboxyl group and a 3 alpha, 7 alpha-dihydroxy system were very effectively 7 alpha-dehydroxylated, whereas 7 beta-hydroxy bile acids resisted 7-dehydroxylation. Oxo bile acids were metabolized at the oxygen function also. Glycine- and taurine-conjugated bile acids were neither deamidated nor 7-dehydroxylated by the bacteria. Thus, side chain conjugation prevents 7-dehydroxylation of bile acids by Eubacterium sp. VPI 12708.
- Subjects :
- Glycochenodeoxycholic Acid metabolism
Glycocholic Acid metabolism
Lithocholic Acid analogs & derivatives
Lithocholic Acid metabolism
Structure-Activity Relationship
Substrate Specificity
Taurochenodeoxycholic Acid metabolism
Taurocholic Acid metabolism
Bile Acids and Salts metabolism
Eubacterium enzymology
Glycine metabolism
Hydroxysteroid Dehydrogenases
Oxidoreductases
Steroid Hydroxylases metabolism
Taurine metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 0021-9258
- Volume :
- 265
- Issue :
- 19
- Database :
- MEDLINE
- Journal :
- The Journal of biological chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 2358447