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Side chain conjugation prevents bacterial 7-dehydroxylation of bile acids.

Authors :
Batta AK
Salen G
Arora R
Shefer S
Batta M
Person A
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.

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