J. Lipid Res.
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Originally published In Press as doi:10.1194/jlr.R500013-JLR200 on November 18, 2005

This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
R500013-JLR200v1
47/2/241    most recent
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Ridlon, J. M.
Right arrow Articles by Hylemon, P. B.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Ridlon, J. M.
Right arrow Articles by Hylemon, P. B.
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati  
What's this?

Journal of Lipid Research, Vol. 47, 241-259, February 2006
Copyright © 2006 by American Society for Biochemistry and Molecular Biology


Review

Bile salt biotransformations by human intestinal bacteria

Jason M. Ridlon, Dae-Joong Kang and Phillip B. Hylemon1

Department of Microbiology/Immunology, Medical College of Virginia, Virginia Commonwealth University, Richmond, VA

Published, JLR Papers in Press, November 18, 2005.

1 To whom correspondence should be addressed. e-mail: hylemon{at}hsc.vcu.edu

Secondary bile acids, produced solely by intestinal bacteria, can accumulate to high levels in the enterohepatic circulation of some individuals and may contribute to the pathogenesis of colon cancer, gallstones, and other gastrointestinal (GI) diseases. Bile salt hydrolysis and hydroxy group dehydrogenation reactions are carried out by a broad spectrum of intestinal anaerobic bacteria, whereas bile acid 7-dehydroxylation appears restricted to a limited number of intestinal anaerobes representing a small fraction of the total colonic flora. Microbial enzymes modifying bile salts differ between species with respect to pH optima, enzyme kinetics, substrate specificity, cellular location, and possibly physiological function. Crystallization, site-directed mutagenesis, and comparisons of protein secondary structure have provided insight into the mechanisms of several bile acid-biotransforming enzymatic reactions. Molecular cloning of genes encoding bile salt-modifying enzymes has facilitated the understanding of the genetic organization of these pathways and is a means of developing probes for the detection of bile salt-modifying bacteria. The potential exists for altering the bile acid pool by targeting key enzymes in the 7{alpha}/ß-dehydroxylation pathway through the development of pharmaceuticals or sequestering bile acids biologically in probiotic bacteria, which may result in their effective removal from the host after excretion.

Supplementary key words bile acids • deoxycholic acid • 7{alpha}-dehydroxylation • gallstone disease • colon cancer • bile salt hydrolase • probiotics • hydroxysteroid dehydrogenase • hydrogen sulfide

Abbreviations: bai, bile acid-inducible; BSH, bile salt hydrolase; CA, cholic acid; CBAH-1, conjugated bile acid hydrolase from C. perfringens; CDCA, chenodeoxycholic acid; DCA, deoxycholic acid; GDCA, glycodeoxycholate; HSDH, hydroxysteroid dehydrogenase; LCA, lithocholic acid; TDCA, taurodeoxycholate; UDCA, ursodeoxycholic acid


Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati    What's this?


This article has been cited by other articles:


Home page
Drug Metab. Dispos.Home page
A. K. Deo and S. M. Bandiera
Identification of Human Hepatic Cytochrome P450 Enzymes Involved in the Biotransformation of Cholic and Chenodeoxycholic Acid
Drug Metab. Dispos., October 1, 2008; 36(10): 1983 - 1991.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
B. V. Jones, M. Begley, C. Hill, C. G. M. Gahan, and J. R. Marchesi
Functional and comparative metagenomic analysis of bile salt hydrolase activity in the human gut microbiome
PNAS, September 9, 2008; 105(36): 13580 - 13585.
[Abstract] [Full Text] [PDF]


Home page
MicrobiologyHome page
J. M. Lambert, R. J. Siezen, W. M. de Vos, and M. Kleerebezem
Improved annotation of conjugated bile acid hydrolase superfamily members in Gram-positive bacteria
Microbiology, August 1, 2008; 154(8): 2492 - 2500.
[Abstract] [Full Text] [PDF]


Home page
Appl. Environ. Microbiol.Home page
J. M. Lambert, R. S. Bongers, W. M. de Vos, and M. Kleerebezem
Functional Analysis of Four Bile Salt Hydrolase and Penicillin Acylase Family Members in Lactobacillus plantarum WCFS1
Appl. Envir. Microbiol., August 1, 2008; 74(15): 4719 - 4726.
[Abstract] [Full Text] [PDF]


Home page
J. Bacteriol.Home page
J. A. Sorg and A. L. Sonenshein
Bile Salts and Glycine as Cogerminants for Clostridium difficile Spores
J. Bacteriol., April 1, 2008; 190(7): 2505 - 2512.
[Abstract] [Full Text] [PDF]


Home page
J. Lipid Res.Home page
G. Kakiyama, H. Tamegai, T. Iida, K. Mitamura, S. Ikegawa, T. Goto, N. Mano, J. Goto, P. Holz, L. R. Hagey, et al.
Isolation and chemical synthesis of a major, novel biliary bile acid in the common wombat (Vombatus ursinus): 15{alpha}-hydroxylithocholic acid
J. Lipid Res., December 1, 2007; 48(12): 2682 - 2692.
[Abstract] [Full Text] [PDF]


Home page
J. Bacteriol.Home page
A. Birkenmaier, J. Holert, H. Erdbrink, H. M. Moeller, A. Friemel, R. Schoenenberger, M. J.-F. Suter, J. Klebensberger, and B. Philipp
Biochemical and Genetic Investigation of Initial Reactions in Aerobic Degradation of the Bile Acid Cholate in Pseudomonas sp. Strain Chol1
J. Bacteriol., October 15, 2007; 189(20): 7165 - 7173.
[Abstract] [Full Text] [PDF]


Home page
CarcinogenesisHome page
C.M. Payne, C. Weber, C. Crowley-Skillicorn, K. Dvorak, H. Bernstein, C. Bernstein, H. Holubec, B. Dvorakova, and H. Garewal
Deoxycholate induces mitochondrial oxidative stress and activates NF-{kappa}B through multiple mechanisms in HCT-116 colon epithelial cells
Carcinogenesis, January 1, 2007; 28(1): 215 - 222.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 All ASBMB Journals   Journal of Biological Chemistry 
 Molecular and Cellular Proteomics   ASBMB Today 
Copyright © 2006 by the American Society for Biochemistry and Molecular Biology.