|
|
||||||||
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Journal of Lipid Research, Vol. 47, 241-259, February 2006
Copyright © 2006 by American Society for Biochemistry and Molecular Biology
Review |
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
/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
-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
![]()
CiteULike
Complore
Connotea
Del.icio.us
Digg
Reddit
Technorati What's this?
This article has been cited by other articles:
![]() |
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] |
||||
![]() |
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] |
||||
![]() |
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] |
||||
![]() |
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] |
||||
![]() |
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] |
||||
![]() |
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] |
||||
![]() |
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] |
||||
![]() |
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 |