|
|
||||||||
Journal of Lipid Research, Vol 23, 1354-1361, Copyright © 1982 by Lipid Research, Inc.
A Roda, LJ Kricka, M DeLuca and AF Hofmann
A simple, rapid, and sensitive bioluminescence method for measuring primary
bile acids has been developed and validated. The method is based on
enzymatic dehydrogenation of bile acids using a bacterial 7
alpha-hydroxysteroid dehydrogenase that is co-immobilized on Sepharose 4B
beads with NADH:FMN oxidoreductase and a bacterial luciferase. The assay is
specific for 7 alpha-hydroxy bile acids and has a detection limit of 0.5
pmol/tube, with a linear range of 0.5-50 pmol/tube. The assay shows good
precision (6-8% intra-assay; 8-10% inter-assay). The values obtained with
the bioluminescence assay showed good agreement with those obtained by
gas-liquid chromatography, radioimmunoassay, or endpoint enzymatic assays.
When applied to the measurement of serum bile acids, there was no
interference from serum albumin, and the effect of other dehydrogenase
activity in serum could be eliminated by heating the sample prior to assay.
Since the method is rapid (1 minute), extremely sensitive (requires only 10
microliters of serum), and specific, it appears to be the best method
currently available for the measurement of serum primary bile acids.
ARTICLES
Bioluminescence measurement of primary bile acids using immobilized 7 alpha-hydroxysteroid dehydrogenase: application to serum bile acids
![]()
CiteULike
Complore
Connotea
Del.icio.us
Digg
Reddit
Technorati What's this?
This article has been cited by other articles:
![]() |
M. L. Ojeda, M. J. Delgado-Villa, R. Llopis, M. L. Murillo, and O. Carreras Lipid Metabolism In Ethanol-Treated Rat Pups and Adults: Effects of Folic Acid Alcohol Alcohol., May 21, 2008; (2008) agn044v1. [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 |