An enzymatic cycling method for the determination of serum total bile acids with recombinant 3alpha-hydroxysteroid dehydrogenase

Biochem Biophys Res Commun. 2005 Jan 7;326(1):87-92. doi: 10.1016/j.bbrc.2004.11.005.

Abstract

A highly sensitive enzymatic cycling method was developed for the serum total bile acids assay. We constructed a prokaryotic expression system to prepare the recombinant 3alpha-hydroxysteroid dehydrogenase in place of the natural enzyme and for the first time used it in the total bile acids assay. The production rate of thio-NADH correlated with the bile acids concentration and was measured by the change of absorbance at 405/660 nm. The enzymatic cycling method could detect 0.22 micromol/L total bile acids in serum. Within-run and between-run imprecisions were 1.2-3.7% and 2.3-4.8%, respectively. The calibration curve for total bile acids in serum was linear between 0.5 and 180 micromol/L. This method was free from interference by bilirubin, hemoglobin, ascorbate, and lactate dehydrogenase. In conclusion, serum total bile acids could be measured by the enzymatic cycling method with recombinant 3alpha-hydroxysteroid dehydrogenase as the tool enzyme.

Publication types

  • Evaluation Study

MeSH terms

  • 3-alpha-Hydroxysteroid Dehydrogenase (B-Specific) / chemistry*
  • 3-alpha-Hydroxysteroid Dehydrogenase (B-Specific) / genetics
  • Animals
  • Bile Acids and Salts / blood*
  • Blood Chemical Analysis / methods*
  • Comamonas testosteroni / enzymology*
  • Comamonas testosteroni / genetics
  • Enzyme-Linked Immunosorbent Assay / methods*
  • Humans
  • Recombinant Proteins / chemistry
  • Reproducibility of Results
  • Sensitivity and Specificity

Substances

  • Bile Acids and Salts
  • Recombinant Proteins
  • 3-alpha-Hydroxysteroid Dehydrogenase (B-Specific)