Journal of Southern Medical University ›› 2005, Vol. 25 ›› Issue (11): 1337-1340.

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Value of bilirubin oxidase and its mutants in the diagnosis of hyperbilirubinemia

ZHANG Lei1, ZHANG Xiao2, LUO Zhi-Ying3   

  1. 1. 华南理工大学化工系生物制药研究室, 广东, 广州, 510640;日本金沢大学化学系, 金沢, 920-1192;
    2. 河南省南阳市第一人民医院小儿科, 河南, 南阳, 473000;
    3. 华南理工大学附属医院, 广东, 广州, 510640
  • Online:2005-11-20 Published:2005-11-20

Abstract: Objective To elucidate the significance of the coordination amino acid residues in bilirubin oxidase (BO) and their kinetic characteristics, and evaluate whether BO mutants may serve as better diagnostic agent for hyperbilirubinemia. Methods The BO mutants I402G and C457S were obtained by site-directed mutagenesis and confirmed by amino acid sequence analysis. Ru-incorporated C457S mutant was obtained by direct incubation of ruthenium compounds with the mutant. The electron paramagnetic resonance (EPR) spectra of the recombinant BO and the mutants were investigated, and the enzyme kinetics of the recombinant BO and I402G mutant were measured with bilirubin as the substrate at 25 ℃. Results The BO mutants were expressed and purified successfully. The mutant I402G showed low enzyme activity, and had C457S virtually no enzyme activity. Nevertheless Ru-incorporation conferred higher enzyme activity to C457S mutant. The enzyme kinetic investigations revealed that the kinetic parameter kcat of the recombinant BO and I402G mutant was 235.8 min-1 and 6.9 min-1, respectively, suggesting higher enzyme activity of the recombinant BO. Conclusions The coordinating amino acids have important significance in maintaining the integrity of active centers and enzyme activities of recombinant BO and its mutants. The enzyme activities of the mutants I402G and C457S are much lower than those of recombinant BO, therefore they are not appropriate for diagnostic purpose. Ru-incorporation facilitates the formation of a new intact active center in C457S mutant, which therefore acquires enzyme activity.

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