Method of reducing measurement error caused by catalase inhibition by azide
Disclosed is a method for reducing measurement errors due to inhibition of catalase by azide in a method for quantification of a component to be measured, in which hydrogen peroxide derived from a component other than the component to be measured is decomposed by a catalase. The method for reducing measurement errors due to inhibition of catalase by azide employs a catalase which has a subunit having a molecular mass of 75 kDa or higher and is derived from a microorganism, when hydrogen peroxide derived from a component other than the component to be measured is decomposed by the catalase followed by quantification of hydrogen peroxide derived from the component to be measured to quantify the component to be measured.
1. A method of reducing measurement errors when hydrogen peroxide derived from a component other than a component to be measured is decomposed by a catalase, comprising the steps of:
decomposing said hydrogen peroxide in the presence of catalase and an azide; and
quantifying hydrogen peroxide derived from the component to be measured to quantify said component to be measured, said measurement errors being due to inhibition of the catalase by an azide, and said catalase comprising a catalase which has a subunit having a molecular mass of 75 kDa or higher and is derived from a microorganism.
2. The method according to claim 1 , wherein said catalase is a catalase having heme d.
3. The method according to claim 1 , wherein said microorganism is an organism of at least one species selected from the group consisting of microorganisms belonging to the genera Podospora, Neurospora, Cladosporium, Emericella, Pleurotus, Deinococcus, Escherichia, Salmonella, Pseudomonas, Bacillus, Mycobacterium, Botryotinia, Claviceps, Aspergillus, Ajellomyces, Agrobacterium, Sinorhizobium, Mesorhizobium, Nosema and Xanthomonas.
4. The method according to claim 3 , wherein said microorganism belongs to Aspergillus.
5. The method according to claim 1 , wherein said component to be measured is neutral fat, HDL cholesterol, LDL cholesterol or creatinine.