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  • Spectrophotometric quantification of lactose in solution with a peroxidase-based enzymatic cascade reaction system.

Spectrophotometric quantification of lactose in solution with a peroxidase-based enzymatic cascade reaction system.

Analytical and bioanalytical chemistry (2011-08-17)
Sara Fornera, Kenjiro Yazawa, Peter Walde
ABSTRACT

A spectrophotometric assay was developed for the quantification of lactose in aqueous solution via a one-pot enzymatic cascade reaction at 25 °C and pH 7.2. Lactose (0.2-1.8 mM), E. coli β-galactosidase (β-Gal), Aspergillus niger glucose oxidase (GOD), horseradish peroxidase (HRP) and o-phenylenediamine (OPD) were incubated, and the increase in absorbance at 417 nm (A (417)) due to the formation of DAP (2,3-diaminophenazine), the dimeric oxidation product of OPD, was followed. The increase in A (417) was found to depend linearly on the initial lactose concentration via three consecutive but simultaneously occurring enzymatic reaction steps catalyzed by β-Gal, GOD, and HRP. No pre-incubation of lactose with β-Gal is needed with this simple lactose assay.

MATERIALS
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Sigma-Aldrich
o-Phenylenediamine, flaked, 99.5%
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o-Phenylenediamine, tablet, 20 mg substrate per tablet
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o-Phenylenediamine dihydrochloride, peroxidase substrate
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o-Phenylenediamine, sublimed, ≥99%
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o-Phenylenediamine, Peroxidase substrate, ≥98.0%, powder
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Sigma-Aldrich
2,3-Diaminophenazine, 90%
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