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• W1427683834 abstract "This chapter discusses the determination of aldehyde oxidase. The reaction catalyzed by aldehyde oxidase is essentially a hydroxylation of the substrate from the elements of water. Hence the role of molecular oxygen is only that of an electron acceptor. Several artificial electron acceptors may be used instead of oxygen. The aerobic oxidation of N 1 -methylnicotinamide (NMN) provides a simple routine assay for the enzyme, as the formation of the pyridone can be measured spectrophotometrically as an increase in absorbance at 300 mμ. The use of ferricyanide as an artificial electron acceptor provides a more general spectrophotometric assay for the enzyme and can be used with a wide variety of substrates. As the rate of ferricyanide reduction is the same aerobically or anaerobically, the ferricyanide assay can be carried out in cuvettes open to air. A unit of enzyme activity is that amount of enzyme, which produces an absorbancy change of 1 per minute per cm at 25° with NMN as substrate in the routine assay. Specific activity is defined in terms of units of activity per milligram of protein." @default.
• W1427683834 created "2016-06-24" @default.
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• W1427683834 date "1966-01-01" @default.
• W1427683834 modified "2023-09-27" @default.
• W1427683834 title "[68] Aldehyde oxidase" @default.
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• W1427683834 doi "https://doi.org/10.1016/0076-6879(66)09075-x" @default.
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