Abstract
An assay for amino acid oxidases is described which is capable of measuring 0.005 μg of enzyme or the oxidation of 0.5 nmole of amino acid. It involves the coupled oxidation of scopoletin by hydrogen peroxide catalyzed by peroxidase and the fluorometric determination of the scopoletin remaining. By the use of this method, it is shown that glycine is a substrate of l-amino acid oxidase.
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