Galactose Oxidase: Applications of the covalently immobilized enzyme in a packed Bed configuration

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Abstract
Galactose oxidase (E.G. 1.1.3.9) was covalently immobilized to chemically modified porous silica particles by reaction of the native enzyme with pendant benzoyl azide groups on the carrier. The enzyme loading on the carrier was 100–150 units per milliliter. The immobilized enzyme was incorporated into a hardware assembly suitable for the determination of galactose or lactose concentrations in complex biological fluids. The prototype instrument as described is suitable for continuous, on‐line monitoring or discrete sample analysis. Reaction conditions can be readily provided which maintain global first order kinetics within the reactor and strict linearity of the procedure over a wide range of sample concentrations. Auto‐inactivation of the immobilized enzyme can be prevented by K3Fe(CN)6 and long‐term reactor stability can be achieved by the periodic application of the reagent to the enzyme reactor in situ.