The design equation for a packed-bed immobilized enzyme reactor is expressed in terms of apparent kinetic parameters and the relationship between the exit concentration of substrate consumed and the logarithm of the exit unconverted fraction of substrate is studied. Agreement of calculated values wi
Galactose Oxidase: Applications of the covalently immobilized enzyme in a packed Bed configuration
β Scribed by S. K. Dahodwala; M. K. Weibel; A. E. Humphrey
- Publisher
- John Wiley and Sons
- Year
- 1976
- Tongue
- English
- Weight
- 690 KB
- Volume
- 18
- Category
- Article
- ISSN
- 0006-3592
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β¦ Synopsis
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 100β150 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, onβline 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. Autoβinactivation of the immobilized enzyme can be prevented by K~3~Fe(CN)~6~ and longβterm reactor stability can be achieved by the periodic application of the reagent to the enzyme reactor in situ.
π SIMILAR VOLUMES
A graphical method of determining the Michaelis-Menten constant free of the external mass transfer resistance for a packed bed immobilized enzyme system was illustrated with examples from 3 different enzyme reactions. The intercept at the ordinate obtained by the straight line extrapolation of data