Abstract
The activity of diaphorase (from Bacillus stearothermophilus) immobilized on glassy carbon (GC) electrodes was determined by analyzing the catalytic currents for oxidation of the immobilized enzyme using digital simulation techniques, which gives the concentration of the active enzyme at the electrode surface. Results show that the immobilization by the cross-linking reaction with glutaraldehyde deactivates the enzyme and only about 10% of the total enzyme remains active at the electrode surface.
Original language | English |
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Pages (from-to) | 337-346 |
Number of pages | 10 |
Journal | Bioelectrochemistry and Bioenergetics |
Volume | 29 |
Issue number | 3 |
DOIs | |
Publication status | Published - 1993 Feb |