Abstract
The field of enzyme electrodes has attracted a great deal of interest in recent years [l-7] and quite a number of papers have appeared dealing with steady state enzyme redox catalysis with a soluble redox mediator in solution [l-6]. Most of these studies, however, involve amperometric techniques and measure the stationary current that generates a flux of mediator at the electrode surface [2]. Under conditions of substrate saturation the steady state kinetics of enzyme reoxidation by the redox mediator can be treated as an extension of the theory of voltammetry for a catalytic mechanism of the type:
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