Electron-Transfer Studies with a New Flavin Adenine Dinucleotide Dependent Glucose Dehydrogenase and Osmium Polymers of Different Redox Potentials

A new extracellular flavin adenine dinucleotide (FAD)-dependent glucose dehydrogenase from Glomerella cingulata (<i>Gc</i>GDH) was electrochemically studied as a recognition element in glucose biosensors. The redox enzyme was recombinantly produced in Pichia pastoris and homogeneously purified, and its glucose-oxidizing properties on spectrographic graphite electrodes were investigated. Six different Os polymers, the redox potentials of which ranged in a broad potential window between +15 and +489 mV versus the normal hydrogen electrode (NHE), were used to immobilize and “wire” <i>Gc</i>GDH to the spectrographic graphite electrode’s surface. The <i>Gc</i>GDH/Os polymer modified electrodes were evaluated by chronoamperometry using flow injection analysis. The current response was investigated using a stepwisely increased applied potential. It was observed that the ratio of <i>Gc</i>GDH/Os polymer and the overall loading of the enzyme electrode significantly affect the performance of the enzyme electrode for glucose oxidation. The best-suited Os polymer [Os(4,4′-dimethyl-2,2′-bipyridine)₂(PVI)Cl]⁺ had a potential of +309 mV versus NHE, and the optimum <i>Gc</i>GDH/Os polymer ratio was 1:2 yielding a maximum current density of 493 μA·cm^–2 at a 30 mM glucose concentration