ChemPlusChem · 2016 · 41 citations · 49 references
EngineeringBiochemistryBiotechnologyBiosensorsNanobiotechnologyNanomaterialsBiosensor DesignElectrochemical BiosensorsElectrode MaterialsEnzymatic BiosensorsNanomaterial-based BiosensorsNanosensorsDirect Electron TransferElectrochemical BiosensingElectrochemical Enzyme BiosensorsModified ElectrodesNanomaterial-enhanced Enzymatic BiosensorsNanomaterial-enhanced Enzyme BiosensorsNanoparticlesRedox Reaction Kinetics
Abstract Efficient conjugation between biomolecules and electrode materials is one of the main challenges in the field of biosensors. Cellobiose dehydrogenase (CDH) is a monomeric enzyme, which consists of two separate domains: one catalytic dehydrogenase domain (DH CDH ) carrying strongly bound flavin adenine dinucleotide (FAD) in the active site and a cytochrome domain (CYT CDH ) carrying a b ‐type heme connected by a flexible linker region. Herein, we report on the development of a lactose biosensor, based on direct electron transfer (DET) from CDH from Phanerochaete sordida ( Ps CDH) electrostatically attached onto polyethyleneimine‐stabilized gold nanoparticles (PEI@AuNPs) used to cover a conventional polycrystalline solid gold disk electrode. PEI@AuNPs were synthesized in aqueous solution using PEI as reducing agent for Au III and as stabilizer for the nanoparticles. The heterogeneous electron‐transfer (ET) rate ( k s ) for the redox reaction of immobilized Ps CDH at the modified electrodes was calculated based on the Laviron theory and was found to be (39.6±2.5) s −1 . The proposed lactose biosensor exhibits good long term stability as well as high and reproducible sensitivity to lactose with a response time less than 5 s and a linear range from 1 to 100 μ m .
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