Oriented Immobilization of a Fully Active Monolayer of Histidine‐Tagged Recombinant Laccase on Modified Gold Electrodes

The formation of a dense monolayer of histidine‐tagged recombinant laccase on gold electrodes by using a short thiol‐NTA linker is described, as well as a kinetic analysis of the process by cyclic voltammetry. From a detailed analysis of the catalytic reduction of dioxygen by laccase in the presence of a one‐electron redox mediator it can be concluded that the immobilized enzyme remains as active as in homogeneous solution.