Abstract
A mesotrione monitoring biosensor was prepared using a nitroreductase (NfrA2) immobilized on a glassy carbon electrode by adsorption on nanoparticles of Mg2Al-NO3 layered double hydroxides (MgAl-NPs). The amperometric transduction process was based on a competitive enzymatic reduction between Fe(CN)63− and mesotrione, both substrates of NfrA2. Indeed in the presence of the NADH cofactor, Fe(CN)63− was enzymatically reduced and the Fe(CN)64− released was then oxidized at the electrode. When mesotrione was added to the electrolyte solution, a competitive enzymatic reaction took place at the NfrA2@MgAl-NPs modified electrode leading to a decrease of the electrocatalytic anodic current. Mesotrione can thus be detected by chronoamperometry at 0.375V/SCE with a sensitivity of 18.4mAM−1cm−2 over a linear concentration range between 5 and 60μM (R2=0.998) and a detection limit (3σ) of 3μM.
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