Abstract

AbstractIn this work, we investigate the immobilization of laccases from Trametes versicolor (TvL) and the small laccase (SLAC) from Streptomyces coelicolor on single‐wall carbon nanotube (SWCNT) surfaces. SLAC may potentially offer improved adsorption on the electrode, thus improving bioelectrocatalytic activity via direct electron transfer (DET). Laccase immobilization on SWCNTs is achieved non‐covalently with a molecular tether (1‐pyrene butanoic acid, succinimidyl ester) that forms an amide bond with an amine group on the laccase surface while the pyrene coordinates to the SWCNT by π–π stacking. In our approach, density functional theory calculations were first used to model the interaction energies between SWCNTs and pyrene to validate an empirical force field, thereafter applied in molecular dynamics (MD) simulations. In the simulated models, the SWCNT was placed near the region of the (type 1) Cu(T1) atom in the laccases, and in proximity to other regions where adsorption seems likely. Calculated interaction energies between the SWCNTs and laccases and distances between the SWCNT surface and the Cu(T1) atom have shown that SWCNTs adsorb more strongly to SLAC than to TvL, and that the separation between the SWCNTs and Cu(T1) atoms is smaller for SLAC than for TvL, having implications for improved DET.

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