4.7 Article

Trametes versicolor laccase activity modulated by the interaction with gold nanoparticles

期刊

ENVIRONMENTAL RESEARCH
卷 237, 期 -, 页码 -

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ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.envres.2023.116920

关键词

Gold nanoparticles; Laccase from Trametes versicolor; Enzyme-nanoparticle interaction; Kinetic study; Naphthol green

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This study investigates the impact of gold nanoparticles on the structure and activity of laccase from Trametes versicolor. It is found that the concentration of nanoparticles and the composition of the medium affect the secondary structure of the enzyme. The binding of nanoparticles leads to conformational changes, and the activity of the enzyme is enhanced at low concentrations of nanoparticles but reduced at high concentrations. The thermal parameters are improved at low nanoparticle concentrations, while the activation energy increases with nanoparticle content. The study also explores the effect of nanoparticles on the decomposition of a recalcitrant dye.
In this study, the impact of gold nanoparticles (AuNPs) on the structure and activity of laccase from Trametes versicolor (Lc) was described. Fluorescence experiments revealed that AuNPs efficiently quench Lc's tryptophan fluorescence by a static and dynamic process. By using differential scanning microcalorimetry and circular dichroism spectroscopy, it was determined how the concentration of nanoparticles and the composition of the medium affected the secondary structure of Lc. The data revealed that upon binding with AuNPs, conformational changes take place mainly in presence of high amounts of nanoparticles. The complex kinetic analysis unveiled the Lc activity enhancement at low concentrations of AuNPs as opposed to the concentrated regime, where it can be reduced by up to 55%. The Michaelis-Menten tests highlighted that the activity of the biocatalyst is closely related to the concentration of AuNPs, while the Selwyn analysis demonstrated that even in a concentrated regime of Lc it is not deactivated regardless of the amount of AuNPs added. The thermal parameters improved by twofold in the presence of low AuNPs concentration, whereas the activation energy increased with AuNPs content, implying that not all collisions are beneficial to the enzyme structure. The effect of AuNPs on the decomposition of a recalcitrant dye (naphthol green B, NG) by Lc was also evaluated, and the Michaelis-Menten model revealed that only the high AuNPs content influenced negatively the Lc activity. The isothermal titration calorimetry revealed that hydrogen bonds are the main intermolecular forces between Lc and AuNPs, while electrostatic interactions are responsible for NG adsorption to AuNPs. The results of the docking analysis show the binding of NG near the copper T1 site of Lc with hydrogen bonds, electrostatic and hydrophobic interactions. The findings of this work provide important knowledge for laccase-based bio-nanoconjugates and their use in the field of environmental remediation.

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