IMPROVED IMMOBILIZATION OF LACCASE ON A GLASSY CARBON ELECTRODE BY ORIENTED COVALENT ATTACHMENT
2014
A laccase from Thermus thermophilus HB27 was reported to be potentially useful in the design of a temperature- controlled biofuel cell. For enhancing its application in different thermal conditions, we engineered a laccase-oriented immobilized electrode. A site-directed mutant N323C of the laccase was constructed. A photometric assay was employed in order to compare the catalytic properties of wild-type laccase and mutant. The mutant was attached to a glass carbon electrode by covalent cross-linking. The electrochemical properties of the immobilized laccase were investigated by cyclic voltammetry. This immobilization allowed the active electrode to function at temperatures up to 95°C. The thermal and pH dependence profiles were similar to those of the soluble enzyme investigated by spectrophotometry.
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