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Entrapment of enzymes and carbon nanotubes in biologically synthesized silica: glucose oxidase-catalyzed direct electron transfer.

作者信息

Ivnitski Dmitri, Artyushkova Kateryna, Rincón Rosalba A, Atanassov Plamen, Luckarift Heather R, Johnson Glenn R

机构信息

Chemical and Nuclear Engineering Department, University of New Mexico, Albuquerque, NM 87131, USA.

出版信息

Small. 2008 Mar;4(3):357-64. doi: 10.1002/smll.200700725.

DOI:10.1002/smll.200700725
PMID:18273853
Abstract

This work demonstrates a new approach for building bioinorganic interfaces by integrating biologically derived silica with single-walled carbon nanotubes to create a conductive matrix for immobilization of enzymes. Such a strategy not only allows simple integration into biodevices but presents an opportunity to intimately interface an enzyme and manifest direct electron transfer features. Biologically synthesized silica/carbon nanotube/enzyme composites are evaluated electrochemically and characterized by means of X-ray photoelectron spectroscopy. Voltammetry of the composites displayed stable oxidation and reduction peaks at an optimal potential close to that of the FAD/FADH(2) cofactor of immobilized glucose oxidase. The immobilized enzyme is stable for a period of one month and retains catalytic activity for the oxidation of glucose. It is demonstrated that the resulting composite can be successfully integrated into functional bioelectrodes for biosensor and biofuel cell applications.

摘要

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