Catalytic Current Based on Direct Electron Transfer Reactions of Enzymes Immobilized onto Carbon Nanotubes

, , , , , and

© 2009 ECS - The Electrochemical Society
, , Citation Masato Tominaga et al 2009 ECS Trans. 16 1 DOI 10.1149/1.3103804

1938-5862/16/38/1

Abstract

Multi-walled and single-walled carbon nanotubes were synthesized on platinum plate (MWCNTs/pt) and gold wire (SWCNTs/Au) electrodes, respectively, using a chemical vapor deposition (CVD) method. These carbon nanotube-modified electrodes were immersed into solutions of glucose oxidase (GOX) and D-fructose dehydrogenase (FDH) to immobilize these enzymes onto the electrode surfaces. After GOX was immobilized onto the MWCNT/Pt electrode, the well-defined catalytic oxidation current was increased from ca. -0.45 V (vs. Ag/AgCl/saturated KCl), which was close to the redox potential of flavin adenine dinucleotide as a prosthetic group of GOX under physiological pH values. Furthermore, catalytic oxidation currents of fructose based on direct heterogeneous electron transfer reactions between FDH and the SWCNT/Pt electrode were observed.

Export citation and abstract BibTeX RIS

10.1149/1.3103804