Tominaga Masato, Nomura Shinya, Taniguchi Isao
Graduate School of Science and Technology, Kumamoto University, Kumamoto 860-8555, Japan.
Biosens Bioelectron. 2009 Jan 1;24(5):1184-8. doi: 10.1016/j.bios.2008.07.002. Epub 2008 Jul 12.
Multi-walled carbon nanotubes (MWCNTs) were synthesized on platinum plate electrodes by the chemical vapor deposition (CVD) method. From the results of X-ray photoelectron spectroscopy and voltammetric investigation, the iron nanoparticles used as a catalyst for the MWCNT synthesis were enclosed with MWCNTs. The MWCNTs synthesized on the Pt plate (MWCNTs/Pt) electrode were immediately immersed into solutions of d-fructose dehydrogenase (FDH) to immobilize the enzyme onto the MWCNTs/Pt electrode surfaces. After the FDH was immobilized onto the MWCNTs/Pt electrode, a well-defined catalytic oxidation current based on FDH was observed from ca. -0.15V (versus Ag/AgCl/sat'd KCl), which was close to the redox potential of heme c as a prosthetic group of FDH. From an analysis of a plot of the catalytic current versus substrate, the calibration range for the fructose concentration was up to ca. 40mmoldm(-3), and the apparent Michaelis-Menten constant was evaluated to be 11+/-1mmoldm(-3).
通过化学气相沉积(CVD)法在铂板电极上合成了多壁碳纳米管(MWCNTs)。根据X射线光电子能谱和伏安法研究结果,用作MWCNT合成催化剂的铁纳米颗粒被MWCNTs包裹。将在铂板(MWCNTs/Pt)电极上合成的MWCNTs立即浸入d-果糖脱氢酶(FDH)溶液中,以将该酶固定在MWCNTs/Pt电极表面。将FDH固定在MWCNTs/Pt电极上后,在约-0.15V(相对于Ag/AgCl/饱和KCl)处观察到基于FDH的明确催化氧化电流,该电位接近作为FDH辅基的血红素c的氧化还原电位。通过分析催化电流与底物的关系图,果糖浓度的校准范围高达约40mmol dm(-3),表观米氏常数经评估为11±1mmol dm(-3)。