Salimi Abdollah, Sharifi Ensiyeh, Noorbakhsh Abdollah, Soltanian Saied
Department of Chemistry, University of Kurdistan, P.O. Box 416, Sanandaj, Iran.
Biophys Chem. 2007 Feb;125(2-3):540-8. doi: 10.1016/j.bpc.2006.11.004. Epub 2006 Nov 23.
Cyclic voltammetry was used for simultaneous formation and immobilization of nickel oxide nano-scale islands and catalase on glassy carbon electrode. Electrodeposited nickel oxide may be a promising material for enzyme immobilization owing to its high biocompatibility and large surface. The catalase films assembled on nickel oxide exhibited a pair of well defined, stable and nearly reversible CV peaks at about -0.05 V vs. SCE at pH 7, characteristic of the heme Fe (III)/Fe (II) redox couple. The formal potential of catalase in nickel oxide film were linearly varied in the range 1-12 with slope of 58.426 mV/pH, indicating that the electron transfer is accompanied by single proton transportation. The electron transfer between catalase and electrode surface, (k(s)) of 3.7(+/-0.1) s(-1) was greatly facilitated in the microenvironment of nickel oxide film. The electrocatalytic reduction of hydrogen peroxide at glassy carbon electrode modified with nickel oxide nano-scale islands and catalase enzyme has been studied. The embedded catalase in NiO nanoparticles showed excellent electrocatalytic activity toward hydrogen peroxide reduction. Also the modified rotating disk electrode shows good analytical performance for amperometric determination of hydrogen peroxide. The resultant catalase/nickel oxide modified glassy carbon electrodes exhibited fast amperometric response (within 2 s) to hydrogen peroxide reduction (with a linear range from 1 microM to 1 mM), excellent stability, long term life and good reproducibility. The apparent Michaelis-Menten constant is calculated to be 0.96(+/-0.05)mM, which shows a large catalytic activity of catalase in the nickel oxide film toward hydrogen peroxide. The excellent electrochemical reversibility of redox couple, high stability, technical simplicity, lake of need for mediators and short preparations times are advantages of this electrode. Finally the activity of biosensor for nitrite reduction was also investigated.
循环伏安法用于在玻碳电极上同时形成并固定氧化镍纳米岛和过氧化氢酶。电沉积的氧化镍因其高生物相容性和大表面积,可能是一种用于酶固定的有前景的材料。组装在氧化镍上的过氧化氢酶膜在pH 7时相对于饱和甘汞电极(SCE)在约-0.05 V处呈现出一对定义明确、稳定且近乎可逆的循环伏安峰,这是血红素铁(III)/铁(II)氧化还原对的特征。氧化镍膜中过氧化氢酶的形式电位在1 - 12范围内呈线性变化,斜率为58.426 mV/pH,表明电子转移伴随着单个质子的传输。在氧化镍膜的微环境中,过氧化氢酶与电极表面之间的电子转移速率常数(k(s))为3.7(±0.1) s(-1),得到了极大促进。研究了用氧化镍纳米岛和过氧化氢酶修饰的玻碳电极上过氧化氢的电催化还原。嵌入氧化镍纳米颗粒中的过氧化氢酶对过氧化氢还原表现出优异的电催化活性。此外,修饰的旋转圆盘电极对过氧化氢的安培测定显示出良好的分析性能。所得的过氧化氢酶/氧化镍修饰玻碳电极对过氧化氢还原表现出快速的安培响应(在2 s内)(线性范围为1 μM至1 mM)、优异的稳定性、长期寿命和良好的重现性。表观米氏常数经计算为0.96(±0.05) mM,这表明氧化镍膜中的过氧化氢酶对过氧化氢具有较大的催化活性。氧化还原对出色的电化学可逆性、高稳定性、技术简单性、无需媒介物以及制备时间短是该电极的优点。最后还研究了该生物传感器对亚硝酸盐还原的活性。