A mediator-free phenol biosensor based on immobilizing tyrosinase to ZnO nanoparticles

被引:150
作者
Li, YF
Liu, ZM
Liu, YL
Yang, YH
Shen, GL
Yu, RQ [1 ]
机构
[1] Hunan Univ, Coll Chem & Chem Engn, State Key Lab Chemo Biosensing & Chemometr, Changsha 410082, Peoples R China
[2] Henan Univ Technol, Coll Chem & Chem Engn, Zhengzhou 450052, Peoples R China
基金
中国国家自然科学基金;
关键词
ZnO nanoparticles; phenol biosensor; tyrosinase;
D O I
10.1016/j.ab.2005.11.017
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A mediator-free phenol biosensor was developed. The low-isoelectric point tyrosinase was adsorbed on the surface of high-isoelectric point ZnO nanoparticles (nano-ZnO) facilitated by the electrostatic interactions and then immobilized on the glassy carbon electrode via the film forming by chitosan. It was found that the nano-ZnO matrix provided an advantageous microenvironment in terms of its favorable isoelectric point for tyrosinase loading and the immobilized tyrosinase retaining its activity to a large extent. Moreover, there is no need to use any other electron mediators. Phenolic compounds were determined by the direct reduction of biocatalytically generated quinone species at -200 mV (vs. saturated calomel electrode). The parameters of the fabrication process and the various experimental variables for the enzyme electrode were optimized. The resulting biosensor can reach 95% of steady-state current within 10 s, and the sensitivity was as high as 182 mu A mmol(-1) L. The linear range for phenol determination was from 1.5 x 10(-7) to 6.5 x 10(-5) mol L-1 with a detection limit of 5.0 x 10(-8) mol L-1 obtained at a signal/noise ratio of 3. In addition, the apparent Michaelis-Menten constant (K-m(app)) and the stability of the enzyme electrode were estimated. The performance of the developed biosensor was compared with that of bio-sensors based on other immobilization matrices. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:33 / 40
页数:8
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