An improved glucose/O2 membrane-less biofuel cell through glucose oxidase purification

被引:51
作者
Gao, Feng [1 ]
Courjean, Olivier [1 ]
Mano, Nicolas [1 ]
机构
[1] Univ Bordeaux, Ctr Rech Paul Pascal, UPR 8641, CNRS, F-33600 Pessac, France
关键词
Biofuel cell; Glucose oxidase; Redox hydrogel; Enzyme purification; Biosensors; DIRECT ELECTRON-TRANSFER; KINETIC-PARAMETERS; ASPERGILLUS-NIGER; ENZYME ELECTRODES; REDOX CENTERS; OXYGEN; LACCASE; ELECTROOXIDATION; DIFFUSION; TRANSPORT;
D O I
10.1016/j.bios.2009.07.015
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
A key objective in any bioelectrochemical systems is to improve the current densities and mass transport limitation. Most of the work is focused on increasing the specific surface of the electrodes or improving the electron transfer between enzymes and electrodes. However, nothing is said about the comparison of purified and non-purified enzyme and their effects on the biosensor efficiency. To illustrate the effect of the enzyme purity, we studied the widely used commercial Glucose Oxidase (GOx) from Aspergillus niger that we are using in our miniature membrane-less biofuel cell. Our results indicate that even if additional compounds contained in the lyophilized enzyme powder do not interfere with its intrinsic catalytic properties, they could prevent a good electron transfer between the enzyme and the electrode surface. By introducing a purified glucose oxidase into a bioelectrocatalyst immobilized on an electrode surface, we show that we can increase the interaction between the enzyme and the redox polymer, forming a better homogenous, leather like gel. At 5 mM glucose concentration and under oxygen atmosphere, the current is three-fold higher when using a purified enzyme than it is when using a non-purified enzyme. Built with this novel anode, we showed that a miniature implantable membrane-less glucose-O-2 biofuel cell could produce, under air, twice the power density that is usually obtained when using a non-purified GOx. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:356 / 361
页数:6
相关论文
共 40 条
[1]   Biofuel Cell Controlled by Enzyme Logic Systems [J].
Amir, Liron ;
Tam, Tsz Kin ;
Pita, Marcos ;
Meijler, Michael M. ;
Alfonta, Lital ;
Katz, Evgeny .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2009, 131 (02) :826-832
[2]   A laccase-glucose oxidase biofuel cell prototype operating in a physiological buffer [J].
Barriere, Frederic ;
Kavanagh, Paul ;
Leech, Donal .
ELECTROCHIMICA ACTA, 2006, 51 (24) :5187-5192
[3]   THEORETICAL TREATMENT OF DIFFUSION AND KINETICS IN AMPEROMETRIC IMMOBILIZED ENZYME ELECTRODES .1. REDOX MEDIATOR ENTRAPPED WITHIN THE FILM [J].
BARTLETT, PN ;
PRATT, KFE .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1995, 397 (1-2) :61-78
[4]   Enzymatic biofuel cells for Implantable and microscale devices [J].
Barton, SC ;
Gallaway, J ;
Atanassov, P .
CHEMICAL REVIEWS, 2004, 104 (10) :4867-4886
[5]   MASS-TRANSPORT AND REACTION KINETIC-PARAMETERS DETERMINED ELECTROCHEMICALLY FOR IMMOBILIZED GLUCOSE-OXIDASE [J].
CASTNER, JF ;
WINGARD, LB .
BIOCHEMISTRY, 1984, 23 (10) :2203-2210
[6]   Enzyme catalysed biofuel cells [J].
Cooney, M. J. ;
Svoboda, V. ;
Lau, C. ;
Martin, G. ;
Minteer, S. D. .
ENERGY & ENVIRONMENTAL SCIENCE, 2008, 1 (03) :320-337
[7]   Design of chitosan gel pore structure: towards enzyme catalyzed flow-through electrodes [J].
Cooney, Michael J. ;
Lau, Carolin ;
Windmeisser, Mona ;
Liaw, Bor Yann ;
Klotzbach, Tamara ;
Minteer, Shelley D. .
JOURNAL OF MATERIALS CHEMISTRY, 2008, 18 (06) :667-674
[8]   Deglycosylation of Glucose Oxidase for Direct and Efficient Glucose Electrooxidation on a Glassy Carbon Electrode [J].
Courjean, Olivier ;
Gao, Feng ;
Mano, Nicolas .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2009, 48 (32) :5897-5899
[9]   Difference in enzyme activity and conformation of glucose oxidase before and after purification [J].
Dai, GL ;
Li, JR ;
Jiang, L .
COLLOIDS AND SURFACES B-BIOINTERFACES, 2002, 24 (3-4) :171-176
[10]   Extracting kinetic parameters for homogeneous [Os(bpy)2ClPyCOOH]+ mediated enzyme reactions from cyclic voltammetry and simulations [J].
Flexer, V. ;
Ielmini, M. V. ;
Calvo, E. J. ;
Bartlett, P. N. .
BIOELECTROCHEMISTRY, 2008, 74 (01) :201-209