Co-immobilization of glucose oxidase and xylose dehydrogenase displayed whole cell on multiwalled carbon nanotube nanocomposite films modified-electrode for simultaneous voltammetric detection of D-glucose and D-xylose

被引:44
|
作者
Li, Liang [1 ,2 ,3 ]
Liang, Bo [2 ,3 ]
Li, Feng [1 ]
Shi, Jianguo [4 ]
Mascini, Marco [5 ]
Lang, Qiaolin [2 ,3 ]
Liu, Aihua [2 ,3 ]
机构
[1] Qingdao Univ Sci & Technol, Coll Environm & Safety Engn, Qingdao 266042, Peoples R China
[2] Chinese Acad Sci, Qingdao Inst Bioenergy & Bioproc Technol, Lab Biosensing, Qingdao 266101, Peoples R China
[3] Chinese Acad Sci, Key Lab Bioenergy, Qingdao 266101, Peoples R China
[4] Shandong Acad Sci, Inst Biol, Key Lab Biosensors Shangdong Prov, Jinan 250014, Peoples R China
[5] Univ Firenze, Dipartimento Chim, I-50019 Sesto Fiorentino, Italy
来源
基金
中国国家自然科学基金;
关键词
Voltammetric biosensor; D-glucose; D-xylose; Simultaneous determination; Glucose oxidase; Xylose dehydrogenase-displayed bacteria; ENZYMATIC-HYDROLYSIS; DIRECT ELECTROCHEMISTRY; ETHANOL-PRODUCTION; ACID PRETREATMENT; DILUTE-ACID; CORN STOVER; BIOSENSOR; BIOMASS; SACCHARIFICATION; FERMENTATION;
D O I
10.1016/j.bios.2012.10.062
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
In this paper, we first report the construction of Nafion/glucose oxidase (GOD)/xylose dehydrogenase displayed bacteria (XDH-bacteria)/multiwalled carbon nanotubes (MWNTs) modified electrode for simultaneous voltammetric determination of D-glucose and D-xylose. The optimal conditions for the immobilized enzymes were established. Both enzymes retained their good stability and activities. In the mixture solution of D-glucose and D-xylose containing coenzyme NAD(+) (the oxidized form of nicotinamide adenine dinucleotide), the Nafion/GOD/XDH-bacteria/MWNTs modified electrode exhibited quasi-reversible oxidation-reduction peak at -0.5 V (vs. saturated calomel electrode, SCE) originating from the catalytic oxidation of D-glucose, and oxidation peak at +0.55 V(vs. SCE) responding to the oxidation of NADH (the reduced form of nicotinamide adenine dinucleotide) by the carbon nanotubes, where NADH is the resultant product of coenzyme NADI(+) involved in the catalysis of D-xylose by XDH-displayed bacteria. For the proposed biosensor, cathodic peak current at -0.5 V was linear with the concentration of D-glucose within the range of 0.25-6 mM with a low detection limit of 0.1 mM D-glucose (S/N =3), and the anodic peak current at +0.55 V was linear with the concentration of D-xylose in the range of 0.25 similar to 4 mM with a low detection limit of 0.1 mM D-xylose (S/N =3). Further, D-xylose and D-glucose did not interfere with each other. 300-fold excess saccharides including D-maltose, D-galactose, D-mannose, D-sucrose, D-fructose, D-cellobiose, and 60-fold excess L-arabinose, and common interfering substances (100-fold excess ascorbic acid, dopamine, uric acid) as well as 300-fold excess D-xylitol did not affect the detection of D-glucose and D-xylose (both 1 mM). Therefore, the proposed biosensor is stable, specific, reproducible, simple, rapid and cost-effective, which holds great potential in real applications. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:156 / 162
页数:7
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  • [1] A selective and sensitive D-xylose electrochemical biosensor based on xylose dehydrogenase displayed on the surface of bacteria and multi-walled carbon nanotubes modified electrode
    Li, Liang
    Liang, Bo
    Shi, Jianguo
    Li, Feng
    Mascini, Marco
    Liu, Aihua
    BIOSENSORS & BIOELECTRONICS, 2012, 33 (01): : 100 - 105