Amperometric L-arginine biosensor based on a novel recombinant arginine deiminase

被引:0
|
作者
Mykhailo T. Zhybak
Lyubov Y. Fayura
Yuriy R. Boretsky
Mykhailo V. Gonchar
Andriy A. Sibirny
Eithne Dempsey
Anthony P. F. Turner
Yaroslav I. Korpan
机构
[1] National Academy of Sciences of Ukraine,Laboratory of Biomolecular Electronics, Institute of Molecular Biology and Genetics
[2] Institute of Cell Biology,Department of Biotechnology and Microbiology
[3] NAS of Ukraine,Centre for Research in Electroanalytical Technologies, Department of Science
[4] Lviv State University of Physical Culture,Biosensors & Bioelectronics Centre
[5] Rzeszow University,undefined
[6] ITT Dublin,undefined
[7] Linköping University,undefined
来源
Microchimica Acta | 2017年 / 184卷
关键词
L-arginine; Ammonium ions; Amperometry; Nafion; Polyaniline; Recombinant enzyme; Plasma samples; Pharmaceuticals;
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学科分类号
摘要
The authors describe an amperometric biosensor for the amino acid L-arginine (L-Arg). It is based on the use of a Nafion/Polyaniline (PANi) composite on a platinum screen-printed electrode (Pt-SPE) using a novel recombinant arginine deiminase isolated from Mycoplasma hominis. The protein was over-expressed, purified and employed as a biorecognition element of the sensor. Enzymatic hydrolysis of L-Arg leads to the formation of ammonium ions which diffuse into the Nafion/PANi layer and induce the electroreduction of PANi at a potential of −0.35 V (vs Ag/AgCl). L-Arg sensitivity is 684 ± 32 A·M−1·m−2, and the apparent Michaelis-Menten constant (KMapp) is 0.31 ± 0.05 mM. The calibration plot is linear over the range 3–200 μM L-Arg, the limit of detection is 1 μM, and the response time (for 90% of the total signal change to occur) is 15 s. The sensor is selective and exhibits good storage stability (> 1 month without loss in signal). The biosensor was applied to the analysis of L-Arg in pharmaceutical samples and of ammonium and L-Arg in spiked human plasma obtained from blood of healthy volunteers and those with a hepatic disorder. Data generated were found to be in good agreement with a reference fluorometric enzymatic assay.
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页码:2679 / 2686
页数:7
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