| HUBÁLEK, Jaromír, Jan HRADECKÝ, Vojtěch ADAM, Olga KRYŠTOFOVÁ, Dalibor HÚSKA, Michal MASAŘÍK, Libuše TRNKOVÁ, Aleš HORNA, Kateřina KLOSOVÁ, Martin ADÁMEK, Josef ZEHNÁLEK and René KIZEK. Spectrometric and voltammetric analysis of urease. Nickel nanoelectrode as an electrochemical sensor. Sensors. Basel, Switzerland: MDPI, 2007, vol. 7, No 7, p. 1238-1255, 17 pp. ISSN 1424-8220. |
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@article{721756,
author = {Hubálek, Jaromír and Hradecký, Jan and Adam, Vojtěch and Kryštofová, Olga and Húska, Dalibor and Masařík, Michal and Trnková, Libuše and Horna, Aleš and Klosová, Kateřina and Adámek, Martin and Zehnálek, Josef and Kizek, René},
article_location = {Basel, Switzerland},
article_number = {7},
keywords = {urease; electrochemical methods; nanotechnology; nanotube; nickel electrode; hanging mercury drop electrode; spectrometry},
language = {eng},
issn = {1424-8220},
journal = {Sensors},
title = {Spectrometric and voltammetric analysis of urease. Nickel nanoelectrode as an electrochemical sensor},
volume = {7},
year = {2007}
}
TY - JOUR
ID - 721756
AU - Hubálek, Jaromír - Hradecký, Jan - Adam, Vojtěch - Kryštofová, Olga - Húska, Dalibor - Masařík, Michal - Trnková, Libuše - Horna, Aleš - Klosová, Kateřina - Adámek, Martin - Zehnálek, Josef - Kizek, René
PY - 2007
TI - Spectrometric and voltammetric analysis of urease. Nickel nanoelectrode as an electrochemical sensor
JF - Sensors
VL - 7
IS - 7
SP - 1238-1255
EP - 1238-1255
PB - MDPI
SN - 14248220
KW - urease
KW - electrochemical methods
KW - nanotechnology
KW - nanotube
KW - nickel electrode
KW - hanging mercury drop electrode
KW - spectrometry
N2 - Urease is the enzyme catalyzing the hydrolysis of urea into carbon dioxide and ammonia. This enzyme is substrate-specific, which means that the enzyme catalyzes the hydrolysis of urea only. This feature is a basic diagnostic criterion used in the determination of many bacteria species. Most of the methods utilized for detection of urease are based on analysis of its enzyme activity, the hydrolysis of urea. The aim of this work was to detect urease indirectly by spectrometric method and directly by voltammetric methods. As spectrometric method we used is called indophenol assay. The sensitivity of detection itself is not sufficient to analyse the samples without pre-concentration steps. Therefore we utilized adsorptive transfer stripping technique coupled with differential pulse voltammetry to detect urease. The influence of accumulation time, pH of supporting electrolyte and concentration of urease on the enzyme peak height was investigated. Under the optimized experimental conditions (0.2 M acetate buffer pH 4.6 and accumulation time of 120 s) the detection limit of urease evaluated as 3 S/N was 200 ng/ml. The activity of urease enzyme depends on the presence of nickel. Thus the influence of nickel(II) ions on electrochemical response of the enzyme was studied. Based on the results obtained the interaction of nickel(II) ions and urease can be determined using electrochemical methods. Therefore we prepared Ni nanoelectrodes to measure urease. The Ni nanoelectrodes was analysed after the template dissolution by scanning electron microscopy. The results shown vertically aligned Ni nanopillars almost covered the electrode surface, whereas the defect places are minor and insignificant in comparison with total electrode surface. We were able to not only detect urease itself but also to distinguish its native and denatured form.
ER -
HUBÁLEK, Jaromír, Jan HRADECKÝ, Vojtěch ADAM, Olga KRYŠTOFOVÁ, Dalibor HÚSKA, Michal MASAŘÍK, Libuše TRNKOVÁ, Aleš HORNA, Kateřina KLOSOVÁ, Martin ADÁMEK, Josef ZEHNÁLEK and René KIZEK. Spectrometric and voltammetric analysis of urease. Nickel nanoelectrode as an electrochemical sensor. \textit{Sensors}. Basel, Switzerland: MDPI, 2007, vol.~7, No~7, p.~1238-1255, 17 pp. ISSN~1424-8220.
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