Urea Biosensors Based on Immobilization of Urease into Two Oppositely Charged Clays (Laponite and Zn−Al Layered Double Hydroxides)

• Published in: Analytical chemistry (Washington) 2002-08, Vol.74 (16), p.4037-4043
• Main Authors: de Melo, J. V, Cosnier, S, Mousty, C, Martelet, C, Jaffrezic-Renault, N
• Format: Article
• Language: English
• Subjects: Aluminum Silicates - chemistry; Biochemistry; Biological and medical sciences; Biosensing Techniques - methods; Biosensing Techniques - standards; Biosensors; Biotechnology; Calibration; Clay; Enzymes, Immobilized; Fundamental and applied biological sciences. Psychology; Membranes; Methods. Procedures. Technologies; Sensitivity and Specificity; Sensors; Urea - analysis; Urease; Various methods and equipments
• ISSN: 0003-2700; 1520-6882
• DOI: 10.1021/ac025627+

Enzyme-based field effect transistors (ENFETs) for urea determination were developed based on the immobilization of urease within two different clay matrixes, one cationic (Laponite) and the other anionic (layered double hydroxide (LDH)), cross-linked with glutaraldehyde. The biosensor based on the enzyme immobilized in Laponite shows a greater sensitivity and smaller dynamic linear range, because the enzymatic reaction is protected from the effect of the buffer capacity of the outer medium. The apparent Michaelis−Menten constant, , is quite similar for both biosensors. Inhibition of the enzyme by sodium tetraborate was investigated. Tetraborate acts as a competitive inhibitor for urease in the two different types of clay, the inhibitor effect being stronger for the LDH/urease biosensor. In particular, the maximum limit of the dynamic linear range extends from 1.4 mM in the absence of the inhibitor to 12 mM in the presence of 0.5 mM tetraborate. The values in the presence of 0.5 mM tetraborate for Laponite and LDH biomembranes were 10 and 62 mM, respectively. Comparison of the inhibition constant values, K i 0.16 and 0.05 mM for Laponite and LDH biosensors, respectively, clearly indicates a stronger enzyme−inhibitor interaction in the LDH/urease biomembrane.