Development of urease and glutamic dehydrogenase amperometric assay for heavy metals screening in polluted samples

An amperometric assay based on urease inactivation has been developed for the screening of heavy metals in environmental samples. The enzyme urease catalyses the hydrolysis of urea and the formation of NH4+ is determined using a NADH-glutamate dehydrogenase coupled reaction system. NADH consumption is monitored anaperometrically using screen-printed three electrode configuration and its oxidation current is then correlated to urease activity. The presence of heavy metals in the samples inhibits the urease activity, resulting in a lower NH4+ production and therefore a decrease in NADH oxidation. The use of metallised carbon electrodes gave a decrease in NADH oxidation potential from +300 mV versus Ag/AgCl compared with >+600 mV for bare carbon electrodes, and thus minimised interferences from oxidizable species present in the samples. Electrodes fouling and possible contamination after reuse and cleaning was also eliminated by using screen-printed disposable electrodes. The linear range obtained for Hg(11) and Cu(11) was 10-100 mug l(-1) with a detection limit of 7.2 mug l(-1) and 8.5 mug l(-1), respectively. Cd(II) and Zn(II) produced enzyme inhibition in the range 1-30 mg l(-1), with limits of detection of 0.3 mg l(-1) for Cd(II) and 0.2 mg l(-1) for Zn(11). Pb(II) did not inactivate the urease enzyme significantly at the studied range (up to 50 mg l(-1)). Coefficients of variation (CV) values were 6-9% in all cases. Application of the assay system to leachate samples gave reliable and accurate toxicity assessments when compared to atomic absorption spectrometry (AAS) and inductively coupled plasma atomic emission spectroscopy (ICP-MS) analysis. This approach provides to be a simple and rapid (15 min, including enzyme inhibition time) method for metal ions detection. (C) 2003 Elsevier B.V. All rights reserved.