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A rapid Electrochemical Procedure for the Determination of Hg(0) Produced by Mercury-Reductase: Application for Monitoring Hg-resistant Bacteria Activity

机译:一种快速电化学测定汞还原酶产生的Hg(0)的方法:在监测耐Hg细菌活性中的应用

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摘要

In this work, gold microelectrodes are employed as traps for the detection of volatilized metallic mercury produced by mercuric reductase (MerA) extracted from an Hg-resistant Pseudo monas putida strain FB1. The enzymatic reduction of Hg (II) to Hg (0) was induced by NADPH cofactor added to the samples. The amount of Hg(0) accumulated on the gold microelectrode surface was determined by anodic stripping voltammetry (ASV) after transferring the gold microelectrode in an aqueous solution containing 0.1 M HNO3 + 1 M KNO3. Electrochemical measurements were combined with spectrofluorometric assays of NADPH consumption to derive an analytical expression for the detection of a relative MerA activity of different samples with respect to that of P. putida. The method developed here was employed for the rapid determination of MerA produced by bacteria harbored in soft tissues of clams (Ruditapes philippinarum), collected in high Hg polluted sediments of Northern Adriatic Sea in Italy.
机译:在这项工作中,金微电极被用作捕集阱,以检测由汞还原酶(MerA)从耐Hg假单胞菌FB1菌株中提取的挥发性金属汞。通过将NADPH辅因子添加到样品中,将Hg(II)酶促还原为Hg(0)。将金微电极转移到含有0.1 M HNO3 + 1 M KNO3的水溶液中后,通过阳极溶出伏安法(ASV)确定在金微电极表面上积累的Hg(0)量。将电化学测量与NADPH消耗量的荧光分光光度测定法相结合,以得出用于检测不同样品相对于恶臭假单胞菌相对MerA活性的分析表达式。本文开发的方法用于快速测定由蛤soft(菲律宾蛤仔)的软组织中存在的细菌产生的MerA,该细菌收集于意大利北亚得里亚海的高汞污染沉积物中。

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