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基于固定化丙氨酸脱氢酶的无试剂安培生物传感器测定铵离子。

Determination of ammonium ion using a reagentless amperometric biosensor based on immobilized alanine dehydrogenase.

机构信息

School of Chemical Sciences and Food Technology, Faculty of Science and Technology, Universiti Kebangsaan Malaysia, Bangi, Selangor 43600, Malaysia.

出版信息

Sensors (Basel). 2011;11(10):9344-60. doi: 10.3390/s111009344. Epub 2011 Sep 29.

Abstract

The use of the enzyme alanine dehydrogenase (AlaDH) for the determination of ammonium ion (NH(4)(+)) usually requires the addition of pyruvate substrate and reduced nicotinamide adenine dinucleotide (NADH) simultaneously to effect the reaction. This addition of reagents is inconvenient when an enzyme biosensor based on AlaDH is used. To resolve the problem, a novel reagentless amperometric biosensor using a stacked methacrylic membrane system coated onto a screen-printed carbon paste electrode (SPE) for NH(4)(+) ion determination is described. A mixture of pyruvate and NADH was immobilized in low molecular weight poly(2-hydroxyethyl methacrylate) (pHEMA) membrane, which was then deposited over a photocured pHEMA membrane (photoHEMA) containing alanine dehydrogenase (AlaDH) enzyme. Due to the enzymatic reaction of AlaDH and the pyruvate substrate, NH(4)(+) was consumed in the process and thus the signal from the electrocatalytic oxidation of NADH at an applied potential of +0.55 V was proportional to the NH(4)(+) ion concentration under optimal conditions. The stacked methacrylate membranes responded rapidly and linearly to changes in NH(4)(+) ion concentrations between 10-100 mM, with a detection limit of 0.18 mM NH(4)(+) ion. The reproducibility of the amperometrical NH(4)(+) biosensor yielded low relative standard deviations between 1.4-4.9%. The stacked membrane biosensor has been successfully applied to the determination of NH(4)(+) ion in spiked river water samples without pretreatment. A good correlation was found between the analytical results for NH(4)(+) obtained from the biosensor and the Nessler spectrophotometric method.

摘要

该酶丙氨酸脱氢酶(AlaDH)用于铵离子(NH(4)(+))的测定通常需要同时添加丙酮酸底物和还原型烟酰胺腺嘌呤二核苷酸(NADH)以进行反应。当使用基于 AlaDH 的酶生物传感器时,这种试剂的添加很不方便。为了解决这个问题,描述了一种新颖的无试剂安培生物传感器,该传感器使用堆叠的甲基丙烯酸酯膜系统涂覆在丝网印刷碳糊电极(SPE)上,用于测定 NH(4)(+)离子。将丙酮酸和 NADH 的混合物固定在低分子量聚(2-羟乙基甲基丙烯酸酯)(pHEMA)膜中,然后将其沉积在含有丙氨酸脱氢酶(AlaDH)酶的光固化 pHEMA 膜(photoHEMA)上。由于 AlaDH 和丙酮酸底物的酶促反应,NH(4)(+)在该过程中被消耗,因此在最佳条件下,施加+0.55 V 的外加电势时,NADH 的电催化氧化的信号与 NH(4)(+)离子浓度成正比。堆叠的甲基丙烯酸酯膜对 10-100 mM 范围内 NH(4)(+)离子浓度的变化快速且线性响应,检测限为 0.18 mM NH(4)(+)离子。安培式 NH(4)(+)生物传感器的重现性在 1.4-4.9%之间产生低相对标准偏差。堆叠膜生物传感器已成功应用于未经预处理的加标河水样品中 NH(4)(+)离子的测定。从生物传感器获得的 NH(4)(+)分析结果与 Nessler 分光光度法之间存在良好的相关性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c718/3231275/a5eab983a449/sensors-11-09344f1.jpg

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