Centre for Metals in Biology, School of Chemistry and Molecular Biosciences, University of Queensland, Brisbane, 4072, Australia.
Anal Chem. 2010 Sep 1;82(17):7374-9. doi: 10.1021/ac101493y.
This paper describes a highly sensitive electrochemical (voltammetric) determination of sulfite using a combination of Starkeya novella sulfite dehydrogenase (SDH), horse heart cytochrome c (cyt c), and a self-assembled monolayer of 11-mercaptoundecanol (MU) cast on a gold electrode. The biosensor was optimized in terms of pH and the ratio of cyt c/SDH. The electrocatalytic oxidation current of sulfite increased linearly from 1 to 6 microM at the enzyme-modified electrode with a correlation coefficient of 0.9995 and an apparent Michaelis constant (K(M,app)) of 43 microM. Using an amperometric method, the low detection limit for sulfite at the enzyme-modified electrode was 44 pM (signal-to-noise ratio = 3). The modified electrode retained a stable response for 3 days while losing only ca. 4% of its initial sensitivity during a 2 week storage period in 50 mM Tris buffer solution at 4 degrees C. The enzyme electrode was successfully used for the determination of sulfite in beer and white wine samples. The results of these electrochemical analyses agreed well with an independent spectrophotometric method using Ellman's reagent, but the detection limit was far superior using the electrochemical method.
本文描述了一种使用斯塔基诺维拉亚硫酸盐脱氢酶(SDH)、马心细胞色素 c(cyt c)和自组装的 11-巯基十一烷醇(MU)单层在金电极上的组合对亚硫酸盐进行高灵敏度电化学(伏安法)测定的方法。该生物传感器在 pH 值和 cyt c/SDH 比例方面进行了优化。在酶修饰电极上,亚硫酸盐的电化学催化氧化电流在 1 至 6 microM 范围内呈线性增加,相关系数为 0.9995,表观米氏常数(K(M,app))为 43 microM。使用电流测定法,酶修饰电极对亚硫酸盐的检测下限为 44 pM(信噪比 = 3)。在 4 摄氏度下,在 50mM Tris 缓冲溶液中储存 2 周期间,修饰电极仅损失约 4%的初始灵敏度,其响应保持稳定 3 天。该酶电极成功用于测定啤酒和白葡萄酒样品中的亚硫酸盐。这些电化学分析的结果与使用 Ellman 试剂的独立分光光度法吻合良好,但电化学法的检测限要好得多。