Iida Y, Ikeda M, Aoto M, Satoh I
Department of Applied Chemistry, Faculty of Engineering, Kanagawa Institute of Technology, 1030 Shimo-Ogino, Atsugi 243-0292, Japan.
Talanta. 2004 Dec 15;64(5):1278-82. doi: 10.1016/j.talanta.2004.06.021.
An acid urease column was applied to a fluorometric flow-injection analysis (FIA) system as a recognition element for determination of urea in rice wines. The acid urease has specific properties of showing its catalytic activity in low pH range and tolerance to ethanol in comparison to those of a urease from jack-beans. The enzymes were covalently immobilized onto porous glass beads with controlled pore size and then, packed into a small polymer column. The flow-type of the biosensing system was assembled with a sample injection valve, the immobilized enzyme column, and a flow-through quartz cell attached to a fluorescent spectrophotometer. Citrate buffer (50mM, pH 5.0) as the carrier solution was continuously pumped through the system. Sample solutions were introduced into the system via a rotary injection valve. A standard urea solution was measured through monitoring variations in fluorescent intensity attributable to fluorescent isoindole derivatives formed by coupling with ammonia molecules released in the enzymatic hydrolysis of urea and orthophthalaldehyde reagents. The fluorescent intensity was measured under the conditions of lambda(ex) = 415nm and lambda(em) = 485nm. A wide, linear relationship was obtained between the concentration of urea (1.0-100muM) and the variation in fluorescent intensity. The monitoring did not suffer from ethanol and various amino acids contained in rice wines. Real samples pretreated with ion exchange resins for removal of endogenous ammonia were introduced into the FIA system and urea in the samples was determined. These results were compared with those obtained with use of an F-kit method. The proposed FIA system should present sensitive, selective and convenient analysis of urea in alcoholic beverages.
将酸性脲酶柱应用于荧光流动注射分析(FIA)系统,作为测定米酒中尿素的识别元件。与刀豆脲酶相比,酸性脲酶具有在低pH范围内显示催化活性和对乙醇有耐受性的特殊性质。将这些酶共价固定在孔径可控的多孔玻璃珠上,然后填充到一个小的聚合物柱中。生物传感系统的流动型由一个进样阀、固定化酶柱和连接到荧光分光光度计的流通式石英池组装而成。以柠檬酸盐缓冲液(50mM,pH 5.0)作为载液连续泵入系统。样品溶液通过旋转进样阀引入系统。通过监测由于尿素酶促水解释放的氨分子与邻苯二甲醛试剂偶联形成的荧光异吲哚衍生物引起的荧光强度变化来测定标准尿素溶液。在激发波长(λex)= 415nm和发射波长(λem)= 485nm的条件下测量荧光强度。尿素浓度(1.0 - 100μM)与荧光强度变化之间获得了较宽的线性关系。该监测不受米酒中乙醇和各种氨基酸的影响。将用离子交换树脂预处理以去除内源性氨的实际样品引入FIA系统并测定样品中的尿素。将这些结果与使用F试剂盒方法获得的结果进行比较。所提出的FIA系统应该能够对酒精饮料中的尿素进行灵敏、选择性和便捷的分析。