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Immobilized Enzyme-Based Microtiter Plate Assay for Ethanol in Alcoholic Beverages

机译:酒精饮料中基于固定化酶的乙醇微量滴定板分析

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摘要

A method for the determination of ethanol using alcohol oxidase (AOD), peroxidase (POD), and 2,2′-azino-bis(3-ethyl-benzthiazoline-6-sulfonic acid) (ABTS) was developed in which those enzymes were separately immobilized on the inside surface of each well of a 96-well microtiter plate. Prior to immobilization, the surface was activated with glutaraldehyde. The activation conditions remarkably affected the activity of the immobilized AOD. A sample solution containing ethanol was first added into the well with immobilized AOD (AOD-well). After 30 min, an aliquot (20 µl) was transferred into the well with immobilized POD containing 180 µl of 2 mM ABTS and the absorbance change at 415 nm for 10 min was measured with a microplate reader. The calibration curve was linear over the range 0.10 - 1.0 mM, and the relative standard deviation (n=5) was 0.8% for 1 mM ethanol. The ethanol concentration in alcoholic beverages, obtained by the present method, agreed well with that by the F-kit method. The AOD-well was reusable for 20 successive determinations.
机译:开发了一种使用乙醇氧化酶(AOD),过氧化物酶(POD)和2,2'-叠氮基双(3-乙基-苯并噻唑啉-6-磺酸)(ABTS)测定乙醇的方法,其中将这些酶分别固定在96孔微量滴定板每个孔的内表面上。固定之前,用戊二醛将表面活化。活化条件显着影响固定化AOD的活性。首先将含有乙醇的样品溶液与固定的AOD(AOD孔)一起添加到孔中。 30分钟后,将等分试样(20微升)转移到含有180微升2 mM ABTS的固定POD的孔中,并用酶标仪测量415 nm下10分钟的吸光度变化。校准曲线在0.10-1.0 mM范围内呈线性,对于1 mM乙醇,相对标准偏差(n = 5)为0.8%。通过本方法获得的含酒精饮料中的乙醇浓度与通过F-kit方法获得的乙醇浓度非常吻合。 AOD孔可重复使用20次。

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