ODA_H_2O_2-HRP偶合反应伏安酶联免疫分析检测植物病毒GFV、TAV和PVY  

Voltammetric Enzyme-linked Immunoassay of GFV,TAV and PVY via an Enzyme-substrate Reaction in the ODA-H_2O_2-HRP System

作　　者：焦奎[1] 韦璐[1] 张书圣[1] 刘澄凡[1] 张成良[2,3] 张作芳[2,3] 刘靖宇 魏澎 

机构地区：[1]青岛化工学院应化系 [2]农业部植物检疫实验所 [3]核工业北京地质研究院

出　　处：《分析测试学报》1998年第2期1-4,共4页Journal of Instrumental Analysis

基　　金：国家自然科学基金;山东省自然科学基金

摘　　要：将邻联茴香胺（ＯＤＡ）＿Ｈ２Ｏ２＿辣根过氧化物酶（ＨＲＰ）偶合反应伏安酶联免疫分析新体系，应用于植物病毒葡萄扇叶病毒（ｇｒａｐｅｖｉｎｅｆａｎｌｅａｆｖｉｒｕｓ，ＧＦＶ）、番茄不孕病毒（ｔｏｍａｔｏａｓｐｅｒｍｙｖｉｒｕｓ，ＴＡＶ）和马铃薯Ｙ病毒（ｐｏｔａｔｏｖｉｒｕｓＹ，ＰＶＹ）的测定。该法对以上各种植物病毒叶澄清液的测定的稀释比均高于酶联免疫吸附分析（ＥＬＩＳＡ）法，检测范围均宽于ＥＬＩＳＡ法。A voltammetric enzyme_linked immunoassay method is described for the detection of grapevine fanleaf virus(GFV),tomato aspermy virus(TAV)and potato virus Y (PVY). Following conjugation of antibodies with horseradish peroxidase,the peroxidase-substrate reaction in the o-dianisidine (ODA)-H_2O_2_horseradish peroxidase (HRP)system yields an end product that can be determined voltammetrically. The highest dilution ratios for the detection of GFV,TAV and PVY in infected leaf saps are 1∶25 000,1∶50 000 and 1∶25 000 000,respectively,while their detection ranges are 1∶10～1∶25 000,1∶10～1∶50 000 and 1∶10～1∶25 000 00,respectively.The sensitivity of the proposed method is higher and the detection range is wider than the conventional enzyme linked immuno-sorbent assay (ELISA)method.

关 键 词：葡萄扇叶病毒 番茄不孕病毒 马铃薯Y病毒 ODA 

分 类 号：S432.41[农业科学—植物病理学]