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开发一种基于多克隆抗体的伏马菌素B(4) 灵敏酶联免疫吸附测定法。

Development of a polyclonal antibody-based sensitive enzyme-linked immunosorbent assay for fumonisin B(4).

作者信息

Christensen H R, Yu F Y, Chu F S

机构信息

Food Research Institute and Department of Food Microbiology and Toxicology, University of Wisconsin-Madison, Madison, Wisconsin 53706, USA.

出版信息

J Agric Food Chem. 2000 May;48(5):1977-84. doi: 10.1021/jf990973m.

Abstract

Polyclonal antibodies (PAb) against fumonisin B(4) (FmB(4)), which have good cross-reactivity with four major fumonisins, were produced by immunizing a rabbit with FmB(4)-keyhole limpet hemocyanin conjugate. A sensitive competitive direct enzyme-linked immunosorbent assay (CD-ELISA) for fumonisins was developed. Because of the limited supply of FmB(4), both FmB(1)-horseradish peroxidase conjugate (HRP) and FmB(3)-HRP were tested as the toxin-enzyme markers in the CD-ELISA. In the FmB(1)-HRP-based CD-ELISA, the concentrations of FmB(1), FmB(2), FmB(3), and FmB(4) causing 50% inhibition of binding of enzyme marker (IC(50)) were 9.0, 2.1, 9.0, and 6.5 ng/mL (or the relative cross-reactivities toward FmB(1), FmB(2), FmB(3), and FmB(4) were 58.5, 309.5, 58.5, and 100%), respectively. In the FmB(3)-HRP-based CD-ELISA, the IC(50) values for FmB(1), FmB(2), FmB(3), and FmB(4) were 7.1, 1.9, 7.6, and 5.3 ng/mL (or the relative cross-reactivities toward FmB(1), FmB(2), FmB(3), and FmB(4) were 74, 280, 70, and 100%), respectively. The FmB(3)-HRP-based CD-ELISA was then used in a series of analytical recovery experiments using Fusarium moniliforme corn culture material spiked with FmB(1) and with clean corn spiked with a FmB(3)/FmB(4)-containing extract. The overall recovery of FmB(1) from culture material in the range of 10-100 ppm was 65%. The detection limit for FmB(1) with clean corn as matrix was between 100 and 500 ppb. F. moniliforme cultures were analyzed with the developed CD-ELISA and a well-established FmB(1) antibody-based ELISA, which is not sensitive to FmB(4). Differences in the fumonisin levels found by the two assays were used as an indication of the presence of FmB(4) in the culture material and, therefore, as a method to identify FmB(4)-producing strains. Using ELISA in combination with HPLC individual B-series fumonisins were quantified. The ELISA developed in the present study would be a useful supplement to FmB(1) antibody-based ELISA for screening of Fusarium strains for the production of major fumonisins.

摘要

通过用伏马毒素B(4)-钥孔戚血蓝蛋白偶联物免疫兔子,制备了对伏马毒素B(4)(FmB(4))具有良好交叉反应性的多克隆抗体(PAb),该抗体与四种主要伏马毒素具有良好的交叉反应性。建立了一种灵敏的伏马毒素竞争性直接酶联免疫吸附测定法(CD-ELISA)。由于FmB(4)的供应有限,FmB(1)-辣根过氧化物酶偶联物(HRP)和FmB(3)-HRP均被用作CD-ELISA中的毒素-酶标记物进行测试。在基于FmB(1)-HRP的CD-ELISA中,导致酶标记物结合抑制50%(IC(50))的FmB(1)、FmB(2)、FmB(3)和FmB(4)的浓度分别为9.0、2.1、9.0和6.5 ng/mL(或对FmB(1)、FmB(2)、FmB(3)和FmB(4)的相对交叉反应性分别为58.5、309.5、58.5和100%)。在基于FmB(3)-HRP的CD-ELISA中,FmB(1)、FmB(2)、FmB(3)和FmB(4)的IC(50)值分别为7.1、1.9、7.6和5.3 ng/mL(或对FmB(1)、FmB(2)、FmB(3)和FmB(4)的相对交叉反应性分别为74、280、70和100%)。然后,基于FmB(3)-HRP的CD-ELISA用于一系列分析回收率实验,这些实验使用接种了FmB(1)的串珠镰刀菌玉米培养材料以及接种了含FmB(3)/FmB(4)提取物的干净玉米。在10 - 100 ppm范围内,培养材料中FmB(1)的总回收率为65%。以干净玉米为基质时,FmB(1)的检测限在100至500 ppb之间。用建立的CD-ELISA和一种成熟的基于FmB(1)抗体的ELISA对串珠镰刀菌培养物进行分析,后者对FmB(4)不敏感。两种测定法所发现的伏马毒素水平差异被用作培养材料中FmB(4)存在的指标,因此,作为一种鉴定产生FmB(4)菌株的方法。结合使用ELISA和HPLC对单个B族伏马毒素进行了定量。本研究中建立的ELISA将是对基于FmB(1)抗体的ELISA的有用补充,用于筛选产生主要伏马毒素的镰刀菌菌株。

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