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抗乳链菌肽多克隆抗体的产生:免疫策略及免疫分析方法的开发

Generation of polyclonal antibodies against nisin: immunization strategies and immunoassay development.

作者信息

Suárez A M, Rodríguez J M, Hernández P E, Azcona-Olivera J I

机构信息

Departmento de Nutrición y Bromatologia III, Facultad de Veterinaria, Universidad Complutense de Madrid, Spain.

出版信息

Appl Environ Microbiol. 1996 Jun;62(6):2117-21. doi: 10.1128/aem.62.6.2117-2121.1996.

Abstract

Murine polyclonal antibodies reactive to the lantibiotic bacteriocin nisin A (nisA) have been produced by immunization with nisA-cholera toxin and nisA-keyhole limpet hemocyanin (nisA-KLH) conjugates. Mice immunized with nisA-cholera toxin developed nisA-specific antibodies with low relative affinities and poor sensitivities, while the immunization of mice with nisA-KLH conjugates resulted in the production of nisA-specific antibodies with high relative affinities and much-increased sensitivities. nisA antibodies could also be readily mass produced in less than 8 weeks in ascites fluid by using the nisA-KLH conjugate. A competitive direct enzyme-linked immunosorbent assay (ELISA) whereby nisA-horseradish peroxidase and free nisA competed for antibody binding was devised. The detection limit for nisA in the competitive direct ELISA with the nisA-KLH-generated antibodies was from 5 to 100 ng/ml, while the amount of free nisA required for 50% antibody binding inhibition ranged from 0.3 to 5 micrograms /ml. Both antisera and ascites polyclonal antibodies cross-reacted with nisZ either in the supernatant of a producer strain or with the pure lantibiotic but did not cross-react at all with non-lantibiotic-type bacteriocins. These polyclonal antibodies should find a wide usage from nisA ELISA analysis in foods and other matrices.

摘要

通过用乳链菌肽 - 霍乱毒素和乳链菌肽 - 钥孔血蓝蛋白(nisA - KLH)偶联物免疫,已产生了对羊毛硫抗生素细菌素乳链菌肽A(nisA)有反应的小鼠多克隆抗体。用nisA - 霍乱毒素免疫的小鼠产生了相对亲和力低且敏感性差的nisA特异性抗体,而用nisA - KLH偶联物免疫小鼠则产生了相对亲和力高且敏感性大大提高的nisA特异性抗体。通过使用nisA - KLH偶联物,还可以在不到8周的时间内从腹水液中轻松大量生产nisA抗体。设计了一种竞争性直接酶联免疫吸附测定(ELISA),其中nisA - 辣根过氧化物酶和游离nisA竞争抗体结合。用nisA - KLH产生的抗体进行的竞争性直接ELISA中,nisA的检测限为5至100 ng/ml,而50%抗体结合抑制所需的游离nisA量为0.3至5微克/毫升。抗血清和腹水多克隆抗体在产生菌的上清液中或与纯羊毛硫抗生素中均与nisZ发生交叉反应,但与非羊毛硫抗生素型细菌素完全不发生交叉反应。这些多克隆抗体在食品和其他基质的nisA ELISA分析中应具有广泛用途。

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