Martínez J M, Martínez M I, Suárez A M, Herranz C, Casaus P, Cintas L M, Rodríguez J M, Hernández P E
Departamento de Nutrición y Bromatología III, Facultad de Veterinaria, Universidad Complutense, 28040 Madrid, Spain.
Appl Environ Microbiol. 1998 Nov;64(11):4536-45. doi: 10.1128/AEM.64.11.4536-4545.1998.
Polyclonal antibodies of predetermined specificity for pediocin PA-1 (pedA1) have been generated by immunization of rabbits with a chemically synthesized C-terminal fragment of this bacteriocin (PH2) conjugated to the carrier protein keyhole limpet hemocyanin (KLH). The sensitivity and specificity of the PH2-KLH-generated antibodies were evaluated by the development of various enzyme-linked immunosorbent assays (ELISAs)-a noncompetitive indirect ELISA (NCI-ELISA), a competitive indirect ELISA (CI-ELISA), and a competitive direct ELISA (CD-ELISA)-and by immunodotting. All immunoassays indicated the existence of pedA1-specific antibodies with high relative affinities and adequate sensitivities in the sera of immunized animals. The limits of detection of pedA1 in MRS medium (Oxoid Ltd., Basingstoke, United Kingdom) were found to be 2.5 microg/ml by immunodotting and 1 microg/ml in the NCI-ELISA. However, the CI-ELISA enhanced the limit of detection of pedA1 to 0.025 microg/ml, while the amount of free pedA1 required for 50% binding inhibition was 10 microg/ml. Moreover, the CD-ELISA increased the affinity of the PH2-KLH-generated antibodies for pedA1; the limit of detection of pedA1 was less than 0.025 microg/ml, and the 50% binding inhibition value was reduced to 0.5 microg of pedA1/ml. All immunoassays and the slot dot assay detected the presence of pedA1 in the supernatant of the producing strain Pediococcus acidilactici 347, with no reactivity or negligible immunoreactivity with the supernatants of other lactic acid bacteria producing or not producing different bacteriocins. The approaches taken for the generation of antibodies and the development of immunoassays could prove useful for the generation and evaluation of antibodies of predetermined specificity for other bacteriocins of interest in the food industry.
通过用与载体蛋白钥孔血蓝蛋白(KLH)偶联的这种细菌素(PH2)的化学合成C末端片段免疫兔子,产生了对片球菌素PA-1(pedA1)具有预定特异性的多克隆抗体。通过开发各种酶联免疫吸附测定法(ELISA)——非竞争性间接ELISA(NCI-ELISA)、竞争性间接ELISA(CI-ELISA)和竞争性直接ELISA(CD-ELISA)以及免疫斑点法,评估了PH2-KLH产生的抗体的敏感性和特异性。所有免疫测定均表明,免疫动物血清中存在具有高相对亲和力和足够敏感性的pedA1特异性抗体。通过免疫斑点法发现,在MRS培养基(英国贝辛斯托克Oxoid有限公司)中pedA1的检测限为2.5微克/毫升,在NCI-ELISA中为1微克/毫升。然而,CI-ELISA将pedA1的检测限提高到0.025微克/毫升,而50%结合抑制所需的游离pedA1量为10微克/毫升。此外,CD-ELISA提高了PH2-KLH产生的抗体对pedA1的亲和力;pedA1的检测限小于0.025微克/毫升,50%结合抑制值降至0.5微克pedA1/毫升。所有免疫测定和狭缝斑点试验均检测到产毒株嗜酸乳杆菌347上清液中存在pedA1,与其他产或不产不同细菌素的乳酸菌上清液无反应或免疫反应可忽略不计。所采用的抗体产生方法和免疫测定开发方法可能对食品工业中其他感兴趣的细菌素产生预定特异性抗体并进行评估有用。