School of Biological Sciences, University of Birmingham, P.O. Box 363, B15 2TT, Birmingham, UK.
Planta. 1991 Feb;183(3):399-408. doi: 10.1007/BF00197739.
Monoclonal antibodies have been raised against haustorial complexes isolated from pea (Pisum sativum L.) leaves infected by the biotrophic powdery mildew fungus Erysiphe pisi D.C. Immuno-localisation studies, using isolated haustorial complexes and infected pea leaf material, have shown that one of the antibodies, designated UB7, binds to fungal wall and plasma membranes present in both haustoria and mycelia. However, a second antibody, UB8, binds specifically to the haustorial plasma membrane, and does not label fungal plasma membranes in mycelia. Western blotting and antigen-modification techniques have shown that UB8 recognises a protein epitope of a 62-kDa antigen. A reduction in molecular weight of this component after endo-F treatment indicates that the antigen is an N-linked glycoprotein. UB7 also recognises a 62-kDa glycoprotein, which is susceptible to endo-F treatment, and the antibody binds to a carbohydrate epitope. Differences in molecular weights of the products after endo-F treatment of antigens show that the 62-kDa glycoproteins recognised by the antibodies are distinct molecules, in accordance with the localisation results. Overall, the results provide evidence for molecular differentiation associated with the development of haustoria in a biotrophic infection.
针对从感染生物营养性白粉菌(Erysiphe pisi D.C.)的豌豆(Pisum sativum L.)叶片中分离出的吸器复合体,已经制备了单克隆抗体。使用分离的吸器复合体和受感染的豌豆叶片材料进行免疫定位研究表明,一种抗体,命名为 UB7,与存在于吸器和菌丝体中的真菌细胞壁和质膜结合。然而,第二种抗体,UB8,特异性结合吸器质膜,而不在菌丝体中的真菌质膜上标记。Western blot 和抗原修饰技术表明,UB8 识别 62kDa 抗原的蛋白表位。endo-F 处理后该成分分子量降低表明该抗原是一种 N 连接糖蛋白。UB7 还识别一种 62kDa 糖蛋白,该蛋白易受 endo-F 处理,并且该抗体结合碳水化合物表位。endo-F 处理抗原后产物分子量的差异表明,抗体识别的 62kDa 糖蛋白是不同的分子,与定位结果一致。总的来说,这些结果为生物侵染中吸器发育相关的分子分化提供了证据。