Abe S, Saito T, Koga T, Ono E, Yanagawa R, Ito T, Kida H, Shimizu Y
Department of Hygiene and Microbiology, Faculty of Veterinary Medicine, Hokkaido University, Sapporo, Japan.
Nihon Juigaku Zasshi. 1990 Feb;52(1):11-8. doi: 10.1292/jvms1939.52.11.
A plasmid gene library of Corynebacterium renale piliated strain No. 109P+ was prepared in Escherichia coli in order to study the chemical structure of the pili of C. renale. Of 3,000 recombinant clones tested, 5 reacted with anti-pili anti-serum. The gene products of these clones reacted with anti-pili monoclonal antibodies 8/4, 5/2 and B20/3 but lacked the reactivity with 13/4. SDS-PAGE analysis revealed that the expressed protein had a molecular mass of 48 kilodalton and deletion analysis showed that the encoding region for this protein was localized within a 1.4 kilobase gene including a promoter sequence. Immunoelectron microscopy showed that mouse antibodies raised to the expressed protein bound to the entire surface of the pili of C. renale. These results indicate that the cloned gene encodes a major structural protein of C. renale pili.
为了研究肾棒状杆菌菌毛的化学结构,构建了肾棒状杆菌109P +菌毛菌株的质粒基因文库,并将其保存在大肠杆菌中。在测试的3000个重组克隆中,有5个与抗菌毛抗血清发生反应。这些克隆的基因产物与抗菌毛单克隆抗体8/4、5/2和B20/3发生反应,但与13/4缺乏反应性。SDS-PAGE分析显示,表达的蛋白质分子量为48千道尔顿,缺失分析表明该蛋白质的编码区域位于一个1.4千碱基的基因内,该基因包括一个启动子序列。免疫电子显微镜显示,针对表达蛋白产生的小鼠抗体与肾棒状杆菌菌毛的整个表面结合。这些结果表明,克隆的基因编码肾棒状杆菌菌毛的一种主要结构蛋白。