Okahashi N, Sasakawa C, Yoshikawa M, Hamada S, Koga T
Department of Bacteriology, University of Tokyo, Japan.
Mol Microbiol. 1989 Feb;3(2):221-8. doi: 10.1111/j.1365-2958.1989.tb01811.x.
The structural gene for a 190 kD protein antigen (PAc) of Streptococcus mutans MT8148 (serotype c) was cloned into the plasmid vector pUC118. SDS-polyacrylamide gel electrophoresis and Western immunoblotting showed that the Escherichia coli harbouring the chimaeric plasmid produced multiple polypeptides of 190-210 kD. Immunodiffusion analysis revealed that the cloned PAc had the same specific determinants as S. mutans PAc. The cloned pac gene was mapped, and its transcriptional orientation was determined by characterizing deletion mutants of the chimaeric plasmid. Southern blot analysis with the cloned gene sequence as a probe revealed the presence of a homologous sequence in DNAs from serotypes e and f S. mutans. PAc-defective mutants were constructed by inserting an erythromycin-resistance gene into the pac gene. The cell-surface hydrophobicity of the mutants was lower than that of the parent strain.
变形链球菌MT8148(血清型c)190kD蛋白抗原(PAc)的结构基因被克隆到质粒载体pUC118中。十二烷基硫酸钠-聚丙烯酰胺凝胶电泳和蛋白质免疫印迹表明,携带嵌合质粒的大肠杆菌产生了190 - 210kD的多种多肽。免疫扩散分析显示,克隆的PAc与变形链球菌PAc具有相同的特异性决定簇。对克隆的pac基因进行了定位,并通过鉴定嵌合质粒的缺失突变体确定了其转录方向。以克隆的基因序列为探针进行的Southern印迹分析表明,在血清型e和f的变形链球菌DNA中存在同源序列。通过将红霉素抗性基因插入pac基因构建了PAc缺陷型突变体。突变体的细胞表面疏水性低于亲本菌株。