Ro M, Naito Y, Okuda K
Department of Microbiology, Tokyo Dental College, Chiba, Japan.
Bull Tokyo Dent Coll. 1995 Feb;36(1):43-8.
We have extracted the cell surface polysaccharide antigen (PS) and protein antigen from an encapsulated and virulent strain of Porphyromonas gingivalis 16-1. The PS was separated from lipopolysaccharide (LPS) by Sephacryl S-300 gel chromatography. It was distinguished from LPS by immunodiffusion with homologous rabbit antiserum. The PS reacted specifically with serogroup b antiserum against P. gingivalis 16-1 and Su63 strains, but not with antisera against serogroup a (ATCC 33277) or serogroup c (W83). The outer membrane protein was extracted with the Zwittergent 3-16 and sarcosyl detergents in a Tris-EDTA buffer. SDS-Page analysis revealed that the extracted protein antigen of P. gingivalis 16-1 contained 2 immunodominant proteins with molecular weights of 41 KDa and 27 KDa.
我们从具荚膜且有毒力的牙龈卟啉单胞菌16 - 1菌株中提取了细胞表面多糖抗原(PS)和蛋白质抗原。通过Sephacryl S - 300凝胶色谱法将PS与脂多糖(LPS)分离。通过与同源兔抗血清进行免疫扩散,将其与LPS区分开来。PS与针对牙龈卟啉单胞菌16 - 1和Su63菌株的b血清群抗血清发生特异性反应,但不与针对a血清群(ATCC 33277)或c血清群(W83)的抗血清反应。在外膜蛋白提取过程中,使用两性离子去污剂Zwittergent 3 - 16和肌氨酸钠在Tris - EDTA缓冲液中进行提取。SDS - 聚丙烯酰胺凝胶电泳分析显示,牙龈卟啉单胞菌16 - 1提取的蛋白质抗原包含2种免疫显性蛋白,分子量分别为41 kDa和27 kDa。