Takada K, Hirasawa M
Department of Microbiology, School of Dentistry at Matsuda, Nihon University, Chiba, Japan.
Microbios. 1998;95(380):35-44.
Escherichia coli-Porphyromonas gingivalis plasmid-shuttle vectors R751::* omega 4, pVOH1, and pVAL-1 were used for isolation of non-pigmented, defective protease, or non-haemolytic activity phenotypes in P. gingivalis. Transfer frequencies for R751::* omega 4, pVOH1, and pVAL-1 varied from 1.7 x 10(-9) to 5.3 x 10(-11) depending on the P. gingivalis 381 and ATCC 33277 strains. Two erythromycin-resistant transconjugants were screened from P. gingivalis 381 and eighteen were screened from ATCC 33277. Among isolated transconjugants, two from ATCC 33277 contained only one transposon insertion, while others included both Tn4351 and R751 sequences. The one transconjugant which contained a single insertion of Tn4351, designated NUM-T14, demonstrated defective pigmentation, and defective protease and haemolytic activities. The other transconjugant, designated NUM-T29, demonstrated defective haemolytic activity, but had black pigmentation and protease activity. Cell surface protein analysis by SDS-PAGE indicated that 40 and 18 kD proteins were lost or reduced and that 45 and 36 kD proteins were made to appear in both NUM-T14 and NUM-T29 transconjugants.
大肠杆菌-牙龈卟啉单胞菌质粒穿梭载体R751::*ω4、pVOH1和pVAL-1用于分离牙龈卟啉单胞菌中无色素、蛋白酶缺陷或无溶血活性的表型。R751::*ω4、pVOH1和pVAL-1的转移频率在1.7×10^(-9)至5.3×10^(-11)之间,具体取决于牙龈卟啉单胞菌381和ATCC 33277菌株。从牙龈卟啉单胞菌381中筛选出两个红霉素抗性接合子,从ATCC 33277中筛选出18个。在分离出的接合子中,来自ATCC 33277的两个仅含有一个转座子插入,而其他的则同时包含Tn4351和R751序列。含有单个Tn4351插入的一个接合子,命名为NUM-T14,表现出色素沉着缺陷、蛋白酶缺陷和溶血活性缺陷。另一个接合子,命名为NUM-T29,表现出溶血活性缺陷,但有黑色色素沉着和蛋白酶活性。通过SDS-PAGE进行的细胞表面蛋白分析表明,NUM-T14和NUM-T29接合子中40和18 kD的蛋白缺失或减少,并且出现了45和36 kD的蛋白。