Kimizuka R, Miura T, Okuda K
Department of Microbiology, Tokyo Dental College, Chiba, Japan.
Microbiol Immunol. 1996;40(10):717-23. doi: 10.1111/j.1348-0421.1996.tb01132.x.
Twenty out of 33 Actinobacillus actinomycetemcomitans strains formed hemolytic colonies on horse blood agar plates under anaerobic conditions. The hemolytic activity found in A. actinomycetemcomitans strain 137HE was examined. This activity was detected in the late exponential to early stationary phases of growth. Human erythrocytes were the most susceptible, followed by rabbit, sheep, horse and swine red blood cells. The majority of activity was detected in the cell-associated vesicle fraction. Zwitterionic detergent 3-[(3-cholamidopropyl)-dimethyl-ammonio]-1-propanesulfonate (CHAPS) extract from whole cells was semipurified by ammonium sulfate precipitation, preparative isoelectric focusing (IEF) and gel-filtration chromatography to yield a major band on sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) with a molecular mass of 12 kDa. Heating at 80 C for 30 min and treatment with proteinase K or trypsin resulted in complete disappearance of the hemolytic activity. Sulphydryl reagents enhanced activity and small amounts of cholesterol inhibited it. In summary, we demonstrated the presence of hemolysin in A. actinomycetemcomitans, and examined and characterized it.
33株伴放线放线杆菌中有20株在厌氧条件下于马血琼脂平板上形成溶血菌落。对伴放线放线杆菌137HE菌株中的溶血活性进行了检测。该活性在生长的指数后期至稳定期早期被检测到。人红细胞最敏感,其次是兔、羊、马和猪的红细胞。大部分活性存在于细胞相关的囊泡部分。通过硫酸铵沉淀、制备性等电聚焦(IEF)和凝胶过滤色谱对全细胞的两性离子去污剂3-[(3-胆酰胺丙基)-二甲基-铵基]-1-丙烷磺酸盐(CHAPS)提取物进行半纯化,以在十二烷基硫酸钠聚丙烯酰胺凝胶电泳(SDS-PAGE)上产生一条主要条带,其分子量为12 kDa。在80℃加热30分钟以及用蛋白酶K或胰蛋白酶处理导致溶血活性完全消失。巯基试剂增强活性,少量胆固醇抑制活性。总之,我们证明了伴放线放线杆菌中存在溶血素,并对其进行了检测和表征。