Sugai M, Komatsuzawa H, Akiyama T, Hong Y M, Oshida T, Miyake Y, Yamaguchi T, Suginaka H
Department of Microbiology, Hiroshima University School of Dentistry, Japan.
J Bacteriol. 1995 Mar;177(6):1491-6. doi: 10.1128/jb.177.6.1491-1496.1995.
Two proteins which are capable of dispersing cell clusters of Staphylococcus aureus have been purified from a S. aureus FDA209P culture supernatant. Both of them were found to have bacteriolytic activity. From the elution profile of column chromatography and Western blot (immunoblot) analysis, one of them was identified as a 51-kDa endo-beta-N-acetylglucosaminidase (GL). The other was a 62-kDa protein on the basis of sodium dodecyl sulfate gel electrophoresis. Analysis of the peptidoglycan fragments following treatment with the 62-kDa protein indicated that this protein is an N-acetylmuramyl-L-alanine amidase (AM). In vitro studies of cluster dispersion activities using S. aureus mutant strains Lyt66 or S. aureus Wood46 grown as clusters demonstrated that these two enzymes act synergistically to disperse clusters into single cells. Antiserum against the 51-kDa GL cross-reacted with the 62-kDa AM, and S. aureus FDA209P grown in the presence of anti-51-kDa-GL immunoglobulin G induced giant clusters. Clusters induced by anti-51-kDa GL and by Cibacron blue F3G-A were dispersed by coincubation with the 51-kDa GL and the 62-kDa AM. Western blot analysis demonstrated that the 51-kDa GL and the 62-kDa AM were missing in culture supernatants of S. aureus Lyt66, Wood46, and RUSAL2 (Tn551 autolysin-defective mutant), which grow in clusters. These results strongly suggest that the 51-kDa GL and 62-kDa AM are involved in cell separation of daughter cells after cell division.
已从金黄色葡萄球菌FDA209P培养上清液中纯化出两种能够分散金黄色葡萄球菌细胞簇的蛋白质。发现它们都具有溶菌活性。根据柱色谱洗脱图谱和蛋白质印迹(免疫印迹)分析,其中一种被鉴定为51 kDa的内切-β-N-乙酰氨基葡萄糖苷酶(GL)。根据十二烷基硫酸钠凝胶电泳,另一种是62 kDa的蛋白质。用62 kDa蛋白质处理后对肽聚糖片段的分析表明,该蛋白质是N-乙酰胞壁酰-L-丙氨酸酰胺酶(AM)。使用以细胞簇形式生长的金黄色葡萄球菌突变株Lyt66或金黄色葡萄球菌Wood46对细胞簇分散活性进行的体外研究表明,这两种酶协同作用将细胞簇分散成单个细胞。针对51 kDa GL的抗血清与62 kDa AM发生交叉反应,在抗51 kDa - GL免疫球蛋白G存在下生长的金黄色葡萄球菌FDA209P诱导形成巨大细胞簇。由抗51 kDa GL和汽巴克隆蓝F3G - A诱导形成的细胞簇通过与51 kDa GL和62 kDa AM共同孵育而分散。蛋白质印迹分析表明,以细胞簇形式生长的金黄色葡萄球菌Lyt66、Wood46和RUSAL2(Tn551自溶素缺陷突变体)的培养上清液中不存在51 kDa GL和62 kDa AM。这些结果有力地表明,51 kDa GL和62 kDa AM参与细胞分裂后子细胞的分离。