Hamada S, Torii M, Kotani S, Tsuchitani Y
Infect Immun. 1981 Apr;32(1):364-72. doi: 10.1128/iai.32.1.364-372.1981.
Streptococcus sanguis isolated from human dental plaque were grown in Todd-Hewitt broth. Cells were collected by centrifugation and lyophilized after extensive washing with water. The cell-associated glucosyltransferase (GTase) activities of S. sanguis strains were assayed with [14C]sucrose. Strain differences in GTase activity were significant within the same serotype or biotype or both. The ability of S. sanguis cells to adhere to smooth glass surfaces was generally weak, irrespective of significant cell-associated GTase activity synthesizing water-insoluble, gel-like glucans. Resting cells of most S. sanguis strains bound extracellular GTase from Streptococcus mutans strain B13 (serotype d), resulting in the strong adherence of the S. sanguis cells to smooth glass surfaces in the presence of sucrose. Conversely, S. mutans B13 cells also could bind extracellular GTase from some strains of S. sanguis examined. The sucrose-dependent adherence of S. mutans cells was not altered, although S. sanguis strains from which the extracellular GTases were obtained did not produce significant adherence in the presence of sucrose. In view of these findings, it was suggested that S. mutans GTase could affect the adherence of S. sanguis to smooth tooth surfaces in the oral cavity.
从人类牙菌斑中分离出的血链球菌在托德-休伊特肉汤中培养。通过离心收集细胞,并用大量水洗后冻干。用血链球菌菌株的细胞相关葡糖基转移酶(GTase)活性以[14C]蔗糖进行测定。在同一血清型或生物型或两者中,GTase活性的菌株差异显著。血链球菌细胞粘附于光滑玻璃表面的能力通常较弱,无论其细胞相关GTase活性是否能合成水不溶性的凝胶状葡聚糖。大多数血链球菌菌株的静息细胞能结合变形链球菌B13菌株(血清型d)的胞外GTase,从而使血链球菌细胞在蔗糖存在下能强烈粘附于光滑玻璃表面。相反,变形链球菌B13细胞也能结合所检测的一些血链球菌菌株的胞外GTase。尽管从其获得胞外GTase的血链球菌菌株在蔗糖存在下不会产生显著的粘附,但变形链球菌细胞的蔗糖依赖性粘附并未改变。鉴于这些发现,有人提出变形链球菌GTase可能会影响血链球菌在口腔中对光滑牙齿表面的粘附。