Osborne R M, Lamberts B L, Meyer T S, Roush A H
J Dent Res. 1976 Jan-Feb;55(1):77-84. doi: 10.1177/00220345760550012801.
This study explored the use of acrylamide gel electrophoretic methods to determine the numbers and types of extracellular sucrose-metabolizing enzymes produced by particular strains of S mutans. Strains HS-6, SL-1, FA-1, and NCTC 10449 were cultured in a chemically defined medium and the extracellular proteins elaborated by the organisms were isolated and subjected to acrylamide gel electrophoresis. Patterns of protein components and sucrose-metabolizing enzymes were then delineated. Three types of sucrose-metabolizing enzymes were observed. One type was involved in the synthesis of polysaccharides that were insolubilized in the gels. Another type was involved in the synthesis of water-soluble polysaccharides. A third type was involved in the splitting of sucrose into reducing sugars without polysaccharide synthesis. Each pattern was distinctive with regard to the numbers, proportions, and types of enzyme components present and their migratory characteristics. From two to at least six components were observed amont the enzyme activity patterns per strain. Extracellular protein patterns showed from 12 to 20 components per strain. Comparative data on growth in the chemically defined medium and Todd-Hewitt broth were also presented. Better growth levels were obtained in all instances with the chemically defined medium over comparable periods of time.
本研究探索了使用丙烯酰胺凝胶电泳法来确定变形链球菌特定菌株产生的细胞外蔗糖代谢酶的数量和类型。将菌株HS-6、SL-1、FA-1和NCTC 10449在化学成分明确的培养基中培养,分离出这些生物体产生的细胞外蛋白质,并进行丙烯酰胺凝胶电泳。然后描绘蛋白质成分和蔗糖代谢酶的图谱。观察到三种类型的蔗糖代谢酶。一种类型参与了凝胶中不溶性多糖的合成。另一种类型参与了水溶性多糖的合成。第三种类型参与了蔗糖分解为还原糖而不合成多糖的过程。每种图谱在存在的酶成分的数量、比例和类型及其迁移特性方面都具有独特性。每个菌株的酶活性图谱中观察到2至至少6个成分。每个菌株的细胞外蛋白质图谱显示有12至20个成分。还给出了在化学成分明确的培养基和托德-休伊特肉汤中生长的比较数据。在可比的时间段内,在所有情况下,使用化学成分明确的培养基都能获得更好的生长水平。