Ciardi J E, Hageage G J, Wittenberger C L
J Dent Res. 1976 Apr;55 Spec No:C87-96. doi: 10.1177/002203457605500330011.
The glucosyltransferases of S mutans 6715 were resolved into two major fractions. One fraction synthesized water-soluble glucans and the other made water-insoluble glucans. Each fraction was found by polyacrylamide gel electrophoresis to be composed of several catalytically active species, apparently glycoprotein in nature. Treatment of the glucosyltransferases with dextranase in the absence of sucrose caused an interconversion of enzyme forms concomitant with a time-dependent loss of enzyme activity, but did not appear to remove significant amounts of the carbohydrate associated with the enzymes. Comparison of enzyme activity patterns on polyacrylamide gels of the five different S mutans serotypes further emphasizes the complexity of the glucosyltransferase system from this group of microorganisms.
变形链球菌6715的葡糖基转移酶可分为两个主要部分。一部分合成水溶性葡聚糖,另一部分合成水不溶性葡聚糖。通过聚丙烯酰胺凝胶电泳发现,每个部分均由几种具有催化活性的物质组成,这些物质在本质上显然是糖蛋白。在没有蔗糖的情况下用葡聚糖酶处理葡糖基转移酶,会导致酶形式的相互转化,并伴随酶活性随时间的丧失,但似乎不会去除与酶相关的大量碳水化合物。对五种不同变形链球菌血清型的聚丙烯酰胺凝胶上的酶活性模式进行比较,进一步强调了这组微生物葡糖基转移酶系统的复杂性。