Janda W M, Kuramitsu H K
Infect Immun. 1978 Jan;19(1):116-22. doi: 10.1128/iai.19.1.116-122.1978.
The production of extracellular and cell-associated glucosyltransferase activity by Streptococcus mutans strain GS-5 was examined during growth on various carbon sources in a chemically defined medium. S. mutans cells produced glucosyltransferase activity only during logarithmic growth when glucose, fructose, mannitol, or sorbitol was the sole carbon source. Cells growing on mannitol or sorbitol produced approximately half as much extracellular glucosyltransferase activity as cells growing on glucose, although the proportions of the glucosyltransferase activity capable of synthesizing insoluble glucans were similar. Cells growing on fructose produced slightly more extracellular glucosyltransferase activity than cells grown on glucose, yet the proportion of the glucosyltransferase activity capable of synthesizing insoluble glucans was again similar to glucose cultures. S. mutans cells growing in the presence of both glucose and mannitol displayed diauxic growth and initial preferential utilization of glucose. Glucosyltransferase enzyme production occurred only during the phases of cell growth in the presence of the two carbon sources. The cell-associated glucosyltransferase activities of glucose-, fructose-, mannitol-, and sorbitol-grown cells were relatively low, yet all the cells were capable of adherence to glass in the presence of sucrose. When glucose-containing cultures of S. mutans were supplemented with sucrose, extracellular glucosyltransferase activity first became cell associated and then appeared to become inactivated, presumably due to the accumulation of insoluble glucans.
在化学限定培养基中,研究了变形链球菌GS-5菌株在多种碳源上生长期间细胞外和细胞相关葡糖基转移酶活性的产生情况。变形链球菌细胞仅在以葡萄糖、果糖、甘露醇或山梨醇作为唯一碳源的对数生长期产生葡糖基转移酶活性。在甘露醇或山梨醇上生长的细胞产生的细胞外葡糖基转移酶活性约为在葡萄糖上生长细胞的一半,尽管能够合成不溶性葡聚糖的葡糖基转移酶活性比例相似。在果糖上生长的细胞产生的细胞外葡糖基转移酶活性略高于在葡萄糖上生长的细胞,然而能够合成不溶性葡聚糖的葡糖基转移酶活性比例再次与葡萄糖培养物相似。在同时存在葡萄糖和甘露醇的情况下生长的变形链球菌细胞呈现双相生长并优先利用葡萄糖。葡糖基转移酶的产生仅发生在两种碳源存在时的细胞生长阶段。在葡萄糖、果糖、甘露醇和山梨醇上生长的细胞的细胞相关葡糖基转移酶活性相对较低,但所有细胞在蔗糖存在下都能够黏附于玻璃。当变形链球菌含葡萄糖的培养物补充蔗糖时,细胞外葡糖基转移酶活性首先与细胞结合,然后似乎失活,推测是由于不溶性葡聚糖的积累。