Chassy B M, Beall J R, Bielawski R M, Porter E V, Donkersloot J A
Infect Immun. 1976 Aug;14(2):408-15. doi: 10.1128/iai.14.2.408-415.1976.
Specific growth rates, growth yields, and the level and cellular distribution of three sucrose-metabolizing enzyme activities were determined for seven oral streptococci (Streptococcus mutans strains E49, BHT, 10449, SL-1, and LM-7, S. sanguis 10558, and S. salivarius 25975). Cultures were grown in a fermentor at pH 6 with either 20 mM glucose or 10 mM sucrose. Generation times varied between 21 and 70 min. Whereas some strains grew 10 to 50% more slowly with sucrose than with glucose, others did not. Growth was always logarithmic, and the growth yields were similar. Glcosyl transferase (EC 2.4.1.5) was largely extracellular; in sucrose cultures it was appreciably lower, but no major shift to a cell-associated form was found. In glucose cultures, the activity varied between 4 and 140 IU per 6-liter culture. The glucan formed was mostly or exclusively water insoluble. Glcosyl transferase was stimulated weakly (60% or less) by various dextrans. Fructosyl transferase (EC 2.4.1.10) was primarily extracellular (except in glucose cultures of S. salivarius) and varied between 0 and 337 IU/culture. In S. salivarius, the extracellular fructosyl transferase was induced by sucrose. In all S. Mutans cultures, the total fructosyl transferase activity was lower after growth with sucrose. All strains had extra- and intracellular invertase (EC 3.2.1.26) activity. Total levels varied between 210 and 3,500 IU/culture. Less extracellular activity was present in sucrose cultures. Only S. salivarius had appreciable activity in the cellular particulate fraction. Invertase activity was significantly higher than the combined glucosyl and fructosyl transferase activities in all cultures.
测定了7种口腔链球菌(变形链球菌E49、BHT、10449、SL-1和LM-7菌株,血链球菌10558,以及唾液链球菌25975)的比生长速率、生长产量以及三种蔗糖代谢酶活性的水平和细胞分布。培养物在pH值为6的发酵罐中生长,分别以20 mM葡萄糖或10 mM蔗糖为碳源。代时在21至70分钟之间变化。虽然一些菌株在以蔗糖为碳源时生长速度比以葡萄糖为碳源时慢10%至50%,但其他菌株则不然。生长始终呈对数增长,且生长产量相似。葡糖基转移酶(EC 2.4.1.5)主要存在于细胞外;在蔗糖培养物中其活性明显较低,但未发现向细胞相关形式的主要转变。在葡萄糖培养物中,每6升培养物的活性在4至140 IU之间。形成的葡聚糖大多或完全不溶于水。各种葡聚糖对葡糖基转移酶的刺激较弱(60%或更低)。果糖基转移酶(EC 2.4.1.10)主要存在于细胞外(唾液链球菌在葡萄糖培养物中除外),每培养物的活性在0至337 IU之间。在唾液链球菌中,细胞外果糖基转移酶由蔗糖诱导。在所有变形链球菌培养物中,以蔗糖生长后总果糖基转移酶活性较低。所有菌株都有细胞外和细胞内转化酶(EC 3.2.1.26)活性。总水平在每培养物210至3500 IU之间变化。蔗糖培养物中的细胞外活性较低。只有唾液链球菌在细胞颗粒部分有明显活性。在所有培养物中,转化酶活性显著高于葡糖基转移酶和果糖基转移酶活性之和。