Kaster A G, Brown L R
Infect Immun. 1983 Nov;42(2):716-20. doi: 10.1128/iai.42.2.716-720.1983.
Three strains of anaerobic, dextranase-producing, gram-positive, rod-shaped bacteria were isolated from human dental plaque associated with root carious lesions. The isolates produced a molar ratio of acetate to lactate from glucose fermentation ranging from 1.1 to 1.9. Each strain also produced fructose-6-phosphate phosphoketolase. The isolates were identified as belonging to the genus Bifidobacterium, but from their carbohydrate fermentation patterns they did not appear to be strains of Bifidobacterium dentium. These microorganisms fermented high-molecular-weight dextrans. A partial characterization of the dextranase activity was included in this study and revealed an extracellular dextranase with a pH optimum of 7.1. Analysis of the dextran degradation products demonstrated the liberation of saccharides larger than 1 glucose unit. It was concluded that this enzyme used an endohydrolytic mode of dextran cleavage.
从与根龋病变相关的人类牙菌斑中分离出三株厌氧、产葡聚糖酶、革兰氏阳性、杆状细菌。这些分离菌株从葡萄糖发酵中产生的乙酸与乳酸的摩尔比在1.1至1.9之间。每株菌株还产生6-磷酸果糖磷酸酮醇酶。这些分离菌株被鉴定为属于双歧杆菌属,但从它们的碳水化合物发酵模式来看,它们似乎不是龋齿双歧杆菌菌株。这些微生物发酵高分子量葡聚糖。本研究对葡聚糖酶活性进行了部分表征,结果显示一种胞外葡聚糖酶的最适pH为7.1。对葡聚糖降解产物的分析表明,释放出的糖类大于1个葡萄糖单位。得出的结论是,这种酶采用葡聚糖内切水解模式进行切割。