Sasaki N, Topitsoglou V, Frostell G
Swed Dent J. 1983;7(4):153-60.
-A method for the determination of acid production from 20-25 mg (wet weight) of Streptococcus mutans and 12-33 mg (wet weight) of human dental plaque is described. After endogenous acid production had been followed, either sorbitol or xylitol or a mixture of sorbitol and xylitol (2:1) was added. After about ten minutes glucose, sucrose or Palatinose were added for a vitality test. Addition of xylitol to the bacterial suspension caused inhibition of acid production from sorbitol by Streptococcus mutans grown on sorbitol or a mixture of sorbitol and glucose. It was also observed that it had a similar effect on acid production from sorbitol in suspensions of dental plaque with few exceptions. On the other hand, Streptococcus mutans cells grown on glucose, sucrose and xylitol media, produced no or insignificant amounts of acid from sorbitol. Streptococcus mutans cells grown on media containing glucose, sucrose, sorbitol and a mixture of sorbitol and glucose generally formed a large amount of acid from glucose and sucrose after the addition of sorbitol and xylitol. However, Streptococcus mutans cells grown on a medium containing xylitol and the mixture of sorbitol and xylitol formed less acid from glucose. The acid production activity from sorbitol in suspensions of dental plaque after the xylitol addition was somewhat lower than the acid production from sorbitol alone (p less than 0.02).
描述了一种测定20 - 25毫克(湿重)变形链球菌和12 - 33毫克(湿重)人牙菌斑产酸量的方法。在追踪内源性产酸后,加入山梨醇或木糖醇或山梨醇与木糖醇的混合物(2:1)。约十分钟后加入葡萄糖、蔗糖或帕拉金糖进行活力测试。向细菌悬液中添加木糖醇会抑制在山梨醇或山梨醇与葡萄糖混合物上生长的变形链球菌由山梨醇产酸。还观察到,除少数例外,它对牙菌斑悬液中由山梨醇产酸也有类似作用。另一方面,在葡萄糖、蔗糖和木糖醇培养基上生长的变形链球菌细胞,由山梨醇产酸量极少或不产酸。在含有葡萄糖、蔗糖、山梨醇以及山梨醇与葡萄糖混合物的培养基上生长的变形链球菌细胞,在添加山梨醇和木糖醇后,通常由葡萄糖和蔗糖产生大量酸。然而,在含有木糖醇以及山梨醇与木糖醇混合物的培养基上生长的变形链球菌细胞,由葡萄糖产酸较少。添加木糖醇后牙菌斑悬液中由山梨醇的产酸活性略低于单独由山梨醇的产酸活性(p小于0.02)。