Iwami Y, Schachtele C F, Yamada T
Department of Oral Biochemistry, Tohoku University School of Dentistry, Sendai, Japan.
J Dent Res. 1995 Sep;74(9):1613-7. doi: 10.1177/00220345950740091801.
We studied the mechanism by which the antimicrobial compound sucrose monolaurate inhibits Streptococcus mutans NCTC 10449 by determining its effect on the rate of acid production from glucose and sucrose and the intracellular and extracellular levels of glycolytic intermediates. Sucrose monolaurate was more effective than either sodium laurate or sodium fluoride in inhibiting acid production at pH 7.0 from glucose. Inhibition of acid production was the same when either glucose or sucrose was the carbon source and in the presence or absence of oxygen. Quantitative analysis of various glycolytic intermediates revealed that the steps inhibited by sucrose monolaurate were the reactions catalyzed by phosphofructokinase and glyceraldehyde 3-phosphate dehydrogenase and/or phosphoglycerate kinase. Since the activities of these enzymes in cell-free extracts were not decreased by the addition of sucrose monolaurate, the inhibition of acid production could not be ascribed to direct effects on the enzymes. A decrease in the rate of acid production with corresponding elevations in the extracellular levels of glycolytic intermediates indicates that sucrose monolaurate inhibits S. mutans by altering the permeability of the cell membrane, which causes a loss of important metabolites.
我们通过测定抗菌化合物月桂酸蔗糖酯对葡萄糖和蔗糖产酸速率以及糖酵解中间产物细胞内和细胞外水平的影响,研究了月桂酸蔗糖酯抑制变形链球菌NCTC 10449的机制。在pH 7.0条件下,月桂酸蔗糖酯在抑制葡萄糖产酸方面比月桂酸钠或氟化钠更有效。当葡萄糖或蔗糖作为碳源时,以及在有氧或无氧条件下,产酸抑制情况相同。对各种糖酵解中间产物的定量分析表明,月桂酸蔗糖酯抑制的步骤是由磷酸果糖激酶、3-磷酸甘油醛脱氢酶和/或磷酸甘油酸激酶催化的反应。由于在无细胞提取物中添加月桂酸蔗糖酯不会降低这些酶的活性,因此产酸抑制不能归因于对酶的直接作用。产酸速率降低,同时糖酵解中间产物细胞外水平相应升高,这表明月桂酸蔗糖酯通过改变细胞膜通透性来抑制变形链球菌,从而导致重要代谢产物的流失。