Pitty L J, Jacques N A
Institute of Dental Research, United Dental Hospital of Sydney, Surry Hills, New South Wales, Australia.
J Gen Microbiol. 1989 Jun;135(6):1431-9. doi: 10.1099/00221287-135-6-1431.
A defined growth medium (designated AP11), in which the concentrations of Na+ and K+ could be altered independently of one another, was developed for Streptococcus salivarius ATCC 25975. The addition of 100 mM-Na+ to AP11-medium containing 25 mM-K+ initially reduced the rate of expression of extracellular glucosyltransferase (GTFe). However, once S. salivarius had adaptated to grow in the presence of 100 mM-Na+, the rate of GTFe expression was stimulated. In fact once adapted to the presence of Na+ in the environment the same increase in the rate of enzyme expression was observed in all batch cultures irrespective of the K+ concentration (2-50 mM). At 2 mM-K+ there was no change in the level of saturation of the membrane lipids when the Na+ concentration was increased from 0 mM to 100 mM. Na+-stimulation of GTFe expression was confirmed in non-proliferating cell suspensions at different K+ concentrations. In non-proliferating cell suspensions, GTFe expression outlined a rectangular hyperbola with respect to K+ concentration when the K+ concentration was stepped up from 2 mM. The increase in GTFe synthesis and secretion was transient and was similar to that previously reported by us in Na+-rich medium, though it did not reach the same high levels. The reduced transient stimulation of GTFe expression correlated both with an enrichment in the saturated fatty acids of the membrane lipids of S. salivarius, and with the fact that the degree of saturation was only slightly reduced when the K+ concentration was stepped up from 2 mM to 50 mM. Needless to say, the final octadecenoic to octadecanoic (C18:1/C18:0) fatty acid ratio retained its direct correlation with the transient increase in GTFe production following the step up in K+ concentration, giving rise to an apparent biphasic plot when combined with that previously reported.
为唾液链球菌ATCC 25975开发了一种特定的生长培养基(命名为AP11),其中Na⁺和K⁺的浓度可以相互独立改变。向含有25 mM - K⁺的AP11培养基中添加100 mM - Na⁺最初会降低细胞外葡糖基转移酶(GTFe)的表达速率。然而,一旦唾液链球菌适应在100 mM - Na⁺存在下生长,GTFe的表达速率就会受到刺激。实际上,一旦适应了环境中Na⁺的存在,在所有分批培养物中都观察到酶表达速率有相同程度的增加,而与K⁺浓度(2 - 50 mM)无关。当K⁺浓度为2 mM时,Na⁺浓度从0 mM增加到100 mM时,膜脂的饱和度水平没有变化。在不同K⁺浓度的非增殖细胞悬液中证实了Na⁺对GTFe表达的刺激作用。在非增殖细胞悬液中,当K⁺浓度从2 mM逐步升高时,GTFe表达相对于K⁺浓度呈现出矩形双曲线。GTFe合成和分泌的增加是短暂的,并且与我们之前在富含Na⁺的培养基中报道的情况相似,尽管没有达到相同的高水平。GTFe表达的短暂刺激减少既与唾液链球菌膜脂中饱和脂肪酸的富集有关,也与当K⁺浓度从2 mM升高到50 mM时饱和度仅略有降低这一事实有关。不用说,最终的十八碳烯酸与十八烷酸(C18:1/C18:0)脂肪酸比率与K⁺浓度升高后GTFe产量的短暂增加仍保持直接相关性,与之前报道的情况相结合时产生了明显的双相图。