Ramos S, Balbín M, Raposo M, Valle E, Pardo L A
Departamento de Biología Funcional, Universidad de Oviedo, Spain.
J Gen Microbiol. 1989 Sep;135(9):2413-22. doi: 10.1099/00221287-135-9-2413.
Addition of glucose or fructose to cells of Saccharomyces cerevisiae adapted to grow in the absence of glucose induced an acidification of the intracellular medium. This acidification appeared to be due to the phosphorylation of the sugar since: (i) glucose analogues which are not efficiently phosphorylated did not induce internal acidification; (ii) glucose addition did not cause internal acidification in a mutant deficient in all the three sugar-phosphorylating enzymes; (iii) fructose did not affect the intracellular pH in a double mutant having only glucokinase activity; (iv) glucose was as effective as fructose in inducing the internal pH drop in a mutant deficient in phosphoglucose isomerase activity; and (v) in strains deficient in two of the three sugar-phosphorylating activities, there was a good correlation between the specific glucose- or fructose-phosphorylating activity of cell extracts and the sugar-induced internal acidification. In addition, in whole cells any of the three yeast sugar kinases were capable of mediating the internal acidification described. Glucose-induced internal acidification was observed even when yeast cells were suspended in growth medium and in cells suspended in buffer containing K+, which supports the possible signalling function of the glucose-induced internal acidification. Evaluation of internal pH by following fluorescence changes of fluorescein-loaded cells indicated that the change in intracellular pH occurred immediately after addition of sugar. The apparent Km for glucose in this process was 2 mM. Changes in both the internal and external pH were determined and it was found that the internal acidification induced by glucose was followed by a partial alkalinization coincident with the initiation of H+ efflux. This reversal of acidification could be due to the activity of the H+-ATPase, since it was inhibited by diethylstilboestrol. Coincidence between internal alkalinization and the H+ efflux was also observed after addition of ethanol.
向适应在无葡萄糖条件下生长的酿酒酵母细胞中添加葡萄糖或果糖会导致细胞内介质酸化。这种酸化似乎是由于糖的磷酸化,因为:(i) 不能有效磷酸化的葡萄糖类似物不会诱导内部酸化;(ii) 添加葡萄糖不会在缺乏所有三种糖磷酸化酶的突变体中引起内部酸化;(iii) 果糖不会影响仅具有葡萄糖激酶活性的双突变体中的细胞内pH;(iv) 在缺乏磷酸葡萄糖异构酶活性的突变体中,葡萄糖在诱导内部pH下降方面与果糖一样有效;以及(v) 在缺乏三种糖磷酸化活性中的两种的菌株中,细胞提取物的特定葡萄糖或果糖磷酸化活性与糖诱导的内部酸化之间存在良好的相关性。此外,在完整细胞中,三种酵母糖激酶中的任何一种都能够介导所述的内部酸化。即使将酵母细胞悬浮在生长培养基中以及悬浮在含有K+的缓冲液中的细胞中,也观察到了葡萄糖诱导的内部酸化,这支持了葡萄糖诱导的内部酸化可能具有的信号传导功能。通过跟踪荧光素负载细胞的荧光变化来评估内部pH,结果表明在添加糖后细胞内pH立即发生变化。此过程中葡萄糖的表观Km为2 mM。测定了内部和外部pH的变化,发现葡萄糖诱导的内部酸化之后是与H+外流开始同时发生的部分碱化。这种酸化的逆转可能是由于H+-ATPase的活性,因为它被己烯雌酚抑制。添加乙醇后也观察到内部碱化与H+外流同时发生。