Sonna L A, Maloney P C
Department of Physiology, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205.
J Membr Biol. 1988 Mar;101(3):267-74. doi: 10.1007/BF01872841.
Resting cells of Staphylococcus aureus displayed a phosphate (Pi) exchange that was induced by growth with glucose 6-phosphate (G6P) or sn-glycerol 3-phosphate (G3P). Pi-loaded membrane vesicles from these cells accumulated 32Pi, 2-deoxyglucose 6-phosphate (2DG6P) or G3P by an electroneutral exchange that required no external source of energy. On the other hand, when vesicles were loaded with morpholinopropane sulfonic acid (MOPS), only transport of 32Pi (and L-histidine) was observed, and in that case transport depended on addition of an oxidizable substrate (DL-lactate). In such MOPS-loaded vesicles, accumulation of the organic phosphates, 2DG6P and G3P, could not be observed until vesicles were preincubated with both Pi and DL-lactate to establish an internal pool of Pi. This trans effect demonstrates that movement of 2DG6P or G3P is based on an antiport (exchange) with internal Pi. Reconstitution of membrane protein allowed a quantitative analysis of Pi-linked exchange. Pi-loaded proteoliposomes and membrane vesicles had comparable activities for the homologous 32Pi: Pi exchange (Kt's of 2.2 and 1.4 mM; Vmax's of 180 and 83 nmol Pi/min per mg protein), indicating that the exchange reaction was recovered intact in the artificial system. Other work showed that heterologous exchange from either G6P- or G3P-grown cells had a preference for 2DG6P (Kt = 27 microM) over G3P (Kt = 1.3 mM) and Pi (Kt = 2.2 mM), suggesting that the same antiporter was induced in both cases. We conclude that 32Pi: Pi exchange exhibited by resting cells reflects operation of an antiporter with high specificity for sugar 6-phosphate.(ABSTRACT TRUNCATED AT 250 WORDS)
金黄色葡萄球菌的静息细胞表现出一种磷酸盐(Pi)交换现象,该现象由葡萄糖6 - 磷酸(G6P)或sn - 甘油3 - 磷酸(G3P)培养诱导产生。来自这些细胞的装载Pi的膜囊泡通过一种无需外部能量源的电中性交换积累32Pi、2 - 脱氧葡萄糖6 - 磷酸(2DG6P)或G3P。另一方面,当膜囊泡装载吗啉丙烷磺酸(MOPS)时,仅观察到32Pi(和L - 组氨酸)的转运,且在这种情况下转运依赖于可氧化底物(DL - 乳酸)的添加。在这种装载MOPS的膜囊泡中,直到膜囊泡与Pi和DL - 乳酸预孵育以建立内部Pi池,才观察到有机磷酸盐2DG6P和G3P的积累。这种转效应表明2DG6P或G3P的转运基于与内部Pi的反向转运(交换)。膜蛋白的重组允许对Pi连接的交换进行定量分析。装载Pi的蛋白脂质体和膜囊泡对于同源的32Pi:Pi交换具有可比的活性(Kt分别为2.2和1.4 mM;Vmax分别为每毫克蛋白质180和83 nmol Pi/分钟),表明交换反应在人工系统中完整恢复。其他研究表明,来自G6P或G3P培养细胞的异源交换对2DG6P(Kt = 27 microM)的偏好高于G3P(Kt = 1.3 mM)和Pi(Kt = 2.2 mM),这表明在两种情况下诱导了相同的反向转运体。我们得出结论,静息细胞表现出的32Pi:Pi交换反映了对糖6 - 磷酸具有高特异性的反向转运体的作用。(摘要截断于250字)