Goto K, Hirata H, Kagawa Y
J Bioenerg Biomembr. 1980 Aug;12(3-4):297-308. doi: 10.1007/BF00744690.
As a first step in the isolation of a stable Na+/H+ antiporter, its reaction in sonicated membrane vesicles of thermophilic bacterium PS3 has been characterized. The sonicated vesicles showed quenching of quinacrine fluorescence in either NADH oxidation or ATP hydrolysis. The quenching was reversed by the addition of Na+, Li+, Mn2+, Cd2+, and Co2+, but not of choline+ or Ca2+, regardless of their counter anions. 22Na+ was taken up into the vesicles by NADH oxidation, and the 22Na+ uptake was inhibited by the addition of an uncoupler. H+ release was observed on addition of Na+ to sonicated vesicles. The magnitude of the pH difference across the membrane induced by NADH oxidation was constant at pH 7.0 to 9.1, but the Na+/H+ antiport was affected by the pH of the medium (optimum pH-8.5). The Km's of the antiporter for Na+ and Li+ were 2.5 and 0.1 mM, respectively, but the Vmax values for the two ions were the same at pH 8.0. In the presence of Li+, no further decrease of fluorescence quenching was observed on addition of Na+ and vice versa. The Na+/H+ antiporter activity in PS3 was stable at 70 degrees C, and the optimum temperature for activity was 55-60 degrees C. In contrast to mesophilic cation/H+ antiporters, this antiporter was not inhibited by a thiol reagent.
作为分离稳定的Na⁺/H⁺反向转运蛋白的第一步,已对其在嗜热细菌PS3的超声破碎膜囊泡中的反应进行了表征。超声破碎的囊泡在NADH氧化或ATP水解过程中显示出奎纳克林荧光猝灭。无论其抗衡阴离子如何,添加Na⁺、Li⁺、Mn²⁺、Cd²⁺和Co²⁺可使猝灭逆转,但添加胆碱⁺或Ca²⁺则不能。通过NADH氧化,²²Na⁺被摄取到囊泡中,添加解偶联剂可抑制²²Na⁺的摄取。向超声破碎的囊泡中添加Na⁺时可观察到H⁺释放。由NADH氧化诱导的跨膜pH差异幅度在pH 7.0至9.1时保持恒定,但Na⁺/H⁺反向转运受培养基pH的影响(最适pH为8.5)。该反向转运蛋白对Na⁺和Li⁺的Km值分别为2.5和0.1 mM,但在pH 8.0时两种离子的Vmax值相同。在存在Li⁺的情况下,添加Na⁺时未观察到荧光猝灭的进一步降低,反之亦然。PS3中的Na⁺/H⁺反向转运蛋白活性在70℃时稳定,活性的最适温度为55 - 60℃。与嗜温阳离子/H⁺反向转运蛋白不同,该反向转运蛋白不受硫醇试剂的抑制。