Bogomolni R A, Baker R A, Lozier R H, Stoeckenius W
Biochim Biophys Acta. 1976 Jul 9;440(1):68-88. doi: 10.1016/0005-2728(76)90114-6.
The purple membrane of Halobacterium halobium acts as a light-driven proton pump, ejecting protons from the cell interior into the medium and generating electrochemical proton gradient across the cell membrane. However, the type response of cells to light as measured with a pH electrode in the medium consists of an initial net inflow of protons which subsides and is then replaced by a net outflow which exponentially approaches a new lower steady state pH level. When the light turned off a small transient acidification occurs before the pH returns to the original dark level. We present experiments suggesting that the initial inflow of protons is triggered by the beginning ejection of protons through the purple membrane and that the initial inflow rate is larger than the continuing light-driven outflow. When the initial inflow has decreased exponentially to a small value, the outflow dominates and causes the net acidification of the medium. The initial inflow is apparently driven by a pre-existing electrochemical gradient across the membrane, which the cells can maintain for extended times in the absence of light and oxygen. Treatments which collapse this gradient such as addition of small concentrations of uncouplers abolish the initial inflow. The triggered inflow occurs through the ATPase and is accompanied by ATP synthesis. Inhibitors of the ATPase such as N,N'-dicyclohexylcarbodiimide (DCCD) inhibit ATP synthesis and abolish the inflow. They also abolish the transient light-off acidification, which is apparently caused by a short burst of ATP hydrolysis before the enzyme is blocked by its endogenous inhibitor. Similar transient inflows and outflows of protons are also observed when anaerobic cells are exposed to short oxygen pulses.
嗜盐菌的紫膜充当光驱动质子泵,将质子从细胞内部泵出到培养基中,在细胞膜上产生电化学质子梯度。然而,用培养基中的pH电极测量的细胞对光的类型响应包括质子的初始净流入,随后净流入减弱,接着被净流出取代,净流出呈指数方式接近新的较低稳态pH水平。当光关闭时,在pH恢复到原始暗水平之前会发生短暂的酸化。我们进行的实验表明,质子的初始流入是由质子通过紫膜开始泵出所触发的,且初始流入速率大于持续的光驱动流出速率。当初始流入呈指数下降到较小值时,流出占主导并导致培养基的净酸化。初始流入显然是由膜上预先存在的电化学梯度驱动的,细胞在无光和无氧条件下可以长时间维持这种梯度。破坏这种梯度的处理,如添加低浓度的解偶联剂,会消除初始流入。触发的流入通过ATP合酶发生,并伴随着ATP合成。ATP合酶抑制剂,如N,N'-二环己基碳二亚胺(DCCD),会抑制ATP合成并消除流入。它们还会消除短暂的光关闭酸化,这显然是由酶被其内源性抑制剂阻断之前的一阵短暂ATP水解引起的。当厌氧细胞暴露于短时间的氧气脉冲时,也会观察到类似的质子短暂流入和流出。