Giannini J L, Briskin D P
Department of Agronomy, University of Illinois, Urbana 61801.
Arch Biochem Biophys. 1988 Feb 1;260(2):653-60. doi: 10.1016/0003-9861(88)90494-8.
The potential role of pyridine nucleotide oxidation in the energization and/or regulation of membrane transport was examined using sealed plasma membrane vesicles isolated from red beet (Beta vulgaris L.) storage tissue. In this system, pyridine nucleotide oxidation, which was enhanced in the presence of ferricyanide, occurred. In the presence or absence of ferricyanide, the oxidation of NADH was several-fold greater than the oxidation of NADPH, indicating that it was the preferred substrate for oxidation in this system. Ferricyanide reduction coupled to NADH oxidation did not require the transmembrane movement of reducing equivalents since ferricyanide incorporated inside the vesicles could not be reduced by NADH added externally to the vesicles, unless the vesicles were made leaky by the addition of 0.05% (v/v) Triton X-100. Using fluorescent probes for the measurement of transmembrane pH gradients and membrane potentials, it was determined that NADH oxidation did not result in the production of a proton electrochemical gradient or have any effect upon the proton electrochemical gradient produced by the plasma membrane H+-ATPase. The oxidation of NADH in the presence of ferricyanide did result in the acidification of the reaction medium. This acidification was unaffected by the addition of Gramicidin D and stimulated by the addition of 0.05% (v/v) Triton X-100, suggesting a scalar (nonvectorial) production of protons in the oxidation/reduction reaction. The results of this study suggest that the oxidation of pyridine nucleotides by plasma membrane vesicles is not related to energization of transport at the plasma membrane or modulation of the activity of the plasma membrane H+-ATPase.
利用从红甜菜(Beta vulgaris L.)贮藏组织中分离得到的密封质膜囊泡,研究了吡啶核苷酸氧化在膜转运的供能和/或调节中的潜在作用。在该系统中,在铁氰化物存在下增强的吡啶核苷酸氧化发生了。无论有无铁氰化物,NADH的氧化都比NADPH的氧化大几倍,表明它是该系统中氧化的首选底物。与NADH氧化偶联的铁氰化物还原不需要还原当量的跨膜移动,因为除非通过添加0.05%(v/v)Triton X-100使囊泡渗漏,否则囊泡内部掺入的铁氰化物不能被外部添加到囊泡中的NADH还原。使用荧光探针测量跨膜pH梯度和膜电位,确定NADH氧化不会导致质子电化学梯度的产生,也不会对质膜H+-ATP酶产生的质子电化学梯度有任何影响。在铁氰化物存在下NADH的氧化确实导致了反应介质的酸化。这种酸化不受短杆菌肽D添加的影响,而受0.05%(v/v)Triton X-100添加的刺激,表明在氧化/还原反应中质子的产生是标量(非矢量)的。本研究结果表明,质膜囊泡对吡啶核苷酸的氧化与质膜转运的供能或质膜H+-ATP酶活性的调节无关。