Andersen Ann Zahle, Poulsen Allan K, Brasen Jens Christian, Olsen Lars Folke
University of Southern Denmark, Department of Biochemistry and Molecular Biology, CelCom, Campusvej 55, 5230 Odense M, Denmark.
Yeast. 2007 Sep;24(9):731-9. doi: 10.1002/yea.1508.
We employed the fluorescent cyanine dye DiOC(2)(3) to measure membrane potential in semi-anaerobic yeast cells under conditions where glycolysis was oscillating. Oscillations in glycolysis were studied by means of the naturally abundant nicotinamide adenine dinucleotide (NADH). We found that the mitochondrial membrane potential was oscillating, and that these oscillations displayed the same frequency and duration as the NADH oscillations. It was confirmed that DiOC(2)(3) localizes itself in the mitochondrial membrane and thus reports qualitative changes solely in mitochondrial membrane potential. Our studies showed that glycolytic oscillations perturb the mitochondrial membrane potential and that the mitochondria do not have any controlling effect on the dynamics of glycolysis under these conditions. Depolarization of the mitochondrial membrane by addition of FCCP quenched mitochondrial membrane potential oscillations and delocalized DiOC(2)(3), while glycolysis continued to oscillate unaffected.
我们使用荧光花青染料DiOC(2)(3)来测量糖酵解振荡条件下半厌氧酵母细胞的膜电位。通过天然丰富的烟酰胺腺嘌呤二核苷酸(NADH)研究糖酵解振荡。我们发现线粒体膜电位在振荡,并且这些振荡与NADH振荡具有相同的频率和持续时间。已证实DiOC(2)(3)定位于线粒体膜中,因此仅报告线粒体膜电位的定性变化。我们的研究表明,糖酵解振荡扰乱线粒体膜电位,并且在这些条件下线粒体对糖酵解动力学没有任何控制作用。添加FCCP使线粒体膜去极化,消除了线粒体膜电位振荡并使DiOC(2)(3)去定位,而糖酵解继续不受影响地振荡。