Skoog C, Kromer U, Mitchell R W, Hoogstraten J, Stephens N L
Am J Physiol. 1978 Jan;234(1):C1-6. doi: 10.1152/ajpcell.1978.234.1.C1.
Studies on oxidative phosphorylation revealed that, in frog skeletal muscle mitochondria (SKMM) from the thigh, the adenosine diphosphate/oxygen ratio (ADP/O) was 2.8 +/- 0.1 SE, and the respiratory control ratio was 9.5 +/- 0.9, with pyruvate/malate as the substrate. Oxygen uptake rate (Qo2) was 225 mumol O2 per minute per gram mitochondrial protein +/- 13; phosphorylation rate (ADP/O X Qo2 X 2) was 1,230 mumol ADP phosphorylation per minute per gram mitochondrial protein +/- 77; and the phosphorylation capacity (phosphorylation rate times tissue mitochondrial protein content) was 3.6 mumol ADP phosphorylated per gram wet weight of muscle +/- 0.2. Tissue mitochondrial protein content was determined by the measurement of nicotinamide adenine dinucleotide (NADH) oxidase activity. Electron microscopy (EM) revealed intact, isolated, energized twisted mitochondria of a condensed form. Frog sartorius muscle mitochondria gave similar oxidative phosphorylation parameters when investigated independently of the rest of the thigh. These values of SKMM respiration from the frog are similar to those values obtained from pigeon and rabbit heart and rat skeletal muscles. However, because of the low NADH-oxidase activity indicating reduced mitochondrial content (this was verified in low-magnification EM pictures), phosphorylation capacity was significantly reduced in frog skeletal muscle mitochondria.
对氧化磷酸化的研究表明,在取自青蛙大腿的骨骼肌线粒体(SKMM)中,以丙酮酸/苹果酸作为底物时,二磷酸腺苷/氧比率(ADP/O)为2.8±0.1(标准误),呼吸控制率为9.5±0.9。氧摄取率(Qo2)为每克线粒体蛋白每分钟225μmol O2±13;磷酸化率(ADP/O×Qo2×2)为每克线粒体蛋白每分钟1230μmol ADP磷酸化±77;磷酸化能力(磷酸化率乘以组织线粒体蛋白含量)为每克肌肉湿重3.6μmol ADP磷酸化±0.2。通过测量烟酰胺腺嘌呤二核苷酸(NADH)氧化酶活性来测定组织线粒体蛋白含量。电子显微镜(EM)显示线粒体完整、分离且呈浓缩形式的活跃扭曲形态。当对青蛙缝匠肌线粒体进行独立于大腿其他部分的研究时,得到了类似的氧化磷酸化参数。青蛙SKMM的这些呼吸值与从鸽子和兔子心脏以及大鼠骨骼肌获得的值相似。然而,由于NADH氧化酶活性较低表明线粒体含量减少(这在低倍EM图像中得到证实),青蛙骨骼肌线粒体中的磷酸化能力显著降低。