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Activity of membrane-bound enzymes exposed to sinusoidally modulated 2450-MHz microwave radiation

机译:暴露于正弦调制的2450 MHz微波辐射下的膜结合酶的活性

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摘要

Membrane-bound enzyme systems were irradiated with sinusoidally modulated microwave radiation in a spectrophotometric apparatus in which enzyme activity was measured during irradiation. The enzymes chosen for study were cytochrome oxidase, a key enzyme in the electron-transport chain that is located in the inner membrane of mitochondria, and adenosine triphosphatase (ATPase) from red-blood-cell membrane, which is involved in maintaining the sodium-potassium balance of the cell. The enzyme systems were prepared from rat tissue and were subjected to 2450-MHz radiation sinusoidally modulated at 16, 30, 90, and 120 Hz; the specific absorption rate was 26 mW g. Temperature was controlled at 25 ± 1.0 °C in all experiments. Irradiation began immediately after initiation of the reaction and continued for several minutes while the reaction rate was being monitored. Cytochrome oxidase activity was measured directly by monitoring the change in absorbance of its substrate, cytochrome c, at 550 nm. Activity of ATPase was measured by a coupled-enzyme system in which the rate of conversion of ATP to ADP was followed at 340 nm by stoichiometric oxidation of NADPH. The enzymes pyruvate kinase and lactate dehydrogenase performed the intermediate steps and were always present in excess so that the activity of ATPase was rate controlling. No statistically significant differences in enzyme activities were obtained between irradiated and control samples at any of the modulation frequencies for either enzyme system.
机译:在分光光度计中用正弦调制的微波辐射辐照膜结合的酶系统,其中在辐照期间测量酶活性。选择用于研究的酶是细胞色素氧化酶(一种位于线粒体内膜中的电子传输链中的关键酶)和来自红细胞膜的腺苷三磷酸酶(ATPase),其参与维持钠-细胞的钾平衡。酶系统是从大鼠组织中制备的,并以1650、30、90和120 Hz进行正弦调制的2450 MHz辐射。比吸收率为26mW g。在所有实验中,温度均控制在25±1.0°C。反应开始后立即开始辐照,并持续几分钟,同时监测反应速率。通过监测其底物细胞色素c在550 nm处吸光度的变化,直接测量了细胞色素氧化酶的活性。 ATP酶的活性通过偶联酶系统测量,其中通过化学计量氧化NADPH来追踪ATP在340 nm处的转化率。丙酮酸激酶和乳酸脱氢酶执行中间步骤,并且总是过量存在,因此ATPase的活性受速率控制。在任一酶系统的任何调制频率下,在辐照样品和对照样品之间均未获得酶活性的统计学显着差异。

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