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首页> 外文期刊>Journal of Neurochemistry: Offical Journal of the International Society for Neurochemistry >Metabolic fate of AMP, IMP, GMP and XMP in the cytosol of rat brain: an experimental and theoretical analysis.
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Metabolic fate of AMP, IMP, GMP and XMP in the cytosol of rat brain: an experimental and theoretical analysis.

机译:大鼠脑胞浆中AMP,IMP,GMP和XMP的代谢命运:实验和理论分析。

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A systematic study of the metabolic fate of AMP, IMP, GMP and XMP (NMP) in the presence of cytosol from rat brain is here presented; the kinetics of both disappearance of NMP, and appearance of their degradation products was followed by HPLC. In the absence of ATP, AMP was preferentially degraded to adenosine with concomitant appearance of inosine and hypoxanthine. In the presence of ATP, AMP was preferentially degraded via IMP. The nucleosides generated in the course of the reactions are further degraded, almost exclusively, via nucleoside phosphorylase using as cofactor the P(i) generated in the reaction mixture. In order to quantify the effect of each one of the enzymes involved in the degradation of NMP, two complementary approaches were followed: (i) the V:(max) and K:(m) values of the enzymes acting in the intermediate steps of the reactions were determined; (ii) these data were introduced into differential equations describing the concentration of the nucleotides and their degradation products as a function of the time of incubation. Factors affecting kinetic parameters of the equation velocity as a function of ATP concentration were introduced when required. The differential equations were solved with the help of Mathematica 3.0. The theoretical method can be used to simulate situations not feasible to be carried out, such as to measure the influence of nM-microM concentrations of ATP on the metabolism of AMP.
机译:本文介绍了在存在来自大鼠脑的胞质溶胶的情况下AMP,IMP,GMP和XMP(NMP)的代谢命运的系统研究; HPLC跟踪NMP消失和其降解产物出现的动力学。在没有ATP的情况下,AMP优先降解为腺苷,并伴随出现肌苷和次黄嘌呤。在ATP存在下,AMP优先通过IMP降解。在反应过程中产生的核苷几乎全部地通过核苷磷酸化酶进一步降解,使用反应混合物中产生的P(i)作为辅因子。为了量化NMP降解所涉及的每种酶的作用,采用了两种互补的方法:(i)在以下中间步骤中起作用的酶的V:(max)和K:(m)值反应已确定; (ii)将这些数据引入微分方程,该微分方程描述了核苷酸浓度及其降解产物随孵育时间的变化。必要时,引入影响方程速度动力学参数随ATP浓度变化的因素。借助Mathematica 3.0解决了微分方程。该理论方法可用于模拟不可行的情况,例如测量nM-microM ATP浓度对AMP代谢的影响。

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