Garfinkel L, Kohn M C, Garfinkel D
Eur J Biochem. 1979 May 2;96(1):183-92. doi: 10.1111/j.1432-1033.1979.tb13028.x.
Recycling of fructose 6-phosphate and fructose 1,6-bisphosphate in the rat liver under gluconeogenic and glycolytic conditions was investigated with a computer model containing representations of the kinetic properties of phosphofructokinase and fructose 1,6-bisphosphatase under realistic physiological conditions. The two enzyme submodels were constructed from data for the isolated enzymes in vitro by formal optimization. Tissue metabolite concentrations were corrected for cytosolic/mitochondrial compartmentation and effects of chelation and protonation equilibria. This model, which mostly considers the behavior of livers from starved rats, predicts negligible recycling under physiologically realistic conditions. Metabolic regulation of fructose 6-phosphate, the magnesium ion concentration and the distribution of adenine nucleotides appear to prevent operation of a 'futile cycle' in vivo. Rate-limiting chemical species were identified by sensitivity analysis.
利用一个计算机模型研究了在糖异生和糖酵解条件下大鼠肝脏中6-磷酸果糖和1,6-二磷酸果糖的循环情况,该模型包含了在实际生理条件下磷酸果糖激酶和1,6-二磷酸果糖酶的动力学特性。这两个酶子模型是通过形式优化从体外分离酶的数据构建而成的。针对细胞溶质/线粒体区室化以及螯合和质子化平衡的影响对组织代谢物浓度进行了校正。该模型主要考虑饥饿大鼠肝脏的行为,预测在生理现实条件下循环可忽略不计。6-磷酸果糖的代谢调节、镁离子浓度和腺嘌呤核苷酸的分布似乎可防止体内“无效循环”的运行。通过敏感性分析确定了限速化学物质。