Schulz A R
Department of Biochemistry and Molecular Biology, Indiana University School of Medicine, Indianapolis, Indiana 46202-5122, USA.
Arch Biochem Biophys. 1998 May 1;353(1):172-80. doi: 10.1006/abbi.1998.0643.
A minimal model of glycogen metabolism in muscle tissue is analyzed in accordance with metabolic control analysis. The model contains two branch points. Rather than contributing to complexity of the analysis, this branching allows expression of the control coefficients in a simplified form. Glucose 6-phosphate is the metabolite at the first branch point, and the analysis is simplified further by the fact that glucose 6-phosphate is the substrate for enzymes which catalyze near-equilibrium reactions. Control of the concentration of glucose 6-phosphate is of interest because of its pivotal location in the metabolic system, but also because it interacts with an allosteric site on glycogen synthase to stimulate glycogen synthase activity. It is shown that the control which the transporter and enzymes involved in glycogen synthesis exert on glycolytic flux is proportional to the control which these components exert on glucose 6-phosphate concentration. Thus, glycolysis plays a major role in control of glucose 6-phosphate concentration. It is concluded that control of glycogen synthesis is not a rigid parameter of any component of this metabolic system. Rather the distribution of control is flexible and shifts from one portion of the system to another in response to shifts in the physiological state. An important element in determining the distribution of control of glycogen synthesis is the change in the sensitivity of the allosteric site of glycogen synthase to glucose 6-phosphate which is brought about by conversion of glycogen synthase to the dephosphorylated, glucose 6-phosphate-independent, state.
根据代谢控制分析方法,对肌肉组织中糖原代谢的一个最小模型进行了分析。该模型包含两个分支点。这种分支结构非但没有增加分析的复杂性,反而使控制系数能够以简化形式表示。6-磷酸葡萄糖是第一个分支点处的代谢物,而且由于6-磷酸葡萄糖是催化近平衡反应的酶的底物,这一事实进一步简化了分析。对6-磷酸葡萄糖浓度的控制备受关注,这不仅是因为它在代谢系统中的关键位置,还因为它与糖原合酶上的一个别构位点相互作用以刺激糖原合酶活性。结果表明,参与糖原合成的转运蛋白和酶对糖酵解通量的控制与这些组分对6-磷酸葡萄糖浓度的控制成正比。因此,糖酵解在6-磷酸葡萄糖浓度的控制中起主要作用。得出的结论是,糖原合成的控制并非该代谢系统任何组分的一个固定参数。相反,控制的分布是灵活的,并会随着生理状态的变化从系统的一部分转移到另一部分。决定糖原合成控制分布的一个重要因素是糖原合酶别构位点对6-磷酸葡萄糖敏感性的变化,这种变化是由糖原合酶转变为去磷酸化的、不依赖6-磷酸葡萄糖的状态所引起的。