Diederichs Frank
Marschweg 10, D-29690 Schwarmstedt, Germany; E-Mail:
Int J Mol Sci. 2010 Aug 12;11(8):2921-61. doi: 10.3390/ijms11082921.
A new formalism to describe metabolic fluxes as well as membrane transport processes was developed. The new flux equations are comparable to other phenomenological laws. Michaelis-Menten like expressions, as well as flux equations of nonequilibrium thermodynamics, can be regarded as special cases of these new equations. For metabolic network modeling, variable conductances and driving forces are required to enable pathway control and to allow a rapid response to perturbations. When applied to oxidative phosphorylation, results of simulations show that whole oxidative phosphorylation cannot be described as a two-flux-system according to nonequilibrium thermodynamics, although all coupled reactions per se fulfill the equations of this theory. Simulations show that activation of ATP-coupled load reactions plus glucose oxidation is brought about by an increase of only two different conductances: a [Ca(2+)] dependent increase of cytosolic load conductances, and an increase of phosphofructokinase conductance by [AMP], which in turn becomes increased through [ADP] generation by those load reactions. In ventricular myocytes, this feedback mechanism is sufficient to increase cellular power output and O(2) consumption several fold, without any appreciable impairment of energetic parameters. Glucose oxidation proceeds near maximal power output, since transformed input and output conductances are nearly equal, yielding an efficiency of about 0.5. This conductance matching is fulfilled also by glucose oxidation of β-cells. But, as a price for the metabolic mechanism of glucose recognition, β-cells have only a limited capability to increase their power output.
一种用于描述代谢通量以及膜转运过程的新形式主义被开发出来。新的通量方程可与其他唯象定律相媲美。米氏(Michaelis-Menten)型表达式以及非平衡热力学的通量方程,都可被视为这些新方程的特殊情况。对于代谢网络建模,需要可变电导和驱动力来实现途径控制,并允许对扰动做出快速响应。当应用于氧化磷酸化时,模拟结果表明,尽管所有耦合反应本身都符合该理论的方程,但整个氧化磷酸化过程不能根据非平衡热力学被描述为双通量系统。模拟表明,ATP耦合的负载反应加葡萄糖氧化的激活仅由两种不同电导的增加引起:一种是依赖于[Ca(2+)]的胞质负载电导增加,另一种是[AMP]使磷酸果糖激酶电导增加,而[AMP]又通过那些负载反应产生[ADP]而增加。在心室肌细胞中,这种反馈机制足以使细胞功率输出和O(2)消耗增加几倍,而不会对能量参数造成任何明显损害。葡萄糖氧化在接近最大功率输出的情况下进行,因为转化后的输入和输出电导几乎相等,效率约为0.5。β细胞的葡萄糖氧化也满足这种电导匹配。但是,作为葡萄糖识别代谢机制的代价,β细胞增加其功率输出的能力有限。