Barrett T W
Physiol Chem Phys. 1982;14(3):249-79.
Chemical parametric excitation is presented as the fundamental mechanism of energy transfer. Together with the Franck-Condon principle, it provides a mechanically sound explanation for enzymatic reaction, nerve excitation, muscle contraction, and electron transfer at a basic level. Intermediate between macroscopic models of membrane asymmetry and molecular models, the new model rests on a systematic approach, proposed here, to organizational aspects of the energy transfer processes. In support, a derivation is given of the chemical analog of the Manley-Rowe power conservation relations for parametrically excited electrical networks. This extension to chemical systems indicates for the first time an explanation of power flow directionality and delegates a pumping role to the enzyme. The generalized Manley-Rowe relations are suggested to be a universal law of nature. In such case, nonlinearity could be attributable to the coupling of three systems by these generalized Manley-Rowe conditions relating flows/reactions/oscillations--even though separately each system might be described by linear (Onsager) relations.
化学参量激发被视为能量转移的基本机制。它与弗兰克 - 康登原理一起,在基础层面上为酶促反应、神经兴奋、肌肉收缩和电子转移提供了一个合理的力学解释。新模型介于膜不对称性的宏观模型和分子模型之间,基于本文提出的一种系统方法,涉及能量转移过程的组织方面。作为支撑,给出了参数激励电网络的曼利 - 罗功率守恒关系的化学类似物的推导。这种对化学系统的扩展首次表明了对功率流方向性的解释,并赋予酶一个泵浦作用。广义的曼利 - 罗关系被认为是自然界的普遍规律。在这种情况下,非线性可能归因于通过这些将流/反应/振荡联系起来的广义曼利 - 罗条件对三个系统的耦合——尽管每个系统单独可能由线性(昂萨格)关系描述。