Himeoka Yusuke, Kirkegaard Julius B, Mitarai Namiko, Krishna Sandeep
Universal Biology Institute, University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, Japan.
The Niels Bohr Institute, University of Copenhagen, Blegdamsvej 17, 2100, Copenhagen, Denmark.
Sci Rep. 2024 Sep 27;14(1):22187. doi: 10.1038/s41598-024-73104-5.
Understanding the relationship between the structure of chemical reaction networks and their reaction dynamics is essential for unveiling the design principles of living organisms. However, while some network-structural features are known to relate to the steady-state characteristics of chemical reaction networks, mathematical frameworks describing the links between out-of-steady-state dynamics and network structure are still underdeveloped. Here, we characterize the out-of-steady-state behavior of a class of artificial chemical reaction networks consisting of the ligation and splitting reactions of polymers. Within this class, we examine minimal networks that can convert a given set of sources (e.g., nutrients) to a specified set of targets (e.g., biomass precursors). By exploring the dynamics of the models with a simple setup, we find three distinct types of relaxation dynamics after perturbation from a steady-state: exponential-, power-law-, and plateau-dominated. We computationally show that we can predict this out-of-steady-state dynamical behavior from just three features computed from the network's stoichiometric matrix, namely, (1) the rank gap, determining the existence of a steady-state; (2) the left null-space, being related to conserved quantities in the dynamics; and (3) the stoichiometric cone, dictating the range of achievable chemical concentrations. We further demonstrate that these three quantities relates to the type of relaxation dynamics of combinations of our minimal networks, larger networks with many redundant pathways, and a real example of a metabolic network. The relationship between the topological features of reaction networks and the relaxation dynamics presented here are useful clues for understanding the design of metabolic reaction networks as well as industrially useful chemical production pathways.
理解化学反应网络的结构与其反应动力学之间的关系对于揭示生物体的设计原理至关重要。然而,虽然已知一些网络结构特征与化学反应网络的稳态特性相关,但描述非稳态动力学与网络结构之间联系的数学框架仍未充分发展。在这里,我们表征了一类由聚合物的连接和分裂反应组成的人工化学反应网络的非稳态行为。在这类网络中,我们研究了能够将给定的一组源(例如营养物质)转化为特定的一组目标(例如生物质前体)的最小网络。通过用简单的设置探索模型的动力学,我们发现在从稳态受到扰动后有三种不同类型的弛豫动力学:指数主导型、幂律主导型和平原主导型。我们通过计算表明,仅从网络化学计量矩阵计算出的三个特征就可以预测这种非稳态动力学行为,即:(1)秩差,决定稳态的存在;(2)左零空间,与动力学中的守恒量有关;(3)化学计量锥,决定可实现的化学浓度范围。我们进一步证明,这三个量与我们的最小网络组合、具有许多冗余途径的更大网络以及一个代谢网络实例的弛豫动力学类型有关。这里呈现的反应网络拓扑特征与弛豫动力学之间的关系是理解代谢反应网络设计以及工业上有用的化学生产途径的有用线索。