核糖核苷酸前生物聚合的平衡和非平衡反应方案

IF 3.1 Q2 CHEMISTRY, MULTIDISCIPLINARY ChemSystemsChem Pub Date : 2023-09-21 DOI:10.1002/syst.202300033
Varun Kitson, Quentin Sanders, Dr. Avinash V. Dass, Prof. Paul G. Higgs
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摘要

生命起源的 RNA 世界理论要求聚合物最初由非生物反应生成。实验研究了 5′-单磷酸盐、2′,3′-环状磷酸盐和 5′-三磷酸盐的聚合反应。我们考虑了溶液聚合的理论模型,以说明这些情况之间的差异。我们考虑了(i)所有单体都进行可逆连接和断裂的基本模式;(ii)2′,3′-环状磷酸盐可以连接,断裂后环状磷酸盐再生的模式;(iii)除了 2′,3′-环状磷酸盐的连接和断裂外,5′-三磷酸酯可以不可逆连接的模式。在(i)和(ii)的情况下,生成键和断开键之间处于平衡稳定状态。在情况(iii)中,单体被外部磷酸源激活,激活的单体形成聚合物,聚合物断裂释放出未激活的单体,在此过程中存在循环反应通量。平均长度可作为浓度的函数来计算。在情况(iii)中,平均长度从由 5′-三磷酸酯控制的低浓度状态转变为由 2′,3′-环磷酸酯控制的高浓度状态。循环反应通量让人联想到新陈代谢。如果 5'-三磷酸盐的形成已经用于 RNA 合成,那么 ATP 随后可能被用于新陈代谢。
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Equilibrium and Non-equilibrium Reaction Schemes for Prebiotic Polymerization of Ribonucleotides

The RNA World theory for the origin of life requires polymers to be generated initially by abiotic reactions. Experiments have studied polymerization of 5′-monophosphates, 2′,3′-cyclic phosphates, and 5′-triphosphates. We consider theoretical models of polymerization in solution illustrating the differences between these cases. We consider (i) a basic model where all monomers undergo reversible joining and breaking; (ii) a model where 2′,3′-cyclic phosphates can join, and breaking regenerates the cyclic phosphate; (iii) a model where 5′-triphosphates can join irreversibly, in addition to the joining and breaking of 2′,3′-cyclic phosphates. In cases (i) and (ii) there is an equilibrium steady state with balance between making and breaking bonds. In case (iii) there is a circular reaction flux in which monomers are activated by an external phosphate source, activated monomers form polymers, and polymers break to release non-activated monomers. The mean length can be calculated as a function of concentration. In case (iii), the mean length switches from a low-concentration regime controlled by the 5′-triphosphates to a high-concentration regime controlled by the 2′,3′-cyclic phosphates. The circular reaction flux is reminiscent of a metabolism. If formation of 5’-triphosphates was already in place for RNA synthesis, ATP could subsequently been coopted for metabolism.

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