Softellect Systems, Inc, 414-300 Ave Des Sommets, Verdun, QC, H3E 2B7, Canada.
Orig Life Evol Biosph. 2022 Dec;52(4):205-232. doi: 10.1007/s11084-022-09632-9. Epub 2022 Nov 18.
We study a very simple linear evolutionary model based on distribution of protocells by total enantiomeric excess and without any mutual inhibition and show that such model can produce two species with values of total enantiomeric excess in each of the species approaching [Formula: see text] when there is a global [Formula: see text] symmetry. We then consider a scenario when there is a small external global asymmetry factor, like weak interaction, and show that only one of the species remains in such a case, and that is the one, which is more efficient in replication. We perform an estimate of the time necessary to reach homochirality in such a model and show that reasonable assumptions lead to an estimate of around 300 thousand years plus or minus a couple of orders of magnitude. Despite this seemingly large time to reach homochirality, the model is immune to racemization because amino acids in the model follow the lifespan of the protocells rather than the time needed to reach homochirality. We show that not needing mutual inhibition in such evolutionary model is due to the difference in the topology of the spaces in which considered model and many known models of biological homochirality operate. Bifurcation-based models operate in disconnected zero-dimensional space (the space is just two points with enantiomeric excess equal [Formula: see text] and [Formula: see text]), whereas considered evolutionary model (in its continuous representation) operates in one-dimensional connected space, that is the whole interval between [Formula: see text] and [Formula: see text] of total enantiomeric excess. We then proceed with the analysis of the replication process in non-homochiral environment and show that replication errors (the probability to attach an amino acid of wrong chirality) result in a smooth decrease of replication time when total enantiomeric excess of the replicated structure moves away from zero. We show that this decrease in replication time is sufficient for considered model to work.
我们研究了一个非常简单的基于原生细胞总对映过量分布的线性进化模型,且没有任何相互抑制作用,并表明当存在全局[Formula: see text]对称时,这样的模型可以产生两种总对映过量接近[Formula: see text]的物种。然后,我们考虑了存在外部全局不对称因素(如弱相互作用)的情况,并表明在这种情况下只有一种物种仍然存在,而且是复制效率更高的那种。我们对这种模型达到同手性所需的时间进行了估计,并表明合理的假设导致了大约 30 万年左右的估计值,加上或减去几个数量级。尽管达到同手性所需的时间似乎很长,但由于模型中的氨基酸遵循原生细胞的寿命而不是达到同手性所需的时间,因此该模型不受外消旋作用的影响。我们表明,在这种进化模型中不需要相互抑制作用,是因为所考虑的模型和许多已知的生物同手性模型的拓扑结构存在差异。基于分支的模型在不连续的零维空间中运行(该空间只有两个点,对映过量分别为[Formula: see text]和[Formula: see text]),而所考虑的进化模型(在其连续表示中)则在一维连续空间中运行,即总对映过量从[Formula: see text]到[Formula: see text]的整个区间。然后,我们继续分析非同手性环境中的复制过程,并表明当被复制结构的总对映过量远离零时,复制错误(即连接错误手性的氨基酸的概率)导致复制时间的平滑减少。我们表明,这种复制时间的减少足以使所考虑的模型发挥作用。