Inducing Homochirality Through Intermediary Catalytic Species: A Stochastic Approach.

A new chiral amplification mechanism based on a stochastic approach is proposed. The mechanism includes five different chemical species, an achiral substrate (A), two chiral forms (L, D), and two intermediary species (LA, DA). The process occurs within a small, semipermeable compartment that can be diffusively coupled with the outside environment.

From a coenzyme-like mechanism to homochirality.

Inspired in a coenzyme-like behavior, an alternative mechanism to induce homochirality within a small vesicle is proposed. The system includes six different chemical species: an achiral substrate A, the enantiomeric forms L and D, a coenzyme E and two intermediate catalytic forms LE and DE. Whereas the coenzyme and the intermediate catalytic forms are trapped within the vesicle, the substrate and the two enantiomeric forms are able to diffuse selectively across the vesicle boundary.

The optimal size of protocells from simple entropic considerations.

Potential constraints on protocell size are developed from simple entropic considerations. To do that, two new different indexes as measures of their structural and dynamic order were developed and applied to an elemental model of the heterotrophic protocell. According to our results, cell size should be a key factor determining the potential of these primitive systems to evolve and consequently to support life.

Constraining the Prebiotic Cell Size Limits in Extremely Hostile Environments: A Dynamical Perspective.

The ability to support a replicator population in an extremely hostile environment is considered in a simple model of a prebiotic cell. We explore from a classical approach how the replicator viability changes as a function of the cell radius. The model includes the interaction between two different species: a substrate that flows from the exterior and a replicator that feeds on the substrate and is readily destroyed in the environment outside the cell.