Molecular chirality is inherent to biology and cellular
chemistry.
In this report, the origin of enantiomeric selectivity is analyzed
from the viewpoint of the “RNA World” model, based on
the autocatalytic turnover of glyceraldehyde as a precursor for simple
sugars, and in particular ribose, as promoted by the formose reaction.
Coupling of formaldehyde and glycolaldehyde produces glyceraldehyde,
which contains a chiral carbon center that is carried through in formation
of the ribose ring. The parity non-conserving weak nuclear interaction
is the only inherently handed property in nature and is herein shown
to be sufficient to differentiate between two enantiomeric forms in
an autocatalytic reaction performed over geologically relevant time
scales, but only in the presence of catalytic metal ions such as divalent
calcium or higher Z alkaline earth elements. This
work details calculations of the magnitude of the effect, the impact
of various geologically available metal ions, the effect of time and
temperature, and their influence on chiral selection in the molecules
of life. Alternative mechanisms are also considered, and a method
of resolving these is proposed.