Life chirality problem can be solved in more steps. A most general question is, why the organisms are accepting the matter and energy in different ways, at second we should explain, why the energy and building blocks molecules differs in chirality, while the third (apparently more difficult question) is, why just the D-sugars and L-amino-acids are accepted by living creatures, but not vice-versa.
The first question isn't so apparent in this moment, but it's connected to dual character of stable forms of matter, which are divided into fermions (female) and boson (male) particles (elements). Both males, both females are occupying their homes/shells/nests, which can be interpreted as sinuses formed by building blocks. In social species, the females are collecting a building blocks, while males are foraging another energy sources preferably. The second question is related to problem, why the building blocks are usually collected from local sources or proximity, while food and energy sources are collected from longer distance and the third problem is related to question, why females tends to forage a food and building blocks, while the males are specialized in collecting of energy sources preferably, usually from outside of their homes.
We can observe an apparent chirality in SU(3) Young polyominos defined in 3D by 2x2x2 Jourdan triade matrix of mutual male/female, mass/energy and proximity/distance dualities, which follows from the fact, the males are movable like energy supplies (a prey) and therefore they appear at the longer distance from homes. This chirality is repeated in many fractal levels, because the fermion particles are serving as a food/energy supplies for subsequent nested levels of food chain.
By AWT the concept of CP invariance violation and chirality of life are closely related by concept of foam, composed of walls/membranes of nonzero thickness. The particles are formed by standing wave packets, spreading along surfaces of these membranes, but the situation of inner and outer surface isn't always very same.
The particles formed by inner gradients of Aether foam membranes are always of higher space-time curvature and mass/energy density, then these outer ones. During condensation of foam the particles formed by inner surfaces will condense into fermions - while the rest of matter will evaporate instead into particles of energy, i.e. the bosons. While total chirality is retained, the evaporating bosons are formed by super-symmetric anti-particles preferably. By AWT during Universe formation (a Big-Bang event) a symmetric graviton foam was formed first. This foam was formed by membranes with (nearly) no preference in concave or convex curvature. The similar foam is formed at the beginning of supercritical fluid condensation.
Whenever the density of graviton foam has increased, a second phase transition has occurred, so called the inflation. During this a system was formed, consisting of nested density fluctuations separated by membranes, composed by adjacent pair of surface gradients. After then the condensation of matter has separated into two branches. A density fluctuations formed by inner walls of foam branes have continued in condensation, forming a dense particles of observable matter. While the second portion of particles has evaporated instead into anti-symmetric bosons, which formed the sparse streaks of dark matter.
We can assume, the very same process has repeated later during life formation. By AWT the life was formed in so-called liposomes, formed by fragmentation of tiny oily droplets at the stormy surface of ancient oceans. Every liposome is very small (i.e. of high surface curvature) and it has a double surface, formed by hydrophobic membranes. In such system, the surface tension phenomena cannot be neglected, because the highly concave surface exhibits so-called superhydrophobicity, so it repels the carbohydrate molecules with many -OH functional groups, which are collected preferably inside of liposome. While the building blocks of organic matter, i.e. the amino-acids with hydrophobic radicals should adsorb at the outer surface of liposome, preferably. This forms natural condition for spatial arrangement of t-RNA components at the phase interface of liposomes. They should probably form spontaneously in thin dispersion of lipids in solution of aminoacids and ribose mixture.
The chirality of liposome follows from so called Hairy ball theorem: every surface of droplet should contain an at least two quantum vortices (an analogy of Cooper pairs condensation in solid state physics) and these vortices are of opposite chirality due the geometry reasons. So that the chiral molecules should separate on both surfaces of liposome by its helicity. For liposomes of larger diameter there is higher number of quantum vortices just at the outer surface of liposome, which is always slightly larger due the nonzero thickness of lipid bilayer (a liposome membrane).
By such way, a chiral organic molecules should obtain their distribution from the very beginning of liposome formation, i.e. it's not accidental, one-shot process depending on panspermia event - but in quite reversible process, which should be replicated in experiments both in supercritical fluid or boson condensate systems, both in liposome dispersions in laboratory conditions. This explanation supports the contemporary models of terrestrial life formation, by which sponges are one of the first multicellular organisms. By AWT the life was formed from liposome foam and the ancient sponges are just another nested phase of it (i.e. sponge of cellular sponge by the same way, like atom nuclei are formed by quantum foam of smaller strings, etc..).
Energy spreads by slowest speed just along foam surfaces, so AWT prefers atemporal fractal foam structures during gradual evolution of complexity over other geometries and the above findings are consistent with this concept.