"Handed-ness", and "racemic: Of or relating to a chemical compound that contains equal quantities of dextrorotatory and levorotatory forms and therefore does not rotate the plane of incident polarized light. ... courtesy of dictionary.com .. more handed-ness" ... I'm sure interesting to some.
Perhaps that's posturing as well, or perhaps these attribues directly address the sanctity of neo-Darwinism; I admit I don't know.
They directly address the issue of multiple biogenesis events.
Specifically, "normal" (laboratory) chemical processes will always produce racemic forms, since there's an even chance of a methyl group attaching to the left side or the right side of any given (symmetric) molecule. Biochemistry appears to be different. Nature has a 'preferred' side; for example, your DNA has a right-handed twist, not the equally plausible but for some reason unfound left-handed version. Similarly, the amino acids that make up your proteins are all levorotary.
We can explain this fairly simply as the result of a single evolutionary coin flip, way back when. The first DNA molecule that happened to form had to be either left- or right-handed, since there's no intermediate choice. But a hypothetical second DNA molecule would only have a 50% chance of being left-handed. If there were a thousand different abiogenesis events that led to the independent creation of DNA, the odds against all the DNA that we see today being left-handed would be the same as the odds of getting heads each time for a thousand coin flips -- essentially negligible.
If, as you suggest, DNA/RNA chemistry was independently reinvented several times, why was it only ever invented on the right side?
We could extend this even further. There's no known reason why left-handed DNA (which we don't have) couldn't work properly with levorotary amino acids (which we do), or why right-hand DNA couldn't work with dextrorotary amino acids. So there's really at least two coin flips involved here.
Similarly, there's really at least twenty coin flips, since there's no known reason why we couldn't use a mixture of dextro- and levorotary acids; biochemistry would probably still be possible with l-cysteine and d-histidine, for example. (In fact, as was pointed out, there are many more than two variations on most amino acids.) But we don't see that combination, either. And the combinations that we do see are the same for all life forms, suggesting a single biogenesis event.
And should separate trees actually exist, how would one differentiate them?
One way was answered above. A tree based on left-handed DNA and dextrorotary amino acids would be notably different, and probably win the Nobel prize for the discoverer. But so far, that doesn't seem to be the case.
ETA: typo fix.
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