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One step further in the understanding the origins of life
M. Pitk¨anen
Email: matpitka6@gmail.com.
http://tgdtheory.com/.
June 20, 2019
Abstract
The group led by Thomas Carell has made an important step in the understanding the
origins of life. They have identified a mechanism leading to the generation of purines A and
G which besides pyrimidines A,T (U) are the basic building bricks of DNA and RNA. The
crucial step is to make the solution involved slightly acidic by adding protons. In TGD based
model of quantum biology this suggest that the protons in the acidic water are dark and that
the attachment of the dark protons to the amines of the amino-pyrimidine transforms them
to ordinary protons and makes the amino-pyrimidine non-reactive. There would be however
one exception: the amine which reacts further to give purines as a reaction product. In this
case the proton would remain dark and the chemical properties of the amine would remain
intact. The TGD based model for cold fusion and the recent results about superdense phase of
hydrogen identifiable in TGD framework as dark proton sequences giving rise to dark nuclear
strings provides support for this picture.
I learned about very interesting discovery related to the problem of understanding how the
basic building bricks of life might have emerged. RNA (DNA) has nucleotides A,G,C,U (T) as
basic building bricks.
The first deep question is how the nucleotides A,G,C,U, and T emerged.
1. There are two types of nucleotides. Pyrimidines C and T/U (see https://en.wikipedia.
org/wiki/Pyrimidine) have single carbon 6-cycle. Purines A and G (see https://en.
wikipedia.org/wiki/Purine) in turn have single 6-single and 5-cycle fused attached to-
gether along one side. Purines are clearly more complex than pyrimidines.
2. U.K. chemist John Sutherland demonstrated a plausible sequence of steps leading to the
emergence of pyrimidines. Purines turned out to be more problematic. Leslie Orgel and
colleagues suggested a possible pathway but it produces purines in too tiny amounts.
Now a group led by Thomas Carell in Ludwig Maximilian University have found a more plau-
sible mechanism [I2] (see http://tinyurl.com/z65kpyo).
1. Carell and colleagues studied the interaction of biomolecule formamido-pyrimidine (FaPy)
with DNA and found that it also reacts to produce purines. Could FaPys have served as
predecessors of purines? (For formamide see https://en.wikipedia.org/wiki/Formamide
and for the class of chemical compounds known as amines see https://en.wikipedia.org/
wiki/Amine).
2. The first step would have been a copious production of amino-pyrimidines containing several
chemical groups known as amines. The problem is that the are so many amines and they
normally react indiscriminantly to produce many different compounds. One wants mostly
purines so that only one critical amine is wanted.
3. When Carell and his team added some acid to the solution to decrease its pH, a miracle
happened. The extra protons from acid attached to the amines of the amino-pyrimidine and
made them non-reactive. There was however one exception: just the amine giving rise to
purine in its reactions! The reactive amine also readily bonded with formic acid acid (see
https://en.wikipedia.org/wiki/Formic_acid) or formamide. Hence it seems that one
big problem has been solved.
1
2
The second challenge is to understand how the building bricks of RNA and DNA combined to
form longer polymers and began to replicate.
1. One prevailing vision is that so called RNA world preceded the recent biology dominated by
DNA. The goal has been to achieve generation of RNA sequence in laboratory. Unlike DNA
RNA sequences are not stable and long sequences are difficult to generate. DNA in turn
replicates only inside cell and the presence of what is known as ordered water seems to be
essential for this.
2. This step might involve new physics and chemistry and I have considered the possibility that
the new physics involves magnetic bodies and dark proton sequences as a representation of
the genetic code at the level of dark nuclear physics. There is no need to add that the fact that
dark proton states provide representations for RNA, DNA, tRNA, and amino-acids [K1, K2]
looks like a miracle and I find still difficult to believe that it is true and for genetic code.
Also the representation of vertebrate code emerges in terms of correspondences of dark proton
states.
This suggests that the replication of DNA and takes place at the level of dark proton sequen-
cies - dark nuclear strings - serving as a dynamical template for the biological replication.
Also transcription and translation would be induced by dark process. Actually all bio-
chemical processes could have as template the dynamics of molecular magnetic bodies and
biochemistry would be kind of shadow of deeper dynamics.
3. There is actually support for dark proton sequences. Quite recently I learned about the
article of Leif Holmlid and Bernhard Kotzias [C1] (see http://tinyurl.com/hxbvfc7) about
the superdense phase of hydrogen. In TGD superdense phase has interpretation as dark
proton sequences at magnetic flux tubes with the Compton length of dark proton coded
by heff /h '211 to electron’s Compton length [L2]. Remarkably, it is reported that the
superdense hydrogen is super-conductor and super-fluid at room temperatures and even
above: this is just what TGD predicts.
The dark protons in TGD inspired quantum biology (see http://tgdtheory.fi/public_
html/articles/geesink.pdf) should have much longer Compton length of order of the
distance between nucleotides in DNA sequences in order to serve as templates for chemical
DNA. This gives a dark Compton length of order '3.3 Angstroms from the fact that there
are 10 codons per 10 nm. This gives heff /h '218 .
One can return back to the first step in the genesis of DNA and RNA. The addition of protons
to the solution used to model prebiotic environment to make it slightly acidic was the key step.
Why?
1. Here cold fusion might help. Cold fusion is claimed to take place in electrolysis involving
ionization and charge separation. The electric fields used in electrolysis induce ionization
and thus charge separation. For me it has however remained a mystery how electric fields,
which are extremely tiny using the typical strength of molecular electric field as standard are
able to induce a charge separation. Of course, every chemist worth of his salt regards this
as totally trivial problem. I am however foolish enough to consider the possibility that some
new physics might be involved.
2. The mechanism causing charge separation could be analogous to or that discovered by Pollack
as he irradiated water bounded by a gel phase [L1] [L1]: in the recent case the electric field
would take the role of irradiation as a feeder of energy. Negatively charged exclusion zones
(EZs) were formed and 1/4 of protons went somewhere.
The TGD proposal is that part of protons went to magnetic flux tubes and formed dark
proton sequences identifiable as dark nuclear strings. The scaled down nuclear binding en-
ergy favours the formation of dark nuclear strings perhaps proceeding as analog of nuclear
chain reaction. This picture allows to ask whether dark proton sequences giving rise to a
fundamental representation of the genetic code could have been present already in water [L3]!
PARTICLE AND NUCLEAR PHYSICS 3
3. How DNA/RNA could have then formed? Could the protons making the solution acidic
be dark so that the proton attaching to the amine would be dark? Could it be that for
all amines except the right one the proton transforms to ordinary proton and destroys the
chemical reactivity. Could the attached dark proton remain dark just for the correct amine
so that the amine would remain reactive and give rise to purine in further reactions? Could
A,G,C,T and U be those purines and pyrimidines - or even more general biomolecules - for
which the attachment to dark proton does not transform it to ordinary proton and in this
manner affect dramatically the chemical properties of the molecule? What is the condition
for the preservation of the darkness of the proton?
REFERENCES
Particle and Nuclear Physics
[C1] Holmlid L and Kotzias B. Phase transition temperatures of 405-725 K in superfluid ultra-
dense hydrogen clusters on metal surfaces. AIP Advances. Available at: http://tinyurl.
com/hxbvfc7, 6(4), 2016.
Biology
[I1] The Fourth Phase of Water : Dr. Gerald Pollack at TEDxGuelphU. Available at: https:
//www.youtube.com/watch?v=i-T7tCMUDXU, 2014.
[I2] Carell T et al. A high-yielding, strictly regioselective prebiotic purine nucleoside formation
pathway. Science. Available at:http://science.sciencemag.org/content/352/6287/833,
352(6287):833–836, 2016.
Books related to TGD
[K1] Pitk¨anen M. Homeopathy in Many-Sheeted Space-Time. In Bio-Systems as Conscious
Holograms. Online book. Available at: http://www.tgdtheory.fi/tgdhtml/holography.
html#homeoc, 2006.
[K2] Pitk¨anen M. Nuclear String Hypothesis. In Hyper-finite Factors and Dark Matter Hier-
archy. Online book. Available at: http://www.tgdtheory.fi/tgdhtml/neuplanck.html#
nuclstring, 2006.
Articles about TGD
[L1] Pitk¨anen M. Pollack’s Findings about Fourth phase of Water : TGD View. Available at:
http://tgdtheory.fi/public_html/articles/PollackYoutube.pdf, 2014.
[L2] Pitk¨anen M. Cold Fusion Again . Available at: http://tgdtheory.fi/public_html/
articles/cfagain.pdf, 2015.
[L3] Pitk¨anen M. More Precise TGD Based View about Quantum Biology and Prebiotic Evolution.
Available at: http://tgdtheory.fi/public_html/articles/geesink.pdf, 2015.