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Pitkänen, M., Potential ”Missing Link” in Chemistry that Led to Life on Earth Discovered

Essay

Potential ”Missing Link” in Chemistry that Led to Life on Earth
Discovered

Matti Pitkänen 1

Abstract

The phosphorylation of short nucleotide sequences, amino-acid sequences, and lipids making possi-
ble formation of small cell membrane like structures is necessary for the formation of larger structures
from their building bricks. As noticed, ribozymes catalyze only dephosphorylation. How RNA was
phosphorylated during RNA era or were the amino-acids present all the time? It was recently dis-
covered that an organic molecule known as diamidophosphate (DAP) having chemical formula could
do the job in presence of water and imidazol. DAP could solve several problems simultaneously: how
the short sequences of RNA (later DNA) and amino-acids emerged, and how the predecessors of cell
membranes emerged. It is not however whether this process could have been fast enough or whether
the slowness only made the first step painful. This problem will be discussed in the sequel.

1 Introduction

In the attempts to understand pre-biology the basic challenge is to understand how the needed short
RNA, DNA, and amino-acid sequences managed to form. Phosphorylation (see http://tinyurl.com/

y732fsd3) is known to be crucial for this process and means energization in standard bio-chemistry. Or-
ganic phosphate (see http://tinyurl.com/cx9ukv9) possesses somewhat mysterious high energy phos-
phate bond, which stores energy and makes possible metabolism: in metabolic ATP with three phosphates
transforms to ADP with two phosphates by giving one phosphate with high energy phosphate bond to
the acceptor molecule, which is therefore phosphorylated.

In the recent biology phosphorylation of various biomolecules such as DNA, RNA, amino-acid se-
quences is catalyzed by proteins known as enzymes known as phosphorylases. Kinase is one particular
enzyme transferring phosphate from ATP to the acceptor molecule. Proteins consist of amino-acids and
would not be present in RNA world, which serves almost as a standard model for the prebiotic period.
Ribozymes are catalysts formed from RNA but they catalyze typically only the reversal of phosphoryla-
tion.

The phosphorylation of short nucleotide sequences and amino-acid sequences, and also lipids making
possible formation of small cell membrane like structures is necessary for the formation of larger structures
from their building bricks. As noticed, ribozymes catalyze only dephosphorylation. How RNA was
phosphorylated during RNA era or were the amino-acid present all the time?

The popular article with the title ”Potential ’missing link’ in chemistry that led to life on Earth dis-
covered” (see http://tinyurl.com/y9s56xnx) tells about a mechanism allowing phosphorylation dur-
ing RNA era in absence of enzymes. The discovery [2] (see http://tinyurl.com/y9kvgl24) is that
an organic molecule known as diamidophosphate (DAP) (see http://tinyurl.com/y88vecs2) having
chemical formula PO2(NH2)−1

2 could do the job in presence of water and imidazol. Imidazol (see
http://tinyurl.com/y8vgfr42) has chemical formulaC3N2H4 and is a molecule possessing aromatic
hetero-cycle consisting of 3 C atoms and 2 N atoms.

Remark: Pyrimidine (see http://tinyurl.com/k3vxl9b) in turn is aromatic hetero-6-cycle con-
sisting of 4 C atoms and 2 N atoms and having formula C4N2H4. DNA (see http://tinyurl.com/

cpndtse) has as basic building bricks phosphates PO−
4 having valence bonds with deoxy-ribose (see

1Correspondence: Matti Pitkänen http://tgdtheory.com/. Address: Rinnekatu 2-4 A8, 03620, Karkkila, Finland. Email:
matpitka6@gamail.com.

ISSN: 2159-046X DNA Decipher Journal www.www.dnadecipher.com

Published by QuantumDream, Inc.

http://tinyurl.com/y732fsd3
http://tinyurl.com/y732fsd3
http://tinyurl.com/cx9ukv9
http://tinyurl.com/y9s56xnx
http://tinyurl.com/y9kvgl24
http://tinyurl.com/y88vecs2
http://tinyurl.com/y8vgfr42
http://tinyurl.com/k3vxl9b
http://tinyurl.com/cpndtse
http://tinyurl.com/cpndtse
http://tgdtheory.com/
mailto:matpitka6@gmail.com


DNA Decipher Journal | December 2017 | Volume 7 | Issue 2 | pp. 129-134 130

Pitkänen, M., Potential ”Missing Link” in Chemistry that Led to Life on Earth Discovered

http://tinyurl.com/qxv9kg8) molecules (containing 5-rings with 4 C atoms and one O). Each sugar
has valence bond with N of nucleoside C, T, A or G. C and T are pyrimidines with single aromatic 6-ring
and A and G are purines obtained by fusing imidazol 5-ring and pyrimidine 6-ring to obtain purine double
ring. By replacing one OH of de-oxyribose of DNA with H one obtains RNA.

DAP could solve several problems simultaneously: how the short sequences of RNA (later DNA) and
amino-acids were formed, and how the predecessors of cell membranes emerged. It is not however clear
to me whether this process could have been fast enough or whether the slowness only made the first step
painful. This finding will be discussed in TGD framework.

2 How could the discovery relate to TGD inspired quantum
biology?

It is interesting to interpret the discovery in TGD framework. The basic question is whether the presence
of dark atoms and electrons in bio-molecule distinguish between atomic physics, in-organic chemistry, and
organic chemistry. Usually organic chemistry is defined to be chemistry of carbon compounds, typically
hydrocarbons. Could it be that the formation of hydrocarbons involves dark variants of proton and
electron identified as heff = n× h variants of ordinary proton and electron?

2.1 From atomic physics to chemistry

How could one proceed from atomic physics to atomic physics to chemistry in TGD framework. The basic
question is how to understand valence bond: it is not at all clear whether mere Schrödinger equation allows
to understand it. Could the emergence of dark electrons allow their delocalization and formation of valence
bonds? It has been known for decades that the heating of rare-earth metals leads to a mysterious loss
of some valence electrons and the explanation would be the energy provided by heating kicks them to
higher energy states by making some valence electrons dark [9]. The explanation would be in terms of
dark electron orbitals for valence electrons which have radii scaled up by factor n2 and are analogous to
Rydberg states identified as orbitals with large value of principal quantum number and having very large
radius.

The dark variants of atoms have binding energy scale reduced by factor 1/n2 so that their formation
requires energy feed (perhaps radiation at required frequencies). One or more valence electrons of ordinary
atom could be dark so that the size of the orbital is scaled up by factor n2. The valence bond central
for chemistry in general and in particular for basic biopolymers could contain dark electrons delocalized
because of larger value of n than for the non-valence electrons. Note that one could be n = n0 > 1 for
ordinary atoms making in principle possible atoms with n < n0 with anomalous large binding energy also
for the filled shells as the findings of Randel Mills indeed suggest [6].

Surprisingly, dark electrons would be essential in ordinary chemistry thought to reduce to standard
model physics! The increase of n reduces binding energy scale and requires energy feed. This would allow
to understand why anabolism (see http://tinyurl.com/c8x8avz) - that is generation of biopolymers
from their building blocks by generating valence bonds - requires energy feed and why catabolism (see
http://tinyurl.com/cbx99fv) - the splitting of biopolymers to their building blocks by splitting the
valence bonds liberates energy.

The valence bonds would be classified by the value of n and it is quite possible that in organic chemistry
the values of n are larger than in in-organic chemistry. Could this mean that valence bonds H and C and
N and O have higher values in bio-chemistry? Also the valence bonds between O and H in water could
have larger value of n.

To sum up, the transition from atomic physics to ordinary chemistry involved generation of dark
electrons associated with valence bonds. The value of n for dark electrons can vary and allow hierarchy
of evolutionary steps with increasingly delocalized valence electrons.

ISSN: 2159-046X DNA Decipher Journal www.www.dnadecipher.com

Published by QuantumDream, Inc.

http://tinyurl.com/qxv9kg8
http://tinyurl.com/c8x8avz
http://tinyurl.com/cbx99fv


DNA Decipher Journal | December 2017 | Volume 7 | Issue 2 | pp. 129-134 131

Pitkänen, M., Potential ”Missing Link” in Chemistry that Led to Life on Earth Discovered

2.2 From chemistry to bio-chemistry

What about the step leading to a genuine bio-chemistry involving genetic code? Magnetic body (MB)
is the basic aspect of biochemistry according to TGD. Pollack effect [1] (see http://tinyurl.com/

y8uxocch) leading to the formation of negatively charged regions - exclusion zones (EZs) - would involve
generation of dark protons at magnetic flux tubes of MB with electrons left to the EZ - possible as
ordinary particles [4]. Also Pollack effect requires feeding of energy, say as irradiation by photons.

DNA is stable against spontaneous hydration only inside cell membrane. This suggests that the EZs of
Pollack containing partially dark water molecules satisfying effectively the stoichiometry H3/2O allowed
to stabilize DNA. Therefore EZs are excellent candidates for the predecessors of cell.

The TGD inspired proposal is that DNA strand for which each phosphate has negative unit charge
is companied by dark analog of DNA consisting of dark protons such that the states of 3-proton units
are in one-one correspondence with DNA, RNA, tRNA and amino-acids and the degeneracies of the
vertebrate genetic code (number of codons coding for given amino-acid) come out correctly [5] (see
http://tinyurl.com/jgfjlbe). A more general picture is that ordinary chemistry is kind of shadow for
the dynamics of dark matter at magnetic flux tubes doing its best to emulate it. This would explain also
why genetic code has also other variants.

It would be the emergence of dark protons with large enough value of n, which would distinguish
between ordinary chemistry and bio-chemistry. Water is basic element of life and hydrogen bonding
is responsible for the formation of water clusters - certainly one of the key aspects of bio-chemistry.
Hydrogen bonds (see http://tinyurl.com/bntn28n) appear between highly electronegative (see http:

//tinyurl.com/pbh6r6c) atoms such as O, N, and F (electronegativity is roughly the tendency to attract
electrons). What distinguishes hydrogen bond from valence bond is that it is proton rather than electron,
which is delocalized. This suggests that the delocalized proton is dark proton at magnetic flux tube
connecting the hydrogen bonded molecules.

2.3 The emergence of metabolism

In the proposed framework the first basic aspect of life would be the generation of dark electrons and
protons using energy feed and their transfer between molecules and their generation by providing the
needed energy.

1. Metabolism (anabolism) would provide the energy needed to transform ordinary atom (that is
electron bound to it) to a dark atom with large value of heff/h = n. This requires energy since the
binding energy is proportional to 1/n2 and reduced in the process. This is quite generally true for
all dark variants of quantum states. One can say that the increase of the complexity of the system
by increasing n characterizing its ”IQ” requires metabolic energy (in adelic physics [10, 11] ”IQ”
has a concrete interpretation as cognitive resources). Therefore the first steps of prebiotic life was
the emergence of energy feed mechanism making possible the increase of n.

2. I have considered the possibility that the period of prebiotic life preceding the the emergence of
chemical storage of energy used dark nucleosynthesis [7] (see http://tinyurl.com/y7u5v7j4) as
the source of metabolic energy. The recently discovered life-like properties [3] in a very simple
system consisting of negatively charged plastic balls in the plasma of Ar+ ions allows to develop
rather detailed ideas about this phase of life [8] (see http://tinyurl.com/yassnhzb).

3. A fundamental question is about the step leading to the chemical storage of metabolic energy to
valence bonds with non-standard value of n. Solar radiation could have generated both negatively
charged EZs identifiable as possible predecessors of cell membrane and valence bonded molecules
storing metabolic energy.

ISSN: 2159-046X DNA Decipher Journal www.www.dnadecipher.com

Published by QuantumDream, Inc.

http://tinyurl.com/y8uxocch
http://tinyurl.com/y8uxocch
http://tinyurl.com/jgfjlbe
http://tinyurl.com/bntn28n
http://tinyurl.com/pbh6r6c
http://tinyurl.com/pbh6r6c
http://tinyurl.com/y7u5v7j4
http://tinyurl.com/yassnhzb


DNA Decipher Journal | December 2017 | Volume 7 | Issue 2 | pp. 129-134 132

Pitkänen, M., Potential ”Missing Link” in Chemistry that Led to Life on Earth Discovered

2.4 About bio-catalysis

Without bio-catalysis biochemical reactions leading to the formation of biopolymers and cell membrane
would be quite too slow. Here phosphorylation enters the game.

1. The TGD based model for bio-catalysis relies on the temporary reduction of heff = n×h liberating
energy kicking the reactants over potential wall. After this step the catalyst - at least in the ideal
situation - receives the energy and the atom becomes dark again.

2. Acid catalyst gives a proton and base catalyst gives an electron. Most bio-catalysts are acid cat-
alysts. The TGD based interpretation should rely on the possibility of dark valence electrons and
dark protons at flux tubes. Since base catalysts are associated with non-organic chemistry, the
identification of the electron given by base catalyst as dark electron looks natural. Acid catalysts
would give dark proton.

Bio-catalysts are usually activated by phosphorylation and de-activated by de-phosphorylation but
there are exceptions to this rule. This can be understood if the catalyst activates a molecule acting as
a switch for a reaction. Catalysts related to phosphorylation are known as phosphotransferasess (see
http://tinyurl.com/y87crqad) and contain kinases transferring phosphate from ATP to the acceptor
molecules.

Phosphatases (see http://tinyurl.com/ybf9onba) remove phosphate from the target molecule: they
are hydrolases (see http://tinyurl.com/y88zayj7) and use water to remove the phosphate and to
hydrate the molecule.

2.4.1 The difference between organic and inorganic phosphates

Phosphate appears as too variants: organic and inorganic.

1. Organic phosphates bound to biomolecules have charge -1. Some electrons of organic phosphate
ion have transformed to valence electrons and are therefore dark. Also some protons - one dark
proton per dark electron to not affect the observed charge in short scales - would be dark and at the
magnetic body of the organic phosphate. Both dark protons and dark electrons would be present
and give rise to somewhat mysterious high energy phosphate bond.

2. Free phosphate in water environment appears in ionized variants HnPOn−4
4 and is regarded as

in-organic and have negative charge 4-n. In inorganic phosphate some dark protons and ordinary
electrons giving rise to the negative charge have combined to hydrogen atoms. The larger the
number of hydrogens is, the higher the level of inorganicity is.

The fractions of variants of free phosphate in water depend on pH characterizing the density of
protons present. Could pH in fact characterize the fraction of dark protons at magnetic flux tubes?
Or could it also characterize the fraction of dark hydrogen atoms present. Similar question applies
to the counterparts of pH for other biologically important ions.

2.4.2 About phosphorylation and the interpretation of DAP

At chemical level phosphorylation attaches phosphate ion to the hydroxyl group (R-OH) of the acceptor
molecule. At deeper level phosphorylation would give dark electron to the acceptor molecule and dark
proton to its MB. Phosphorylation would increase the quantum coherence length: the formation of short
RNA, amino-acid sequences and of cell membrane like structures would be a basic example of this.

What about the interpretation of the role of DAP in this framework? DAP has charge -1 as also the
phosphate bound to DNA and RNA have (in ATP the outermost phosphate has charge -2). DAP is very
similar to the phosphate in DNA and RNA and expected to carry high energy phosphate bond. In TGD
framework it would possess both dark valence electrons and dark protons at magnetic flux tubes with

ISSN: 2159-046X DNA Decipher Journal www.www.dnadecipher.com

Published by QuantumDream, Inc.

http://tinyurl.com/y87crqad
http://tinyurl.com/ybf9onba
http://tinyurl.com/y88zayj7


DNA Decipher Journal | December 2017 | Volume 7 | Issue 2 | pp. 129-134 133

Pitkänen, M., Potential ”Missing Link” in Chemistry that Led to Life on Earth Discovered

only one ordinary electron responsible for the charge of DAP. Due to the properties of phosphatase the
phosphorylation would be very simple process at the level of dark electron and proton. Hence DAP and
imidazole could make possible the phosphorylation.

2.4.3 About dephosphorylation and phosphoryl transfer

The scanning of web shows that some sources talk of dephosphorylation and some sources about phos-
phoryl transfer reactions and it remained unclear to me whether the two terms really have the same
meaning. In any case, in TGD framework one can distinguish between these notion. Dephosphorylation
could mean either phosphoryl transfer (transfer of phosphate between donor and acceptor molecules) or
”dropping” of organic phosphate to water environment and giving it negative additional negative charge
(the transfer would be now to water environment) and making it inorganic.

1. Phosphoryl would transfer removes PO−
4 group and presumably also the associated dark proton

from the target and transfers them to the acceptor molecule and its MB. I have proposed that
reconnection of flux tubes transforms the flux tubes entering to the donor molecule to that associated
with the acceptor molecule so that dark proton is automatically transferred. In ATP-ADP process
the phosphate group and presumably also the dark proton and electron would be transferred to the
acceptor molecule from ATP. ADP is dephosphorylated and acceptor phosphorylated.

2. In ”dropping” the outcome would be in-organic phosphate denoted by Pi, which is a mixture of
HPO−2

4 and H2PO−1
4 . One interpretation is that 1 or 2 dark protons from magnetic flux tubes

have transformed to ordinary protons and combined with electrons to form hydrogen atoms. This
operation would reduce the number of dark particle and thus the ”evolutionary level” of the system.

Dephosphorylation is known to lead to a decomposition of the donor molecule to smaller structures,
indicating the reduction of heff/h = n and thus of quantum coherence length. In RNA world dephos-
phorylation would be catalyzed by ribozymes and in some important cases also in the recent biology.
Dephosphorylation would reduce quantum coherence length and lead to the decomposition of structures
to smaller ones: mRNA splicing is one example of this. Catabolism of nutrients and the decay process of
dead organic matter provide further basic examples.

Catabolism (see http://tinyurl.com/cbx99fv) of nutrients and the decay process of dead organic
matter suggest what happens. In the first preliminary step of catabolism catalysts are involved. At the
second step of catabolism inorganic phosphate is formed, which suggests that the number of dark protons
is reduced in the process. This conforms with the reduction of the value of heff/h = n.

References

[1] The Fourth Phase of Water : Dr. Gerald Pollack at TEDxGuelphU. Available at: https://www.

youtube.com/watch?v=i-T7tCMUDXU, 2014.

[2] Gibard C et al. Phosphorylation, oligomerization and self-assembly in water under potential prebiotic
conditions. Nature Chemistry. doi:10.1038/nchem.2878, 2017.

[3] Gogia G and Burton JC. Emergent Bistability and Switching in a Nonequilibrium Crystal. arXiv.org.
Available at: http://tinyurl.com/ychho4l8, 2017.

[4] Pitkänen M. Pollack’s Findings about Fourth phase of Water : TGD View. Available at: http:

//tgdtheory.fi/public_html/articles/PollackYoutube.pdf, 2014.

[5] Pitkänen M. About Physical Representations of Genetic Code in Terms of Dark Nuclear Strings.
Available at: http://tgdtheory.fi/public_html/articles/genecodemodels.pdf, 2016.

ISSN: 2159-046X DNA Decipher Journal www.www.dnadecipher.com

Published by QuantumDream, Inc.

http://tinyurl.com/cbx99fv
https://www.youtube.com/watch?v=i-T7tCMUDXU
https://www.youtube.com/watch?v=i-T7tCMUDXU
http://tinyurl.com/ychho4l8
http://tgdtheory.fi/public_html/articles/PollackYoutube.pdf
http://tgdtheory.fi/public_html/articles/PollackYoutube.pdf
http://tgdtheory.fi/public_html/articles/genecodemodels.pdf


DNA Decipher Journal | December 2017 | Volume 7 | Issue 2 | pp. 129-134 134

Pitkänen, M., Potential ”Missing Link” in Chemistry that Led to Life on Earth Discovered

[6] Pitkänen M. Hydrinos again. Available at: http://tgdtheory.fi/public_html/articles/

Millsagain.pdf, 2016.

[7] Pitkänen M. Cold fusion, low energy nuclear reactions, or dark nuclear synthesis? Available at:
http://tgdtheory.fi/public_html/articles/krivit.pdf, 2017.

[8] Pitkänen M. Life-like properties observed in a very simple system. Available at: http://tgdtheory.
fi/public_html/articles/plasticballs.pdf, 2017.

[9] Pitkänen M. Mysteriously disappearing valence electrons of rare Earth metals and hierarchy of
Planck constants. Available at: http://tgdtheory.fi/public_html/articles/rareearth.pdf,
2017.

[10] Pitkänen M. Philosophy of Adelic Physics. In Trends and Mathematical Methods in Interdisci-
plinary Mathematical Sciences, pages 241–319. Springer.Available at: https://link.springer.

com/chapter/10.1007/978-3-319-55612-3_11, 2017.

[11] Pitkänen M. Philosophy of Adelic Physics. Available at: http://tgdtheory.fi/public_html/

articles/adelephysics.pdf, 2017.

ISSN: 2159-046X DNA Decipher Journal www.www.dnadecipher.com

Published by QuantumDream, Inc.

http://tgdtheory.fi/public_html/articles/Millsagain.pdf
http://tgdtheory.fi/public_html/articles/Millsagain.pdf
http://tgdtheory.fi/public_html/articles/krivit.pdf
http://tgdtheory.fi/public_html/articles/plasticballs.pdf
http://tgdtheory.fi/public_html/articles/plasticballs.pdf
http://tgdtheory.fi/public_html/articles/rareearth.pdf
https://link.springer.com/chapter/10.1007/978-3-319-55612-3_11
https://link.springer.com/chapter/10.1007/978-3-319-55612-3_11
http://tgdtheory.fi/public_html/articles/adelephysics.pdf
http://tgdtheory.fi/public_html/articles/adelephysics.pdf

	Introduction
	How could the discovery relate to TGD inspired quantum biology?
	From atomic physics to chemistry
	From chemistry to bio-chemistry
	The emergence of metabolism
	About bio-catalysis
	The difference between organic and inorganic phosphates
	About phosphorylation and the interpretation of DAP
	About dephosphorylation and phosphoryl transfer



