Gravity Driven Cosmological Evolution and the Origin of Life



Hypothesis

Driven by reaction to the Big Bang in a fully deterministic process directed at opposing expansion of space/time, gravity generates a logically sequential set of energy/matter transitions leading to and incorporating intelligent life.

Background

At present origin-of-life science is largely a hit or miss affair lacking any overall theory or guiding principle, with the result that almost any suggestion concerning some possible precursor physics or chemistry can be considered potentially relevant. This proposal, in contrast, offers a coherent and rigidly deterministic framework governing the mechanisms of cosmological evolution which extends to all classes of energy transduction reactions from astrophysical to biochemical. If proven correct, therefore, the effect would be to focus and organize investigation into strictly circumscribed relevant subjects, thereby shortening the research effort by at least several decades.
This hypothesis addresses relationships between cosmological expansion, evolution, life and origins. The basic principle demands that in order to understand life it is essential first to view it in its context, that of an expanding universe. What is the connection between life and expansion? To answer this question we need to consider gravitational attraction as a reaction to, and therefore generated by, universal expansion. The forcible curving or distortion of space/time by Big Bang expansion generates an equal and opposite counter-force, gravity, which as a result acts as if to return energy/matter to its primordial state in a singularity. Since the universe appears to be expanding at an increasing rate, clearly gravitational forces are frustrated in that they are not powerful enough to counter the energy released by the Big Bang and re-condense it in its entirety in a single locality. Gravity is therefore obliged to follow more circuitous routes to accretion. If, having established these principles, we then consider the situation of intelligent organisms 1011 years or so from now, when energy/matter density will have attenuated to an extreme degree, we see that being critically dependent on a sufficient concentration of energy/matter, organisms will be obliged to act as agents of the gravitational force and develop mechanisms, such as manipulation of black hole dynamics, to attract energy/matter and maintain it in their vicinity. This fact suggests the intriguing possibility that live organisms may actually be, in a physical sense, creations or extensions of universal gravitation – robots compelled, with no particular outcome assured, to control the expansion of space/time through a directed ability to analyze and manipulate the cosmos, at least locally. Does gravitational accretion actually have the potential to spawn such a high degree of complexity? In order to appreciate the organizing, creative capacity of gravitation one need only consider its ability to acquire an amorphous cloud of hydrogen atoms and to manipulate it by accretion alone in order to generate the structural and functional complexity of the myriad astrophysical objects now seen to populate our universe. Further examination of this intellectually and emotionally challenging hypothesis does indeed reveal a logically coherent sequence of obligate structures and processes, a continuous series of phase transitions historically generated by graduated increases in condensation of matter accompanied by their cognate energy transduction mechanisms leading to the generation of biological functionality. One of the crucial evolutionary transitions is the repeated frustration of energy/matter accretion into black holes by interceding supernova events with a resulting redistribution of elements, including radioactive isotopes. These radioisotopes eventually settle in inner planetary bodies and following fractionation, gather in placer deposits under pressures of 1-3 GPa. In such a highly energetic environment, driven by a powerful flux of a-, b- and g-particles, the biogenic elements, CHNOPS, will be rapidly generated by de novo nucleosynthesis through activation of triple alpha reactions and the CNO cycle normally associated with stellar cores. Held in close confinement under supercritical conditions, these elements will then be obliged to assemble in stable energy storing and transduction structures – cyclic peptides, polyamines and chromophores including porphyrins, FMN, NTP, cAMP and highly conserved very small catalytic micro RNAs consisting of two or three nucleotides, e.g. cyclic diguanylic acid. Such reactions are clearly non-trivial as we now know that low molecular weight signalling modulators and nucleic acids regulate a diverse array of biological metabolic functions, catalyzing various types of polymerization reactions as well as bond formation including C-C bonds. The primary characteristic of these micro RNAs is that they are catalytic, meaning that they possess the ability to acquire energy and use it to manipulate their environment in specifically directed ways, an essential step on the road to life.



Report and Conclusions

Could life be the result of random chemical “accidents” or is it more likely to be rooted deterministically in the fundamental physics of cosmological evolution? Our current knowledge of the intricacy and complexity of biological function, together with hints of its aetiology, clearly render the isolated chemical accident or serendipitous hypothesis impossible to sustain. Furthermore attempts over many decades to determine a point of origin for life, the standard approach, have met with little success because they ignore the increasing evidence for continuity and tight entaglement which characterizes global evolutionary processes. In other words, there can not be a specific point of origin for life apart from the Big Bang itself. So the question is – What are the physical processes which would generate biological function as well as the qualifier we label intelligence?  In order to understand life it is essential first to view it in its context, that of an expanding universe and, as described in the Summary, this context leads us to consider the situation of intelligent organisms 1011 years or so from now, when energy/matter density
r(z) will have attenuated to an extreme degree. At that point our critical dependence on a sufficient concentration of energy/matter will oblige organisms to develop mechanisms which attract energy/matter and maintain it in their vicinity, leading to a surprising interpretation of the nature of organisms as extensions of the gravitational force. To be more precise, according to this intellectually and emotionally challenging view, we are robots literally generated by gravity and programmed to undertake the tasks it is unable to accomplish in its primordial physical state. Our mission, whether or not we wish to accept it, is to comprehend the mechanisms of time dilation and cosmological expansion so as to manipulate and perhaps eventually control them. Can this interpretation of life survive rigorous examination?

The first step in answering this question involves understanding gravitational attraction as a reaction to, and therefore generated by, universal expansion. The forcible curving or distortion of space/time by Big Bang expansion generates an equal and opposite counter force, gravity, which as a result acts as if to return energy/matter to its original state in a singularity. If we can accept this notion, the rest follows logically. This procedure involves tracing, step by step, the progress and consequences of the gravitational force as it is exerted through time on energy/matter in the universe.

Since the universe appears to be expanding at an increasing rate, clearly gravitational forces are frustrated in that they are not powerful enough to counter the energy released by the Big Bang and re-condense it in its entirety into a single locality. As a consequence gravity is obliged to take a more circuitous route to accretion. Fortunately it is still able to attract and condense, at least locally, limited quantities of matter which can evolve into galaxies and eventually into solar systems. At this point we can already begin to appreciate the creative, organizing potential of gravitation – the ability to acquire an amorphous cloud of hydrogen atoms and manipulate it by accretion alone to create structurally and functionally complex astrophysical objects. This process of structuring by gravitational accretion and condensation continues gradually in stellar cores of intermediate mass, creating step by step all the stable elements up to iron, making use of the fundamental particles and interactions to bind them into increasingly dense, massive and complex but relatively stable units. In larger stars where gravitational forces are powerful enough, this condensation continues unopposed until a black hole singularity is reached – gravitation has finally achieved its “goal”, as far as it can under the circumstances. But in smaller stars, those which end their nucleosynthetic phase with a mass between 1.4 and 3 solar masses, gravitational forces are not strong enough and the result is a Type II core collapse Supernova – gravitation is again frustrated, having been prevented from reaching its ultimate goal. This is good news since the events that follow are what makes our universe interesting because gravitation still continues to exert its influence, only now through more devious and complex mechanisms. The universe would be an exceedingly dull place if all stars ended their active lives with more than three solar masses.

Following a Supernova explosion, gravitation gradually starts to shed its purely compressive character and begins a long metamorphosis through an endless series of phase transitions which, to be more precise, we would refer to as energy transformations or transductions. The first transition, in a great compressive thrust, consists in transducing the gravitational potential of the collapsing star, as it bounces off its iron and neutron core, into a compact shock front. As this wave travels through the star’s outer layers it delivers a compressive force highly magnified by its compactness, forcing together numbers of free nuclei of various masses, along with free protons and neutrons. The wave travels on leaving behind an expanding gas cloud composed not only of all the elements up to iron but also a range of newly synthesized heavier elements and their isotopes, many of which contain a large excess of neutrons. Some of these nuclei are as a result unstable since they contain more protons and neutrons than their binding energies can control, and they immediately start to decay by ejecting excess particles in a process, radioactivity, that must continue until they finally reach a low energy, stably bound structural configuration. The generation of radioactivity is the second major transduction of gravitational energy. The supernova explosion then causes these radioactive isotopes to act as vectors storing and transporting excess gravitational energy throughout the ISM.

During solar system formation, as molecular clouds condense under the effect of gravitational contraction, heavier elements fall in toward the center of gravity with the result that neutron-rich radioactive nuclei are strongly represented in the inner planets as they form, which is why they have become an important element of the Earth’s crust. There is clear evidence that short-lived nuclides were originally present on Earth, with initial abundances in general many times their present values. Similarly longer lived isotopes, for example
235U, are believed to have been 100 times more abundant than at present. Another long lived isotope, Thorium, 232Th, is about four times more abundant than uranium in the Earth’s crust and is in addition present in uranium ores. Following the decline of radioactive isotopes since the formation of the Earth, concentrations of radiogenic nuclides, the products of decay, have increased at rates depending on the different half-lives of their precursors, considerably complicating the radioactive landscape. Subsequently, geochemical, hydrothermal and other gravitationally driven geological fractionation processes tended to concentrate radioactive nuclides in deep crustal placer deposits. Along with the fact that radionuclides were considerably more abundant in the Archaean Earth, these processes created compact centers of powerful radiogenic decay pressure.

Radionuclides can undergo many possible modes of decay depending on the particular characteristics of the species in question, however the three principal types concerning us here are alpha, beta and gamma emission. A most important characteristic of
a-particles, Helium nuclei 4He2+, is that a given nuclide will emit them at certain discrete energy levels exclusively. For example 238U emits alphas of 5.2 MeV only, while 235U emits alphas of 4.39 MeV and 4.56 MeV in fixed proportions. b-decay is considerably more complex, but the most significant result is emission of electrons over a wide spectrum of energies with, however, a characteristic maximum energy for each nuclide. Typical b-electron emission energies range from several keV to a few MeV. g-ray photons are also emitted at certain defined energy levels characteristic of each nuclide, commonly in the multi-MeV range.

The kinetic energy levels of these emissions constitute a significant feature as surprisingly they lie within the energy range of the universe approximately one second after the Big Bang, during the era of nucleosynthesis. They also correspond to temperatures between 10
9K and 1010K obtaining in the core of a large star in which iron is being synthesized. Given the conditions of energy, pressure and confinement described above, it is reasonable to conclude that processes such as the triple alpha reaction and the CNO cycle operating at temperatures between 107K and 108K, which we normally associate with stellar core nucleosynthesis, could easily have occurred on Earth although clearly not at rates occurring in stellar cores. These processes would have generated, in a highly confined locale, all the biogenic elements, C, H, N, O, P, S along with others including some transition metals, by de novo nucleosynthesis, constituting the third major transduction of gravitational energy.

There are many indicators supporting this thesis and hinting at a probable link between radioactivity and biosynthesis. For example there is the fact that all known uranium deposits are enveloped in thick layers of carbonaceous bitumens containing kerite crystals composed of C, H, N, O and S. Kerite’s fibrous structure and properties are very similar to those of simple organisms and its chemical composition is nearly identical to that of proteins. Significantly, it also contains 13 of the 20 amino acids of living cells. There is in addition the interesting connection between fossil stromatolites, colonies of primitive cyanobacteria, and uranium deposits, frequently found in close association with each other.

The next phase of prebiotic evolution is more problematic as it involves the structuring and cooperative action of complex molecules. In support of this phase we invoke many experimental investigations performed in recent decades, demonstrating that, given biogenic elements as a substrate, irradiation from various sources does result in synthesis of an array of complex compounds with molecular weights up to approximately 80 kDa. Most significantly not only have several amino acids been thus produced but also all five DNA/RNA based nucleotides. Also included were formic acid, oxalic acid and formaldehyde, all potential precursors for synthesis of more complex organic compounds such as carbohydrates. Polymerization and cyclization reactions were commonplace. These data lend compelling support to the idea that radiation can indeed act as a particle and energy source driving such bonding reactions.

As a result we can qualify the process of molecular bonding to be the fourth major transduction of gravitational energy.

Significant as these processes may be, however, they do not come close to solving the fundamental problems of organization, coordination and self-primed action displayed by living organisms. How and why do prebiotic reactions, no matter how complex, move on from the physico-chemical to the bio-functional realm?   What is the precise sequence of steps and motive force directing molecular reactions along the path to metabolic autonomy?

The first point to retain from the brief history of energy/matter we have reviewed above is that, whether it concerns fundamental particles or complex molecules, matter does not exist in isolation. It is a social unit, functioning in groups. Furthermore every unit of matter has an identity, a history and a memory of that history. In a paper entitled Computational Capacity of the Universe published in October 2001, Seth Lloyd, then at MIT, says:

“Merely by existing all physical systems register information, and by evolving dynamically in time they transform and process that information. The laws of physics determine the amount of information that a physical system can register and the number of elementary logic operations that a system can perform… It is known that fundamental interactions between … particles allow the performance of logic operations… and every time those particles interact they perform one or more elementary operations…”

In other words, by its very existence matter contains information, and that information is its history – the state it’s in now as well as all the influences it ever absorbed in order to reach that state. That history or memory is held in and by the structure of matter, in its electronic configuration, which is continuously being broadcast in the form of electromagnetic waves forming an exquisitely fine and detailed image not only of the matter in question but also of the environmental pressures being exerted on it. This fact is what allows us to investigate the nature of our cosmos, from elementary particles to proteins to galaxies. In precisely the same way as they communicate with us through our specially designed sensors, particles communicate with each other, that is to say that they radiate their message to whichever other particle is able to sense, absorb and register it. We shall qualify this energy and information radiation as the fifth major transduction of gravitational energy.

Matter is therefore constantly interacting with other parts of its environment in a relationship one could characterize as a flow of stresses, with each particle seeking to establish a state of equilibrium or even dominance within its own zone of influence. Stress, and stress response, are complex multi-level phenomena with internal as well as external components but for our purposes we can say that any configurational shift or change imposed on matter is the result of a stress, and that change or adjustment is its response. Stress response adjustment usually occurs in a hierarchical sequence or cascade, unless the stress is very mild and fleeting. Response cascades unfold in a time sequence, the initial protective nonspecific response being a rapid one of flight or when possible, erection of an impervious shield. This is then followed by a more leisurely specific sensing and analysis of the stress, allowing its effects to be absorbed and a corresponding configurational adjustment to be made. The stress is thereby integrated into the particle’s structural memory. At that point, if the stress is disturbing enough and if the stressed particle can muster a requisite amount of energy, it can broadcast a message back in a directed reaction utilizing the data about the stressor it has just absorbed. This can alter the stressor so as to either render it less disturbing or neutralize it by forcing it to partake in a state of equilibrium. Further levels of response could see the stressor absorbed in its entirety to become part not only of the stressed particle’s structural memory but also of its energy/matter resources, a metabolic response. So much for theory – now how does this relate to the radiogenic micro-environments of the Early Archaean Earth?

As there is little we can find in the literature relevant to evolutionary high pressure radiochemistry or radiophysics, we shall be obliged to proceed largely by analogy. Clearly therefore we are entering the realm of speculation, and it is particularly from this point on that experimental investigation is required.

The principal feature of confined radiogenic deposits is obviously the extremely high energy environment which totally dominates and drives all reactions. Under these circumstances, although molecular bonding may be strongly encouraged, bonds will tend to be disrupted almost as soon as they are formed, the perfect paradigm for a stressful environment leading, as in the biological realm, to rapid evolutionary species divergence. This competition-driven evolutionary process has been convincingly demonstrated recently (Mulkidjanian et al. 2003) by Monte Carlo simulation of a sugar phosphate polymerization reaction in the presence of nitrogenous bases under intense UV radiation. The conclusion reached by this investigation was that accumulation of the first polynucleotides could be explained by darwinian selection of biopolymers most effectively resistant to (UV) radiation. We could extend these results to the case of radioactive bombardment in which survivors in the short term would be molecules which can rapidly attain stability for reasonable periods while effectively absorbing beta and gamma radiation. There are in fact two possible adaptive responses dealing with such an attack: one would be to assume a configuration able to store excess energy, in other words to tolerate considerable instability, without disintegrating. Another method would be to adopt a structure which rapidly ejects surplus energy in a controlled and directed action, without suffering damage or alteration in the process. The ideal structure would combine both responses, as in a catalytic reaction. An interesting, perhaps essential, characteristic of such existing structures is that they preserve their integrity by constantly metabolising energetic particles, maintaining what one could term a state of controlled instability, a more appropriate term might be dynamic stability, which is arguably the defining state characterizing biological systems. Molecules of this type have been synthesized for industrial purposes and are therefore convenient in order to draw comparisons with natural analogs.

Industrial application of such structures in recent years has focused on design and production of organic electro-optic (EO) materials and devices based on chromophores with a large dipole moment. Organic EO chromophores are dipolar charge-transfer (transduction) molecules consisting of an electron donor, an electron acceptor, and a pi-electron bridge providing communication between the two moieties but more significantly also providing a variable energy storage structure. These molecules are of interest to science because they act as antennae, absorbing photons of specific wavelengths which can be precisely selected by effecting appropriate structural adjustments. This means that precise amounts of energy can be introduced simply by irradiation and stored, transported or channelled for delivery in the required form to a designated location. Examples of such uses are numerous and surprisingly diverse, including memory storage, switching and logic devices, optical fiber communications, electro-optic circuitry, photoactive polymer films and dyes, bio-sensors and many others.

One of the most remarkable features of this effort to develop efficient synthetic chromophores is the consistent emergence of the same small number of almost identical structures in the various labs around the world and their striking resemblance to forms found in nature. Among the chromophores with the greatest polarizability and absorption cross section, the most efficient were found to be asymmetrical units with a heterocyclic purine nucleoside acceptor and a pentose ring for electron storage. All that is missing is a phosphate donor to make up ATP or a DNA/RNA nucleotide. Other commonly derived structures closely resemble a straight chain tetrapyrrole or a short length of DNA/RNA backbone with sulfur atoms in place of phosphates. Furthermore it was found that two-photon excitation of certain dyes provides a means of activating chemical or physical processes with extremely high spatial resolution. The large driving force available for electron transfer reactions, even to relatively weak acceptors, allow this type of molecule to function as a highly efficient and precise polymerization initiator. This effect will drive the synthetis of more complex morphologies including long chain polymers allowing virtually infinite data storage capacity.

In the situation of radiogenic pockets on the Archaean Earth, small heterocyclic molecules as described above, probably combined with conjugated chains, would tend to be synthesized as a result of constant bombardment by beta and gamma particles, and be competitively selected in the first instance according to their efficiency in metabolizing and directing highly energetic photons and electrons. This phase would most probably be followed by evolution of macrocycles, a step particularly applicable to the tetrapyrrole-like structures which will cyclize to form porphyrins, one of the most ubiquitous and highly conserved molecules in the biological realm, precisely because they are so efficient at processing photons and electrons. Also generated because of their energy transduction efficiency would be low molecular weight nucleic acids and other highly conserved very small catalytic micro RNAs composed of two or three nucleotides, e.g. cyclic diguanylic acid with two nucleotides joined in a macrocycle by phosphodiester bonds. Such small-molecule modulators and nucleic acids are now known to regulate a diverse array of metabolic functions and, without mediation of enzymes, directly to catalyze various types of bond formation including C-C bonds. We shall characterize the synthesis of directed charge storage and transfer molecules as the sixth transduction of gravitational energy.

Assuming that, in this high energy bath, a selection of such polymeric, cyclic and macrocyclic catalytic molecules manage to establish a state of dynamic stability, the common adaptive response directed toward stress neutralization by mutual equilibration of the molecules would result in a process of symbiotic mutualism. In such a phase, all unsuitable or non-complementary species would be eliminated, leaving a series of complementary cooperative molecules, each and every one partaking in maintaining mutual stability in what will have become a functioning system. This system is driven by the need to precisely control and process the constant pressure emanating from its radiogenic environment, in a high energy photosynthetic analog. We shall characterize the process of symbiotic equilibration by mutual charge neutralization to be the seventh major transduction of gravitational energy.

The question now is – What species of molecule would tend to form mutually stabilizing associations under these conditions and why? Tackling the last part of the question first, obviously species associate because each one provides some element which the other(s) need in order to maintain equilibrium over time. Summarizing the various points raised above, maintaining a state of temporal dynamic equilibrium, the primary requirement for continued existence of any system, demands that species fulfill the following specification:

1.       Species must acquire, store and transduce energy in order to maintain a state of dynamic equilibrium both internally and externally.

2.       Based on No.1 above, species will sense, acquire and store environmental data in their structure.

3.       Based on Nos. 1 and 2 above, species must organize this energy and data so as to permit manipulation and reconfiguration of their environment, both internal and external, necessary for an effective stress analysis and response leading toward equilibrium.

4.       Due to continuously developing environmental conditions, species must organize and maintain encoded in their structure a readily accessible permanently updated and expanding database along with updated environment-manipulation mechanisms.

Based on the above four points we can hazard a definition of the term “fittest” as it applies to entities involved in competitive darwinian adaptation, as follows:

The fittest entity is that which has rapid access to the most complete and accurate data base concerning its environment, internal and external, both proximate and remote. It must in addition be able to treat these data combinatorially to create the largest repertoire of coherent and relevant responses to stimuli in the shortest possible time as well as to devise an appropriate, broadly anticipatory, longer term response strategy the result of which must enable the entity to make use of or to manipulate its environment so as to secure its own short and long term existence.

Given this demanding specification it is logical to suppose that molecules which evolve an aptitude for performing one of these tasks will tend to associate with molecules better suited to one or more of the others. Under conditions of high energy flux, as mentioned above molecules with an aptitude for energy capture and transduction would form in the first instance and be rapidly selected. Some of these molecules would be chromophores strongly resembling RNA nucleosides and might well polymerize and cyclize to resemble di- or tri-guanylic acid, structures exhibiting considerable catalytic and regulatory activity. The shortcoming of such molecules, however, is an extremely poor memory capacity, limited by the repeated use of just four different base configurations linked by an invariant backbone. Unable to satisfy condition 4, none of the other higher tasks could be accomplished. The tendency therefore would be to associate with a more varied or variable molecule or polymer having the potential to be organized as a readily accessible database while also exhibiting complementary recognition and binding sites. Which molecule satisfies these requirements?

Organic molecules displaying the greatest morphological variation include sugars, lipids and amino acids, all of which were represented in the results of irradiation experiments mentioned above and, incidentally, form associations with nucleic acids in modern living cells. These molecules possess conspicuously different structural characteristics suited to their individual functions. Lipids consist mainly of long conjugated unvarying hydrophobic linear chains with variable heads able to bond covalently. Such molecules can hold some information, particularly in the head moiety, but the uniformity of the tail section is too limiting for this purpose. The structure of sugars, on the other hand, is so varied, forming no readily discernible pattern, that using them as a database would pose virtually insuperable packing, access and reading problems. The structure of amino acids is ideal for encoding data because of its simple invariant polar head, the peptide group, combined with the highly variable side chains displaying differing electrostatic properties while maintaining compact, regular configurations. The ready adoption of specifically determined secondary, tertiary and quarternary configurations, although also true of nucleic acids and sugars to a limited extent, adds significantly to the encryption potential of amino acids.

It now seems reasonable to suggest that the primordial function of radiogenetically synthesized molecules was to sense and record environmental data. This task could initially have been accomplished by cyclic peptides which would have formed as a chromophore-like analog under steady bombardment by energetic gamma photons. These could have acted as both sensors of the environment and catalytic activators of their own transcription or polymerization, as is seen in NodD and related proteins secreted by modern symbiotic rhizobia. Many such small cyclic peptides exist today in vivo, e.g. nodularin or microcystin, and in vitro, e.g. RAFT molecules or beta-turn mimics containing as few as two residues. Particularly interesting is the design of beta-turn mimics as bioactive cyclic peptides where they function either as scaffolds or as molecular recognition sites. The role of beta-turns in peptide-enzyme recognition and receptor reactions is clearly not trivial and would seem to be related to their postulated origins.

Cyclic nucleic acids (CNA) would also be synthesized as described above and initially would compete with cyclic peptides (CP) and polyamines having a similar structure. It is interesting to note that in small CNAs such as diguanylic acid the backbone lies inside the circle with bases turned outward for obvious reasons of steric hindrance, so that they bear a superficial morphological resemblance to small CPs with consequently related functions. As is the case in modern organisms, competing antigens frequently evolve into symbionts, and this would occur with CNAs and CPs as their respective functionalities were exploited. At this point CNAs would have been drafted into a symbiotic association with CPs, acting as environmental sensors and catalytic activators, while still retaining some memory function. Equally peptides would then be free to act principally as databases, a role to which they are better suited particularly as they eventually polymerize to become linear, while they still retain a catalytic enzymatic function “learned” in their cyclic phase.

How would the interaction between these species evolve over the long term? In the first place, if CPs lose their cyclic morphology they can no longer act as energy transducing chromophores, at which point CNAs and micro RNAs take over the sensor, polymerase and catalytic functions required to enlarge the peptide database. Large cyclic peptides break down to become linear, their polymerization regulated by CNAs and micro RNAs. The essential state subsisting now between peptides and nucleic acids (NAs) is that of symbiotic mutualism, each having specialized in a particular function complementary to the other: NAs supply energy with its cognate environmental data to the peptides, which in turn store this data first simply by polymerizing and eventually by adopting secondary and tertiary conformations.

An interesting by-product of NA polymerization of peptides is determination of amino acid (AA) chirality. Why are almost all natural AAs L – enantiomers? Asymmetric synthesis requires a means of distinguishing one enantiomer from the other but this distinction can only be made by molecules which are themselves chiral. Nucleotides possess several sources of asymmetry, in particular axial, backbone and phosphorus chirality. Most important though could be the role of the imidazole ring, acting as both ligand and catalyst, which has the remarkable property of being electronically tunable by varying its substituent molecules and surprisingly also by application of high atmospheric pressure which has the effect of considerably enhancing enantioselectivity, to be discussed below. Furthermore electronic tuning of ligands is known to have a dramatic effect on selectivity, particularly in the case of metal-catalyzed reactions, which may well be involved in prebiotic AA synthesis.

We shall now adress the effects of high atmospheric pressure chemistry on prebiotic evolution. Many of the reactions discussed above concerning asymmetric catalysis were first characterized under conditions of supercriticality involving various solvents including water, CO2, CHF3 and other classes of organic solvents. Investigation of supercritical (SC) fluids over the last few decades has provided a wealth of data relevant to the origins of biologically active molecules, although in practice the pressures applied have seldom exceeded 100 MPa. As a result of liquid solvents’ very low compressibility, pressure has little effect on the enantioselectivity of asymmetric catalysis in them except at extremely high levels. However the high compressibilities of SCFs, especially near their critical point, allow pressure effects to be more readily achieved and precisely controlled. Under the right conditions of temperature and pressure enantiomeric excess (ee) can reach close to 100%.

Supercritical fluids can be defined as fluids or solvents above their critical temperatures and atmospheric pressures, possessing properties between those of liquids and gases, with densities similar to liquids while viscosities and diffusivities are closer to those of gases. Apart from their effects on enantioselectivity they have many important characteristics relevant to this discussion. Pressure effects in particular are quite dramatic, fundamentally changing the electronic character and physical properties of most solvents. Water, for instance, with a critical pressure of 22 MPa at 647 K, can be pressure-tuned to behave like almost any organic solvent of low dielectric constant, generating chemistry in a single fluid phase that would otherwise require a multiphase system under conventional conditions. SC water has the capability to dissolve organic compounds, with the significant exception of enzymes, while simultaneously retaining an active state of high hydrolysis performance, acting as solvent, reactant and catalyst in organic chemical reactions. The character of water under supercritical conditions changes from one that supports only ionic species at ambient conditions to one that dissolves paraffins, aromatics, gases and salts, partly as a result of the shift of dielectric constant from 78 to approximately 6 at critical. The ion product, or dissociation constant, for SC water as it approaches the critical point is about 3 orders of magnitude higher than it is for ambient water. It therefore generates a higher H+ and OH- ion concentration than liquid water. As such SC water is an effective medium for both acid- and base-catalyzed reactions with organic compounds. The dissociation of water near its critical point generates a sufficiently high H+ concentration that some acid-catalyzed organic reactions actually proceed without the presence of any acid, with resulting hydronium ions being the primary catalytic agents. In fact approaching the critical point, the density of any supercritical fluid becomes extremely sensitive to even minor changes in temperature and especially pressure and this affects several fundamental properties including dielectric constant, pH, polarity, viscosity, diffusivity, solubility, mass transfer rates, activation volume and rates, enantioselectivity, electrostriction and electron attachment rates. As a result, it has been found that under certain conditions of supercriticality chemical reaction rates can be accelerated by several orders of magnitude, a fact with profound implications for prebiotic molecular evolution. Reaction rates are classically controlled by catalysts. What is the connection between catalysts and supercriticality?

The ideal catalyst generates significantly accelerated reactions, often enhanced by a high degree of selectivity. In the world of biochemistry, this role is generally filled by enzymes, which may be proteins or nucleic acids or more likely both in tandem, frequently with the participation of cofactors such as transition metal ions. In the prebiotic world, the role of catalyst was probably occupied by gravity-generated high “atmospheric” pressure exerted on molecules in solution under conditions of supercriticality, which we shall characterize as the eighth major transduction of gravitational energy. How do SC fluids and enzymes produce their catalytic effects? Are their mechanisms fundamentally identical or totally disparate? Can the first evolve into the second?

The textbook description of biological catalysis states that enzymes reduce the energy required to surmount the barrier between reactants and products, thereby leading to accelerated reaction rates. The mechanism of this concept known as transition state theory (TST) is little understood. Recently the theory itself has been brought into question and fundamentally modified by the demonstration that quantum tunneling is responsible for catalytic action in a growing number of enzymes and may prove to be a general strategy used by all enzymes catalysing highly energetic transformations with large activation barriers. In fact the majority of enzymes catalyze by hydrogen transfer in some form, including proton movements in acid/base catalysis, hydride transfer in redox catalysis or radical transfer. How do these biological enzymatic transformations relate to inorganic catalysis? It is certainly not coincidental that H-transfer in inorganic non-biological systems also occurs by vibrationally assisted quantum tunneling as a means of proton transfer in metals or, for instance, along hydrogen bonds in benzoic acid dimer and similar reactions. How are these transfers effected and more significantly, how are they controlled, in biological as well as in non-biological systems?

Many hypotheses analyzing the factors contributing to catalytic potential have been proposed but definitive experimental investigation in support of these concepts has been sadly lacking. The basic problem remains elucidation of the mechanisms of energy transduction by charge transfer which relies on controlling two essential components: relative distances and positioning of reactants. This principle known as orbital steering has been shown to play a major quantitative role in the catalytic power of enzymes accounting under the right conditions for rate acceleration by many orders of magnitude. There are naturally many secondary influences on reaction rates but these only come into play if the fundamentals are also satified. One of the most significant secondary states concerns application of external fields that may couple to the transfer particle’s dipole moment. Experiments provide evidence that pressure-driven external fields can direct optimal orientation of overlap in reacting orbitals thus directing both angular positioning and distance. This would be particularly important in tunneling effects which rely crucially on distance between donor and acceptor. As H-tunneling occurs over relatively short distances (
≈ 0.5 Å), high pressure in inorganic systems would clearly be a major factor in achieving the necessary molecular compression. In biological systems a key feature of the thermal vibration or dynamic barrier model is the role of protein motion in transiently compressing the width of potential energy barriers, thereby promoting tunneling reactions. We can therefore see that, in providing a mechanism for controlled charge transfer by orbital steering, high pressure under supercritical conditions can be considered as a general physical analog of enzymatic or at least catalytic function, greatly accelerating as well as directing molecular reactions.

At this point we must be conscious of the fact that we have wandered well away from direct gravity-driven effects into the realm of biological function which is dominated by electrostatic forces. How can we justify a hypothesis which demands that gravitational effects undergo a “phase transition” to processes driven by electrostatics? How can electrostatics suddenly come into the picture? What is the link, if any exists, between these two apparently different forces? To answer this question we must return to the Big Bang and Grand Unification (GU). Under GU, of course, the four fundamental forces - strong, weak, electromagnetic and gravity – are all united, but only at extremely high energies obtaining immediately after the BB. Furthermore until recently gravity has managed to stay firmly out of any proposed unification scheme – until recently, that is. Today (2004) it is probably safe to say that this is no longer true.

In the course of the last five years or so enough confirmed evidence has accumulated to justify the statements which now follow. Several investigators have, over the years, proposed unification schemes but the one which appears most coherent and convincing is authored by Dr. Myron W. Evans and his colleagues at A.I.A.S. (www.aias.us). His approach expresses the gravitational and electromagnetic field in terms of the geometry of spacetime, thus unifying the description of these fields within General Relativity. The metric therefore becomes the fundamental potential field for both gravitation and electromagnetism. In a private communication Dr. Evans says – “AIAS has proven that electromagnetism and gravitation are parts of the same field, described by the tetrad form of differential geometry…The AIAS website describes papers suggesting new experiments designed to detect the influence of gravitation on electrostatics”. He goes on to demonstrate that the electric field strength between charged particles (electrostatic field) originates in their acceleration due to gravity and is therefore a purely gravitational effect. In his 2002 paper entitled Electromagnetic Energy from Curved Spacetime Dr. Evans says – “In this paper Einstein’s perturbation method is applied to General Relativity to demonstrate the existence of the B(3) field for a simple metric corresponding to an expanding universe. The result is used to derive an expression for the electromagnetic energy density due to B(3) and to show that in principle energy density can be obtained from curved spacetime without source charges being present”. Elsewhere he states that as gravitational and electromagnetic fields are both generated by the curvature (expansion) of spacetime, “This means that one field can be converted into another and that gravitation can give rise to electromagnetism and vice-versa”. Dr. Evans has thus completed the conceptual framework begun by Einstein concerning the unified geometrization of the four fundamental forces, and demonstrated conclusively that they all stem from the expansion with concomitant spin and curvature of spacetime. Here we demonstrate that life, as a functional extension of gravity, also is a direct consequence of spacetime expansion, spin and curvature, thereby establishing the principle of the geometrization of life and unifying it with the other fundamental forces of nature.

With this essential background information we can now return to our investigation of the relationship between cyclic peptides (CP), a term in which we shall include polyamines, and cyclic nucleic acids (CNA), which we interrupted on page 8 in order to discuss supercriticality. Beyond the supposition that evolutionary processes affecting CPs and CNAs would be vastly accelerated under supercritical conditions it is difficult to be more precise, exposing an important subject for experimental investigation. Nevertheless clues to functional associations between these molecular types can be found by examining highly conserved small RNA/protein complexes, the ribonucleoproteins (RNP), and in particular the signal recognition particles (SRP), universally conserved complexes found in all domains of life. Recent advances in X-ray crystallography, NMR and related imaging technologies have permitted dramatic insights into the structure and function of RNPs as well as many other biological molecules. One of the major discoveries concerns the fact that proteins invariably function in intimate association with nucleic acids either in the form of RNA or as small molecules such as GTP or ATP,  frequently both. The RNA world of recent years has turned out to be largely an RNP world, the classic example naturally being the ribosome comprising over 70 different proteins and several classes of RNAs. What is the nature of the relationship and interaction between these two molecules? Why do they need each other in order to function?

Examining proteins first, it has now been convincingly demonstrated that these molecules exist as modular units, each type dedicated to performing a certain limited and highly specific class of function. It would appear that such modules probably originated as small molecules responding to a specific stress such as temperature, pressure, pH, etc. In time they speciated, becoming more selective and forming diverse population types, now known as domains. More complex functions are accomplished not by larger proteins but by assemblies of several complementary domains, each of which is assigned its specific role in a precisely targeted and coordinated mechanism. How is this synchronization achieved?

In order to answer this question it is revealing to examine SRPs. Their precise cellular functions are not relevant to this discussion, but what is interesting is that they exhibit most of the significant characteristics of the protein/RNA connection. In higher eukaryotes SRP holds six different proteins retained by an RNA acting as a scaffold consisting of ~300 nucleotides. The secondary structure of the RNA moiety is shaped somewhat like a backbone or a nerve cell with the roots (synapses), stem (axon) and branches (dendrites) each attached to one of the various proteins. If the stem were cut in the middle, the complex would form two separate domains, each of which performs a clearly differentiated but complementary function. In fact if the RNA were disassembled into its component parts each attached to its cognate protein and then reassembled, we would probably have a simplified picture of the evolutionary origin of such complexes. The RNA moiety clearly plays a “nervous system” type of role in assembling, guiding and coordinating the proteins in their eventual catalytic or enzymatic function.

Another revealing example of the protein/RNA connection consists of the highly conserved Sm proteins which are always associated with U-rich RNA sequences. The protein moiety functions in a heptameric doughnut-shaped ring formation with part of the RNA moiety forming a smaller ring inside the central 15Å cavity. Each of seven RNA uridines make stacking contacts with aromatic residues projecting into the inner cavity, reading the instructions contained within the Sm structure and processing that information in order to carry out its cognate function. It is particularly interesting that certain Sm-like proteins, specifically E. coli Hfq which plays wide-ranging roles in RNA metabolism, reciprocate in this relationship by acting as an RNA chaperone, inducing structural changes in mRNA, thereby helping to maintain the RNA’s specific functionality.

In a series of recent papers (Lai et al., 2003) it has been reported that certain RNA sequences can act as sensors of various environmental factors, in particular temperature or the presence of specific small metabolites and cofactors. This information could then be relayed to selected proteins for storage and later reference, or as was actually determined in these investigations, it is used by the RNA to directly regulate the transcription or translation of associated mRNA, including itself. These RNAs, known as riboswitches, thereby simultaneously perform both sensing and regulatory functions without the mediation of any proteins, similarly to miRNAs, clearly demonstrating that the principal function of protein is information storage rather than molecular activation. This intimate relationship between sensing and regulating on the one hand, and environmental state-and-response data storage on the other, between RNA and protein, seems to be at the core of biological function. It would appear furthermore that each needs the other in order to achieve its active tertiary or higher order structure, suggesting that their respective structures probably evolved together as physically and functionally bound units.

During this stage of evolution electrostatic forces finally establish their domination over biomolecular interactions, a highly complex subject which unfortunately remains poorly understood in spite of being the focus of considerable investigation. A simple definition of electrostatics would state that it concerns the interaction of positive and negative charges at rest or moving at low speeds such that their fields are not affected. The problem is that, like gravity, as they unfold electrostatic forces take on many different and subtle forms, occasionally producing quite counter-intuitive effects. Added to that is the fact that intricately structured biomolecules such as those we have been discussing generate highly complex and mobile electronic fields. Nevertheless if we are to understand the coevolution of peptides and nucleic acids, even at a very simple level, we must come to grips with the subject.

The first point to consider is the fundamental force causing positive and negative charges to interact, which is of course the tendency toward equilibration, the search for stability. To understand this force we again turn to GU and the geometry of curved spacetime. Curvature, the tension-stress caused by expansion, as we saw above gives rise to reactions manifested as gravity and electric charge. Response to tension will result in a minimization of charge in accordance with the Evans Principle of Least Curvature, an effect which causes positive and negative (opposite) charges to relieve stress by neutralizing each other. This stress-relieving neutralizing response is so basic that it is probably at the root of all forces and events, but it becomes most apparent in molecular and biomolecular interactions. Any charge by definition seeks to be equilibrated, to be counterbalanced or neutralized, and will therefore naturally tend to combine with its opposite charge and to avoid any like charge which would increase its imbalance pushing it further away from neutrality. This may seem obvious but it bears repeating because it is the basis for all biomolecular interactions and, with the added element of selection, it forms the stress-responses-selection triad (SRS), the mechanism leading to molecular and biological evolution.

Molecular biologists have come to give electrostatic interactions different names such as van der Waals, induced dipole, hydrogen bond, dispersion forces, etc. according to their particular range, energy, circumstances and effects, as if they were separate and distinct forces in their own right, thus adding confusion to an already complicated situation. Adding further to the difficulty is the fact that biological reactions occur in solvent which of course drastically alters the charge environment and has far reaching solvation effects of its own. The most significant of these is the so-called hydrophobic effect which is due largely to the charge-related energetic structure of the bulk solvent, in most cases water.

We can now pick up the discussion on page 10 concerning interactions of nucleic acids and peptides including polyamines which are likely to have originated as amino acid precursors. One of the significant energetic features of these two sets of molecules is that nucleic acids are highly negatively charged, particularly at the backbone phosphates, while polyamines are highly positively charged, this charge being concentrated on the mobile amine and amide moieties. Many amino acids also carry significant mobile positive charges, in particular at the guanidium moiety of arginine closely resembling a polyamine, as well as at their amino ends, so that these two sets of molecules, peptides and nucleic acids, will tend naturally to complement each other, at least partially neutralizing each other’s charge. Also available for attenuating charge are various elements such as salts, monovalent and multivalent metal cations and of course water itself, whose hydration shells are quite effective at screening charge while remaining mobile and loosely bound, thereby permitting more stable reactions to take place by replacement of water molecules.

In the Hadean and early Archaean high-pressure radiogenic environment, highly reactive radicals and ionic species will inevitably abound exerting considerable stress on many molecules. In particular beta and gamma bombardment lead to rapid radiolysis of water releasing free electrons and OH- hydroxyl radicals. The .OH generated by these reactions can abstract a hydrogen from the ribose sugar of RNA and DNA backbones leading to cleavage of the phosphodiester bonds. The long term result, in accordance with the SRS principle, will be darwinian selection favoring those nucleic acids whose negatively charged backbones are best and most rapidly protected, either by metal cations such as Mg2+ or by polyamines or of course by peptides, thus tending to drive these molecules together in a symbiotic relationship. In modern cells polyamines are present in millimolar concentrations and, together with magnesium ions, account for the majority of intracellular cationic charges. Clearly charge neutralization of intracellular anions, in particular those of DNA and RNA, are among their most important physiological roles, however polyamine binding also has profound effects on nucleic acid structure, causing bending, folding and transitions to different forms. The process of charge neutralization is undoubtedly also at the origin of protein folding whereby susceptible scissile bonds exposed to solvent are protected by complementary moieties within the same molecule. These conformational changes directly affect binding and as a result influence enzymatic function. Most interestingly, it has also been found that polyamines promote and increase rates of RNA polymerization.

RNA backbone charge-stress and neutralization processes would therefore appear to be at the origin of biomolecular functional evolution. As nucleic acids and peptides, with the active participation of waters, metal cations, salts, and polyamines, evolve new mechanisms and conformations increasing their stability, both in isolation and as a complex, the evolutionary history of these events is recorded in their physical and electronic structure. The molecular structure best able to store complex information is, as discussed previously, that of peptides which as a result constitute an accessible data bank containing a complete memory of the stresses and successful responses experienced by the molecules. This process involves nucleic acids receiving stress signals which may be briefly stored or instantly transmitted to their cognate peptides which in turn may make the structural adjustments necessary to neutralize or compensate for the particular stress. The most efficient and successful RNA-peptide complexes will survive the SRS elimination process and thereby maintain a record of these events.

Stress-charge excitation transfer to peptide…relaxation…release.

The question we now need to examine is this – Can the cyclic nucleic acids and peptides discussed earlier emerge from radiogenic supercritical conditions to evolve into catalytic systems able to function in ambient conditions? Why and how do they emerge from these high energy conditions?


Proposal Objectives

The objectives of this proposal generally include those of the NASA Astrobiology Roadmap but seek to go further, first in demonstrating the existence of a process linking life directly to the Big Bang and second in providing evidence indicating that biological function stems deterministically from the fundamental physics of cosmological evolution. Use of the term deterministic means that every step in this process is logically and sequentially guided both in its mechanism and its direction, at no point relying on the exercise of possibilities or probabilities. Synthesis of the molecular precursors and generating mechanisms leading to biological function are explored from an entirely new perspective, that of gravitationally driven condensation. It is suggested that this putative metamechanism, generated by and in reaction to the Big Bang and directed at opposing subsequent cosmological expansion, accounts for all the structures and cognate processes displayed by the universe, including galaxies, molecules and living organisms.

The immediate objective of this proposal would be to test the initial claims of the cited hypothesis, particularly those concerning de novo nucleosynthesis of the biogenic elements, CHNOPS, followed by chromophore, cyclic peptide (polyamine) and nucleotide synthesis, under high pressure supercritical and radiogenic conditions.

Technical Approach and Methodology

Suggestions are made below for the performance of exclusively ground based theoretical and experimental investigations testing the relevance of this hypothesis to those physical and chemical principles which underly the origins and evolution of life.
It should be made clear from the outset that to elucidate all the stages of evolution at the molecular level, starting from formation of solar systems and proceeding up to the emergence of recognizable ab initio biological function, must be a process which will at best occupy scientists for many decades and will necessarily be highly interdisciplinary, employing specialists in several domains.

Although this proposal attempts to cover the entire evolutionary process at a general theoretical level, at the experimental investigation level only the initial critical steps will be mentioned. These steps are concerned exclusively with high pressure radioactive chemistry and may possibly involve design and construction of bespoke equipment. One of the major problems facing this equipment is the need to flush solvents through a flow reactor system continuously under high pressure without stopping or interrupting the experimental procedure, while at all times maintaining a safe radiation shield.

The initial experiments will be designed to reproduce conditions in the Earth’s crust about 600 million years after its formation, or about 4 Gyr ago. It will be particularly important to arrive at an accurate definition of crustal radiological conditions at that time and of the evolution of these conditions as radiogenic isotopes accumulate.


Plan of Initial Experimental Investigation

Experimental investigation of these putative phenomena would be aimed at establishing the degree to which they actually do occur as predicted and would require an initial research program designed to focus mainly on the procedures listed below. The purpose of these procedures would be to simulate gravitational pressure and radiological conditions in the Archaean Earth’s crust as well as their subsequent evolutionary history.

1.       PHASE I – Simulate high pressure radiochemical reactions under various conditions of pressure and temperature in the presence of selected elements and compounds including water and other solvents. The purpose of this step would be to determine the elements and species of molecular structures synthesized and the character of bonds formed in confined high energy and high pressure radiogenic environments.

2.       PHASE II – Using molecules generated in Phase I, impose accelerated reduction of radiogenic energy and pressure to simulate changing conditions over geological time. The purpose of this step would be to characterize the effect of an evolving radiogenic environment on molecular structures and reactions.

3.       PHASE III - Using molecules generated in Phases I and II again by varying environmental conditions, characterize the reaction kinetics and mechanisms determining structural responses to various types of radiogenic environmental stress.

4.       PHASE IV – Using molecules generated in Phases I and II, determine mechanisms for encoding and storing information relative to specific environmental stress factors in molecular structures and for accessing these data in order to permit adaptation by eliciting targeted stress responses through variations of structural configuration.

5.       PHASE V – Following the results of Phase IV, further reduce energy regime until equilibrium is reached and molecules are observed to react by influencing and eventually controlling previously dominant environmental stress factors.

Once the radiogenic energy regime has reached equilibrium levels, further investigation will be needed to determine how heterogeneous molecular systems encode, store and access large databases on environmental conditions to elicit targeted stress responses. It will also be necessary to characterize the mechanisms using these databases and directed at manipulating the environment specifically to extract energy and matter required to substitute for the reduced radiogenic input. These investigations will clearly involve many more phases of highly interdisciplinary intensive research lasting a considerable time which, needless to say, at this point it would be difficult to estimate.