QUANTUM ENGINEERING #70: HOW DID NATURE DESIGN HER SEMICONDUCTORS?

Listen to the video and you'll get one level of complexity. The blog below will give you a new perspective to see on the same topic.

Stoping light in cells is a feature of cellular design and not a bug.

Cellular stress increases bio-photon release, why? 

Prokaryotes release 5000 time more light than eukaryotes. Eukaryotes release more light when they are stressed. Do eukaryotic cells use this excess light in some way we do not yet understand?

Yes, I believe they do. It has to do with biological chip design on the topological insulator chips inside of cells.  It is a process of biological photolithography.

Manipulating the flow of light in a material at small scales is a specialty of cells loaded with hydrated carbon-based semiconductors.  Why?  Doing so allows for complexity development under low-power situations.   In a semiconductor, electrons can, in principle, move freely, but an external magnetic field can stop this motion. The circular movement of the ATPase caused by the magnetic field stops conduction, and as such, electrons can only exist in the material if they have very specific energies. The energy level corresponds to the light frequencies that excite these electrons by the photoelectric effect.  These energy levels are called Landau levels, and they are characteristics of electrons operating in a magnetic field.  These forces are operating right around the mitochondria creating a force field of action that allows for quantum mechanical process life needs.  You must open your eyes to new data to see the magic inside of cells.

NATURE'S MAGNETS ARE IONS EJECTED FROM THE CORE OF STARS.

This implies that all biological magnets used in mitochondria and cells come from things that make light. This is axiomatic and critical in showing how physics trumps biochemistry in controlling how life unfolds below the cell level.

Since manganese has a nuclear spin of 5/2 and a nuclear magnetic moment of 3.4687, spectral lines of Mn II show it has a hyperfine structure (HFS). Manganese has one stable isotope with a mass number of 55. The ground electronic configuration of Mn II is 3d5(6S)4s (Sansonetti & Martin 2005). This specific electronic configuration allows cells to create SOD2 from excess oxygen from mtDNA metabolism.

It reveals the queerest aspects of Nature that remain hidden from the biologists and biochemists. Manganese is not a particularly common element on Earth. It is the 12th most common element in the rocks of Earth. However, where it is concentrated reveals the quantum biological story of the evolution of prokaryotes and their lives before oxygen filled the ionosphere. The most incredible abundance of manganese is ferromanganese nodules and crusts along the ocean floor. Marine chemical processes and microorganisms (prokaryotes) capture dissolved manganese in seawater, which is precipitated on the ocean floor. Once captured, the prokaryotes could use the element to create a spectra and a magnet to drive biology using light DIRECTLY from matter.

It should immediately stimulate your neurons to recall that Prokaryotes emit 5000 times more light than eukaryotes. It would help if you remembered that prokaryotes populated our ocean long before eukaryotes ever appeared on Earth. This mechanism is ancient. It is not holistic! It is not alternative medicine. In fact, it is native biology, and it reveals that centralized science and medicine are the real alternative versions of events created by the minds of man in his labs. It is directly related to the organizational plans buried in Nature.

Shannon's theory of Information has told us that unusual things make excellent information carriers in computing machines. The ground electronic configuration of Mn II is 3d5(6S)4s, a superb information carrier with evolutionary severe weight. Phosgene is a chemical that puts an acetyl group on the aromatic amino acid tyrosine, and this small biochemical change blocks the electronic transition and blocks the flow of information in mitochondria. It blocks the Mn redox cycling between ESR-silent Mn(III) and ESR-active Mn(II) required for superoxide dismutation. Many people do not know that ESR silent Mn(lll) is the source of many of the critical evolutionary porphyrins of life. High spin Mn(lll) has an electronic configuration 3d4(6S)4s. Nature used the D shell electronic configuration of Mn as her signal for SOD2 production. Let that level of complexity sink in while you still think biochemistry is "the main controller" in your cells.

High spin Mn(III) is the archetypal of such non-Kramers ions. Mono and polynuclear Mn(all) are of central importance in biological systems that use heme-based proteins like SOD2, catalase, and photosystem II, while Mn(III) porphyrins phthalocyanines have been used as building blocks in the construction of molecule-based magnets. This has huge implications for how life operates below the cell level. Soon you'll learn about that level because it is not in your biology books and not in any medical textbooks. That is how vital Turin's serendipitous finding was for the Ivory Tower. Some of us already knew biology was driven by changing the electronic configuration of ions using light.

For example life is flexible.  How does QED happen during mechanical deformations in life?  Generally, mechanical deformation stops conduction in semiconductors or topologic insulators like graphene; those type of materials turn into an insulator in this case and consequently the electrons become fixed in their lattice & are bound to Landau levels.  

Does light act like electrons since they are linked by the photoelectric effect?  Yes.  A photonic crystal, like cell water, normally consists of a regular—two dimensional—pattern of holes, as one would expect to see in a silicon layer on a chip.  Breaking this regularity in water in precisely the right manner will deform the array and consequently lock the photons inside the cell. This is how we create Landau levels for photons.

Implications?  Once you slow light down in a crystal, you can steer it to where you need it.  So, increasing your metabolism increases the biophoton creation in the mitochondria.  Then, cell water captures it and drives it to the biochemical boxcars.  In Landau levels, light waves no longer move; they do not flow through the crystal either but stand still. This shows that the deformation of liquid crystalline water can have a similar effect on photons as a magnetic field on electrons.  By altering the deformation pattern, research has shown you can establish various types of effective magnetic fields in one material.  This can be used to do physiological work. As a result, photons can move through certain parts of the material but not in others. Hence, life seems to have an ability to steer light on a liquid crystalline surface.  

Stopping light in its tracks to steer biophotons begins to show us how organs really function on our semiconductive chips built by Nature. The ability to stop light gives cells a new biological ability that mimics on-chip applications. This ability can explain how smells and words can go from sensations to visual imagery in working memory. It likely will explain consciousness, memory, and how holography forms in water. 

What does this look like on silicon?

HYPERLINK

Slowing light in water was a critical evolutionary step that existed before Nature invented DNA. Ferrodoxins and aromatic amino acids were in our primative oceans. How did it happen?

How do I see a quantum cell using this physics? 

Although a magnetic field doesn't directly affect the photons of light, a magnet does distort the medium through which light passes and thereby “bends” the light rays indirectly. This is used inside cells where mitochondria and melanin are in close proximity. Cells take advantage of every option Nature provides to transform energy. When defective oxidative phosphorylation is present, it adjusts the cell's stress response like the mammalian DAMP program.

Aging isn’t driven by ROS, as doctors are taught to believe. Many now think the DAMP Program drives it. I feel sunlight controls all the DAMP molecules. I believe slowing light down in cells is linked to healthspan and aging. Why do I say this? Aging and cancer share some common origins and hallmarks, such as genomic instability. Sunlight exposure creates genomic stability to quiet epigenetic programming and lower cell protein turnover. Recent advances indicate that damage-associated molecular pattern molecules (DAMPs) such as high mobility group box 1, histones, S100, and heat shock proteins play location-dependent roles inside and outside the cell.

Mitochondria under stress via the DAMP program respond by transforming more ATP to bend light to compensate for the stress.  Why does it do this?   Light travels through space-time along a geodesic – the shortest possible path between two points on a curved surface.  Making more ATP means the ATPase spins faster than 9000 RPM and this increases the magnetic strength in the cell. This magnetic flux is used to make the stressor hormetic. It drives adaptive changes in cells by altering the epigenome.

SUMMARY

When water superconduction is broken in you due to modern life, you must rely on the rapid recycling of ATP from the pathways I mentioned in the EMF-4 blog.  This means that glycolysis and the PPP will be the metabolism the cell will have to rely on when there is a proton problem.  When you live in a world only powered by ATP, your sleep is the first thing to go south.  Initially, it becomes poor before it totally fails,  and you get diagnosed with sleep apnea.  As it goes on more chronically without proper treatment,  you eventually die from right-sided congestive heart disease and pulmonary hypertension.  Yes, in total sleep failure, you get a specific kind of heart failure preceded by a fatal heart arrhythmia.  This rhythm modern cardiology knows about but still has not made the link to it. I have it because of the loss of water proton conduction.

When your sleep fails, your gene transcription falls off., and your mitochondria are liberating more light than they should and making more ATP than they should. This activates the DAMP program in cells.

The DAMP program provides interaction platforms at molecular levels linked to common hallmarks of aging and cancer. They can act as inducers, sensors, and mediators of stress through individual plasma membrane receptors, intracellular recognition receptors (e.g., advanced glycosylation end product-specific receptors, AIM2-like receptors, RIG-I-like receptors, and NOD1-like receptors, and toll-like receptors), or following endocytic uptake. Thus, the DAMP Hypothesis is novel and complements other theories that explain the features of aging. Aging is not a disease. It is a feature of quantum cell design. DAMPs represent ideal biomarkers of aging and provide an attractive target for interventions in aging and age-associated diseases. DAMP phenotype = a loss of energy at the electronic level in the cell. A loss of energy/information leads to a loss of time in your life.  

Chronically pumping in light to cells from the sun allows you to remain in a “zero entropy state” of health.   When quantum timing is off, life dies because it has to rely on ATP regeneration and recycling systems (EMF-4) which are only designed to support non-complex life like Archaea and Eubacteria……not a matrix with a complex nervous system in its head.

Cells that use water superconduction live far from equilibrium all the time. Cells are dissipative forms of plasma that allow for exotic physics to occur daily as light and dark act on the cell.   A zero entropy state defines what a perfect equilibrium is,  in case you are wondering.  Thermal energies, particularly at cellular equilibrium, possess no information potential at all to help biochemical reactants meet and react, whereas an excitation or resonance of a specific frequency at a certain temperature where no other excitation of the same energy exists in a system far from equilibrium  (a cell) not only has just the requisite information to do the work but the inherent power to do it as well. 

This power is built into its coherent cytostructural design and not into its mechanistic reactions found in a modern biochemistry textbook. The living organisms' cytostructure provides the motive force of attraction using the power of semiconduction between appropriate bio-reactive moieties. In turn, this enables efficient energy transfers to take place simultaneously without time ever being a major player in those reactions. In essence, time can stand still in a zero-entropy system because light is not moving inside your cells due to the physics of ions and matter in cells in how they are atomically organized.  

When this system gets any disorder (entropy) placed into it, we call this inflammation, randomness, or chaos increase, and the result is a process called aging.  It does appear that order comes with chaos.  This chaos is accounted for in a cell by its telomere length becoming shorter.  The shorter the telomere, the more molecular chaos is present and, hence, the older the living organism is.  This links leptin resistance to aging and shorter telomere lengths.  When life is constructed in a quantum fashion, ‘information’ is not something apart from the energy. It is accounted for in functional design and organization.

CITES

https://www.picardlab.org/uploads/7/7/8/4/77845210/s42255-023-00968-8.pdf

https://www.nature.com/articles/s41566-024-01412-3

https://www.youtube.com/watch?v=IKPC64n_U0s&t=114s