DNA and cell communication via magneticscalar waves, a possible basic principle of theB io resonance Me thod?

Prof. Dr.-lng. Konstantin Meyl, Radolfzell, Germany

DNA generates a longitudinal wave that propagates in the direction of the magneticfield vector. Computed frequencies from the structure of DNA agree with those ofbiophoton radiation.The optimisation of efficiency by minimising the conduction losses leads to thedouble-he l ix s t ructure of DNA\

The vortex model of the magnetic scalar wave not only covers many observedstructures within the cell nucleus perfectly, but also explains the hyperboloidchannels in the matrix when two cells communicate with each other.

Potential vortices are an essential component of scalar waves", as discovered in7 990. The basic approach for an extended field theory was confirmed in 2009 withthe discovery of magnetic monopoles^^. This provides the opportunity to explain thephysical basis of life\With this first introduction of the magnetic scalar wave, it becomes clear that such awave is suitable to use genetic code chemically stored in the base pairs of the genesand electrically modulate them, so as to ^^piggyback^' information from the cellnucleus to another cell. At the receiving end, the reverse process takes place and thetransported information is converted back into a chemical structure. The necessaryenergy required to power the chemical process is provided by the magnetic scalarw a v e i t s e l f .

C e l l c o m m u n i c a t i o n

When two cel ls communicate wi th oneanother, when the information read in onecell is written to another, the question is howdoes the process of reading and writing andthe transfer of genetic information operatefrom a technical viewpoint.

Hydrogen bonds hold together electricallypolarised base pairs in a DNA strand bymeans of Coulomb force. To achieve this

polarisation, these hydrogen bonds mustbe disconnected and this requires electricalfield lines directed radially outwards. I amspeaking here of a field vortex.

Since the magnetic field vector liesperpendicular to the electrical, it inevitablypoints axially towards the DNA strand. Sothe movement of the field vortex towardsthe magnetic field results in a longitudinalwave, which we refer to as a magneticscalar wave (Fig. 1).

52nd International Congress for Bicom Therapists, 28 to 30 April in Fuldo, Germany

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Sugar-phosphate backbone

Hel ical co i l = 3.4 nm

Fig. 1: Field distribution of the electrical field (E)and magnetic flow density (B) in thedoub le he l i xV = speed of the DNA wavec = speed of light

(= vortex speed)

The biochemistty of the cell nucleus, thesubject of outstanding research, prescribesin practical terms what we need to lookfor ' .

"The coding areas in a DNA strand, the so-called genes, make up at most 10% of thetotal DNA ("exons"). The remaining DNA(90%), known as "introns", consists ofuncoded DNA. Introns were initiallyregarded as meaningless rubbish. Todaybiologists and geneticists believe that therole of this uncoded DNA lies in exposingthe coded areas and regulating how genesexpress themselves"̂ .

Yet introns could also hove a completelydifferent function which we will examine inmore detail in part 2.

The electrical field of the 4 bases

As we know, DNA is coiled into a doublehelix with a clockwise sense of rotation(type A or B). The two polynucleotidestrands have opposing polarity. Hydrogenbonds form between the bases wherebyadenine always forms a base pair withthymine and guanine forms a base pairwith cytosine^. They make up the characterset for genetic information.

Chemists distinguish between the fourbases by means of their structure whileengineers, on the other hand, woulddifferentiate on the basis of the different

charges. The electrical charges are verylow yet the distances are too, with the resultthat extremely high electrical field strengthscan occur, measured in volts per meter.

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When at rest the hydrogen bonds followthe field strength and neutralise thedifference in electrical charge between thebase pairs. DNA behaves outwardly in aneutral manner and , conversely, remainsunaffected by external electrical fields.

Due to the helical structure of the fieldvortex the field lines are not self-contained,however. They advance in a spirallingmotion, similar to a circularly polarisedwave (Fig. 2).

Only during the selection process are thehydrogen bonds briefly suspended and thebase pair separated slightly allowing thesequence of the open charges to be read.This requires a higher electrical fieldstrength. The magnetic scalar wave (Fig. 1)is, for example, capable of providing therequired voltage. Moreover, this is the onlytype of wave where the field vectors of theelectrical field point radially outwards as aprerequisite for interaction with theelectrical charge of the bases. The result isa modulation which is transferred on by thew a v e .

The circularly polarised double helix

The longitudinal wave used here ispropagated in the direction of the magneticfield vector. Consequently magnetic forcesdevelop between the vortex fields and theseare responsible for the creation of wavenodes as well as for the wave advancing.

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The vortex speed (speed of light c) spiralson along the external line. Since the path ismore than twice the length as a result,propagating this field information indirection x produces a longitudinal wavetravelling at 140,000 km/s. This is derivedfrom the geometrical dimensions'*, firstly, ofthe diameter of the helix (2 nm) and,secondly, of the distance in direction x(3.4 nm} measured through one full helicalturn (Fig. 1).

T h e w a v e l e n g t h o f t h e D N A w a v e

The next question is to determine thefrequency and wavelength of themodulated wave running in the direction ofthe magnetic field vector. The observedtendency for the helix to wrap itself like acoil with two twists around sphericalproteins, known as histones, providesvaluable information here.

It is obvious that the two twists correspondto half the period. Consequently the transferfrom one histone to the next always occursin a wave node and therefore correspondsto half the wavelength. If one coil carriesthe positive half wave, then theneighbouring coil is responsible for thenegative and vice versa. The aifernatingdirection of twist from one coil to the nextconfirms that this assumption is correct!

The length of the DNA strand of both twistscan be determined in two ways.

An average coil diameter of 10 nm isassumed for the nucleosome core particlesconsisting of the coil body (histone) and theDNA molecule wrapped around it^. Themolecular length of a twist in the centre ofthe DNA thread is therefore (7T-10) nm andthe wavelength with 4 twists distributedover 2 histones:

^DNA = 1 26 nm .

The values cited in the technical literaturediffer in some cases, as a result of thedegree of concentration of the molecule.Error analysis would help to limit thepossible range of fluctuation.

Published data observed with the help ofX-ray structural analysis provide valuableinformation for enabling the toleranceband to be estimated^. For the secondcomputation we must count the base pairs.

A nucleosome core particle has 146 bp(base pairs), enough for slightly less than1.8 twists while a full twist consists of 83bp, the two together therefore making up166 bp. Additional base pairs are requiredfor the transfer from one "coil bod/' to thenext. Unfortunately no reliable data areavailable on this. The high packing densitymakes it difficult to count within thecondensed chromatin fibre (Fig. 3). In anopen, uncondensed fibre the count is200 bp^

V

Repeatedafter 200 bp

Fig. 3: The open "decompressed" structure of aDNA strand indicating the direction of twist

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The helix progresses along its central axisby 0.332 nm per base pair*^. Multiplied bythe number of base pairs, the maximumand minimum wavelength, depending onthe degree of concentration, is therefore:

AoNAlmax) = 200 bp-2-0.332 = 132.8 nm^DNA(m'n) = 180 bp-2-0.332 = 119.5 nm

or, assuming a spread:

^DNA = 126 nm ± 6 nm

Speed of propagation vq^a and wavelengthAdna determine, in turn, the frequency ofthe DNA wove:

r ^foNA = VDHA/ADNA = 140-10V126-10-'foNA =(1-11 ± 0.06)10'^ Hz

{= UV radiation)where c/2.14 = 140-10"^ m/s

as average speed of the DNA wave

E v a l u a t i o n

The values determined here apply primarilyto B -DNA.

The important result that, at frequenciesaround 10^® Hz, the DNA wove consists ofUV radiation accords with experience fromprevious measurements.

Prof. Popp speaks in terms of biophotonsand demonstrates that the extremely weakUV light transmitted by cells can bedetected using highly sensitivephotomultipliers'.

In his research Prof. Heine surveyed tunnelstructures of the ground substance of theextracellular matrix and the values hedetermined match the wavelengthcalculated here^°.

Once again we see two scientistsinvestigating the same topic of cellcommunication without incorporating theother's results in their own research,despite overwhelming agreement in theirresults.

The reason could be that Popp places cellradiation at 126 nm in the range of thespeed of light whereas Heine works on thebasis of structure-borne sound as the speedof propagation. The latter view is probablycloser to reality yet there must be anexplanation and it lies in the nature ofmagnetic scalar waves.

Longitudinal waves have no fixed speed ofpropagation and consequently no fixedfrequency, but instead produce theobovementioned noise^'. If we wish tocharacterise them, we have to use thewavelength for this. This does not changeeven if the wave is slowed down to lowerspeedsV The speed of propagation is inturn dependent on the properties of themedium carrying the longitudinal wave.

L i t e r a t u r e

1 -1: Meyl, K: DNA- und Zellfunk, Eine feldphysikoiische Erklarung derZellkommunlkation uber mognetische Skolorwelien [DNA- and Cell Radio.Communication of cells explained by field physics including magnetic scalarwaves], INDEL Verl. (www.etzs.de) 2010

1 -2: Meyl, K; DNA and Cell Radio, Double helix structure and cell communicationexplained by field physics, 2nd World DNA Day - China, 2011, conf. proc. p. 145

2: from L. Fredholm: „Die Entdeckung der molekularen Struktur der DNA -Die Doppel-Helix" [The discovery of the molecular structure of DNA - thedouble helix]. Science, 9/2003

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3: Karp, Gerald: Cell and Molecular Biology, 4"" ed. 2005, (Molekulare Zellbiologie,1st German edition 2005), Springer Verlag, ISBN 3-540-23857-3

4-1: ditto. (Karp, Gerald), p. 5034-2: Jaenicke, L (ed.): Molekularblologle der Zelle [Molecular biology of the cell],

1st German edition, VCH Verlag,Weinheim, ISBN 3-527-26350-0, p. 109

5: Lewin, Benjamin: Genes IV, Oxford University Press, Cambridge 1990,ISBN 0-19-854268-2, page 421

6-1: Alberts, Bray, Lewis, Raff, Roberts, Watson: The Cell, 3'"^ ed. Garland Publishing,N.Y. 1994, ISBN 0-8153-1619-4, p. 345

6-2: Karp, Gerald: Molekulare Zellbiologie [Cell and Molecular Biology],1st German edition 2005, Springer Verlag, p. 620

7: Alberts, Bray, Lewis, Raff, Roberts, Watson: The Cell, 3'^^ ed. Garland Publishing,N.Y. 1994, ISBN 0-8153-1619-4, p. 343

8: Sinden, R.R.: DNA structure and function. Academic Press, T' ed. 1994. pp. 398.I S B N 0 - 1 2 - 6 4 5 7 5 0 - 6

9: Popp, A.F.: Neue Horizonte in der Medizin [New Horizons in Medicine], 2nd ed.Haug Verlag Heidelberg 1987

10: Heine, Hartmut: Lehrbuch der biologischen Medizin. Grundregulation undExtrazellulare Matrix [Textbook of Biological Medicine. Ground Regulation andExtracellular Matrix], 2nd ed. 1997, Hippokrates Verlag Stuttgart, p. 56

11: Meyl, K: Widerspruchsfreie Elektrodynamik. Die groBe Einheitliche Theoriewinkt, wenn neu entdeckte Potentialwirbel im Dielektrikum das Vektorpotentialersetzen. [Consistent electrodynamics. The great universal theory beckonswhen newly discovered potential vortices in the dielectric replace potentialvector.] INDEL-Verlag 2009, ISBN 978-3-940703-14-9

12-1: D.J.P. Morris et al.: Magnetische Monopole in magnetischem Festkorper entdeckt[Magnetic monopoles discovered in magnetic solid], press statement on 3.9.09 bythe Helmholtz-Gemeinschaft e.V. Berlin, and:

12-2: Dirac Strings and Magnetic Monopoles in the Spin Ice Dy2Ti207, Science16 October 2009, Vol. 326. no. 5951, pp. 411-414;

Additional publications (essays, books, CDs, DVDs) available atwww.meyl.eu (or in the shop of www.etzs.de

This scientific paper was first presented under the title "DNA and Cell Radio, double helixstructure and cell communications explained by field physics" on 26 April 2011 in Dalian,China. The author was also admitted as a member of the programme committee at thesecond World DNA Congress, attended by 10 Nobel prize winners amongst others.Prof. Meyl was also Chair of Track 2.7 and was appointed to the scientific advisory body ofthe World Congress, an indication of the scientific community's official recognition at thehighest level of his research into scalar waves.

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