3) EMC is observed only in some solutions of the leachate with high moisture content. For example, solutions from 10-9 to 10-18 certain drugs filtrates (E). coli.
4) In the case of the M. pirum separated single gene (adgezin, previously cloned and sekvenirovannyj) was able to call EMC. Because the gene was cloned into two pieces, each individual piece was able to produce EMC, that suggests, that short DNA sequence sufficient for the production of signals. Similarly,, short DNA sequence of HIV (104 base pairs) It was easy for EMC.
5) Some bacteria do not produce EMC: as in the case of probiotic bacteria, such as Lactobacillus, as well as some laboratory species (E). coli, used as a vector kloniruûŝego.
6) These studies have been extended to viruses, Although not all the viral family were studied. Like EMC were found in some exogenous retroviruses (HIV, leukemia), hepatitis viruses (hepatitis B, (C)) and influenza a (culture in vitro). On the whole, EMC (and the accompanying spinor field? PG) It is made 20 nm filtrates viral suspensions or èkstragirovannymi DNA. The question remains for RNA viruses (hepatitis C, flu): whether RNA mature viral particles EMC source or not? In the case of HIV RNA are EMC virus particles, but the provirusnymi are made of DNA, present in the infected cells. In the case of EMC bacteria produced filtrates 100 nm, 20 nm but not filtrates, that shows the, that the size of the structures, generating EMC varies between 20 and 100 nm. This justifies the name of nanostructures. This research is likely to suggest, What we are dealing with nanostructures, consisting of water. Has been used highly purified water, However, you cannot delete the role the slightest traces of impurities. EMC is production stable to: Rnase activity, DNKazy (Although this destroys the DNA in the EMC), Protease (Proteinase k), Detergent (LTOS). However, they are sensitive to high temperature (more than 70° c) and low temperature (-80ºS).
This sensitivity is reduced with purified DNA sequences short. Technical conditions for the occurrence of EMS are shown in the following list:
– Filtering: 450/100 nm for bacterial DNA, 450/20 nm for viral DNA
Figure 3. The transfer of genetic information from the DNA in the water through the electromagnetic waves.
– Solution with great breeding water
– Mechanical stirring (Vortex) between each solution
– Extremely low-frequency excitation (KNČ) electromagnetic environment, starting from a very low value in 7Hz. Excite does not occur, When the system is protected by MU-metal cage.
