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Volume 4
Trends in Green Chemistry
ISSN: 2471-9889
Page 79
JOINT EVENT
Environmental Chemistry 2018 &
Green Technologies 2018
September 20-22, 2018
September 20-22, 2018 Berlin, Germany
&
7
th
Edition of International Conference on
Green Energy, Green Engineering and Technology
8
th
International Conference on
Environmental Chemistry and Engineering
Correlation between all the relevant bioprocesses of the genotype and phenotype
Emma A Tumasyan
Republic of Armenia
D
osage being result of interaction of two parameters – energy (conditions by agents) and time (dosage) = E (energy) x T
(time), as instrument brings about result. Analyses of modeling of results according to the method of dialectics “cause
and consequence” reveal a number of patterns: discreetness, continuity, homogeneity, heterogeneity, relativity, discontinuity,
abruptness, spontaneity and correlation between genotype and phenotype in the organism
in vivo
that characterize sufficient
and necessary factor to approve the quantum theory of
E. Schrödinger
that the mechanism of the biological process
in vivo
.
Based on this we can more deeply imagine the relationship between all bio-processes of the genotype and phenotype. It is
known that genotypic and phenotypic processes are biochemical, morphological, physiological, etc. All these bioprocesses
separately occur with the complete kinetics of frequency rate min-max-min. The relationship between these bioprocesses
is due to alternation, discreteness, continuity, relativity, spasmodic nature and correlation, which as a result are revealed by
the method of dose-effect - D=E
I,C
x T. Figure 1 presents the genotypic processes: different biochemical processes A1, A2,
A3, etc.; different morphological processes B1, B2, B3, etc.; different physiological processes C1, C2, C3, etc. The phenotypic
processes are presented: different biochemical processes a1, a2, a3, etc.; different morphological processes b1, b2, b3, etc.;
different physiological processes c1, c2, c3, etc. The property of alternation of these bioprocesses is carried out in this way:
A1→ A2→ A3, etc.; B1→ B2→ B3, etc.; C1→ C2→ C3, etc.; a1→ a2→ a3, etc.; b1→ b2→ b3, etc.; c1→ c2→ c3, etc., by the effect of
doses intervals, respectively [0-D1], [0-D2], [0-D3], etc., which provide discreteness, continuity, relativity, spasmodic nature
of these bioprocesses. The dose interval [0-D1] provides the bioprocesses A1, B1, C1, a1, b1, c1, with complete kinetics, at the
same time taking frequency rate min–max–min; the dose interval [0-D2] provides the bioprocesses A2, B2, C2, a2, b2, c2, with
complete kinetics, at the same time taking frequency rate min–max–min; the dose interval [0-D3] provides the bioprocesses
A3, B3, C3, a3, b3, c3, with complete kinetics, at the same time taking frequency rate min–max–min, i.e. the dose interval
[0-D] reveals the correlation between the relevant bioprocesses. In sum, we can conclude, that the revealed regularities of the
bioprocesses of the genotype and phenotype carry out the life cycle of the organism
in vivo
.
Figure :
Complete life cycle (min-max-min) occurred by genotypic, phenotypic, physiological bioprocesses which are interrelated by the regularities of
discontinuity, continuity, homogeneity, heterogeneity, relativity, successiveness and abruptness.
Recent Publications
1. Tumasyan E A (2017) Quantum transfer as a mechanism of the mutation
in vivo
. Science Stays True Here. Biological
and Chemical Research 254-264.
2. Djordjevic Y B (2014) Markov chain-like quantum biological modeling of mutations, aging and evolution. Life (Basel)
5(3):1518-1538.
Emma A Tumasyan, Trends in Green chem 2018, Volume 4
DOI: 10.21767/2471-9889-C2-012