Cell Language Theory, The: Connecting Mind And Matter

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126 The Cell Language Theory: Connecting Mind and Matter

b2861 The Cell Language Theory: Connecting Mind and Matter “6x9”

apparently can vary from 8 to 12 depending on organisms (see Figures 3.35
and 3.36). In addition, the most significant deficiency of the chemiosmotic
model, from the theoretical point of view, is the lack of any enzymologi-
cally realistic molecular mechanism of generating the proton-motive
force, comparable to the one depicted in Figure 3.30.

3.3.4 A Comparison Between the Chemiosmotic and Conformon
Models of Oxidative Phosphorylation
A visual comparison between the chemiosmotic and conformon models of
oxphos is given in Figure 3.34. There are three essential differences
between these two models:

(1) The absence in the former and the presence in the latter of the con-
cept of conformons, the molecular mechanisms postulated to underly
all bioenergetic processes in the living cell (see process 4 in Figure
3.29 and Section 3.4).
(2) The transmembrane proton gradient as the primary cause for ATP
synthesis in the former and as caused by the conformon in the latter
(compare processes 3 and 4 in Figure 3.29).
(3) Of the two possible mechanisms for coupling respiration and phos-
phorylation reactions, namely via the intra-membrane proton move-
ment (i.e., step 2 followed by step 4 in Figure 3.29) and the
trans-membrane proton movement (i.e., step 3 in Figure 3.29) fol-
lowed by the bulk phase proton-driven shifting of the equilibrium
reaction, ADP + Pi + H+ ↔ ATP + H 2 O, toward ATP synthesis), only
the latter of which is being utilized by the chemiosmotic model (see
Figure 3.32b).

I have long been a critic of the chemiosmotic hypothesis [7, 14, 25],
primarily because the model does not propose any fundamental theories
nor principles concerning the molecular mechanisms underlying oxidative
phosphorylation and photophosphorylation. Besides, even if the chemios-
motic hypothesis proves to be phenomenologically correct, it cannot rep-
resent a universal principle of biological energy coupling, because there
are membrane-independent (and hence non-osmotic) energy-coupled

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