scholarly journals Entropy Production and Its Application to the Coupled Nonequilibrium Processes of ATP Synthesis

Entropy ◽  
2019 ◽  
Vol 21 (8) ◽  
pp. 746 ◽  
Author(s):  
Sunil Nath

Starting from the universal concept of entropy production, a large number of new results are obtained and a wealth of novel thermodynamic, kinetic, and molecular mechanistic insights are provided into the coupling of oxidation and ATP synthesis in the vital process of oxidative phosphorylation (OX PHOS). The total dissipation, Φ , in OX PHOS with succinate as respiratory substrate is quantified from measurements, and the partitioning of Φ into the elementary components of ATP synthesis, leak, slip, and other losses is evaluated for the first time. The thermodynamic efficiency, η , of the coupled process is calculated from the data on Φ and shown to agree well with linear nonequilibrium thermodynamic calculations. Equations for the P/O ratio based on total oxygen consumed and extra oxygen consumed are derived from first principles and the source of basal (state 4) mitochondrial respiration is postulated from molecular mechanistic considerations based on Nath’s two-ion theory of energy coupling within the torsional mechanism of energy transduction and ATP synthesis. The degree of coupling, q , between oxidation and ATP synthesis is determined from the experimental data and the irreversible thermodynamics analysis. The optimality of biological free energy converters is explored in considerable detail based on (i) the standard biothermodynamic approach, and (ii) a new biothermokinetic approach developed in this work, and an effective solution that is shown to arise from consideration of the molecular aspects in Nath’s theory is formulated. New experimental data in state 4 with uncouplers and redox inhibitors of OX PHOS and on respiratory control in the physiological state 3 with ADP and uncouplers are presented. These experimental observations are shown to be incompatible with Mitchell’s chemiosmotic theory. A novel scheme of coupling based on Nath’s two-ion theory of energy coupling within the torsional mechanism is proposed and shown to explain the data and also pass the test of consistency with the thermodynamics, taking us beyond the chemiosmotic theory. It is concluded that, twenty years since its first proposal, Nath’s torsional mechanism of energy transduction and ATP synthesis is now well poised to catalyze the progress of experimental and theoretical research in this interdisciplinary field.

Author(s):  
Zhasur Kulmukhamedov ◽  
Ravshan Khikmatov ◽  
Alisher Saidumarov ◽  
Yulduz Kulmukhamedova

The manuscript proposes analytical methods for calculating fuel economy and traction-speed properties when modeling the movement of cargo-carrying vehicles on real routes, based on theoretical and experimental studies in a hot and dry climate, which allows for determining the efficiency of cargo-carrying vehicles objectively in terms of traction and speed, fuel and economic indicators. Using the statistical processing of experimental, theoretical research data, the authors calculate the coefficient X2, which allows for evaluating the adequacy of the mathematical model and experimental data. As an example, the manuscript provides for an assessment of fuel economy and traction and speed properties. The authors presented the results in graphs for the ease of evaluating the effect of external temperature on fuel consumption and the average speed of a road train. The authors’ methodology allows for determining the efficiency of cargo-carrying vehicles in a hot and dry climate.


2018 ◽  
Author(s):  
A. Arango-Restrepo ◽  
J.M. Rubi ◽  
D. Barragán

AbstractWe show that the structural evolution of enzymes is largely influenced by the entropy produced in the enzymatic process. We have computed this quantity for the case in which the process has unstable and metastable intermediate states. By assuming that the kinetics takes place along a potential barrier, we have found that the behavior of the total entropy produced is a non-monotonic function of the intermediate state energy. By diminishing the number of metastable intermediate states, the total entropy produced decreases and consequently the enzyme kinetics and the thermodynamic efficiency are enhanced. Minimizing locally the total entropy produced for an enzymatic process with metastable intermediate states, the kinetics and the thermodynamic efficiency are raised. In contrast, in the absence of metastable intermediate states, a maximum of the entropy produced results in an improvement of the kinetic performance although the thermodynamic efficiency diminishes. Our results show that the enzymatic evolution proceeds not only to enhance the kinetics but also to optimize the total entropy produced.


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