Nonequilibrium Steady State of a Nanometric Biochemical System:  Determining the Thermodynamic Driving Force from Single Enzyme Turnover Time Traces

Nano Letters ◽  
2005 ◽  
Vol 5 (12) ◽  
pp. 2373-2378 ◽  
Author(s):  
Wei Min ◽  
Liang Jiang ◽  
Ji Yu ◽  
S. C. Kou ◽  
Hong Qian ◽  
...  

Molecules ◽  
2020 ◽  
Vol 25 (3) ◽  
pp. 699 ◽  
Author(s):  
Miloslav Pekař

Molar balances of continuous and batch reacting systems with a simple reaction are analyzed from the point of view of finding relationships between the thermodynamic driving force and the chemical reaction rate. Special attention is focused on the steady state, which has been the core subject of previous similar work. It is argued that such relationships should also contain, besides the thermodynamic driving force, a kinetic factor, and are of a specific form for a specific reacting system. More general analysis is provided by means of the non-equilibrium thermodynamics of linear fluid mixtures. Then, the driving force can be expressed either in the Gibbs energy (affinity) form or on the basis of chemical potentials. The relationships can be generally interpreted in terms of force, resistance and flux.



2020 ◽  
Author(s):  
Miloslav Pekař

Molar balances of continuous and batch reacting systems with a simple reaction are analyzed from the point of view of finding relationships between the thermodynamic driving force and the chemical reaction rate. Special attention is focused on steady state, which has been the core subject of previous similar work. It is argued that such relationships should contain, besides the thermodynamic driving force, also a kinetic factor, and are of a specific form for a specific reacting system. More general analysis is provided by means of the non-equilibrium thermodynamics of linear fluid mixtures. Then, the driving force can be expressed either in Gibbs energy (affinity) form or on the basis of chemical potentials. The relationships can be generally interpreted in terms of force-resistance-flux.



2021 ◽  
Author(s):  
David W. Mulder ◽  
John W. Peters ◽  
Simone Raugei

Under steady state conditions, the differential stability of reaction intermediates can alter the rate and the direction of a catalytic process regardless the overall underlying thermodynamic driving force.



2020 ◽  
Author(s):  
Miloslav Pekař

Molar balances of continuous and batch reacting systems with a simple reaction are analyzed from the point of view of finding relationships between the thermodynamic driving force and the chemical reaction rate. Special attention is focused on steady state, which has been the core subject of previous similar work. It is argued that such relationships should contain, besides the thermodynamic driving force, also a kinetic factor, and are of a specific form for a specific reacting system. More general analysis is provided by means of the non-equilibrium thermodynamics of linear fluid mixtures. Then, the driving force can be expressed either in Gibbs energy (affinity) form or on the basis of chemical potentials. The relationships can be generally interpreted in terms of force-resistance-flux.



2019 ◽  
Author(s):  
Miloslav Pekař

Molar balances of continuous and batch reacting systems with a simple reaction are analyzed from the point of view of finding relationships between the thermodynamic driving force and the chemical reaction rate. Special attention is focused on steady state, which has been the core subject of previous similar work. It is argued that such relationships should contain, besides the thermodynamic driving force, also a kinetic factor, and are of a specific form for a specific reacting system. More general analysis is provided by means of the non-equilibrium thermodynamics of linear fluid mixtures. Then, the driving force can be expressed either in Gibbs energy (affinity) form or on the basis of chemical potentials. The relationships can be generally interpreted in terms of force-resistance-flux.





2016 ◽  
Vol 113 (4) ◽  
pp. 48001 ◽  
Author(s):  
Andrew Mellor ◽  
Mauro Mobilia ◽  
R. K. P. Zia


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