Template:Correction NAD and H+: Difference between revisions

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== Hydrogen ion ambiguities in the electron transfer system ==
== Hydrogen ion ambiguities in the electron transfer system ==


Β  Communicated by [[Gnaiger E]] (2023-10-04)
Β  Communicated by [[Gnaiger E]] (2023-10-08) last update 2023-11-10


:::: Electron (e<sup>-</sup>) transfer linked to hydrogen ion (H<sup>+</sup>) transfer is a fundamental concept in the field of bioenergetics, critical for understanding redox-coupled energy transformations. However, the current literature contains ambiguities regarding H<sup>+</sup> formation on the negative side of bioenergetic membranes, such as the matrix side of the mitochondrial inner membrane, during oxidative phosphorylation (OXPHOS). This uncertainty arises particularly when examining the oxidation of reduced nicotinamide adenine dinucleotide NADH by respiratory Complex I or succinate by Complex II. The graphical representations depicting putative H<sup>+</sup> formation in these redox reactions conflict with chemiosmotic coupling stoichiometries between H<sup>+</sup> translocation across the coupling membrane and electron transfer to oxygen. The oxidized NAD<sup>+</sup> is distinguished from NAD<sup>+</sup> indicating nicotinamide adenine dinucleotide independent of oxidation state. Clarity in this complex area is essential to prevent confusion, especially given the increasing number of interdisciplinary publications on bioenergetics related to diagnostic and clinical applications of OXPHOS analysis.
:::: Electron (e<sup>-</sup>) transfer linked to hydrogen ion (hydron; H<sup>+</sup>) transfer is a fundamental concept in the field of bioenergetics, critical for understanding redox-coupled energy transformations. Β 
[[File:Ambiguity alert H+.png|left|80px]]
:::: However, the current literature contains inconsistencies regarding H<sup>+</sup> formation on the negative side of bioenergetic membranes, such as the matrix side of the mitochondrial inner membrane, when NADH is oxidized during oxidative phosphorylation (OXPHOS). Ambiguities arise when examining the oxidation of NADH by respiratory Complex I or succinate by Complex II.
[[File:Ambiguity alert e-.png|left|70px]]
:::: Oxidation of NADH or succinate involves a two-electron transfer of 2{H<sup>+</sup>+e<sup>-</sup>} to FMN or FAD, respectively. Figures indicating a single electron e<sup>-</sup> transferred from NADH or succinate lack accuracy.Β 
[[File:Ambiguity alert NAD.png|left|60px]]
:::: The oxidized NAD<sup>+</sup> is distinguished from NAD indicating nicotinamide adenine dinucleotide independent of oxidation state. Β 
:::: NADH + H<sup>+</sup> β†’ NAD<sup>+</sup> +2{H<sup>+</sup>+e<sup>-</sup>}Β  is the oxidation half-reaction in this H<sup>+</sup>-linked electron transfer represented as 2{H<sup>+</sup>+e<sup>-</sup>} ([[Gnaiger 2023 MitoFit CII |Gnaiger 2023]]). Putative H<sup>+</sup> formation shown as NADH β†’ NAD<sup>+</sup> + H<sup>+</sup> conflicts with chemiosmotic coupling stoichiometries between H<sup>+</sup> translocation across the coupling membrane and electron transfer to oxygen. Ensuring clarity in this complex field is imperative to tackle the apparent ambiguity crisis and prevent confusion, particularly in light of the increasing number of interdisciplinary publications on bioenergetics concerning diagnostic and clinical applications of OXPHOS analysis.


[[Category:Ambiguidity crisis - NAD and H+]]
[[Category:Ambiguity crisis - NAD and H+]]

Latest revision as of 04:15, 10 November 2023

Hydrogen ion ambiguities in the electron transfer system

Communicated by Gnaiger E (2023-10-08) last update 2023-11-10
Electron (e-) transfer linked to hydrogen ion (hydron; H+) transfer is a fundamental concept in the field of bioenergetics, critical for understanding redox-coupled energy transformations.
Ambiguity alert H+.png
However, the current literature contains inconsistencies regarding H+ formation on the negative side of bioenergetic membranes, such as the matrix side of the mitochondrial inner membrane, when NADH is oxidized during oxidative phosphorylation (OXPHOS). Ambiguities arise when examining the oxidation of NADH by respiratory Complex I or succinate by Complex II.
Ambiguity alert e-.png
Oxidation of NADH or succinate involves a two-electron transfer of 2{H++e-} to FMN or FAD, respectively. Figures indicating a single electron e- transferred from NADH or succinate lack accuracy.
Ambiguity alert NAD.png
The oxidized NAD+ is distinguished from NAD indicating nicotinamide adenine dinucleotide independent of oxidation state.
NADH + H+ β†’ NAD+ +2{H++e-} is the oxidation half-reaction in this H+-linked electron transfer represented as 2{H++e-} (Gnaiger 2023). Putative H+ formation shown as NADH β†’ NAD+ + H+ conflicts with chemiosmotic coupling stoichiometries between H+ translocation across the coupling membrane and electron transfer to oxygen. Ensuring clarity in this complex field is imperative to tackle the apparent ambiguity crisis and prevent confusion, particularly in light of the increasing number of interdisciplinary publications on bioenergetics concerning diagnostic and clinical applications of OXPHOS analysis.
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