Additive effect of convergent electron flow: Difference between revisions

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Electron flow converges at the [[Q-junction]] from respiratory Complexes I and II ([[CI+II e-input]]), [[glycerophosphate dehydrogenase]] and [[electron-transferring flavoprotein]].  Convergent electron flow corresponds to the operation of the [[TCA cycle]] and mitochondrial substrate supply in vivo.   
Electron flow converges at the '''Q-junction''' from respiratory Complexes I and II ([[CI+II e-input]]), [[glycerophosphate dehydrogenase]] and [[electron-transferring flavoprotein]].  Convergent electron flow corresponds to the operation of the [[TCA cycle]] and mitochondrial substrate supply in vivo.   
==Additive effect==
==Additive effect==
Convergent electron flow simultaneously through CI+II into the [[Q-junction]] supports higher [[OXPHOS]] and [[ETS]] capacities than separate electron flow through either CI or CII.  Physiological substrate combinations supporting convergent CI+II e-input are required for reconstitution of intracellular [[TCA cycle]] function.  The convergent CI+II effect may be completely or partially additive, suggesting that conventional bioenergetic protocols with [[mt-preparations]] have underestimated cellular OXPHOS capacities.
Convergent electron flow simultaneously through CI+II into the [[Q-junction]] supports higher [[OXPHOS]] and [[ETS]] capacities than separate electron flow through either CI or CII.  Physiological substrate combinations supporting convergent CI+II e-input are required for reconstitution of intracellular [[TCA cycle]] function.  The convergent CI+II effect may be completely or partially additive, suggesting that conventional bioenergetic protocols with [[mt-preparations]] have underestimated cellular OXPHOS capacities.

Revision as of 15:20, 15 August 2010

Electron flow converges at the Q-junction from respiratory Complexes I and II (CI+II e-input), glycerophosphate dehydrogenase and electron-transferring flavoprotein. Convergent electron flow corresponds to the operation of the TCA cycle and mitochondrial substrate supply in vivo.

Additive effect

Convergent electron flow simultaneously through CI+II into the Q-junction supports higher OXPHOS and ETS capacities than separate electron flow through either CI or CII. Physiological substrate combinations supporting convergent CI+II e-input are required for reconstitution of intracellular TCA cycle function. The convergent CI+II effect may be completely or partially additive, suggesting that conventional bioenergetic protocols with mt-preparations have underestimated cellular OXPHOS capacities.

References

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