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Difference between revisions of "PM-pathway control state"

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[[Pyruvate]] (P) is oxidatively decarboxylated to acetyl-CoA and CO<sub>2</sub>, yielding [[NADH]] catalyzed by pyruvate dehydrogenase. [[Malate]] (M) is oxidized to oxaloacetate by mt-malate dehydrogenase located in the mitochondrial matrix. Condensation of oxaloacate with acetyl-CoA yields citrate (citrate synthase). 2-oxoglutarate (Ξ±-ketoglutarate) is formed from isocitrate (isocitrate dehydrogenase).
[[Pyruvate]] (P) is oxidatively decarboxylated to acetyl-CoA and CO<sub>2</sub>, yielding [[NADH]] catalyzed by pyruvate dehydrogenase. [[Malate]] (M) is oxidized to oxaloacetate by mt-malate dehydrogenase located in the mitochondrial matrix. Condensation of oxaloacate with acetyl-CoA yields citrate (citrate synthase). 2-oxoglutarate (Ξ±-ketoglutarate) is formed from isocitrate (isocitrate dehydrogenase).
|info=[[Gnaiger 2014 MitoPathways |Gnaiger 2014 MitoPathways - Chapter 3.2]]
|info=[[Gnaiger 2020 BEC MitoPathways]]
}}
}}
{{MitoPedia concepts
{{MitoPedia concepts
|mitopedia concept=SUIT state
|mitopedia concept=SUIT state
}}
}}
[[File:PM.jpg|right|400px|link=Gnaiger 2014 MitoPathways |Gnaiger 2014 MitoPathways - Chapter 3.2]]
[[File:PM.jpg|right|400px|link=Gnaiger 2020 BEC MitoPathways |Gnaiger 2020 BEC MitoPathways]]


== PM<sub>''L''</sub> ==
== PM<sub>''L''</sub> ==

Revision as of 20:12, 1 January 2021


high-resolution terminology - matching measurements at high-resolution


PM-pathway control state

Description

PM

PM: Pyruvate & Malate.

MitoPathway control state: NADH Electron transfer-pathway state

SUIT protocol: 1PM;2D;3U;4G;5S;6Oct;7Rot;8Gp- - SUIT_RP1

Pyruvate (P) is oxidatively decarboxylated to acetyl-CoA and CO2, yielding NADH catalyzed by pyruvate dehydrogenase. Malate (M) is oxidized to oxaloacetate by mt-malate dehydrogenase located in the mitochondrial matrix. Condensation of oxaloacate with acetyl-CoA yields citrate (citrate synthase). 2-oxoglutarate (Ξ±-ketoglutarate) is formed from isocitrate (isocitrate dehydrogenase).

Abbreviation: PM

Reference: Gnaiger 2020 BEC MitoPathways


MitoPedia concepts: SUIT state 

Gnaiger 2020 BEC MitoPathways

PML

LEAK state (L) with PM as N-linked substrates can be evaluated in the following SUIT protocols:


PMP

OXPHOS state (P) with PM as N-linked substrates can be evaluated in the following SUIT protocols:

PME

ET state (E) with PM as N-linked substrates can be evaluated in the following SUIT protocols:


Linear coupling control in the N-pathway control state: L – P - E

  • L - P
OXPHOS-coupling efficiency (P-L or β‰ˆP control factor), jβ‰ˆP = β‰ˆP/P = (P-L)/P = 1-L/P, is measured in the N-linked pathway state, with defined coupling sites (CI, CIII, CIV) and at high flux.
  • P - E
CCCP is titrated stepwise to maximum flux, to evaluate limitation of OXPHOS by the phosphorylation system, expressed as the apparent excess E-P capacity factor (E-P coupling control factor), jExP = (E-P)/E = 1-P/E. If jExP>0, then the E-L coupling efficiency rather than the OXPHOS-coupling efficiency is the proper expression of coupling, jβ‰ˆE = β‰ˆE/E = (E-L)/E = 1-L/E.


Discussion

The Pyruvate anaplerotic pathway control state (pyruvate alone) is not an ET-pathway competent substrate state in most mt-preparations, since acetyl-CoA accumulates without the co-substrate (oxaloacetate) of citrate synthase.
The Malate-anaplerotic pathway control state (M alone) is not an ET-pathway competent substrate state in many mt-preparations, since oxaloacetate accumulates without the co-substrate (acetyl-CoA) of citrate synthase.