Complex II ambiguities: Difference between revisions
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{{MitoPedia | {{MitoPedia | ||
|abbr=CII ambiguities | |abbr=CII ambiguities | ||
|description="The substrate of CII is succinate, which is oxidized forming fumarate while reducing flavin adenine dinucleotide FAD to FADH2, with further electron transfer to the quinone pool. Whereas reduced NADH is a substrate of Complex I linked to dehydrogenases of the TCA cycle and mt-matrix upstream of CI, reduced FADH2 is a product of Complex II with downstream electron flow from CII to Q" ( | |description=The [[Succinate pathway]] is represented in the literature in some cases with a surprising error which warrants an analysis of '''Complex II ambiguities'''. For clarification: "The substrate of CII is succinate, which is oxidized forming fumarate while reducing flavin adenine dinucleotide FAD to FADH2, with further electron transfer to the quinone pool. Whereas reduced NADH is a substrate of Complex I linked to dehydrogenases of the TCA cycle and mt-matrix upstream of CI, reduced FADH2 is a product of Complex II with downstream electron flow from CII to Q" (quote from Gnaiger 2020). | ||
|info=Gnaiger E (2020) Mitochondrial pathways and respiratory control. An introduction to OXPHOS analysis. 5th ed. Bioenerg Commun 2020.2. https://doi.org/10.26124/bec:2020-0002 | |info=Gnaiger E (2020) Mitochondrial pathways and respiratory control. An introduction to OXPHOS analysis. 5th ed. Bioenerg Commun 2020.2. https://doi.org/10.26124/bec:2020-0002 | ||
}} | }} | ||
== FADH<sub>2</sub> and S-pathway == | |||
[[File:Yepez 2018 PLOS One Fig1B.jpg|400px|right|link=Yepez 2018 PLOS One]] | |||
:::* FADH<sub>2</sub> appears in several publications as the substrate of CII in the forward direction of the Krebs cycle. This commonly found error requires correction. For clarification, see page 48 in [[Gnaiger_2020_BEC_MitoPathways |Gnaiger (2020)]]. | |||
::::* [[Arnold 2022 J Biol Chem]] | |||
::::* [[Martinez-Reyes 2020 Nat Commun]] | |||
::::* [[Yepez 2018 PLOS One]] | |||
::::* [[DeBerardinis 2016 Sci Adv]] | |||
::::* [[Sanchez 2001 Br J Pharmacol]] | |||
== CII and fatty acid oxidation == | |||
:::: "Since mitochondrial Complex II also participates in the oxidation of fatty acids (6), .." (quote from [ Lemmi et al 1990]). | |||
::::::* Ref 6: Tzagoloff A (1982) Mitochondria. Plenum, New York. | |||
{{MitoPedia concepts | {{MitoPedia concepts | ||
|mitopedia concept=MiP concept | |mitopedia concept=MiP concept | ||
}} | }} | ||
{{MitoPedia topics | {{MitoPedia topics | ||
|mitopedia topic=Enzyme, Substrate and metabolite | |mitopedia topic=Enzyme, Substrate and metabolite | ||
}} | }} | ||
Revision as of 18:11, 15 February 2023
Description
The Succinate pathway is represented in the literature in some cases with a surprising error which warrants an analysis of Complex II ambiguities. For clarification: "The substrate of CII is succinate, which is oxidized forming fumarate while reducing flavin adenine dinucleotide FAD to FADH2, with further electron transfer to the quinone pool. Whereas reduced NADH is a substrate of Complex I linked to dehydrogenases of the TCA cycle and mt-matrix upstream of CI, reduced FADH2 is a product of Complex II with downstream electron flow from CII to Q" (quote from Gnaiger 2020).
Abbreviation: CII ambiguities
Reference: Gnaiger E (2020) Mitochondrial pathways and respiratory control. An introduction to OXPHOS analysis. 5th ed. Bioenerg Commun 2020.2. https://doi.org/10.26124/bec:2020-0002
FADH2 and S-pathway
- FADH2 appears in several publications as the substrate of CII in the forward direction of the Krebs cycle. This commonly found error requires correction. For clarification, see page 48 in Gnaiger (2020).
CII and fatty acid oxidation
- "Since mitochondrial Complex II also participates in the oxidation of fatty acids (6), .." (quote from [ Lemmi et al 1990]).
- Ref 6: Tzagoloff A (1982) Mitochondria. Plenum, New York.
- "Since mitochondrial Complex II also participates in the oxidation of fatty acids (6), .." (quote from [ Lemmi et al 1990]).
MitoPedia concepts: MiP concept
MitoPedia topics:
Enzyme,
Substrate and metabolite