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Difference between revisions of "Flux control efficiency"

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{{MitoPedia
{{MitoPedia
|abbr=''FCC''
|abbr=''FCC''
|description='''Flux control capacities''' express the control of respiration by a metabolic variable, ''X'', as a fractional change of flux, Ξ”''j'' (normalized, dimensionless). ''Z'' is the [[reference state]] with high (stimulated or un-inhibited) flux; ''Y'' is the [[background state]] at low flux, upon which ''X'' acts.Β  This yields the flux control ratio ''j<sub>Y</sub>''=''Y/Z''),
|description='''Flux control capacities''' express the control of respiration by a metabolic variable, ''X'', as a fractional change of flux from ''Y'' to ''Z'', Ξ”''j'' (normalized for ''Z'', dimensionless). ''Z'' is the [[reference state]] with high (stimulated or un-inhibited) flux; ''Y'' is the [[background state]] at low flux, upon which ''X'' acts.Β  This yields the flux control ratio ''j<sub>Y</sub>''=''Y/Z''),


:: Ξ”''j<sub>Z-Y</sub>'' = (''Z-Y'')/''Z'' = 1-''j<sub>Y</sub>''
:: Ξ”''j<sub>Z-Y</sub>'' = (''Z-Y'')/''Z'' = 1-''j<sub>Y</sub>''
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|mitopedia topic=Respiratory state, Respiratory control ratio
|mitopedia topic=Respiratory state, Respiratory control ratio
}}
}}
== Metabolic control variable, respiratory states and flux control capacities ==
== Metabolic control variable, respiratory states and flux control capacities ==



Revision as of 22:03, 4 August 2013


high-resolution terminology - matching measurements at high-resolution


Flux control efficiency

Description

Flux control capacities express the control of respiration by a metabolic variable, X, as a fractional change of flux from Y to Z, Ξ”j (normalized for Z, dimensionless). Z is the reference state with high (stimulated or un-inhibited) flux; Y is the background state at low flux, upon which X acts. This yields the flux control ratio jY=Y/Z),

Ξ”jZ-Y = (Z-Y)/Z = 1-jY

Complementary to the concept of flux control ratios and analogous to elasticities of metabolic control analysis, the flux control capacity of X upon background Y is expressed as the change of flux from Y to Z normalized for the reference state Z.

Abbreviation: FCC

Reference: Gnaiger 2013 Abstract MiP2013


MitoPedia methods: Respirometry 


MitoPedia topics: "Respiratory state" is not in the list (Enzyme, Medium, Inhibitor, Substrate and metabolite, Uncoupler, Sample preparation, Permeabilization agent, EAGLE, MitoGlobal Organizations, MitoGlobal Centres, ...) of allowed values for the "MitoPedia topic" property. Respiratory state"Respiratory state" is not in the list (Enzyme, Medium, Inhibitor, Substrate and metabolite, Uncoupler, Sample preparation, Permeabilization agent, EAGLE, MitoGlobal Organizations, MitoGlobal Centres, ...) of allowed values for the "MitoPedia topic" property., "Respiratory control ratio" is not in the list (Enzyme, Medium, Inhibitor, Substrate and metabolite, Uncoupler, Sample preparation, Permeabilization agent, EAGLE, MitoGlobal Organizations, MitoGlobal Centres, ...) of allowed values for the "MitoPedia topic" property. Respiratory control ratio"Respiratory control ratio" is not in the list (Enzyme, Medium, Inhibitor, Substrate and metabolite, Uncoupler, Sample preparation, Permeabilization agent, EAGLE, MitoGlobal Organizations, MitoGlobal Centres, ...) of allowed values for the "MitoPedia topic" property. 

Metabolic control variable, respiratory states and flux control capacities

A metabolic control variable, X, is either added (stimulation, activation) or removed (reversal of inhibition) to yield a high flux in thereference state, Z, from the background state, Y. X, Y and Z denote the metabolic control variable (X) or respiratory state (Y, Z) and the corresponding respiratory fluxes, X=Z-Y. Experimentally, inhibitors are added rather than removed (-X); then Y is the background state in the presence of the inhibitor.


Substrate control capacity

Substrate control capacities express the relative change of oxygen flux in response to a transition of substrate availability in a defined coupling state.


Coupling control capacity

Coupling control capacities are determined in an ETS-competent substrate state.