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Difference between revisions of "Oxygen flux"

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{{MitoPedia
{{MitoPedia
|abbr=''J''<sub>O2</sub>
|abbr=''J''<sub>O2</sub>
|description='''Oxygen flux''', ''J''<sub>O2</sub>, is a [[specific quantity]]. Oxygen flux is [[oxygen flow]], ''I''<sub>O2</sub> [mol·s<sup>-1</sup> per system], divided by system size.  Flux may be volume-specific (flow per volume [pmol·s<sup>-1</sup>·ml<sup>-1</sup>]), mass-specific (flow per mass [pmol·s<sup>-1</sup>·mg<sup>-1</sup>]), or marker-specific (e.g. flow per mtDNA). Oxygen flux (e.g. per body mass, or per cell mass) is distinguished from oxygen flow (per subject, or per million cells).
|description='''Oxygen flux''', ''J''<sub>O<sub>2</sub></sub>, is a [[specific quantity]]. Oxygen [[flux]] is [[oxygen flow]], ''I''<sub>O<sub>2</sub></sub> [mol·s<sup>-1</sup> per system] (an [[extensive quantity]]), divided by system size.  Flux may be volume-specific (flow per volume [pmol·s<sup>-1</sup>·mL<sup>-1</sup>]), mass-specific (flow per mass [pmol·s<sup>-1</sup>·mg<sup>-1</sup>]), or marker-specific (flow per mtEU). Oxygen flux (''e.g.'', per body mass, or per cell volume) is distinguished from oxygen flow (per number of objects, such as cells), ''I''<sub>O<sub>2</sub></sub> [mol·s<sup>-1</sup>·x<sup>-1</sup>].  These are different forms of [[normalization of rate]].
|info=[[Gnaiger 2014 MitoPathways]], [[Gnaiger 1993 PAC]], [[Renner_2003_Biochim_Biophys_Acta]]
|info=[[BEC 2020.1]], [[Gnaiger 2020 BEC MitoPathways]], [[Gnaiger 1993 Pure Appl Chem]], [[Renner 2003 Biochim  Biophys Acta]]
|type=Respiration
}}
}}
{{MitoPedia concepts
Contributed by [[Gnaiger E]] (2020-01-15)
|mitopedia concept=MitoFit Quality Control System
 
|type=Respiration
== Which SI units should be used? ==
}}
 
{{MitoPedia methods
:::* '''The SI unit for volume'''
|mitopedia method=Respirometry
:::::: 1000 L = 1 m<sup>3</sup>
|type=Respiration
:::::: 1 L = 1 dm<sup>3</sup>
}}
:::::: 1 mL = 1 cm<sup>3</sup>
{{MitoPedia SUIT|type=Respiration
:::::: 1 µL = 1 mm<sup>3</sup>
}}
 
{{MitoPedia topics|type=Respiration
:::* '''Convert various units of volume-specific oxygen flux''', ''J''<sub>O<sub>2</sub></sub>, to '''SI units''' [nmol·s<sup>-1</sup>·L<sup>-1</sup>] = [pmol·s<sup>-1</sup>·mL<sup>-1</sup>]
}}
 
{{Labeling
:::::: 1 µmol O<sub>2</sub>∙min<sup>-1</sup>∙L<sup>-1</sup> ∙ [1000 nmol∙(1 µmol)<sup>-1</sup>] ∙ [1 min∙(60 s)<sup>-1</sup>] = 16.67 nmol O<sub>2</sub>∙s<sup>-1</sup>∙L<sup>-1</sup>
|discipline=Mitochondrial Physiology
:::::: 1 nmol O<sub>2</sub>∙min<sup>-1</sup>∙mL<sup>-1</sup> ∙ [1000 pmol∙(1 nmol)<sup>-1</sup>] ∙ [1 min∙(60 s)<sup>-1</sup>] = 16.67 pmol O<sub>2</sub>∙s<sup>-1</sup>∙mL<sup>-1</sup>
|kinetics=Oxygen
:::::: 1 nmol O<sub>2</sub>∙h<sup>-1</sup>∙mL<sup>-1</sup> ∙ [1000 pmol∙(1 nmol)<sup>-1</sup>] ∙ [1 min∙(60 s)<sup>-1</sup>] ∙ [1 h∙(60 min)<sup>-1</sup>] = 0.2778 pmol O<sub>2</sub>∙s<sup>-1</sup>∙mL<sup>-1</sup>
|instruments=Theory
 
|type=Respiration
:::::: 1 natom O∙s<sup>-1</sup>∙L<sup>-1</sup> ∙ [1 nmol O<sub>2</sub>∙(2 natm O)<sup>-1</sup>] = 0.5 nmol O<sub>2</sub>∙s<sup>-1</sup>∙L<sup>-1</sup>
}}
:::::: 1 natom O∙min<sup>-1</sup>∙L<sup>-1</sup> ∙ [1000 pmol O<sub>2</sub>∙(2 natom O)<sup>-1</sup>] ∙ [1 min∙(60 s)<sup>-1</sup>] = 8.33 pmol O<sub>2</sub>∙s<sup>-1</sup>∙L<sup>-1</sup>
== Oxygen flux in open O2k-Chamber ==
 
{{Technical support integrated}}
:::* '''Convert [[VO2max |''V''<sub>O<sub>2</sub>max/''M''</sub>]] from ergometric to SI units'''
{{#set:Technical service=O2 signal|Technical service=Chamber}}
:::::: 1 mL O<sub>2</sub>∙min<sup>-1</sup>∙kg<sup>-1</sup> (at [[STPD]]) ∙ [1000 µmol∙(22.392 mL)<sup>-1</sup>] ∙ [1 min∙(60 s)<sup>-1</sup>] = 0.744 µmol O<sub>2</sub>∙s<sup>-1</sup>∙kg<sup>-1</sup>
In an [[open chamber]] of the O2k the liquid phase in the chamber (aqueous medium) is in equilibrium with the atmosphere. All oxygen consumed by the polarographic oxygen sensor ([[POS]]) is immediately replaced from the atmosphere. The oxygen signal therefore has to be constant and the (negative) time derivative of the oxygen signal, called "O2 slope uncorr." in DatLab, has to be zero. The background corrected oxygen flux is meaningless for the open chamber situation. This is because the background correction at air saturation subtracts the consumption of oxygen by the sensor from the negative slope, when diffusion into and out of the chamber is zero at air saturation. Therefore, the background-corrected oxygen flux in the open chamber at air saturation is shown as a negative value. To avoid this apparent artefact, the "O2 slope uncorr." is selected to be shown while the chamber is open. Only Graph Layouts that display "O2 slope uncorr." are suitable for assessing the stability of the oxygen signal when the chamber is open. Such Layouts are:
 
* 01 Calibration Exp Gr3-Temp
:::* There is a difference between '''oxygen flux per volume''' and '''oxygen concentration change per time'''
* 02 Background Experiment
* 04 Flux per Volume uncorrected
* Z Trouble Shooting


The observation of a zero flux with an open chamber is an important performance parameter. It indicates that thermal stability and equilibrium of oxygen between the gas and aqueous phases have been reached. Therefore no experiment should be started before a zero "O2 slope uncorr." has been reached with an open chamber. The suggested criterion for signal stability is a "O2 slope uncorr." between -1 pmol/(s ml) and + 1 pmol/(s ml).
:::::: The oxygen concentration change per time (= rate of concentration change) is expressed in units [µmol O<sub>2</sub>∙L<sup>-1</sup>∙s<sup>-1</sup>].
:::::::: By definition the rate of concentration change is zero in an open system at steady-state, when the concentration in the system does not change at any respiratory flux by the sample enclosed in the open system.  


:::::: Oxygen flux per volume (= volume-specific oxygen flux) is expressed in units [µmol O<sub>2</sub>∙s<sup>-1</sup>∙L<sup>-1</sup>] or [nmol O<sub>2</sub>∙s<sup>-1</sup>∙L<sup>-1</sup>]
:::::::: By definition the volume-specific oxygen flux is the [[advancement]] of reaction per volume of the reaction chamber.


'''Problem'''
:::::: Oxygen flux per mass (= mass-specific oxygen flux) is expressed in units [µmol O<sub>2</sub>∙s<sup>-1</sup>∙kg<sup>-1</sup>] = [pmol O<sub>2</sub>∙s<sup>-1</sup>∙mg<sup>-1</sup>]
:* The "O2 slope uncorr." does not reach the interval +/- 1 pmol/(s ml) even after a prolonged time (1 to 2 hours).
:::::::: By definition the mass-specific oxygen flux is the [[advancement]] of reaction per mass of the sample enclosed in the reaction chamber.  


'''Solutions'''
== References ==
:* The oxygen level in the gas phase may not correspond to air. Move the stopper upwards to exchange the gas phase and insert it partially using the [[Stopper-Spacer]] as a guide.
{{#ask:[[Additional label::Oxygen flux]]
:* The "O2 slope uncorr." is always calculated from the calibrated O2 signal. Check the [[MiPNet19.18D O2k-Calibration |POS calibration]].
| mainlabel=Bioblast link
:* Observe the [[Raw signal]] and check if it is in the expected range
|?Has title=Reference
:* If the raw signal is unstable, and thereby creating an apparent O2 flux, follow the instructions for [[Locating a problem]].
|?Was published in year=Year
|format=broadtable
|limit=5000
|offset=0
|sort=Has title
|order=ascending
}}


'''See also'''
{{Template:Keywords: Normalization}}
:» [[MiPNet19.18D O2k-Calibration]]
:» [[MiPNet06.03 POS-Calibration-SOP]]
:» [[MiPNet19.18E O2 Flux Analysis]]
:» [[MiPNet14.06 InstrumentalO2Background]]


[[Category:Technical service]]
{{MitoPedia concepts
|mitopedia concept=MiP concept, Ergodynamics
}}
{{MitoPedia methods
|mitopedia method=Respirometry
}}

Latest revision as of 01:14, 31 December 2020


high-resolution terminology - matching measurements at high-resolution


Oxygen flux

Description

Oxygen flux, JO2, is a specific quantity. Oxygen flux is oxygen flow, IO2 [mol·s-1 per system] (an extensive quantity), divided by system size. Flux may be volume-specific (flow per volume [pmol·s-1·mL-1]), mass-specific (flow per mass [pmol·s-1·mg-1]), or marker-specific (flow per mtEU). Oxygen flux (e.g., per body mass, or per cell volume) is distinguished from oxygen flow (per number of objects, such as cells), IO2 [mol·s-1·x-1]. These are different forms of normalization of rate.

Abbreviation: JO2

Reference: BEC 2020.1, Gnaiger 2020 BEC MitoPathways, Gnaiger 1993 Pure Appl Chem, Renner 2003 Biochim Biophys Acta

Contributed by Gnaiger E (2020-01-15)

Which SI units should be used?

  • The SI unit for volume
1000 L = 1 m3
1 L = 1 dm3
1 mL = 1 cm3
1 µL = 1 mm3
  • Convert various units of volume-specific oxygen flux, JO2, to SI units [nmol·s-1·L-1] = [pmol·s-1·mL-1]
1 µmol O2∙min-1∙L-1 ∙ [1000 nmol∙(1 µmol)-1] ∙ [1 min∙(60 s)-1] = 16.67 nmol O2∙s-1∙L-1
1 nmol O2∙min-1∙mL-1 ∙ [1000 pmol∙(1 nmol)-1] ∙ [1 min∙(60 s)-1] = 16.67 pmol O2∙s-1∙mL-1
1 nmol O2∙h-1∙mL-1 ∙ [1000 pmol∙(1 nmol)-1] ∙ [1 min∙(60 s)-1] ∙ [1 h∙(60 min)-1] = 0.2778 pmol O2∙s-1∙mL-1
1 natom O∙s-1∙L-1 ∙ [1 nmol O2∙(2 natm O)-1] = 0.5 nmol O2∙s-1∙L-1
1 natom O∙min-1∙L-1 ∙ [1000 pmol O2∙(2 natom O)-1] ∙ [1 min∙(60 s)-1] = 8.33 pmol O2∙s-1∙L-1
  • Convert VO2max/M from ergometric to SI units
1 mL O2∙min-1∙kg-1 (at STPD) ∙ [1000 µmol∙(22.392 mL)-1] ∙ [1 min∙(60 s)-1] = 0.744 µmol O2∙s-1∙kg-1
  • There is a difference between oxygen flux per volume and oxygen concentration change per time
The oxygen concentration change per time (= rate of concentration change) is expressed in units [µmol O2∙L-1∙s-1].
By definition the rate of concentration change is zero in an open system at steady-state, when the concentration in the system does not change at any respiratory flux by the sample enclosed in the open system.
Oxygen flux per volume (= volume-specific oxygen flux) is expressed in units [µmol O2∙s-1∙L-1] or [nmol O2∙s-1∙L-1]
By definition the volume-specific oxygen flux is the advancement of reaction per volume of the reaction chamber.
Oxygen flux per mass (= mass-specific oxygen flux) is expressed in units [µmol O2∙s-1∙kg-1] = [pmol O2∙s-1∙mg-1]
By definition the mass-specific oxygen flux is the advancement of reaction per mass of the sample enclosed in the reaction chamber.

References

Bioblast linkReferenceYear
Gnaiger E et al ― MitoEAGLE Task Group (2020) Mitochondrial physiology. Bioenerg Commun 2020.1. https://doi.org/10.26124/bec:2020-0001.v12020


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MitoPedia concepts: MiP concept, Ergodynamics 


MitoPedia methods: Respirometry