Team:Evry/Model3

From 2013.igem.org

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&nbsp;<img src="https://static.igem.org/mediawiki/2013/7/72/Reg1.png" height="30px"/><br/>
&nbsp;<img src="https://static.igem.org/mediawiki/2013/7/72/Reg1.png" height="30px"/><br/>
We reduced this equation to:<br/>
We reduced this equation to:<br/>
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<img src="https://static.igem.org/mediawiki/2013/e/e8/Reg2.png"/><br/>
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<img src="https://static.igem.org/mediawiki/2013/e/e8/Reg2.png" height="30px"/><br/>
Which is not annoying, since we just have to divide our [FeFur] by to to get the real complex concentration.<br/>
Which is not annoying, since we just have to divide our [FeFur] by to to get the real complex concentration.<br/>
We can easily write down both the formation (v) and the dissociation (v') speed:<br/>
We can easily write down both the formation (v) and the dissociation (v') speed:<br/>
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<img src="https://static.igem.org/mediawiki/2013/f/fe/Reg3.png"/><br/>
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<img src="https://static.igem.org/mediawiki/2013/f/fe/Reg3.png" height="30px"/><br/>
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<img src="https://static.igem.org/mediawiki/2013/8/84/Reg4.png"/><br/>
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<img src="https://static.igem.org/mediawiki/2013/8/84/Reg4.png" height="30px"/><br/>
We chose to model the iron input in the bacteria using a linear function of the external iron concentration <i>Ferext</i>, the factor <i>p</i> being the cell-wall permeability for iron.<br/>
We chose to model the iron input in the bacteria using a linear function of the external iron concentration <i>Ferext</i>, the factor <i>p</i> being the cell-wall permeability for iron.<br/>
The FUR on the other hand, is produced by the bacteria. It's evolution can also be considered linerar, using a mean production rate <i>Fur0</i>.<br/>
The FUR on the other hand, is produced by the bacteria. It's evolution can also be considered linerar, using a mean production rate <i>Fur0</i>.<br/>
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<img src="https://static.igem.org/mediawiki/2013/5/51/Regfer.png"/><br/>
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<img src="https://static.igem.org/mediawiki/2013/5/51/Regfer.png" height="30px"/><br/>
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<img src="https://static.igem.org/mediawiki/2013/6/68/Regfur.png"/><br/>
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<img src="https://static.igem.org/mediawiki/2013/6/68/Regfur.png" height="30px"/><br/>
In this model, we only track the free Fe-FUR and not those which are attached to a FUR Binding Site. As <i>LacI</i> is the number of inhibited LacI, we can use this number to express how much Fe-FUR does bind to a FBS per unit of time.<br/>
In this model, we only track the free Fe-FUR and not those which are attached to a FUR Binding Site. As <i>LacI</i> is the number of inhibited LacI, we can use this number to express how much Fe-FUR does bind to a FBS per unit of time.<br/>
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<img src="https://static.igem.org/mediawiki/2013/6/6d/Regfefur.png"/>
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<img src="https://static.igem.org/mediawiki/2013/6/6d/Regfefur.png" height="30px"/>
</p>
</p>

Revision as of 16:27, 4 October 2013

Iron coli project

Metabolic model

Overview

Enzymes regulation:
This regulation is based on two consecutives inhibitions, which, in the end, is an activator with a certain delay. The model will follow this principle.

Assumptions

Model Description

Variables:

  • [Fe] : Iron concentration inside the bacteria
  • [Fur] : FUR concentration inside the bacteria
  • [FeFur] : Iron-FUR complex concentration inside the bacteria
  • LacI : Number of inhibited LacI
  • LacO : Number of non-inhibited LacO
  • [mRNA]: mRNA (from LacO) concentration
  • [Enz] : Enzyme concentration : EntA,-B,-C,-D,-E,-F
All those concentrations are expressed in mmol/L

Parameters table:

Fe, FUR and FeFUR:
The iron-FUR complex is simply formed that way:
 
We reduced this equation to:

Which is not annoying, since we just have to divide our [FeFur] by to to get the real complex concentration.
We can easily write down both the formation (v) and the dissociation (v') speed:


We chose to model the iron input in the bacteria using a linear function of the external iron concentration Ferext, the factor p being the cell-wall permeability for iron.
The FUR on the other hand, is produced by the bacteria. It's evolution can also be considered linerar, using a mean production rate Fur0.


In this model, we only track the free Fe-FUR and not those which are attached to a FUR Binding Site. As LacI is the number of inhibited LacI, we can use this number to express how much Fe-FUR does bind to a FBS per unit of time.

Results

Conclusion

References: