Team:Evry/Modelmeta1
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We reduced this equation to:<br/> | We reduced this equation to:<br/> | ||
<img src="https://static.igem.org/mediawiki/2013/e/e8/Reg2.png"/><br/> | <img src="https://static.igem.org/mediawiki/2013/e/e8/Reg2.png"/><br/> | ||
- | Which is not annoying, since we just have to divide our [FeFur] by | + | Which is not annoying, since we just have to divide our [FeFur] by two to get the real complex concentration.<br/> |
- | We can easily write down both the formation (v) and the dissociation (v') | + | We can easily write down both the formation (v) and the dissociation (v') speeds:<br/> |
<img src="https://static.igem.org/mediawiki/2013/f/fe/Reg3.png"/><br/> | <img src="https://static.igem.org/mediawiki/2013/f/fe/Reg3.png"/><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. Its evolution can also be considered as linear, using a mean production rate <i>Fur0</i>.<br/> | + | The FUR on the other hand is produced by the bacteria. Its evolution can also be considered as linear, using a mean production rate of <i>Fur0</i>.<br/> |
<img src="https://static.igem.org/mediawiki/2013/5/51/Regfer.png"/><br/> | <img src="https://static.igem.org/mediawiki/2013/5/51/Regfer.png"/><br/> | ||
- | <img src="https://static.igem.org/mediawiki/2013/6/68/Regfur.png"/>< | + | <img src="https://static.igem.org/mediawiki/2013/6/68/Regfur.png"/> |
- | + | </p> | |
- | + | <p> | |
- | + | In this model, we only track the free Fe-FUR complex and not those attached to a FUR Binding Site. <i>FBS</i> is the number of inhibited Fur Binding Sites.<br/> | |
- | < | + | |
- | In this model, we only track the free Fe-FUR complex and not those attached to a FUR Binding Site. | + | |
<img src="https://static.igem.org/mediawiki/2013/6/6d/Regfefur.png"/> | <img src="https://static.igem.org/mediawiki/2013/6/6d/Regfefur.png"/> | ||
</p> | </p> |
Revision as of 15:10, 27 October 2013
Sensor Model
Introduction
In order to determine our Iron Coli's enterobactin production rate, we first have to know how much time our bacteria will take to sense the ambient iron. So, this first part of the Enterobactin production model focuses on the synthetic sensing system our team implemented in the bacteria.
Observations
As shown on the Figure 1, our sensing system relies on a FUR Binding Site (FBS). In order to easily model the sensing delay and analyse its results, the first construction is composed of a GFP placed right after the FBS.
Goals
Our goal in this part of the model is to create a generic FBS-related sensing model so that:
- We can determine the iron-sensing delay of our bacteria
- The model can can be reused by other iron related projects
Materials and methods
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 two to get the real complex concentration.
We can easily write down both the formation (v) and the dissociation (v') speeds:
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. Its evolution can also be considered as linear, using a mean production rate of Fur0.
In this model, we only track the free Fe-FUR complex and not those attached to a FUR Binding Site. FBS is the number of inhibited Fur Binding Sites.
Results
Conclusion
Models and scripts
References: