Team:Evry/ent prod

From 2013.igem.org

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In order to determine our <b><span style="color:#bb8900">Iron</span><span style="color:#7B0000"> Coli</span></b>'s enterobactin production rate, we modelize the different systems uses in our project: the iron sensor, the inverter system and the chelator system.We then divided this model in 3 differents parts.<br/>
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In order to determine our <b><span style="color:#bb8900">Iron</span><span style="color:#7B0000"> Coli</span></b>'s enterobactin production rate, we modeled the different systems used in our project: the iron sensor, the inverter system and the chelator system.<br/>
The first part focuses on the synthetic <a href="https://2013.igem.org/Team:Evry/Sensor">sensing system</a>, the second on our <a href="https://2013.igem.org/Team:Evry/Inverter">inverter system</a> our team implemented in the bacteria. The last part intagrate those previous parts with the chemical reactions leading to the enterobactin production.
The first part focuses on the synthetic <a href="https://2013.igem.org/Team:Evry/Sensor">sensing system</a>, the second on our <a href="https://2013.igem.org/Team:Evry/Inverter">inverter system</a> our team implemented in the bacteria. The last part intagrate those previous parts with the chemical reactions leading to the enterobactin production.
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<h2>Sensor model</h2>
<h2>Sensor model</h2>
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We first modeled the iron absorption of a hemochromatosic patient using ODEs.
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We first modeled the sensing system using ODEs, with the help of experimental results to tune one of our parameters.
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<h2>Inverter model</h2>
<h2>Inverter model</h2>
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We then used the disease model as a base to develop our flush treatment model. It aims to answer the following question:<br/>
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We then used the sensor model as a base and build an inverter model downstream. This model allowed us to answer the following question:<br/>
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<em>"Is it possible to chelate a significant amount of iron with a flush strategy?"</em>
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<em>"Which plasmid's copy should we prioritize in our bacteria?"</em>
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<h2>Enterobactin production model</h2>
<h2>Enterobactin production model</h2>
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We then used the disease model as a base to develop our flush treatment model. It aims to answer the following question:<br/>
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As a final step, we combined the sensor model and the inverter model, and added an enzymatic reactions model to annswer this final question:<br/>
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<em>"Is it possible to chelate a significant amount of iron with a flush strategy?"</em>
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<em> "How much time is needed for our bacteria to start producing enterobactins from the moment they sense the iron?"</em>
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<a href="https://2013.igem.org/Team:Evry/Modelmeta3">Here is the link to the enterobactin production model</a>.
<a href="https://2013.igem.org/Team:Evry/Modelmeta3">Here is the link to the enterobactin production model</a>.
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Revision as of 02:40, 29 October 2013

Iron coli project

Enterobactin production model overview

Introduction

Ent

In order to determine our Iron Coli's enterobactin production rate, we modeled the different systems used in our project: the iron sensor, the inverter system and the chelator system.
The first part focuses on the synthetic sensing system, the second on our inverter system our team implemented in the bacteria. The last part intagrate those previous parts with the chemical reactions leading to the enterobactin production.

Sensor model

We first modeled the sensing system using ODEs, with the help of experimental results to tune one of our parameters.

Here is the link to the sensor model.

Inverter model

We then used the sensor model as a base and build an inverter model downstream. This model allowed us to answer the following question:
"Which plasmid's copy should we prioritize in our bacteria?"

Here is the link to the inverter model.

Enterobactin production model

As a final step, we combined the sensor model and the inverter model, and added an enzymatic reactions model to annswer this final question:
"How much time is needed for our bacteria to start producing enterobactins from the moment they sense the iron?"

Here is the link to the enterobactin production model.