Team:Paris Saclay/Modeling

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<p>Here we only reveal 2 kinds of reporter protein(green and red) in the model. In anaerobic condition, FNR active lead to the production the green reporter protein but suppress the exprission of the red one. In aerobic condition, FNR is inactivated by oxygen, there is no production of green protein, on the contrary the red reporter protein is synthized. </p>
<p>Here we only reveal 2 kinds of reporter protein(green and red) in the model. In anaerobic condition, FNR active lead to the production the green reporter protein but suppress the exprission of the red one. In aerobic condition, FNR is inactivated by oxygen, there is no production of green protein, on the contrary the red reporter protein is synthized. </p>
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[[User:Zyi|Zyi]] 11:58, 1 October 2013 (CDT)
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Revision as of 16:58, 1 October 2013

Contents

Introduction

Those words could give you the first impression of our modeling.

What do we model?

The degradation of PCBs demands multi bio-chemical reactions performing successively in aerobic or anaerobic condition. The regulator FNR is the key to control the processus. In different condition, FNR activated or desactivated, and foster or prevent some gene expression. So our super bacterium PCBs buster can be regulated by our will,and does the right thing at the right time.

This modeling is about the simulation of FNR aero/anaerobic regulation system that we have successfully achieved in our experiments. Briefly, we try to build bio-informatically a model which can reveal the alternate expression of FNR and its reporter, a virtuel system include bio-chemical phenomenons from the translation of fnr to the production of reporter protein.

What’s our purpose for this modeling?

The main aim of our modeling is recreate the aero/anaerobic reporter protein expression system. By alternating the oxygen concentration, active or inactive FNR combines (or not) with potential sensor gene sequence and make blue or red color. Our job is to see if we can observe the alternating red and blue curve when we change the oxygen condition.

How do we model?

As the research of FNR regulation system is a well-studied territory, we found some excellent scientific paper in library especially [http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2867928/ Regulation of Aerobic to Anaerobic Transitions by the FNR cycle in Escherichia coli by Dean A.Tolla and Michael A.Savageau]. They have built successfully a differential equation system. And in our modeling we decided to redo what they have done but use a different method: a stochastic system created by new modeling tool: Hsim.

What does our model look like?

In our modele, we try to establish a virtual space of a bacterium form. Inside of this bacterium, we simulate different reactions of different molecules. The simulation shows our virtual bacterium acting as same as in our experiments.

PSecolivert.jpg PSecolirouge.jpg
In anaerobic condition
In aerobic condition

Here we only reveal 2 kinds of reporter protein(green and red) in the model. In anaerobic condition, FNR active lead to the production the green reporter protein but suppress the exprission of the red one. In aerobic condition, FNR is inactivated by oxygen, there is no production of green protein, on the contrary the red reporter protein is synthized.

Zyi 11:58, 1 October 2013 (CDT)