Team:Grenoble-EMSE-LSU/Project/Instrumentation

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                                     <h2 id="Box">The Box</h2>
                                     <h2 id="Box">The Box</h2>
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                                       <p align="center"><object width="480" height="360"><param name="movie" value="//www.youtube.com/v/OY0-y8JZme0?version=3&amp;hl=fr_FR"></param><param name="allowFullScreen" value="true"></param><param name="allowscriptaccess" value="always"></param><embed src="//www.youtube.com/v/OY0-y8JZme0?version=3&amp;hl=fr_FR" type="application/x-shockwave-flash" width="480" height="360" allowscriptaccess="always" allowfullscreen="true"></embed></object></p>
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                                       <p align="center"><object width="480" height="360"><param name="movie" value="//www.youtube.com/v/OY0-y8JZme0?version=3&amp;hl=fr_FR"></param><param name="allowFullScreen" value="true"></param><param name="allowscriptaccess" value="always"></param><embed src="//www.youtube.com/v/OY0-y8JZme0?version=3&amp;hl=fr_FR" type="application/x-shockwave-flash" width="480" height="360" allowscriptaccess="always" allowfullscreen="true"></embed></object></br></br></p>
                                       <p>Our device is built in such a way that the user <strong>just</strong> needs to <strong>input the concentration of living cells</strong> he wants and put <strong>the Erlenmeyer with our engineered bacteria</strong>. From that moment the device works in <strong>standalone mode</strong>. Firstly our device measures <a href="https://2013.igem.org/Team:Grenoble-EMSE-LSU/Project/Instrumentation/Fluo#Fluo">the red fluorescence</a> of the culture that will be <strong>the baseline</strong>. Then it induces the <a href="https://2013.igem.org/Team:Grenoble-EMSE-LSU/Project/Biology#KR">KillerRed</a> protein using <a href="https://2013.igem.org/Team:Grenoble-EMSE-LSU/Project/Biology/KR">the red light inducible promoter</a>. Every <strong>5 minutes</strong>, Talk’E.Coli measures the level of red fluorescence of the culture and consequently of KillerRed. With <strong>these measurements and the parameters given by <a href="https://2013.igem.org/Team:Grenoble-EMSE-LSU/Project/Modelling/Parameters">the model</a></strong> it can calculate the moment when it needs to activate the ROS emissions with white light to stabilize the living cell concentration. The main asset of the device is that even if there is a lower increase of the concentration of KillerRed or if the killing rate is higher since it measures every 5 minutes the red fluorescence it can adjust exactly the light intensity to correct these rates.</br></br></p>
                                       <p>Our device is built in such a way that the user <strong>just</strong> needs to <strong>input the concentration of living cells</strong> he wants and put <strong>the Erlenmeyer with our engineered bacteria</strong>. From that moment the device works in <strong>standalone mode</strong>. Firstly our device measures <a href="https://2013.igem.org/Team:Grenoble-EMSE-LSU/Project/Instrumentation/Fluo#Fluo">the red fluorescence</a> of the culture that will be <strong>the baseline</strong>. Then it induces the <a href="https://2013.igem.org/Team:Grenoble-EMSE-LSU/Project/Biology#KR">KillerRed</a> protein using <a href="https://2013.igem.org/Team:Grenoble-EMSE-LSU/Project/Biology/KR">the red light inducible promoter</a>. Every <strong>5 minutes</strong>, Talk’E.Coli measures the level of red fluorescence of the culture and consequently of KillerRed. With <strong>these measurements and the parameters given by <a href="https://2013.igem.org/Team:Grenoble-EMSE-LSU/Project/Modelling/Parameters">the model</a></strong> it can calculate the moment when it needs to activate the ROS emissions with white light to stabilize the living cell concentration. The main asset of the device is that even if there is a lower increase of the concentration of KillerRed or if the killing rate is higher since it measures every 5 minutes the red fluorescence it can adjust exactly the light intensity to correct these rates.</br></br></p>
<p>Firstly we will explain the choice of the different components, then the several experiences we did to find the most accurate parameters for each part of the device : <a href="https://2013.igem.org/Team:Grenoble-EMSE-LSU/Project/Instrumentation/Fluo#Photodiode">the photodiode and Arduino</a>, <a href="https://2013.igem.org/Team:Grenoble-EMSE-LSU/Project/Instrumentation/Fluo#Fluo">fluorescence measurement</a>, <a href="https://2013.igem.org/Team:Grenoble-EMSE-LSU/Project/Instrumentation/Fluo#Electronic">the electronic circuit</a>, <a href="https://2013.igem.org/Team:Grenoble-EMSE-LSU/Project/Instrumentation/Fluo#Servo">the servomotor</a>. All these elements were then integrated in <a href="https://2013.igem.org/Team:Grenoble-EMSE-LSU/Project/Instrumentation/Fluo#Box">the box</a> that we designed and built.</p>
<p>Firstly we will explain the choice of the different components, then the several experiences we did to find the most accurate parameters for each part of the device : <a href="https://2013.igem.org/Team:Grenoble-EMSE-LSU/Project/Instrumentation/Fluo#Photodiode">the photodiode and Arduino</a>, <a href="https://2013.igem.org/Team:Grenoble-EMSE-LSU/Project/Instrumentation/Fluo#Fluo">fluorescence measurement</a>, <a href="https://2013.igem.org/Team:Grenoble-EMSE-LSU/Project/Instrumentation/Fluo#Electronic">the electronic circuit</a>, <a href="https://2013.igem.org/Team:Grenoble-EMSE-LSU/Project/Instrumentation/Fluo#Servo">the servomotor</a>. All these elements were then integrated in <a href="https://2013.igem.org/Team:Grenoble-EMSE-LSU/Project/Instrumentation/Fluo#Box">the box</a> that we designed and built.</p>

Revision as of 09:01, 4 October 2013

Grenoble-EMSE-LSU, iGEM


Grenoble-EMSE-LSU, iGEM

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