Team:Grenoble-EMSE-LSU/Project/Instrumentation

From 2013.igem.org

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<h1>TalkE'coli - Our device</h1>
<h1>TalkE'coli - Our device</h1>
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<p>Our project aims to <strong>control the concentration of living bacteria in a culture</strong>. To do so, we designed a genetic network allowing light controlled cell growth. In addition, we built a device in order to send and receive light signals from the bacterial culture. We have thus to create a means of communication from cell to machine and from machine to cell. For cell to machine communication, we chose to measure the red fluorescence of KillerRed. A first function of our device is to excite and measure fluorescence intensity thanks to a light source, excitation/emission optics and a photodiode. In this way, our bacteria will be able to talk to our device. For machine to cell communication, we will use red light to activate a light-inducible promoter that triggers KillerRed production and white light to generate ROS thanks to KillerRed phototoxic activity. In our system, the rate of KillerRed production and the number of living cells will be controlled by the intensity of the red and white light beams. A second function of our device is therefore to generate controlled light intensities at different wavelengths. In this way, our device will be able to talk to our bacteria. Firstly we will explain the choice of the different components by giving an overview of the device, then the several experiences we did to find the most accurate parameters for each part of the device : <a href=#Photodiode>the photodiode</a>, <a href=#Arduino>Arduino</a>, <a href=#Fluo>fluorescence measurement</a>, <a href=#Electronic>the electronic circuit</a>, <a href=#Servo>the servomotor</a>. All these elements were then integrated in <a href=#Box>the box</a> that we designed and built.</p>
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<p>Our project aims to <strong>control the concentration of living bacteria in a culture</strong>. To do so, we designed a genetic network allowing light controlled cell growth. In addition, we built a device in order to send and receive light signals from the bacterial culture. We have thus to create a means of communication from cell to machine and from machine to cell. For cell to machine communication, we chose to measure the red fluorescence of KillerRed. A first function of our device is to excite and measure fluorescence intensity thanks to a light source, excitation/emission optics and a photodiode. In this way, our bacteria will be able to talk to our device. For machine to cell communication, we will use red light to activate a light-inducible promoter that triggers KillerRed production and white light to generate ROS thanks to KillerRed phototoxic activity. In our system, the rate of KillerRed production and the number of living cells will be controlled by the intensity of the red and white light beams. A second function of our device is therefore to generate controlled light intensities at different wavelengths. In this way, our device will be able to talk to our bacteria. Firstly we will explain the choice of the different components by giving an <a href="#Overview">overview of the device</a>, then the several experiences we did to find the most accurate parameters for each part of the device : <a href=#Photodiode>the photodiode</a>, <a href=#Arduino>Arduino</a>, <a href=#Fluo>fluorescence measurement</a>, <a href=#Electronic>the electronic circuit</a>, <a href=#Servo>the servomotor</a>. All these elements were then integrated in <a href=#Box>the box</a> that we designed and built.</p>
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<h2 id="Component">The components</h2>
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<h2 id="Overview">Overview of the device</h2>
<p>To record light intensity, we were inspired by the E. glometer of the Cambridge team of iGEM 2010.<br>
<p>To record light intensity, we were inspired by the E. glometer of the Cambridge team of iGEM 2010.<br>

Revision as of 18:04, 30 September 2013

Grenoble-EMSE-LSU, iGEM


Grenoble-EMSE-LSU, iGEM

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