Team:Grenoble-EMSE-LSU/Project/Device
From 2013.igem.org
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<h1>Talk'E.coli - Our device</h1> | <h1>Talk'E.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 created a genetic network but to control the cell culture without employing <strong>any human means</strong> we needed to create <strong>a device</strong>. We have thus to create a means of communication from cell to machine and from machine to cell. To create the first one, we chose the red fluorescence protein KillerRed as a reporter protein. The first condition that our device needs to fulfill is to generate fluorescence thanks to a light source and a couple of excitation and emission filters and be able to measure its intensity. With these conditions our bacteria will be able to talk to our device. Then for the other way, the machine needs to send messages to the bacteria in order for them to know what to do – produce KillerRed or die. This is possible thanks to the inducible promoter and the property of KillerRed. Therefore our device must emit red light to induce the KillerRed production and white light to generate ROS with KillerRed. That means our device will be able to emit light to different wavelengths. But thanks to the modeling we know that the number of living cells can be controlled by the intensity of the white light, this is another condition our machine needs to satisfy. 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=#Photodiode>the photodiode</a>, <a href=#Arduino>Arduino</a>, <a href=#Fluo>florescence measurement</a>, <a href=#Electronic>the electronic circuit</a>, <a href=#Servo>the servomotor</a> and of course <a href=#Box>the box</a>.</p> | <p>Our project aims to <strong>control the concentration of living bacteria in a culture</strong>. To do so, we created a genetic network but to control the cell culture without employing <strong>any human means</strong> we needed to create <strong>a device</strong>. We have thus to create a means of communication from cell to machine and from machine to cell. To create the first one, we chose the red fluorescence protein KillerRed as a reporter protein. The first condition that our device needs to fulfill is to generate fluorescence thanks to a light source and a couple of excitation and emission filters and be able to measure its intensity. With these conditions our bacteria will be able to talk to our device. Then for the other way, the machine needs to send messages to the bacteria in order for them to know what to do – produce KillerRed or die. This is possible thanks to the inducible promoter and the property of KillerRed. Therefore our device must emit red light to induce the KillerRed production and white light to generate ROS with KillerRed. That means our device will be able to emit light to different wavelengths. But thanks to the modeling we know that the number of living cells can be controlled by the intensity of the white light, this is another condition our machine needs to satisfy. 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=#Photodiode>the photodiode</a>, <a href=#Arduino>Arduino</a>, <a href=#Fluo>florescence measurement</a>, <a href=#Electronic>the electronic circuit</a>, <a href=#Servo>the servomotor</a> and of course <a href=#Box>the box</a>.</p> | ||
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<h2 id="Arduino">Arduino</h2> | <h2 id="Arduino">Arduino</h2> | ||
<p>Arduino is used to translate the frequency given by the photodiode in irrandiance that gives us the light intensity. The algorithm is quite simple. It counts the number of high levels (samples) and the duration of the measurement (length) and with these two elements it makes this calculation:</br></br> | <p>Arduino is used to translate the frequency given by the photodiode in irrandiance that gives us the light intensity. The algorithm is quite simple. It counts the number of high levels (samples) and the duration of the measurement (length) and with these two elements it makes this calculation:</br></br> | ||
- | <strong>Irradiance=frequency/(frequency scaling)= samples/(frequency scaling × length)</strong></br></br> | + | <strong>Irradiance=frequency/(frequency scaling)= samples/(frequency scaling × length)</strong></br></br></p> |
+ | <p align="center"><img src="https://static.igem.org/mediawiki/2013/2/22/Algo_photodiode.PNG" alt="algo_photodiode" width="500px" /></p> | ||
+ | <p> | ||
To know if this program works, a function generator was plug in one of the digital input of Arduino instead of the photodiode. By changing the frequency of the square signal sent by the generator and measuring several times the frequency with Arduino and compare the measures to the frequency given by an oscilloscope, we can calculate the accuracy of the program.</br> | To know if this program works, a function generator was plug in one of the digital input of Arduino instead of the photodiode. By changing the frequency of the square signal sent by the generator and measuring several times the frequency with Arduino and compare the measures to the frequency given by an oscilloscope, we can calculate the accuracy of the program.</br> | ||
If the algorithm is right, the curve should follow the equation x=y, which means that Arduino and the oscilloscope measure the same frequencies.</br></br></p> | If the algorithm is right, the curve should follow the equation x=y, which means that Arduino and the oscilloscope measure the same frequencies.</br></br></p> |
Latest revision as of 08:31, 24 September 2013