Team:Grenoble-EMSE-LSU

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                                     <img src="https://static.igem.org/mediawiki/2013/9/9a/1ere_version_image.png" alt="Project overview" width="600px" />
                                     <img src="https://static.igem.org/mediawiki/2013/9/9a/1ere_version_image.png" alt="Project overview" width="600px" />
                                  
                                  
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                                 Our system utilizes Escherichia coli (E. coli) bacteria that are producing the photosensitizing protein KillerRed (KR).  When illuminated with light, the KR fluorescent protein (580/630nm) produces Reactive Oxygen Species (ROS).  These species irreversibly damage cell proteins, membranes, and DNA, ultimately leading to cell death [2].  Bacterial growth is monitored by measuring the fluorescence of cells containing KillerRed, and population control can be achieved by modulating the amount of ROS produced inside the bacteria with light stimulation.  Since the amount of ROS produced is closely related to the amount of intracellular KillerRed, a photosensitive system [3] was developed to regulate the concentration of this protein.<br><br>
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                                 Our system utilizes <em>Escherichia coli (E. coli)</em> bacteria that are producing the photosensitizing protein KillerRed (KR).  When illuminated with light, the KR fluorescent protein (580/630nm) produces Reactive Oxygen Species (ROS).  These species irreversibly damage cell proteins, membranes, and DNA, ultimately leading to cell death [2].  Bacterial growth is monitored by measuring the fluorescence of cells containing KillerRed, and population control can be achieved by modulating the amount of ROS produced inside the bacteria with light stimulation.  Since the amount of ROS produced is closely related to the amount of intracellular KillerRed, a photosensitive system [3] was developed to regulate the concentration of this protein.<br><br>
                                 The results given by our current biological experiments have enabled us to build a mathematical model that can help predict the amount of living cells within our culture and their growth rate in a specific set of experimental conditions such as:  light intensity, illumination time, and concentration of intracellular KillerRed protein.  The model was further implemented on a microcontroller, directing our electronic system Talk’E. Coli. This device, equipped with different light sources and a photodiode, can then be used to regulate cell population and growth to any arbitrary level within natural limits.<br><br>
                                 The results given by our current biological experiments have enabled us to build a mathematical model that can help predict the amount of living cells within our culture and their growth rate in a specific set of experimental conditions such as:  light intensity, illumination time, and concentration of intracellular KillerRed protein.  The model was further implemented on a microcontroller, directing our electronic system Talk’E. Coli. This device, equipped with different light sources and a photodiode, can then be used to regulate cell population and growth to any arbitrary level within natural limits.<br><br>
                                 <em>References:</em><br>
                                 <em>References:</em><br>

Revision as of 11:15, 9 August 2013

Grenoble-EMSE-LSU, iGEM


Grenoble-EMSE-LSU, iGEM

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