Difference between revisions of "Team:Chalmers-Gothenburg/Theory"

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<a href="https://2015.igem.org/Team:Chalmers-Gothenburg/Project"><li>PROJECT
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<a href="https://2015.igem.org/Team:Chalmers-Gothenburg/Theory"><li>Theory</li></a>
 
<a href="https://2015.igem.org/Team:Chalmers-Gothenburg/Theory"><li>Theory</li></a>
 
<a href="https://2015.igem.org/Team:Chalmers-Gothenburg/Protocols"><li>Protocols</li></a>   
 
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<a href="https://2015.igem.org/Team:Chalmers-Gothenburg/Project Results"><li>Project Results</li></a>
 
<a href="https://2015.igem.org/Team:Chalmers-Gothenburg/Project Results"><li>Project Results</li></a>
 
<a href="https://2015.igem.org/Team:Chalmers-Gothenburg/BioBricks"><li>BioBricks</li></a>   
 
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<h1>Our Team</h1>
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<h1> Project </h1>
 
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<p>We are Team Chalmers-Gothenburg, a group of students with different backgrounds but a common interest in Synthetic biology. Chalmers University is a well-known technical university in Gothenburg, the second largest city in Sweden located on the beautiful but rainy west coast. </p>
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<p>The team is composed of 15 students with backgrounds in several different fields, including Biotechnology, Chemistry, Physics and Computational Science. This broad range of knowledge has given us the possibility to face challenges with different perspectives. Therefore teamwork and cooperation are of great importance for our team and every person in the team is crucial for a successful result.</p>
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To integrate the different parts of the project and to avoid miscommunication, we have deliberately chosen not to divide into groups with specific tasks. Instead most of the team members have been involved in both lab work and human practices. However, the lab work has been divided into three main groups focusing on each of our three systems.
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No matter how much we enjoy working in our lab, we have also arranged team building activities outside the lab almost every week which has made the summer even more fun.</p>
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<h1>OVERVEIW</H1>
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<p>Contaminations – a problem you definitely want to get rid of as quick as possible. It can destroy your product and lower the efficiency of the process, which in the end may lead to higher expenses. We have created a great system for both finding and combating contaminations in bioreactors, automatically! Our intention was to deal with the hard process in finding unwanted cells in bioreactors and our solution is an innovative system that is both time and material efficient. With our project you no longer need to worry about long analytic times and if your product is pure enough, it will all be taken care of directly in the process! Do you know what the best part is? The system is really cool and can be used for so much more!</p>
 
<p>Contaminations – a problem you definitely want to get rid of as quick as possible. It can destroy your product and lower the efficiency of the process, which in the end may lead to higher expenses. We have created a great system for both finding and combating contaminations in bioreactors, automatically! Our intention was to deal with the hard process in finding unwanted cells in bioreactors and our solution is an innovative system that is both time and material efficient. With our project you no longer need to worry about long analytic times and if your product is pure enough, it will all be taken care of directly in the process! Do you know what the best part is? The system is really cool and can be used for so much more!</p>
  
 
<p>Our project presents a solution for dealing with contamination in bioreactors. We have found a way to detect and deal with contamination without wasting product in the tank. The solution could be used both for academic and industrial use. We have designed a two system solution that we have implemented in Saccharomyces cerevisiae, a solution that is both efficient and timesaving. The systems are based on one detection system that gives a fluorescent signal when a contaminant is present and one DNA-repair-system. The detection system uses pheromone detection to sense the present of a contaminant and uses an intracellular cascade reaction to send out a RFP-signal. The repair system is based on a system from the bacterium Deinococcus radiodurans and repairs blunt DNA-cuts, which are hard for the cell to repair. This system makes it possible to irradiate the tank with UV-irradiation that will kill the contaminant but not the yeast. These systems together with a safety switch for use in research will be presented in detail in this chapter.</p>
 
<p>Our project presents a solution for dealing with contamination in bioreactors. We have found a way to detect and deal with contamination without wasting product in the tank. The solution could be used both for academic and industrial use. We have designed a two system solution that we have implemented in Saccharomyces cerevisiae, a solution that is both efficient and timesaving. The systems are based on one detection system that gives a fluorescent signal when a contaminant is present and one DNA-repair-system. The detection system uses pheromone detection to sense the present of a contaminant and uses an intracellular cascade reaction to send out a RFP-signal. The repair system is based on a system from the bacterium Deinococcus radiodurans and repairs blunt DNA-cuts, which are hard for the cell to repair. This system makes it possible to irradiate the tank with UV-irradiation that will kill the contaminant but not the yeast. These systems together with a safety switch for use in research will be presented in detail in this chapter.</p>
 
<h2>Detection</H2>
 
 
<h2>Repair</H2>
 
 
<h2>Safety Switch</H2>
 

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Project

Contaminations – a problem you definitely want to get rid of as quick as possible. It can destroy your product and lower the efficiency of the process, which in the end may lead to higher expenses. We have created a great system for both finding and combating contaminations in bioreactors, automatically! Our intention was to deal with the hard process in finding unwanted cells in bioreactors and our solution is an innovative system that is both time and material efficient. With our project you no longer need to worry about long analytic times and if your product is pure enough, it will all be taken care of directly in the process! Do you know what the best part is? The system is really cool and can be used for so much more!

Our project presents a solution for dealing with contamination in bioreactors. We have found a way to detect and deal with contamination without wasting product in the tank. The solution could be used both for academic and industrial use. We have designed a two system solution that we have implemented in Saccharomyces cerevisiae, a solution that is both efficient and timesaving. The systems are based on one detection system that gives a fluorescent signal when a contaminant is present and one DNA-repair-system. The detection system uses pheromone detection to sense the present of a contaminant and uses an intracellular cascade reaction to send out a RFP-signal. The repair system is based on a system from the bacterium Deinococcus radiodurans and repairs blunt DNA-cuts, which are hard for the cell to repair. This system makes it possible to irradiate the tank with UV-irradiation that will kill the contaminant but not the yeast. These systems together with a safety switch for use in research will be presented in detail in this chapter.