Difference between revisions of "Team:Edinburgh UG"

 
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     <title>Full Slider - Start Bootstrap Template</title>
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     <title>Edinburgh iGEM 2018</title>
  
 
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         <h1>Full Slider by Start Bootstrap</h1>
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            <h2>MaxED OOT</h2>
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           file.</p>
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            <p>We are an interdisciplinary team of undergraduate students hailing from the University of Edinburgh in Scotland. This summer our research is focused on Maxicell formation in E. coli. We aim to provide improved characterization to facilitate the use of Maxicells - achromosomal E. coli cells  - as a safe and minimalistic chassis for future use in Synthetic Biology. We intend to quantify the time frame in which Maxicells can continue to express protein, the active metabolic time frame, by producing reporters for the intracellular concentration of important metabolites such as ATP. In addition we wish to attenuate the improvements in biosafety offered by a non-reproducing chassis via amber suppression and recoding, a DNA degrading killswitch, and replacement of standard antibiotic-mediated resistance to prevent advantageous horizontal gene transfer. The resulting novel chassis raises many compelling questions both philosophically; as to our definitions of what constitutes a living cell and legally in terms of the current legislation governing the use of GMOs outside of the laboratory setting.</p>
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          <p> We believe that our project meets <font color="gold">Gold</font> <a href="https://2018.igem.org/Team:Edinburgh_UG/Medal_Criteria"> Medal Criteria. </a>  
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Latest revision as of 00:58, 18 October 2018

Edinburgh iGEM 2018

MaxED OOT

We are an interdisciplinary team of undergraduate students hailing from the University of Edinburgh in Scotland. This summer our research is focused on Maxicell formation in E. coli. We aim to provide improved characterization to facilitate the use of Maxicells - achromosomal E. coli cells - as a safe and minimalistic chassis for future use in Synthetic Biology. We intend to quantify the time frame in which Maxicells can continue to express protein, the active metabolic time frame, by producing reporters for the intracellular concentration of important metabolites such as ATP. In addition we wish to attenuate the improvements in biosafety offered by a non-reproducing chassis via amber suppression and recoding, a DNA degrading killswitch, and replacement of standard antibiotic-mediated resistance to prevent advantageous horizontal gene transfer. The resulting novel chassis raises many compelling questions both philosophically; as to our definitions of what constitutes a living cell and legally in terms of the current legislation governing the use of GMOs outside of the laboratory setting.

We believe that our project meets Gold Medal Criteria.

Contact EdiGEM18

Feel free to leave us a comment on social media!