Difference between revisions of "Team:Edinburgh UG"
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<a class="dropdown-item" href="https://2018.igem.org/Team:Edinburgh_UG/Parts">Parts Overview</a> | <a class="dropdown-item" href="https://2018.igem.org/Team:Edinburgh_UG/Parts">Parts Overview</a> | ||
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| − | + | <a class="dropdown-item" href="https://2018.igem.org/Team:Edinburgh_UG/Basic_Part">Basic Parts</a> | |
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<a class="nav-link" href="https://2018.igem.org/Team:Edinburgh_UG/Safety">Safety <span class="sr-only">(current)</span></a> | <a class="nav-link" href="https://2018.igem.org/Team:Edinburgh_UG/Safety">Safety <span class="sr-only">(current)</span></a> | ||
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| − | <a class="nav-link | + | <a class="nav-link" href="https://2018.igem.org/Team:Edinburgh_UG/Human_Practices">Human Practices <span class="sr-only">(current)</span></a> |
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<a class="nav-link" href="https://igem.org/2018_Judging_Form?team=Edinburgh_UG">Judging Form <span class="sr-only">(current)</span></a> | <a class="nav-link" href="https://igem.org/2018_Judging_Form?team=Edinburgh_UG">Judging Form <span class="sr-only">(current)</span></a> | ||
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| + | <a class="nav-link" href="https://2018.igem.org/Team:Edinburgh_UG/Medal_Criteria">Medal Criteria<span class="sr-only">(current)</span></a> | ||
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| − | <h2> | + | <h2>MaxED OOT</h2> |
| − | <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 | + | <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> |
| + | <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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<span class="network-name">Twitter</span> | <span class="network-name">Twitter</span> | ||
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| + | <a href="https://www.instagram.com/igemedinburgh/" class="btn btn-default btn-lg"> | ||
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| + | <span class="network-name">Instagram</span> | ||
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Latest revision as of 00:58, 18 October 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.
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