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<li class=""><a class="dropdown-item" href="https://2018.igem.org/Team:Waterloo/Engagement"><span>Engagement</span></a></li> | <li class=""><a class="dropdown-item" href="https://2018.igem.org/Team:Waterloo/Engagement"><span>Engagement</span></a></li> | ||
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− | <li class=""><a class="dropdown-item" href="https://2018.igem.org/Team:Waterloo/ | + | <li class=""><a class="dropdown-item" href="https://2018.igem.org/Team:Waterloo/IAT"><span>Iat</span></a></li> |
</li> | </li> | ||
<li class=""><a class="dropdown-item" href="https://2018.igem.org/Team:Waterloo/Societal_Considerations"><span>Societal Considerations</span></a></li> | <li class=""><a class="dropdown-item" href="https://2018.igem.org/Team:Waterloo/Societal_Considerations"><span>Societal Considerations</span></a></li> | ||
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<div class="row"><div class="col"><div class="content-main"><p>This year, our team biobricked the MetE gene into a cassette with LacI promoter: | <div class="row"><div class="col"><div class="content-main"><p>This year, our team biobricked the MetE gene into a cassette with LacI promoter: | ||
<a href="http://parts.igem.org/Part:BBa_K2573000">BBa_K2573000</a>. This can be cloned into a methionine auxotroph to restore its ability to produce methionine. The MetE coding sequence can also be PCR amplified out of this biobrick and assembled into a new plasmid for a variety of applications. For instance, it can be put under the control of an optogenetic promoter/system (like CcaS/R or pDawn). </p> | <a href="http://parts.igem.org/Part:BBa_K2573000">BBa_K2573000</a>. This can be cloned into a methionine auxotroph to restore its ability to produce methionine. The MetE coding sequence can also be PCR amplified out of this biobrick and assembled into a new plasmid for a variety of applications. For instance, it can be put under the control of an optogenetic promoter/system (like CcaS/R or pDawn). </p> | ||
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<td> Name <td> Type <td> Description <td> Designer <td> length | <td> Name <td> Type <td> Description <td> Designer <td> length | ||
<tr> | <tr> | ||
− | <td> <a href="http://parts.igem.org/Part:BBa_K2573000" > BBa_K2573000 </a> <td> Composite <td> MetE coding sequence in cassete with LacI promoter <td> Amanda Kuang <td> 2658 </ | + | <td> <a href="http://parts.igem.org/Part:BBa_K2573000" > BBa_K2573000 </a> <td> Composite <td> MetE coding sequence in cassete with LacI promoter <td> Amanda Kuang <td> 2658 |
+ | |||
+ | </table> | ||
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{{Waterloo/footer}} | {{Waterloo/footer}} |
Revision as of 01:35, 18 October 2018
Parts
This year, our team biobricked the MetE gene into a cassette with LacI promoter: BBa_K2573000. This can be cloned into a methionine auxotroph to restore its ability to produce methionine. The MetE coding sequence can also be PCR amplified out of this biobrick and assembled into a new plasmid for a variety of applications. For instance, it can be put under the control of an optogenetic promoter/system (like CcaS/R or pDawn).