Difference between revisions of "Team:Waterloo/Meet the Microbes"
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<li class=""><a class="dropdown-item" href="https://2018.igem.org/Team:Waterloo/Experiments"><span>Experiments</span></a></li> | <li class=""><a class="dropdown-item" href="https://2018.igem.org/Team:Waterloo/Experiments"><span>Experiments</span></a></li> | ||
</li> | </li> | ||
| − | <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/Interlab"><span>Interlab</span></a></li> |
</li> | </li> | ||
<li class=""><a class="dropdown-item" href="https://2018.igem.org/Team:Waterloo/Demonstrate"><span>Demonstrate</span></a></li> | <li class=""><a class="dropdown-item" href="https://2018.igem.org/Team:Waterloo/Demonstrate"><span>Demonstrate</span></a></li> | ||
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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> | ||
</li> | </li> | ||
| − | <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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</ul> | </ul> | ||
| − | <li class="dropdown nav-item"><a href="#" class="nav-link dropdown-toggle nav-link" data-toggle="dropdown" role="button" aria-haspopup="true" aria-expanded="false"> | + | <li class="dropdown nav-item"><a href="#" class="nav-link dropdown-toggle nav-link" data-toggle="dropdown" role="button" aria-haspopup="true" aria-expanded="false">Dry Lab<span class="caret"></span></a> |
<ul class="dropdown-menu"> | <ul class="dropdown-menu"> | ||
| + | <li class=""><a class="dropdown-item" href="https://2018.igem.org/Team:Waterloo/Model"><span>Model</span></a></li> | ||
| + | </li> | ||
<li class=""><a class="dropdown-item" href="https://2018.igem.org/Team:Waterloo/Software"><span>Software</span></a></li> | <li class=""><a class="dropdown-item" href="https://2018.igem.org/Team:Waterloo/Software"><span>Software</span></a></li> | ||
</li> | </li> | ||
| − | <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/Automation"><span>Automation</span></a></li> |
| + | </li> | ||
| + | <li class=""><a class="dropdown-item" href="https://2018.igem.org/Team:Waterloo/Turbidostat"><span>Turbidostat</span></a></li> | ||
</li> | </li> | ||
</ul> | </ul> | ||
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| − | <div class="row"><div class="col"><div class="content-main"></div></div></div> | + | <div class="row"><div class="col"><div class="content-main"><p><img align="left" src="https://static.igem.org/mediawiki/2018/a/a9/T--Waterloo--MeetMicro_JT2CcaSR.png"></p> |
| + | <p><strong>Strain</strong>: <em>Escherichia coli</em> <a href="https://www.addgene.org/80403/">JT2 SKA974</a>. This strain has been engineered for optogenetic control using CcaS/R. Its genomic MetE gene is under control of the CcaS/R promoter. It also has a Kanamycin resistance gene in its genome. </p> | ||
| + | <p><strong>Plasmids</strong>:</p> | ||
| + | <ul> | ||
| + | <li><a href="https://www.addgene.org/63197/">pSR43.6r</a> (CcaS, its photoreceptor, p15A origin of replication)</li> | ||
| + | <li><a href="https://www.addgene.org/63176/">pSR58.6</a> (CcaR, sfGFP under the CcaR promoter, ColeI origin of replication)<ul> | ||
| + | <li>Note that we made two versions of this strain. One contains both these plasmids, unaltered, and was used for characterization | ||
| + | experiments. We cut GFP out of pSR58.6 for the second version of this strain, and used it for non-characterization experiments. </li> | ||
| + | </ul> | ||
| + | </li> | ||
| + | </ul> | ||
| + | <p><strong>Antibiotic Resistance(s)</strong>: Kanamycin, Spectinomycin, Chloramphenicol </p> | ||
| + | <p><strong>Fluorescent Marker</strong>: GFP in the characterization version of this strain, only expressed when CcaS/R is activated.</p> | ||
| + | <p><strong>Can produce methionine?</strong> Yes, but only when CcaS/R is activated. </p> | ||
| + | <hr> | ||
| + | <p><img align="left" src="https://static.igem.org/mediawiki/2018/5/56/T--Waterloo--MeetMicro_JT2.png"></p> | ||
| + | <p><strong>Strain</strong>: <em>Escherichia coli</em> <a href="https://www.addgene.org/80403/">JT2 SKA974</a>. </p> | ||
| + | <p>This strain has been engineered for optogenetic control using CcaS/R. </p> | ||
| + | <p>Its genomic MetE gene is under control of the CcaS/R promoter. </p> | ||
| + | <p>It also has a Kanamycin resistance gene in its genome. </p> | ||
| + | <p><strong>Plasmids</strong>: None</p> | ||
| + | <p><strong>Antibiotic Resistance(s)</strong>: Kanamycin</p> | ||
| + | <p><strong>Fluorescent Marker</strong>: None</p> | ||
| + | <p><strong>Can produce methionine?</strong> No </p> | ||
| + | <hr> | ||
| + | <p><img align="left" src="https://static.igem.org/mediawiki/2018/c/c9/T--Waterloo--MeetMicro_GFP.png"></p> | ||
| + | <p><strong>Strain</strong>: <em>Escherichia coli</em> DH5alpha </p> | ||
| + | <p><strong>Plasmids</strong>:</p> | ||
| + | <ul> | ||
| + | <li><a href="http://parts.igem.org/Part:BBa_E0040">BBa_E0040 in pSB1C3</a> (GFP biobrick, ColeI origin of replication)</li> | ||
| + | <li>a plasmid we constructed that has Spectinomycin resistance and p15A origin of replication</li> | ||
| + | </ul> | ||
| + | <p><strong>Antibiotic Resistance(s)</strong>: Spectinomycin, Chloramphenicol </p> | ||
| + | <p><strong>Fluorescent Marker</strong>: GFP, constitutively expressed. </p> | ||
| + | <p><strong>Can produce methionine?</strong>: Yes, with wild type genomic MetE gene. </p> | ||
| + | <hr> | ||
| + | <p><img align="left" src="https://static.igem.org/mediawiki/2018/9/92/T--Waterloo--MeetMicro_dh5.png"></p> | ||
| + | <p><strong>Strain</strong>: <em>Escherichia coli</em> DH5alpha</p> | ||
| + | <p><strong>Plasmids</strong>: None</p> | ||
| + | <p><strong>Antibiotic Resistance(s)</strong> None</p> | ||
| + | <p><strong>Fluorescent Marker</strong> None</p> | ||
| + | <p><strong>Can produce methionine?</strong> Yes, with wild type genomic MetE gene. </p> | ||
| + | </div></div></div> | ||
</div> | </div> | ||
</html> | </html> | ||
{{Waterloo/footer}} | {{Waterloo/footer}} | ||
Latest revision as of 05:09, 1 December 2018
Meet the Microbes
Strain: Escherichia coli JT2 SKA974. This strain has been engineered for optogenetic control using CcaS/R. Its genomic MetE gene is under control of the CcaS/R promoter. It also has a Kanamycin resistance gene in its genome.
Plasmids:
- pSR43.6r (CcaS, its photoreceptor, p15A origin of replication)
- pSR58.6 (CcaR, sfGFP under the CcaR promoter, ColeI origin of replication)
- Note that we made two versions of this strain. One contains both these plasmids, unaltered, and was used for characterization experiments. We cut GFP out of pSR58.6 for the second version of this strain, and used it for non-characterization experiments.
Antibiotic Resistance(s): Kanamycin, Spectinomycin, Chloramphenicol
Fluorescent Marker: GFP in the characterization version of this strain, only expressed when CcaS/R is activated.
Can produce methionine? Yes, but only when CcaS/R is activated.
Strain: Escherichia coli JT2 SKA974.
This strain has been engineered for optogenetic control using CcaS/R.
Its genomic MetE gene is under control of the CcaS/R promoter.
It also has a Kanamycin resistance gene in its genome.
Plasmids: None
Antibiotic Resistance(s): Kanamycin
Fluorescent Marker: None
Can produce methionine? No
Strain: Escherichia coli DH5alpha
Plasmids:
- BBa_E0040 in pSB1C3 (GFP biobrick, ColeI origin of replication)
- a plasmid we constructed that has Spectinomycin resistance and p15A origin of replication
Antibiotic Resistance(s): Spectinomycin, Chloramphenicol
Fluorescent Marker: GFP, constitutively expressed.
Can produce methionine?: Yes, with wild type genomic MetE gene.
Strain: Escherichia coli DH5alpha
Plasmids: None
Antibiotic Resistance(s) None
Fluorescent Marker None
Can produce methionine? Yes, with wild type genomic MetE gene.