Team:Calgary/Project/DataPage

From 2013.igem.org

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<h2>Further characterization and improvement of parts already in the registry</h2>
<h2>Further characterization and improvement of parts already in the registry</h2>
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<ul><li> Submitted optimized parts of TALE-A and TALE-B (Slovenia 2012) for use in <i>E. coli </i> by removing the eukaryotic kozak sequence and nuclear localization signal, codon optimizing it for expression in <i>E. coli </i> and finally adding a KasI restriction site in the composite part such that future teams can essentially plasmid switch their own TALEs into our system. Also fixed a mutation in TALE-B.
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<ul><li> Submitted optimized parts of TALE-A (<a href="http://parts.igem.org/wiki/index.php?title=Part:BBa_K1189022"><span class="Green"><b>Bba_ K1189022</b></span></a>) and TALE-B (<a href="http://parts.igem.org/wiki/index.php?title=Part:BBa_K1189023"><span class="Green"><b>Bba_ K1189023</b></span></a>) (Slovenia 2012) for use in <i>E. coli </i> by removing the eukaryotic kozak sequence and nuclear localization signal, codon optimizing it for expression in <i>E. coli </i> and finally adding a KasI restriction site in the composite part such that future teams can essentially plasmid switch their own TALEs into our system. Also fixed a mutation in TALE-B.
<li>Submitted multiple composite parts of both TALEs with his-6 tags for easy purification, as well as with linkers and our two reporters: Beta-lactamase and ferritin.</li>  
<li>Submitted multiple composite parts of both TALEs with his-6 tags for easy purification, as well as with linkers and our two reporters: Beta-lactamase and ferritin.</li>  

Revision as of 03:03, 28 September 2013

Data Page

Characterization of new parts submitted to the Registry

  • Submitted two new reporters to the registry: Beta-lactamase (Bba_ K1189008) and Recombinant Human Ferritin (Bba_ K1189008) . We submitted these parts alone, with 6-his tags and lacI inducible promoters and fused to TALE-A (Slovenia 2012).
  • Expressed Ferritin (Bba_ K1189008)), which possesses 24 subunits, and showed successful chemical conversion of our expressed protein into Prussian blue ferritin. We also showed that this part could feasibly be used as a reporter in a nitrocellulose test-strip system.
  • Expressed and purified beta lactamase both with and without TALE-A (Bba_ K1189007) and (Bba_ K1189031) and characterized the functionality of these Biobricks as a reporter using both pH and ampicillin resistance assays.

Further characterization and improvement of parts already in the registry