Difference between revisions of "Team:Toronto/Results"

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<li><a href="https://2016.igem.org/Team:Toronto/HP-Gold"><span>gold</span></a></li>
 
<li><a href="https://2016.igem.org/Team:Toronto/HP-Gold"><span>gold</span></a></li>
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<li><a href="https://2016.igem.org/Team:Toronto/HP-Impact"><span>impact</span></a></li>
 
 
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<li><a href="https://2016.igem.org/Team:Toronto/Integrated_Practices"><span>integrated_practices</span></a></li>
 
<li><a href="https://2016.igem.org/Team:Toronto/Integrated_Practices"><span>integrated_practices</span></a></li>

Revision as of 14:58, 19 October 2016

Results

Success

Discussion

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Figure 2: 3D Absorbance graph for CPRG assay

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Figure 3: 2D Absorbance graph for CPRG assa

We expected to see a linear increase correlated to increase in the concentration. However, instead, we observed a sudden decrease in expression levels after 0.5uM. This became more pronounced over time, resulting a Range Detector Circuit.

We suspect that there is an inherent edge that represses the expression after a certain threshold. This would produce the circuit shown in Figure 4. We speculated that this effect might be minimum for cell free extracts that contain minimal enzymes.

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Figure 4: computational explanation for the CPRG assay

Not so successful

  • Cell-free assay required more time and troubleshooting.

Future plans

  • Make cell-free assays work.

The iGEM Toronto 2016 team was successful at modifying an naturally existing transcription factor, GolS (natively found in Salmonella enterica), to contain certain mutations that have been found to cause CueR (a copper-response factor in Escherichia coli)to increase sensitivity to gold and significantly decrease it's sensitivity to copper. This modification was due to an amino acid change from proline to alanine at site 118. This successful synthetic change can be found composite BioBricks, Long GolS P118A (BBa_K2048002) compared to the unchanged Long GolS (BBa_K2048001).