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Team:University College London/Module 5/Results
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Revision as of 13:59, 21 September 2012
Module 5: Salt Tolerance
Description | Design | Construction | Characterisation | Modelling | Results | Conclusions
Characterisation of BBa_K729005 (IrrE)
From our results, we observed that E. Coli transformed with the IrrE gene exhibit greater salt tolerance than their non-transformed counterparts. This is revealed in the greater OD the cells grow to in high salt media, as well as their increased growth rates in the exponential growth phase. Our results are consistent with the results obtained in the original paper, establishing the fact that our cells are indeed expressing the IrrE global regulator.
Characterisation of BBa_K398108 for Comparison
We have observed that the results we have obtained for the characterisation of K398108 are consistent with those of the TU Delft '10 iGEM team. From the growth curves obtained (see graph below), an increase growth rate during the exponential phase is observed in E. Coli expressing BBa_K398108 as opposed to the wild type when the salt concentration of the media is elevated.
However, while we have managed to replicate the results of the TU Delft '10 iGEM team, we question the viability of this BioBrick for conferring salt tolerance in E. Coli. While the growth rate is improved for the cells expressing the BioBrick, the overall exponential growth phase does not - from our results, the final OD of the cells in the stationary phase is not higher than that of the wild-type.
Examining the literature, a better gauge of salt tolerance can be found via an increase in OD over the wild type cells in increased salt concentrations, which this BioBrick has not been shown to do. As such, the choice to use K398108 to confer salt tolerance on our cells would remain questionable at best.
