"
Team:Harvard/flavor/results
From 2010.igem.org
Mtheilmann (Talk | contribs) |
Mtheilmann (Talk | contribs) |
||
| Line 7: | Line 7: | ||
<h1>Results</h1> | <h1>Results</h1> | ||
<img href=”image location:> | <img href=”image location:> | ||
| + | |||
| + | <p> | ||
| + | The two flavors that are currently ready for transformation into plants are the "taste-inverter" <u>miraculin</u> and the sweetener <u>brazzein</u>. Given the long time-frame of plant transformation we used two different assays in <i>E. Coli</i> to confirm that our proteins could indeed be transcribed and translated. The results of those assays are shown here. | ||
| + | </p> | ||
| + | |||
<h2>Confirmation with <i>YFP-2x</i> Tags</h2> | <h2>Confirmation with <i>YFP-2x</i> Tags</h2> | ||
<p> | <p> | ||
| - | In order to confirm that the Miraculin and Brazzein are able to be expressed in <i>E. Coli</i> we attached a <i>YFP-2x</i> tag sequence to the termini of both proteins. The proteins were placed under an IPTG-expressible promoter and used spectrophotometry to determine the level of YFP fluorescence against a baseline, untagged protein. Figure 1 shows relative-fluorescence at times post induction. In all circumstances the levels of YFP-fluorescence increased | + | In order to confirm that the Miraculin and Brazzein are able to be expressed in <i>E. Coli</i> we attached a <i>YFP-2x</i> tag sequence to the termini of both proteins. The proteins were placed under an IPTG-expressible promoter and used spectrophotometry to determine the level of YFP fluorescence against a baseline, untagged protein. Figure 1 shows relative-fluorescence at times post induction. In all circumstances the levels of YFP-fluorescence increased. |
</p> | </p> | ||
| Line 35: | Line 40: | ||
<p> | <p> | ||
| - | A western blot assay was performed to check for <i>E. Coli</i> expression of | + | A western blot assay was performed to check for <i>E. Coli</i> expression of Miraculin and Brazzein. Proteins tagged at either the N- or C- terminus were placed under the control of an IPTG-inducible promoter. In the miraculin assay, no protein expression was seen. It is possible that the protein does not express well in <i>E. Coli</i>, or that the plant-specific codon optimization of the proteins resulted in reduced expressibility. Brazzein, specifically C-terminus tagged brazzein was seen to be highly expressed in <i>E. Coli</i>. |
</p> | </p> | ||
Revision as of 06:11, 25 October 2010
Results
The two flavors that are currently ready for transformation into plants are the "taste-inverter" miraculin and the sweetener brazzein. Given the long time-frame of plant transformation we used two different assays in E. Coli to confirm that our proteins could indeed be transcribed and translated. The results of those assays are shown here.
Confirmation with YFP-2x Tags
In order to confirm that the Miraculin and Brazzein are able to be expressed in E. Coli we attached a YFP-2x tag sequence to the termini of both proteins. The proteins were placed under an IPTG-expressible promoter and used spectrophotometry to determine the level of YFP fluorescence against a baseline, untagged protein. Figure 1 shows relative-fluorescence at times post induction. In all circumstances the levels of YFP-fluorescence increased.
|
Figure 1 click to enlarge 
|
|
Confirmation with Western Blot
A western blot assay was performed to check for E. Coli expression of Miraculin and Brazzein. Proteins tagged at either the N- or C- terminus were placed under the control of an IPTG-inducible promoter. In the miraculin assay, no protein expression was seen. It is possible that the protein does not express well in E. Coli, or that the plant-specific codon optimization of the proteins resulted in reduced expressibility. Brazzein, specifically C-terminus tagged brazzein was seen to be highly expressed in E. Coli.
|
Figure 2 click to enlarge 
|
|
