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Team:Harvard/results
From 2010.igem.org
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<a class="labnotebook" name="parts"><h2>Parts</h2></a> | <a class="labnotebook" name="parts"><h2>Parts</h2></a> | ||
| - | <p>We transformed 11 completed vectors into Arabidopsis. A complete list of these parts and other parts built and submitted to the registry, please check out our <a href="https://2010.igem.org/Team:Harvard/parts">parts</a> page.</p> | + | <p style="width;600px;">We transformed 11 completed vectors into Arabidopsis. A complete list of these parts and other parts built and submitted to the registry, please check out our <a href="https://2010.igem.org/Team:Harvard/parts">parts</a> page.</p> |
<a class="labnotebook" name="plants"><h2>Plants</h2> | <a class="labnotebook" name="plants"><h2>Plants</h2> | ||
| - | <p>We raised Arabidopsis plants with the help of Kurt Schellenberg and the Mathews lab at the Harvard Herbarium and transformed them through the agrobacterium flower dip. For more detailed protocol and photos of the procedure, check out our <a href="https://2010.igem.org/Team:Harvard/vectors/agrotoplants">plant protocols page</a>. The transformed plants produced seeds, which we harvested, dried, and plated onto selective agar plates. In the first few days after plating, all the seeds sprout.</p> | + | <p style="width;600px;">We raised Arabidopsis plants with the help of Kurt Schellenberg and the Mathews lab at the Harvard Herbarium and transformed them through the agrobacterium flower dip. For more detailed protocol and photos of the procedure, check out our <a href="https://2010.igem.org/Team:Harvard/vectors/agrotoplants">plant protocols page</a>. The transformed plants produced seeds, which we harvested, dried, and plated onto selective agar plates. In the first few days after plating, all the seeds sprout.</p> |
<p>Day 1:</p> | <p>Day 1:</p> | ||
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<a class="labnotebook" name="future"><h2>Future Directions</h2> | <a class="labnotebook" name="future"><h2>Future Directions</h2> | ||
| - | <p>Because plants take a long time to grow, we were unfortunately unable to verify the function of out parts in Arabidopsis. Stay updated with our results after the Jamboree by checking out our <a href="http://openwetware.org/wiki/IGEM:Harvard/2010">OpenWetWare page</a>. | + | <p style="width;600px;">Because plants take a long time to grow, we were unfortunately unable to verify the function of out parts in Arabidopsis. Stay updated with our results after the Jamboree by checking out our <a href="http://openwetware.org/wiki/IGEM:Harvard/2010">OpenWetWare page</a>. |
Revision as of 12:31, 25 October 2010
Results
FlavorThe 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.
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Figure 1 click to enlarge 
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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.
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Figure 2 click to enlarge 
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Genetic Fence
Induction of Barnase (death gene) reduces cell growth
We characterized the activity of Barnase on an inducible plasmid constructed by UC Berkeley for iGEM 2007 (part I716408C). This contruct works by expressing background levels of Barstar with Barnase controlled by an arabinose inducible promoter such that it will overwhelm Barstar when induced. Higher levels of Barnase expression resulted in lower rates of growth in the bacteria, affirming the principle of Barnase-based growth control for the genetic fence, and confirming the results from Berkeley 2007. We characterized the growth repression of Barnase under a range of arabinose inducer concentrations.
Our results show that expression of Barnase is effective in reducing cell growth, suggesting that Barnase will enable the genetic fence to prevent growth of iGarden plants outside of their designated areas.
Parts
We transformed 11 completed vectors into Arabidopsis. A complete list of these parts and other parts built and submitted to the registry, please check out our parts page.
Plants
We raised Arabidopsis plants with the help of Kurt Schellenberg and the Mathews lab at the Harvard Herbarium and transformed them through the agrobacterium flower dip. For more detailed protocol and photos of the procedure, check out our plant protocols page. The transformed plants produced seeds, which we harvested, dried, and plated onto selective agar plates. In the first few days after plating, all the seeds sprout.
Day 1:
Day 2:
Day 3:
Future Directions
Because plants take a long time to grow, we were unfortunately unable to verify the function of out parts in Arabidopsis. Stay updated with our results after the Jamboree by checking out our OpenWetWare page.
