Difference between revisions of "Team:US AFRL CarrollHS/Improve"

 
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<h1>Improve</h1>
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<p>For teams seeking to improve upon a previous part or project, you should document all of your work on this page. Please remember to include all part measurement and characterization data on the part page on the Registry. Please include a link to your improved part on this page.</p>
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<h3>Gold Medal Criterion #2</h3>
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<p><b>Standard Tracks:</b> Create a new part that has a functional improvement upon an existing BioBrick part. The sequences of the new and existing parts must be different. You must perform experiments with both parts to demonstrate this improvement.  Document the experimental characterization on the Part's Main Page on the Registry for both the existing and new parts. Both the new and existing Main Page of each Part’s Registry entry must reference each other. Submit a sample of the new part to the Registry.
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The existing part must NOT be from your 2018 part number range and must be different from the part documented in bronze #4.
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<b>Special Tracks:</b> Improve the function of an existing iGEM project (that your current team did not originally create) and display your achievement on your wiki.</p>
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<div class="row"><p>As part of the gold medal criteria to improve a previous years part, the team decided to improve on British Columbia’s (2013) three parts (BBa_K1129003, BBa_K1129042, and BBa_K1129039) to create the “flavor” of cinnamon through the production of the molecule cinnamaldehyde. These three parts created enzymes to break down the naturally produced, in E. coli., molecule phenylalanine into cinnamaldehyde. Our team decided to take these three separate parts and combine them into a singular part for easier use and cloning. Two ribosomal binding sites were also added in front of the second two parts in order to increase the efficiency of the production of the enzymes to create the cinnamaldehyde (The first part did not need an RBS as the promoter had one attached). In the context of this year’s project, this part would be used in order to produce the cinnamaldehyde molecule as a means of killing off bacteria and fungi that contaminate biofuels in containment systems. This molecule will also kill off the bacteria that is producing it, effectively causing it to be the bacteria’s killswitch. This will ensure that the engineered bacteria will not begin to contaminate the containment system as well. However, due to the part ending up around 5 kb and time constraints, the team was unsuccessful at cloning the part into the iGEM backbone in time for submission and it was not submitted.
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Latest revision as of 21:46, 17 October 2018

Improve

As part of the gold medal criteria to improve a previous years part, the team decided to improve on British Columbia’s (2013) three parts (BBa_K1129003, BBa_K1129042, and BBa_K1129039) to create the “flavor” of cinnamon through the production of the molecule cinnamaldehyde. These three parts created enzymes to break down the naturally produced, in E. coli., molecule phenylalanine into cinnamaldehyde. Our team decided to take these three separate parts and combine them into a singular part for easier use and cloning. Two ribosomal binding sites were also added in front of the second two parts in order to increase the efficiency of the production of the enzymes to create the cinnamaldehyde (The first part did not need an RBS as the promoter had one attached). In the context of this year’s project, this part would be used in order to produce the cinnamaldehyde molecule as a means of killing off bacteria and fungi that contaminate biofuels in containment systems. This molecule will also kill off the bacteria that is producing it, effectively causing it to be the bacteria’s killswitch. This will ensure that the engineered bacteria will not begin to contaminate the containment system as well. However, due to the part ending up around 5 kb and time constraints, the team was unsuccessful at cloning the part into the iGEM backbone in time for submission and it was not submitted.