Team:BV CAPS Kansas/Project/Future

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<p>Our plan for future projects!</p>
<p>Our plan for future projects!</p>
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We chose this project because of its ability to be scalable. Next year, we can make more parts with various promoters and ribosomal binding sites. To characterize the parts better, we will be using a pyruvate kinase assay and gas chromatography. We also want to examine optimal conditions of cyanobacteria, including experimentation with CO<sub>2</sub> limitation to reroute Acetyl-CoA usage in the cell to the alkane pathway. Furthermore, we plan on making a more in-depth and accurate TinkerCell model to show the amount of resources directed into specific pathways in the cell and how we are trying to change that usage. We would also like to expand our community outreach by expanding a BiobBuilder.
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In the future, the 2014 iGEM team will be continuing with this project idea, and expanding the use of it. We are hoping to make great improvements next year!<br><br> <ol>
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<li>Next year, we can make more parts with various promoters and ribosomal binding sites.</li><br>
 +
<li>To characterize the parts better, we will be using a pyruvate kinase assay and gas chromatography.</li><br>
 +
<li>We also want to examine optimal conditions of cyanobacteria, including experimentation with CO<sub>2</sub> limitation to reroute Acetyl-CoA usage in the cell to the alkane pathway.</li><br>
 +
<li>Furthermore, we plan on making a more in-depth and accurate TinkerCell model to show the amount of resources directed into specific pathways in the cell and how we are trying to change that usage.</li><br>
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<li>We would also like to expand our community outreach by expanding a BioBuilder.</li><br>
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Latest revision as of 18:50, 21 June 2013

Team:BV CAPS Kansas Team Page Code Testing 2 - 2013hs.igem.org

BV CAPS iGEM Tweets

Thanks!

Future

Our plan for future projects!

In the future, the 2014 iGEM team will be continuing with this project idea, and expanding the use of it. We are hoping to make great improvements next year!

  1. Next year, we can make more parts with various promoters and ribosomal binding sites.

  2. To characterize the parts better, we will be using a pyruvate kinase assay and gas chromatography.

  3. We also want to examine optimal conditions of cyanobacteria, including experimentation with CO2 limitation to reroute Acetyl-CoA usage in the cell to the alkane pathway.

  4. Furthermore, we plan on making a more in-depth and accurate TinkerCell model to show the amount of resources directed into specific pathways in the cell and how we are trying to change that usage.

  5. We would also like to expand our community outreach by expanding a BioBuilder.

Retrieved from "https://2013hs.igem.org/Team:BV_CAPS_Kansas/Project/Future"

Retrieved from "http://2013hs.igem.org/Team:BV_CAPS_Kansas/Project/Future"