Difference between revisions of "Team:Georgia State/Description"
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<h5>Bacto-ink!</h5> | <h5>Bacto-ink!</h5> | ||
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Our bacteria will be engineered to be used as a viable alternative to printer ink as well as pen ink. They will be transformed with fusion proteins composed of a cellulose binding domain(CBD) and a chroma protein, blue and red. The CBD will allow the bacteria to bind to paper and the various chroma proteins will give the ink color. | Our bacteria will be engineered to be used as a viable alternative to printer ink as well as pen ink. They will be transformed with fusion proteins composed of a cellulose binding domain(CBD) and a chroma protein, blue and red. The CBD will allow the bacteria to bind to paper and the various chroma proteins will give the ink color. | ||
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<h5>Horseshoe Crab Factor-C Detection Spray</h5> | <h5>Horseshoe Crab Factor-C Detection Spray</h5> | ||
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<h5>Bacteria vs. Tobacco, Mambalgin-1 Production Showdown! </h5> | <h5>Bacteria vs. Tobacco, Mambalgin-1 Production Showdown! </h5> | ||
<p>We will engineer two different chassis systems to produce a eukaryotic analgesic protein derived from Dendroaspis polylepis. The first will consist of transformed Escherichia coli that will assemble our protein and localize it to the periplasm. This method should allow for more efficient disulfide bond formation due to the periplasm's oxidizing environment. Furthermore, this strategy will reduce the labor required to isolate our protein during purification. Meanwhile, the second system will consist of Agrobacterium transfected Nicotiana benthamiana plants. The infiltrated leaves will produce our protein of interest over several days. Then, the leaves will be collected, macerated and further purified to isolate the protein product. Finally, by using two systems that differ by domain, we can determine which organism-based chassis is superior for producing our protein of interest. | <p>We will engineer two different chassis systems to produce a eukaryotic analgesic protein derived from Dendroaspis polylepis. The first will consist of transformed Escherichia coli that will assemble our protein and localize it to the periplasm. This method should allow for more efficient disulfide bond formation due to the periplasm's oxidizing environment. Furthermore, this strategy will reduce the labor required to isolate our protein during purification. Meanwhile, the second system will consist of Agrobacterium transfected Nicotiana benthamiana plants. The infiltrated leaves will produce our protein of interest over several days. Then, the leaves will be collected, macerated and further purified to isolate the protein product. Finally, by using two systems that differ by domain, we can determine which organism-based chassis is superior for producing our protein of interest. | ||
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Revision as of 20:38, 30 June 2017
Georgia_State
Bacto-ink!
Our bacteria will be engineered to be used as a viable alternative to printer ink as well as pen ink. They will be transformed with fusion proteins composed of a cellulose binding domain(CBD) and a chroma protein, blue and red. The CBD will allow the bacteria to bind to paper and the various chroma proteins will give the ink color.
Horseshoe Crab Factor-C Detection Spray
We will synthetically produce the factor C protein from the horseshoe crab blood and create a detection system that detects gram negative bacteria without the harvesting of horseshoe crabs.
Bacteria vs. Tobacco, Mambalgin-1 Production Showdown!
We will engineer two different chassis systems to produce a eukaryotic analgesic protein derived from Dendroaspis polylepis. The first will consist of transformed Escherichia coli that will assemble our protein and localize it to the periplasm. This method should allow for more efficient disulfide bond formation due to the periplasm's oxidizing environment. Furthermore, this strategy will reduce the labor required to isolate our protein during purification. Meanwhile, the second system will consist of Agrobacterium transfected Nicotiana benthamiana plants. The infiltrated leaves will produce our protein of interest over several days. Then, the leaves will be collected, macerated and further purified to isolate the protein product. Finally, by using two systems that differ by domain, we can determine which organism-based chassis is superior for producing our protein of interest.
