Team:WPI-Worcester/ATF1
From 2014.igem.org
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- | <h4>Characterization of the Efficiency of the ATF1 Enzyme | + | |
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+ | <h9>Characterization of the Efficiency of the ATF1 Enzyme | ||
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The ATF1 enzyme converts isoamyl alcohol to isoamyl acetate, which gives off a strong banana odor. The conversion of isoamyl alcohol to isoamyl acetate can be monitored using gas chromatography and mass spectroscopy. Thus, the efficiency of the ATF1 enzyme can be characterized.</p> | The ATF1 enzyme converts isoamyl alcohol to isoamyl acetate, which gives off a strong banana odor. The conversion of isoamyl alcohol to isoamyl acetate can be monitored using gas chromatography and mass spectroscopy. Thus, the efficiency of the ATF1 enzyme can be characterized.</p> | ||
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- | < | + | <h9>Quantification of ATF1 through Gas Chromatography and Mass Spectroscopy |
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<li> Although inducible by arsenic, cells appear to die off after the concentration of arsenite exceeds 5uM</li> | <li> Although inducible by arsenic, cells appear to die off after the concentration of arsenite exceeds 5uM</li> | ||
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+ | <li> Yields of isoamyl acetate were improved slightly when there was less open air within the incubation tubes </li> | ||
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Revision as of 17:00, 17 October 2014
Team:WPI-Worcester
From 2014.igem.org
Better Biobrick Characterization
The ATF1 enzyme converts isoamyl alcohol to isoamyl acetate, which gives off a strong banana odor. The conversion of isoamyl alcohol to isoamyl acetate can be monitored using gas chromatography and mass spectroscopy. Thus, the efficiency of the ATF1 enzyme can be characterized.
We have constructed two different biobricks that include the ATF1 gene. The first biobrick, K1423007, is a construct consisting of an arsenic inducible promoter, a ribosome binding site, the ATF1 gene, and a double terminator. The second biobrick, K1423008, consists of a high strength constitutive promoter, a ribosome binding site, the ATF1 gene, and the double terminator.
BBa_K1243007: Inducible Banana Odor Generator
BBa_K1243008: Constitutive Banana Odor Generator
In order to efficiently quantify the performance of these two constructs, we designed and performed a number of experiments based around E.Coli with the constitutive promoter plasmid, and E.Coli with the arsenic inducible promoter. The full protocol is located in our protocol section, and can be located through this link. Some findings through these experiments revealed that:
Our final Experimental procedure combined our best practices across our previous experiments.