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Our Results |
This summer, we have conducted the following experiments regarding the biofuels in bacteria project.
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CALIBRATION CURVE FOR N-BUTANOL HEXANE EXTRACTION |
The calibration curve was designed to determine how much 1-butanol was extracted by hexane. This was performed using gas chromatography. This method of measurement is a common type of chromatography used in analytical chemistry for analyzing vaporized compounds without decomposition.
The most common method of detection is flame ionization detection and is sensitive to a wide variety of compounds. This was the ideal measurement device for 1-butanol measurement.
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n-Butanol Production |
We concluded that the mutant strain produced a significantly higher amount of 1-butanol than the wild type. These results were extrapolated from three samples and three hexane extractions from the same culture.
This allows us to control for errors in the extraction and measurement, but not for potential variations between independent cultures. The mutant strain of E. coli (JCL) produced a yield of 128.08 +/-5.4 ug/ml/OD; the wild type (DH5 alpha) strain of E. coli produced a yield of 93.81+/- 1.5 ug/ml/OD per cell.
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Confirmation of the Benefit of Ter Function of 1-Butanol Production |
The ter gene originally from Treponema denticola is a trans-2-enl-CoA reductase. Its functional portion of this project is to convert an intermediate of Crotonyl-CoA into Butyryl-CoA.
This part has been submitted to the parts registry and is proven to be functional as our assay with the final project shows a statistically significant production of 1-butanol. We have proven that the use of this gene in the circuit does in fact allow the transformed cell to produce the desired product. Since the gene is NADH dependent, we can presume that the NADH-surplus mutant strain generates feeds into this gene and produces a higher net result of 1-butanol. |
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Parts Submission |
RUiGEM2012 -- Parts sent to the Registry
<groupparts>iGEM2012 Rutgers</groupparts>
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