Team:UCSF/Violacein Results
From 2012.igem.org
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<li>Strain 2:pcdfDuet+VioDC</li> | <li>Strain 2:pcdfDuet+VioDC</li> | ||
<li>Strain 3: pcdfDuet:VioABE+VioDC (full operon)</li> | <li>Strain 3: pcdfDuet:VioABE+VioDC (full operon)</li> | ||
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<P> | <P> | ||
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<regulartext> | <regulartext> | ||
While other teams and papers have reported that extracting pigment from cultures is the best way to perform analysis and quantification, several different solvents have been reported. The 2009 Cambridge iGEM team used acetone to extract, so we tested extraction of violacen from Strain 3 (full violacein operon) using acetone as well as methanol and ethanol. <p> | While other teams and papers have reported that extracting pigment from cultures is the best way to perform analysis and quantification, several different solvents have been reported. The 2009 Cambridge iGEM team used acetone to extract, so we tested extraction of violacen from Strain 3 (full violacein operon) using acetone as well as methanol and ethanol. <p> |
Revision as of 03:31, 4 October 2012
Strain 1, which only has the first half of the enzymes necessary to produce violacein is still able to produce a green pigment. When the pigment is extracted from cells, the wavelength scan shown in dark blue is obtained.
Strain 2, which has the second half of the violacein pathway, produces no pigment. This is expected because without the first half of the pathway, no pigment can be produced.
Strain 3, which contains the entire violacein operon produces a wavelength scan similar to our standard obtained from Sigma-Aldrich, with violacein having a maximum absorbance near 575nm.
Co-Culture: Strain 1 and Strain 2 grown together (red line) produce a wavelength scan that indicates production of violacein.