Difference between revisions of "Part:BBa K323135:Experience"
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[[Image:Sloviolaceingraph.JPG|left|thumb|300px| '''Figure: Violacein concentrations measured at various times through the experiment.''' The results above show that cultures containing the DNA program produce violacein more rapidly and efficiently.]] | [[Image:Sloviolaceingraph.JPG|left|thumb|300px| '''Figure: Violacein concentrations measured at various times through the experiment.''' The results above show that cultures containing the DNA program produce violacein more rapidly and efficiently.]] | ||
− | [[Image:Sloviolaceinhistogram.JPG|center|thumb| | + | [[Image:Sloviolaceinhistogram.JPG|center|thumb|400px| '''Figure: Violacein concentrations at the end of the experiment.''' Measuring the concentration of violacein in extracts of the incubated cultures determined the highest yield of violacein in the culture with the DNA program. The production was increased 6-fold in comparison with the culture without a DNA program. A significant disctintion from the culture with the scrambled program is also notable, which implies that a correct arrangement of enzymes on the DNA program is important for the speed of the reaction.]] |
By measuring the concentrations of violacein in the extracts of taken samples, we determined that the speed and yield of violacein production in our system increased 6-fold in comparison to an ''E. coli'' strain containing plasmids with a scrambled DNA program or without a DNA program. | By measuring the concentrations of violacein in the extracts of taken samples, we determined that the speed and yield of violacein production in our system increased 6-fold in comparison to an ''E. coli'' strain containing plasmids with a scrambled DNA program or without a DNA program. |
Revision as of 03:40, 27 October 2010
Cells containing plasmids with Part:BBa_K323135 and Part:BBa_K323132 were transformed with Part:BBa_K323066, Part:BBa_K323153 and a commercial pBluescript plasmid without a DNA program. Cultures were incubated at 30°C for several days and samples were taken at various times. Violacein was extraced from individual samples to analyze the products and evaluate the yield of violacein production.
By measuring the concentrations of violacein in the extracts of taken samples, we determined that the speed and yield of violacein production in our system increased 6-fold in comparison to an E. coli strain containing plasmids with a scrambled DNA program or without a DNA program.
In addition, the 2010 iGEM team Slovenia have shown that a DNA program-mediated biosynthesis decreases formation of an unwanted side product deoxychromoviridans. We have analysed the products of the vio operon (Part:Bba_K274002) with HPLC, TLC and mass spectrometry (for detailed description see the 2010 iGEM team Slovenia [http://2010.igem.org/Team:Slovenia/METHODS_and_PARTS wiki]).
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UNIQf436db55f9b35005-partinfo-00000000-QINU UNIQf436db55f9b35005-partinfo-00000001-QINU