Difference between revisions of "Part:BBa K323132:Experience"
(→User Reviews) |
|||
(One intermediate revision by one other user not shown) | |||
Line 5: | Line 5: | ||
[[Image:Sloviolaceincultures.JPG|left|thumb|380px| '''Figure: Bacterial cultures carrying parts BBa_K323135 and BBa_K323132 and containing a DNA program or a scrambled DNA program or no DNA program.''' Cultures of bacteria carrying parts [[Part:BBa_K323132]], [[Part:BBa_K323135]] and | [[Image:Sloviolaceincultures.JPG|left|thumb|380px| '''Figure: Bacterial cultures carrying parts BBa_K323135 and BBa_K323132 and containing a DNA program or a scrambled DNA program or no DNA program.''' Cultures of bacteria carrying parts [[Part:BBa_K323132]], [[Part:BBa_K323135]] and | ||
1.) plasmid containing a DNA program [[Part:BBa_K323066]] (left), | 1.) plasmid containing a DNA program [[Part:BBa_K323066]] (left), | ||
− | 2.) plasmid containing a scrambled DNA program [[Part:BBa_K323153]] | + | 2.) plasmid containing a scrambled DNA program [[Part:BBa_K323153]] (middle) |
− | and 3.) plasmid without a DNA program | + | and 3.) plasmid without a DNA program (right) |
were incubated at 30°C in a Luria Bertani media. The color of the culture containing the plasmid with the DNA program is notably more purple than the color of other two cultures.]] | were incubated at 30°C in a Luria Bertani media. The color of the culture containing the plasmid with the DNA program is notably more purple than the color of other two cultures.]] | ||
Line 136: | Line 136: | ||
<!-- End of the user review template --> | <!-- End of the user review template --> | ||
<!-- DON'T DELETE --><partinfo>BBa_K323132 EndReviews</partinfo> | <!-- DON'T DELETE --><partinfo>BBa_K323132 EndReviews</partinfo> | ||
+ | |||
+ | Karina Arnesen, undergraduate, Alberta iGEM 2010 | ||
+ | |||
+ | Transformed from the 2011 registry shipment and Digested with NotI. The only bands visible are at 2kb (backbone) and ~ 850bps (wrong size for the insert). |
Latest revision as of 21:50, 28 June 2011
E.coli containing parts Part:BBa_K323135 and Part:BBa_K323132 were transformed with Part:BBa_K323066 or Part:BBa_K323153 or a 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 yield of violacein production in our system (DNA-guided biosynthesis) increased 6-fold in comparison to an E. coli strain containing a plasmid without a DNA program.
In addition, the 2010 iGEM team Slovenia has 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]).
Applications of BBa_K323132
User Reviews
UNIQd5fbe98fefc58893-partinfo-00000000-QINU UNIQd5fbe98fefc58893-partinfo-00000001-QINU
Karina Arnesen, undergraduate, Alberta iGEM 2010
Transformed from the 2011 registry shipment and Digested with NotI. The only bands visible are at 2kb (backbone) and ~ 850bps (wrong size for the insert).