Difference between revisions of "Part:BBa K3269001:Experience"
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| − | + | In order to validate that our part performs its intended function of providing a visual fluorescent output that is in some way proportional to the UV dose given to the cell, we exposed E. coli K-12 cells transformed with our part (BBa_K3269001) in a pSB1A3 backbone with our UV-C handlamp at 11.9 W/m^2 for increments 0, 4, and 10 seconds. Negative and positive controls for fluorescence were also clones, the positive having a constitutive promoter upstream of GFP (BBa_K3269002) and the negative only having the uvrA promoter and no GFP(BBa_K3269003). Cells were inoculated in LB with ampicillin the night before and then diluted to an OD of 0.1, and were then allowed to grow up to ~0.4. Directly after exposure in the 96-well plate, cells were then placed in a plate reader, which measured their fluorescence over a 3 hour period, taking Fluorescence and OD600 measurements every 3 minutes. | |
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Sadly, our results suggest that there is no significant difference in induction at any of the UV doses for our part BBa_K3269001. This is most likely because we only exposed it to UV transiently as opposed to continuously. Possible improvements could include the addition of an Anderson promoter to recruit more transcription machinery, as well as a stronger RBS to raise levels of protein expression. | Sadly, our results suggest that there is no significant difference in induction at any of the UV doses for our part BBa_K3269001. This is most likely because we only exposed it to UV transiently as opposed to continuously. Possible improvements could include the addition of an Anderson promoter to recruit more transcription machinery, as well as a stronger RBS to raise levels of protein expression. | ||
Revision as of 03:35, 21 October 2019
In order to validate that our part performs its intended function of providing a visual fluorescent output that is in some way proportional to the UV dose given to the cell, we exposed E. coli K-12 cells transformed with our part (BBa_K3269001) in a pSB1A3 backbone with our UV-C handlamp at 11.9 W/m^2 for increments 0, 4, and 10 seconds. Negative and positive controls for fluorescence were also clones, the positive having a constitutive promoter upstream of GFP (BBa_K3269002) and the negative only having the uvrA promoter and no GFP(BBa_K3269003). Cells were inoculated in LB with ampicillin the night before and then diluted to an OD of 0.1, and were then allowed to grow up to ~0.4. Directly after exposure in the 96-well plate, cells were then placed in a plate reader, which measured their fluorescence over a 3 hour period, taking Fluorescence and OD600 measurements every 3 minutes.
Sadly, our results suggest that there is no significant difference in induction at any of the UV doses for our part BBa_K3269001. This is most likely because we only exposed it to UV transiently as opposed to continuously. Possible improvements could include the addition of an Anderson promoter to recruit more transcription machinery, as well as a stronger RBS to raise levels of protein expression.
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UNIQ30702e112fcef067-partinfo-00000000-QINU UNIQ30702e112fcef067-partinfo-00000001-QINU