Difference between revisions of "Part:BBa R0071:Experience"
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===Improvement=== | ===Improvement=== | ||
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[[Image:Improved_Prhl_Promoter_Assay_Result.png|thumb|center|600px|<b>Fig. 1.</b> Fluorescence intensity detected by flow cytometer]] | [[Image:Improved_Prhl_Promoter_Assay_Result.png|thumb|center|600px|<b>Fig. 1.</b> Fluorescence intensity detected by flow cytometer]] | ||
Revision as of 22:44, 14 October 2016
Improvement
iGEM 2016 Tokyo_tech
iGEM 2014 Tokyo_Tech
We, Tokyo Tech 2014, improved Prhl Promoter (BBa_R0071) by changing LuxR binding site of Plux Promoter to RhlR binding site.
We dsigned new Prhl promoter
We measured the GFP expression with the four different promoters (Prhl : BBa_R0071, Prhl(RR) : BBa_K1529320, Prhl(LR) : BBa_K1529310 and Prhl(RL) : BBa_K1529300) by flow cytometer. Each promoter was tested in the presence and also in the absence of C4HSL.
Fig. 1 shows the fluorescence intensity detected by flow cytometer.
From the result, when induced by C4HSL, Prhl(RR) promoter showed higher maximum expression level and higher leak than the original Prhl promoter (BBa_R0071).
Although Prhl(RL) promoter had lower maximum expression level compared to Prhl(RR) promoter, it had the highest induced/not-induced ratio.
This means Prhl(RL) promoter has little leak.
Therefore, we can say that Prhl(RL):BBa_K1529300 promoter is the best improved Prhl promoter due to the advantages of less leak and higher expression level.
For more information, see [http://2014.igem.org/Team:Tokyo_Tech/Experiment/Prhl_reporter_assay our work in Tokyo_Tech 2014 wiki].
Applications of BBa_R0071
User Reviews
UNIQ413ce642cbb7c8a7-partinfo-00000005-QINU UNIQ413ce642cbb7c8a7-partinfo-00000006-QINU
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No review score entered. Northwestern 2011 |
The 2011 Northwestern iGEM team used this promoter as a unit within our Pseudomonas Aeruginosa biosensor. When this RhlR/C4-HSL regulated promoter is induced at varying concentrations of C4-HSL, we observed GFP fluorescence in accordance to the graph below.
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