Difference between revisions of "Part:BBa K1529321"

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[[Image:Improved_Prhl(RL)_Promoter_Assay_Result.png|thumb|center|600px|<b>Fig. 3.</b> Fluorescence intensity detected by flow cytometer]]
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[[Image:Improved_Prhl(RR)_Promoter_Assay_Result.png|thumb|center|600px|<b>Fig. 3.</b> Fluorescence intensity detected by flow cytometer]]
 
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Revision as of 11:07, 20 October 2014

Prhl(RR)_GFP

This part is Prhl(RR) promoter regulating GFP. Prhl(RR) is a promoter that is activated by C4HSL-RhlR complex.
We improved Prhl (BBa_R0071) by changing a LuxR binding site of Plux (BBa_R0062) to a RhlR binding site. (Fig. 1.)
The bottom structures of LuxR and RhlR are similar to each other, so RhlR can also bind to Lux Box. (Fig. 2.)

We constructed this part to characterize the function of the Prhl(RR) promoter (BBa_K1529310), by inserting Prhl(RR) promoter upstream of a GFP coding sequence.

Fig. 1. Our newly designed promoter
Fig. 2. Difference between LuxR and RhlR


By using reporter cells that contain Prhl(RR)-GFP, we measured the fluorescence intensity of the cells induced by C4HSL.
Through an induction assay, we found that our new Prhl(RL) promoter was actually activated by C4HSL-RhlR complex and had high induced/not-induced ratio(Fig. 3.).
This means Prhl(RL) promoter has the higher expression level while keeping the low leakage.

We can say that Prhl(RL) promoter is the best improved Prhl promoter due to the advantages of less leak and higher expression level.


Fig. 3. Fluorescence intensity detected by flow cytometer


For more information, see [http://2014.igem.org/Team:Tokyo_Tech/Experiment/Prhl_reporter_assay our work in Tokyo_Tech 2014 wiki].

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BglII site found at 90
    Illegal BamHI site found at 78
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI.rc site found at 777