Difference between revisions of "Part:BBa K1529321"

 
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<partinfo>BBa_K1529321 short</partinfo>
 
<partinfo>BBa_K1529321 short</partinfo>
  
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Prhl(a) is a promoter that is activated by C4HSL (Fig. 1).<br>
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On the downstream of the promoter, GFP is inserted as a reporter.<br>
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[[Image:titech2013_parts_K1139150_main_Fig1.jpg|thumb|center|250px|<b>Fig. 1.</b> Our newly designed hybrid promoter]]
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To characterize the function of the <i>Prhl(a)</i> promoter (<partinfo>BBa_K1529320</partinfo>), we constructed this part Prhl(a)_GFP (<partinfo>BBa_K1529321</partinfo>) by inserting ''rhl(a)'' promoter upstream of a GFP coding sequence. By using reporter cells that contain Prhl(a)-GFP, we measured the fluorescence intensity of the cells induced by C4HSL (Fig. 2). <br>
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We saw that our new ''rhl(a)'' promoter was actually activated by C4HSL through an induction assay (Fig. 3).<br>
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[[Image:titech2013_parts_K1139150_main_Fig2.jpg|thumb|left|310px|<b>Fig. 2.</b> Fluorescence intensity detected by flow cytometer]]
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[[Image:titech2013_parts_K1139150_main_Fig3.jpg|thumb|none|240px|<b>Fig. 3.</b> Comparison of N99 and JM2.300]]
  
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For more information, see [http://2013.igem.org/Team:Tokyo_Tech/Experiment/RM-lac_Hybrid_Promoter_Assay our work in Tokyo_Tech 2013 wiki].
  
 
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Revision as of 15:52, 2 October 2014

Prhl(RR)_GFP

Prhl(a) is a promoter that is activated by C4HSL (Fig. 1).
On the downstream of the promoter, GFP is inserted as a reporter.

Fig. 1. Our newly designed hybrid promoter

To characterize the function of the Prhl(a) promoter (BBa_K1529320), we constructed this part Prhl(a)_GFP (BBa_K1529321) by inserting rhl(a) promoter upstream of a GFP coding sequence. By using reporter cells that contain Prhl(a)-GFP, we measured the fluorescence intensity of the cells induced by C4HSL (Fig. 2).
We saw that our new rhl(a) promoter was actually activated by C4HSL through an induction assay (Fig. 3).

Fig. 2. Fluorescence intensity detected by flow cytometer
Fig. 3. Comparison of N99 and JM2.300


For more information, see [http://2013.igem.org/Team:Tokyo_Tech/Experiment/RM-lac_Hybrid_Promoter_Assay our work in Tokyo_Tech 2013 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