Difference between revisions of "Part:BBa K2036013"
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<partinfo>BBa_K2036013 parameters</partinfo>
 
<partinfo>BBa_K2036013 parameters</partinfo>
 
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<h2>Protein&promoter</h2>
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<p>--CII and pRE</p>
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<br>
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<p>
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CII (BBa_K2036000) functions as a transcriptional activator to direct promoter RE, so we constructed CII-TT-pRE-RBS-GFP-LVAssrAtag as test group and pRE-RBS-GFPLVAssrAtag as CK to see if CII efficiently activate pRE.
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</p>
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<br>
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[[File:T--HUST-China--CII-pRE_plate.png|800px|thumb|center|Fig2: According to the Flourescence measurement curve above, we can see clearly that GFP level increased over time and it showed significant difference from CK.]]
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<br>
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[[File:T--HUST-China--Experiments-CII-pRE_Flou-detec.png|800px|thumb|center|Fig3: We also did Fluorescence microscope detection after 30, 120 and 240 minutes induction. According to the figture below, we can tell qualitively that pRE leakage are at relative low level and CII can efficiently activate the promoter.]]
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<h2>Protein&protein reaction</h2>
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<p>
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We had submitted and documented RBS-CIII-RBS-CIII-RBS-CII-TT-pRE-RBS-GFP-LVAssrAtag (BBa_K2036014) and RBS-CII-RBS-CII-RBS-CII-TT-pRE-RBS-GFP-LVAssrAtag (BBa_K2036015). These two parts were to test whether CIII can protect CII from being degraded by Ftsh by competitive inhibition.
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</p>
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<br>
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[[File:T--HUST-China--CIII%26Ftsh.png|800px|thumb|center|Fig4: According to the Flourescence measurement curve above, we can see clearly that GFP level of CIII test circuit increased over time and it showed significant difference from two control groups. It indicates that tandomly expressed CIII can efficiently protect CII from being degraded by Ftsh. ]]

Revision as of 16:55, 19 October 2016


RBS-CII-TT-pRE-RBS-GFP-LVAssrAtag

It is a GFP regulationary circuits. When CII is expressed it can further activate GFP and forming a Switching Lag-times. HUST-China 2016 build this part to characterize CII and pRE interaction with a control group:pRE-GFP-LVAssrAtag ( BBa_K2036011). And we also construct a tandem expression of CII (BBa_K2036015)to figure out if the flouresence level will come up with CII.

Fig1:CII&pRE interaction characterization circuits

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI.rc site found at 1168


Protein&promoter

--CII and pRE


CII (BBa_K2036000) functions as a transcriptional activator to direct promoter RE, so we constructed CII-TT-pRE-RBS-GFP-LVAssrAtag as test group and pRE-RBS-GFPLVAssrAtag as CK to see if CII efficiently activate pRE.


Fig2: According to the Flourescence measurement curve above, we can see clearly that GFP level increased over time and it showed significant difference from CK.


Fig3: We also did Fluorescence microscope detection after 30, 120 and 240 minutes induction. According to the figture below, we can tell qualitively that pRE leakage are at relative low level and CII can efficiently activate the promoter.

Protein&protein reaction

We had submitted and documented RBS-CIII-RBS-CIII-RBS-CII-TT-pRE-RBS-GFP-LVAssrAtag (BBa_K2036014) and RBS-CII-RBS-CII-RBS-CII-TT-pRE-RBS-GFP-LVAssrAtag (BBa_K2036015). These two parts were to test whether CIII can protect CII from being degraded by Ftsh by competitive inhibition.


Fig4: According to the Flourescence measurement curve above, we can see clearly that GFP level of CIII test circuit increased over time and it showed significant difference from two control groups. It indicates that tandomly expressed CIII can efficiently protect CII from being degraded by Ftsh.