Difference between revisions of "Part:BBa K2036007"
Line 3: | Line 3: | ||
<partinfo>BBa_K2036007 short</partinfo> | <partinfo>BBa_K2036007 short</partinfo> | ||
− | CII is a transcriptional activator of pRE, but it is normally degrade by Ftsh, and in this case, | + | CII is a transcriptional activator of pRE, but it is normally degrade by Ftsh, and in this case,tandem expression is useful to activate pRE. |
<h2>Protein&promoter</h2> | <h2>Protein&promoter</h2> | ||
Line 14: | Line 14: | ||
[[File:T--HUST-China--CII-pRE_plate.png|800px|thumb|center|Fig1: According to the Fluorescence measurement curve above, we can see clearly that GFP level increased over time and it showed significant difference from CK.]] | [[File:T--HUST-China--CII-pRE_plate.png|800px|thumb|center|Fig1: According to the Fluorescence measurement curve above, we can see clearly that GFP level increased over time and it showed significant difference from CK.]] | ||
<br> | <br> | ||
− | [[File:T--HUST-China--Experiments-CII-pRE_Flou-detec.png|800px|thumb|center|Fig2: We also did Fluorescence microscope detection after 30, 120 and 240 minutes' induction. According to the | + | [[File:T--HUST-China--Experiments-CII-pRE_Flou-detec.png|800px|thumb|center|Fig2: We also did Fluorescence microscope detection after 30, 120 and 240 minutes' induction. According to the figure above, we can tell qualitatively that pRE leakage are at relative low level and CII can efficiently activate the promoter.]] |
<h2>Protein&protein reaction</h2> | <h2>Protein&protein reaction</h2> | ||
Line 21: | Line 21: | ||
</p> | </p> | ||
<br> | <br> | ||
− | [[File:T--HUST-China--CIII%26Ftsh.png|800px|thumb|center|Fig3: According to the Fluorescence measurement curve above, we can see clearly that GFP intensity of the CIII test circuit increases over time and it shows significant difference from two control groups. It indicates that | + | [[File:T--HUST-China--CIII%26Ftsh.png|800px|thumb|center|Fig3: According to the Fluorescence measurement curve above, we can see clearly that GFP intensity of the CIII test circuit increases over time and it shows significant difference from two control groups. It indicates that tandemly expressed CIII can efficiently protect CII from being degraded by Ftsh. ]] |
<!-- Add more about the biology of this part here | <!-- Add more about the biology of this part here |
Revision as of 05:03, 25 October 2016
RBS-CII-RBS-CII, tandem expression
CII is a transcriptional activator of pRE, but it is normally degrade by Ftsh, and in this case,tandem expression is useful to activate pRE.
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 the test group and pRE-RBS-GFP-LVAssrAtag as CK to see whether CII efficiently activates pRE.
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 constructed to test whether CIII can protect CII from being degraded by Ftsh by competitive inhibition.
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]