Difference between revisions of "Part:BBa K2036012"
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− | [[File:T--HUST-China--CIII%26Ftsh.png|800px|thumb|center|Fig3: 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 | + | [[File:T--HUST-China--CIII%26Ftsh.png|800px|thumb|center|Fig3: 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 tandemly expressed CIII can efficiently protect CII from being degraded by Ftsh. ]] |
Revision as of 05:05, 25 October 2016
RBS-CII-TT
CII (BBa_K2036000 ) is a regulatory gene derived from bacteriaphage lambda. It is an activate pRE's expression. And it can be normally degrade by Ftsh in E.coli. This part is designed as CII expression frame with RBS ahead and terminator behind.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Protein&promoter
--CII and pRE
CII (BBa_K2036000) functions as a transcriptional activator to direct promoter pRE, 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.
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.