Part:BBa_K1741006
sfGFP under short rhamnose promoter (very weak)
From rhaBAD1 promoter we removed both CRP binding sites. It seems likely thatt RhaS binding site has been also affected, so however the resulting promoter is still induced by rhamnose, the induction is very weak.
Design
Legend:
RhaWT - rhamnose wild type
Rha1 - [BBa_K1741005]
Rha2 - [BBa_K1741006]
Our wild type rhamnose promoter is commercially available. However, we had to modify it to remove EcoRI restriction site to fit BioBrick standards. We achieved it by a single point mutation of cytosine to thymine - that is how Rha1 was created. Next, we decided to further minimize the promoter sequence by removing the CRP site - we called this contstruct Rha2.
Results
Legend:
RhaWT - rhamnose wild type
Rha1 - [BBa_K1741005]
Rha2 - [BBa_K1741006]
The sfGFP fluorescence [RFU] was measured using Tecan fluorometer.
All three rhamnose promoters are induced by rhamnose and repressed by glucose. Turns out that single point mutation in EcoRI restriction site in Rha1 significantly increased the activity of the promoter as comapred to the wild type construct. Rha2 is a weak promoter, perfect for people who would like to manufacture small amount of the protein of interest.
We also checked the tightness of our promoters.
All of our promoters are induced only by their respective sugars with a small exception of xylose promoters being slightly induced by arabinose and arabinose promoters being slightly induced by xylose. All of our promoters are repressed by glucose.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI.rc site found at 148
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