Part:BBa_K2120201
mutated ptet-2
tetR repressible promoter. The function is similar with pTet BBa_R0040. We mutated the -35 region and selected one with lower strength.It can be used to control the expression of toxin proteins to avoid leaking out.
A series of Ptet promoters
We designed a killer switch controlled by TetR repressor. When the concentration of inhibitors reduces to a threshold, the downstream in-promoter Ptet will start the transcription of killer gene. After measuring the original promoter strength [Part:BBa_R0040], we found that the activity is too high to be well controlled for expressing killer genes. So we mutated the original promoter and got 4 mutants with lower activity.
Design
We analyzed the promoter region and decided to mutated the -35 region through designing random primers. It can at most ensure the change of promoter’s background activity and maintain the promoter’s character since the tightly binding region with repressor is well-conserved while the tightly binding region with RNA polymerase is changed .
Characterization using RFP
The four mutated promoters were characterized using RFP to measure the level of gene expression. Cells were grown in 1.5 mL tube in LB culture medium. The host we used is E.coli TOP10.
Results
Cells showed Red fluorescence under fluorescence microscopy. Quantitative measurement was carried out through enzyme-labeled instrument. It turned out that the highest activity of mutants is about 500, while the common activity is about 200. The original promoter is 9000.
We have submitted four mutated promoters [BBa_K2120200; BBa_K2120201; BBa_K2120202 ; BBa_K2120203], here we listed the mutation in -35 region:
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]
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