![](https://parts.igem.org/images/partbypart/icon_composite.png)
Part:BBa_K4604018
piG_02b (tetR_riboK12_mazF_mTurq)
BioBrick piG_02b is a plasmid consisting of the tet promoter/repressor, an AdoCbl riboswitch, mazF fused togther with mTurquoise and the rrnB terminator. The backbone we used in the experiments is pGGAselect. The tet promoter is a BioBrick from iGEM Freiburg 2022 (BBa_K4229059). This is an improved version of BioBrick BBa_K4604017.
Characterization
To indirectly check for mazF-mTurquoise expression a fluorescent measurement was done and compared to BBa_K4604019, namely piG_03.
Next, a growth assay was performed comparing this BioBrick to <a href="https://parts.igem.org/Part:BBa_K4604019">BBa_K4604019</a></html>, namely piG_03.
We also performed a western blot to detect MazF expresion.
In conclusion, we did not observe significant cell death or growth inhibition when measuring OD600 (figure 2) even for higher DOX concentrations. Unfortunately, we were not able to evaluate the CFUs from this experiment because there was a bacterial lawn on the plates due to the high growth rate. Those experiments were repeated three times without any growth inhibition or cell death observed. However, when we measured fluorescence we saw an increase in fluorescence with higher DOX concentrations (Figure 1). This would suggest that the lack of cell death is not due to missing expression. This was also confirmed by western blot (Figure 3) where we detected bands for both toxin-mTurquoise fusion as well as the toxin alone. However, the increase in the intensity of the bands with higher DOX concentrations was only mild. We hypothesized that this could be the result of a subculture in our glycerol stock that either does not produce Toxin or has found a way to inhibit Toxin expression.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 710
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 883
Illegal AgeI site found at 1376 - 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 2250
None |