Part:BBa_K1493003
Fusaric acid induced promoter + GFP
Promoter fusaric acid inducible
Usage and Biology
A fusaric acid efflux pump within Pseudomonas putida is encoded by an operon consisting of four genes. We found that this operon is controlled by a LysR-type gene (pp1262) which is located upstream of the operon. This gene inhibits the binding of RNA polymerase to the promoter in the intergenic region between pp1262 and the operon. Fusaric acid blocks this inhibition, allowing activity of the operon. (See figure 1) Hence, pp1262 and the intergenic region are isolated and put into BioBrick form, effectively acting as a Fusaric Acid inducible Promoter (FAiP).
A growth experiment was set up, using M9 medium. In this experiment both the WT and transformed P. putida containing the BBa_K1493000 BioBrick are grown in a 96-wells plate with 0, 85, 170, 255, 340 and 425µM (0, 15, 30, 45, 60 and 75µg/ml) fusaric acid. Furthermore, E. coli DH5α cells (WT and BBa_K741002) were also grown in the same plate, but without fusaric acid. The transformed E. coli has a well characterized promoter with the same GFP gene downstream. By comparing the fluorescence of our fusaric acid induced promoter at different fusaric acid concentrations to this constitutive promoter, a characterization can be performed.
*Significantly different from WT with p<0.05
The measurement is based on GFP fluorescence in P. putida at increased concentrations of fusaric acid to prove and characterize the activity of the fusaric acid induced promoter, BBa_K1493000. For comparison, the well characterized pLac promoter (BBa_K741002, uninduced by IPTG) was used to quantify the activity of this promoter at different concentrations of fusaric acid. Our fusaric acid inducible promoter does not respond to low concentrations up to 170µM. From 255µM and up, the activity increases. The maximum measured activity of the promoter is 0.21 RPU at 425µM.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal XhoI site found at 1049
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 855
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 928
Features
This BioBrick consists of the fusaric acid inducible promoter and the BBa_I13504 reporter BioBrick. This BioBrick can only be used in any microorganism that has resistance to fusaric acid. For testing and characterizing, we used Pseudomonas putida. This gene contains an illegal restriction site PstI at the repressor gene, so don't use this restriction enzyme when working with this gene.
A similar functioning BioBrick can be found here: https://parts.igem.org/Part:BBa_K1493000
This BioBrick without a reporter GFP can be found here: https://parts.igem.org/Part:BBa_K1493002
For more information on the functioning of this BioBrick, please check: http://2014.igem.org/Team:Wageningen_UR/project/fungal_sensing
References
Hu, R.-M., et al., An Inducible Fusaric Acid Tripartite Efflux Pump Contributes to the Fusaric Acid Resistance in Stenotrophomonas maltophilia. PLoS ONE, 2012. 7(12): p. e51053.
Nelson, K.E., et al., Complete genome sequence and comparative analysis of the metabolically versatile Pseudomonas putida KT2440. Environmental microbiology, 2002. 4(12): p. 799-808.
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