Difference between revisions of "Part:BBa K3725110"
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====CHARACTERIZATION==== | ====CHARACTERIZATION==== | ||
− | Utilizing the | + | Utilizing the phosphate range of 0-100μM and characterization protocol (See: [https://2021.igem.org/Team:Lambert_GA/Pho#:~:text=Engineering%20Success%20page.-,Characterization%20Protocol,-The%20failed%20characterization Modified Protocol]), we characterized the BBa_K3725110 phosphate sensor. As seen in Figure, the characterization data yielded insignificant levels of fluorescence, thus leading us to conclude that the promoter is not sensitive enough to extracellular phosphate levels. |
Revision as of 20:28, 17 December 2021
PhoA Promoter with GFP Reporter
DESIGN
The inducible promoter BBa_K1682012, created by 2015 HKUST-Rice iGEM, was originally made to control the expression of the PhoA alkaline phosphatase gene following activation by the phosphorylated PhoB transcription factor.
CHARACTERIZATION
Utilizing the phosphate range of 0-100μM and characterization protocol (See: Modified Protocol), we characterized the BBa_K3725110 phosphate sensor. As seen in Figure, the characterization data yielded insignificant levels of fluorescence, thus leading us to conclude that the promoter is not sensitive enough to extracellular phosphate levels.
Assembly Compatibility:
- 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 BsaI.rc site found at 741