Difference between revisions of "Part:BBa K3733023"
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<p>BBa_K3733022: https://parts.igem.org/Part:BBa_K3733022 </p> | <p>BBa_K3733022: https://parts.igem.org/Part:BBa_K3733022 </p> | ||
<p>BBa_K3733023: https://parts.igem.org/Part:BBa_K3733023 </p> | <p>BBa_K3733023: https://parts.igem.org/Part:BBa_K3733023 </p> | ||
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<p>BBa_K3733028: https://parts.igem.org/Part:BBa_K3733028 </p> | <p>BBa_K3733028: https://parts.igem.org/Part:BBa_K3733028 </p> | ||
<p>BBa_K3733029: https://parts.igem.org/Part:BBa_K3733029 </p> | <p>BBa_K3733029: https://parts.igem.org/Part:BBa_K3733029 </p> |
Latest revision as of 17:17, 21 October 2021
The nitrate sensor(J23109-B0033) system with neGFP
The NarXL is a the two-component signal system in E.coli, which each constitute a sensor histidine kinase and a response regulator. The NarX is sensor histidine kinase, which can phosphorylate NarL in response to nitrate and nitrite. And then the phosphorylated NarL will binding the site and activate the transcription of PyeaR promoter. So in this nitrate sensor system, we use J23109 (weak promoter) and B0033 (weak RBS) to produce NarX and NarL. When we add different concentrations of nitrate, and measurement the fluorescence intensity to reflect the expression level of PyeaR promoter.
Usage and Biology
The NarX/NarL two component system(TCS) can be activated if the concentration of nitrate is enough. So this NarX/NarL TCS can be designed the nitrate sensor with the PyeaR promoter. When there is enough nitrate, the NarX will change configuration and then phosphorylate. After that, the phosphorylated NarX will transport the phosphate group to NarL. Last, the phosphorylated NarL will bind to the certain sequence of PyeaR, and it acts as a transcription factor, which can active the downstream of PyeaR to transcription.
In this part, we use the combination is J23109 -B0033. The promoter J23109 is the weak promoter, and B0033 is also a weak RBS.
To learn more about nitrate sensor system, a collection of this kind of nitrate sensor system were constructed.
BBa_K3733015: https://parts.igem.org/Part:BBa_K3733015
BBa_K3733016: https://parts.igem.org/Part:BBa_K3733016
BBa_K3733017: https://parts.igem.org/Part:BBa_K3733017
BBa_K3733018: https://parts.igem.org/Part:BBa_K3733018
BBa_K3733019: https://parts.igem.org/Part:BBa_K3733019
BBa_K3733020: https://parts.igem.org/Part:BBa_K3733020
BBa_K3733021: https://parts.igem.org/Part:BBa_K3733021
BBa_K3733022: https://parts.igem.org/Part:BBa_K3733022
BBa_K3733023: https://parts.igem.org/Part:BBa_K3733023
BBa_K3733028: https://parts.igem.org/Part:BBa_K3733028
BBa_K3733029: https://parts.igem.org/Part:BBa_K3733029
BBa_K3733030: https://parts.igem.org/Part:BBa_K3733030
BBa_K3733031: https://parts.igem.org/Part:BBa_K3733031
Functional Parameters
For the nitrate sensor sensitivity testing, we transformed the constructed plasmid with nitrate sensor into E.coli DH5α and BL21. The E.coli strain was cultured at 37°C overnight, and then diluted to OD600 = 0.4. And then, culture bacteria at 37°C for 2 hours, the potassium nitrate solution that has been serially diluted were add. After 8 hours inducing, we detected the expression of the neGFP by microplate reader.
In this combination, there is lower expression in the inactivated nitrate sensor system in E.coli DH5α than BL21. While, two strains have the same expression at the highest concentration.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 7
Illegal NheI site found at 30 - 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 2017
Illegal BglII site found at 2185 - 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal AgeI site found at 2769
Illegal AgeI site found at 2892 - 1000COMPATIBLE WITH RFC[1000]