Difference between revisions of "Part:BBa K3408009"
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We used constitutive promoter P<sub>liaG</sub> to transcribe trigger RNA all the time. And we also used P<sub>CⅠ</sub> as a constitutive promoter to transcribe switch RNA. If our Toehold switch could work normally, GFP could be translated and we could see green bacteria in our culture medium. | We used constitutive promoter P<sub>liaG</sub> to transcribe trigger RNA all the time. And we also used P<sub>CⅠ</sub> as a constitutive promoter to transcribe switch RNA. If our Toehold switch could work normally, GFP could be translated and we could see green bacteria in our culture medium. | ||
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The pWB980-DB is digested with enzyme EcoRI and PstI. The target fragment of the promoter, RBS, gene of phytase and terminator of this device are synthesized by the biotechnology company with 6×His tags added. Add EcoRI and PstI restriction sites to both ends of the target fragment respectively. Connect the target fragment to the plasmid vector fragment to construct the expression vector PliaG- trigger RNA-PCⅠ-switch RNA-GFP. | The pWB980-DB is digested with enzyme EcoRI and PstI. The target fragment of the promoter, RBS, gene of phytase and terminator of this device are synthesized by the biotechnology company with 6×His tags added. Add EcoRI and PstI restriction sites to both ends of the target fragment respectively. Connect the target fragment to the plasmid vector fragment to construct the expression vector PliaG- trigger RNA-PCⅠ-switch RNA-GFP. | ||
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Revision as of 17:02, 18 October 2020
PliaG-trigger RNA-B0015-PCⅠ-switch RNA-GFP-B0015
We used constitutive promoter PliaG to transcribe trigger RNA all the time. And we also used PCⅠ as a constitutive promoter to transcribe switch RNA. If our Toehold switch could work normally, GFP could be translated and we could see green bacteria in our culture medium.
1. Experimental methods
1.1 Construction of the expression vector
The pWB980-DB is digested with enzyme EcoRI and PstI. The target fragment of the promoter, RBS, gene of phytase and terminator of this device are synthesized by the biotechnology company with 6×His tags added. Add EcoRI and PstI restriction sites to both ends of the target fragment respectively. Connect the target fragment to the plasmid vector fragment to construct the expression vector PliaG- trigger RNA-PCⅠ-switch RNA-GFP.
Plasmid profile
Fig.1. The expression vector of device PliaG- trigger RNA-PCⅠ-switch RNA-GFP
1.2. Construction and screening of recombinant engineered bacteria
Using B. subtilis WB800N as the expression host, the secretion expression vector pWB980-DB was transformed by electro-transformation. Inoculate them on LB solid medium coated with 10μg/mL kanamycin, and incubate them overnight at 37°C. Send transformants to biotechnology company for sequencing.
1.3 Characterization experiment
Take 2 bottles of 50ml LB liquid medium with 10μg/mL kanamycin. 10μg/mL kanamycin is added to the one used for the test group while the other used for the control group is not. Test group in which engineered bacteria is successfully transformed, and control group in which pWB980-DB is transformed, are inoculated by the same amount bacteria. After culturing them for a period of time, use the fluorescence microscope to observe the presence of fluorescence in the test group and the control group.
2. Expected results
Fluorescence can be observed in the test group but not in the negative control group.
The negative control group The test group
Fig.2. Expected results: different expressions of fluorescence between the control group and the test group.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 239
Illegal BglII site found at 461 - 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 1190