Difference between revisions of "Part:BBa K4119003"
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− | + | In this part of our project, the key promoter vgb was a microaerobic induced promoter of Vitreoscilla hemoglobin gene. Considering the gene compatibility difference between different host bacteria, we designed the pMTL-Pvgb-bs2 plasmid to determine whether the promoter vgb could work normally in Clostridium tyrobutyricum by detecting the fluorescent expression intensity of fluorescent protein Bs2. | |
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Revision as of 14:09, 12 October 2022
Pvgb-Bs2-Cpa fdx terminator
In this part of our project, the key promoter vgb was a microaerobic induced promoter of Vitreoscilla hemoglobin gene. Considering the gene compatibility difference between different host bacteria, we designed the pMTL-Pvgb-bs2 plasmid to determine whether the promoter vgb could work normally in Clostridium tyrobutyricum by detecting the fluorescent expression intensity of fluorescent protein Bs2.
Results:
The test group: the fluorescence intensity is relatively high
The control group: the fluorescence intensity is lower compared to the test group
Sequence and Features
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal PstI site found at 350
- 12INCOMPATIBLE WITH RFC[12]Illegal PstI site found at 350
- 21COMPATIBLE WITH RFC[21]
- 23INCOMPATIBLE WITH RFC[23]Illegal PstI site found at 350
- 25INCOMPATIBLE WITH RFC[25]Illegal PstI site found at 350
- 1000COMPATIBLE WITH RFC[1000]