Difference between revisions of "Part:BBa K1031521"
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− | <p>For detailed information concerning HpaR and | + | <p>For detailed information concerning HpaR and Pg promoter, please visit <a href="http://2013.igem.org/Team:Peking/Project/BioSensors/HpaR">2013 Peking iGEM Biosensor HpaR</a></p> |
<img src="https://static.igem.org/mediawiki/igem.org/c/c9/Peking_Logo.jpg" style="width:960px;"/> | <img src="https://static.igem.org/mediawiki/igem.org/c/c9/Peking_Logo.jpg" style="width:960px;"/> | ||
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− | <img src="https://static.igem.org/mediawiki/igem.org/9/93/Peking2013_HpaRFig5.jpg" | + | <img src="https://static.igem.org/mediawiki/igem.org/9/93/Peking2013_HpaRFig5.jpg" style="width:700px; margin-left:120px" /> |
+ | <p style="text-align:center"><b>Fig 1</b> Structure of the intergenic region between hpaR and hpaG (Galán, B. et al, 2003). The elements of the promoters are enclosed by square. Especially, two OPRs responsible for HpaR binding are marked. The transcription direction of hpaR and hpaG are indicated with arrows. The IHF and CRP sites are marked respectively. | ||
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− | ''Pc'' promoter J23106 is selected to initiate the transcription of hpaR. Based on this circuit, we constructed a library of RBS (Ribosome Binding Site) for tunning for expression level of reporter gene sfGFP ('''Fig 2'''). K1031521 is composed of three elements, Pg promoter regulated by HpaR, RBS | + | ''Pc'' promoter J23106 is selected to initiate the transcription of hpaR. Based on this circuit, we constructed a library of RBS (Ribosome Binding Site) for tunning for expression level of reporter gene sfGFP ('''Fig 2'''). K1031521 is composed of three elements, Pg promoter regulated by HpaR, RBS <html><a href="https://parts.igem.org/Part:BBa_B0032">B0032</a></html> and reporter gene sfGFP. However, we haven`t got the obvious induction ratio. It is hypothesized that several overall-controlling sites are located in the promoter. Bacteria will control strictly the expression of the relative genes in rich condition. |
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− | <img src="https://static.igem.org/mediawiki/igem.org/b/bc/Peking2013_part_32-Pg_HpaR.png" | + | <img src="https://static.igem.org/mediawiki/igem.org/b/bc/Peking2013_part_32-Pg_HpaR.png" style="width:400px; margin-left:250px" /> |
+ | <p style="text-align:center"><b>Fig 2</b> Construction of reporter circuit. The orange arrow represents <i>Pg</i> promoter. The green oval stands for RBS B0032. sfGFP coding sequence is shown with dark blue, while terminator B0015 is in dark red. | ||
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Latest revision as of 04:23, 28 September 2013
Pg-B0032-sfGFP-Terminator (HpaR)
For detailed information concerning HpaR and Pg promoter, please visit 2013 Peking iGEM Biosensor HpaR
Structure
The structure of Pr and Pg promoters are complex, for they are adjacent and many transcription factors besides HpaR including IHF and CRP participate. Pr and Pg are in the opposite direction. The two binding sites for HpaR, OPR1 and OPR2, perform obvious synergistic effect, making the two operons, hpaR and hpaGEDFHI coordinate with each other on transcription level (Fig 1)
Fig 1 Structure of the intergenic region between hpaR and hpaG (Galán, B. et al, 2003). The elements of the promoters are enclosed by square. Especially, two OPRs responsible for HpaR binding are marked. The transcription direction of hpaR and hpaG are indicated with arrows. The IHF and CRP sites are marked respectively.
Sequence and Features
Sequence and Features
- 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 SapI.rc site found at 265
Construction and tunning
Pc promoter J23106 is selected to initiate the transcription of hpaR. Based on this circuit, we constructed a library of RBS (Ribosome Binding Site) for tunning for expression level of reporter gene sfGFP (Fig 2). K1031521 is composed of three elements, Pg promoter regulated by HpaR, RBS B0032 and reporter gene sfGFP. However, we haven`t got the obvious induction ratio. It is hypothesized that several overall-controlling sites are located in the promoter. Bacteria will control strictly the expression of the relative genes in rich condition.
Fig 2 Construction of reporter circuit. The orange arrow represents Pg promoter. The green oval stands for RBS B0032. sfGFP coding sequence is shown with dark blue, while terminator B0015 is in dark red.