Difference between revisions of "Part:BBa K1413024"
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===Usage and Biology=== | ===Usage and Biology=== | ||
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<span class='h3bb'>Sequence and Features</span> | <span class='h3bb'>Sequence and Features</span> | ||
<partinfo>BBa_K1413024 SequenceAndFeatures</partinfo> | <partinfo>BBa_K1413024 SequenceAndFeatures</partinfo> |
Revision as of 22:13, 1 November 2014
bphR1-RBS-RFP-Terminator
This part is composed by bphR1 promoter (BBa_K1155001), from Pseudomonas pseudoalcaligenes KF707, which allows the transcription of the genes of biphenyl degradation, the RBS (BBa_B0034), RFP gene (BBa_E1010) and terminator (BBa_B0015). In our project, genes of degradation was replaced by RFP gene to detect the compound.
Mechanism explanation: In absence of PCBs, bphR2 (BBa_K1413021) is bound to bphR1 promoter which activate the transcription of RFP but in very low expression. In presence of PCBs, when compound diffuses into the media, it binds to bphr2 protein which undergoes a conformational change that permits to activate more stronger bphR1 promoter and increase the transcription of RFP.
Usage and Biology
Combinated with the part BBa_K1413023, it could be used like PCB biosensor.
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 156
Illegal BamHI site found at 239
Illegal XhoI site found at 46 - 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal AgeI site found at 883
Illegal AgeI site found at 995 - 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI.rc site found at 139