Difference between revisions of "Part:BBa K831017"
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Fluorescence reporter that responds to the presence of 3OH-PAME (Quorum Sensing signal). | Fluorescence reporter that responds to the presence of 3OH-PAME (Quorum Sensing signal). | ||
| − | <!-- Add more about the biology of this part here | + | <!-- Add more about the biology of this part here--> |
PxpsR is the promoter region of xpsR (PxpsR) wich integrates different signals including phcA. Therefore, expression of genes regulated by XpsR may be correlated with threshold concentrations of 3 OH-PAME an exclusive quorum sensing signal of R. solanacearum. This biobrick comprises the upstream region of xpsR gene including the two binding boxes of phcA, the -35 and -10 conserved boxes and excluding the native RBS. | PxpsR is the promoter region of xpsR (PxpsR) wich integrates different signals including phcA. Therefore, expression of genes regulated by XpsR may be correlated with threshold concentrations of 3 OH-PAME an exclusive quorum sensing signal of R. solanacearum. This biobrick comprises the upstream region of xpsR gene including the two binding boxes of phcA, the -35 and -10 conserved boxes and excluding the native RBS. | ||
Revision as of 14:57, 1 October 2012
PxpsR-EYFP
Fluorescence reporter that responds to the presence of 3OH-PAME (Quorum Sensing signal).
PxpsR is the promoter region of xpsR (PxpsR) wich integrates different signals including phcA. Therefore, expression of genes regulated by XpsR may be correlated with threshold concentrations of 3 OH-PAME an exclusive quorum sensing signal of R. solanacearum. This biobrick comprises the upstream region of xpsR gene including the two binding boxes of phcA, the -35 and -10 conserved boxes and excluding the native RBS.
Usage and Biology
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 65
Illegal NgoMIV site found at 312 - 1000COMPATIBLE WITH RFC[1000]
Functional Characterization
To assess the fuctionality of our part Escherichia coli K12 DH5a were transformed with part BBa_K831017
Bacterial strains were photographed while using Differential Interference Contrast (DIC) microscopy and Fluorescence microscopy using FITC filter. Bacteria transformed with PxpsR-eYFP construct show basal levels of expression of the reporter while none of the bacteria transformed with the promotorless EYFP show fluorescence. High background levels in the promotorless EYFP are due to the autoflorescence of the LB medium and the high exposition time.
