Difference between revisions of "Part:BBa K4156118"
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Characterization details can be found at: | Characterization details can be found at: | ||
− | pCadC-TP901:<html><a style="padding: 0px; margin: 0px;" href="https://parts.igem.org/Part: | + | |
− | pCadC-TP901-φ174E:<html><a style="padding: 0px; margin: 0px;" href="https://parts.igem.org/Part: | + | pCadC-TP901:<html><a style="padding: 0px; margin: 0px;" href="https://parts.igem.org/Part:BBa_K4156099"> BBa_K4156099 </a></html> |
− | pLldR-TP901:<html><a style="padding: 0px; margin: 0px;" href="https://parts.igem.org/Part: | + | |
− | pLldR-TP901-φ174E:<html><a style="padding: 0px; margin: 0px;" href="https://parts.igem.org/Part: | + | pCadC-TP901-φ174E:<html><a style="padding: 0px; margin: 0px;" href="https://parts.igem.org/Part:BBa_K4156100"> BBa_K4156100 </a></html> |
− | pPepT-TP901:<html><a style="padding: 0px; margin: 0px;" href="https://parts.igem.org/Part: | + | |
− | pPepT-TP901-φ174E:<html><a style="padding: 0px; margin: 0px;" href="https://parts.igem.org/Part: | + | pLldR-TP901:<html><a style="padding: 0px; margin: 0px;" href="https://parts.igem.org/Part:BBa_K4156104"> BBa_K4156104 </a></html> |
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+ | pLldR-TP901-φ174E:<html><a style="padding: 0px; margin: 0px;" href="https://parts.igem.org/Part:BBa_K4156105"> BBa_K4156105 </a></html> | ||
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+ | pPepT-TP901:<html><a style="padding: 0px; margin: 0px;" href="https://parts.igem.org/Part:BBa_K4156108"> BBa_K4156108 </a></html> | ||
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+ | pPepT-TP901-φ174E:<html><a style="padding: 0px; margin: 0px;" href="https://parts.igem.org/Part:BBa_K4156109"> BBa_K4156109 </a></html> | ||
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Latest revision as of 02:04, 12 October 2022
XOR gate-mRFP
XOR gate-mRFP consists of an XOR logic gate ( BBa_K4156117 ) and a downstream RFP sequence to test the performance of the XOR gate by detecting the red fluorescent signal.
Usage and Biology
We introduced a dual vector system in the same strain. The XOR gate-mRFP is located on pSB4C5, while its upstream promoter and corresponding TP901/BxB1 integrase are located on another plasmid, pSB1A3, which are resistant to chloramphenicol and ampicillin, respectively. Through the expression of red fluorescent protein in the dual vector system, we can monitor the change of red fluorescent signal of the recombinant vector to test the performance of XOR gate.
Characterization
We used three different promoter combinations with XOR gate-mRFP to characterize the performance of the promoter and TP901-coupled logic gates, as well as the effect of the addition of lysis genes.
Characterization details can be found at:
pCadC-TP901: BBa_K4156099
pCadC-TP901-φ174E: BBa_K4156100
pLldR-TP901: BBa_K4156104
pLldR-TP901-φ174E: BBa_K4156105
pPepT-TP901: BBa_K4156108
pPepT-TP901-φ174E: BBa_K4156109
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 104
Illegal AgeI site found at 1097
Illegal AgeI site found at 1209 - 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 124
Illegal BsaI.rc site found at 351