Part:BBa_K4115046:Design
NS3-2-KanR-J23101-B0034-LuxR-B0015-Lux pR-B0034-sfGFP-B0015-NS3-1
- 10INCOMPATIBLE WITH RFC[10]Illegal PstI site found at 507
Illegal PstI site found at 4261 - 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 1167
Illegal NheI site found at 1190
Illegal PstI site found at 507
Illegal PstI site found at 4261 - 21COMPATIBLE WITH RFC[21]
- 23INCOMPATIBLE WITH RFC[23]Illegal PstI site found at 507
Illegal PstI site found at 4261 - 25INCOMPATIBLE WITH RFC[25]Illegal PstI site found at 507
Illegal PstI site found at 4261 - 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 2145
Design Notes
We use sfGFP as a reporter gene to detect whether LuxR is functional when responding to the AHL signal in HL7942. It is the first step in our demonstration that Escherichia coli and Synechococcus can communicate through quorum sensing signals.
Source
The sequence of LuxR is achieved from the article 'Tools for engineering coordinated system behaviour in synthetic microbial consortia'[1]. The sequence of sfGFP(BBa_K4115000) is designed by our team. Most components in the composite part are synthesized by the company and then we integrate them into the backbone of PUC57.
References
[1] Kylilis, N., Tuza, Z.A., Stan, GB. et al. Tools for engineering coordinated system behaviour in synthetic microbial consortia. Nat Commun 9, 2677 (2018). https://doi.org/10.1038/s41467-018-05046-2