Regulatory

Part:BBa_K3747301

Designed by: Riemer van der Vliet   Group: iGEM21_Wageningen_UR   (2021-10-21)


Plux/lac_dE

Plux/lac_dE hybrid promotor

Sequence and Features


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal SpeI site found at 583
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal SpeI site found at 583
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal SpeI site found at 583
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal SpeI site found at 583
  • 1000
    COMPATIBLE WITH RFC[1000]


By combining multiple operator sites in a promoter region, a “hybrid promoter” can be created that responds to multiple input signals. This creates a logic transcriptional AND gate, of which the dynamic range can be further tuned by changing -35 and -10 sites. This E. coli promoter, Plux/lac, was developed by Chen et al. (2018) [1] and contains operator sites for LacI repression and LuxR activation. Transcription is fully activated when LacI is absent and LuxR is present. Different -10 sites “E” and “F” influence the transcription rate when only one of the two input signals is present (Figure 1).


T--Wageningen_UR--wetlab_MKS_HP.png


References

1. Y. Chen, J. M. L. Ho, D. L. Shis, et al., Tuning the dynamic range of bacterial promoters regulated by ligand-inducible transcription factors. Nat. Commun. 9, 1–8 (2018).

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