RBS

Part:BBa_K2680561

Designed by: Julia Urban   Group: iGEM18_William_and_Mary   (2018-10-17)


BCD8

BCD8

Our team characterized the BCD8 RBS in the genetic context of the luxI gene.

Measurment

We characterized this RBS in the genetic context of luxI. We built a fusion of the first 36 nucleotides of the LuxI synthase with sfGFP to characterize the relative strength of our deployed RBS in the context of the LuxI coding sequence. To quantify this output we measured the fluorescence using microplate reader FlexStation3 (Molecular Devices) with excitation wavelength 485nm and emission wavelength 510nm. We conducted measurements in different time points after the induction with aTc, using different concentrations of the inducer.

BCD8 luxI sfGFP iGEM Ath 22.png

'Figure 1: Characterization of BCD8 RBS in the genetic context of luxI'

Comparison of BCDs Ath22.png

'Figure 2: Characterization of BCDs our team tested in the genetic context of luxI'


Athens2022-RBS-COMPARISON.png

'Figure 3: Characterization of all the RBS our team tested in the genetic context of luxI'


Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]


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