Regulatory

Part:BBa_J100303

Designed by: Emilie Uffman   Group: Campbell M Lab   (2016-09-08)


PmanP

The PmanP promoter, when induced by mannose, increases the beta-galactosidase activity of bacteria, which thus increases the expression of lacZ by four to seven-fold. In this experiment, we are using a 0.2% concentration of mannose in order to test the induction of transcription.


Induction of pMAN promoter in V. natriegens

(Characterized by iGEM Groningen-2019)

The mannose inducible promoter is part of the pJOE8889 plasmid and controls the expression of the Cas9 enzyme. Since we designed all CRISPR components to work with this plasmid we also had to make sure that Cas9 would be expressed upon addition of mannose. There are no reports in the literature on the use of this promoter so we characterized it with the reporter mCherry. Moreover, V. natriegens cannot utilize mannose as a carbon source. Addition of 1 (w/v) % led to a 2.5 fold increase of expression within 12 hours.

BBa J100303.png

Figure 1: pMAN is used in the pJOE8889 to control the expression of Cas9. In order to characterize this promoter we built it with mCherry and quantified the induction with mannose in V. natriegens.

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]


[edit]
Categories
Parameters
None