Composite

Part:BBa_K101006

Designed by: Ellen Martin   Group: iGEM08_Minnesota   (2008-07-28)

Construct with TetR/p22mnt promoter, RBS, RFP, Terminator

The promoter contains binding sites for both TetR and p22mnt. RBS is the ribosomal binding site. RFP is the red fluorescent protein, which is a reporter gene. The terminator will terminate transcription.

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BglII site found at 42
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]


The device has a dual promoter which is repressed by tetR and p22mnt. The input is aTc and output is fluorescence as gene for mRFP (BBa_J61002) is cloned downstream to the dually repressed promoter.

Input: aTc

Output: Red Fluorescence

Experiment

Characteristic

Value

Promoter Activity in TOP 10 cells

Maximum Fluorescence

277006.0 (Normalized fluorescence at OD600 ~1.0) 3 hours after the growth.

Growth of culture in LB media

Doubling time of the recombinant cells

~ 25 Minutes

Response time (after addition of IPTG)

~20 Minutes

Compatibility
Chassis: Device has been shown to work in BBa_J61002, BBa_B0034, and BBa_B0015

Plasmids: Device has been shown to work in pSB3K3

[edit]
Categories
Parameters
None