Generator

Part:BBa_K1783000:Design

Designed by: Iowis Zhu   Group: iGEM15_UMaryland   (2015-06-03)
Revision as of 20:32, 12 August 2015 by HHeLiBeBCNOFNe (Talk | contribs) (→‎Design Notes)


Miraculin Generator


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 125
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BamHI site found at 65
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]


Design Notes

Parts were assembled using 3A assembly of K206000 (pBAD promoter) and K1033120 (RBS-Miraculin), following the iGEM protocol. Since both parts were in the pSB1C3 backbone, we initially assembled the final construct in the pSB1A3 backbone, then moved the composite part into the pSB1C3 backbone using RE cloning.

Restriction Enzyme cloning: Double digest of pSB1C3 backbone + K1783000 of EcoRI-HF and PstI-HF (1 unit each) for 1 hr. Ligation with T4 DNA Ligase overnight

DH5α was used as the cell strain for transformations.

Source

All parts are from previous BioBricks. pBAD promoter is from E. coli, while Miraculin gene comes from S. dulcificum.

References