Device

Part:BBa_K2207997:Design

Designed by: Junming Qian   Group: iGEM17_ZJU-China   (2017-10-23)


2,4-DAPG PhlABCD Cluster with T7 promoter and Double Terminator


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal XhoI site found at 672
    Illegal XhoI site found at 1538
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal NgoMIV site found at 85
    Illegal NgoMIV site found at 372
    Illegal AgeI site found at 1847
    Illegal AgeI site found at 1875
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI.rc site found at 3725


Design Notes

We used T7 promoter to improve the enzymes level in cell to synthesis DAPG heterologously.


Source

The coding sequence was pcr from Pseudomonas fluorescens 2P24, promoter and terminator were got from igem stock.

References