Plasmid_Backbone

Part:BBa_M11421:Design

Designed by: Amanda Romero   Group: UtahState BE5930 - S09 UtahState BE5930 - S10   (2010-04-26)


Streptomyces Shuttle Vetor Thiostrepton Resistance


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Plasmid lacks a prefix.
    Plasmid lacks a suffix.
    Illegal EcoRI site found at 11868
    Illegal SpeI site found at 2
    Illegal PstI site found at 16
    Illegal NotI site found at 9
    Illegal NotI site found at 2075
    Illegal NotI site found at 2201
    Illegal NotI site found at 2294
    Illegal NotI site found at 3386
    Illegal NotI site found at 3415
    Illegal NotI site found at 4123
  • 21
    INCOMPATIBLE WITH RFC[21]
    Plasmid lacks a prefix.
    Plasmid lacks a suffix.
    Illegal EcoRI site found at 11868
    Illegal XhoI site found at 1559
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal prefix found at 11868
    Illegal suffix found at 2
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal prefix found at 11868
    Plasmid lacks a suffix.
    Illegal XbaI site found at 11883
    Illegal SpeI site found at 2
    Illegal PstI site found at 16
    Illegal NgoMIV site found at 719
    Illegal NgoMIV site found at 1513
    Illegal NgoMIV site found at 2851
    Illegal NgoMIV site found at 3630
    Illegal NgoMIV site found at 4000
    Illegal NgoMIV site found at 5732
    Illegal NgoMIV site found at 5789
    Illegal AgeI site found at 603
    Illegal AgeI site found at 1794
    Illegal AgeI site found at 6577
    Illegal AgeI site found at 7386
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Plasmid lacks a prefix.
    Plasmid lacks a suffix.
    Illegal BsaI site found at 4594
    Illegal BsaI site found at 5422
    Illegal BsaI.rc site found at 1503
    Illegal BsaI.rc site found at 5082
    Illegal BsaI.rc site found at 6380
    Illegal BsaI.rc site found at 10933
    Illegal SapI.rc site found at 241


Design Notes

This is a shuttle vector for Streptomyces.


Source

This originated from the plasmid pRM5. Site-directed mutagenesis was used to remove specific restriction sites to make it biobrick compatible.

References