Composite

Part:BBa_K1973032

Designed by: José Martín Gómez   Group: iGEM16_UPO-Sevilla   (2016-10-14)


miniTn7BBGm-nahR-Psal-nasF-epi

nahR (Pseudomonas putida, see BBa_K1031610) is expressed under the constitutive Pr promoter. It encodes a regulatory protein that activates the Psal promoter (see BBa_J61051) in the presence of salicylate. epi (BBa_K1973030) is expressed from the Psal promoter in the presence of this molecule. nasF (see BBa_K1973001) is an attenuator of transcription elongation (terminator) from Klebsiella pneumoniae that decreases the basal expression from the Psal promoter. The miniTn7 tool allows the stable integration of this module in the chromosome of a wide range of bacteria (see https://parts.igem.org/Genome_Integration).

Sequence and Features


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal prefix found in sequence at 4367
    Illegal suffix found in sequence at 1
    Illegal SpeI site found at 6052
    Illegal PstI site found at 6066
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal EcoRI site found at 4367
    Illegal SpeI site found at 2
    Illegal SpeI site found at 6052
    Illegal PstI site found at 16
    Illegal PstI site found at 6066
    Illegal NotI site found at 9
    Illegal NotI site found at 4373
    Illegal NotI site found at 6059
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal EcoRI site found at 4367
    Illegal BglII site found at 3051
    Illegal BglII site found at 3322
    Illegal BglII site found at 3608
    Illegal BglII site found at 4972
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal prefix found in sequence at 4367
    Illegal suffix found in sequence at 2
    Illegal SpeI site found at 6052
    Illegal PstI site found at 6066
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal prefix found in sequence at 4367
    Illegal XbaI site found at 4382
    Illegal SpeI site found at 2
    Illegal SpeI site found at 6052
    Illegal PstI site found at 16
    Illegal PstI site found at 6066
    Illegal NgoMIV site found at 4804
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI site found at 1681
    Illegal SapI.rc site found at 2763


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