Device

Part:BBa_K2629000:Design

Designed by: Elise Aubert   Group: iGEM18_Grenoble-Alpes   (2018-09-07)
Revision as of 08:14, 7 September 2018 by Registry (Talk | contribs)

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Pseudomonas aeruginosa detector part - it activation allows the detection of 36bp of Pseudomonas aer


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal NgoMIV site found at 39
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal SapI site found at 1


Design Notes

The probe is designed in order to detect a fragment less than 100 bp. The aim is to create a single strand window that enable the perfect hybridization of our choosen target. It is made by: → Two restrictions enzymes producing cohesives end, SphI and NgoMIV, which goal is to remove the little sequence in between on the bottom strand and thus create a perfect complementarity with the target. But at the end we trust that using PCR linearization could reduce the background of uncut plasmid. → Twi nicking enzymes, Nt.BspQ1 and Nb.BssS1, enzymes that cut one strand of the double DNA strand.



Source

The aim is to detect a small fragment of Pseudomonas aeruginosa DNA. The target was found in ProC gene (822bp) from PAO1 strain (GenBank : AAG03782.1) located in PA0393 locus. The target is located between nucleotide 766 and nucleotide 802. ProC is an housekeeping gene found in all Pseudomonas aeruginosa strains and not linked in pathogenic behavior of Pseudomonas aeruginosa.


References