Difference between revisions of "Part:BBa J61025"

 
 
(2 intermediate revisions by one other user not shown)
Line 1: Line 1:
 +
ULB-Brussels : as far as we can tell, the DNA present in the registry isn't good. This biobrick as it exists doesn't confer Chloramphenicol resistance. We sent a duplicate of this part to the registry : [https://parts.igem.org/Part:BBa_K551000].
  
 
__NOTOC__
 
__NOTOC__
 
<partinfo>BBa_J61025 short</partinfo>
 
<partinfo>BBa_J61025 short</partinfo>
 +
 +
  
 
Cassette for knockins or knockouts with chloramphenicol selection.  The cassette can be removed by introduction of flp recombinase expressing helper plasmid pCP20 leaving behind a single FRT site scar.
 
Cassette for knockins or knockouts with chloramphenicol selection.  The cassette can be removed by introduction of flp recombinase expressing helper plasmid pCP20 leaving behind a single FRT site scar.
  
 +
pSB1A2-Bca9007
 +
 +
{{JCA_Arkin-TranspositionKnockinTools}}
  
 
<!-- Add more about the biology of this part here
 
<!-- Add more about the biology of this part here

Latest revision as of 14:46, 21 September 2011

ULB-Brussels : as far as we can tell, the DNA present in the registry isn't good. This biobrick as it exists doesn't confer Chloramphenicol resistance. We sent a duplicate of this part to the registry : [1].


[FRT][CmR][FRT]


Cassette for knockins or knockouts with chloramphenicol selection. The cassette can be removed by introduction of flp recombinase expressing helper plasmid pCP20 leaving behind a single FRT site scar.

pSB1A2-Bca9007

This part belongs to a family useful for the construction of transposons and knockin cassettes.

FRT The FRT sequence is the recombination substrate for Flp recombinase. Like the Cre/Lox system, sequences flanked by FRT sites oriented in the same direction get excised by expression of Flp. Cassettes flanked by FRT allow the introduction of selectable markers into the genome followed by subsequent removal by the recombinase.

Tn5 The two Tn5 elements are the substrates for the Tnp transposase in both orientations. Sequences flanked by the two Tn5 elements (in opposing orientation) are mobilizable elements. In the presence of Tnp, they are excised from their plasmid and introduced randomly into the genome or plasmids present in the cell.

Tnp The gene for a high-activity mutant of Tn5 transposase.

OriTr Special strains of E. coli with remnants of the RP4 plasmid, including Rlambda (part ) and BW20767, can transfer plasmids with oriTr (part J01003) to diverse species of bacteria.

OriTf Special strains of E. coli with remanants of the F plasmid, such as J23055, can transfer plasmids with oriTf (part J01002) to other E. coli.

R6K A conditional origin of transfer requiring the pir gene expressed in trans.

Construction of Transposon Plasmids
Transposition mutagenesis is usually carried out by mating a donor strain containing a transposon on a plasmid into a recipient strain. The plasmid with the transposon and transposase transfers to the recipient strain, the transposon is excised from the plasmid, and inserts randomly into the genome. A selectable marker in the transposon and in the recipient strain allows selection of cells receiving the transposon over both the donor and recipient strain.

Construction of the transposon donor strain requires a conjugative donor strain harboring a plasmid with the following elements:

  • A conjugative origin of transfer
  • A conditional origin of replication, usually R6K, so that the plasmids cannot replicate within the recipient strain (so no second origin of replication)
  • A transposon containing a selectable marker flanked by Tn5 ends
  • The transposase gene

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]