Difference between revisions of "Part:BBa K1413043"

(Usage and Biology)
(Usage and Biology)
 
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===Usage and Biology===
 
===Usage and Biology===
This part is extract to plasmid pNK2 (see BBa_K1413044). This part is used to insert the transposon in genome of some bacteria like BL21 and Pseudovibrio denitrificans.
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This part was extracted from pNK2 plasmid (see BBa_K1413044). This part was used to insert the transposon in the genome of bacteria like E. coli and Pseudovibrio denitrificans.
  
  
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Picture of an electrophorese gel samples come from the PCR which amplify the kanamycineR cassette. All clones have the insertion of the transposon. The Control, Pseudovibrio denitrificans, do not the insertion as expected.
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Picture of an electrophoresis gel of the PCR which amplifies the kanamycine resistance cassette. The template of this PCR was Pseudovibrion denetrificans genome after electroporation of the transposon plasmid pNK2, control was P. denetrificans without electroporation. As expected, all clones have the insertion of the transposon, except the control.  
  
  

Latest revision as of 18:18, 2 November 2014

Transposase Tn10

This part is the coding sequence for the transposase Tn10. A cut-and-paste mechanism where the transposase allows insertion of a transposon randomly in the genome. The transposon must be surrounded by IS10 sequences.


Usage and Biology

This part was extracted from pNK2 plasmid (see BBa_K1413044). This part was used to insert the transposon in the genome of bacteria like E. coli and Pseudovibrio denitrificans.


Picture of an electrophoresis gel of the PCR which amplifies the kanamycine resistance cassette. The template of this PCR was Pseudovibrion denetrificans genome after electroporation of the transposon plasmid pNK2, control was P. denetrificans without electroporation. As expected, all clones have the insertion of the transposon, except the control.



Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 244
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]


References

-Bender, J., & Kleckner, N. (1988). Genetic Evidence That TnlO Transposes by a Nonreplicative Mechanism, 45, 801–815
-Crellin, P., & Chalmers, R. (2001). Protein±DNA contacts and conformational changes in the Tn 10 transpososome during assembly and activation for cleavage, 20(14).