Composite

Part:BBa_K5109001

Designed by: Lisa Faccincani   Group: iGEM24_Uni-Padua-IT   (2024-09-22)
Revision as of 14:40, 27 September 2024 by Lisafaccincani (Talk | contribs)


Dehalogenase type II intracellular expression tool

This part is a tool created for the inducible expression of enzymes of interest, in this case the enzyme is Dehalogenase type II. The part is structured with the biobrick prefix and suffix at the ends, allowing cloning via RFC 10. The chosen promoter is pTac (BBa K864400), an inducible promoter consisting of the sequence of pTac and LacO: the sequence includes the Lac Operon, repressing the expression in presence of LacI protein, and allowing it in presence of IPTG inducer. This part is to be used in bacterial strains already containing a gene cassette for constitutive LacI expression, or in alternative, to be cloned inside strains via co-trasformation with a plasmid carrying the LacI expression cassette. This way expression of the enzyme is blocked until IPTG is added. If the trascription is not blocked, constitutive expression of the enzyme of interest has shown to interfere with the growth of cells, preventing the formation of colonies. RBS.1 (BBa_B0030) is a strong RBS, based on Ron Weiss thesis. It presents a high non-modularity with promoters and protein coding parts. Dehalogenase type II (BBa_K5109009) is a coding sequence of a Dehalogenase enzyme to which we added bases at the ends, to insert the sequence of some desired restriction sites. We obtained the sequence from the previous work of USAFA 2020 team: thanks to their work, the sequence which comes originally from Delftia acidovorans, has been codon optimized for the expression in Escherichia coli.


Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BamHI site found at 772
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI site found at 778
    Illegal BsaI.rc site found at 804


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Categories
Parameters
None