Difference between revisions of "Part:BBa K1980000:Design"
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===Design Notes===
 
===Design Notes===
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The part is codon optimised for E. coli. A native <i>E. coli</i> TAT sequence has been added in place of the original host TAT sequence in an attempt to make the protein go to the periplasm. The E. coli TAT sequence from CueO in particular was chosen only because it is quite short and CueO is also involved in copper homeostasis.  There is a hexahistidine purification tag on C-terminus in order to purify the protein whilst preserving the N-terminal TAT sequence.
+
The part is codon optimised for E. coli. A native <i>E. coli</i> TAT sequence has been added in place of the original host TAT sequence in an attempt to make the protein go to the periplasm. The <i>E. coli</i> TAT sequence from CueO in particular was chosen only because it is quite short and CueO is also involved in copper homeostasis.  There is a hexahistidine purification tag on C-terminus in order to purify the protein whilst preserving the N-terminal TAT sequence.
  
  
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===Source===
 
===Source===
  
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The source organism for the main protein sequence is Methylosinus trichosporium OB3b. The TAT sequence originate from E. coli multi copper oxidase enzyme CueO. We ordered it as codon optimised DNA from IDT.
+
The source organism for the main protein sequence is <i>Methylosinus trichosporium OB3b</i>. The TAT sequence originate from <i>E. coli</i> multi-copper oxidase enzyme CueO. We ordered it as codon optimised DNA from IDT.
  
 
===References===
 
===References===

Revision as of 20:21, 12 October 2016


TAT Copper Storage Protein 1


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]


Design Notes

The part is codon optimised for E. coli. A native E. coli TAT sequence has been added in place of the original host TAT sequence in an attempt to make the protein go to the periplasm. The E. coli TAT sequence from CueO in particular was chosen only because it is quite short and CueO is also involved in copper homeostasis. There is a hexahistidine purification tag on C-terminus in order to purify the protein whilst preserving the N-terminal TAT sequence.


Source

The source organism for the main protein sequence is Methylosinus trichosporium OB3b. The TAT sequence originate from E. coli multi-copper oxidase enzyme CueO. We ordered it as codon optimised DNA from IDT.

References