Difference between revisions of "Part:BBa K2607002:Design"

 
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===Design Notes===
 
===Design Notes===
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To be added
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This part is assembled as improvement of B0034-Blue Florescent Protein (BFP) (BBa_K592024). Our established part consists of these following features:
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<ul>
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<li>lacI regulated promoter (BBa_R0010) in the upstream</li>
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<li>Double terminator (BBa_B0010 and BBa_B0012) in the downstream</li>
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<li>SalI restriction site between the promoter and ribosome binding site</li>
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<li>NdeI restriction site between the ribosome binding site and coding sequence</li>
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<li>Modified blue fluorescence protein coding sequence to eliminate SalI restriction site in the middle without altering amino acid sequence</li></ul>
  
 
===Source===
 
===Source===
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We constructed this part with help of references from several previous parts (e.g. BBa_R0010, BBa_B0010, BBa_B0012, BBa_K592100, and BBa_K592024). As for the protein itself, it is derived from modification of <i>Aequoria victoria</i>'s green fluorescent protein (GFP).
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To be added
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===References===
 
===References===
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[http://www.ncbi.nlm.nih.gov/pubmed/18940671] Subach OM, Gundorov IS, et al. (2008). Conversion of red fluorescent protein into a bright blue probe. Chem Biol 15(10): 1116-24.

Latest revision as of 17:34, 14 October 2018


Improved Blue Fluorescent Protein (BFP)


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

This part is assembled as improvement of B0034-Blue Florescent Protein (BFP) (BBa_K592024). Our established part consists of these following features:

  • lacI regulated promoter (BBa_R0010) in the upstream
  • Double terminator (BBa_B0010 and BBa_B0012) in the downstream
  • SalI restriction site between the promoter and ribosome binding site
  • NdeI restriction site between the ribosome binding site and coding sequence
  • Modified blue fluorescence protein coding sequence to eliminate SalI restriction site in the middle without altering amino acid sequence

Source

We constructed this part with help of references from several previous parts (e.g. BBa_R0010, BBa_B0010, BBa_B0012, BBa_K592100, and BBa_K592024). As for the protein itself, it is derived from modification of Aequoria victoria's green fluorescent protein (GFP).

References

[http://www.ncbi.nlm.nih.gov/pubmed/18940671] Subach OM, Gundorov IS, et al. (2008). Conversion of red fluorescent protein into a bright blue probe. Chem Biol 15(10): 1116-24.