Coding

Part:BBa_K3381003:Design

Designed by: Alina Arvisais   Group: iGEM20_Waterloo   (2020-10-20)
Revision as of 23:42, 20 October 2020 by Registry (Talk | contribs)

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FutA1-CBM2a (fusion)


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 496
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BglII site found at 46
    Illegal BamHI site found at 1493
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]


Design Notes

The His-tag and TEV linker sequences were codon optimized for *E. coli*, removing all cut sites for RFc 10 and NdeI/BamHI (required for cloning into pET 11a). Then a 5-poly-AT + NdeI prefix and a BamHI + 5-poly-AT suffix was added to facilitate cloning into the pET 11a vector by standard assembly. Lastly, the prefix and suffix for RFc 10 were appended.



Source

Sources of DNA sequences, in order of occurrence in the fusion protein from N' to C': His-tag and TEV linker sequence: Retrieved from His-tag and TEV linker that occurs in bacterial expression vector pMCSG7: https://plasmid.med.harvard.edu/PlasmidRepository/file/sequence/pMCSG7.gb Sequence of FUTA1 (iron-binding domain) retrieved from Genbank (Synechocystis species PCC 6803): https://www.ncbi.nlm.nih.gov/nuccore/BA000022.2?from=291626&to=292708 Sequence of the CBM linker domain was back-translated from its amino acid sequence, which was retrieved from the following paper describing a natural occurrence of the linker in a protein with a cellulose-binding domain: https://www.jbc.org/content/293/34/13006.full Sequence of CBM2a (cellulose-binding domain) retrieved from DNA sequence of BBa_K863101 (Cellulose-binding domain of Cellulomonas fimi exoglucanase): https://parts.igem.org/Part:BBa_K863101


References