Difference between revisions of "Part:BBa K4121052:Design"
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Enter the source of this part：
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We get sequences of the promoter from Eukaryotic promoter database(EPD), the sequences of CDS and the terminator from National Center for Biotechnology Information(NCBI).
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__NOTOC__
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Enter any design considerations：We used the "Goldengate" method for the ligation of the basic parts, We introduced recognition sites and cleavage sites for the type IIs restriction endonuclease BsmBI at both ends of the Basic Parts to ensure that the Basic Parts could be ligated successfully, and changed the location of the recognition sites and cleavage sites so that the BsmBI would not cut repeatedly.
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<partinfo>BBa_K4121052 short</partinfo>
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<partinfo>BBa_K4121052 SequenceAndFeatures</partinfo>
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===Design Notes===
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We used the "Goldengate" method for the ligation of the basic parts, We introduced recognition sites and cleavage sites for the type IIs restriction endonuclease BsmBI at both ends of the Basic Parts to ensure that the Basic Parts could be ligated successfully, and changed the location of the recognition sites and cleavage sites so that the BsmBI would not cut repeatedly.
 
To avoid homologous recombination in Saccharomyces cerevisiae, we substitute different promoters and terminators.
 
To avoid homologous recombination in Saccharomyces cerevisiae, we substitute different promoters and terminators.
 
Please refer to" Design" part of the Wiki for detailed experimental design.
 
Please refer to" Design" part of the Wiki for detailed experimental design.
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===Source===
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We get sequences of the promoter from Eukaryotic promoter database(EPD), the sequences of CDS and the terminator from National Center for Biotechnology Information(NCBI).
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===References===

Revision as of 09:36, 12 October 2022


Expression cassette of TmCrtE with constitutive promoter


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal XbaI site found at 728
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BglII site found at 590
    Illegal BglII site found at 731
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal XbaI site found at 728
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal XbaI site found at 728
  • 1000
    COMPATIBLE WITH RFC[1000]


Design Notes

We used the "Goldengate" method for the ligation of the basic parts, We introduced recognition sites and cleavage sites for the type IIs restriction endonuclease BsmBI at both ends of the Basic Parts to ensure that the Basic Parts could be ligated successfully, and changed the location of the recognition sites and cleavage sites so that the BsmBI would not cut repeatedly. To avoid homologous recombination in Saccharomyces cerevisiae, we substitute different promoters and terminators. Please refer to" Design" part of the Wiki for detailed experimental design.


Source

We get sequences of the promoter from Eukaryotic promoter database(EPD), the sequences of CDS and the terminator from National Center for Biotechnology Information(NCBI).


References