Difference between revisions of "Part:BBa K4475000"

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<partinfo>BBa_K4475000 short</partinfo>
 
<partinfo>BBa_K4475000 short</partinfo>
  
This is the full exon only coding sequence for the CTB1 enzyme in the fungus cercospora beticola. The enzyme is the first in a multi step pathway for the production of cercosporin, a reactive oxygen species producing toxin. FSU's iGEM team is looking to synthesize CTB1 in yeast as a proof of concept for cercosporin pathway expression in a non-native and scalable organism, with the goal of producing cercosporin to combat algal blooms. The sequence has been codon optimized for Saccharomyces cerevisiae.
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This is the full exon only coding sequence for the CTB1 enzyme in the fungus cercospora beticola. The enzyme is the first in a multi step pathway for the production of cercosporin, a reactive oxygen species producing toxin. FSU's iGEM team is looking to synthesize CTB1 in yeast as a proof of concept for cercosporin pathway expression in a non-native and scalable organism, with the goal of producing cercosporin to combat algal blooms. The sequence has been codon optimized for Saccharomyces cerevisiae. An HA tag is embedded on the N-terminus for expression verification.
  
 
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Revision as of 23:58, 18 July 2022


CTB1 Gene from Cercospora beticola

This is the full exon only coding sequence for the CTB1 enzyme in the fungus cercospora beticola. The enzyme is the first in a multi step pathway for the production of cercosporin, a reactive oxygen species producing toxin. FSU's iGEM team is looking to synthesize CTB1 in yeast as a proof of concept for cercosporin pathway expression in a non-native and scalable organism, with the goal of producing cercosporin to combat algal blooms. The sequence has been codon optimized for Saccharomyces cerevisiae. An HA tag is embedded on the N-terminus for expression verification.

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BglII site found at 3532
    Illegal BamHI site found at 3441
    Illegal BamHI site found at 5614
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal NgoMIV site found at 6121
    Illegal AgeI site found at 4195
  • 1000
    COMPATIBLE WITH RFC[1000]