Difference between revisions of "Part:BBa K4475000"

Revision as of 03:36, 19 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 coding 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]

@@ Line 3: / Line 3: @@
 <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. An HA tag is embedded on the N-terminus for expression verification.
+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 coding sequence has been codon optimized for Saccharomyces cerevisiae. An HA tag is embedded on the N-terminus for expression verification.
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