Difference between revisions of "Part:BBa K2944001"
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<partinfo>BBa_K2944001 short</partinfo> | <partinfo>BBa_K2944001 short</partinfo> | ||
− | Glucose oxidase from Aspergillus niger was codon optimized for transcription in Saccharomyces cerevisiae. Glucose oxidase catalyzes the oxidation of glucose to D-glucono-1,5-lactone and hydrogen peroxide. Original sequence was obtained from BBa_K2238000 and then codon optimized, but retains the | + | Glucose oxidase from Aspergillus niger was codon optimized for transcription in <i>Saccharomyces cerevisiae</i>. Glucose oxidase catalyzes the oxidation of glucose to D-glucono-1,5-lactone and hydrogen peroxide. Original sequence was obtained from BBa_K2238000 and then codon optimized, but retains the His<sub>6</sub>-tag for purification. |
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+ | This part is also flanked by assembly scars on both sides, between the promoter and the gene (5'-agatct-3') and as well between the gene and the terminator (5'-atcctaactcgag-3') | ||
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Latest revision as of 03:08, 22 October 2019
Glucose oxidase optimized for Saccharomyces cerevisiae
Glucose oxidase from Aspergillus niger was codon optimized for transcription in Saccharomyces cerevisiae. Glucose oxidase catalyzes the oxidation of glucose to D-glucono-1,5-lactone and hydrogen peroxide. Original sequence was obtained from BBa_K2238000 and then codon optimized, but retains the His6-tag for purification.
This part is also flanked by assembly scars on both sides, between the promoter and the gene (5'-agatct-3') and as well between the gene and the terminator (5'-atcctaactcgag-3')
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 1
Illegal BamHI site found at 42
Illegal BamHI site found at 352
Illegal XhoI site found at 1916 - 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 376
Illegal BsaI.rc site found at 1594