Difference between revisions of "Part:BBa K1149050:Design"
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===Source=== | ===Source=== | ||
− | + | <p>team: Imperial College 2013 iGEM Team </p> | |
− | Imperial | + | <p>organism: Ralstonia pickettii</p> |
===References=== | ===References=== |
Latest revision as of 13:38, 27 September 2013
Bdh2 (intracellular)
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 125
- 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 65
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal AgeI site found at 181
Illegal AgeI site found at 1126 - 1000COMPATIBLE WITH RFC[1000]
Design Notes
We removed secretion tag to make intracellular. While doing this, we linearised the plasmid with PCR to exclude the secretion tag in construct BBa_K1149013. Then, we did blunt ended ligation to circularize the plasmid again. During the ligation, 3 nucleatodes disappeared fron the scar between the RBS and the start of the bdh2 gene. Therefore the scar is "TAC" istead of the regular "tactag".
Source
team: Imperial College 2013 iGEM Team
organism: Ralstonia pickettii
References
Characterization of Two 3-Hydroxybutyrate Dehydrogenases in Poly(3-Hydroxybutyrate)-Degradable Bacterium, Ralstonia pickettii T1 , Masahiko Takanashi and Terumi Saito, 2006