DNA
Part:BBa_K1732000:Design
Designed by: Donna Lee Group: iGEM15_Carnegie_Mellon (2015-09-03)
J23100-PelB-GlucHCO-B0015
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 7
Illegal NheI site found at 30 - 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 546
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 115
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
This sequence is codon optimized for E.coli.
The plasmid was used to produce Gaussia princeps luciferase proteins that would express luminescence when reacted with an optimal concentration of 3-4 uM of coelenterazine.
Sequence contains a PelB leader sequence which suggested that the Gaussia princeps luciferase proteins would be secreted into the expected location of the periplasmic space. Howeverm the observed location of the proteins was extracellular (in the media).
Source
Engineered from XXXXXXXX. Provided by the Bruchez lab at Carnegie Mellon.