Coding
Part:BBa_K4212000:Design
Designed by: Shirin Bamezai Group: iGEM22_Imperial_College_London (2022-09-29)
CotG_ChiS
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal EcoRI site found at 849
- 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 849
- 21INCOMPATIBLE WITH RFC[21]Illegal EcoRI site found at 849
Illegal BamHI site found at 834 - 23INCOMPATIBLE WITH RFC[23]Illegal EcoRI site found at 849
- 25INCOMPATIBLE WITH RFC[25]Illegal EcoRI site found at 849
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
This is a direct tandem C'terminal fusion.
Source
The CotG CDS comes from the genome of B. subtilis, and was produced through genome amplification with appropriately designed primers. The chitinase protein sequence comes from the B. pumilus, however this was codon-optimised for B. subtilis and synthesized as a gBlock (IDT). The individual CDSs were also either ordered or amplified with Type IIS restriction sites on either end, to enable scarless fusion as a single CDS in a level 0 plasmid within a Golden Gate system.