Device
Part:BBa_K4593021:Design
Designed by: Jianfei Song Group: iGEM23_BNDS-China (2023-10-08)
S. aureus in vivo elimination apparatus for B. subtilis
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 439
Illegal BglII site found at 6064
Illegal BamHI site found at 1323
Illegal XhoI site found at 2618 - 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 5716
Illegal NgoMIV site found at 6548
Illegal NgoMIV site found at 7222
Illegal AgeI site found at 3117
Illegal AgeI site found at 3255
Illegal AgeI site found at 5585
Illegal AgeI site found at 6692
Illegal AgeI site found at 6920
Illegal AgeI site found at 7091
Illegal AgeI site found at 7204 - 1000COMPATIBLE WITH RFC[1000]
Design Notes
The promoter and RBS of the circuit are optimized for protein expression in B. subtilis. However, further codon optimization might be needed to achieve the full potential for expression level.
The P2 promoter shows a high background expression in E. coli, but the detection device should function as intended in B. subtilis, as previous research showed that the same design works in closely related gram-positive bacteria (Bacillus megaterium)[5]. However, we don't have enough time to test this design.
For the initial version designed for the expression in E.coli, see BBa_K4593020.
Source
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