Part:BBa_K2739010:Design
Hybrid promoter-PhaCB-Bktb
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 7
Illegal NheI site found at 30
Illegal NheI site found at 69
Illegal NheI site found at 92 - 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 1041
Illegal BglII site found at 1866 - 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 347
Illegal NgoMIV site found at 418
Illegal NgoMIV site found at 1018
Illegal NgoMIV site found at 1330
Illegal NgoMIV site found at 1609
Illegal NgoMIV site found at 2768 - 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 2836
Illegal BsaI site found at 3898
Design Notes
This is a composite part, which developed based on the BBa_K2739008 (Btkb) and BBa_K2739011 (Hybrid-promoter-phaCB).
For the Bktb part, its length is 1185bp and excess the 1kb length limit of the IDT sponsor limitation to be generated. Therefore two overlapped fragments of Bktb were then designed and generated by IDT. A set of PCR primer were then design to generate the whole Bktb through the PCR amplification.
Figure 1. B1 and B2 fragments were codon-optimised for E. coli and synthesised by IDT. The 696 bp overlap was in green and restriction enzyme sites were coloured by red. Two pairs of primers were ordered from IDT to amplify bktB, among which B1 forward primer and B2 reverse primer were used to amplify bktB fragments.
BBa_K2739011 (Hybrid-promoter-phaCB) is created using the BBa_K1149051 (Hybrid promoter-phaCAB) as the template. A set of primer is designed to cut the phaA from the BBa_K934001 (phaC1-A-B1) biobrick and then ligated back.
Source
BBa_K2739008 (Btkb) used in the part were created through IDT. The part of the btkb original sequence would be accessed in NCBI: NC_015726.1. Bktb sequence is codon optimised by IDT.
Hybrid-promoter-phaCB was developed from BBa_K1149051.
References
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