Part:BBa_K3726046:Design
BOH1_C_Lv1
- 10INCOMPATIBLE WITH RFC[10]Illegal PstI site found at 1723
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 431
Illegal NheI site found at 454
Illegal NheI site found at 729
Illegal NheI site found at 957
Illegal PstI site found at 1723 - 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 2057
Illegal BglII site found at 2174
Illegal BglII site found at 4593
Illegal XhoI site found at 3277
Illegal XhoI site found at 4120 - 23INCOMPATIBLE WITH RFC[23]Illegal PstI site found at 1723
- 25INCOMPATIBLE WITH RFC[25]Illegal PstI site found at 1723
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
The part is a MoClo Lv.1 part, assembled in in the acceptor Lv1 entry vector whose ori is âBBa_K2560036â, and it's resistance cassette is âBBa_K3726039â (MARK_Lv0_AmpR). This part has been assembled following the marburg collection standard, then the transcriptional unit is flanked by the part 5'Con3 âBBa_K2560067â in its upstream region will allow the assembly of a Lv2 construct following the marburg collection standard. And by the part âBBa_K3726105â 3CON5(H)_NS1(mod)-down (PCC 11801) in its downstream region, which is a homology region for homologous recombination within the genome of PCC 11801.
Source
This construct has been made by golden gate reaction.
References
X. Liu, R. Miao, P. Lindberg and P. Lindblad, "Modular engineering for efficient photosynthetic biosynthesis of 1-butanol from CO2in cyanobacteria", 2021.