Difference between revisions of "Part:BBa K3726046:Design"
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+ | __NOTOC__ | ||
+ | <partinfo>BBa_K3726046 short</partinfo> | ||
+ | <partinfo>BBa_K3726046 SequenceAndFeatures</partinfo> | ||
+ | |||
+ | |||
+ | ===Design Notes=== | ||
+ | |||
+ | The part is a MoClo Lv.1 part, assembled in in the acceptor Lv1 entry vector whose ori is “BBa_K2560036”, and it's resistance cassette is “BBa_K3726039” (MARK_Lv0_AmpR). This part has been assembled following the marburg collection standard, then the transcriptional unit is flanked by the part 5'Con3 | ||
+ | “BBa_K2560067” in its upstream region will allow the assembly of a Lv2 construct following the marburg collection standard. And by the part “BBa_K3726105” 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. |
Latest revision as of 22:38, 19 October 2021
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 “BBa_K2560036”, and it's resistance cassette is “BBa_K3726039” (MARK_Lv0_AmpR). This part has been assembled following the marburg collection standard, then the transcriptional unit is flanked by the part 5'Con3 “BBa_K2560067” in its upstream region will allow the assembly of a Lv2 construct following the marburg collection standard. And by the part “BBa_K3726105” 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.