Difference between revisions of "Part:BBa K4759077:Design"
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===Source=== | ===Source=== | ||
− | ferredoxin reductase PetH | + | ferredoxin reductase PetH and ferredoxin PetF are from the algae (Synechocystis PCC 6803) |
===References=== | ===References=== |
Latest revision as of 02:38, 12 October 2023
petH-RBS2-petF(D21F)-linker-GFP1-10
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal EcoRI site found at 1249
- 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 1249
Illegal NotI site found at 1022 - 21INCOMPATIBLE WITH RFC[21]Illegal EcoRI site found at 1249
Illegal BglII site found at 1560
Illegal BglII site found at 2229
Illegal BamHI site found at 1243 - 23INCOMPATIBLE WITH RFC[23]Illegal EcoRI site found at 1249
- 25INCOMPATIBLE WITH RFC[25]Illegal EcoRI site found at 1249
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
To rapidly screen the most compatible redox chaperone with Olep, a novel redox chaperone sensor was constructed to measure the interaction force between Olep and the redox chaperone based on bimolecular fluorescence complementation techniques. The sensor uses a superfolded green fluorescent protein (sfGFP), and sfGFP is divided into sfGFP-1-10 and sfGFP-11 without fluorescence. The interaction between sfGFP-1-10 and sfGFP-11 pulls down the distance in space. We performed site-directed mutagenesis of petF (D21F)and ligated GFP1-10 at the C terminus of PetF.
Source
ferredoxin reductase PetH and ferredoxin PetF are from the algae (Synechocystis PCC 6803)