Difference between revisions of "Part:BBa K3720003"
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Quantitative measurements were not possible because the laboratory facilities did not allow us to prepare a luminometer. | Quantitative measurements were not possible because the laboratory facilities did not allow us to prepare a luminometer. | ||
As shown in the photo, the pipette which carbon monoxide was injected showed a change in color. | As shown in the photo, the pipette which carbon monoxide was injected showed a change in color. | ||
− | <p>[[File:T--Qdai-- | + | <p>[[File:T--Qdai--result1.png|800px|thumb|center|figure. 1 Color changes in bacterial culture Left: LB medium+luciferin Right: LB medium+luciferin+CO gas]] </p> |
<!-- Add more about the biology of this part here | <!-- Add more about the biology of this part here | ||
===Usage and Biology=== | ===Usage and Biology=== |
Revision as of 13:30, 21 October 2021
Firefly luciferase with pCooM, RBS (weak), and double terminator
When used in combination with CooA, it is possible to create a light emitting mechanism that reacts with carbon monoxide. Culture pBEST incorporating this part in LD medium and transfer 20㎕ to a 1.5-ml tube. Then, 0.5㎕ of D-luciferin was added, CO was injected, and luminescence was measured. Quantitative measurements were not possible because the laboratory facilities did not allow us to prepare a luminometer. As shown in the photo, the pipette which carbon monoxide was injected showed a change in color.
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI.rc site found at 900