Difference between revisions of "Part:BBa K3018000"
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<partinfo>BBa_K3018000 parameters</partinfo> | <partinfo>BBa_K3018000 parameters</partinfo> | ||
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+ | <h1><b>Tongji_China 2019 Characterization</b></h1> | ||
+ | <br/> | ||
+ | All characterizations are performed in plasmid pET-28a(+), strain E. coli BL21(DE3). | ||
+ | <br/> | ||
+ | <b>Function Validation</b> | ||
+ | To validate the function of this part in E. coli BL21(DE3), we transformed pET-28a(+)-bFMO into E. coli BL21(DE3). Bacte and induced with IPTG (final concentration: 0.5mM) . Culture without induction was used as control. | ||
+ | <br/> | ||
+ | [[Image:T--Tongji_China--pET-28a(+)-bFMO_induced_plate.jpg|left|400px|thumb|Dark blue clones on LB plate with IPTG]] | ||
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+ | [[Image:T--Tongji_China--indigores.jpg|left|400px|thumb|Validation of function. Tube on the left was induced with IPTG, on the right was not induced as control. This figure shows a significant difference in color between induced group and control group, indicates the production of indigo. The result supports that this part can work in BL21(DE3).]] | ||
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+ | [[Image:T--Tongji_China--indigo_powder.jpg|left|400px|thumb|Indigo powder extracted from culture medium]] | ||
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+ | [[Image:T--Tongji_China--tjindigo.jpg|left|400px|thumb|Tubes containing blue culture medium, color comes from IPTG induction. Tubes organized in the shape of TJ]] | ||
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Revision as of 22:57, 21 October 2019
Bacterial flavin-containing monooxydase, codon-optimized
This part encodes a bacterial flavin-containing monooxygenase(bFMO), which can catalyze the oxidation of indole. We had the codon-optimized for E. coli. You can use this part to produce indigo through indoxyl and leucoindigo in E. coli. Indigo is a hydrophobic blue dye; the expression of functional FMO can be estimated by the color of culture solution. Clones on LB plates should be blue when it works.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Tongji_China 2019 Characterization
All characterizations are performed in plasmid pET-28a(+), strain E. coli BL21(DE3).
Function Validation
To validate the function of this part in E. coli BL21(DE3), we transformed pET-28a(+)-bFMO into E. coli BL21(DE3). Bacte and induced with IPTG (final concentration: 0.5mM) . Culture without induction was used as control.