Difference between revisions of "Part:BBa K1916102"
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==Characterization== | ==Characterization== | ||
− | The ara-inducible system was cloned into pSB1C3 and co-transformed into DH5-alpha cells along with a plasmid containing heme oxygenase and PcyA. After growing the cells to OD=0.9-1 in Terrific Broth, the cultures were induced with increasing levels of arabinose to study the vibrancy of the cells once harvested. | + | The ara-inducible system was cloned into pSB1C3 and co-transformed into DH5-alpha cells along with a plasmid containing heme oxygenase and PcyA. After growing the cells to OD=0.9-1 in Terrific Broth, the cultures were induced with increasing levels of arabinose to study the vibrancy of the cells once harvested (Fig.1). |
[[Image:K1916102_cyan_induction.jpeg|600px|thumb|left|Fig.1 Pellets of cells expressing Cyan7427, spun down 4 hrs after being induced by different concentrations of arabinose.]] | [[Image:K1916102_cyan_induction.jpeg|600px|thumb|left|Fig.1 Pellets of cells expressing Cyan7427, spun down 4 hrs after being induced by different concentrations of arabinose.]] | ||
Revision as of 07:10, 25 October 2016
Ara-Inducible Cyan7427_1390g3 Expression System
A GAF domain of the cyanobacteriochrome (CBCR) Cyan7427_1390 with an intein/chitin-binding domain fused to the C-terminus for purification. Expression regulated by a pBAD promoter. As with most CBCRs, NpF requires a phycocyanobilin co-factor, and must therefore be expressed in a system with heme oxygenase (BBa_I15008) and PcyA (BBa_I15009). Cyan7427_1390g3 expresses well in E. coli and cells appear vibrant blue-green under normal light.
Characterization
The ara-inducible system was cloned into pSB1C3 and co-transformed into DH5-alpha cells along with a plasmid containing heme oxygenase and PcyA. After growing the cells to OD=0.9-1 in Terrific Broth, the cultures were induced with increasing levels of arabinose to study the vibrancy of the cells once harvested (Fig.1).
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 125
- 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 65
Illegal BamHI site found at 731 - 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 1251
Illegal AgeI site found at 1341 - 1000COMPATIBLE WITH RFC[1000]