Part:BBa_K4192130
Plac-RBS-yf1-RBS-fixJ-Pfixk2-RBS-mcherry
The gene yf1, fixJ and PfixK2 make up the system of blue light regulation. Under dark conditions, phosphate groups are transferred from Yf1 protein to FixJ protein, and the phosphorylated FixJ protein activates the PfixK2 promoter, which in turn activates downstream gene expression. Under light induction, the phosphorylation of Fixj protein was blocked and the expression of genes regulated by the PfixK2 promoter was suppressed.The mCherry protein emits red fluorescence to characterize the efficiency of control elements in regulating gene expression.
Usage
Light control system can regulate gene expression by light intensity. MCherry has an excitation wavelength of 580nm and an emission wavelength of 610nm. Quantitative detection of mcherry can be achieved by detecting the optical signal at 610nm. This composite part was constructed to test the ability of the original light control system to regulate gene expression compared with the light control system containing yf1 mutation(BBa_K4192132).
Biology
In the absence of light, FixL first undergoes autophosphorylation at histidine at position 29, and then transfers the phosphate moiety to its homologous, noncovalently bound response regulator FixJ. Phosphorylated FixJ binds to homologous promoters to activate transcription; In the presence of light, FixJ cannot be phosphorylated, no longer binds to the promoter, and transcriptional activity is downregulated.[1]
Fig.1 the principle of light control system
References
- Möglich, A., R.A. Ayers and K. Moffat, Design and Signaling Mechanism of Light-Regulated Histidine Kinases. Journal of Molecular Biology, 2009. 385(5): p. 1433-1444.
Sequence and Features
- 10INCOMPATIBLE WITH RFC[10]Illegal SpeI site found at 210
Illegal SpeI site found at 1361
Illegal SpeI site found at 2257 - 12INCOMPATIBLE WITH RFC[12]Illegal SpeI site found at 210
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Illegal SpeI site found at 1361
Illegal SpeI site found at 2257 - 25INCOMPATIBLE WITH RFC[25]Illegal SpeI site found at 210
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Illegal SpeI site found at 2257
Illegal NgoMIV site found at 764
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Illegal AgeI site found at 478
Illegal AgeI site found at 1618 - 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 1507
Illegal BsaI.rc site found at 377
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