Freiburg07/report light sensor

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Contents

Towards optical signal processing in E. coli

iGEM team Freiburg

Introduction

Phytochrome A (PhyA) is a member of the phytochrome family of red/far-red photoreceptors. These photoreceptors are involved in a wide range of developmental responses in plants. It changes between two stable conformations, the Pr (red light absorbing) and Pfr (far-red light absorbing) form. Red light causes a conformational switch into the Pfr form and far-red light switches PhyA into the Pr form. The conformational change is induced by PCB, a tetrapyrrole which rotates by light radiation. Fhy1 is a protein which binds PhyA under light conditions, enable us to use this protein-protein interaction. In plants Fhy1 is responsable for nuclear accumulation of PhyA in case of light exposure. In our case it wasn´t neccessary to use the full Fhy1 protein, that is why we restriced to the PhyA binding domain of Fhy1. We choose two different sizes of the Fhy1 fragment, a small version and a big one. Our goal was to show the interaction of both by performing a FRET, fusing CFP to PhyA and YFP to Fhy1.

PhyA - Fhy1 Interaction and light cycle

Materials and Methods

Cloning of constructs:

PhyA Insert was gained by PCR from plasmid D153ah-phyA using 5´ (5´-TATCGACGAA TTCGCGGCCG CTTCTAGAAA GAGGAGAAAT
TAACTATGTC AGGCTCTAGG CCGAC-3´) and 3´ (5´- AACGATCACT AGTTCCGCCG TGATGGTGAT GGTGGCCTCC GTTATCGAGT TCCACCTCCT TA-3´) primers.
Fhy1 Insert1 was gained by PCR from pGADT7 using 5´ (5´-TATCGACGCT AGCGATTACA TCTATGGGAC TCAGA-3´) and 3´
(5´-AACGATCGGC GCGCCCAGCA TTAGCGTTGA GAAGTAT-3´) primers.
Fhy1 Insert2 was gained by PCR from pGADT7 using 5´ (5´-TATCGACGCT AGCAGTAGTA ATGCTGCTAA GTTTGT-3`) and 3´
(5´-AACGATCGGC GCGCCCAGCA TTAGCGTTGA GAAGTAT-3´) primers.

PhyA Insert was digested with EcoRI and SpeI, the CFP containing plasmid pAR200-cJunCFP as well. Fhy1 Insert1 was digested with AscI and NheI, the YFP containing plasmid pAR200-YFP-Dummy (for N-terminal fusion) and pAR200-cFOS-YFP (for C-terminal fusion) as well. All vector plasmids were provided by our laboratory.

Insert and Vector fragments were ligated. The purified DNA was used for a transformation in E. coli. The E. coli DNA was purified and sequenzed.

Results

Under construction...

Discussion

The PhyA - Fhy1 light sensing system is a promising approach for regulating protein/enzyme activity by light stimulation. Of course we need evidence for the correct arrangement, given by the CFP and YFP fusion. Gaining a FRET would help us to be sure about the arrangement for split enzymes. These parts could be fused to PhyA and Fhy1 and get a complementation of the enzyme by light.

References

Hiltbrunner A, Tscheuschler A, Viczian A, Kunkel T, Kircher S, Schäfer E. "FHY1 and FHL act together to mediate nuclear accumulation of the phytochrome A photoreceptor." Plant Cell Physiol. 2006 Aug;47(8):1023-34.

Hiltbrunner A, Viczian A, Bury E, Tscheuschler A, Kircher S, Toth R, Honsberger A, Nagy F, Fankhauser C, Schäfer E "Nuclear accumulation of the phytochrome A photoreceptor requires FHY1." Curr Biol. 2005 Dec 6;15(23):2125-30.

Gambetta GA, Lagarias JC "Genetic engineering of phytochrome biosynthesis in bacteria." Proc Natl Acad Sci U S A. 2001 Sep 11;98(19):10566-71.

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