Team:ETHZ Basel/Biology/Archeal Light Receptor
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In ''Natronobacterium pharaonis'', the NpSRII contains a domain of seven membrane-spanning helices, which carry out two distinct functions: Firstly, they serve as photo-inducible ion-pumps and secondly, as actors in the chemotaxis signaling network. This was proposed by Spudich et al. in 2001. | In ''Natronobacterium pharaonis'', the NpSRII contains a domain of seven membrane-spanning helices, which carry out two distinct functions: Firstly, they serve as photo-inducible ion-pumps and secondly, as actors in the chemotaxis signaling network. This was proposed by Spudich et al. in 2001. | ||
- | Encouraged by this work, we cloned the archean photoreceptor NpSRII as biobrick into the standardized vector pSB1C3 | + | Encouraged by this work, we cloned the archean photoreceptor NpSRII as biobrick into the standardized vector pSB1C3 [http://partsregistry.org/Part:BBa_K220001 BBa_K22001]. For the expression (and experimental purposes), we used pACT3 (BamHI/HindIII) as plasmid backbone, which has a CmR gene (Chloramphenicol resistance) and is IPTG-inducibile (Isopropyl-ß-D-thiogalactopyranosid). |
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=Primers for pACT3= | =Primers for pACT3= |
Revision as of 15:43, 17 October 2010
Archean Light Receptor
Parallely to the light-sensitive Pif3/PhyB-system, another implementation strategy caught our attention: The generation of our E. lemming by the fusion of an archean photoreceptor to a bacterial chemotactic transducer. This was successfully demonstrated by Jung et al. in 2001 [1], who fused the Natronobacterium pharaonis NpSRII (Np seven-transmembrane retinylidene photoreceptor sensory rhodopsins II) and their cognate transducer HtrII to the cytoplasmic domain of the chemotaxis transducer EcTsr of Escherichia coli.
Rhodopsins are photoreactive, membrane-embedded proteins, which are found not only in archaea, but in eubacteria and microbes as well. In Natronobacterium pharaonis, the NpSRII contains a domain of seven membrane-spanning helices, which carry out two distinct functions: Firstly, they serve as photo-inducible ion-pumps and secondly, as actors in the chemotaxis signaling network. This was proposed by Spudich et al. in 2001.
Encouraged by this work, we cloned the archean photoreceptor NpSRII as biobrick into the standardized vector pSB1C3 [http://partsregistry.org/Part:BBa_K220001 BBa_K22001]. For the expression (and experimental purposes), we used pACT3 (BamHI/HindIII) as plasmid backbone, which has a CmR gene (Chloramphenicol resistance) and is IPTG-inducibile (Isopropyl-ß-D-thiogalactopyranosid).
Primers for pACT3
Name: AR-BamHI-forward Scale: 0.04 umol Purification: Desalted 5' Mod.: None Inner Mod.: None 3' Mod.: None Type: DNA Sequence (5'-3'): GTG GAT CCA AGG AGA TAT ACA TAT GGT TGG TCT GAC CAC CCT G Length: 43 Aliquots: NONE
Name: AR-Hind-reverse
Scale: Genomics
Purification: Desalted
5' Mod.: None
Inner Mod.: None
3' Mod.: None
Type: DNA
Sequence (5'-3'): GCA AGC TTT TAA CCG CTA TAA ATT G
Length: 25
Aliquots: NONE
Sequence
Chrystal structure of NpSRII
Sensory Rhodopsin II photocycle
References
[1] Jung, Spudich, Trivedi and Spudich: An archaeal photosignal-transducing module mediates phototaxis in Escherichia coli. Journal of bacteriology. 2001; 21.
[2] Hartmut Luecke1 and Brigitte Schobert, Janos K. Lanyi, Elena N. Spudich, John L. Spudich. Crystal Structure of Sensory Rhodopsin II at 2.4 Angstroms: Insights into Color Tuning and Transducer Interaction. Science Express. 2001; 293;5534
[3] Shimono K, Iwamoto M, Sumi M, Kamo N.: Functional expression of pharaonis photorhodopsin in Escherichia coli. FEBS Lett 1997; 22
[4] Michael Hein, Ansgar A. Wegener,† Martin Engelhard,† and Friedrich Siebert. Time-Resolved FTIR Studies of Sensory Rhodopsin II (NpSRII) from Natronobacterium pharaonis: Implications for Proton Transport and Receptor Activation. Biophys J. 2003; 84
[5]Igor Chizhov, Georg Schmies, Ralf Seidel, Jens R. Sydor, Beate Lüttenberg and Martin Engelhard.The Photophobic Receptor from Natronobacterium pharaonis: Temperature and pH Dependencies of the Photocycle of Sensory Rhodopsin II. Biophysical Journal. 1898; 75(2)