Part:BBa_K343003
NpSopII-NpHtrII-StTar (M-fusion)
Sensory Rhodopsin II bluelight receptor fused to its transducer, HtrII, with a 27 BP linker region. This is fused to Salmonella enterica serovar typhimurium chemotaxis protein Tar, so that the protein effectively couples the input from the receptor to the chemotaxis pathway and reduces the amount of phosphorylated CheY, which results in a lowered tumbling frequency. The fusion between HtrII and Tsr is an M-fusion in the HAMP domain, which is supposed to give it maximum activity.
Sequencing confirmed that the sequence is identical to the found in the article by Jung, Spudich E, Trivedi and Spudich J in the article: An Archaeal Photosignal-Transducing Module Mediates Phototaxis in Escherichia coli. (1)
Background
The mechanism of bacterial motility
Phototaxis is naturally not present in E.Coli, so that the wildtype does not change it's motility in response to light. The bacteria do move in response to different chemical gradients, so called chemotaxis. By this ability the cell can choose whether it wants tu "run" or "tumble", which are the 2 modes of bacterial propulsion known. When running the bacteria just go in a straight line. When the bacteria tumble they will randomly reorientate themselves, until the mode is switched back to run and they run off into another direction. The cells use these mechanisms so that they will increase the rate of tumbling in an unfavorable environment, so that they tumble a lot and thereby get away from the unfavorable environment. In a favorable environment the bacteria will reduce their tumbling frequency so as they won't leave the good environment they are in at the moment.
The bacterial propulsion works with the help of flagellae, small bacterial motors that rotate. The 6 - 8 flagella of E. Coli bacteria will rotate counter clockwise when being in "run-mode" and three of them will bundle up to create one big flagellum. This results in a smooth-straight line pattern of movement. When the bacteria tumble the flagellae rotate clockwise, which breaks the bigger bundle up and makes the flagella whip around randomly instead of their normal rotation.
Molecular mechanism of the photosensor
The photosensor acts directly on the tumbling frequency by effecting E. Coli's normal chemotaxis pathway.
Usage
When exposed to bluelight, the sensory rhodopsin II will undergo a change in ultrastructure, which is being transduced through HtrII on to the Tar domain. This influences the cell's normal chemotaxis pathway, so that it will decrease the amount of phosphorylated CheY and thereby decrease the tumbling frequency of the cell.
The part requires retinal to work in E.Coli. This can be achieved through adding retinal to the liquid growth medium and/or the plates. Currently we are doing experiments on wether the part also functions with an internal retinal source, ie retinal synthesis in E. Coli.
Results
Bacteria containing this part will exhibit a lowered tumbling rate when exposed to blue light (wavelengths around 350nm - 450nm). This was analysed with the help of video microscopy and the open source software [http://db.cse.ohio-state.edu/CellTrack/ "CellTrack"]. The individual cells trajectory was tracked and their speed measured. The tracking results are as follows:
From left to right, trajectory of: E.Coli with photosensor exposed to blue light, E.Coli with photosensor exposed to red light and E.Coli Mg1655 Wildtype exposed to blue light: (Blue dots show the location of the cell in the given frame, so the number of dots equals the number of frames from the sample.)
The phototaxic bacteria move more in a straight line when exposed to bluelight, as can be seen when comparing the trajectories of the thee bacteria given earlier. These were taken from a batch of 10 cells tracked per sample.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NotI site found at 1783
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 73
Illegal NgoMIV site found at 331
Illegal AgeI site found at 1585 - 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 1027
Illegal BsaI.rc site found at 1300
Illegal SapI site found at 801
Illegal SapI.rc site found at 1801
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