Team:Cambridge/Bioluminescence/Bacterial Luciferases

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{{:Team:Cambridge/Templates/headerbar|colour=#fb5c2b|title=Project Vibrio: Introduction}}
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{{:Team:Cambridge/Templates/headerbar|colour=#386abc|title=Project Vibrio: Introduction}}
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{{:Team:Cambridge/Templates/RightImage|image=Cambridge-Photobacterium_plate.JPG|caption=One of the plates of <i>V. phosphoreum</i> we prepared.}}
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'''Project Vibrio''' was designed to create BioBricks from genes involved in bacterial bioluminescence.  
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'''Project Vibrio''' was designed to complement Project Firefly, by using bacterial lux operons to do what had been impossible with firefly luciferases:
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* Emission of blue light to fill the gap in our spectrum of emission wavelengths.
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* Substrate production within E. coli, avoiding the need for external addition of substrates, such as luciferin.
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Bacterial lux operons can be found in a range of [https://2010.igem.org/Team:Cambridge/Bioluminescence/Background natural bioluminescent bacteria].
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==Natural bioluminescent bacteria==
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{{:Team:Cambridge/Templates/RightImage|image=Tide.jpg|caption=Wave glowing with bioluminescent micro-organisms}}
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Bioluminescence is a trait found in a number of marine bacteria. Some strains use their ability to emit light to form symbiotic relationships. A number of deep sea fish and squids have specialised <em>light organs</em> which harbour populations of bacteria that help their hosts by emitting light.  One such example is the partnership between the Hawaiian Bobtail squid <em>(Euprymna scolopes)</em> and the bacterium <em>Vibrio fischeri</em>.  
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==Pathway==
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At night squid hunt high in the water column, attacking their prey from above.  The squid uses the light produced by its symbionts to hide the shadow it casts when hunting in top waters in clear moonlit nights. An elaborate light sensing and shutter system adjusts the light output to the light that falls on the squid's back.
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Bacterial lux operons emit light using five enzymes:
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*<i>luxA</i> and <i>luxB</i> form the luciferase of the system, they emit light using the substrate <b>tetradecanal</b>
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*<i>luxC</i>, <i>luxD</i> and <i>luxE</i> are involved in the biosynthesis of tetradecanal from readily available substrates
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==Bioluminescent species==
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Bioluminescent bacterial species can differ markedly in their lifestyles. Vibrio Harveyi is a free living marine bacterium, while Xenorhabdus luminescens is a symbiont of terrestrial nematodes.
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The Cambridge team is looking into these bacterial luciferases:
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* <i>Vibrio fischeri</i> forms symbioses with squid to prevent the squid from casting a shadow on moonlit nights. Due to this their lux proteins are non-functional above 30 degrees
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The light-generating chemical reactions in bioluminescent bacteria are catalysed by enzymes expressed from so-called lux genes. These genes encode not only the bacterial luciferase, but also the enzymes required for the synthesis of fatty aldehydes, which are the substrates for the reaction. In the bacterial genome, the lux genes occur clustered in the [https://2010.igem.org/Team:Cambridge/Bioluminescence/Background lux operon].
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* <i>Vibrio (formerly Photobacterium) phosphoreum</i> emits a very blue light, perhaps partly through its use of [http://partsregistry.org/Part:BBa_K216007 lumazine]
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==Our work==
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{{:Team:Cambridge/Templates/RightImage|image=Phosphoreum_bright.jpg|caption=Our workspace illuminated by'' Vibrio phosphoreum'', a bacterium we investigated}}
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To complement 'Project Firefly', we intended to use the lux operon from ''Vibrio fischeri'' for the following three purposes:
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* Emission of blue light to complete our spectrum of emission wavelengths.
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* Substrate production within E. coli, avoiding the need for addition of external substrates, such as luciferin.
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* Design of a biosensor output device that can be combined with various input systems.
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Bacterial lux operons encode five enzymes involved in the light-generating pathway. In nature, the lux genes appear to be repressed by the [https://2010.igem.org/Team:Cambridge/Bioluminescence/Background nucleoid protein, H-NS], and occur under [https://2010.igem.org/Team:Cambridge/Bioluminescence/Background quorum sensing control]. We wished to relieve repression by H-NS to achieve brighter light outputs. We furthermore removed quorum sensing control to facilitate use of the part in biosensors under different regulatory inputs.
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Latest revision as of 03:00, 28 October 2010