Team:Macquarie Australia/Project

From 2010.igem.org

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<h2>Aim</h2>
<h2>Aim</h2>
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The aim of our project is to introduce ''D. radiodurans'' and ''A. tumefaciens'' bacteriophytochromes into ''E. coli'' which have the potential to be used as molecular light switches in response to red and far-red light. Comparison and analysis of the phosphorylated peptides in recombinant ''E. coli'' will also be considered.
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The aim of our project is to introduce Deinococcus radiodurans and Agrobacterium tumefaciens bacteriophytochromes into E. coli which have the potential to be used as molecular light switches in response to red and far-red light. Comparison and analysis of the phosphorylated peptides in recombinant E. coli can also be considered in the future.
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<h2>Abstract </h2><p>
<h2>Abstract </h2><p>
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Photoreceptors are utilized by almost every organism to adapt to their ambient light environment (Karniol and Vierstra, 2003). Bacteriophytochrome photoreceptors are members of the phytochrome superfamily. They are a highly specialized group of photoreceptor proteins that have been observed in plants, fungi and bacteria (Halliday, 2004). <p><p>
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Photoreceptors are utilized by almost every organism to adapt to their ambient light environment. <p><p>
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Bacteriophytochromes allow bacteria to detect light and respond according to the changing light environment. Light detection is achieved by rapid photo-conversion between two stable isoforms; a red light absorbing form (Pr) and a far-red light bsorbing form (Pfr). <p><p>
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Our aim is to engineer a novel reversible molecular ‘light switch’ within E. coli by introducing a photoreceptor from non-photosynthetic bacteria (D. radiodurans and A. tumafaciens). <p><p>
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Both bacteriophytochrome isoforms (referred to as BphP1 and BphP2) often contain an N-terminal chromophore binding domain (CBD) and a C-terminal two-component histidine kinase motif. Bacteriophytochromes use biliverdin as the chromophore which is directly synthesized from heme by heme oxygenase and covalently binds to CBD (Karniol and Vierstra, 2003). This photo-conversion happens when initially synthesized Pr form is excited with red light and is converted to Pfr whose activity is repressed by far-red light resulting in rapid reversing of Pfr to Pr. Thus this rapid interconversion between the two forms of allows them to act as "photoreversible switches".<p><p>
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By cloning the bacteriophytochorome coupled with heme-oxygenase, an enzyme that produces biliverdin from heme, the created colonies are able to respond to red and far-red light environmments. <p><p>
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In this study we aim to introduce bacteriophytochromes from two bacterial species (''Deinococcus radiodurans'' and ''Agrobacterium tumafaciens'') into ''Escherichia coli''. When the bacteriophytochromes covalently attach biliverdin the ''E. coli'' cells would have the capacity to switch from blue to green colour under red light dense and far-red light dense environments, respectively. Therefore recombinant ''E. Coli'' can be potentially used as a light switch. This action is also expected to activate other signalling cascades resulting in the synthesis of new phosphorylated peptides in ''E. coli''. Comparison and analysis of those phosphorylated peptides in recombinant ''E. coli'' bacteriophytochrome is further considered.<p><p>
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This novel approach results in the colour of the E. coli ‘switching’ from blue to green.<p><p>
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Our E. coli chameleon will serve as a fundamental ‘bio-brick’ for future applications by providing a simple and photo-reversible switch. <p><p>
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Revision as of 01:03, 5 October 2010

Aim

The aim of our project is to introduce Deinococcus radiodurans and Agrobacterium tumefaciens bacteriophytochromes into E. coli which have the potential to be used as molecular light switches in response to red and far-red light. Comparison and analysis of the phosphorylated peptides in recombinant E. coli can also be considered in the future.

Abstract

Photoreceptors are utilized by almost every organism to adapt to their ambient light environment.

Our aim is to engineer a novel reversible molecular ‘light switch’ within E. coli by introducing a photoreceptor from non-photosynthetic bacteria (D. radiodurans and A. tumafaciens).

By cloning the bacteriophytochorome coupled with heme-oxygenase, an enzyme that produces biliverdin from heme, the created colonies are able to respond to red and far-red light environmments.

This novel approach results in the colour of the E. coli ‘switching’ from blue to green.

Our E. coli chameleon will serve as a fundamental ‘bio-brick’ for future applications by providing a simple and photo-reversible switch.