Team:Glasgow/Parts

From 2011.igem.org

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<h1>Parts</h1>
<h1>Parts</h1>
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The 2011 University of Glasgow team has submitted 9 novel biobricks.  You can find out more about these below, or by visiting the Registry Page.  If you are interested in finding out about the safety reviews of these biobricks then please visit our Biobrick Safety Page, which can be accessed <a href=https://2011.igem.org/Team:Glasgow/Safetybiobricks>here.</a> <br/>
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The 2011 University of Glasgow team has submitted a number of novel biobricks, ranging from reporters with more functionality than GFP to our novel biofilm chassis.  You can find out more about these by using the links below.  <br/><Br/><br/><Br/>
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<a href=https://2011.igem.org/Team:Glasgow/PDE>Phosphodiesterase</a><br/>
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<a href=https://2011.igem.org/Team:Glasgow/mcs>Multiple Cloning Site</a><br/>
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<a href=https://2011.igem.org/Team:Glasgow/LOV2>LOV2 and iLOV</a><br/>
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<a href=https://2011.igem.org/Team:Glasgow/Parts/Latherin>Latherin</a><br/>
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<a href=https://2011.igem.org/Team:Glasgow/Ranaspumin2>Ranaspumin-2</a><br/>
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<a href=https://2011.igem.org/Team:Glasgow/Nissle><i>E.coli</i> Nissle 1917</a></td>
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<img src=https://static.igem.org/mediawiki/2011/thumb/2/27/Lovlleaf-pola-annotated.jpg/493px-Lovlleaf-pola-annotated.jpg width=250 height=250>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
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<img src=https://static.igem.org/mediawiki/2011/thumb/5/55/Untitled-pola-annotated.jpg/493px-Untitled-pola-annotated.jpg width=275 height=275>
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Alternatively, to visit the Registry page for each of our biobricks, please use the table below.  <br/><br/> If you are interested in finding out about the safety reviews of these biobricks then please visit our Biobrick Safety Page, which can be accessed <a href="https://2011.igem.org/Team:Glasgow/Safetybiobricks">here.</a> <br/>
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<h1>Phosphodiesterase</h1>
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<b>Phosphodiesterase (<a href=http://partsregistry.org/Part:BBa_k660300>Part BBa_K660300</a>)<br/><br/></b>
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Phosphodiesterases are a family of enzymes naturally present in microorganisms, which break phosphodiester bonds. The specific enzyme we are using breaks the phosphodiester bond in the second messenger nucleotide, cyclic digaunylate (cyclic-di-GMP). Cyclic-di-GMP is important in many bacterial processes, including biofilm formation and motility. The enzyme regulates signal transduction by controlling levels of the signalling molecule in cells.<br/><br/>
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This enzyme was amplified from the genome of <i>Pseudomonas aeruginosa</i> PA01.  The enzyme contains a domain (vieA) which specifically targets the cyclic-di-GMP molecule.
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We are using the enzyme to control the levels of cyclic-di-GMP within the cell. We expect that the targeted expression of phosphodesiterase could be used to interfere with biofilm formation or to trigger dispersal.<br/><br/>
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Due to the number of processes in which cyclic-di-GMP is used by prokarytes, we hope that future iGEM teams will find diverse uses for it.<br/><br/>
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<b>Phosphodiesterase with 6xHIS Tag (<a href=http://partsregistry.org/Part:BBa_k660301>Part BBa_K660301</a>)</b><br/><br/>
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We have also created a version of the phosphodiesterase biobrick with a 6xHIS tag. This can be used for affinity purification.
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<b>References & Further Reading:</b><br/><br/>
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"The EAL Domain Protein VieA Is a Cyclic Diguanylate Phosphodiesterase" which can be accessed here <a href=http://www.jbc.org/content/280/39/33324.abstract>here.</a><br /><br />
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"A blue light-inducible phosphodiesterase activity in the cyanobacterium <i>Synechococcus elongates</i>" which can be accessed <a href=http://www.ncbi.nlm.nih.gov/pubmed/20408974>here.</a>
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<h1>Novel Reporters</h1>
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We have submitted two novel reporters to the registry, LOV2 and iLOV. Read on to find out about the exciting advantages these reporters have over GFP derived flourescent proteins.  <br/><br/>
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<b>LOV2 (<a href=http://partsregistry.org/Part:BBa_K660000>Part:BBa_K660000</a>)<br/><br/></b>
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The LOV (Light-Oxygen-Voltage) domain is a photoreceptor that responds to blue light. In nature it was first found to be involved in the phototropism response in plants and has since been found to be present in fungi and bacteria also. It has been shown to be coupled to many domains, for example phosphodiesterase or kinases.
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We are using it as a reporter due to its ability to function in anoxic conditions. This is particularly useful in biofilms and is a function that fluorescent proteins derived from GFP do not have.
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<b>LOV2 with 6xHIS tag (<a href=http://partsregistry.org/Part:BBa_K660001>Part:BBa_K60001</a>)</b>
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We have also created a version of the LOV2 biobrick with a 6xHIS tag. This can be used for affinity purification.
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<b>iLOV (<a href=http://partsregistry.org/Part:BBa_K660004>Part:BBa_K660004</a>)</b>
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iLOV is a version of LOV2 that has been altered through site directed mutagenesis and DNA shuffling.  iLOV has the same function and uses as LOV2, but contains mutations that caused increased intensity in brightness.<br/><Br/>
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As a reporter, it is advantageous over GFP derived fluorescent proteins for a number of reasons.  Firstly, it is small in size so can be used when tagging proteins.  It also recovers quickly from photobleaching. Uniquely, it has the ability to function  in anoxic conditions.
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<b>References & Further Reading:</b><br/><br/>
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"LOV (light, oxygen, or voltage) domains of the blue-light photoreceptor phototropin (nph1): Binding sites for the chromophore flavin mononucleotide" which can be accessed <a href=http://www.pnas.org/content/96/15/8779.short>here.</a><br /><br />
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"The LOV Domain Family:  Photoresponsive Signaling Modules Coupled to Diverse Output Domains" which can be accessed <a href=http://pubs.acs.org/doi/abs/10.1021/bi026978l>here.</a><br /><br />
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"Information on the LOV Domain" by Dr John Christie which can be accessed <a href=http://www.photobiology.info/Christie.html>here.</a><Br /><br/>
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"The photoreversible fluorescent protein iLOV outperforms GFP as a reporter of plant virus infection" which can be accessed <a href=http://www.pnas.org/content/105/50/20038.short>here.</a><br/>
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<h1>Surfactant Proteins</h1>
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We have developed biobricks of surfactant proteins, Ranaspumin and Latherin, which have been investigated for their antimicrobial activity.
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<b>Ranaspumin (RSN2) (<a href=http://partsregistry.org/Part:BBa_K660100>Part:BBa_K660100</a>)</b>
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Ranaspumin is a protein found in the foam nests of the Túngara Frog <i>(Engystomops pustulosus).</i> In nature it is used to protect and incubate the fertilized eggs of the frog.<br/><Br/> It has natural antimicrobial and antibiofilm activity.<br/><br/>
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Ranaspumin has a <a href=http://www.cell.com/biophysj/abstract/S0006-3495%2809%2900792-9>unique amino acid sequence.</a>
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<b>Ranspumin (RSN2) with 6xHIS tag (<a href=http://partsregistry.org/Part:BBa_K660101>Part:BBa_K660101</a></b>
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We have also created a version of Ranaspumin (RSN2) biobrick with a 6xHIS tag. This can be used for affinity purification.
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<b>References & Further Reading:</b>
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"Ranaspumin-2: Structure and Function of a Surfactant Protein from the Foam Nests of a Tropical Frog" which can be accessed <a href=http://www.sciencedirect.com/science/article/pii/S0006349509007929>here.</a><br /><br />
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"Biofoams and natural protein surfactants" which can be accessed <a href=http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2954283/>here.</a>
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<b>Latherin (<a href=http://partsregistry.org/Part:BBa_K660200>Part:BBa_K660200</a>)</b>
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Latherin is a surfactant protein that was originally isolated from horse sweat. Its normal biological function is temperature regulation and is believed to function by enhancing evaporation from the pelt. Due to its ability to bind to hydrophobic surfaces, the protein is being investigated for its possible ability to aid in breaking up biofilms.<br/><br/>
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We are using latherin to aid in dispersal of biofilms, which is a natural property of the protein.
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<b>Latherin with 6xHIS tag (<a href=http://partsregistry.org/Part:BBa_K660201>Part:BBa_K660201</a>)</b>
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We have also created a version of Latherin with a 6xHIS tag. This can be used for affinity purification.
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<b>References & Further Reading:</b><br/><br/>
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"Latherin: A Surfactant Protein of Horse Sweat and Saliva" which can be accessed <a href=http://www.plosone.org/article/info:doi%2F10.1371%2Fjournal.pone.0005726>here</a><br /><br />
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"Isolation and characterization of latherin, a surface-active protein from horse sweat" which can be accessed <a href=http://www.ncbi.nlm.nih.gov/sites/entrez?db=pubmed&cmd=search&term=3753435>here.</a><br /><br />
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"Biochemical characterization and surfactant properties of horse allergens" which can be accessed <a href=http://www.ncbi.nlm.nih.gov/sites/entrez?db=pubmed&cmd=search&term=11358533>here.</a><Br /><br />
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"Latherin and other biocompatible surfactant proteins" which can be accessed <a href=http://www.biochemsoctrans.org/bst/039/bst0391017.htm>here</a><br />
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===Parts===
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New for iGEM 2010 is the ''groupparts'' tag.  This tag will generate a table with all of the parts that your team adds to your team sandbox.  Note that if you want to document a part you need to document it on the [http://partsregistry.org Registry], not on your team wiki.
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<groupparts>iGEM010 Glasgow</groupparts>
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Latest revision as of 13:08, 21 September 2011


Parts

The 2011 University of Glasgow team has submitted a number of novel biobricks, ranging from reporters with more functionality than GFP to our novel biofilm chassis. You can find out more about these by using the links below.



Phosphodiesterase
Multiple Cloning Site
LOV2 and iLOV
Latherin
Ranaspumin-2
E.coli Nissle 1917

        




Alternatively, to visit the Registry page for each of our biobricks, please use the table below.

If you are interested in finding out about the safety reviews of these biobricks then please visit our Biobrick Safety Page, which can be accessed here.


<groupparts>iGEM011 Glasgow</groupparts>


Retrieved from "http://2011.igem.org/Team:Glasgow/Parts"