Team:Reading/Parts

From 2014.igem.org

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<!--Our parts-->
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<h3 class="title"> Our parts</h3>
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Synechocystis
Synechocystis
is done by modifying the chromosome,
is done by modifying the chromosome,
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rather than inserting plasmids. Synechocystis is na
+
rather than inserting plasmids. Synechocystis is naturally transformable, and will
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turally transformable, and will
+
undergo homologous recombination between its chromosome and a plasmid
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undergo homologous recombination between its chromo
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containing a homologous region. This means that plasmids for insertion or
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some and a plasmid
+
deletion need to have regions of ~500 to ~1000bp either side of the inserted
-
containing a homologous region. This means that pla
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sequence, making modifications time consuming or costly depending on your
-
smids for insertion or
+
method of plasmid construction. We will therefore submit all our BioBricks for
-
deletion need to have regions of ~500 to ~1000bp ei
+
insertions and deletions to the registry. All of these will contain Kanamycin
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ther side of the inserted
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resistance for simple selection of transformants.  
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sequence, making modifications time consuming or co
+
-
stly depending on your
+
-
method of plasmid construction. We will therefore s
+
-
ubmit all our BioBricks for
+
-
insertions and deletions to the registry. All of th
+
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ese will contain Kanamycin
+
-
resistance for selecting transformants.  
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<br />
<br />
<br />
<br />
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The mechanism for each of the BioBricks is the same
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<center><img src="https://static.igem.org/mediawiki/2014/6/6c/Matt_bg11plate_1.jpg" width=600px></center>
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. They will undergo
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<br />
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recombination with the region that they share homol
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<center>Above: Wild-type <i>Synechocystis</i> transformed with a plasmid carrying kanamycin resistance.</center>
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ogy with. Knockouts will
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<br />
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undergo recombination with the specified gene, repl
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<br />
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acing it will kanamycin
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The mechanism for each of the BioBricks is the same. They will undergo
-
resistance. Insertions will undergo recombination w
+
recombination with the region that they share homology with. Knockouts will
-
ith a region of the
+
undergo recombination with the specified gene, replacing it with kanamycin resistance. Insertions will undergo recombination with a region of the
chromosome that is not important for the metabolic
chromosome that is not important for the metabolic
-
conditions we are using, and
+
conditions we are using, and will insert the gene of interest along with a kanamycin resistance gene.  
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will insert the gene of interest and a kanamycin re
+
-
sistance gene.  
+
<br />
<br />
<br />
<br />
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We are creating 7 BioBricks that will be submitted
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We are creating 4 BioBricks that will be submitted
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to registry, consisting of 4
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to registry, consisting of 2
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deletions and 3 insertions, in addition to improvin
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deletions (<a href="http://parts.igem.org/Part:BBa_K1476003" title="Go to PsaD wiki page">PsaD</a> and <a href="http://parts.igem.org/Part:BBa_K1476000" title="Go to PilT1 wiki page">PilT1</a>) and 2 insertions (<a href="http://parts.igem.org/Part:BBa_K1476004" title="Go to PetF wiki page">PetF</a> and <a href="http://parts.igem.org/Part:BBa_K1476001" title="Go to PilA1 wiki Page">PilA1</a>). Background information on the aim of these parts can be
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g characterization of an
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found in our <a href="https://2014.igem.org/Team:Reading/Project" title="Go to project section">project section</a>. <br />
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existing BioBrick. Background information on the ai
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<br />
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m of these parts can be
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found in our “Project” section.  
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<tr><td colspan="3" > <h3> Parts Table</h3></td></tr>
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<tr><td><h3 class="title"> Reading iGEM 2014 parts</h3></td>
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<td></td>
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<tr><td width="45%" colspan="3"  valign="top">
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Any parts your team has created will appear in this table below:</td></tr>
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</table>
</table>

Latest revision as of 00:31, 18 October 2014

University of Reading
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Our parts

Genetic modification in Synechocystis is done by modifying the chromosome, rather than inserting plasmids. Synechocystis is naturally transformable, and will undergo homologous recombination between its chromosome and a plasmid containing a homologous region. This means that plasmids for insertion or deletion need to have regions of ~500 to ~1000bp either side of the inserted sequence, making modifications time consuming or costly depending on your method of plasmid construction. We will therefore submit all our BioBricks for insertions and deletions to the registry. All of these will contain Kanamycin resistance for simple selection of transformants.


Above: Wild-type Synechocystis transformed with a plasmid carrying kanamycin resistance.


The mechanism for each of the BioBricks is the same. They will undergo recombination with the region that they share homology with. Knockouts will undergo recombination with the specified gene, replacing it with kanamycin resistance. Insertions will undergo recombination with a region of the chromosome that is not important for the metabolic conditions we are using, and will insert the gene of interest along with a kanamycin resistance gene.

We are creating 4 BioBricks that will be submitted to registry, consisting of 2 deletions (PsaD and PilT1) and 2 insertions (PetF and PilA1). Background information on the aim of these parts can be found in our project section.

Reading iGEM 2014 parts

<groupparts>iGEM013 Reading</groupparts>

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rusynbioigem@gmail.com

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