Team:Imperial College London/Project Gene Future

From 2011.igem.org

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<p><b>1. 16s rRNA of the bacteria grown up from sterile and non-sterile soil will be sequenced to determine the bacterial species present.</b>
<p><b>1. 16s rRNA of the bacteria grown up from sterile and non-sterile soil will be sequenced to determine the bacterial species present.</b>
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<p>This sequencing will allow us to confirm that the bacteria we were able to rescue from soil are indeed <i>E. coli</i>. This will hopefully confirm that our bacteria have been able to retain their plasmids for over a month while exposed to competition from other soil microorganisms.
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<p><b>2. Replicates of the soil experiment will be analysed for expression of sfGFP.</p></b>
<p><b>2. Replicates of the soil experiment will be analysed for expression of sfGFP.</p></b>
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<p>This will allow us to establish statistical significance of our results. At present, we need to test replicates for the presence and functionality of the GFP gene.</p>
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Revision as of 23:04, 21 September 2011




Module 3: Gene Guard

Containment is a serious issue concerning the release of genetically modified organisms (GMOs) into the environment. To prevent horizontal gene transfer of the genes we are expressing in our chassis, we have developed a system based on the genes encoding holin, anti-holin and endolysin. We are engineering anti-holin into the genome of our chassis, where it acts as an anti-toxin, and holin and endolysin on plasmid DNA. In the event of horizontal gene transfer with a soil bacterium, holin and endolysin will be transferred without anti-holin, rendering the recipient cell non-viable and effectively containing the Auxin Xpress and Phyto-Route genes in our chassis.




Future Work

To carry on the work on the Gene Guard module, there are a number of steps we would take in the immediate future and others that form part of our long term plan.

Short-term plans

1. 16s rRNA of the bacteria grown up from sterile and non-sterile soil will be sequenced to determine the bacterial species present.

This sequencing will allow us to confirm that the bacteria we were able to rescue from soil are indeed E. coli. This will hopefully confirm that our bacteria have been able to retain their plasmids for over a month while exposed to competition from other soil microorganisms.

2. Replicates of the soil experiment will be analysed for expression of sfGFP.

This will allow us to establish statistical significance of our results. At present, we need to test replicates for the presence and functionality of the GFP gene.

3.

Long-term plans

1. Alternative to antibiotic resistance

During the assembly and testing of this module,

2.

3.Testing and implementation in the field.