IGEM:Paris Bettencourt 2012/Notebooks/Delay group: Difference between revisions

From OpenWetWare
Jump to navigationJump to search
No edit summary
Line 8: Line 8:
  ! [[IGEM:Paris_Bettencourt_2012/Previous_Biosafety_iGEM_Projects | Previous Biosafety iGEM projects]]
  ! [[IGEM:Paris_Bettencourt_2012/Previous_Biosafety_iGEM_Projects | Previous Biosafety iGEM projects]]
|}
|}




Line 19: Line 17:
Here we report the idea we have, and how we could make them real.
Here we report the idea we have, and how we could make them real.


===Alginate beads===
=Alginate beads=
Here, we would place alginate beads, with controlled alginate matrix size into the capsule. The alginate beads contains theophylline, that would act as an activator of a [http://en.wikipedia.org/wiki/Riboswitch| riboswitch] that would repress gene expression [1]. This riboswitch would be fused into the 5'-UTR of the gene we want to repress (see figure 1). That gene would be one of the [http://en.wikipedia.org/wiki/Colicin| colicin] gene, that can diffuse and kill other ''Enterobacteriaceae''. The colicine gene is under Rpos promoter which is activated when bacteria is on stationary phase. So, bacteria  will die on stationary phase and when theophylline is under a certain threshold, thanks to its diffusion through beads and capsule.
Here, we would place alginate beads, with controlled alginate matrix size into the capsule. The alginate beads contains theophylline, that would act as an activator of a [http://en.wikipedia.org/wiki/Riboswitch| riboswitch] that would repress gene expression [1]. This riboswitch would be fused into the 5'-UTR of the gene we want to repress (see figure 1). That gene would be one of the [http://en.wikipedia.org/wiki/Colicin| colicin] gene, that can diffuse and kill other ''Enterobacteriaceae''. The colicine gene is under Rpos promoter which is activated when bacteria is on stationary phase. So, bacteria  will die on stationary phase and when theophylline is under a certain threshold, thanks to its diffusion through beads and capsule.


Line 25: Line 23:
<center>Figure 1 : Theophylline riboswitch, adapted from [1]</center>
<center>Figure 1 : Theophylline riboswitch, adapted from [1]</center>


== References ==  
= References =
1. Topp, S. & Gallivan, J.P. Riboswitches in unexpected places -€” A synthetic riboswitch in a protein coding region. RNA journal 2498-2503 (2008) [http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2590966/| Paper]
1. Topp, S. & Gallivan, J.P. Riboswitches in unexpected places -€” A synthetic riboswitch in a protein coding region. RNA journal 2498-2503 (2008) [http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2590966/| Paper]

Revision as of 08:00, 25 June 2012

Notebook Design Roadmap Meetings and to-dos Protocols Bibliography Previous Biosafety iGEM projects


Delay group

The aim of that subproject is to find a way to launch the destruction of either the construction or the organism after a certain laps of time.

Here we report the idea we have, and how we could make them real.

Alginate beads

Here, we would place alginate beads, with controlled alginate matrix size into the capsule. The alginate beads contains theophylline, that would act as an activator of a riboswitch that would repress gene expression [1]. This riboswitch would be fused into the 5'-UTR of the gene we want to repress (see figure 1). That gene would be one of the colicin gene, that can diffuse and kill other Enterobacteriaceae. The colicine gene is under Rpos promoter which is activated when bacteria is on stationary phase. So, bacteria will die on stationary phase and when theophylline is under a certain threshold, thanks to its diffusion through beads and capsule.

Figure 1 : Theophylline riboswitch, adapted from [1]

References

1. Topp, S. & Gallivan, J.P. Riboswitches in unexpected places -€” A synthetic riboswitch in a protein coding region. RNA journal 2498-2503 (2008) Paper