Future Prospects

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<h4><font face="Broadway, Verdana">Possible Future Work</font></h4>
<h4><font face="Broadway, Verdana">Possible Future Work</font></h4>
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*Mutatuional nalysis must be performed to turn our plasmids into BioBricks and this includes mutations of Pst and other sites.
+
*Mutational nalysis must be performed to turn our plasmids into BioBricks and this includes mutations of Pst and other sites.
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*Work mustbe done to further understand the interesting formations we saw.
+
*Work must be done to further understand the interesting formations we saw.
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*More inductions must be done to understand exactly the fluorescence patrtern.
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*More inductions must be done to understand exactly the fluorescence pattern.
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*More understanding regarding stability of the protein products is required.
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*More understanding regarding stability of the protein products will be investigated.
<h4><font face="Broadway, Verdana">Possible Future Work in the field</font></h4>
<h4><font face="Broadway, Verdana">Possible Future Work in the field</font></h4>
Fos and Jun complementation and half YFP can have a variety of applications. One that we were thinking about was to fuse either Fos or Jun with an element of the flagella and that would stick to the membrane of a next cell, hence forming a chain. By fusing to different membrane proteins, eventually one could use bacteria as building blocks for entire strucures that work in synchrony. What still has to be worked out is their short life span.
Fos and Jun complementation and half YFP can have a variety of applications. One that we were thinking about was to fuse either Fos or Jun with an element of the flagella and that would stick to the membrane of a next cell, hence forming a chain. By fusing to different membrane proteins, eventually one could use bacteria as building blocks for entire strucures that work in synchrony. What still has to be worked out is their short life span.

Revision as of 12:54, 4 November 2006

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Contents

Fluorescence complementation

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Conclusions

Fos Jun Complementation is indeed happening. However, the induction of bacteria does not last a long time, breaks at room temperature within a few hours. Also it is not quite sure whether the cells are touching while the complementation takes place or are simply close to each other.

Possible Future Work

  • Mutational nalysis must be performed to turn our plasmids into BioBricks and this includes mutations of Pst and other sites.
  • Work must be done to further understand the interesting formations we saw.
  • More inductions must be done to understand exactly the fluorescence pattern.
  • More understanding regarding stability of the protein products will be investigated.

Possible Future Work in the field

Fos and Jun complementation and half YFP can have a variety of applications. One that we were thinking about was to fuse either Fos or Jun with an element of the flagella and that would stick to the membrane of a next cell, hence forming a chain. By fusing to different membrane proteins, eventually one could use bacteria as building blocks for entire strucures that work in synchrony. What still has to be worked out is their short life span.

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