Team:Cambridge/Description
From 2010.igem.org
(Difference between revisions)
(→Preliminary description) |
(REDIRECT) |
||
(3 intermediate revisions not shown) | |||
Line 1: | Line 1: | ||
+ | #REDIRECT [[Team:Cambridge]] | ||
+ | |||
{{:Team:Cambridge/Templates/header}} | {{:Team:Cambridge/Templates/header}} | ||
=Preliminary description= | =Preliminary description= | ||
Line 7: | Line 9: | ||
* Partially reconstruct the biosynthetic pathway of luciferin | * Partially reconstruct the biosynthetic pathway of luciferin | ||
* Create a biobrick for the induction of quiescence in ''E. coli'' | * Create a biobrick for the induction of quiescence in ''E. coli'' | ||
- | * Improve the existing switching mechanism for quiescence | + | * Improve the existing switching mechanism for quiescence using aptamers |
- | Our focus will shift over the course of the project, and objectives may be added and removed, but the end goal ideally is to have a strain of ''E. coli'' which will stop growing and start emitting light | + | Our focus will shift over the course of the project, and objectives may be added and removed, but the end goal ideally is to have a strain of ''E. coli'' which will stop growing and start emitting light on a trigger. |
+ | |||
+ | |||
+ | |||
+ | |||
+ | |||
+ | |||
+ | |||
+ | |||
+ | |||
+ | <html> </html> | ||
{{:Team:Cambridge/Templates/footer}} | {{:Team:Cambridge/Templates/footer}} |
Latest revision as of 22:31, 4 August 2010
- REDIRECT Team:Cambridge
Preliminary description
The Cambridge iGEM team will be investigating bioluminescence and quiescence in E. coli. Our broad targets will be to:
- Maximise light output from bacterial or firefly luciferase
- Characterise a device with a known transfer function between PoPs input and light output
- Partially reconstruct the biosynthetic pathway of luciferin
- Create a biobrick for the induction of quiescence in E. coli
- Improve the existing switching mechanism for quiescence using aptamers
Our focus will shift over the course of the project, and objectives may be added and removed, but the end goal ideally is to have a strain of E. coli which will stop growing and start emitting light on a trigger.