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Team:Groningen/Future
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* Reusing the bacteria by moving them to another container and using Sb to accelerate As efflux ([[Team:Groningen/Literature#Meng2004|Meng2004]]). | * Reusing the bacteria by moving them to another container and using Sb to accelerate As efflux ([[Team:Groningen/Literature#Meng2004|Meng2004]]). | ||
* Demonstrating the presence of arsenic by putting Luciferase under regulation of ArsR. | * Demonstrating the presence of arsenic by putting Luciferase under regulation of ArsR. | ||
| + | * Use hydrophobic chaplin proteins to keep the bacteria floating on the surface of the medium (it won't help them to start floating) | ||
| + | ** This might be used to start bouyancy with GVP and keep them on the surface of the medium with these proteins. These proteins origin from Gram positive bacteria, which may cause problems. Information may be asked from: Dennis Klaassen (MolMic). | ||
Revision as of 10:04, 23 July 2009
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Ideas for future work (TODO references):
- Reusing the bacteria by moving them to another container and using Sb to accelerate As efflux (Meng2004).
- Demonstrating the presence of arsenic by putting Luciferase under regulation of ArsR.
- Use hydrophobic chaplin proteins to keep the bacteria floating on the surface of the medium (it won't help them to start floating)
- This might be used to start bouyancy with GVP and keep them on the surface of the medium with these proteins. These proteins origin from Gram positive bacteria, which may cause problems. Information may be asked from: Dennis Klaassen (MolMic).
Retrieved from "http://2009.igem.org/Team:Groningen/Future"
