Team:EPF Lausanne/Project asaia

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In this page we want to summarize the main properties coming out from our experiments.
In this page we want to summarize the main properties coming out from our experiments.
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=New Chassis=
= Doubling Time =
= Doubling Time =

Revision as of 16:53, 25 October 2010



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One of the main goals of our project is to establish Asaia as a new chassis. Hence, we will make a lot of characterization experiment, so that other teams will be able to quickly and efficiently engineer new and more potent Asaia strains.

Among the bacteria that naturally live in the mosquito's intestinal tract, we chose the bacteria Asaia because of its high rate of transmission between mosquitoes. Indeed, it seems that Asaia is transmitted horizontally (from one mosquito to another) but also vertically (from parent to offspring). These properties of Asaia make it a really good candidate for our project. Indeed, a lot of mosquitoes would have to be infected with our engineered Asaia before any significant reductions of malaria transmission could occur.

We believe it could be a really good instrument in the fight against malaria and other mosquito-borne diseases.


In this page we want to summarize the main properties coming out from our experiments.

Contents

New Chassis

Doubling Time

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We measured the growth curve of Asaia at differents pH (ph2-pH7) and at 30°C and 37°C to figure out the optimal growth conditions. We found that the optimal Temperature is 30°C, and the optimal pH is 5. At this conditions we measured a doubling time of 2h40min.


Graph growth curve2.jpg

Antibiotic resistance

We characterized Asaia's properties against various antibiotics. We had noticed previously that Asaia is naturally resistant to Amphicillin (Amp) and Chloroamphenicol (Cm) to the standard concentrations for E. coli. We tested the behaviour of Asaia to 7 others antibiotic like Tetracyclin (Tet) and Kanamycin (Kan) at various concentrations.



Graph Resistance2.jpg

Compatibility with E. coli

We noticed that the Origin of replication of Asaia is compatible with E. coli, but the opposite is not true. The origin of replication of E. coli isn't compatible with Asaia. Thus, we had to add Asaia's origin of replication to all our parts so they would function in both Asaia and E. coli







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