Team:Chiba/Sender experiments/Senders(XL10Gold) T9002(JW1908)
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==design== | ==design== | ||
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===='''Receiver'''==== | ===='''Receiver'''==== |
Revision as of 17:46, 29 October 2008
Home | The Team | The Project | Parts Submitted to the Registry | Reference | Notebook | Acknowledgements |
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design
Receiver
- [http://partsregistry.org/Part:BBa_T9002 BBa_T9002 (Express GFP in response to AHL)]
Method
- Transformed Senders into E.coli strains(JW1908) and Receiver into E.coli strain(JW1908).
- Inoculated them independently in liquid media. Incubated at 37°C 12h
- Mixed them.
- Incubated at 37°C.
- Measured intensity of green fluorescence at regular time intervals.
Results
Reaction temparature:37°C
- センダーの培養液:500μL、レシーバの培養液:500μL
Reaction temparature:30°C
- センダーの培養液:500μL、レシーバの培養液:500μL
Reaction temparature:25°C
センダーの培養液:500μL、レシーバの培養液:500μL
Left:
- 蛍光強度が、30°C,37°Cに比べて極端に低く,Sendersの培養液を添加しなかった反応液と差がほとんどなかった.LuxI,LasI,RhlI,LuxR,GFPすべての発現量が減っていたためと考えた.
- LuxI,RhlIの培養液を,混ぜた反応液に比べて,LasIの培養液を混ぜた反応液は,最大蛍光強度が小さかった(約1/2).
Right:
- RhlIにLVAtagのついているものは,LVAtagのついていないものに比べて最大蛍光強度が小さかった.
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