Team:Chiba/Sender experiments/Senders(XL10Gold) T9002(JW1908)

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Revision as of 17:53, 29 October 2008

Method

1. Transformed Senders into E.coli strains(JW1908) and Receiver into E.coli strain(JW1908).
2. Inoculated them independently in liquid media. Incubated at 37°C 12h
3. Mixed them.
4. Incubated at 37°C.
5. Measured intensity of green fluorescence at regular time intervals.

more details...

Results

Reaction temparature:37°C

• センダーの培養液：500μL、レシーバの培養液：500μL

Fig.　　
E.coli strain,BBa_K084007:XL10Gold,BBa_T9002:JW1908,37°C,Receiver cells/Sender cells = 1.

Fig.　　
E.coli strain,BBa_K084007:XL10Gold,BBa_T9002:JW1908,37°C,Receiver cells/Sender cells = 1.

Fig.　　
E.coli strain,BBa_K084007:XL10Gold,BBa_T9002:JW1908,37°C,Receiver cells/Sender cells = 1.

Reaction temparature:30°C

• センダーの培養液：500μL、レシーバの培養液：500μL

Fig.　　
E.coli strain,BBa_K084007:XL10Gold,BBa_T9002:JW1908,30°C,Receiver cells/Sender cells = 1.

Fig.　　
E.coli strain,BBa_K084007:XL10Gold,BBa_T9002:JW1908,30°C,Receiver cells/Sender cells = 1.

Reaction temparature:25°C

センダーの培養液：500μL、レシーバの培養液：500μL

Fig.
E.coli strain,Senders:XL10Gold,BBa_T9002:JW1908,25°C,Receiver cells/Sender cells = 1.

Fig.
　E.coli strain,Senders:XL10Gold,BBa_T9002:JW1908,25°C,Receiver cells/Sender cells = 1.

Left:

1. 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.
2. 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:

1. 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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