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

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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.


    • 結果
      • LuxI(BBa_K084012),RhlI(BBa_K084008)は活性。蛍光強度は500に達した。LasI(BBa_K084007)は目標としている蛍光強度200に届かなかった。
    • 考察
    • 結果
    • 考察
    • 結果
    • 考察

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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