Team:Chiba/Experiments:/LuxR mutant
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+ | ==LuxR mutant (Under Planning== | ||
+ | ===Design=== | ||
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[[Image:Receiver switch mLuxR chiba.jpg|left]] | [[Image:Receiver switch mLuxR chiba.jpg|left]] | ||
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===Design=== | ===Design=== |
Revision as of 20:20, 29 October 2008
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LuxR mutant (Under Planning
Design
English:
日本語:私たちはmutated Receiverを用いることで、AHL感受性の違う2種類(WTと変異体)のレシーバーを用意し、delay-timeのバリエーションを増やした。
- a greater response to 3OC6HSL[http://authors.library.caltech.edu/5553/ (3)]
- a increase in sensitivity to 3OC12HSL[http://mic.sgmjournals.org/cgi/content/abstract/151/11/3589 (4)].
Receiver experiments details
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LuxR mutant (Under construction)
レシーバータンパク質であるLuxRに変異を入れることで応答感度を上下させる(5),(6)
LuxR mutant (Under Plannning)
Design
Collins et.al. described the hyper-sensitive variants of luxR to AHL.(Collins, C. H., Arnold, F. H. & Leadbetter, J. R. Directed evolution of Vibrio fischeri LuxR for increased sensitivity to a broad spectrum of acyl-homoserine lactones. Mol. Microbiol. 55, 712–723
LuxRに変異を入れることでLuxRのAHLに対する感受性を変えることができると報告されている。(1),(2)
- Ile45PheとするとAHLに対する感受性が約10倍上昇する(1)
- Leu42AlaとするとAHLに対する感受性が1/15に減少する(2)
- Leu42SerとするとAHLに対する感受性が1/1000に減少する(2)
Design
Collins et.al. described the hyper-sensitive variants of luxR to AHL.(Collins, C. H., Arnold, F. H. & Leadbetter, J. R. Directed evolution of Vibrio fischeri LuxR for increased sensitivity to a broad spectrum of acyl-homoserine lactones. Mol. Microbiol. 55, 712–723 (2005))
私たちはmutated Receiverを用いることで、AHL感受性の違う2種類(WTと変異体)のレシーバーを用意し、delay-timeのバリエーションを増やした。 (小林)
Method
- Sender
- [http://partsregistry.org/Part:BBa_S03623 BBa_S03623 (AHL auto inucer)]
- Receivers
- mutant LuxR Receiver
- WT LuxR Receiver ([http://partsregistry.org/Part:BBa_S03623 BBa_T9002 ])
LuxR mutantsとWT LuxRのディレイタイムはfollowing procedureによってanalyzeした。
- Transformed sender (Ptet-luxI), mutant LuxR Receiver (Ptet-mLuxR-Plux-GFP) and WT LuxR Receiver ()into E coli strains (BW⊿FliC)
- Inoculated Sender, WT Receiver (wild type luxR/BW⊿FliC) and mutated Receiver (1point mutation/BW⊿FliC) in liquid media for 12 h at 37℃.
- Inoculated again in liquid media upto about OD600=2 at 37℃
- Washed Senders and receiver.
- Mixed them. (Sender:Receiver=1000μL:1000μL)
- Incubated at 30°C.
- Measured intensity of green fluorescence at regular time intervals.
Result
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