Team:Chiba/Project

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*We created a mutant library of LuxR (size = 8000) with the use of error-prone PCR and incorporated the resulting coding regions into expression vectors.
*We created a mutant library of LuxR (size = 8000) with the use of error-prone PCR and incorporated the resulting coding regions into expression vectors.
*The vectors were then transformed into a strain of E.coli BW1226 cells harboring plux-gfp and grew approximately 200 colonies.
*The vectors were then transformed into a strain of E.coli BW1226 cells harboring plux-gfp and grew approximately 200 colonies.
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*The colonies were lifted off the agar plate with a nitrocellulose filter and transfered to a plate containing AHL in order to observe the evolution of GFP fluorescence over time (Fig. 3).
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*The colonies were lifted off the agar plate with a nitrocellulose filter and transfered to a plate containing AHL in order to observe the evolution of GFP fluorescence over time (Fig. 4).
*We selected 13 colonies that were slow to display fluorescence, which we designated as delyaed-LuxR mutants.
*We selected 13 colonies that were slow to display fluorescence, which we designated as delyaed-LuxR mutants.
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[[Image:chiba09_exp2.png|frame|center|Fig. 3 ]]
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[[Image:chiba09_exp2.png|frame|center|Fig. 4 display fluorescence]]
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Revision as of 23:33, 21 October 2009

E.coli Time Manager


Home The Team Parts Reference Notebook Protocols Links Acknowledgements Contact

The Project

1, Introduction

2, Project Design

3, Experiments, Results & Discussion

3-1, Making LuxR Mutants

3-2, Characterization of LuxR Mutants

3-3, Demonstration

5, Conclusions

Introduction

Implementing a "Timer" Function!

  • Our project is to make a sort of "timer", where gene activation is triggered after a certain time.
  • Our approach to this goal is to create a series of transcription factors (TFs) that can be activated by the same inducer molecule but with a different sensitivity. In an environment where the inducer concentration gradually levels up, these TFs switches on one by one according to the order of sensitivity.
  • We believe such collection of such TF variants would be useful for the timing control in biological function at will, and thereby contribute to the synthetic biology & iGEM community.
  • Using a set of TF variants, we aimed to draw an "animated picture": a picture that pop up one by one.

Fig. 1 Completion drawing of our bacterial timer

Project Design

Fig. 2 Function of LuxR :(1)LuxR protein generation, (2)AHL binding domain, (3)dimerization, (4)DNA binding domain
  • 私たちはタイマーを創るためにLuxRを利用する。
  • LuxRはcell-cellcommunicationで使われるタンパクである。
  • LuxRは細胞内でFig. 2にしめすとおりに働く。
  • 私たちはLuxRに変異を入れることで、スイッチングのdelayを数種類入れられると考えた。


Experiments, Results & Discussion

Making delayed-LuxR mutants

Experiments

Fig. Y Directed evolution to get some delayed-LuxR mutants
  • We created a mutant library of LuxR (size = 8000) with the use of error-prone PCR and incorporated the resulting coding regions into expression vectors.
  • The vectors were then transformed into a strain of E.coli BW1226 cells harboring plux-gfp and grew approximately 200 colonies.
  • The colonies were lifted off the agar plate with a nitrocellulose filter and transfered to a plate containing AHL in order to observe the evolution of GFP fluorescence over time (Fig. 4).
  • We selected 13 colonies that were slow to display fluorescence, which we designated as delyaed-LuxR mutants.
Fig. 4 display fluorescence


  • 変異が入った場所は以下の通り。
Fig.
  • リガンド（AHL）結合ドメイン／DNA結合ドメイン、どちらに変異が入っても、Delay変異体の表現型を与えた。

Characterization of LuxR Mutants

Fig. Characterization of LuxR Mutants

Experiments

  1. LuxR WT, Mutant（13種）とpLux-GFPのプラスミドが2つトランスフォーメーションされたJW1226株を12h@37℃液体培養。
  2. Cultureを48ピンでNCフィルタへ植菌し、フィルタを固体培地にのせて12h@37℃で培養。
  3. AHLの濃度を0, 1, 10, 100, 1000 nMでふった固体培地に、NCフィルタを移動。
  4. この時を測定開始点とし、30分毎に4時間蛍光の上がり方を目視で確認。
  • フナコシのUVGL-58のlong waveは365 nm


Results and Discussion

  • pickした13個のクローンの転写活性化速度を，再度transformして確認し，最終的に8個の速度バリエーションのluxR変異体を得た。
100 nM培地での応答の遅れについての結果
Fig.時間依存
  • 一番GFP強度の上がり方がばらついた100 nM　AHL培地の写真。
  • 応答速度の異なる以下のようなタイプのMutantを確認できた。
    • スイッチが入るタイミングが違うモノ
    • スイッチが入ってもなかなか蛍光強度が上がらないモノ


ＡＨＬ濃度を振った場合の、６ｈ後の蛍光強度の差についての結果
Fig.濃度依存
  • スイッチングが起こる濃度がＷＴと異なるMutantを得ることができた。
  • 変異がはいっている部分がほとんど同じである#4と#7の間に、以下のような差が見られた。
    • 4 : 10 nM AHLで蛍光がみられる。
    • 7 : 100 nM AHLで蛍光がみられる。


Demonstration

  1. Double-Transformed (pUC-LuxR Mutants series-ColE1 and pLux-GFPuv-P15A) and cultured on LB-Amp-Cm-plate. (37°C,12h)
  2. Pick and cultured in 10mL of LB-Amp-Cm (37°C,12h).
  3. Drawing picture with those liquid culture on nitrocellulose Filter.
  4. Those nitrocellulose Filter placed on LB-Amp-Cm-plate.
  5. Cultured at 37°C, 12h.
  6. Transfer pictures on special plate.
  7. Exposed to UV (385nm) light once every 30 minutes to observe GFP fluorescence.

T=0

T=130 min

T=150 min

T=180 min

T=230 min

T=260 min

T=300 min

T=360 min


  • For the determination of best condition for E coli painting, Click here!

Conclusions

  • By using error-prone PCR, we have created a LuxR library.
  • With a simple and convenient screening method, we have isolated various LuxR mutants which confer delayed switching behavior in GFP signals.
  • By introducing these LuxR variants together with reporter genes (such as GFP) under the control of Lux promoter, we created bacteria 'ink's that develop their color with unique delay-time.
  • We conducted painting with these bacteria inks thereby created animated pictures.
  • Characterization of LuxR mutants is ongoing. But our preliminary data showed that some of the variants turned out to be the one with less sensitivity to AHLs, and others seemed to be as sensitive as wild-type LuxR but seemed less efficient somewhere in the downstream process.
  • We created variety of Biobricks during the course of this projects. Some of them are characterized and sent to the HQ, and many more are almost ready for shipping!
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