Team:Tokyo Tech/Experiment/Crosstalk Confirmation Assay

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<h1>Crosstalk Confirmation Assay
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<p style="line-height:0em; text-indent:0em;" name="top">Crosstalk Confirmation Assay</p>
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</h1>
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</div>
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<h3>1. Introduction
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<div class="box">
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</h3>
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<h1>1. Introduction </h1>
 +
 
<h2>
<h2>
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<p>Our goal in this project is to construct a system to suppress crosstalk by 3OC12HSL-LasR complex on lux promoter. We thought that we could prove that our system precisely works only after we obtain data of crosstalk happening by ourselves. Therefore, we confirmed that crosstalk is really happening by the following assay.
+
<p>Our goal in this project is to construct a system to circumvent crosstalk by 3OC12HSL-LasR complex on lux promoter. We thought that we could prove that our system precisely works only after we obtain data of crosstalk happening by ourselves. Therefore, we confirmed that crosstalk really happened by the following assay.
</p>
</p>
</h2>
</h2>
-
<h3>2. Summary of the experiment
+
<h1>2. Summary of the experiment </h1>
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</h3>
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<h2>
<h2>
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<p>Our purpose is to confirm 3OC12HSL-LasR complex really activates lux promoter. We prepared four plasmids shown in below (Fig. 4-1). We checked what would happen when we add intercellular molecules 3OC6HSL and 3OC12HSL.
+
<p>Our purpose is to confirm 3OC12HSL-LasR complex really activates lux promoter. We prepared four plasmid sets shown in below (Fig. 3-1-1). We checked what would happen when we added intercellular molecules 3OC6HSL and 3OC12HSL to these plasmid sets.
</p>
</p>
We prepared twelve conditions as follow.<br>
We prepared twelve conditions as follow.<br>
-
A-1) Culture containing Ptrc-lasR and Plas-GFP cell with 3OC6HSL induction<br>
+
<blockquote>
-
A-2) Culture containing Ptrc-lasR and Plas-GFP cell with 3OC12HSL induction<br>
+
<li>A-1) Culture containing Ptrc-<i>lasR</i> and Plas-<i>GFP</i> cell with 3OC6HSL induction
-
A-3) Culture containing PtrclasR and Plas-GFP cell with DMSO ( no induction)<br>
+
<li>A-2) Culture containing Ptrc-<i>lasR</i> and Plas-<i>GFP</i> cell with 3OC12HSL induction
-
<br>
+
<li>A-3) Culture containing Ptrc-<i>lasR</i> and Plas-<i>GFP</i> cell with DMSO ( no induction)
-
B-1) Culture containing Ptrc-lasR and Plux-GFP cell with 3OC6HSL induction<br>
+
<br><br>
-
B-2) Culture containing Ptrc-lasR and Plux-GFP cell with 3OC12HSL induction<br>
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<li>B-1) Culture containing Ptrc-<i>lasR</i> and Plux-<i>GFP</i> cell with 3OC6HSL induction
-
B-3) Culture containing Ptrc-lasR and Plux-GFP cell with DMSO (no induction)<br>
+
<li>B-2) Culture containing Ptrc-<i>lasR</i> and Plux-<i>GFP</i> cell with 3OC12HSL induction
-
<br>
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<li>B-3) Culture containing Ptrc-<i>lasR</i> and Plux-<i>GFP</i> cell with DMSO (no induction)
-
C-1) Culture containing Ptrc-luxR and Plas-GFP cell with 3OC6HSL induction<br>
+
<br><br>
-
C-2) Culture containing Ptrc-luxR and Plas-GFP cell with 3OC12HSL induction<br>
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<li>C-1) Culture containing Ptrc-<i>luxR</i> and Plas-<i>GFP</i> cell with 3OC6HSL induction
-
C-3) Culture containing Ptrc-luxR and Plas-GFP cell with DMSO (no induction)<br>
+
<li>C-2) Culture containing Ptrc-<i>luxR</i> and Plas-<i>GFP</i> cell with 3OC12HSL induction
-
<br>
+
<li>C-3) Culture containing Ptrc-<i>luxR</i> and Plas-<i>GFP</i> cell with DMSO (no induction)
-
D-1) Culture containing Ptrc-luxR and Plux-GFP cell with 3OC6HSL induction<br>
+
<br><br>
-
D-2) Culture containing Ptrc-luxR and Plux-GFP cell with 3OC12HSL induction<br>
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<li>D-1) Culture containing Ptrc-<i>luxR</i> and Plux-<i>GFP</i> cell with 3OC6HSL induction
-
D-3) Culture containing Ptrc-luxR and Plux-GFP cell with DMSO (no induction)<br>
+
<li>D-2) Culture containing Ptrc-<i>luxR</i> and Plux-<i>GFP</i> cell with 3OC12HSL induction
-
<br>
+
<li>D-3) Culture containing Ptrc-<i>luxR</i> and Plux-<i>GFP</i> cell with DMSO (no induction)
-
Positive control and negative control are similarly operated.<br>
+
<br><br>
 +
<li>Positive control and negative control are similarly operated.
 +
</blockquote>
</h2>
</h2>
-
<h3>3. Results of Prediction
+
 
-
</h3>
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<h1>3. Prediction</h1>
<h2>
<h2>
-
<p>If the GFP expression level of B-2) is as high as that of A-2), it is confirmed that 3OC12HSL-LasR complex crosstalk is occurred.
+
<p>If the GFP expression level of B-2) is as high as that of A-2), it shows that 3OC12HSL-LasR complex crosstalk happened.
</p>
</p>
</h2>
</h2>
-
<h3>4. Materials and Methods
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<h1>4. Materials and Methods </h1>
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</h3>
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<h3>4-1. Construction </h3>
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<font size="5">Construction  
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-
</font>
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<h2>
<h2>
-
<p>We used protein LasR or LuxR with constitutive promoter as regulator plasmids, and protein GFP under las promoter or lux promoter as reporter plasmids. Making pairs from 2 regulators and 2 repressors, we had to prepare 4 plasmid sets. These sets are transformed into different cells (Gray KM et al., 1994).
+
<p>We used <i>lasR</i> or <i>luxR</i> with constitutive promoter as a regulator and <i>GFP</i> understream of <i>las</i> promoter or <i>lux</i> promoter as a reporter. Making pairs from 2 regulators and 2 repressors, we had to prepare four plasmid sets. These sets are transformed into different cells (Gray KM et al., 1994).
</p>
</p>
-
[[Image:Titech2013_CrosstalkConfirmationAssay_3-1_1.jpg|500px|thumb|center|Fig. 4-1. Circuit of the crosstalk confirmation assay]]
+
[[Image:Titech2013_CrosstalkConfirmationAssay_3-1_1.jpg|500px|thumb|center|Fig. 3-1-1. Circuit of the crosstalk confirmation assay]]
-
<p>To construct plasmids in above, we ligated Ptrc-RBS-lasR-TT or Ptrc-RBS-luxR-TT as the regulator, and Plas-RBS-GFP-TT or Plux-RBS-GFP-TT as the reporter plasmid.<br><br>
+
<p>To construct plasmids above, we ligated Ptrc-RBS-<i>lasR</i>-TT or Ptrc-RBS-<i>luxR</i>-TT as the regulator, and Plas-RBS-<i>GFP</i>-TT or Plux-RBS-<i>GFP</i>-TT as the reporter plasmid.<blockquote>
-
•Regulator: pSB6A1-Ptrc-lasR / Reporter: pSB3K3-Plas-GFP (JM2.300)…Ptrc-lasR and Plas-GFP cell<br>
+
<li>Regulator: pSB6A1-Ptrc-<i>lasR</i> / Reporter: pSB3K3-Plas-<i>GFP</i> (JM2.300)…Ptrc-<i>lasR</i> and Plas-<i>GFP</i> cell
-
•Regulator: pSB6A1-Ptrc-lasR / Reporter: pSB3K3-Plux-GFP (JM2.300)…Ptrc-lasR and Plux-GFP cell<br>
+
<li>Regulator: pSB6A1-Ptrc-<i>lasR</i> / Reporter: pSB3K3-Plux-<i>GFP</i> (JM2.300)…Ptrc-<i>lasR</i> and Plux-<i>GFP</i> cell
-
•Regulator: pSB6A1-Ptrc-luxR / Reporter: pSB3K3-Plas-GFP (JM2.300)…Ptrc-luxR and Plas-GFP cell<br>
+
<li>Regulator: pSB6A1-Ptrc-<i>luxR</i> / Reporter: pSB3K3-Plas-<i>GFP</i> (JM2.300)…Ptrc-<i>luxR</i> and Plas-<i>GFP</i> cell
-
•Regulator: pSB6A1-Ptrc-luxR / Reporter: pSB3K3-Plux-GFP (JM2.300)…Ptrc-luxR and Plux-GFP cell<br>
+
<li>Regulator: pSB6A1-Ptrc-<i>luxR</i> / Reporter: pSB3K3-Plux-<i>GFP</i> (JM2.300)…Ptrc-<i>luxR</i> and Plux-<i>GFP</i> cell
-
•pSB6A1-Ptet-GFP(JM2.300)…positive control<br>
+
<li>pSB6A1-Ptet-<i>GFP</i> (JM2.300)…positive control
-
•pSB6A1-Promoter less-GFP(JM2.300)…negative control<br>
+
<li>pSB6A1-Promoterless-<i>GFP</i> (JM2.300)…negative control
-
</p></h2>
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</blockquote></p></h2>
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<font size="5">Strain</font>
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<h3>4-2. Strain </h3>
<h2>
<h2>
-
&nbsp;&nbsp;&nbsp;•JM2.300
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&nbsp;&nbsp;&nbsp;JM2.300
</h2>
</h2>
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<font size="5">
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<h3>4-3. Protocol </h3>
-
Protocol</font>
+
<h2>
<h2>
-
<p>
+
<blockquote>
-
1. O/N -> FC -> Induction<br>
+
<b>1. O/N -> FC -> Induction</b>
-
1.1 Prepare overnight culture of each cell (GFP posi, GFP nega, sample) at 37°C for 12 h. (=> O/N)<br>
+
</blockquote>
-
1.2 Take 30 microL (from GFP posi, GFP nega, sample) of the overnight culture of inducer cell into LB (3 mL) + antibiotics (Amp 50 microg/mL+ Kan 30 microg/mL).  (=> Fresh Culture)<br>
+
 
-
1.3 Incubate the flesh culture of cells (GFP posi, GFP nega, sample) until the observed OD600 reaches around 0.50.<br>
+
<p><blockquote>
-
1.4 Dilute the flesh culture in 1:5 by the following conditions:<br>
+
1.1 Prepare overnight culture of each cell (GFP posi, GFP nega, and samples) at 37°C for 12 h. <br> (=> O/N)
-
...LB (3 mL) + antibiotics (Amp 50 microg/mL + Kan 30 microg/mL) + 5 microM 3OC6HSL (3 microL)<br>
+
</blockquote></p>
-
...LB (3 mL) + antibiotics (Amp 50 microg/mL + Kan 30 microg/mL) + 5 microM 3OC12HSL (3 microL)<br>
+
<p><blockquote>
-
...LB (3 mL) + antibiotics (Amp 50 microg/mL + Kan 30 microg/mL) + 5 microM DMSO (3 microL)<br>
+
1.2 Take 30 µL (from GFP posi, GFP nega, sample) of the overnight culture of inducer cell into LB (3 mL) + antibiotics (Amp 50 µg/mL+ Kan 30 µg/mL).<br> (=> Fresh Culture)
-
1.5 Incubate the flesh culture of diluted inducer cell for 4 h at 37°C.  (=> Induction)<br>
+
</blockquote></p>
-
</p>
+
<p><blockquote>
 +
1.3 Incubate the flesh culture of cells (GFP posi, GFP nega, sample) until the observed OD600 reaches around 0.50.
 +
</blockquote></p>
 +
<p><blockquote>
 +
1.4 Dilute the flesh culture by the following conditions:
 +
<blockquote>LB (3 mL) + antibiotics (Amp 50 µg/mL + Kan 30 µg/mL)<br> + 5 µM 3OC6HSL (3 µL)</blockquote>
 +
<blockquote>LB (3 mL) + antibiotics (Amp 50 µg/mL + Kan 30 µg/mL)<br> + 5 µM 3OC12HSL (3 µL)</blockquote>
 +
<blockquote>LB (3 mL) + antibiotics (Amp 50 µg/mL + Kan 30 µg/mL)<br> + 5 µM DMSO (3 µL)</blockquote>
 +
</blockquote></p>
 +
 
 +
<p><blockquote>
 +
1.5 Incubate the flesh culture of diluted inducer cell for 4 h at 37°C.<br> (=> Induction)
 +
</blockquote></p>
<br>
<br>
-
<p>
+
 
-
2. Measurement (Flow cytometer)<br>
+
<blockquote>
-
2.1 Measure all samples' OD600.<br>
+
<b>2. Measurement (Flow cytometer)</b>
-
2.2 Dilute all samples with 1X PBS to keep OD600 in the range from 0.2 to 0.5.<br>
+
</blockquote>
-
2.3 Take 1 mL (from all samples) into a disposal tube (for flow cytometer).<br>
+
 
-
2.4 Centrifuge them at 9000 g, 4°C, 1 min. and take their supernatant away.<br>
+
<p><blockquote>
-
2.5 Suspend all samples with 1 mL 1X PBS.<br>
+
2.1 Measure all samples' OD600.
-
2.6 Measure all samples.<br>
+
</blockquote></p>
-
2.7 Save and organize data.<br>
+
<p><blockquote>
-
</p>
+
2.2 Dilute all samples with 1X PBS to keep OD600 in the range from 0.2 to 0.5.
 +
</blockquote></p>
 +
<p><blockquote>
 +
2.3 Take 1 mL (from all samples) into a disposable tube (for flow cytometer).
 +
</blockquote></p>
 +
<p><blockquote>
 +
2.4 Centrifuge them at 9,000g, 4°C, 1 min. and take their supernatant away.
 +
</blockquote></p>
 +
<p><blockquote>
 +
2.5 Suspend all samples with 1 mL 1X PBS.
 +
</blockquote></p>
 +
<p><blockquote>
 +
2.6 Measure all samples.
 +
</blockquote></p>
 +
<p><blockquote>
 +
2.7 Save and organize data.
 +
</blockquote></p>
</h2>
</h2>
-
<h3>5. Result of the assay
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<h1>5. Results of the assay </h1>
-
</h3>
+
-
[[Image:Titech2013_CrosstalkConfirmationAssay_3-1_2.jpg|500px|thumb|center|Fig. 5-1. Crosstalk confirmation result]]
+
-
 
+
<h2>
<h2>
-
<p>From above chart (Fig. 5-1), it turns out the following.  las promoter is activated by 3OC12HSL-LasR complex.  Similarly, lux promoter is activated by 3OC12HSL-LasR complex, too.  From this result we confirm that crosstalk by 3OC12HSL-LasR complex really happens.
+
[[Image:Titech2013_CrosstalkConfirmationAssay_3-1_2.jpg|500px|thumb|center|Fig. 3-1-2. Crosstalk confirmation results]]
-
</p>
+
</h2>
</h2>
-
<h3>6. Reference
 
-
</h3>
 
<h2>
<h2>
-
1. Gray KM, Passador L (1994) Interchangeability and specificity of components from the quorum-sensing regulatory systems of Vibrio fischeri and Pseudomonas aeruginosa.  Journal of bacteriology 176(10): 3076–3080.
+
<p>Fig. 3-1-2 shows the following, <i>las</i> promoter is activated by 3OC12HSL-LasR complex.  Similarly, <i>lux</i> promoter is activated by 3OC12HSL-LasR complex, too.  From this result we confirmed that crosstalk by 3OC12HSL-LasR complex really happened.
 +
</p>
 +
</h2>
 +
<h1>6. Reference </h1>
 +
<h2><OL><LI>
 +
Gray KM, Passador L (1994) Interchangeability and specificity of components from the quorum-sensing regulatory systems of Vibrio fischeri and Pseudomonas aeruginosa.  Journal of bacteriology 176(10): 3076–3080.</LI></OL>
</h2>
</h2>
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-
 
-
 
-
 
-
 
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</div><br>
</div><br>
 +
<html><div align="center"><a href="https://2013.igem.org/Team:Tokyo_Tech/Experiment/Crosstalk_Confirmation_Assay#top"><img src="https://static.igem.org/mediawiki/2013/f/f0/Titeh2013_backtotop.png" width="200px"></a></div></html>
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Latest revision as of 02:59, 29 October 2013


Crosstalk Confirmation Assay

Contents

1. Introduction

Our goal in this project is to construct a system to circumvent crosstalk by 3OC12HSL-LasR complex on lux promoter. We thought that we could prove that our system precisely works only after we obtain data of crosstalk happening by ourselves. Therefore, we confirmed that crosstalk really happened by the following assay.

2. Summary of the experiment

Our purpose is to confirm 3OC12HSL-LasR complex really activates lux promoter. We prepared four plasmid sets shown in below (Fig. 3-1-1). We checked what would happen when we added intercellular molecules 3OC6HSL and 3OC12HSL to these plasmid sets.

We prepared twelve conditions as follow.

  • A-1) Culture containing Ptrc-lasR and Plas-GFP cell with 3OC6HSL induction
  • A-2) Culture containing Ptrc-lasR and Plas-GFP cell with 3OC12HSL induction
  • A-3) Culture containing Ptrc-lasR and Plas-GFP cell with DMSO ( no induction)

  • B-1) Culture containing Ptrc-lasR and Plux-GFP cell with 3OC6HSL induction
  • B-2) Culture containing Ptrc-lasR and Plux-GFP cell with 3OC12HSL induction
  • B-3) Culture containing Ptrc-lasR and Plux-GFP cell with DMSO (no induction)

  • C-1) Culture containing Ptrc-luxR and Plas-GFP cell with 3OC6HSL induction
  • C-2) Culture containing Ptrc-luxR and Plas-GFP cell with 3OC12HSL induction
  • C-3) Culture containing Ptrc-luxR and Plas-GFP cell with DMSO (no induction)

  • D-1) Culture containing Ptrc-luxR and Plux-GFP cell with 3OC6HSL induction
  • D-2) Culture containing Ptrc-luxR and Plux-GFP cell with 3OC12HSL induction
  • D-3) Culture containing Ptrc-luxR and Plux-GFP cell with DMSO (no induction)

  • Positive control and negative control are similarly operated.
  • 3. Prediction

    If the GFP expression level of B-2) is as high as that of A-2), it shows that 3OC12HSL-LasR complex crosstalk happened.

    4. Materials and Methods

    4-1. Construction

    We used lasR or luxR with constitutive promoter as a regulator and GFP understream of las promoter or lux promoter as a reporter. Making pairs from 2 regulators and 2 repressors, we had to prepare four plasmid sets. These sets are transformed into different cells (Gray KM et al., 1994).

    Fig. 3-1-1. Circuit of the crosstalk confirmation assay

    To construct plasmids above, we ligated Ptrc-RBS-lasR-TT or Ptrc-RBS-luxR-TT as the regulator, and Plas-RBS-GFP-TT or Plux-RBS-GFP-TT as the reporter plasmid.

  • Regulator: pSB6A1-Ptrc-lasR / Reporter: pSB3K3-Plas-GFP (JM2.300)…Ptrc-lasR and Plas-GFP cell
  • Regulator: pSB6A1-Ptrc-lasR / Reporter: pSB3K3-Plux-GFP (JM2.300)…Ptrc-lasR and Plux-GFP cell
  • Regulator: pSB6A1-Ptrc-luxR / Reporter: pSB3K3-Plas-GFP (JM2.300)…Ptrc-luxR and Plas-GFP cell
  • Regulator: pSB6A1-Ptrc-luxR / Reporter: pSB3K3-Plux-GFP (JM2.300)…Ptrc-luxR and Plux-GFP cell
  • pSB6A1-Ptet-GFP (JM2.300)…positive control
  • pSB6A1-Promoterless-GFP (JM2.300)…negative control
  • 4-2. Strain

       JM2.300

    4-3. Protocol

    1. O/N -> FC -> Induction

    1.1 Prepare overnight culture of each cell (GFP posi, GFP nega, and samples) at 37°C for 12 h.
    (=> O/N)

    1.2 Take 30 µL (from GFP posi, GFP nega, sample) of the overnight culture of inducer cell into LB (3 mL) + antibiotics (Amp 50 µg/mL+ Kan 30 µg/mL).
    (=> Fresh Culture)

    1.3 Incubate the flesh culture of cells (GFP posi, GFP nega, sample) until the observed OD600 reaches around 0.50.

    1.4 Dilute the flesh culture by the following conditions:
    LB (3 mL) + antibiotics (Amp 50 µg/mL + Kan 30 µg/mL)
    + 5 µM 3OC6HSL (3 µL)
    LB (3 mL) + antibiotics (Amp 50 µg/mL + Kan 30 µg/mL)
    + 5 µM 3OC12HSL (3 µL)
    LB (3 mL) + antibiotics (Amp 50 µg/mL + Kan 30 µg/mL)
    + 5 µM DMSO (3 µL)

    1.5 Incubate the flesh culture of diluted inducer cell for 4 h at 37°C.
    (=> Induction)


    2. Measurement (Flow cytometer)

    2.1 Measure all samples' OD600.

    2.2 Dilute all samples with 1X PBS to keep OD600 in the range from 0.2 to 0.5.

    2.3 Take 1 mL (from all samples) into a disposable tube (for flow cytometer).

    2.4 Centrifuge them at 9,000g, 4°C, 1 min. and take their supernatant away.

    2.5 Suspend all samples with 1 mL 1X PBS.

    2.6 Measure all samples.

    2.7 Save and organize data.

    5. Results of the assay

    Fig. 3-1-2. Crosstalk confirmation results

    Fig. 3-1-2 shows the following, las promoter is activated by 3OC12HSL-LasR complex. Similarly, lux promoter is activated by 3OC12HSL-LasR complex, too. From this result we confirmed that crosstalk by 3OC12HSL-LasR complex really happened.

    6. Reference

    1. Gray KM, Passador L (1994) Interchangeability and specificity of components from the quorum-sensing regulatory systems of Vibrio fischeri and Pseudomonas aeruginosa. Journal of bacteriology 176(10): 3076–3080.