Difference between revisions of "Team:McMasterU/DNAzyme"

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<div class = "band">
 
<h1>Protocols</h1>
 
<h1>Protocols</h1>
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<br>
 
 
<h2>Testing Fluorescence of Bacterial Plates</h2>
 
<h2>Testing Fluorescence of Bacterial Plates</h2>
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<strong>Date:</strong> May 18
+
<p><strong>Date:</strong> May 18 <br /> <strong>Reagents:</strong></p>
−
<br>
+
<ul>
−
<strong>Reagents:</strong>
+
 
<li>3x DNAzyme stock: 13.35 uL (200nM final concentration)</li>
 
<li>3x DNAzyme stock: 13.35 uL (200nM final concentration)</li>
 
<li>2x selection buffer (150uL)</li>
 
<li>2x selection buffer (150uL)</li>
 
<li>dH2O: 136.65uL</li>
 
<li>dH2O: 136.65uL</li>
−
<br>
+
</ul>
−
 
+
<p><br /> <strong>Protocol:</strong></p>
−
<strong>Protocol:</strong>
+
 
<ol>
 
<ol>
 
<li>The DNAzyme stock solution in the previous slide was created in an Eppendorf tube.</li>
 
<li>The DNAzyme stock solution in the previous slide was created in an Eppendorf tube.</li>
 
<li>100 uL of DNAzyme stock solution was pipetted into Plates 1,2, and 3. A hockey stick was used to spread the solution over the surface.</li>
 
<li>100 uL of DNAzyme stock solution was pipetted into Plates 1,2, and 3. A hockey stick was used to spread the solution over the surface.</li>
 
<li>Plates 1-3 were left for 5 minutes to dry (with plate lids on).</li>
 
<li>Plates 1-3 were left for 5 minutes to dry (with plate lids on).</li>
−
<li>A disposable inoculation loop was used to streak nothing onto Plates 1 and 5. </li>
+
<li>A disposable inoculation loop was used to streak nothing onto Plates 1 and 5.</li>
 
<li>Disposable inoculation loops were used to streak E. coli on Plates 2 and 4 and B. subtilis on Plate 3.</li>
 
<li>Disposable inoculation loops were used to streak E. coli on Plates 2 and 4 and B. subtilis on Plate 3.</li>
 
<li>Plates were placed upside down in an incubator at 37℃.</li>
 
<li>Plates were placed upside down in an incubator at 37℃.</li>
 
</ol>
 
</ol>
−
 
+
<p><strong>Plates Segmentation:</strong></p>
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<strong>Plates Segmentation:</strong>
+
<ul>
 
<li>only DNAzyme</li>
 
<li>only DNAzyme</li>
 
<li>E. coli with DNAzyme</li>
 
<li>E. coli with DNAzyme</li>
Line 26: Line 28:
 
<li>E. coli only</li>
 
<li>E. coli only</li>
 
<li>Nothing</li>
 
<li>Nothing</li>
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+
</ul>
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<br><br>
+
<p><br /><br /></p>
−
 
+
 
<h2>Fluorophore Concentrations</h2>
 
<h2>Fluorophore Concentrations</h2>
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<strong>Date:</strong> May 23
+
<p><strong>Date:</strong> May 23 <br /> <strong>Reagents:</strong></p>
−
<br>
+
<ul>
−
<strong>Reagents:</strong>
+
 
<li>FDNA</li>
 
<li>FDNA</li>
 
<li>dH2O</li>
 
<li>dH2O</li>
Line 38: Line 38:
 
<li>LB agar plates</li>
 
<li>LB agar plates</li>
 
<li>UV box</li>
 
<li>UV box</li>
−
 
+
</ul>
−
<br>
+
<p><br /> <strong>Protocol:</strong></p>
−
<strong>Protocol:</strong>
+
 
<ol>
 
<ol>
 
<li>7 different concentrations of fluorescent DNA with the fluorophore were created. These concentrations were 0, 100, 250, 500, 1000, 2500, and 5000 nM.</li>
 
<li>7 different concentrations of fluorescent DNA with the fluorophore were created. These concentrations were 0, 100, 250, 500, 1000, 2500, and 5000 nM.</li>
 
<li>10 uL from each of the concentrations were dropped into the middle of a quadrant on a plate.</li>
 
<li>10 uL from each of the concentrations were dropped into the middle of a quadrant on a plate.</li>
 
<li>A hockey stick was used on each quadrant to spread the fluorescent DNA.
 
<li>A hockey stick was used on each quadrant to spread the fluorescent DNA.
−
<ul>*Did not spread because the dot of solution had set into the agar and therefore did not spread with the hockey stick. This time we dotted the plates and immediately used the hockey stick after putting each dot onto each quadrant.</ul></li>
+
<ul>*Did not spread because the dot of solution had set into the agar and therefore did not spread with the hockey stick. This time we dotted the plates and immediately used the hockey stick after putting each dot onto each quadrant.</ul>
 +
</li>
 
</ol>
 
</ol>
−
 
+
<p><br /><br /></p>
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<br><br>
+
<h2>Optimizing Concentrations &amp; Cleavage</h2>
−
 
+
<p><br /> <strong>Date of Experiment:</strong> May 26 </p>
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<h2>Optimizing Concentrations & Cleavage</h2>
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−
<br>
+
−
<Strong>Date of Experiment:</strong> May 26
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−
<br>
+
 
<h3>Materials/Reagents:</h3>
 
<h3>Materials/Reagents:</h3>
 
<ul>
 
<ul>
 
<li>3 agar plates</li>
 
<li>3 agar plates</li>
−
</ul>
 
 
<li>100uL of:
 
<li>100uL of:
 
<ul>
 
<ul>
 
<li>2.5uM FDNA, 5.0uM FDNA</li>
 
<li>2.5uM FDNA, 5.0uM FDNA</li>
 
<li>2.5uM FQ substrate (RS28), 5.0uM FQ substrate (RS28)</li>
 
<li>2.5uM FQ substrate (RS28), 5.0uM FQ substrate (RS28)</li>
−
<li>Gycerol stock of E.coli</li></ul>
+
<li>Gycerol stock of E.coli</li>
−
<br>
+
</ul>
−
 
+
<br />
 
<h3>Protocol:</h3>
 
<h3>Protocol:</h3>
−
<br>
+
<br />
 
<ol>
 
<ol>
 
<li>3 plates were split into quadrants with 25uL FDNA and FQ substrate stock on each quadrant:
 
<li>3 plates were split into quadrants with 25uL FDNA and FQ substrate stock on each quadrant:
Line 73: Line 68:
 
<li>Plate 2 (2.5uM): FQ substrate, negative, FQ substrate + 0.5uM 0.2uM NaOh, FDNA</li>
 
<li>Plate 2 (2.5uM): FQ substrate, negative, FQ substrate + 0.5uM 0.2uM NaOh, FDNA</li>
 
<li>Plate 3 (5.0uM): FQ substrate, negative, FQ substrate with 0.5uM 0.2M NaOH, FDNA</li>
 
<li>Plate 3 (5.0uM): FQ substrate, negative, FQ substrate with 0.5uM 0.2M NaOH, FDNA</li>
−
</ul></li>
+
</ul>
 +
</li>
 
<li>E. coli was streaked onto its designated quadrants on plate 1</li>
 
<li>E. coli was streaked onto its designated quadrants on plate 1</li>
 
<li>Plate 2 and 3 were checked under blue light for fluorescence after NaOH applied for 15 minutes</li>
 
<li>Plate 2 and 3 were checked under blue light for fluorescence after NaOH applied for 15 minutes</li>
Line 82: Line 78:
 
<li>520 BP CY2, ECL+, Blue FAM Emission Filter</li>
 
<li>520 BP CY2, ECL+, Blue FAM Emission Filter</li>
 
<li>Emission Filter</li>
 
<li>Emission Filter</li>
−
</ul></li>
+
</ul>
 +
</li>
 
</ol>
 
</ol>
−
 
 
<h2>Experiment 1.a - M9 vs LB Autofluorescence via Agar Thickness</h2>
 
<h2>Experiment 1.a - M9 vs LB Autofluorescence via Agar Thickness</h2>
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<br>
+
<br /> <strong>Date of Experiment:</strong> June 12-13 <br /> <strong>Goal:</strong> Testing different thicknesses of M9 and LB plates to find the minimal autofluorescence. Determine the optimal medium (M9 vs LB) and the optimal volume/thickness <br /> <strong>Different thicknesses by volume spread on a 5 mL plate:</strong> 5 mL, 3.5 mL, 2.5 mL, 1 mL <br /> <strong>Materials:</strong>
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<strong>Date of Experiment:</strong> June 12-13
+
−
<br>
+
−
<strong>Goal:</strong> Testing different thicknesses of M9 and LB plates to find the minimal autofluorescence. Determine the optimal medium (M9 vs LB) and the optimal volume/thickness  
+
−
<br>
+
−
<strong>Different thicknesses by volume spread on a 5 mL plate:</strong> 5 mL, 3.5 mL, 2.5 mL, 1 mL
+
−
 
+
−
<br>
+
−
<strong>Materials:</strong>  
+
 
<ul>
 
<ul>
−
<li>LB (12 mL) & M9 (12 mL)</li>
+
<li>LB (12 mL) &amp; M9 (12 mL)</li>
−
<li>Small plates (typically 5 mL agar capacity) </li>
+
<li>Small plates (typically 5 mL agar capacity)</li>
−
<li>UV light & Typhoon Imaging </li>
+
<li>UV light &amp; Typhoon Imaging</li>
 
<li>FDNA</li>
 
<li>FDNA</li>
 
</ul>
 
</ul>
−
<br>
+
<br /> <strong>Protocols: </strong> <br />
−
 
+
−
<strong>Protocols: </strong>
+
−
<br>
+
 
<ol>
 
<ol>
−
<li>Make 200 mL stock of M9 <i>(http://www.thelabrat.com/protocols/m9minimal.shtml) (http://www.protocolsonline.com/recipes/media/m9-medium-5x/)</i>  
+
<li>Make 200 mL stock of M9 <em>(http://www.thelabrat.com/protocols/m9minimal.shtml) (http://www.protocolsonline.com/recipes/media/m9-medium-5x/)</em>
−
<ol>  
+
<ol>
−
<li>Make M9 salts:
+
<li>Make M9 salts:
−
    <ol>
+
<ol>
−
  <li>Aliquote 160 ml H2O and add:
+
<li>Aliquote 160 ml H2O and add:
−
      <ul>
+
<ul>
−
      <li>12.8 g Na2HPO4-7H2O</li>
+
<li>12.8 g Na2HPO4-7H2O</li>
−
      <li>3.0 g KH2PO4</li>
+
<li>3.0 g KH2PO4</li>
−
      <li>0.50 g NaCl</li>
+
<li>0.50 g NaCl</li>
−
      <li>1.0g NH4Cl</li>
+
<li>1.0g NH4Cl</li>
−
      </ul>
+
</ul>
−
    </li>
+
</li>
−
   
+
<li>Stir until dissolved &amp; Adjust to 200 ml with distilled H2O</li>
−
    <li>Stir until dissolved & Adjust to 200 ml with distilled H2O</li>
+
<li>Sterilize by autoclaving</li>
−
    <li>Sterilize by autoclaving</li>
+
<li>Add 4 ml of 20% glucose (or other carbon source) - filter sterilize separately
−
    <li>Add 4 ml of 20% glucose (or other carbon source) - filter sterilize separately  
+
<ul>
−
      <ul>
+
<li>8 mL of glucose (12.16 g)</li>
−
        <li>8 mL of glucose (12.16 g)</li>
+
<li>32 mL of water</li>
−
        <li>32 mL of water</li>
+
</ul>
−
      </ul>
+
</li>
−
    </li>
+
 
<li>Measure ~140 ml of distilled H2O (sterile)</li>
 
<li>Measure ~140 ml of distilled H2O (sterile)</li>
 
<li>Add 0.4 ml of 1M MgSO4 (sterile)</li>
 
<li>Add 0.4 ml of 1M MgSO4 (sterile)</li>
−
<li>Add 20 ul of 1M CaCl2 (sterile) </li>
+
<li>Add 20 ul of 1M CaCl2 (sterile)</li>
 
<li>Adjust to 200ml with distill H2O</li>
 
<li>Adjust to 200ml with distill H2O</li>
−
<li>Autoclave from b to f first and then mix with M9 salt solution of step i. </li>
+
<li>Autoclave from b to f first and then mix with M9 salt solution of step i.</li>
 
<li>Add 40 ml of M9 salts</li>
 
<li>Add 40 ml of M9 salts</li>
 
</ol>
 
</ol>
−
  </li></ol>
+
</li>
−
 
+
</ol>
−
<i>Note: M9 media ratios are 16:4:0.4 respectively for MgSO4 solution, M9 salts and glucose. MgSO4+water+agar solution expires 2 weeks after first use.</i>
+
<em>Note: M9 media ratios are 16:4:0.4 respectively for MgSO4 solution, M9 salts and glucose. MgSO4+water+agar solution expires 2 weeks after first use.</em> </li>
−
<br>
+
−
 
+
 
<li>Melt LB (12 mL) with microwave</li>
 
<li>Melt LB (12 mL) with microwave</li>
 
<li>Pour M9 and LB into the small plates each with a different thickness:
 
<li>Pour M9 and LB into the small plates each with a different thickness:
 
<ul>
 
<ul>
−
<li>5 mL</li>
+
<li>5 mL</li>
−
<li>3.5 mL</li>
+
<li>3.5 mL</li>
−
<li>2.5 mL</li>
+
<li>2.5 mL</li>
−
<li>1.5 mL</li>
+
<li>1.5 mL</li>
 
</ul>
 
</ul>
−
 
+
</li>
 
<li>Drop 2.5 uM of 20 uL of FDNA in one corner of each plate</li>
 
<li>Drop 2.5 uM of 20 uL of FDNA in one corner of each plate</li>
 
<li>Negative control:
 
<li>Negative control:
 
<ul>
 
<ul>
 
<li>blank plate, no M9 or LB</li>
 
<li>blank plate, no M9 or LB</li>
−
<li>Leaving 2 plates without FDNA but with 5 mL of each medium </li>
+
<li>Leaving 2 plates without FDNA but with 5 mL of each medium</li>
 
</ul>
 
</ul>
−
<li>Observe under UV light & Typhoon Imaging  
+
</li>
 +
<li>Observe under UV light &amp; Typhoon Imaging</li>
 
</ol>
 
</ol>
−
 
+
<br /> <br />
−
<br>
+
<h2>Experiment 1.b. Optimal pH of M9 Media for Cell Growth</h2>
−
<br>
+
<br /> <strong>Date of Experiment:</strong> June 12-13 <br /> <strong>Purpose:</strong> To determine the effect of pH change on E. coli bacterial growth and autofluorescence on M9 and LB plates. <br />
−
<h2>Experiment 1.b. Optimal pH of M9 Media for Cell Growth </h2>
+
<h3>Reagents</h3>
−
<br>
+
−
<strong>Date of Experiment:</strong> June 12-13
+
−
<br>
+
−
<strong>Purpose:</strong> To determine the effect of pH change on E. coli bacterial growth
+
−
and autofluorescence on M9 and LB plates.
+
−
<br>
+
−
 
+
−
<h3>Reagents</h3>  
+
 
<ul>
 
<ul>
 
<li>LB Media</li>
 
<li>LB Media</li>
 
<li>M9 Media</li>
 
<li>M9 Media</li>
 
<li>E. coli cells from glycerol stock</li>
 
<li>E. coli cells from glycerol stock</li>
−
<li>NaOH (0.2 M) </li>
+
<li>NaOH (0.2 M)</li>
 
<li>Small agar plates</li>
 
<li>Small agar plates</li>
 
<li>Disposable wire loop</li>
 
<li>Disposable wire loop</li>
 
</ul>
 
</ul>
−
 
+
<br />
−
<br>
+
 
<h3>Protocol:</h3>
 
<h3>Protocol:</h3>
 
<ol>
 
<ol>
−
<li>Create M9 stock media at pH range: control (7), Plate 1 (7.2), Plate 2 (7.6), Plate 3 (8.0), Plate 4 (8.5) by adding volumes of 0.2 M NaOH and checking with a pH meter.
+
<li>Create M9 stock media at pH range: control (7), Plate 1 (7.2), Plate 2 (7.6), Plate 3 (8.0), Plate 4 (8.5) by adding volumes of 0.2 M NaOH and checking with a pH meter.
−
 
+
<ul>
−
<ul>
+
<li>Control Plate: No NaOH added, pH measured to be 7.0</li>
−
<li>Control Plate: No NaOH added, pH measured to be 7.0 </li>
+
<li>Plate 1: 300 uL of NaOH added, 7.2 pH</li>
−
<li>Plate 1: 300 uL of NaOH added, 7.2 pH </li>
+
<li>Plate 2: 750 uL of NaOH added, 7.6 pH</li>
−
<li>Plate 2: 750 uL of NaOH added, 7.6 pH </li>
+
<li>Plate 3: 1500 uL of NaOH added, 8.0 pH</li>
−
<li>Plate 3: 1500 uL of NaOH added, 8.0 pH </li>
+
<li>Plate 4: 1800 uL of NaOH added, 8.5 pH</li>
−
<li>Plate 4: 1800 uL of NaOH added, 8.5 pH </li>
+
</ul>
−
</ul>
+
<p><em> *Note: We poured 2.5 mL of M9 solution out after each plate&rsquo;s pH was measured, thus the total volume of solution that NaOH is added to gradually decreases by 2.5 mL each time, impacting the concentration of NaOH in each plate <br />*Note: pH measured in 40 degrees Celsius solution (M9 solidifies quickly at room temperature). Pour 5 M9 media plates (one for each pH value) at the desired thickness as determined in the previous experiment. (Thickness found to be 2.5 mL of M9 for the small plates) </em></p>
−
<p><i>
+
</li>
−
*Note: We poured 2.5 mL of M9 solution out after each plate’s pH was measured, thus the total volume of solution that NaOH is added to gradually decreases by 2.5 mL each time, impacting the concentration of NaOH in each plate
+
<li>Using a disposable wire loop, plate E. coli cells in a specific streaking pattern across the plate quadrant for bacteria streaking.</li>
−
<br>*Note: pH measured in 40 degrees Celsius solution (M9 solidifies quickly at room temperature).
+
<li>Add FQ substrate spot (2.5 uM, 10uL) onto the FQ quadrant of the plate (bottom left in photo)
−
Pour 5 M9 media plates (one for each pH value) at the desired thickness as determined in the previous experiment. (Thickness found to be 2.5 mL of M9 for the small plates)
+
<ul>
−
</p></i>  
+
<li>Positive control: Plate bacteria on unaltered M9 (control plate).</li>
−
 
+
<li>Negative control: No bacteria on unaltered plate (see negative quadrant of each plate)</li>
−
<li>Using a disposable wire loop, plate E. coli cells in a specific streaking pattern across the plate quadrant for bacteria streaking.
+
</ul>
−
<li>Add FQ substrate spot (2.5 uM, 10uL) onto the FQ quadrant of the plate (bottom left in photo)
+
</li>
−
<ul>
+
−
<li>Positive control: Plate bacteria on unaltered M9 (control plate).</li>  
+
−
<li>Negative control: No bacteria on unaltered plate (see negative quadrant of each plate) </li>
+
−
</ul>
+
−
</li>  
+
−
 
+
 
<li>Incubate bacteria at 37 degrees Celsius for 12 hours.
 
<li>Incubate bacteria at 37 degrees Celsius for 12 hours.
−
<ol>
 
−
  <li>We streaked E coli cells at 11:30 AM, June 13, 2017 and put all plates in the incubator at 11:57 AM on the same day. </li>
 
−
  <li>We checked on bacterial growth and FQ cleavage using UV and typhoon imaging at 4:00 PM of the same day (1st interval check). </li>
 
−
  <li>Incubate again overnight. </li>
 
−
  <li>Check growth and cleavage next morning.</li>
 
−
</ol>
 
−
</li>
 
−
 
−
<li>Check bacterial growth and fluorescence of plates using the Typhoon Imager.
 
 
<ol>
 
<ol>
−
 
+
<li>We streaked E coli cells at 11:30 AM, June 13, 2017 and put all plates in the incubator at 11:57 AM on the same day.</li>
−
<br><br>
+
<li>We checked on bacterial growth and FQ cleavage using UV and typhoon imaging at 4:00 PM of the same day (1st interval check).</li>
 +
<li>Incubate again overnight.</li>
 +
<li>Check growth and cleavage next morning.</li>
 +
</ol>
 +
</li>
 +
<li>Check bacterial growth and fluorescence of plates using the Typhoon Imager.<br /><br />
 
<h2>Exp 1.c. Cell Detection Using DNAzyme in M9</h2>
 
<h2>Exp 1.c. Cell Detection Using DNAzyme in M9</h2>
−
<br>
+
<br /><strong>Date of Experiment:</strong>
−
<strong>Date of Experiment:</strong> June 14-15, 2017
+
<ol>
−
<br>
+
<ol>June 14-15, 2017</ol>
−
<strong>Purpose:</strong> To observe the effectiveness of DNAzyme in M9 with the pH of 8 to detect E. coli colonies. This is within the optimal range mentioned in “A Sensitive DNA Enzyme-Based Fluorescent Assay for Bacterial Detection (Aguirre et al.)
+
</ol>
−
<br>
+
<br /><strong>Purpose:</strong>
−
 
+
<ol>
−
<h3>Materials & Reagents:</h3>
+
<ol>To observe the effectiveness of DNAzyme in M9 with the pH of 8 to detect E. coli colonies. This is within the optimal range mentioned in &ldquo;A Sensitive DNA Enzyme-Based Fluorescent Assay for Bacterial Detection (Aguirre et al.)</ol>
−
<ul>  
+
</ol>
−
<li>UV box & Typhoon imager</li>
+
<br />
 +
<h3>Materials &amp; Reagents:</h3>
 +
<ol>
 +
<ol>
 +
<ul>
 +
<li>UV box &amp; Typhoon imager</li>
 
<li>Incubator</li>
 
<li>Incubator</li>
 
<li>Small agar plates</li>
 
<li>Small agar plates</li>
 
<li>Disposable wire loop</li>
 
<li>Disposable wire loop</li>
−
<br>
+
</ul>
 +
</ol>
 +
</ol>
 +
<br />
 +
<ol>
 +
<ol>
 +
<ul>
 
<li>E. Coli cells from glycerol stock (K12 3)</li>
 
<li>E. Coli cells from glycerol stock (K12 3)</li>
 
<li>DNAzyme (RFD-EC1) 2.245 uM</li>
 
<li>DNAzyme (RFD-EC1) 2.245 uM</li>
Line 238: Line 213:
 
<li>M9 solution</li>
 
<li>M9 solution</li>
 
</ul>
 
</ul>
−
<br>
+
</ol>
−
 
+
</ol>
 +
<br />
 
<h3>Protocol:</h3>
 
<h3>Protocol:</h3>
 +
<ol>
 +
<ol>
 
<ol>
 
<ol>
 
<li>Prepare two M9 plates at pH 8</li>
 
<li>Prepare two M9 plates at pH 8</li>
 
<li>Streak E. coli cells onto the plate suing a wire loop into 3 quadrants</li>
 
<li>Streak E. coli cells onto the plate suing a wire loop into 3 quadrants</li>
−
<img src="http://paste.pics/27B4V"
+
</ol>
−
alt="E coli plate wire loop 1">
+
</ol>
−
<ul><li>The streaking pattern should look like this.</li></ul>
+
</ol>
 +
<img src="http://paste.pics/27B4V" alt="E coli plate wire loop 1" />
 +
<ol>
 +
<ol>
 +
<ol>
 +
<ul>
 +
<li>The streaking pattern should look like this.</li>
 +
</ul>
 
<li>Prepare DNAzyme SB (5 uL of stock + 5 uL of 2x SB)</li>
 
<li>Prepare DNAzyme SB (5 uL of stock + 5 uL of 2x SB)</li>
 
<li>Place in incubator (37 degrees celsius) overnight</li>
 
<li>Place in incubator (37 degrees celsius) overnight</li>
 
<li>Drop DNAzyme and FQ into the different quadrants as shown:
 
<li>Drop DNAzyme and FQ into the different quadrants as shown:
−
<ul>
+
<ul>
−
  <li>Quadrant:
+
<li>Quadrant:
−
  <ul>
+
<ul>
−
    <li> 1.Cell + DNAzyme (4.454 uL)</li>
+
<li>1.Cell + DNAzyme (4.454 uL)</li>
−
    <li> 2. Cell + FQ (4 uL diluted)</li>
+
<li>2. Cell + FQ (4 uL diluted)</li>
−
    <li> 3. Cell only</li>
+
<li>3. Cell only</li>
−
    <li> 4. FQ (4 uL) + NaOH (enough to cover FQ ~2 uL)</li>
+
<li>4. FQ (4 uL) + NaOH (enough to cover FQ ~2 uL)</li>
−
  </ul></li>
+
</ul>
−
  </ul>
+
</li>
−
<li>Afterwards, put in box (don’t expose to light)</li>
+
</ul>
 +
</li>
 +
<li>Afterwards, put in box (don&rsquo;t expose to light)</li>
 
<li>For quadrant 4, let FQ be cleaved over time and add HCl (2 uL) to neutralize right before screening.</li>
 
<li>For quadrant 4, let FQ be cleaved over time and add HCl (2 uL) to neutralize right before screening.</li>
 
<li>After ~5 hours, observe plate under UV light and record observations</li>
 
<li>After ~5 hours, observe plate under UV light and record observations</li>
 
<li>Analyze fluorescence using the typhoon imager to view any other sources of fluorescence</li>
 
<li>Analyze fluorescence using the typhoon imager to view any other sources of fluorescence</li>
−
 
+
<li><br /><br />
−
<br><br>
+
<h2>Experiment 2.a. Differing [NaOH] for Positive Control</h2>
−
<h2>Experiment 2.a. Differing [NaOH] for Positive Control </h2>
+
<br /> <strong>Date of Experiment:</strong> June 19-20, 2017 <br /> <strong>Purpose:</strong>To ensure that NaOH can cleave the FQ substrate so that we have a reliable positive control in future experiments. <br />
−
<br>
+
−
<strong>Date of Experiment:</strong> June 19-20, 2017  
+
−
<br>
+
−
<strong>Purpose:</strong>To ensure that NaOH can cleave the FQ substrate so that we have a reliable positive control in future experiments.  
+
−
<br>
+
 
<h3>Reagents:</h3>
 
<h3>Reagents:</h3>
 
<ul>
 
<ul>
−
<li>NaOH (varying concentrations)</li>
+
<li>NaOH (varying concentrations)</li>
−
<li>FQ substrate (2.5 uM)</li>
+
<li>FQ substrate (2.5 uM)</li>
−
<li>Eppendorf tubes</li>
+
<li>Eppendorf tubes</li>
−
<li>UV light</li>
+
<li>UV light</li>
−
<li>Typhoon imager</li>
+
<li>Typhoon imager</li>
 
</ul>
 
</ul>
−
<br>
+
<br />
 
<h3>Protocol:</h3>
 
<h3>Protocol:</h3>
 
<ol>
 
<ol>
−
<li>Add 6uL of FQ substrate to 5 separate Eppendorf tubes.</li>
+
<ol>
−
<li>Dilute the NaOH stock to the appropriate concentrations for use.</li>
+
<li>Add 6uL of FQ substrate to 5 separate Eppendorf tubes.</li>
−
<li>Add 4uL of NaOH to each tube with concentrations as described in the table below:</li>
+
<li>Dilute the NaOH stock to the appropriate concentrations for use.</li>
−
 
+
<li>Add 4uL of NaOH to each tube with concentrations as described in the table below:</li>
 +
</ol>
 +
</ol>
 
<table>
 
<table>
−
<tr>
+
<tbody>
−
  <th>Tube #</th>
+
<tr>
−
  <td>1</td>
+
<th>Tube #</th>
−
  <td>2</td>
+
<td>1</td>
−
  <td>3</td>
+
<td>2</td>
−
  <td>4</td>
+
<td>3</td>
−
  <td>5</td>
+
<td>4</td>
−
</tr>
+
<td>5</td>
−
<tr>
+
</tr>
−
  <th>[NaOH]</th>
+
<tr>
−
  <td>0.2</td>
+
<th>[NaOH]</th>
−
  <td>0.4</td>
+
<td>0.2</td>
−
  <td>0.6</td>
+
<td>0.4</td>
−
  <td>0.8</td>
+
<td>0.6</td>
−
  <td>1.0</td>
+
<td>0.8</td>
−
</tr>
+
<td>1.0</td>
 +
</tr>
 +
</tbody>
 
</table>
 
</table>
−
 
+
<ol>
−
<li>Let tubes sit for 30 minutes, then observe fluorescence using the UV box in the cold room.</li>
+
<ol>
−
<li>Transfer 10 uL of NaOH+FQ sub as well as 10uL FDNA control onto labeled quadrants of M9 media plates as drawn below:</li>
+
<li>Let tubes sit for 30 minutes, then observe fluorescence using the UV box in the cold room.</li>
−
  <img src="http://paste.pics/27B5T"
+
<li>Transfer 10 uL of NaOH+FQ sub as well as 10uL FDNA control onto labeled quadrants of M9 media plates as drawn below:</li>
−
  alt="NaOH Plate formations">
+
 
</ol>
 
</ol>
−
 
+
</ol>
−
<br><br>
+
<img src="http://paste.pics/27B5T" alt="NaOH Plate formations" /><br /><br />
 
<h2>Exp 2.b. Testing DNAzyme Sensitivity</h2>
 
<h2>Exp 2.b. Testing DNAzyme Sensitivity</h2>
−
<br>
+
<br /> <strong>Date of Experiment:</strong> June 22-25 <strong>Purpose:</strong> Proof of concept that RFD-EC1 probe is specific only to E. coli that express the RNAse I enzyme
−
<strong>Date of Experiment:</strong> June 22-25
+
−
<strong>Purpose:</strong> Proof of concept that RFD-EC1 probe is specific only to E. coli that express the RNAse I enzyme
+
 
<h3>Setup:</h3>
 
<h3>Setup:</h3>
−
<ul>
+
<ul>
 
<li>E. coli K12 + DNAzyme (4.45 uL of 2.245 uM)</li>
 
<li>E. coli K12 + DNAzyme (4.45 uL of 2.245 uM)</li>
 
<li>E. coli K12 (delta RNAseI) + DNAzyme (4.45 uL of 2.245 uM)</li>
 
<li>E. coli K12 (delta RNAseI) + DNAzyme (4.45 uL of 2.245 uM)</li>
 
<li>FDNA (4 uL of 2.5 uM)</li>
 
<li>FDNA (4 uL of 2.5 uM)</li>
 
<li>Nothing
 
<li>Nothing
−
<ul>
+
<ul>
−
<li>Bacteria was streaked on each plate in respective quadrants and grown overnight.
+
<li>Bacteria was streaked on each plate in respective quadrants and grown overnight. next morning: DNAzyme was dropped on cells and FDNA was dropped on 3rd quadrant. The M9 media is pH 8, 2.5 mL.</li>
−
next morning: DNAzyme was dropped on cells and FDNA was dropped on 3rd quadrant.
+
</ul>
−
The M9 media is pH 8, 2.5 mL.</li>
+
−
</ul>  
+
 
</li>
 
</li>
 
</ul>
 
</ul>
−
 
+
<br /><br />
−
<br><br>
+
 
<h2>Exp 3a Reducing Colony Formation Time</h2>
 
<h2>Exp 3a Reducing Colony Formation Time</h2>
−
<br>
+
<br /> <strong>Date of Experiment:</strong> June 29, 2017 <br /> <strong>Purpose:</strong> To determine the minimum amount of time required for E. coli bacterial growth (minimum colony size) to be detectable through fluorescence on M9 plates using UV light. <br />
−
<strong>Date of Experiment:</strong> June 29, 2017
+
<h3>Materials &amp; Reagents:</h3>
−
<br>
+
−
<strong>Purpose:</strong> To determine the minimum amount of time required for E. coli bacterial growth (minimum colony size) to be detectable through fluorescence on M9 plates using UV light.
+
−
<br>
+
−
<h3>Materials & Reagents: </h3>
+
 
<ul>
 
<ul>
−
<li>UV box</li>
+
<li>UV box</li>
−
<li>Typhoon imager</li>
+
<li>Typhoon imager</li>
−
<li>Incubator</li>
+
<li>Incubator</li>
−
<li>2 M9 plates at pH 7</li>
+
<li>2 M9 plates at pH 7</li>
−
<li>E. Coli cells from glycerol stocks (K12) </li>
+
<li>E. Coli cells from glycerol stocks (K12)</li>
−
<li>DNAzyme (RFD-EC1) concentration of 50 pM </li>
+
<li>DNAzyme (RFD-EC1) concentration of 50 pM</li>
−
<li>2.5 uM FDNA</li>
+
<li>2.5 uM FDNA</li>
 
</ul>
 
</ul>
−
<br>
+
<br />
−
 
+
 
<h3>Protocol:</h3>
 
<h3>Protocol:</h3>
 
<ol>
 
<ol>
 
<li>Prepare one M9 plate at pH 7
 
<li>Prepare one M9 plate at pH 7
 
<ul>
 
<ul>
−
<li>Label one plate with quadrants: E. coli + DNAzyme, FDNA, E Coli, DNAzyme</li>
+
<li>Label one plate with quadrants: E. coli + DNAzyme, FDNA, E Coli, DNAzyme</li>
−
<li>Label second plate with DNAzyme + E coli, FDNA, E Coli, DNAzyme</li>
+
<li>Label second plate with DNAzyme + E coli, FDNA, E Coli, DNAzyme</li>
 
</ul>
 
</ul>
 
</li>
 
</li>
−
 
 
<li>Spread 7.24uL DNAzyme on plates and the second plate quadrant E coli + DNAzyme</li>
 
<li>Spread 7.24uL DNAzyme on plates and the second plate quadrant E coli + DNAzyme</li>
 
<li>Streak E. Coli cells onto both plates
 
<li>Streak E. Coli cells onto both plates
−
<ul>
+
<ul>
−
  <li>Drop 7.24uL DNAzyme onto first plate</li>
+
<li>Drop 7.24uL DNAzyme onto first plate</li>
−
  <li>Drop 20uL FDNA on both plates
+
<li>Drop 20uL FDNA on both plates
−
<ul><li>*make sure FDNA does not come in contact with too much light</ul></li>
+
<ul>
−
</li>  
+
<li>*make sure FDNA does not come in contact with too much light</li>
 
</ul>
 
</ul>
 
</li>
 
</li>
−
 
+
</ul>
 +
</li>
 +
</ol>
 +
</li>
 
<li>Place in incubator (37 degrees celsius)</li>
 
<li>Place in incubator (37 degrees celsius)</li>
 
<li>Do an initial scan after 30min</li>
 
<li>Do an initial scan after 30min</li>
Line 375: Line 352:
 
<li>Determine the minimum time needed to confirm the presence of E. Coli bacteria.</li>
 
<li>Determine the minimum time needed to confirm the presence of E. Coli bacteria.</li>
 
</ol>
 
</ol>
−
 
+
</ol>
−
<br><br>
+
</ol>
 +
<br /><br />
 
<h2>Exp 3b DNAzyme Specificity</h2>
 
<h2>Exp 3b DNAzyme Specificity</h2>
−
<strong>Date of Experiment:</strong> July 5
+
<strong>Date of Experiment:</strong>
−
 
+
<ol>
 +
<ol>July 5</ol>
 +
</ol>
 
<h3>Reagents:</h3>
 
<h3>Reagents:</h3>
 +
<ol>
 +
<ol>
 
<ul>
 
<ul>
 
<li>DNAzyme (50 pmol)</li>
 
<li>DNAzyme (50 pmol)</li>
Line 391: Line 373:
 
<li>Leuconostoc mesenteroides glycerol stock</li>
 
<li>Leuconostoc mesenteroides glycerol stock</li>
 
<li>Another bacteria glycerol stock</li>
 
<li>Another bacteria glycerol stock</li>
−
<li>UV lightbox & Typhoon Imager</li>
+
<li>UV lightbox &amp; Typhoon Imager</li>
 
<li>M9 Media plates 4cm diameter</li>
 
<li>M9 Media plates 4cm diameter</li>
 
</ul>
 
</ul>
−
 
+
</ol>
 +
</ol>
 
<h3>Protocol:</h3>
 
<h3>Protocol:</h3>
 
<ol>
 
<ol>
−
<li>Label 4 M9 pH 7.0-7.2, 2.5mL plates as depicted. </li>
+
<ol>
 +
<ol>
 +
<li>Label 4 M9 pH 7.0-7.2, 2.5mL plates as depicted.</li>
 
<li>Streak bacteria in pattern shown with a 10uL pipette tip (exception: for plate 1 use a 2uL pipette tip) @ 4:30pm</li>
 
<li>Streak bacteria in pattern shown with a 10uL pipette tip (exception: for plate 1 use a 2uL pipette tip) @ 4:30pm</li>
 
<li>Leave plates upside down in a 37 degree Celsius incubator overnight (until 9:30am next morning)</li>
 
<li>Leave plates upside down in a 37 degree Celsius incubator overnight (until 9:30am next morning)</li>
 
<li>Drop 7.24 uL of 6.9 uM DNAzyme (effective concentration: 50pmol). To ensure less spreading drop 3.62 uL (2x).</li>
 
<li>Drop 7.24 uL of 6.9 uM DNAzyme (effective concentration: 50pmol). To ensure less spreading drop 3.62 uL (2x).</li>
 
</ol>
 
</ol>
−
 
+
</ol>
−
<br><br>
+
</ol>
 +
<br /><br />
 
<h2>Exp 3c Bacterial Mixture</h2>
 
<h2>Exp 3c Bacterial Mixture</h2>
−
<strong>Date of Experiment:</strong> July 7
+
<strong>Date of Experiment:</strong>
−
<strong>Purpose:</strong> To determine whether the RFD-EC1 DNAzyme can detect E. coli while in a sample of multiple different species of bacteria.
+
<ol>
−
<br>
+
<ol>July 7</ol>
−
<h3>Materials/Reagents: </h3>
+
</ol>
 +
<strong>Purpose:</strong>
 +
<ol>
 +
<ol>To determine whether the RFD-EC1 DNAzyme can detect E. coli while in a sample of multiple different species of bacteria.</ol>
 +
</ol>
 +
<br />
 +
<h3>Materials/Reagents:</h3>
 +
<ol>
 +
<ol>
 
<ul>
 
<ul>
−
<li>E. coli (K12) cells </li>
+
<li>E. coli (K12) cells</li>
−
<li>B. subtilis cells </li>
+
<li>B. subtilis cells</li>
 
<li>Serratia Fonticola cells</li>
 
<li>Serratia Fonticola cells</li>
 
<li>Brevundimonas diminuta cells</li>
 
<li>Brevundimonas diminuta cells</li>
−
<li>New M9 media solution of pH 7.0-7.2 </li>
+
<li>New M9 media solution of pH 7.0-7.2</li>
 
<li>Plates (4cm diameter)</li>
 
<li>Plates (4cm diameter)</li>
 
<li>DNAzyme probe (50 picomol per quadrant)</li>
 
<li>DNAzyme probe (50 picomol per quadrant)</li>
 
</ul>
 
</ul>
−
<br>
+
</ol>
−
 
+
</ol>
−
<h3>Protocol: </h3>
+
<br />
 +
<h3>Protocol:</h3>
 
<ol>
 
<ol>
−
<li>Plate 2 plates (one with DNAzyme spread before cell growth, another with DNAzyme dropped after cell growth) with M9 solution and separate into 3 quadrants  
+
<ol>
−
<ul>
+
<ol>
−
  <li>Negative control of nothing </li>
+
<li>Plate 2 plates (one with DNAzyme spread before cell growth, another with DNAzyme dropped after cell growth) with M9 solution and separate into 3 quadrants
−
  <li>Positive control of E. coli + DNAzyme </li>
+
<ul>
−
  <li>4 distinct streaks of E. coli, Serratia Fonticola, B subtilis, and Brevundimonas diminuta  
+
<li>Negative control of nothing</li>
−
    <ul>
+
<li>Positive control of E. coli + DNAzyme</li>
−
    <li>Make sure each bacteria streak is in a unique pattern to identify which bacteria strain reacted in the end </li>
+
<li>4 distinct streaks of E. coli, Serratia Fonticola, B subtilis, and Brevundimonas diminuta
−
    </ul>  
+
<ul>
−
  </ul>
+
<li>Make sure each bacteria streak is in a unique pattern to identify which bacteria strain reacted in the end</li>
−
</li>
+
</ul>
−
<img src="http://paste.pics/27BAU" alt="Specificity Plate Test">
+
</li>
−
 
+
</ul>
−
<li>Grow the cells overnight </li>
+
</li>
−
<li>UV image next morning to ensure cells have grown </li>
+
</ol>
−
<li>For plate with label “DNAzyme drop after”, drop and spread 50 picomoles of DNAzyme probe on the positive control and experiment quadrants  
+
</ol>
−
<ol>
+
</ol>
−
  <li>Plate: “DNAzyme to be dropped after"</li>
+
<img src="http://paste.pics/27BAU" alt="Specificity Plate Test" />
−
  <li>For that, we'll need to drop a larger volume of DNAzyme so we'll use DNAzyme Eppendorf labelled 2.245 uM that's a larger volume and lighter in color (that's the one we diluted with water)</li>
+
<ol>
−
  <li>To get 50 picomoles, dilute 20.46 uL of DNAzyme with 20.46 uL of 2x buffer and pour the total volume of 40.9198 uL over the 2 non-negative control quadrants (3/4 of the plate).</li>
+
<ol>
−
  <li>(volume may be a lot but the thing is, I kind of need to flood the surface area of the quadrants since I can't spread with hockey sticks - will shift cells - and I need to cover the entire area since I drew cells in thin lines over a large surface area)</li>
+
<li>Grow the cells overnight</li>
−
  <li>If volume is too large, we can drop half of the mixed solution (20.46 uL) first, let set, and drop the other half again as a second layer</li>
+
<li>UV image next morning to ensure cells have grown</li>
−
</ol>
+
<li>For plate with label &ldquo;DNAzyme drop after&rdquo;, drop and spread 50 picomoles of DNAzyme probe on the positive control and experiment quadrants
−
 
+
<ol>
 +
<li>Plate: &ldquo;DNAzyme to be dropped after"</li>
 +
<li>For that, we'll need to drop a larger volume of DNAzyme so we'll use DNAzyme Eppendorf labelled 2.245 uM that's a larger volume and lighter in color (that's the one we diluted with water)</li>
 +
<li>To get 50 picomoles, dilute 20.46 uL of DNAzyme with 20.46 uL of 2x buffer and pour the total volume of 40.9198 uL over the 2 non-negative control quadrants (3/4 of the plate).</li>
 +
<li>(volume may be a lot but the thing is, I kind of need to flood the surface area of the quadrants since I can't spread with hockey sticks - will shift cells - and I need to cover the entire area since I drew cells in thin lines over a large surface area)</li>
 +
<li>If volume is too large, we can drop half of the mixed solution (20.46 uL) first, let set, and drop the other half again as a second layer</li>
 +
</ol>
 +
</li>
 
<li>Let sit for 30 minutes to 1 hour for DNAzyme to set</li>
 
<li>Let sit for 30 minutes to 1 hour for DNAzyme to set</li>
−
 
+
<li>UV and Typhoon image to see which bacteria species cleaved DNAzyme probe
−
<li>UV and Typhoon image to see which bacteria species cleaved DNAzyme probe  
+
<ul>
−
<ul>
+
<li>See if presence of other bacteria interferes with the fluorescence compared to the positive control
−
<li>See if presence of other bacteria interferes with the fluorescence compared to the positive control  
+
<ul>
−
  <ul>
+
<li>If brighter bc other bacterial autofluorescence or dimmer bc of lower concentration of target E. coli bacteria strain</li>
−
<li>If brighter bc other bacterial autofluorescence or dimmer bc of lower concentration of target E. coli bacteria strain
+
</ul>
−
</li></li></ul></ul>
+
 
</li>
 
</li>
−
 
+
</ul>
−
<br><br>
+
</li>
 +
<li><br /><br />
 
<h2>Fluorescence detecting wavelength</h2>
 
<h2>Fluorescence detecting wavelength</h2>
−
<br>
+
<br /> <strong>Date of experiment:</strong> July 25, 2017 <strong>Purpose:</strong> To find out which wavelength best detects fluorescence from the cleavage of DNAzyme in the presence of E. coli K12 bacteria
−
<strong>Date of experiment:</strong> July 25, 2017
+
−
<strong>Purpose:</strong> To find out which wavelength best detects fluorescence from the cleavage of DNAzyme in the presence of E. coli K12 bacteria
+
−
 
+
 
<h3>Reagents/Materials:</h3>
 
<h3>Reagents/Materials:</h3>
 
<ul>
 
<ul>
Line 472: Line 471:
 
<li>Typhoon imager</li>
 
<li>Typhoon imager</li>
 
</ul>
 
</ul>
−
 
+
<br />
−
<br>
+
 
<h3>Protocol:</h3>
 
<h3>Protocol:</h3>
 
<ol>
 
<ol>
Line 479: Line 477:
 
<li>Label 2 plates with quadrants: K12, delta RNAse, negative, FDNA</li>
 
<li>Label 2 plates with quadrants: K12, delta RNAse, negative, FDNA</li>
 
<li>In one eppendorf tube, insert 11.45 uL 2xSB, 10uL K12 cells, 1.45uL DNAzyme</li>
 
<li>In one eppendorf tube, insert 11.45 uL 2xSB, 10uL K12 cells, 1.45uL DNAzyme</li>
−
<li>Repeat step 3 in a separate eppendorf tube but instead inserting 10uL delta RNAse
+
<li>Repeat step 3 in a separate eppendorf tube but instead inserting 10uL delta RNAse <em>*** make sure to add DNAzyme last (SB may cause unintentional cleavage)</em></li>
−
<i>*** make sure to add DNAzyme last (SB may cause unintentional cleavage)</i></li>
+
 
<li>Place both eppendorf tubes in an incubator for at least 30 minutes</li>
 
<li>Place both eppendorf tubes in an incubator for at least 30 minutes</li>
 
<li>Remove tubes from incubator and drop 10uL from both tubes onto its labeled quadrant on the plate letting it slightly spread</li>
 
<li>Remove tubes from incubator and drop 10uL from both tubes onto its labeled quadrant on the plate letting it slightly spread</li>
Line 486: Line 483:
 
<li>Image under UV and typhoon to observe fluorescence</li>
 
<li>Image under UV and typhoon to observe fluorescence</li>
 
</ol>
 
</ol>
−
 
+
<br /><br />
−
<br><br>
+
−
 
+
 
<h2>Optimal DNAzyme Concentration</h2>
 
<h2>Optimal DNAzyme Concentration</h2>
−
<br>
+
<br /> <strong>Date of experiment:</strong> July 25, 2017 <strong>Experiment done by:</strong> Audrey <br /> <strong>Purpose:</strong> After discovering the optimal number of bacterial cells needed for visible DNAzyme cleavage, this experiment will find the minimal number/concentration of DNAzyme to show distinguishable fluorescence
−
<strong>Date of experiment:</strong> July 25, 2017
+
−
<strong>Experiment done by:</strong> Audrey
+
−
<br>
+
−
<strong>Purpose:</strong> After discovering the optimal number of bacterial cells needed for visible DNAzyme cleavage, this experiment will find the minimal number/concentration of DNAzyme to show distinguishable fluorescence
+
−
 
+
 
<h3>Reagents/materials:</h3>
 
<h3>Reagents/materials:</h3>
 +
<ul>
 
<ul>
 
<ul>
 
<li>13.8 uM DNAzyme</li>
 
<li>13.8 uM DNAzyme</li>
Line 506: Line 497:
 
<li>UV box</li>
 
<li>UV box</li>
 
<li>Typhoon imager</li>
 
<li>Typhoon imager</li>
−
<ul>
+
</ul>
−
 
+
</ul>
 
<h3>Protocol:</h3>
 
<h3>Protocol:</h3>
 +
<ul>
 +
<ul>
 +
<ul>
 
<ol>
 
<ol>
 
<li>Grow K12 in liquid culture until it reaches a cell count of 10^8 cells/mL</li>
 
<li>Grow K12 in liquid culture until it reaches a cell count of 10^8 cells/mL</li>
−
<li>Label eppendorf tubes: 10pmol DNAzyme, 20pmol DNAzyme, 30pmol DNAzyme, 40pmol DNAzyme, FDNA
+
<li>Label eppendorf tubes: 10pmol DNAzyme, 20pmol DNAzyme, 30pmol DNAzyme, 40pmol DNAzyme, FDNA In 4 separate eppendorf tubes, drop 10uL of cells and the following amount of reagent:
−
In 4 separate eppendorf tubes, drop 10uL of cells and the following amount of reagent:
+
<ul>
−
<ul>
+
<li>10pmol DNAzyme: 10.73uL SB + 0.75uL DNAzyme</li>
−
  <li>10pmol DNAzyme: 10.73uL SB + 0.75uL DNAzyme</li>
+
<li>20pmol DNAzyme: 11.45uL SB + 1.45uL DNAzyme</li>
−
  <li>20pmol DNAzyme: 11.45uL SB + 1.45uL DNAzyme</li>
+
<li>30pmol DNAzyme: 12.17uL SB + 2.174uL DNAzyme</li>
−
  <li>30pmol DNAzyme: 12.17uL SB + 2.174uL DNAzyme</li>
+
<li>40pmol DNAzyme: 12.90uL SB + 2.90uL DNAzyme</li>
−
  <li>40pmol DNAzyme: 12.90uL SB + 2.90uL DNAzyme</li>
+
</ul>
−
</ul>
+
 
</li>
 
</li>
−
<i>*** make sure to add DNAzyme last (SB may cause unintentional cleavage)</i>
+
</ol>
−
 
+
</ul>
 +
</ul>
 +
</ul>
 +
<em>*** make sure to add DNAzyme last (SB may cause unintentional cleavage)</em>
 +
<ul>
 +
<ul>
 +
<ul>
 +
<ol>
 
<li>Place eppendorf tubes in an incubator for at least 30 minutes</li>
 
<li>Place eppendorf tubes in an incubator for at least 30 minutes</li>
 
<li>Label 2 plates with quadrants:
 
<li>Label 2 plates with quadrants:
−
<ul>
+
<ul>
−
  <li>10pmol, 20pmol, DNAzyme, FDNA</li>
+
<li>10pmol, 20pmol, DNAzyme, FDNA</li>
−
  <li>30pmol, 40pmol, DNAzyme, FDNA</li>
+
<li>30pmol, 40pmol, DNAzyme, FDNA</li>
−
</ul>
+
</ul>
 
</li>
 
</li>
 
<li>Remove tubes from incubator and drop 10uL from tubes onto its labeled quadrant on the plate letting it slightly spread</li>
 
<li>Remove tubes from incubator and drop 10uL from tubes onto its labeled quadrant on the plate letting it slightly spread</li>
Line 534: Line 534:
 
<li>Image under UV and typhoon to observe fluorescence</li>
 
<li>Image under UV and typhoon to observe fluorescence</li>
 
</ol>
 
</ol>
−
 
+
</ul>
−
<br><br>
+
</ul>
 +
</ul>
 +
<br /><br />
 
<h2>Quantifying Autofluorescence</h2>
 
<h2>Quantifying Autofluorescence</h2>
−
<br>
+
<br /><strong>Date of experiment:</strong>
−
<strong>Date of experiment:</strong> July 27, 2017
+
<ul>
−
<strong>Purpose:</strong> It is unsure whether strong fluorescence is partially due to autofluorescence generated from cells and/or the DNAzyme. This experiment will gather numerical data on fluorescence to determine how much autofluorescence exists in different concentrations of bacteria.
+
<ul>
−
 
+
<ul>July 27, 2017</ul>
−
<br>
+
</ul>
 +
</ul>
 +
<strong>Purpose:</strong>
 +
<ul>
 +
<ul>
 +
<ul>It is unsure whether strong fluorescence is partially due to autofluorescence generated from cells and/or the DNAzyme. This experiment will gather numerical data on fluorescence to determine how much autofluorescence exists in different concentrations of bacteria.</ul>
 +
</ul>
 +
</ul>
 +
<br />
 
<h3>Reagents/materials:</h3>
 
<h3>Reagents/materials:</h3>
 
<ul>
 
<ul>
−
<li>13.8 uM DNAzyme</li>
+
<ul>
−
<li>2x selection buffer</li>
+
<ul>
−
<li>E. coli K12 (10^8 cells/mL) liquid culture</li>
+
<ul>
−
<li>2 M9 plates</li>
+
<li>13.8 uM DNAzyme</li>
−
<li>5 Eppendorf tubes</li>
+
<li>2x selection buffer</li>
−
<li>UV box & Typhoon imager</li>
+
<li>E. coli K12 (10^8 cells/mL) liquid culture</li>
 +
<li>2 M9 plates</li>
 +
<li>5 Eppendorf tubes</li>
 +
<li>UV box &amp; Typhoon imager</li>
 
</ul>
 
</ul>
−
<br>
+
</ul>
 +
</ul>
 +
</ul>
 +
<br />
 
<h3>Protocol:</h3>
 
<h3>Protocol:</h3>
 +
<ul>
 +
<ul>
 +
<ul>
 
<ol>
 
<ol>
 
<li>Grow K12 in liquid culture until it reaches a cell count of 10^8 cells/mL</li>
 
<li>Grow K12 in liquid culture until it reaches a cell count of 10^8 cells/mL</li>
 
<li>Dilute liquid culture to 10^6 cells/mL and 10^4 cells/mL</li>
 
<li>Dilute liquid culture to 10^6 cells/mL and 10^4 cells/mL</li>
 
<li>Take 10uL of 10^8 cells/mL and place into a new eppendorf tube. Do the same with 10^6, 10^4 cells/mL</li>
 
<li>Take 10uL of 10^8 cells/mL and place into a new eppendorf tube. Do the same with 10^6, 10^4 cells/mL</li>
−
<li>Pipette 11.45uL of selection buffer into each tube and 1.45uL DNAzyme.  
+
<li>Pipette 11.45uL of selection buffer into each tube and 1.45uL DNAzyme. <em>*** make sure to add DNAzyme last (SB may cause unintentional cleavage)</em></li>
−
<i>*** make sure to add DNAzyme last (SB may cause unintentional cleavage)</i></li>
+
 
<li>Place eppendorf tubes in an incubator for at least 30 minutes</li>
 
<li>Place eppendorf tubes in an incubator for at least 30 minutes</li>
 
<li>Label 3 plates with quadrants: DNAzyme + cells, cells, DNAzyme, negative</li>
 
<li>Label 3 plates with quadrants: DNAzyme + cells, cells, DNAzyme, negative</li>
 
<li>Label each plate so it corresponds to one of the three different cell counts (10^6, 10^4, 10^2 cells)</li>
 
<li>Label each plate so it corresponds to one of the three different cell counts (10^6, 10^4, 10^2 cells)</li>
−
<li>Drop 10uL of the liquid cultures with different concentrations into the “cells” quadrant in the plate that’s labeled with its cell count</li>
+
<li>Drop 10uL of the liquid cultures with different concentrations into the &ldquo;cells&rdquo; quadrant in the plate that&rsquo;s labeled with its cell count</li>
 
<li>Drop 1.45uL DNAzyme separately onto its quadrant and let it spread</li>
 
<li>Drop 1.45uL DNAzyme separately onto its quadrant and let it spread</li>
 
<li>Remove tubes from incubator and drop 10uL from tubes onto its labeled quadrant on the plate letting it slightly spread</li>
 
<li>Remove tubes from incubator and drop 10uL from tubes onto its labeled quadrant on the plate letting it slightly spread</li>
 
<li>Image under UV and typhoon to observe fluorescence</li>
 
<li>Image under UV and typhoon to observe fluorescence</li>
 
</ol>
 
</ol>
−
 
+
</ul>
−
<br><br>
+
</ul>
 +
</ul>
 +
<br /><br />
 
<h2>Fluorescing Colonies</h2>
 
<h2>Fluorescing Colonies</h2>
−
<br>
+
<br /><strong>Date of experiment:</strong>
−
<strong>Date of experiment:</strong> July 28, 2017
+
<ul>
−
<strong>Purpose:</strong> Before performing the timepoint experiment, it must be confirmed whether the DNAzyme will fluoresce when dropped onto a colony of E.coli K12
+
<ul>
−
 
+
<ul>July 28, 2017</ul>
−
<br>
+
</ul>
 +
</ul>
 +
<strong>Purpose:</strong>
 +
<ul>
 +
<ul>
 +
<ul>Before performing the timepoint experiment, it must be confirmed whether the DNAzyme will fluoresce when dropped onto a colony of E.coli K12</ul>
 +
</ul>
 +
</ul>
 +
<br />
 
<h3>Reagents/materials:</h3>
 
<h3>Reagents/materials:</h3>
 +
<ul>
 +
<ul>
 +
<ul>
 
<ul>
 
<ul>
 
<li>13.8 uM DNAzyme</li>
 
<li>13.8 uM DNAzyme</li>
Line 583: Line 614:
 
<li>2 M9 plates</li>
 
<li>2 M9 plates</li>
 
<li>1 Eppendorf tube</li>
 
<li>1 Eppendorf tube</li>
−
<li>UV box & Typhoon imager</li>
+
<li>UV box &amp; Typhoon imager</li>
 
</ul>
 
</ul>
−
 
+
</ul>
−
<br>
+
</ul>
 +
</ul>
 +
<br />
 
<h3>Protocol:</h3>
 
<h3>Protocol:</h3>
 +
<ul>
 +
<ul>
 +
<ul>
 
<ol>
 
<ol>
 
<li>Streak both bacteria onto separate plates labeled: E.coli K12 and delta RNAse</li>
 
<li>Streak both bacteria onto separate plates labeled: E.coli K12 and delta RNAse</li>
Line 597: Line 633:
 
<li>Remove plates from incubator and image under UV and typhoon for observations</li>
 
<li>Remove plates from incubator and image under UV and typhoon for observations</li>
 
</ol>
 
</ol>
−
 
+
</ul>
−
<br><br>
+
</ul>
 +
</ul>
 +
<br /><br />
 
<h2>DNAzyme Autofluorescence</h2>
 
<h2>DNAzyme Autofluorescence</h2>
−
<strong>Date of experiment:</strong> July 31, 2017
+
<strong>Date of experiment:</strong>
−
<strong>Purpose:</strong> As the DNAzyme shows excessive autofluorescence, it was important to see how much DNAzyme could be added to produce the least amount of autofluorescence, but the most cleavage in the presence of E. coli K12.
+
<ul>
−
 
+
<ul>
−
<br>
+
<ul>July 31, 2017</ul>
 +
</ul>
 +
</ul>
 +
<strong>Purpose:</strong>
 +
<ul>
 +
<ul>
 +
<ul>As the DNAzyme shows excessive autofluorescence, it was important to see how much DNAzyme could be added to produce the least amount of autofluorescence, but the most cleavage in the presence of E. coli K12.</ul>
 +
</ul>
 +
</ul>
 +
<br />
 
<h3>Reagents/materials:</h3>
 
<h3>Reagents/materials:</h3>
 +
<ul>
 +
<ul>
 +
<ul>
 
<ul>
 
<ul>
 
<li>13.8 uM DNAzyme</li>
 
<li>13.8 uM DNAzyme</li>
Line 613: Line 663:
 
<li>UV box</li>
 
<li>UV box</li>
 
<li>Typhoon imager</li>
 
<li>Typhoon imager</li>
−
<ul>
+
</ul>
−
 
+
</ul>
 +
</ul>
 +
</ul>
 
<h3>Protocol:</h3>
 
<h3>Protocol:</h3>
 +
<ul>
 +
<ul>
 +
<ul>
 +
<ul>
 +
<ul>
 
<ol>
 
<ol>
 
<li>Dilute DNAzyme using liquid M9 media in 4 separate eppendorf tubes to obtain the following amounts: 5, 10, 20, 30, 40 pmol</li>
 
<li>Dilute DNAzyme using liquid M9 media in 4 separate eppendorf tubes to obtain the following amounts: 5, 10, 20, 30, 40 pmol</li>
Line 624: Line 681:
 
<li>Drop FDNA (positive control) and FQ (negative control) onto its quadrant and image to observe fluorescence</li>
 
<li>Drop FDNA (positive control) and FQ (negative control) onto its quadrant and image to observe fluorescence</li>
 
</ol>
 
</ol>
−
 
+
</ul>
−
<br><hr>
+
</ul>
 +
</ul>
 +
</ul>
 +
</ul>
 +
<br /><hr />
 
<h1>New DNAzyme Stock</h1>
 
<h1>New DNAzyme Stock</h1>
 
<h2>Bacterial Autofluorescence</h2>
 
<h2>Bacterial Autofluorescence</h2>
−
<br>
+
<br /><strong>Purpose:</strong>
−
<strong>Purpose:</strong> To explore the effect bacterial autofluorescence may be having on experiments, to quantify bacterial autofluorescence so as to minimize it in future experiments.
+
<ul>
−
<br>
+
<ul>
 +
<ul>
 +
<ul>
 +
<ul>To explore the effect bacterial autofluorescence may be having on experiments, to quantify bacterial autofluorescence so as to minimize it in future experiments.</ul>
 +
</ul>
 +
</ul>
 +
</ul>
 +
</ul>
 +
<br />
 
<h3>Setup:</h3>
 
<h3>Setup:</h3>
 +
<ul>
 +
<ul>
 +
<ul>
 +
<ul>
 +
<ul>
 
<ul>
 
<ul>
 
<li>Eppendorf tubes: (4)</li>
 
<li>Eppendorf tubes: (4)</li>
Line 640: Line 714:
 
<li>Typhoon Imager</li>
 
<li>Typhoon Imager</li>
 
</ul>
 
</ul>
−
<br>
+
</ul>
 +
</ul>
 +
</ul>
 +
</ul>
 +
</ul>
 +
<br />
 
<h3>Protocol:</h3>
 
<h3>Protocol:</h3>
 +
<ul>
 +
<ul>
 +
<ul>
 +
<ul>
 +
<ul>
 
<ol>
 
<ol>
 
<li>Make 4 dilutions for E. coli K12. This will be 10^9 cells/mL, 10^7 cells/mL, 10^6 cells/mL, and 10^5 cells/mL (4 tubes in total).</li>
 
<li>Make 4 dilutions for E. coli K12. This will be 10^9 cells/mL, 10^7 cells/mL, 10^6 cells/mL, and 10^5 cells/mL (4 tubes in total).</li>
Line 650: Line 734:
 
<li>The next morning (SHOULD BE EXACTLY 16 HOURS AFTER, PLAN ACCORDINGLY), image under UV and Typhoon.</li>
 
<li>The next morning (SHOULD BE EXACTLY 16 HOURS AFTER, PLAN ACCORDINGLY), image under UV and Typhoon.</li>
 
</ol>
 
</ol>
−
 
+
</ul>
−
<br><br>
+
</ul>
 +
</ul>
 +
</ul>
 +
</ul>
 +
<br /><br />
 
<h2>DNAzyme Autofluorescence</h2>
 
<h2>DNAzyme Autofluorescence</h2>
−
<br>
+
<br /><strong>Date:</strong>
−
<strong>Date:</strong> August 21, 2017
+
<ul>
−
<strong>Purpose:</strong> To quantify and minimize the amount of autofluorescence produced from the DNAzyme.
+
<ul>
−
<br>
+
<ul>
 +
<ul>
 +
<ul>August 21, 2017</ul>
 +
</ul>
 +
</ul>
 +
</ul>
 +
</ul>
 +
<strong>Purpose:</strong>
 +
<ul>
 +
<ul>
 +
<ul>
 +
<ul>
 +
<ul>To quantify and minimize the amount of autofluorescence produced from the DNAzyme.</ul>
 +
</ul>
 +
</ul>
 +
</ul>
 +
</ul>
 +
<br />
 
<h3>Setup:</h3>
 
<h3>Setup:</h3>
 
<ul>
 
<ul>
−
<li>Plates from the previous experiment can be used (the empty quadrants (8)) </li>
+
<ul>
 +
<ul>
 +
<ul>
 +
<ul>
 +
<ul>
 +
<li>Plates from the previous experiment can be used (the empty quadrants (8))</li>
 
<li>DNAzyme</li>
 
<li>DNAzyme</li>
 
<li>2X SB</li>
 
<li>2X SB</li>
Line 665: Line 775:
 
<li>Typhoon Imager</li>
 
<li>Typhoon Imager</li>
 
</ul>
 
</ul>
−
+
</ul>
−
<br>
+
</ul>
 +
</ul>
 +
</ul>
 +
</ul>
 +
<br />
 
<h3>Protocol:</h3>
 
<h3>Protocol:</h3>
 +
<ul>
 +
<ul>
 +
<ul>
 +
<ul>
 +
<ul>
 
<ol>
 
<ol>
 
<li>After completing the bacterial experiment (2), utilize the empty quadrants (4).</li>
 
<li>After completing the bacterial experiment (2), utilize the empty quadrants (4).</li>
Line 674: Line 793:
 
<li>Plate the 5uL in the empty quadrants of the bacterial plates. Incubate right side up for 1hr at 37 degrees Celsius and image under UV and with the Typhoon.Incubate for another hour and image again under Typhoon.</li>
 
<li>Plate the 5uL in the empty quadrants of the bacterial plates. Incubate right side up for 1hr at 37 degrees Celsius and image under UV and with the Typhoon.Incubate for another hour and image again under Typhoon.</li>
 
</ol>
 
</ol>
−
 
+
</ul>
−
<br><br>
+
</ul>
 +
</ul>
 +
</ul>
 +
</ul>
 +
<br /><br />
 
<h2>Optimal Response</h2>
 
<h2>Optimal Response</h2>
−
<br>
+
<br /><strong>Date:</strong>
−
<strong>Date:</strong> August 21, 2017
+
<ul>
−
<strong>Purpose:</strong> To generate the optimal response for the DNAzyme to detect E. coli K12 while minimizing all autofluorescence.
+
<ul>
−
<br>
+
<ul>
 +
<ul>
 +
<ul>August 21, 2017</ul>
 +
</ul>
 +
</ul>
 +
</ul>
 +
</ul>
 +
<strong>Purpose:</strong>
 +
<ul>
 +
<ul>
 +
<ul>
 +
<ul>
 +
<ul>To generate the optimal response for the DNAzyme to detect E. coli K12 while minimizing all autofluorescence.</ul>
 +
</ul>
 +
</ul>
 +
</ul>
 +
</ul>
 +
<br />
 
<h3>Setup:</h3>
 
<h3>Setup:</h3>
 +
<ul>
 +
<ul>
 +
<ul>
 +
<ul>
 +
<ul>
 
<ul>
 
<ul>
 
<li>DNAzyme: pmol/5uL, pmol/5uL, pmol/5uL, pmol/5uL</li>
 
<li>DNAzyme: pmol/5uL, pmol/5uL, pmol/5uL, pmol/5uL</li>
 
<li>E. coli K12 cells on plates from experiment (2)</li>
 
<li>E. coli K12 cells on plates from experiment (2)</li>
 
<li>E. coli K12 delta RNase cells from experiment (2)</li>
 
<li>E. coli K12 delta RNase cells from experiment (2)</li>
−
<li>UV Imager & Typhoon Imager</li>
+
<li>UV Imager &amp; Typhoon Imager</li>
 
</ul>
 
</ul>
−
<br>
+
</ul>
 +
</ul>
 +
</ul>
 +
</ul>
 +
</ul>
 +
<br />
 
<h3>Protocol:</h3>
 
<h3>Protocol:</h3>
 +
<ul>
 +
<ul>
 +
<ul>
 +
<ul>
 +
<ul>
 
<ol>
 
<ol>
 
<li>On the same day as the bacterial autofluorescence experiment Day 2, once results are obtained for that experiment, do this experiment.</li>
 
<li>On the same day as the bacterial autofluorescence experiment Day 2, once results are obtained for that experiment, do this experiment.</li>
Line 696: Line 851:
 
<li>Image again at 2 hrs with the Typhoon Imager.</li>
 
<li>Image again at 2 hrs with the Typhoon Imager.</li>
 
</ol>
 
</ol>
−
 
+
</ul>
−
<br>
+
</ul>
 +
</ul>
 +
</ul>
 +
</ul>
 +
<br />
 
<h2>DNAzyme Specificity</h2>
 
<h2>DNAzyme Specificity</h2>
−
<strong>Date:</strong> August 21, 2017
+
<strong>Date:</strong>
−
<strong>Purpose:</strong> To verify the specificity of the DNAzyme solely for E. coli K12, and to show the inability to cleave against other bacterial species.
+
<ul>
−
<br>
+
<ul>
 +
<ul>
 +
<ul>
 +
<ul>August 21, 2017</ul>
 +
</ul>
 +
</ul>
 +
</ul>
 +
</ul>
 +
<strong>Purpose:</strong>
 +
<ul>
 +
<ul>
 +
<ul>
 +
<ul>
 +
<ul>To verify the specificity of the DNAzyme solely for E. coli K12, and to show the inability to cleave against other bacterial species.</ul>
 +
</ul>
 +
</ul>
 +
</ul>
 +
</ul>
 +
<br />
 
<h3>Setup:</h3>
 
<h3>Setup:</h3>
 +
<ul>
 +
<ul>
 +
<ul>
 +
<ul>
 +
<ul>
 
<ul>
 
<ul>
 
<li>E. coli K12 (10^8 cells/mL)</li>
 
<li>E. coli K12 (10^8 cells/mL)</li>
Line 714: Line 896:
 
<li>FDNA (10uM)</li>
 
<li>FDNA (10uM)</li>
 
<li>M9 plates</li>
 
<li>M9 plates</li>
−
<li>UV Imager & Typhoon Imager</li>
+
<li>UV Imager &amp; Typhoon Imager</li>
 
</ul>
 
</ul>
−
<br>
+
</ul>
 +
</ul>
 +
</ul>
 +
</ul>
 +
</ul>
 +
<br />
 
<h3>Protocol:</h3>
 
<h3>Protocol:</h3>
 +
<ul>
 +
<ul>
 +
<ul>
 +
<ul>
 +
<ul>
 
<ol>
 
<ol>
 
<li>Grow overnight liquid cultures in M9 media of each bacterial species.</li>
 
<li>Grow overnight liquid cultures in M9 media of each bacterial species.</li>
 
<li>Plate 30uL of cells (10^4 cells) on each quadrant and grow for 16 hours at 37 degrees Celsius. Remember to put cell cultures back in the fridge after use!</li>
 
<li>Plate 30uL of cells (10^4 cells) on each quadrant and grow for 16 hours at 37 degrees Celsius. Remember to put cell cultures back in the fridge after use!</li>
−
<li>After the 16 hours, drop the 5uL of DNAzyme on an individual colony of each bacterial species. </li>
+
<li>After the 16 hours, drop the 5uL of DNAzyme on an individual colony of each bacterial species.</li>
 
<li>Incubate right side up for 1hr and UV image and Typhoon image.</li>
 
<li>Incubate right side up for 1hr and UV image and Typhoon image.</li>
 
<li>Incubate for another hour and Typhoon Image.</li>
 
<li>Incubate for another hour and Typhoon Image.</li>
 
</ol>
 
</ol>
−
 
+
</ul>
−
<br>
+
</ul>
 +
</ul>
 +
</ul>
 +
</ul>
 +
<br />
 
<h2>Tracking Fluorescence Over Time</h2>
 
<h2>Tracking Fluorescence Over Time</h2>
−
<strong>Date:</strong> August 21, 2017
+
<strong>Date:</strong>
−
<strong>Purpose:</strong> To quantify DNAzyme fluorescence over time and determine whether the addition of selection buffer impacts fluorescence results.
+
<ul>
−
<br>
+
<ul>
 +
<ul>
 +
<ul>
 +
<ul>August 21, 2017</ul>
 +
</ul>
 +
</ul>
 +
</ul>
 +
</ul>
 +
<strong>Purpose:</strong>
 +
<ul>
 +
<ul>
 +
<ul>
 +
<ul>
 +
<ul>To quantify DNAzyme fluorescence over time and determine whether the addition of selection buffer impacts fluorescence results.</ul>
 +
</ul>
 +
</ul>
 +
</ul>
 +
</ul>
 +
<br />
 
<h3>Setup:</h3>
 
<h3>Setup:</h3>
 +
<ul>
 +
<ul>
 +
<ul>
 +
<ul>
 +
<ul>
 
<ul>
 
<ul>
 
<li>E. coli K12</li>
 
<li>E. coli K12</li>
Line 739: Line 958:
 
<li>UV Imager</li>
 
<li>UV Imager</li>
 
<li>M9 plates</li>
 
<li>M9 plates</li>
−
<ul>
+
</ul>
−
<br>
+
</ul>
 +
</ul>
 +
</ul>
 +
</ul>
 +
</ul>
 +
<br />
 
<h3>Protocol:</h3>
 
<h3>Protocol:</h3>
 +
<ul>
 +
<ul>
 +
<ul>
 +
<ul>
 +
<ul>
 +
<ul>
 +
<ul>
 
<ol>
 
<ol>
 
<li>Incubate E. coli cells at 37 degrees Celsius until a density of /mL</li>
 
<li>Incubate E. coli cells at 37 degrees Celsius until a density of /mL</li>
Line 751: Line 982:
 
<li>Label all results and post them here.</li>
 
<li>Label all results and post them here.</li>
 
</ol>
 
</ol>
−
 
+
</ul>
−
 
+
</ul>
−
<br><hr>
+
</ul>
−
<h1>Experiments Redone Without Selection Buffer </h1>
+
</ul>
−
<br>
+
</ul>
−
<strong>Date of Experiment:</strong> September 28  
+
</ul>
−
<strong>Purpose:</strong> To prove the specificity of the DNAzyme and supply appropriate measurements for data analysis.  
+
</ul>
−
<br>
+
<br /><hr />
 +
<h1>Experiments Redone Without Selection Buffer</h1>
 +
<br /><strong>Date of Experiment:</strong>
 +
<ul>
 +
<ul>
 +
<ul>
 +
<ul>
 +
<ul>
 +
<ul>
 +
<ul>September 28</ul>
 +
</ul>
 +
</ul>
 +
</ul>
 +
</ul>
 +
</ul>
 +
</ul>
 +
<strong>Purpose:</strong>
 +
<ul>
 +
<ul>
 +
<ul>
 +
<ul>
 +
<ul>
 +
<ul>
 +
<ul>To prove the specificity of the DNAzyme and supply appropriate measurements for data analysis.</ul>
 +
</ul>
 +
</ul>
 +
</ul>
 +
</ul>
 +
</ul>
 +
</ul>
 +
<br />
 
<h3>Materials:</h3>
 
<h3>Materials:</h3>
 +
<ul>
 +
<ul>
 +
<ul>
 +
<ul>
 +
<ul>
 +
<ul>
 +
<ul>
 
<ul>
 
<ul>
 
<li>M9 plates</li>
 
<li>M9 plates</li>
−
<li>E. coli K12 & E. coli K12 delta RNase</li>
+
<li>E. coli K12 &amp; E. coli K12 delta RNase</li>
 
<li>B. subtilis</li>
 
<li>B. subtilis</li>
 
<li>A. xylosoxidans</li>
 
<li>A. xylosoxidans</li>
Line 768: Line 1,036:
 
<li>S. fonticola</li>
 
<li>S. fonticola</li>
 
</ul>
 
</ul>
−
<br>
+
</ul>
 +
</ul>
 +
</ul>
 +
</ul>
 +
</ul>
 +
</ul>
 +
</ul>
 +
<br />
 
<h3>Protocols:</h3>
 
<h3>Protocols:</h3>
−
<ol>  
+
<ul>
 +
<ul>
 +
<ul>
 +
<ul>
 +
<ul>
 +
<ul>
 +
<ul>
 +
<ol>
 
<li>Culture all bacteria in liquid M9 media overnight</li>
 
<li>Culture all bacteria in liquid M9 media overnight</li>
 
<li>Look at the OD for bacteria and calculate cell density (around 10^8-10^9 cells/mL).</li>
 
<li>Look at the OD for bacteria and calculate cell density (around 10^8-10^9 cells/mL).</li>
−
<li>Dilute cells as necessary and plate 30uL onto a quadrant of a plate. 3 quadrants bacteria, one quadrant empty (for negative control).  
+
<li>Dilute cells as necessary and plate 30uL onto a quadrant of a plate. 3 quadrants bacteria, one quadrant empty (for negative control). <em>*made replicates to verify results</em></li>
−
<i>*made replicates to verify results</i></li>
+
 
<li>Put the plates in the incubator upside down for 16 hrs exactly</li>
 
<li>Put the plates in the incubator upside down for 16 hrs exactly</li>
 
<li>An hour before removing the plates from the incubator, prepare the DNAzyme (the optimal amount per 5uL).</li>
 
<li>An hour before removing the plates from the incubator, prepare the DNAzyme (the optimal amount per 5uL).</li>
Line 780: Line 1,061:
 
<li>Incubate with the DNAzyme for 1 hour and then image with the typhoon imager.</li>
 
<li>Incubate with the DNAzyme for 1 hour and then image with the typhoon imager.</li>
 
</ol>
 
</ol>
−
 
+
</ul>
−
<br>
+
</ul>
−
<hr>
+
</ul>
−
<h1>Enzyme Kinetics & 96 Well Plate</h1>
+
</ul>
−
<br>
+
</ul>
 +
</ul>
 +
</ul>
 +
<br /><hr />
 +
<h1>Enzyme Kinetics &amp; 96 Well Plate</h1>
 +
<br />
 
<h2>Without Selection Buffer</h2>
 
<h2>Without Selection Buffer</h2>
−
<strong>Date:</strong> September 25
+
<strong>Date:</strong>
−
<br>
+
<ul>
 +
<ul>
 +
<ul>
 +
<ul>
 +
<ul>
 +
<ul>
 +
<ul>September 25</ul>
 +
</ul>
 +
</ul>
 +
</ul>
 +
</ul>
 +
</ul>
 +
</ul>
 +
<br />
 
<h3>Materials:</h3>
 
<h3>Materials:</h3>
 +
<ul>
 +
<ul>
 +
<ul>
 +
<ul>
 +
<ul>
 +
<ul>
 +
<ul>
 
<ul>
 
<ul>
 
<li>96-well plate (black-clear bottom)</li>
 
<li>96-well plate (black-clear bottom)</li>
Line 796: Line 1,102:
 
<li>DNAzyme (RFD-EC1)</li>
 
<li>DNAzyme (RFD-EC1)</li>
 
</ul>
 
</ul>
−
<br>
+
</ul>
 +
</ul>
 +
</ul>
 +
</ul>
 +
</ul>
 +
</ul>
 +
</ul>
 +
<br />
 
<h3>Protocol:</h3>
 
<h3>Protocol:</h3>
 +
<ul>
 +
<ul>
 +
<ul>
 +
<ul>
 +
<ul>
 +
<ul>
 +
<ul>
 
<ol>
 
<ol>
 
<li>Grow a liquid culture of E. coli bacteria in liquid M9 overnight in a shaker incubator</li>
 
<li>Grow a liquid culture of E. coli bacteria in liquid M9 overnight in a shaker incubator</li>
Line 803: Line 1,123:
 
<li>Dilute with liquid M9 (if necessary) to obtain a cell concentration of 10^7cells/mL or 10^4cells/uL</li>
 
<li>Dilute with liquid M9 (if necessary) to obtain a cell concentration of 10^7cells/mL or 10^4cells/uL</li>
 
<li>Transfer 100uL of cells to wells A1 and C1</li>
 
<li>Transfer 100uL of cells to wells A1 and C1</li>
−
<li>Do a serial dilution and transfer 10uL across the wells (e.g. from A1 to A2, A2 to A3, etc)
+
<li>Do a serial dilution and transfer 10uL across the wells (e.g. from A1 to A2, A2 to A3, etc) *once you&rsquo;ve reached row 6, take out 10uL but DO NOT put into row 7</li>
−
*once you’ve reached row 6, take out 10uL but DO NOT put into row 7</li>
+
 
<li>At this point, 90uL should be the volume in every well used for this experiment</li>
 
<li>At this point, 90uL should be the volume in every well used for this experiment</li>
 
<li>Dilute using sterile distilled water (if necessary) to reach a concentration of 4uM</li>
 
<li>Dilute using sterile distilled water (if necessary) to reach a concentration of 4uM</li>
Line 810: Line 1,129:
 
<li>Scan immediately in plate reader to observe kinetics</li>
 
<li>Scan immediately in plate reader to observe kinetics</li>
 
</ol>
 
</ol>
−
 
+
</ul>
−
<br>
+
</ul>
 +
</ul>
 +
</ul>
 +
</ul>
 +
</ul>
 +
</ul>
 +
<br />
 
<h2>With Selection Buffer (Replicates)</h2>
 
<h2>With Selection Buffer (Replicates)</h2>
−
<strong>Date:</strong> October 5
+
<strong>Date:</strong>
 +
<ul>
 +
<ul>
 +
<ul>
 +
<ul>
 +
<ul>
 +
<ul>
 +
<ul>October 5</ul>
 +
</ul>
 +
</ul>
 +
</ul>
 +
</ul>
 +
</ul>
 +
</ul>
 
<h3>Materials:</h3>
 
<h3>Materials:</h3>
 +
<ul>
 +
<ul>
 +
<ul>
 +
<ul>
 +
<ul>
 +
<ul>
 +
<ul>
 
<ul>
 
<ul>
 
<li>Everything else listed in previous experiment (including selection buffer)</li>
 
<li>Everything else listed in previous experiment (including selection buffer)</li>
 
</ul>
 
</ul>
−
<br>
+
</ul>
 +
</ul>
 +
</ul>
 +
</ul>
 +
</ul>
 +
</ul>
 +
</ul>
 +
<br />
 
<h3>Protocol:</h3>
 
<h3>Protocol:</h3>
−
<ol><li>Repeat all steps in previous experiment on a new plate doing triplicates to verify data and create error bars (used rows A to F)</li></ol>
+
<ul>
−
 
+
<ul>
−
<br>
+
<ul>
−
<hr>
+
<ul>
 +
<ul>
 +
<ul>
 +
<ul>
 +
<ol>
 +
<li>Repeat all steps in previous experiment on a new plate doing triplicates to verify data and create error bars (used rows A to F)</li>
 +
</ol>
 +
</ul>
 +
</ul>
 +
</ul>
 +
</ul>
 +
</ul>
 +
</ul>
 +
</ul>
 +
<br /><hr />
 
<h1>DNAzyme Ligation Protocol</h1>
 
<h1>DNAzyme Ligation Protocol</h1>
−
<br>
+
<br /><strong>Date:</strong>
−
<strong>Date:</strong> Repeat performances throughout summer to replenish and refine DNAzyme stock.  
+
<ul>
−
<br>
+
<ul>
 +
<ul>
 +
<ul>
 +
<ul>
 +
<ul>
 +
<ul>Repeat performances throughout summer to replenish and refine DNAzyme stock.</ul>
 +
</ul>
 +
</ul>
 +
</ul>
 +
</ul>
 +
</ul>
 +
</ul>
 +
<br />
 
<h2>Protocol</h2>
 
<h2>Protocol</h2>
−
<br>
+
<br />
−
 
+
 
<table>
 
<table>
−
<tr>
+
<tbody>
−
  <th> </th>
+
<tr>
−
  <th>Absorbance (OD600)</th>
+
<th>Absorbance (OD600)</th>
−
  <th>Concentration (initial)</th>
+
<th>Concentration (initial)</th>
−
  <th>Molecular Weight</th>
+
<th>Molecular Weight</th>
−
  <th>Concentration by Weight</th>
+
<th>Concentration by Weight</th>
−
  <th>Concentration by Lambert-Beers</th>
+
<th>Concentration by Lambert-Beers</th>
−
</tr>
+
</tr>
−
<tr>
+
<tr>
−
  <th>Template Short Strand</th>
+
<th>Template Short Strand</th>
−
  <td>Ex:22.31A</td>
+
<td>Ex:22.31A</td>
−
  <td>Ex: 730 ng/uL</td>
+
<td>Ex: 730 ng/uL</td>
−
  <td>7884.2 g/mol</td>
+
<td>7884.2 g/mol</td>
−
  <td>Calculated by example:90.4 uM</td>
+
<td>Calculated by example:90.4 uM</td>
−
  <td>Calculated by example:92.6 u</td>
+
<td>Calculated by example:92.6 u</td>
−
</tr>
+
</tr>
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+
</tbody>
−
 
+
</table>
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</li>
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</ol>
 
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</li>
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{{:Template:McMasterU_Footer}}

Revision as of 02:38, 28 October 2017

Protocols

Testing Fluorescence of Bacterial Plates

Date: May 18
Reagents:

  • 3x DNAzyme stock: 13.35 uL (200nM final concentration)
  • 2x selection buffer (150uL)
  • dH2O: 136.65uL


Protocol:

  1. The DNAzyme stock solution in the previous slide was created in an Eppendorf tube.
  2. 100 uL of DNAzyme stock solution was pipetted into Plates 1,2, and 3. A hockey stick was used to spread the solution over the surface.
  3. Plates 1-3 were left for 5 minutes to dry (with plate lids on).
  4. A disposable inoculation loop was used to streak nothing onto Plates 1 and 5.
  5. Disposable inoculation loops were used to streak E. coli on Plates 2 and 4 and B. subtilis on Plate 3.
  6. Plates were placed upside down in an incubator at 37℃.

Plates Segmentation:

  • only DNAzyme
  • E. coli with DNAzyme
  • B. subtilis with DNAzyme
  • E. coli only
  • Nothing



Fluorophore Concentrations

Date: May 23
Reagents:

  • FDNA
  • dH2O
  • Hockey stick
  • LB agar plates
  • UV box


Protocol:

  1. 7 different concentrations of fluorescent DNA with the fluorophore were created. These concentrations were 0, 100, 250, 500, 1000, 2500, and 5000 nM.
  2. 10 uL from each of the concentrations were dropped into the middle of a quadrant on a plate.
  3. A hockey stick was used on each quadrant to spread the fluorescent DNA.
      *Did not spread because the dot of solution had set into the agar and therefore did not spread with the hockey stick. This time we dotted the plates and immediately used the hockey stick after putting each dot onto each quadrant.



Optimizing Concentrations & Cleavage


Date of Experiment: May 26

Materials/Reagents:

  • 3 agar plates
  • 100uL of:
    • 2.5uM FDNA, 5.0uM FDNA
    • 2.5uM FQ substrate (RS28), 5.0uM FQ substrate (RS28)
    • Gycerol stock of E.coli

    Protocol:


    1. 3 plates were split into quadrants with 25uL FDNA and FQ substrate stock on each quadrant:
      • Plate 1 (2.5uM): FDNA, Negative, E. coli, FDNA + E. coli
      • Plate 2 (2.5uM): FQ substrate, negative, FQ substrate + 0.5uM 0.2uM NaOh, FDNA
      • Plate 3 (5.0uM): FQ substrate, negative, FQ substrate with 0.5uM 0.2M NaOH, FDNA
    2. E. coli was streaked onto its designated quadrants on plate 1
    3. Plate 2 and 3 were checked under blue light for fluorescence after NaOH applied for 15 minutes
    4. All plates were placed in 37C incubator overnight
    5. Plates were visualized using the Typhoon. The following scans were performed using the blue laser (488nm):
      • 526 SP Fluorescein, Cy2, AlexaFlour488 Emission Filter
      • 520 BP CY2, ECL+, Blue FAM Emission Filter
      • Emission Filter

    Experiment 1.a - M9 vs LB Autofluorescence via Agar Thickness


    Date of Experiment: June 12-13
    Goal: Testing different thicknesses of M9 and LB plates to find the minimal autofluorescence. Determine the optimal medium (M9 vs LB) and the optimal volume/thickness
    Different thicknesses by volume spread on a 5 mL plate: 5 mL, 3.5 mL, 2.5 mL, 1 mL
    Materials:
    • LB (12 mL) & M9 (12 mL)
    • Small plates (typically 5 mL agar capacity)
    • UV light & Typhoon Imaging
    • FDNA

    Protocols:
    1. Make 200 mL stock of M9 (http://www.thelabrat.com/protocols/m9minimal.shtml) (http://www.protocolsonline.com/recipes/media/m9-medium-5x/)
      1. Make M9 salts:
        1. Aliquote 160 ml H2O and add:
          • 12.8 g Na2HPO4-7H2O
          • 3.0 g KH2PO4
          • 0.50 g NaCl
          • 1.0g NH4Cl
        2. Stir until dissolved & Adjust to 200 ml with distilled H2O
        3. Sterilize by autoclaving
        4. Add 4 ml of 20% glucose (or other carbon source) - filter sterilize separately
          • 8 mL of glucose (12.16 g)
          • 32 mL of water
        5. Measure ~140 ml of distilled H2O (sterile)
        6. Add 0.4 ml of 1M MgSO4 (sterile)
        7. Add 20 ul of 1M CaCl2 (sterile)
        8. Adjust to 200ml with distill H2O
        9. Autoclave from b to f first and then mix with M9 salt solution of step i.
        10. Add 40 ml of M9 salts
      Note: M9 media ratios are 16:4:0.4 respectively for MgSO4 solution, M9 salts and glucose. MgSO4+water+agar solution expires 2 weeks after first use.
    2. Melt LB (12 mL) with microwave
    3. Pour M9 and LB into the small plates each with a different thickness:
      • 5 mL
      • 3.5 mL
      • 2.5 mL
      • 1.5 mL
    4. Drop 2.5 uM of 20 uL of FDNA in one corner of each plate
    5. Negative control:
      • blank plate, no M9 or LB
      • Leaving 2 plates without FDNA but with 5 mL of each medium
    6. Observe under UV light & Typhoon Imaging


    Experiment 1.b. Optimal pH of M9 Media for Cell Growth


    Date of Experiment: June 12-13
    Purpose: To determine the effect of pH change on E. coli bacterial growth and autofluorescence on M9 and LB plates.

    Reagents

    • LB Media
    • M9 Media
    • E. coli cells from glycerol stock
    • NaOH (0.2 M)
    • Small agar plates
    • Disposable wire loop

    Protocol:

    1. Create M9 stock media at pH range: control (7), Plate 1 (7.2), Plate 2 (7.6), Plate 3 (8.0), Plate 4 (8.5) by adding volumes of 0.2 M NaOH and checking with a pH meter.
      • Control Plate: No NaOH added, pH measured to be 7.0
      • Plate 1: 300 uL of NaOH added, 7.2 pH
      • Plate 2: 750 uL of NaOH added, 7.6 pH
      • Plate 3: 1500 uL of NaOH added, 8.0 pH
      • Plate 4: 1800 uL of NaOH added, 8.5 pH

      *Note: We poured 2.5 mL of M9 solution out after each plate’s pH was measured, thus the total volume of solution that NaOH is added to gradually decreases by 2.5 mL each time, impacting the concentration of NaOH in each plate
      *Note: pH measured in 40 degrees Celsius solution (M9 solidifies quickly at room temperature). Pour 5 M9 media plates (one for each pH value) at the desired thickness as determined in the previous experiment. (Thickness found to be 2.5 mL of M9 for the small plates)

    2. Using a disposable wire loop, plate E. coli cells in a specific streaking pattern across the plate quadrant for bacteria streaking.
    3. Add FQ substrate spot (2.5 uM, 10uL) onto the FQ quadrant of the plate (bottom left in photo)
      • Positive control: Plate bacteria on unaltered M9 (control plate).
      • Negative control: No bacteria on unaltered plate (see negative quadrant of each plate)
    4. Incubate bacteria at 37 degrees Celsius for 12 hours.
      1. We streaked E coli cells at 11:30 AM, June 13, 2017 and put all plates in the incubator at 11:57 AM on the same day.
      2. We checked on bacterial growth and FQ cleavage using UV and typhoon imaging at 4:00 PM of the same day (1st interval check).
      3. Incubate again overnight.
      4. Check growth and cleavage next morning.
    5. Check bacterial growth and fluorescence of plates using the Typhoon Imager.

      Exp 1.c. Cell Detection Using DNAzyme in M9


      Date of Experiment:
          June 14-15, 2017

      Purpose:
          To observe the effectiveness of DNAzyme in M9 with the pH of 8 to detect E. coli colonies. This is within the optimal range mentioned in “A Sensitive DNA Enzyme-Based Fluorescent Assay for Bacterial Detection (Aguirre et al.)

      Materials & Reagents:

          • UV box & Typhoon imager
          • Incubator
          • Small agar plates
          • Disposable wire loop

          • E. Coli cells from glycerol stock (K12 3)
          • DNAzyme (RFD-EC1) 2.245 uM
          • Selection buffer
          • FQ (2.5 uM)
          • NaOH (0.2 M)
          • HCl (0.2 M)
          • M9 solution

      Protocol:

          1. Prepare two M9 plates at pH 8
          2. Streak E. coli cells onto the plate suing a wire loop into 3 quadrants
      E coli plate wire loop 1
            • The streaking pattern should look like this.
          1. Prepare DNAzyme SB (5 uL of stock + 5 uL of 2x SB)
          2. Place in incubator (37 degrees celsius) overnight
          3. Drop DNAzyme and FQ into the different quadrants as shown:
            • Quadrant:
              • 1.Cell + DNAzyme (4.454 uL)
              • 2. Cell + FQ (4 uL diluted)
              • 3. Cell only
              • 4. FQ (4 uL) + NaOH (enough to cover FQ ~2 uL)
          4. Afterwards, put in box (don’t expose to light)
          5. For quadrant 4, let FQ be cleaved over time and add HCl (2 uL) to neutralize right before screening.
          6. After ~5 hours, observe plate under UV light and record observations
          7. Analyze fluorescence using the typhoon imager to view any other sources of fluorescence


          8. Experiment 2.a. Differing [NaOH] for Positive Control


            Date of Experiment: June 19-20, 2017
            Purpose:To ensure that NaOH can cleave the FQ substrate so that we have a reliable positive control in future experiments.

            Reagents:

            • NaOH (varying concentrations)
            • FQ substrate (2.5 uM)
            • Eppendorf tubes
            • UV light
            • Typhoon imager

            Protocol:

              1. Add 6uL of FQ substrate to 5 separate Eppendorf tubes.
              2. Dilute the NaOH stock to the appropriate concentrations for use.
              3. Add 4uL of NaOH to each tube with concentrations as described in the table below:
            Tube # 1 2 3 4 5
            [NaOH] 0.2 0.4 0.6 0.8 1.0
              1. Let tubes sit for 30 minutes, then observe fluorescence using the UV box in the cold room.
              2. Transfer 10 uL of NaOH+FQ sub as well as 10uL FDNA control onto labeled quadrants of M9 media plates as drawn below:
            NaOH Plate formations

            Exp 2.b. Testing DNAzyme Sensitivity


            Date of Experiment: June 22-25 Purpose: Proof of concept that RFD-EC1 probe is specific only to E. coli that express the RNAse I enzyme

            Setup:

            • E. coli K12 + DNAzyme (4.45 uL of 2.245 uM)
            • E. coli K12 (delta RNAseI) + DNAzyme (4.45 uL of 2.245 uM)
            • FDNA (4 uL of 2.5 uM)
            • Nothing
              • Bacteria was streaked on each plate in respective quadrants and grown overnight. next morning: DNAzyme was dropped on cells and FDNA was dropped on 3rd quadrant. The M9 media is pH 8, 2.5 mL.


            Exp 3a Reducing Colony Formation Time


            Date of Experiment: June 29, 2017
            Purpose: To determine the minimum amount of time required for E. coli bacterial growth (minimum colony size) to be detectable through fluorescence on M9 plates using UV light.

            Materials & Reagents:

            • UV box
            • Typhoon imager
            • Incubator
            • 2 M9 plates at pH 7
            • E. Coli cells from glycerol stocks (K12)
            • DNAzyme (RFD-EC1) concentration of 50 pM
            • 2.5 uM FDNA

            Protocol:

            1. Prepare one M9 plate at pH 7
              • Label one plate with quadrants: E. coli + DNAzyme, FDNA, E Coli, DNAzyme
              • Label second plate with DNAzyme + E coli, FDNA, E Coli, DNAzyme
            2. Spread 7.24uL DNAzyme on plates and the second plate quadrant E coli + DNAzyme
            3. Streak E. Coli cells onto both plates
              • Drop 7.24uL DNAzyme onto first plate
              • Drop 20uL FDNA on both plates
                • *make sure FDNA does not come in contact with too much light
          9. Place in incubator (37 degrees celsius)
          10. Do an initial scan after 30min
          11. After ~2 hours, observe plate under UV light and record observations
          12. Analyze possible fluorescence using the typhoon imager (ensure DNAzyme is functioning normally)
          13. Place plate back in incubator and take plate out every 1-2 hours (time dependent on how much fluorescence is visible) to view under UV light. Record time and observations.
          14. Determine the minimum time needed to confirm the presence of E. Coli bacteria.


      Exp 3b DNAzyme Specificity

      Date of Experiment:
          July 5

      Reagents:

          • DNAzyme (50 pmol)
          • E. coli K12 glycerol stock
          • B. subtilis glycerol stock
          • Brevundimonas diminuta glycerol stock
          • Hafnia alvei glycerol stock
          • Achromobacter xylosoxidans glycerol stock
          • Serratia fonticola glycerol stock
          • Leuconostoc mesenteroides glycerol stock
          • Another bacteria glycerol stock
          • UV lightbox & Typhoon Imager
          • M9 Media plates 4cm diameter

      Protocol:

          1. Label 4 M9 pH 7.0-7.2, 2.5mL plates as depicted.
          2. Streak bacteria in pattern shown with a 10uL pipette tip (exception: for plate 1 use a 2uL pipette tip) @ 4:30pm
          3. Leave plates upside down in a 37 degree Celsius incubator overnight (until 9:30am next morning)
          4. Drop 7.24 uL of 6.9 uM DNAzyme (effective concentration: 50pmol). To ensure less spreading drop 3.62 uL (2x).


      Exp 3c Bacterial Mixture

      Date of Experiment:
          July 7
      Purpose:
          To determine whether the RFD-EC1 DNAzyme can detect E. coli while in a sample of multiple different species of bacteria.

      Materials/Reagents:

          • E. coli (K12) cells
          • B. subtilis cells
          • Serratia Fonticola cells
          • Brevundimonas diminuta cells
          • New M9 media solution of pH 7.0-7.2
          • Plates (4cm diameter)
          • DNAzyme probe (50 picomol per quadrant)

      Protocol:

          1. Plate 2 plates (one with DNAzyme spread before cell growth, another with DNAzyme dropped after cell growth) with M9 solution and separate into 3 quadrants
            • Negative control of nothing
            • Positive control of E. coli + DNAzyme
            • 4 distinct streaks of E. coli, Serratia Fonticola, B subtilis, and Brevundimonas diminuta
              • Make sure each bacteria streak is in a unique pattern to identify which bacteria strain reacted in the end
      Specificity Plate Test
        1. Grow the cells overnight
        2. UV image next morning to ensure cells have grown
        3. For plate with label “DNAzyme drop after”, drop and spread 50 picomoles of DNAzyme probe on the positive control and experiment quadrants
          1. Plate: “DNAzyme to be dropped after"
          2. For that, we'll need to drop a larger volume of DNAzyme so we'll use DNAzyme Eppendorf labelled 2.245 uM that's a larger volume and lighter in color (that's the one we diluted with water)
          3. To get 50 picomoles, dilute 20.46 uL of DNAzyme with 20.46 uL of 2x buffer and pour the total volume of 40.9198 uL over the 2 non-negative control quadrants (3/4 of the plate).
          4. (volume may be a lot but the thing is, I kind of need to flood the surface area of the quadrants since I can't spread with hockey sticks - will shift cells - and I need to cover the entire area since I drew cells in thin lines over a large surface area)
          5. If volume is too large, we can drop half of the mixed solution (20.46 uL) first, let set, and drop the other half again as a second layer
        4. Let sit for 30 minutes to 1 hour for DNAzyme to set
        5. UV and Typhoon image to see which bacteria species cleaved DNAzyme probe
          • See if presence of other bacteria interferes with the fluorescence compared to the positive control
            • If brighter bc other bacterial autofluorescence or dimmer bc of lower concentration of target E. coli bacteria strain


        6. Fluorescence detecting wavelength


          Date of experiment: July 25, 2017 Purpose: To find out which wavelength best detects fluorescence from the cleavage of DNAzyme in the presence of E. coli K12 bacteria

          Reagents/Materials:

          • 13.8 uM DNAzyme
          • 2x selection buffer
          • E. coli K12 and delta RNAse
          • 100uM FDNA
          • 2 M9 plates
          • 5 Eppendorf tubes
          • UV box
          • Typhoon imager

          Protocol:

          1. Grow K12 and delta RNAse in liquid culture until both reach a count of 10^8 cells/mL
          2. Label 2 plates with quadrants: K12, delta RNAse, negative, FDNA
          3. In one eppendorf tube, insert 11.45 uL 2xSB, 10uL K12 cells, 1.45uL DNAzyme
          4. Repeat step 3 in a separate eppendorf tube but instead inserting 10uL delta RNAse *** make sure to add DNAzyme last (SB may cause unintentional cleavage)
          5. Place both eppendorf tubes in an incubator for at least 30 minutes
          6. Remove tubes from incubator and drop 10uL from both tubes onto its labeled quadrant on the plate letting it slightly spread
          7. Perform a 1:10 dilution of FDNA in an eppendorf tube using sterile water and drop 2uL onto its quadrant
          8. Image under UV and typhoon to observe fluorescence


          Optimal DNAzyme Concentration


          Date of experiment: July 25, 2017 Experiment done by: Audrey
          Purpose: After discovering the optimal number of bacterial cells needed for visible DNAzyme cleavage, this experiment will find the minimal number/concentration of DNAzyme to show distinguishable fluorescence

          Reagents/materials:

            • 13.8 uM DNAzyme
            • 2x selection buffer
            • E. coli K12
            • 100uM FDNA
            • 2 M9 plates
            • 5 Eppendorf tubes
            • UV box
            • Typhoon imager

          Protocol:

                1. Grow K12 in liquid culture until it reaches a cell count of 10^8 cells/mL
                2. Label eppendorf tubes: 10pmol DNAzyme, 20pmol DNAzyme, 30pmol DNAzyme, 40pmol DNAzyme, FDNA In 4 separate eppendorf tubes, drop 10uL of cells and the following amount of reagent:
                  • 10pmol DNAzyme: 10.73uL SB + 0.75uL DNAzyme
                  • 20pmol DNAzyme: 11.45uL SB + 1.45uL DNAzyme
                  • 30pmol DNAzyme: 12.17uL SB + 2.174uL DNAzyme
                  • 40pmol DNAzyme: 12.90uL SB + 2.90uL DNAzyme
          *** make sure to add DNAzyme last (SB may cause unintentional cleavage)
                1. Place eppendorf tubes in an incubator for at least 30 minutes
                2. Label 2 plates with quadrants:
                  • 10pmol, 20pmol, DNAzyme, FDNA
                  • 30pmol, 40pmol, DNAzyme, FDNA
                3. Remove tubes from incubator and drop 10uL from tubes onto its labeled quadrant on the plate letting it slightly spread
                4. Drop 5uL DNAzyme separately onto its quadrant (to check for autofluorescence)
                5. Perform a 1:10 dilution of FDNA in an eppendorf tube using sterile water and drop 2uL from the tube onto the plate with the lower cell count. Drop 4uL onto plate with the higher cell count.
                6. Image under UV and typhoon to observe fluorescence


          Quantifying Autofluorescence


          Date of experiment:
                July 27, 2017
          Purpose:
                It is unsure whether strong fluorescence is partially due to autofluorescence generated from cells and/or the DNAzyme. This experiment will gather numerical data on fluorescence to determine how much autofluorescence exists in different concentrations of bacteria.

          Reagents/materials:

                • 13.8 uM DNAzyme
                • 2x selection buffer
                • E. coli K12 (10^8 cells/mL) liquid culture
                • 2 M9 plates
                • 5 Eppendorf tubes
                • UV box & Typhoon imager

          Protocol:

                1. Grow K12 in liquid culture until it reaches a cell count of 10^8 cells/mL
                2. Dilute liquid culture to 10^6 cells/mL and 10^4 cells/mL
                3. Take 10uL of 10^8 cells/mL and place into a new eppendorf tube. Do the same with 10^6, 10^4 cells/mL
                4. Pipette 11.45uL of selection buffer into each tube and 1.45uL DNAzyme. *** make sure to add DNAzyme last (SB may cause unintentional cleavage)
                5. Place eppendorf tubes in an incubator for at least 30 minutes
                6. Label 3 plates with quadrants: DNAzyme + cells, cells, DNAzyme, negative
                7. Label each plate so it corresponds to one of the three different cell counts (10^6, 10^4, 10^2 cells)
                8. Drop 10uL of the liquid cultures with different concentrations into the “cells” quadrant in the plate that’s labeled with its cell count
                9. Drop 1.45uL DNAzyme separately onto its quadrant and let it spread
                10. Remove tubes from incubator and drop 10uL from tubes onto its labeled quadrant on the plate letting it slightly spread
                11. Image under UV and typhoon to observe fluorescence


          Fluorescing Colonies


          Date of experiment:
                July 28, 2017
          Purpose:
                Before performing the timepoint experiment, it must be confirmed whether the DNAzyme will fluoresce when dropped onto a colony of E.coli K12

          Reagents/materials:

                • 13.8 uM DNAzyme
                • 2x selection buffer
                • E. coli K12 (10^8 cells/mL) liquid culture
                • Delta RNAse (10^8 cells/mL) liquid culture
                • 2 M9 plates
                • 1 Eppendorf tube
                • UV box & Typhoon imager

          Protocol:

                1. Streak both bacteria onto separate plates labeled: E.coli K12 and delta RNAse
                2. Place in incubator and let it grow for a day (~20 hours) until isolated colonies form and are noticeable
                3. In an eppendorf tube, add 1.45uL 2x selection buffer and 1.45uL DNAzyme
                4. Take plates out of incubator and take 1.45uL from the eppendorf to drop on top of individual colonies in the E.coli K12 plate
                5. Repeat step 4 for the delta RNAse plate
                6. Place both plates in the incubator and set it rest for ~20min
                7. Remove plates from incubator and image under UV and typhoon for observations


          DNAzyme Autofluorescence

          Date of experiment:
                July 31, 2017
          Purpose:
                As the DNAzyme shows excessive autofluorescence, it was important to see how much DNAzyme could be added to produce the least amount of autofluorescence, but the most cleavage in the presence of E. coli K12.

          Reagents/materials:

                • 13.8 uM DNAzyme
                • 2x selection buffer
                • E. coli K12 (10^8 cells/mL) liquid culture
                • 2 M9 plates
                • 6 Eppendorf tubes
                • UV box
                • Typhoon imager

          Protocol:

                    1. Dilute DNAzyme using liquid M9 media in 4 separate eppendorf tubes to obtain the following amounts: 5, 10, 20, 30, 40 pmol
                    2. Drop 20 uL onto quadrants and spread evenly using a hockey stick.
                    3. Let the DNAzyme set for a few minutes then image to observe autofluorescence
                    4. Streak bacteria onto each quadrant to grow colonies
                    5. Place in incubator overnight
                    6. Drop FDNA (positive control) and FQ (negative control) onto its quadrant and image to observe fluorescence

          New DNAzyme Stock

          Bacterial Autofluorescence


          Purpose:
                    To explore the effect bacterial autofluorescence may be having on experiments, to quantify bacterial autofluorescence so as to minimize it in future experiments.

          Setup:

                    • Eppendorf tubes: (4)
                    • E. coli K12
                    • Bacterial Spreading Sticks (4)
                    • M9 Plates (4)
                    • UV Imager
                    • Typhoon Imager

          Protocol:

                    1. Make 4 dilutions for E. coli K12. This will be 10^9 cells/mL, 10^7 cells/mL, 10^6 cells/mL, and 10^5 cells/mL (4 tubes in total).
                    2. Transfer 30uL of each of these to a new separate Eppendorf tube.
                    3. Image under UV immediately and after 30 minutes of incubation.
                    4. Before the 1hr mark, plate and spread (with hockey stick) all of these bacteria separately.
                    5. Incubate plates overnight at 37 degrees Celsius upside down.
                    6. The next morning (SHOULD BE EXACTLY 16 HOURS AFTER, PLAN ACCORDINGLY), image under UV and Typhoon.


          DNAzyme Autofluorescence


          Date:
                    August 21, 2017
          Purpose:
                    To quantify and minimize the amount of autofluorescence produced from the DNAzyme.

          Setup:

                    • Plates from the previous experiment can be used (the empty quadrants (8))
                    • DNAzyme
                    • 2X SB
                    • UV Imager
                    • Typhoon Imager

          Protocol:

                    1. After completing the bacterial experiment (2), utilize the empty quadrants (4).
                    2. Make DNAzyme dilutions: 40pmol/5uL,30pmol/5uL, 20pmol/5uL, 10pmol/5uL. = 8pmol/uL, 6pmol/uL, 4pmol/uL, 2pmol/uL
                    3. Put 5uL of these into separate Eppendorf tubes. Image under UV immediately.
                    4. Plate the 5uL in the empty quadrants of the bacterial plates. Incubate right side up for 1hr at 37 degrees Celsius and image under UV and with the Typhoon.Incubate for another hour and image again under Typhoon.


          Optimal Response


          Date:
                    August 21, 2017
          Purpose:
                    To generate the optimal response for the DNAzyme to detect E. coli K12 while minimizing all autofluorescence.

          Setup:

                    • DNAzyme: pmol/5uL, pmol/5uL, pmol/5uL, pmol/5uL
                    • E. coli K12 cells on plates from experiment (2)
                    • E. coli K12 delta RNase cells from experiment (2)
                    • UV Imager & Typhoon Imager

          Protocol:

                    1. On the same day as the bacterial autofluorescence experiment Day 2, once results are obtained for that experiment, do this experiment.
                    2. Drop the 5uL of each DNAzyme amount on individual colonies of E. coli K12 and E. coli K12 delta RNase for each bacterial number. BE SURE TO KEEP TRACK HOW MUCH DNAZYME IS PUT ON WHICH COLONY!
                    3. Incubate the plates right side up for 1 hr, then image under UV and Typhoon Image.
                    4. Image again at 2 hrs with the Typhoon Imager.

          DNAzyme Specificity

          Date:
                    August 21, 2017
          Purpose:
                    To verify the specificity of the DNAzyme solely for E. coli K12, and to show the inability to cleave against other bacterial species.

          Setup:

                    • E. coli K12 (10^8 cells/mL)
                    • E. coli K12 delta RNase (10^8 cells/mL)
                    • Bacillus subtilis (10^8 cells/mL)
                    • Hafnia alvei (10^7 cells/mL)
                    • Achromobacter xylosoxidans (10^7 cells/mL)
                    • Serratia fonticola (10^7 cells/mL)
                    • DNAzyme (A)
                    • 2X SB
                    • FDNA (10uM)
                    • M9 plates
                    • UV Imager & Typhoon Imager

          Protocol:

                    1. Grow overnight liquid cultures in M9 media of each bacterial species.
                    2. Plate 30uL of cells (10^4 cells) on each quadrant and grow for 16 hours at 37 degrees Celsius. Remember to put cell cultures back in the fridge after use!
                    3. After the 16 hours, drop the 5uL of DNAzyme on an individual colony of each bacterial species.
                    4. Incubate right side up for 1hr and UV image and Typhoon image.
                    5. Incubate for another hour and Typhoon Image.

          Tracking Fluorescence Over Time

          Date:
                    August 21, 2017
          Purpose:
                    To quantify DNAzyme fluorescence over time and determine whether the addition of selection buffer impacts fluorescence results.

          Setup:

                    • E. coli K12
                    • DNAzyme (40pmol/5uL)
                    • 2X SB
                    • Typhoon Imager
                    • UV Imager
                    • M9 plates

          Protocol:

                        1. Incubate E. coli cells at 37 degrees Celsius until a density of /mL
                        2. Plate 30uL of cells and let grow for 16 hours at 37 degrees Celsius.
                        3. Drop 5uL of DNAzyme (pmol) + 5uL 2xSB on a colony.
                        4. Drop 5uL of DNAzyme (pmol) + 5uL water on another separate colony.
                        5. UV image immediately. Typhoon Image Immediately.
                        6. Typhoon Image after 30 minutes, 1hr, 2hrs, 3hrs, 4hrs, and 5 hrs.
                        7. Label all results and post them here.

          Experiments Redone Without Selection Buffer


          Date of Experiment:
                        September 28
          Purpose:
                        To prove the specificity of the DNAzyme and supply appropriate measurements for data analysis.

          Materials:

                        • M9 plates
                        • E. coli K12 & E. coli K12 delta RNase
                        • B. subtilis
                        • A. xylosoxidans
                        • H. alvei
                        • S. fonticola

          Protocols:

                        1. Culture all bacteria in liquid M9 media overnight
                        2. Look at the OD for bacteria and calculate cell density (around 10^8-10^9 cells/mL).
                        3. Dilute cells as necessary and plate 30uL onto a quadrant of a plate. 3 quadrants bacteria, one quadrant empty (for negative control). *made replicates to verify results
                        4. Put the plates in the incubator upside down for 16 hrs exactly
                        5. An hour before removing the plates from the incubator, prepare the DNAzyme (the optimal amount per 5uL).
                        6. Drop the 5uL of DNAzyme onto each bacterial quadrant as and one control quadrant
                        7. Incubate with the DNAzyme for 1 hour and then image with the typhoon imager.

          Enzyme Kinetics & 96 Well Plate


          Without Selection Buffer

          Date:
                        September 25

          Materials:

                        • 96-well plate (black-clear bottom)
                        • E. coli K12 (at least at 10^7cells/mL or 10^4cells/uL)
                        • Liquid M9
                        • Autoclaved distilled water
                        • DNAzyme (RFD-EC1)

          Protocol:

                        1. Grow a liquid culture of E. coli bacteria in liquid M9 overnight in a shaker incubator
                        2. Pipette 90uL of liquid M9 from A2-7 and C2-7
                        3. Dilute with liquid M9 (if necessary) to obtain a cell concentration of 10^7cells/mL or 10^4cells/uL
                        4. Transfer 100uL of cells to wells A1 and C1
                        5. Do a serial dilution and transfer 10uL across the wells (e.g. from A1 to A2, A2 to A3, etc) *once you’ve reached row 6, take out 10uL but DO NOT put into row 7
                        6. At this point, 90uL should be the volume in every well used for this experiment
                        7. Dilute using sterile distilled water (if necessary) to reach a concentration of 4uM
                        8. Using a multichannel pipette, drop 10uL of DNAzyme into the upper row (A1-7)
                        9. Scan immediately in plate reader to observe kinetics

          With Selection Buffer (Replicates)

          Date:
                        October 5

          Materials:

                        • Everything else listed in previous experiment (including selection buffer)

          Protocol:

                        1. Repeat all steps in previous experiment on a new plate doing triplicates to verify data and create error bars (used rows A to F)

          DNAzyme Ligation Protocol


          Date:
                        Repeat performances throughout summer to replenish and refine DNAzyme stock.

          Protocol


          Absorbance (OD600) Concentration (initial) Molecular Weight Concentration by Weight Concentration by Lambert-Beers
          Template Short Strand Ex:22.31A Ex: 730 ng/uL 7884.2 g/mol Calculated by example:90.4 uM Calculated by example:92.6 u