Team:Paris Bettencourt/Protocols

From 2014.igem.org

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<h3>CaCl2 Competent Cells</h3>
<h3>CaCl2 Competent Cells</h3>
<p>This protocol makes 4 ml of competent cells, and can be easily scaled up to make more. The cells are typically stored in 110 ul aliquots, so this will make about 35 tubes. A typical transformation uses 20 ul of cells.</p>
<p>This protocol makes 4 ml of competent cells, and can be easily scaled up to make more. The cells are typically stored in 110 ul aliquots, so this will make about 35 tubes. A typical transformation uses 20 ul of cells.</p>
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  <li>Aliquot into pre-chilled Eppendorf tubes. Use immediately or store at -80ºC.<br />
  <li>Aliquot into pre-chilled Eppendorf tubes. Use immediately or store at -80ºC.<br />
    Note: Frozen cells are only good once.Do not refreeze cells once thawed.</li>
    Note: Frozen cells are only good once.Do not refreeze cells once thawed.</li>
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    <div id="prot3" class="protocol">
 
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      <h2>Glycerol Stocks </h2>
 
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      <p><ol>
 
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  <li>Pick Single colonies from agar plates
 
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  <li>Innoculate 5ml LB broth overnight.
 
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  <li>Add 750ml of overnight culture to 250ml of 60% glycerol in a cryotube.
 
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  <li>Make two sets of Glycerol stocks freeze one at -20ºC and the other at -80ºC.
 
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  <li>Collect the drop after 30 - 45 minutes.<br />
  <li>Collect the drop after 30 - 45 minutes.<br />
    The volume will change, but the DNA is not lost.
    The volume will change, but the DNA is not lost.
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    <div id="prot5" class="protocol">
 
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      <h2> Miniprep </h2>
 
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      <h3>Miniprep using <i>Thermo Scientific GeneJET Plasmid Miniprep Kit</i></h3>
 
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      <p>All centrifugations should be carried out in a table-top microcentrifuge at sup12000 x g
 
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<ol>
 
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  <li>Resuspend the pelleted cells in 250 ul of the Resuspension Solution. Transfer the cell suspension to a microcentrifuge tube. The bacteria should be resuspended completely by vortexing or pipetting up and down until no cell clumps remain.</br>
 
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    <b><i>Note</i></b>. Ensure RNase A has been added to the Resuspension Solution.
 
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  </li>
 
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  <li>Add 250 ul of the Lysis Solution and mix thoroughly by inverting the tube 4-6 times until the solution becomes viscous and slightly clear.</br>
 
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    <b><i>Note</i></b>. Do not vortex to avoid shearing of chromosomal DNA. Do not incubate for more than 5 min to avoid denaturation of supercoiled plasmid DNA.</br>
 
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  </li>
 
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  <li>Add 350 ul of the Neutralization Solution and mix immediately and thoroughly by inverting the tube 4-6 times.</br>
 
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    <b><i>Note</i></b>.
 
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    It is important to mix thoroughly and gently after the addition of the Neutralization Solution to avoid localized precipitation of bacterial cell debris. The neutralized bacterial lysate should become cloudy.
 
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  </li>
 
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  <li>Centrifuge for 5 min to pellet cell debris and chromosomal DNA.
 
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  </li>
 
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  <li>Transfer the supernatant to the supplied GeneJET spin column by decanting or pipetting. Avoid disturbing or transferring the white precipitate.
 
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  </li>
 
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  <li>Centrifuge for 1 min. Discard the flow-through and place the column back into the same collection tube.<br />
 
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    <b><i>Note</i></b>.Do not add bleach to the flow-through.
 
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  </li>
 
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  <li>Add 500 ul of the Wash Solution (diluted with ethanol) to the GeneJET spin column. Centrifuge for 30-60 seconds and discard the flow-through. Place the column back into the same collection tube.
 
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  </li>
 
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  <li>Repeat the wash procedure (step 7) using 500 ul of the Wash Solution.
 
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  </li>
 
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  <li>Discard the flow-through and centrifuge for an additional 1 min to remove residual Wash Solution. This step is essential to avoid residual ethanol in plasmid preps.
 
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  </li>
 
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  <li>Transfer the GeneJETspin column into a fresh 1.5 ml microcentrifuge tube. Add 50 ul of the Elution Bufferto the center of GeneJET spin column membrane to elute the plasmid DNA. Take care not to contact the membrane with the pipette tip. Incubate for 2 min at room tempera ture and centrifuge for 2 min.</br>
 
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    <b><i>Note</i></b>.
 
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    An additional elution step (<i>optional</i>) with Elution Buffer or water will recover residual DNA from the membrane and increase the overall yield by 10-20%. For elution of plasmids or cosmids sup20 kb, prewarm Elution Buffer to 70&deg;C before applying to silica membrane.
 
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  </li>
 
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  <li>Discard the column and store the purified plasmid DNA at -20&deg;C.
 
  </li>
  </li>
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Revision as of 13:27, 19 August 2014

Paris Bettencourt 2014

Heat Shock Transformation of E. coli

This protocol can be used to transform chemically competent (i.e. from CaCl2) with a miniprepped plasmid or a ligation product.

Note: Never vortex competent cells. Mix cells by gentle shaking.

  1. Thaw competent cells on ice. These can be prepared using the CaCl2 protocol.
  2. Place 20 ul of cells in a pre-chilled Eppendorf tube.
    • For an Intact Vector: Add 0.5 ul or less to the chilled cells
    • For a Ligation Product: Add 2-3 ul to the chilled cells.
  3. Mix gently by flicking the tube.
  4. Chill on ice for 10 minutes. This step is optional, but can improve yields when transforming a ligation product.
  5. Heat shock at 42 °C for 30 seconds.
  6. Return to ice for 2 minutes.
  7. Add 200 ul LB medium and recover the cells by shaking at 37 °C.
    Another rich medium can substitute for the recovery.
    The recovery time varies with the antibiotic selection.
    Ampicillin: 15-30 minutes
    Kanamycin or Spectinomycin: 30-60 minutes
    Chloramphenicol: 60-120 minutes
  8. Plate out the cells on selective LB.
    Use glass beads to spread the cells.
    The volume of cells plated depends on what is being transformed.
    • For an Intact Vector: High transformation efficiencies are expected. Plating out 10 ul of recovered cells should produce many colonies.
    • For a Ligation Product: Lower transformation efficiencies are expected. Therefore you can plate the entire 200 ul volume of recovered cells.
    Note: 200 ul is the maximum volume of liquid that an LB plate can absorb.
  9. Incubate at 37 °C. Transformants should appear within 12 hrs.

CaCl2 Competent Cells

This protocol makes 4 ml of competent cells, and can be easily scaled up to make more. The cells are typically stored in 110 ul aliquots, so this will make about 35 tubes. A typical transformation uses 20 ul of cells.

Note: Never vortex competent cells. Resuspend by pipetting with large Pasteur pipettes.

  1. The night before, inoculate a 5 ml culture and grow overnight with selection.
  2. The day of the experiment dilute cells ~ 1:200 into selective media.
    For this example add 250 ul to 50 ml of selective media.
    Note: The protocol is easily scaled to increase the number of cells.
  3. Grow the cells to an OD600 of 0.6 – 0.7.
    Use a large flask, 500ml, for good aeration.
    Use a baffled flask for fastest growth.
    This takes about 3 hours depending on the cells.
    Medium-heavy cloudiness by eye is fine.
  4. Spin down the cells at 4 ºC, 4000 rpm, 15 minutes. Note: Keep the cells at 4 ºC from now on.
  5. Resuspend cells in 15 ml, ice-cold 100 mM CaCl2. Leave on ice 4 hours to overnight.
  6. Spin down the cells at 4 ºC, 4000 rpm, 15 minutes.
  7. Resuspend cells in 4 ml, ice-cold 100 mM CaCl2 + 15% glycerol.
  8. Aliquot into pre-chilled Eppendorf tubes. Use immediately or store at -80ºC.
    Note: Frozen cells are only good once.Do not refreeze cells once thawed.

Electroporation

Preparation of Electrocompetent Cells

Competent cells should never be vortexted, as this will cause them to lyse and release salts into the media. Resuspend cells by pipeting up and down with a large pasteur pipet. Once they are chilled, cells should be continuously cold.

  1. The night before the transformation, start an overnight culture of cells.
    5 ml LB Amp.
  2. The day of the transformation, dilute the cells 100X. 100 ml LB Amp.
    Grow at 30°C for about 90 minutes.
  3. Harvest the cells.
    When the cells reach an OD600 of between 0.6 and 0.8.
    Split the culture into 2x 50 ml falcon tubes, on ice.
    Centrifuge at 4 °C for 10 min at 4000 rpm.
  4. Wash and combine the cells.
    Remove the supernatant.
    Resuspend the cells in 2x 25 ml of ice cold water.
    Combine the volumes in a single 50 ml falcon tube.
  5. Wash the cells 2 more times.
    Centrifuge at 4 °C for 10 min at 4000 rpm.
    Resuspend in 50 ml of ice cold water.
    Repeat.
  6. Wash and concentrate the cells for electroporation.
    Centrifuge at 4 °C for 10 min at 4000 rpm.
    Resuspend in 1-2 ml of ice cold water.
    We will use 200 ul of washed cells per transformation.

Dialysis of PCR or Digestion Products

DNA for electroporation must be free of salts to avoid arcing.

  1. Float a filter in a Petri dish filled with water.
    Millipore membrane filter 0.025 uM.
  2. Pipet one drop of PCR product onto the filter.
    200 ng is needed per transformation.
    20 - 100 ul fits well on one filter.
  3. Collect the drop after 30 - 45 minutes.
    The volume will change, but the DNA is not lost.

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