Preparation of MS media for Arabidopsis thaliana

For 500 ml of MS (Murashige-Skoog) media measure:

• 5 g of sucrose
• 2.2 g of basal MS salt (Sigma-Aldrich)
• 4 g of agar
• 5 ml of Vitamin stock mix (Gamblor stock solution)
• 500 ml of distilled water

1. Mix all the components, except the agar, in constant agitation.
2. Adjust the pH to 5.7 ± 0.1.
3. Add the agar and mix gently and heat until it reaches 65 – 70 °C. (Do not boil or autoclave)
4. Pour the agar in plates, let them cool and store at 4 °C.

Preparation of Antibiotic stocks

• Cloramphenicol Stock:

1. Weight 10 mg of lyophilized antibiotic for each ml of stock solution.
2. Dissolve in ethanol and mix gently (It is possible to use Vortex)

• Kanamicin Stock:

1. Weight 50 mg of lyophilized antibiotic for each ml of stock solution.
2. Dissolve in distilled water and mix gently (It is possible to use Vortex).

• Ampicilin Stock:

1. Weight 100 mg of liophylized antibiotic for each ml of stock solution.
2. Dissolve in distilled water and mix gently (It is possible to use Vortex).
3. For each 2 ml of media use 1 ul of stock antibiotic.

Therefore the working concentration for each antibiotic (for use in and Agrobacterium tumefaciens and E. coli) will be:
1. Cloramphenicol: 5ul/ml
2. Kanamicin: 25 ul/ml
3. Ampicilin: 50 ul/ml

CaCl2 Competent Cells

1. Streak out frozen glycerol stock of bacterial cells (Top10, DH5α, etc.) onto an LB plate (no antibiotics since these cells do not have a plasmid in them). Work sterile. Grow plate overnight at 37°C.
2. Make sure to autoclave 1 L LB (or your preferred media), 1 L of 100 mM CaCl2, 1 L of 100 mM MgCl2, 100 mL of 85 mM CaCl2, 15% glycerol v/v, 4 centrifuge bottles and caps, lots of microfuge tubes
3. Chill overnight at 4°C 100 mM CaCl2, 100 mM MgCl2, 85 mM CaCl2, 15% glycerol v/v
4. Prepare starter culture of cells
5. Select a single colony of E. coli from fresh LB plate and inoculate a 10 mL starter culture of LB (or your preferred media – no antibiotics). Grow culture at 37°C in shaker overnight.
6. For the next day, inoculate 1 L of LB media with 10 mL starter culture and grow in 37°C shaker.
7. Measure the OD600 every hour, then every 15-20 minutes when the OD getsabove 0.2.
8. When the OD600 reaches 0.35-0.4, immediately put the cells on ice. Chill the culture for 20-30 minutes, swirling occasionally to ensure even cooling. Place centrifuge bottles on ice at this time.
9. (Spin #1) Split the 1 L culture into four parts by pouring about 250 mL into ice cold centrifuge bottles. Harvest the cells by centrifugation at 3000g for 15 minutes at 4°C.
10. Decant the supernatant and gently resuspend each pellet in about 100 mL of ice cold MgCl2. Combine all suspensions into one centrifuge bottle. Make sure to prepare a blank bottle as a balance.
11. (Spin #2) Harvest the cells by centrifugation at 2000g in the refrigerated centrifuge (~3000 rpm) for 15 minutes at 4°C.
12. Decant the supernatant and resuspend the pellet in about 200 mL of ice cold CaCl2. Keep this suspension on ice for at least 20 minutes. Start putting 1.5 mL microfuge tubes on ice if not already chilled.
13. (Spin #3) Harvest the cells by centrifugation at 2000g (~3000 rpm) for 15 minutes at 4°C. At this step, rinse a 50 mL conical tube with ddH2O and chill on ice.
14. Decant the supernatant and resuspend the pellet in ~50 mL of ice cold 85 mM CaCl2, 15% glycerol. Transfer the suspension to the 50 mL conical tube.
15. (Spin #4) Harvest the cells by centrifugation at 1000g (~2100) for 15 minutes at 4°C.
16. Decant the supernatant and resuspend the pellet in 2 mL of ice cold 85 mM CaCl2, 15% glycerol. The final OD600 of the suspended cells should be ~200-250.
17. Aliquot 50 μL into sterile 1.5 mL microfuge tubes and snap freeze with liquid nitrogen. Store frozen cells in the -80°C freezer.

Heat Shock Transformation of E. coli

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. (Optional)
5. Heat shock at 42 °C for 50 seconds.
6. Incubate on ice for 2 minutes.
7. Add 200 ul LB, Terrific or SOC medium and recover the cells by shaking at 37 °C.
8. The recovery time varies with the antibiotic selection.
   • Ampicillin: 15-30 minutes
   • Kanamycin or Spectinomycin: 30-60 minutes
   • Chloramphenicol: 60-120 minutes
9. 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.
10. Incubate at 37 °C. Transformants should appear within 8 – 16 hrs.

Transformation by 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.
3. Grow at 30°C for about 90 minutes.
4. Harvest the cells. When the cells reach an OD600 of between 0.6 and 0.8.
5. Split the culture into 2x 50 ml falcon tubes, on ice.
6. Centrifuge at 4 °C for 10 min at 4000 rpm.
7. Wash and combine the cells.
8. Remove the supernatant.
9. Resuspend the cells in 2x 25 ml of ice cold water.
10. Combine the volumes in a single 50 ml falcon tube.
11. Wash the cells 2 more times.
12. Centrifuge at 4 °C for 10 min at 4000 rpm.
13. Resuspend in 50 ml of ice cold water.
14. Repeat.
15. Wash and concentrate the cells for electroporation.
16. Centrifuge at 4 °C for 10 min at 4000 rpm.
17. Resuspend in 1-2 ml of ice cold water.
18. We will use 200 ul of washed cells per transformation.

Dialysis of PCR or Digestion Products

1. DNA for electroporation must be free of salts to avoid arcing.
2. Float a filter in a Petri dish filled with water.
3. Millipore membrane filter 0.025 uM.
4. Pipet one drop of PCR product onto the filter.
5. 200 ng is needed per transformation.
6. 20 - 100 ul fits well on one filter.
7. Collect the drop after 30 - 45 minutes.
8. The volume will change, but the DNA is not lost.

Gel Purification

Gel purification using Thermo Scientific GeneJET Gel Extraction Kit

All centrifugations should be carried out in a table-top microcentrifuge at sup12000 x g

1. Excise gel slice containing the DNA fragment using a clean scalpel or razor blade. Cut as close to the DNA as possible to minimize the gel volume. Place the gel slice into a pre-weighed 1.5 ml tube and weigh. Record the weight of the gel slice.
   Note. If the purified fragment will be used for cloning reactions, avoid damaging the DNA through UV light exposure. Minimize UV exposure to a few seconds or keep the gel slice on a glass or plastic plate during UV illumination.
2. Add 1:1 volume of Binding Buffer to the gel slice (volume: weight)(e.g., add 100 ul of Binding Buffer for every 100 mg of agarose gel).
   Note. For gels with an agarose content greater than 2%, a dd 2:1 volumes of Binding Buffer to the gel slice.
3. Incubate the gel mixture at 50-60°C for 10 min or until the gel slice is completely dissolved. Mix the tube by inversion every few minutes to facilitate the melting process. Ensure that the gel is completely dissolved. Vortex the gel mixture briefly before loading on the column. Check the color of the solution. A yellow color indicates an optimal pH for DNA binding. If the color of the solution is orange or violet, add 10 ul of 3 M sodium acetate, pH 5.2 solution and mix. The color of the mix will become yellow.
4. Optional: use this step only when DNA fragment is inf 500 bp or sup10 kb long. If the DNA fragment is inf 500 bp, add a 1:2 volume of 100% isopropanol to the so lubilized gel solution (e.g. 100 ul of isopropanol should be added to 100 mg gel slice solubilized in 100 ul of Binding Buffer). Mix thoroughly. If the DNA fragment is sup10 kb , add a 1:2 volume of water to the solubilized gel solution (e.g. 100 ul of water should be added to 100 mg gel slice solubilized in 100 ul of Binding Buffer). Mix thoroughly.
5. Transfer up to 800 ul of the solubilized gel solution (from step 3 or 4) to the GeneJET purification column. Centrifuge for 1 min. Discard the flow-through and place the column back into the same collection tube.
   Note. If the total volume exceeds 800 ul, the solution can be added to the column in stages. After each application, centrifuge the column for 30-60 s and discard the flow-through aftereach spin. Repeat until the entire volume has been applied to the column membrane. Do not exceed 1 g of total agarose gel per column.
6. Optional: use this additional binding step only if the purified DNA will be used for sequencing. Add 100 ul of Binding Buffer to the GeneJET purification column. Centrifuge for 1 min. Discard the flow-through and place the column back into the same collection tube.
7. Centrifuge the empty GeneJET purification column for an additional 1 min to completely remove residual wash buffer.
   Note. This step is essential to avoid residual ethanol in the purified DNA solution. The presence of ethanol in the DNA sample may inhibit downstream enzymatic reactions.
8. Transfer the GeneJET purification column into a clean 1.5 ml microcentrifuge tube (not included). Add 50 ul of Elution Buffer to the center of the purification column membrane. Centrifuge for 1 min.
   Note. For low DNA amounts the elution volumes can be reduced to increase DNA concentration. An elution volume between 20-50 ul does not significantly reduce the DNA yield. However, elution volumes less than 10 ul are not recommended. If DNA fragment is sup10 kb, prewarm Elution Buffer to 65°C before applying to column. If the elution volume is 10 ul and DNA amount is inf5 ug, incubate column for 1 min at room temperature before centrifugation.
9. Discard the GeneJET purification column and store the purified DNA at -20°C.

P1 Transduction

This protocol uses a phage to transfer a marker from a donor strain to a recipient strain. The phage head packages about 90 kb of DNA, so donor DNA near the marker is also transferred. Note that this can cause problems if you are working with several markers that are very close together.

Lysate preparation

Note: P1 phage should be stored at 4 C. It can't be frozen.

1. The night before, start a 5 mL culture of the donor strain in selective LB.
2. The day of, dilute the donor strain 1:100 into Phage Lysis medium.
   • 50 ul of cells in 5 mL LB
   • 50 uL of 20% Glucose
   • 50 uL of 1M MgSO4
   • 25 ul of 1M CaCl2
   • No antibiotics
3. Incubate at 37 C for 1 hour.
4. Add 50 ul of P1 phage lysate
   Monitor the culture for 1-3 hours.
   The culture should become cloudy, then clear following lysis.
5. Add 500 ul of chloroform to the lysate and vortex.
6. Centrifuge at max speed for 1 minute to clear the cell debris.
   Collect the supernatant.
7. Phage lysate can be stored indefinitely at 4 C. Freezing will destroy the phage.

Transduction

1. The night before, start a 5 ml culture of the recipient strain in selective LB.
2. The day of, harvest the cells by centrifugation.
   6000 rpm for 2 min.
3. Resuspend in original culture volume in 5 mL Phage Infection LB.
   
   • 5 mL LB
   • 50 uL of 1M MgSO4
   • 25 ul of 1M CaCl2
4. Transfer 100 uL of donor P1 lysate per transformation to a 1.5 mL tube.
   Incubate at 37 C for 30 minutes.
   This allows the residual chloroform to evaporate.
5. Set up 4 reactions for each transduction
   1. 100 uL Donor Lysate
   2. 10 uL Donor Lysate
   3. 100 uL Donor Lysate
   4. 100 uL Plain Lb
   100 uL Recipient Cells 190 uL Recipient Cells 100 uL Plain LB 100 uL Recipient Cells
6. Incubate at 37 C for 30 minutes.
7. Stop the infection with 200 uL of 1 M Sodium Citrate (pH 5.5).
8. Add 1 mL LB and recover the cells for 1-2 hours.
9. Spin the cells down and resuspend for plating.
   100 ul LB + 10 uL of 1 M Sodium Citrate (pH 5.5)
10. Plate on selective LB.

Colony PCR

1. Pick a single colony into 30ul of nuclease-free H20. (Fresh colonies grown that day work best, but they can also come from 4 C).
2. Boil for 10 minutes at 100C.
3. Centrifuge (find G) for 1 min. 1ul of this can be used directly for PCR. Best if used directly, but can also be stored at 4C for a few days.

PCR Reaction

Keep all the reagents at 4C while preparing the mixture. Pre-heat the thermocycler to 95C and transfer your reaction directly from 4 C.

Thermocycler Protocol: NEB Quick-Load

Preparation of LB liquid broth

LB is our standard rich media. Directions are on the bottle.

1. Add 12.5g of LB broth powder to a 1L glass bottle.
2. Add 500ml of osmotic water.
3. Autoclave

Preparation of LB Agar

LB agar is our standard rich media for plating. Directions are taken from the bottle.

1. Add 20 g of LB agar powder to a 1 L glass bottle
2. Add 500 ml of osmotic water.
3. Autoclave

Making LB Agar plates

1. Melt LBA in microwave (~8 min).
2. Don’t burn yourself. Most Antibiotics are thermo sensitive so allow agar to cool to approximately 56º C before adding antibiotics.
3. Add antibiotics if required
4. Add 15-25 ml of LBA into each plate. You can get more plates with less agar in each plate, but the plates will desiccate faster and cannot be stored as long.
5. Allow the plates to set.
6. Dry them 45' under the flow hood, with the lid open.

Gel Electrophoresis

Standard 1% agarose gel

Agarose gels are commonly used in concentrations between 0.7 to 2% depending on the size of bands needed to be separated. Simply adjust the amount of starting agarose to %g/100mL TAE e.g. 2g/100mL will give 2%.

1. Measure out 1g of agarose
2. Pour agarose powder into a microwavable flask along with 100mL of 1xTAE
3. Microwave for 1-3mins (until the agarose has dissolved completely and there is a nice rolling boil). Caution HOT! Be careful stirring, eruptive boiling can occur.
4. Let agarose solution cool down for 5min.
5. Pour the agarose into a gel tray with the suitable well comb in place (pour slowly to avoid bubbles which will disrupt the gel).
6. Place newly poured gel at 4°C for 10-15 minutes or let sit at room temperature for 20-30 minutes, until the gel has completely solidified.
7. Once solidified, remove the comb and place the gel into the electrophoresis unit (gel box).
8. Fill the gel box with 1xTAE buffer.
9. Carefully load GeneRuler 100bp Plus DNA weight ladder into the first lane of the gel.
10. Carefully load your samples into the additional wells of the gel.
11. Run the gel at 50-150V until the dye line is approximately 75-80% of the way down the gel.
12. Turn off the power, disconnect the electrodes from the power source and then carefully remove the gel from the gel box.
13. Place the gel into a container filled with 100ml of 1xTAE running buffer and 5μL of EtBr for 5 minutes.
14. Use any device that has UV light to visualize the DNA fragments.

J774 macrophages cell culture

We cultured the cells in T75 flasks for cell culture. Cells were incubated at 37oC in a humidified, 5% CO2.

Preparation of a complete media

1. Take RPMI 1640 medium supplemented with Glutamine
2. Add 10% of foetal bovine serum
3. Add 1% of antibiotics (penicillin/streptomycin/Amphotercin B)
4. Add 1% HEPES
5. Add 1% pyruvate sodium.

Passaging the cells

Passage the J774 cells 2 times a week using a scratcher.

1. Pipet out the media from the flask
2. Add a 5 mL of a fresh complete media
3. Scratch the cells
4. Count the cells them under the microscope

Froze cells for conservation

1. Pipet the media out of the Flask
2. Add 5 mL of new media
3. Scratch the cells
4. Centrifuge the scratched cells at 4000 rpm during 5 minutes
5. Resuspend the pellet in DMSO 1/5, Foetal bovine serum 4/5.
6. Put in cryotubes at - 80°C.

Cells counting

1. Take 10µL of cells
2. Add 90µL of trypan blue
3. Count the cells under the microscope(if you count all the cells in the grid it corresponds to 1µL) If there is so many cells, dilute them in RPMI.
4. Calculate your amount of cells/µL (don't forget to multiplicate by 10 to take into account the dilution factor)