Streamlined Purification of Plasmid DNA From Prokaryotic Cultures

1. Lysate Clearance

1. Grow E. coli cultures transformed with desired plasmid DNA in deep well plates (1 mL of culture/well) in Luria Broth with appropriate antibiotic overnight at 37 °C with shaking.
2. Pellet E. coli in culture plate at 5,000 x g for 10 minutes, then decant supernatant.
3. Resuspend each pellet in 100 μL Resuspension Buffer (50 mM Tris-HCl, pH 8.0, 10 mM EDTA,100 μg/mL RNase A).
4. Add 100 μL/well Lysis Buffer (200 mM NaOH, 1% SDS) and shake using plate shaker for 2 minutes.
5. Add 100 μL/well Neutralization Buffer (3.0 M Potassium Acetate, pH 5.5) and shake for 2 minutes.
6. Transfer cell lysate to lysate clarification plate.
7. Place DNA binding plate on top of 350 μL collection plate and place into bottom of vacuum manifold. Assemble vacuum manifold (see Figure 1).
8. Place lysate clarification plate on top of vacuum apparatus.
9. Apply vacuum at 10 in. Hg (0.34 bar) and collect filtrate into DNA binding plate. Do not use vacuum greater than 12 in. Hg. (0.41 bar).
10. Disassemble vacuum manifold. Place 2 mL waste collection plate in bottom of apparatus.

2. DNA Binding

1. Move the DNA binding plate to the top of the manifold (see Figure 2).
2. Add 300 μL/well Binding Buffer (6 M Guanidine-HCl) and pipette up and down to mix.
3. Apply vacuum [~ 5 in. Hg (0.17 bar) for slow vacuum] and discard filtrate. DNA is now bound to membrane.
4. Wash with 400 μL/well of Wash Buffer (80% Ethanol).
5. Apply vacuum, then discard the filtrate. Discard unnecessary if using 2 mL collection plate or filtering directly to waste.
6. Repeat wash once.
7. Blot bottom of filter plate on absorbent towel to dry.
8. Apply vacuum once more for 5-10 minutes to ensure removal of residual alcohol.
9. Blot bottom to ensure removal of ethanol droplets.

3. DNA Elution

1. Add 70 μL/well Elution Buffer (10 mM Tris-HCl, pH 8.0, 1 mM EDTA). If higher DNA concentration is desired, volume can be reduced to 50 μL/well, but the average total yield will be lower.
2. Incubate the plate at room temperature for one minute.
3. Purified DNA can be eluted by either vacuum or centrifugation.
4. Vacuum method: Place clean collection plate (DNase, RNase free) into vacuum manifold. Place filter plate on top of vacuum manifold, apply vacuum at 15 in. Hg (0.5 bar) for 1 minute until all elution buffer has passed through the DNA binding plate. Collect purified DNA (see Figure 3).
5. Centrifugation method: Place purification filter plate on top of clean collection plate and centrifuge at 1,000 x g for 5 minutes.

4. Quantitative and Qualitative Analyses

1. Measure OD_260/280, calculate concentration of purified DNA.
2. Perform agarose gel analysis of the purified pDNA.

5. Representative Results

E. coli lysate clarified using traditional centrifugation and Pall AcroPrep Advance lysate clarification Filter Plates showed appreciable reduction of debris from starting material. (Figure 4).

Plasmid DNA at three concentrations was spiked into TE buffer and passed through the AcroPrep Advance lysate clarification filter plate. A comparison of plasmid DNA concentration, pre- and post-filtration, shows ~100% recovery (Figure 5) at all three concentrations.

To demonstrate the recovery of DNA from clarified E. coli lysate, plasmid DNA was spiked into crude lysate and then clarified by filtration. The same plasmid DNA was added to cell lysate following filtration. Electrophoresis was performed on aliquots from each sample (Figure 6). A single, clear band of similar intensity from each sample demonstrates little if any DNA loss during the filtration-based clarification step.

Cultures of E. coli containing pCAT plasmid DNA were purified from E. coli lysates using Pall’s 350 μL and 1 mL DNA binding Filter Plates, as well as two other brands of 350 μL DNA binding plates. All purifications were performed as specified in the manufacturer’s recommended protocol. The highest DNA concentration and total yield are seen from Pall’s 1 mL AcroPrep Advance DNA purification filter plate (Figure 7 and Table 2).

Although Competitor W also shows high DNA concentration (155 ng/μL), total DNA yield is the lowest (4.7 μg/well) due to the low recovery volume, ~30 μL. Competitor M gave the lowest concentration of DNA at 108 ng/μL with a total yield of 5.6 μg/well.

Agarose gel analysis of purified pCAT DNA from the three different DNA binding plates is shown in Figure 8. Each collected sample volume was adjusted to 65 μL to correct for differences in recovery volume prior to electrophoresis. All samples show supercoiled plasmid DNA, but DNA yield from each of the Filter Plates varies.

Figure 9 shows the prepared DNA is all in supercoiled form and has similar concentration.

Figure 1. Assembly of Vacuum Manifold for Lysate Clarification.

Figure 2. Assembly of Vacuum Manifold for DNA Binding.

Figure 3. Assembly of Vacuum Manifold for Vacuum Elution.

Figure 4. Filtration simplifies sample clarification. Triplicate samples of 300 μL of crude lysate clarified by vacuum filtration (350 μL AcroPrep Advance lysate clarification filter plate) or traditional centrifugation. OD₃₂₀ measured before and after clarification.

Figure 5. Full recovery of pDNA after passage through AcroPrep Advance lysate clarification filter plate. 300 μL TE buffer spiked with pCAT at 25, 50 and 100 μg/mL. DNA concentration and recovery calculated from OD₂₆₀ before and after filtration, N = 2.

Figure 6. Recovery of pCAT DNA after clarification. Equal amounts of pUC19 spiked into lysate before or after clarification, then diluted 1 to 10 in TE buffer. Loaded 2 μL/lane on 1.2% Agarose gel.

Figure 7. Higher plasmid DNA yield per well with pall Acroprep Advance DNA binding filter plate than competitor plates. pCAT plasmid DNA yield (OD₂₆₀) using indicated DNA purification plates with 1 mL (Pall and Competitor M) or 1.5 mL (Competitor W) overnight culture of DH5α. Purification using plate manufacturer’s recommended protocol. Error bars indicate standard error (n > 6).

Figure 8. Agarose gel analysis of pCAT DNA purified on indicated DNA binding plate. 1.2% agarose gel electrophoresis of the purified pDNA. Pooled samples from three separate purifications, eluate adjusted to 65 μL after purification, diluted 1:10. Loaded 2 μL per lane.

Figure 9. Quality and recovery of pure dna similar when centrifuge or vacuum methods are used for final eluate collection agarose gel electrophoresis of the purified pDNA. The manufacturer’s recommended protocol for AcroPrep Advance Filter Plates was followed for pDNA purification. Elution was performed by centrifuge at 1,000 x g for 5 minutes or vacuum with 15 in. Hg (0.5 bar) for 2 minutes.