Extraction of Yeast High-Molecular-Weight Genomic DNA 

The protocol requires four different solutions (called Solution 1 through Solution 4 below). Prepare each as directed and filter sterilize them. Solutions 1 through 3 are stored at 4°C. Solution 4 is stored at room temperature.

The recipes below assume that you have various stock solutions available. These stocks are listed in the Materials section of the protocol and will need to be made first. The recipes also may be recalculated to accommodate different starting materials.

Solution 1: EDTA and 2-ME

A	B	C
Final Solution	Stock Solutions	For 100 ml
40 mM EDTA	0.5 M EDTA pH 8.0	8 ml
90 mM 2-ME	Stock bottle acquired from supplier	0.69 ml
Purified water		To 100 ml total volume

Solution 2: Sorbitol/EDTA/DTT (add Zymolyase just before use)

A	B	C
Final Solution	Stock Solutions	For 100 ml
~ 1 M Sorbitol	1 M Sorbitol	100 ml
1 mM EDTA	0.5 M EDTA, pH 8.0	200 μl
3 mM DTT	1 M DTT	300 μl
2 mg/ml Zymolyase	Powder	Weigh as much Zymolyase as needed for that day. Dissolve in Solution 2 just before use.

Solution 3: Tris-HCl/NaCl/MgCl2/2-ME ₂/2-ME

A	B	C
Final Solution	Stock Solutions	For 100 ml
10 mM Tris-HCl, pH 8.0	1 M Tris-HCl, pH 8.0	1 ml
100 mM NaCl	5 M NaCl	2 ml
10 mM MgCl2	1 M MgCl2	1 ml
2 mM 2-ME	Stock bottle acquired from supplier	15 μl
Purified water		To 100 ml total volume

Solution 4: Tris-HCl/NaCl/Sodium Dodecyl Sulfate (SDS)/EDTA

A	B	C
Final Solution	Stock Solutions	For 100 ml
50 mM Tris-HCl, pH 8.0	1 M Tris-HCl, pH 8.0	5 ml
1 M NaCl	5 M NaCl	20 ml
2% SDS	10% SDS	20 ml
50 mM EDTA, pH 8.0	0.5 M EDTA, pH 8.0	10 ml
Purified water		To 100 ml total volume

Buffer-Saturated Phenol/Chloroform (1:1) Mixture

Add equal volumes of buffer-saturated phenol and chloroform to a clean glass bottle. Close the bottle tightly and mix by inversion. Ensure that the cap does not have a liner that will be dissolved by either phenol or chloroform. Store the bottle at 4°C .

Grow the yeast strain on an agar plate, streaking for isolated colonies. Incubate the plate as appropriate for the species. Store the stock plate at 4°C for no more than 1 week.

Inoculate a single, representative colony into a sterile Erlenmeyer flask that contains appropriate liquid growth medium. Incubate the flask to reach early stationary phase of the growth curve. Incubation conditions will vary with the species. Zymolyase digestion is more efficient for cells recovered from earlier stages of the growth curve.

On the day of the extraction, set up a 30°C water bath as well as a 45°C water bath or heating block.

Warm the bottle containing Solution 4 at 45°C to dissolve the SDS.

Place tube racks, pipettes, solutions and other small equipment in the fume hood. Solutions that contain 2-ME, DTT, phenol or chloroform should be opened in the fume hood.

Collect the yeast cells from the culture flask by centrifugation. Many yeast species will pellet after centrifugation at 3000 x g for 0h 5m 0s. Adjust the g force and time according to the species.

Remove the culture supernatant into a biohazard waste beaker for autoclaving prior to disposal.

Resuspend the cell pellet in 5mL Solution 1. Incubate 0h 5m 0s at room temperature.

Repeat the centrifugation step to pellet the cells. Remove the culture supernatant and set aside for appropriate disposal.

Resuspend the cell pellet in 5mL of Solution 2 (into which 10mg Zymolyase was dissolved). Place the tube into a 30°C water bath. Incubate for at least 0h 40m 0s with gentle shaking (approximately 100 rpm). Gentle shaking is intended to discourage the cells from pelleting.

Optional step: Place 2µL of the Zymolyase prep onto a microscope slide with and without 2µL of 10% SDS. Spheroplasts will burst in the presence of SDS, making the SDS-treated sample look quite different than the untreated sample. If the samples look alike, spheroplasts have not been formed yet. Continue the 30°C incubation step.

Centrifuge to collect the spheroplasts. Carefully pour off the supernatant and set aside for appropriate disposal.

Gently resuspend the spheroplasts in 2mL of Solution 3. Spheroplasts are fragile. Prematurely releasing the DNA and harsh pipetting will shear the DNA.

Add 2mL of Solution 4 and mix gently by inversion. Solution 4 contains SDS and will burst the spheroplasts. Handling the prep roughly or pipetting the sample at this point in the protocol will shear the DNA and result in a lower-quality preparation. Your patience and gentle handling of the prep will be rewarded with beautiful high-molecular-weight genomic DNA for procedures such as long-read genome sequencing. If all you want is a genomic DNA prep for PCR amplification of short sequences, it is fine to rush through these steps.

Incubate the tube at 45°C for 0h 10m 0s, gently inverting the tube several times over the course of the incubation period.

Add 2mL of phenol/chloroform to the tube. Invert gently until the mixture is homogeneous. Centrifuge the tube for 0h 5m 0s at 3000 x g. The phenol/chloroform extraction step may be repeated or completed just once.

Remove the upper aqueous phase to a fresh tube sacrificing yield for the sake of purity. Add 2-3 volumes of isopropanol to the aqueous phase to precipitate the genomic DNA. Mix gently by inversion. If you started the prep with 50 ml of yeast cells, there is a sufficient quantity of DNA that you should see the DNA fall out of solution. Mixing by inversion will create a stringy precipitate or pellet that can be scooped out of the tube using a sterile pipet tip or sterile wooden stick. If you started the prep with a smaller number of cells, centrifuge to pellet the DNA and discard the isopropanol supernatant into the correct waste container.

Add 0.5mL Tris-EDTA pH 8.0 (1x TE buffer) to the DNA pellet. Allow the DNA to dissolve into the solution over the course of several hours or overnight. Do not pipet the DNA to resuspend it. Pipetting will cause shearing and a lower-quality DNA prep.

RNase treatment is needed to remove RNA from the genomic DNA prep. RNase may be added to the DNA pellet as it is dissolving in the TE buffer.

Optional step: Proteinase K treatment is often required before genomic DNA will be accepted for long-read DNA sequencing. Proteinase K treatment may be completed after the RNase treatment following manufacturer's instructions.

Extract the sample with phenol/chloroform and precipitate with isopropanol as described above. Resuspend the DNA pellet in a buffer appropriate for the next steps in your experimental plan.

Agarose gel electrophoresis can be used to check the quality of your DNA prep. Select an appropriate size marker that can help you to demonstrate the size and quality of your DNA. My laboratory routinely gets DNA >50 kb without evidence of shearing from this protocol. The preps are used successfully for long-read genome sequencing.