Ethanol Precipitation of DNA and RNA: How it Works
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DNA and RNA are hydrophilic (water-loving) molecules and, therefore, soluble in water. Ethanol precipitation of DNA and RNA works by adding salt and ethanol to a DNA solution, which makes the DNA less hydrophilic, causing it to precipitate out.
What is Ethanol Precipitation of DNA?
Ethanol precipitation is a commonly used technique for concentrating and de-salting nucleic acid (DNA or RNA) preparations in an aqueous solution.
The basic procedure is that salt and ethanol are added to the aqueous solution, which forces the precipitation of nucleic acids out of the solution. After precipitation, the nucleic acids can then be separated from the rest of the solution by centrifugation. The pellet is then washed in cold 70% ethanol. After a further centrifugation step, the ethanol is removed and the nucleic acid pellet is allowed to dry before resuspending in a clean aqueous buffer.
So how does this work?
It’s All About Solubility…
First, we need to know why nucleic acids are soluble in water. Water is a polar molecule – it has a partial negative charge near the oxygen atom due to the unshared pairs of electrons, and partial positive charges near the hydrogen atoms. Because of these charges, polar molecules like DNA or RNA can interact electrostatically with the water molecules, allowing them to easily dissolve in water. Polar molecules can therefore be described as hydrophilic and non-polar molecules, which can’t easily interact with water molecules, are hydrophobic. Nucleic acids are hydrophilic due to the negatively charged phosphate (PO4–) groups along the sugar-phosphate backbone.
The Role of Salt…
OK, so back to the protocol. The role of salt in the protocol is to neutralize the charges on the sugar-phosphate backbone. A commonly used salt is sodium acetate. In solution, sodium acetate breaks up into Na+ and [CH3COO]–. The positively charged sodium ions neutralize the negative charge on the PO4– groups on the nucleic acids, making the molecule far less hydrophilic and, therefore, much less soluble in water.
The Role of Ethanol…
The electrostatic attraction between the Na+ ions in solution and the PO4– ions are dictated by Coulomb’s Law, which is affected by the dielectric constant of the solution. Water has a high dielectric constant, which makes it fairly difficult for the Na+ and PO4– to come together. Ethanol, on the other hand, has a much lower dielectric constant, making it much easier for Na+ to interact with the PO4–. This shields its charge and makes the nucleic acid less hydrophilic, thus causing it to drop out of the solution.
The Role of Temperature…
Incubation of the nucleic acid/salt/ethanol mixture at low temperatures (e.g. –20° or –80°C) is commonly cited as a necessary step in protocols. However, according to Maniatis et al. (Molecular Cloning, A Laboratory Manual 2nd Edition… 2nd edition?? – I need to get a newer version!), this is not required, as nucleic acids at concentrations as low as 20 ng/mL will precipitate at 0–4°C, so incubation for 15–30 minutes on ice is sufficient.
The Wash Step With 70% Ethanol…
This step is to wash any residual salt away from the pelleted DNA.
A Few Tips on Ethanol Precipitation…
- Choice of salt
- Use sodium acetate (0.3 M final conc, pH 5.2) for routine DNA precipitation.
- Use sodium chloride (0.2 M final conc) for DNA samples containing SDS, since NaCl keeps SDS soluble in 70% ethanol so that it doesn’t precipitate with the DNA.
- Use lithium chloride (0.8 M final conc) for RNA. Since 2.5–3 volumes of ethanol are needed for RNA precipitation and LiCl is more soluble in ethanol than sodium acetate, it will not precipitate. But beware – chloride ions will inhibit protein synthesis and DNA polymerase, so LiCl is no good for RNA preps for in vitro translation or reverse transcription. In these cases, use sodium acetate.
- Use ammonium acetate (2 M final conc) for the removal of dNTPs, but do not use it for the preparation of DNA for T4 polynucleotide kinase reactions as ammonium ions inhibit the enzyme.
- To increase the yield in precipitations of low concentration or small nucleic acid pieces (less than 100 nucleotides)
- Add MgCl2 to a final concentration of 0.01 M.
- Increase the time of incubation on ice before centrifugation to 1 hour.
This explanation should bring you up to speed on how ethanol precipitation works. If you want to learn more about the ins and outs of ethanol precipitation and other DNA clean-up approaches, you might want to check these out…
More Articles on Ethanol Precipitation
- Ethanol precipitation – DNA vs Isopropanol
- How to get the perfect pellet after DNA/RNA ethanol precipitation
Originally published December 4, 2007. Reviewed and republished March 2021.
How can DNA extraction without ethanol?
You can use isopropanol to precipitate DNA – see our article DNA Precipitation: Ethanol vs. Isopropanol for more information here: https://bitesizebio.com/2839/dna-precipitation-ethanol-vs-isopropanol/
The link to “How to get the perfect pellet after DNA/RNA ethanol precipitation”
Seems dead. Should be
Thanks, we’ve fixed this link now!
Let’s say that disrupted cells and cell free DNA are placed into 90ml of 95% ethanol at room temperature, how would you go about extracting the DNA directly from the ethanol?
its coooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooool……but a doubt why dna called dna
DeoxyriboNucleic Acid… in other words, DNA has the sugar deoxyribose, and obviously, it’s a nucleic acid.
Thank you very much for your great article. How can we cite your article? I could not find the date published?