Efficiency of DNA extraction from the leaves of the common oak (Q. robur L.) and the needles of the Scots pine (P. sylvestris L.)

The extraction of high-quality DNA from tissues of woody plants, such as English oak (Quercus robur L.) and Scots pine (Pinus sylvestris L.), is challenging due to the high content of secondary metabolites (polyphenols, polysac-charides). These compounds co-extract with nucleic acids and inhibit downstream molecular genetic analyses. The aim of this work was a comparative evaluation of the efficiency of different DNA extraction methods (a modified CTAB protocol, a CTAB protocol with additional cleanup, and two commercial kits: the SKYSuper Plant Genomic DNA Kit and D-Plants) for obtaining DNA samples suitable for further research. The quality of the DNA preparations was as-sessed spectrophotometrically by the absorbance ratios A260/A280 (to assess protein contamination) and A260/A230 (to assess contamination by polysaccharides and polyphenols), electrophoretically (to visualize DNA integrity and the presence of impurities), and quantitatively. Functional suitability was tested via PCR amplification. For Scots pine nee-dles, the D-Plants kit demonstrated consistently high quality of the preparations (A260/A280 = 1.87 ± 0.33; A260/A230 = 1.95 ± 0.09) and 100% PCR efficiency. The SKYSuper kit showed the highest DNA yield but also signs of degradation (A260/A280 > 2.0) and low PCR efficiency (<50%). The classic CTAB method was the most economi-cal but required mandatory additional cleanup for polysaccharides. For English oak leaves, only the D-Plants kit yield-ed PCR-suitable DNA (80% efficiency), although the yield was very low (0.15 μg), resulting in a high cost per 1 μg of DNA. The other methods, including CTAB with cleanup, failed to produce a functional preparation (0% PCR efficien-cy). The D-Plants kit is the optimal solution for tasks requiring high-quality DNA (PCR, sequencing) for pine. For large-scale screening of pine, the classic CTAB method with subsequent cleanup is preferable. For English oak, none of the tested methods yielded a satisfactory result, indicating the need to develop specialized protocols including PVP pre-treatment steps.

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Publication Details

Journal
Forestry Engineering Journal
Published
2025-09-28
DOI
https://doi.org/10.34220/issn.2222-7962/2025.3/6
Primary Topic
Forest ecology and management
Type
article
Field-Weighted Citation Impact
0.00

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article

Efficiency of DNA extraction from the leaves of the common oak (Q. robur L.) and the needles of the Scots pine (P. sylvestris L.)

Ekaterina Trapeznikova, Sergey Matveev
Forestry Engineering Journal
Forest ecology and management
article

Efficiency of DNA extraction from the leaves of the common oak (Q. robur L.) and the needles of the Scots pine (P. sylvestris L.)

Ekaterina Trapeznikova, Sergey Matveev
article en

Abstract

The extraction of high-quality DNA from tissues of woody plants, such as English oak (Quercus robur L.) and Scots pine (Pinus sylvestris L.), is challenging due to the high content of secondary metabolites (polyphenols, polysac-charides). These compounds co-extract with nucleic acids and inhibit downstream molecular genetic analyses. The aim of this work was a comparative evaluation of the efficiency of different DNA extraction methods (a modified CTAB protocol, a CTAB protocol with additional cleanup, and two commercial kits: the SKYSuper Plant Genomic DNA Kit and D-Plants) for obtaining DNA samples suitable for further research. The quality of the DNA preparations was as-sessed spectrophotometrically by the absorbance ratios A260/A280 (to assess protein contamination) and A260/A230 (to assess contamination by polysaccharides and polyphenols), electrophoretically (to visualize DNA integrity and the presence of impurities), and quantitatively. Functional suitability was tested via PCR amplification. For Scots pine nee-dles, the D-Plants kit demonstrated consistently high quality of the preparations (A260/A280 = 1.87 ± 0.33; A260/A230 = 1.95 ± 0.09) and 100% PCR efficiency. The SKYSuper kit showed the highest DNA yield but also signs of degradation (A260/A280 > 2.0) and low PCR efficiency (<50%). The classic CTAB method was the most economi-cal but required mandatory additional cleanup for polysaccharides. For English oak leaves, only the D-Plants kit yield-ed PCR-suitable DNA (80% efficiency), although the yield was very low (0.15 μg), resulting in a high cost per 1 μg of DNA. The other methods, including CTAB with cleanup, failed to produce a functional preparation (0% PCR efficien-cy). The D-Plants kit is the optimal solution for tasks requiring high-quality DNA (PCR, sequencing) for pine. For large-scale screening of pine, the classic CTAB method with subsequent cleanup is preferable. For English oak, none of the tested methods yielded a satisfactory result, indicating the need to develop specialized protocols including PVP pre-treatment steps.

Forestry Engineering Journal
Voronezh State University of Forestry and Technologies (RU)
Russian Science Foundation
Openalex Percentile: Top 73%
Forest ecology and management
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