Evidence map›Paper›PMID 40569330›Full record

ArticleMolecular biology reports2025

Improved genomic DNA extraction from citrus species using a modified CTAB method.

Komaljeet Gill, Shivanti Negi, Pankaj Kumar, Mohammad Irfan

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Article in Molecular biology reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

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10citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

10 citing papers in PubMed.

  1. Article
  2. Mechanism of Terpene Formation inInternational journal of molecular sciences · 2026
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  6. A novelFrontiers in plant science · 2026
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  7. The complete chloroplast genome sequence ofMitochondrial DNA. Part B, Resources · 2026
    Article
  8. Article
  9. Article
  10. Article
4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Komaljeet Gill *Department of Biotechnology, Dr. Yashwant Singh Parmar University of Horticulture and Forestry, Solan, Himachal Pradesh, India. singh.komal2111@gmail.com.
Shivanti Negi *Department of Biotechnology, Dr. Yashwant Singh Parmar University of Horticulture and Forestry, Solan, Himachal Pradesh, India.
Pankaj Kumar *Department of Biotechnology, Dr. Yashwant Singh Parmar University of Horticulture and Forestry, Solan, Himachal Pradesh, India. pksharmabiotech@gmail.com.ORCID http://orcid.org/0000-0002-2275-9144
Mohammad IrfanPlant Biology Section, School of Integrative Plant Science, Cornell University, Ithaca, NY, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCitrus species are recalcitrant to DNA extraction due to high levels of polysaccharides, polyphenols, and secondary metabolites that interfere with DNA yield and purity. This study presents an optimized cetyltrimethylammonium bromide (CTAB)-based protocol for efficient genomic DNA isolation from citrus leaves.

methodsLeaf tissues were ground in liquid nitrogen and extracted using a CTAB buffer supplemented with 2% β-mercaptoethanol and 2% polyvinylpyrrolidone. Contaminants were removed by two rounds of phenol: chloroform: isoamyl alcohol (25:24:1) extraction. RNase A treatment was applied, followed by DNA precipitation using cold isopropanol. DNA quality was assessed by A260/280 absorbance ratios and agarose gel electrophoresis. Statistical comparisons were made using the Mann-Whitney U test, Cohen's d, and bootstrap resampling.

resultsThe modified protocol yielded high-molecular-weight DNA with A260/280 ratios ranging from 1.78 to 1.98, indicating high purity. Electrophoresis confirmed intact DNA with minimal RNA contamination. DNA yield and band intensity were significantly higher than with the conventional method (p < 0.001, Cohen's d = -2.10). A positive correlation (r = 0.23) was observed between yield and band intensity. Bootstrap confidence intervals for mean band intensity were 0.11-0.20 (conventional) and 2.91-4.84 (modified).

conclusionThe optimized CTAB protocol provides a simple, cost-effective, and reproducible method for high-quality genomic DNA extraction from citrus, suitable for PCR, genotyping, and sequencing applications.

Indexed as

CitrusDNA, PlantCetrimoniumCetrimonium CompoundsGenome, PlantPlant LeavesCetrimoniumCetrimonium CompoundsDNA, PlantCitrusCTAB methodDNA isolationDNA qualityDNA yieldGel electrophoresisStatistical analysis

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.