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An optimized high-quality DNA isolation protocol for spodoptera frugiperda J. E. smith (Lepidoptera: Noctuidae).
Marín, Diana Victoria; Castillo, Diana Katherine; López-Lavalle, Luis Augusto Becerra; Chalarca, Jairo Rodríguez; Pérez, Cristo Rafael.
Afiliação
  • Marín DV; Universidad Nacional de Colombia, Sede Palmira, Palmira, Valle del Cauca, Colombia.
  • Castillo DK; The Alliance of Bioversity International and the International Center for Tropical Agriculture (CIAT), Recta Cali-Palmira km 17, Valle del Cauca, Colombia.
  • López-Lavalle LAB; The Alliance of Bioversity International and the International Center for Tropical Agriculture (CIAT), Recta Cali-Palmira km 17, Valle del Cauca, Colombia.
  • Chalarca JR; The Alliance of Bioversity International and the International Center for Tropical Agriculture (CIAT), Recta Cali-Palmira km 17, Valle del Cauca, Colombia.
  • Pérez CR; The Alliance of Bioversity International and the International Center for Tropical Agriculture (CIAT), Recta Cali-Palmira km 17, Valle del Cauca, Colombia.
MethodsX ; 8: 101255, 2021.
Article em En | MEDLINE | ID: mdl-34434778
ABSTRACT
An optimized high-quality DNA isolation protocol was developed using body segment tissue from the Fall Armyworm (Spodoptera frugiperda), that will allow documenting genetic variability based on biotypes, facilitating studies on the appearance, distribution and population dynamics of the fall armyworm at the molecular level. The resulting protocol is an easy-to-use, timesaving method that can rapidly achieve high quality, high-yielding total genomic DNA, using chemicals and everyday consumables available in a molecular laboratory. This new method of DNA extraction avoids the contamination of polysaccharides, salts, phenols, proteins and other cellular by-products that can interfere with subsequent reactions. DNA purity estimates reveal A260 A280 ratios greater than 1.9, which were evidenced by quality test on agarose gel, observing complete integrity and high purity of the resulting samples, and yielded 30-99 µg/g of total DNA. Therefore, the quality of the DNA produced from this extraction is suitable for subsequent molecular applications (i) next generation whole genome sequencing, (ii) conventional polymerase chain reaction for genotyping, (iii) barcodes and (iv) gene cloning. In addition, to become an anticipating diagnostic tool for invasive lepidopteran larval stages•The resulting protocol is an easy-to-use time-saving method.•This new extraction method prevents contamination from polysaccharides, salts, phenols, proteins, and other cellular sub-products.•DNA purity estimations reveal A260A280 ratios above 1.9.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Guideline Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Guideline Idioma: En Ano de publicação: 2021 Tipo de documento: Article