2020
DOI: 10.17816/ecogen12977
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Modern approach of structuring the variety diversity of the naked and covered forms of cultural oats (Avena sativa L.)

Abstract: Background. Structuring and phenotyping genetic diversity is an important aspect of the work with breeding sources and materials. In the Introduction, the authors pointed out the role of N.I. Vavilovs scientific foresight in defining the topical trend in researching the genetic diversity of a crop, particularly the analysis of its biochemical composition. As the target of their research, the authors chose biochemical characters identifiable in the process of metabolomic analysis conducted by means of gas chrom… Show more

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Cited by 17 publications
(8 citation statements)
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“…Primary and secondary metabolites were analyzed using gas chromatography with mass spectrometry according to a published protocol [58]. The ground sample (40-50 mg) was mixed with methanol at a ratio of 1:10 (w:v); the sample was infused for no less than 30 days at 5-6 • C; the resulting extract was centrifuged at 14,000 rpm for 10 min;100 µL of the extract was dried on a CentriVap Concentrator (Labconco, Kansas, MI, USA); then 20 µL of tricosane solution in pyridine (concentration: 1 µg/µL) was added to the sample as an internal standard, and the result was silylated with 50 µL of N,O-bis(trimethylsilyl)trifluoroacetamide for 40 min at 100 • C. The sample (1.2 µL) was separated using an HP-5MS capillary column (5% phenyl 95% methylpolysiloxane, 30.0 m, 250.00 µm, 0.25 µm; Agilent Technologies, Palo Alto, CA, USA) on an Agilent 6850 gas chromatograph with a quadrupole mass selective detector (Agilent 5975B VL MSD, Agilent Technologies).…”
Section: Gc-ms Analysismentioning
confidence: 99%
“…Primary and secondary metabolites were analyzed using gas chromatography with mass spectrometry according to a published protocol [58]. The ground sample (40-50 mg) was mixed with methanol at a ratio of 1:10 (w:v); the sample was infused for no less than 30 days at 5-6 • C; the resulting extract was centrifuged at 14,000 rpm for 10 min;100 µL of the extract was dried on a CentriVap Concentrator (Labconco, Kansas, MI, USA); then 20 µL of tricosane solution in pyridine (concentration: 1 µg/µL) was added to the sample as an internal standard, and the result was silylated with 50 µL of N,O-bis(trimethylsilyl)trifluoroacetamide for 40 min at 100 • C. The sample (1.2 µL) was separated using an HP-5MS capillary column (5% phenyl 95% methylpolysiloxane, 30.0 m, 250.00 µm, 0.25 µm; Agilent Technologies, Palo Alto, CA, USA) on an Agilent 6850 gas chromatograph with a quadrupole mass selective detector (Agilent 5975B VL MSD, Agilent Technologies).…”
Section: Gc-ms Analysismentioning
confidence: 99%
“…A study aimed at identifying biochemical differences (metabolite markers) among naked and hulled oat cultivars for subsequent phenotyping the varietal gene pool of common oat was accomplished by Loskutov et al [ 96 ]. The naked oat forms were found to have a higher content of hydroxybenzoic acids, and the hulled forms contained more phenols.…”
Section: Study Of Oat and Barley Accessions From The Vir Global Collection For The Content Of Bioactive Components In Grainmentioning
confidence: 99%
“…et Sold. ), which differ from each other in their morphological characteristics, biochemical properties and resistance to abiotic and biotic factors, were described (Kobylyansky, Soldatov, 1994;Loskutov et al, 2020). The relatively high resistance of naked oats to Fusarium infection of grain, in comparison with husked oats, has been repeatedly noted (Tekauz et al, 2008;Yan et al, 2010;Gagkaeva et al, 2013;Martin et al, 2018;Chropová et al, 2020).…”
Section: Introductionmentioning
confidence: 97%