2017
DOI: 10.17513/mjpfi.12010
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Study of the Domestic Breeding Winter Rape Morphogenetic Potential Using in Vitro Culture

Abstract: Проведена оптимизация условий индукции каллусогенеза и регенерации побегов озимого рапса сорта Северянин из гипокотилей 14-дневных проростков. Учитывались следующие параметры культивирования растений в условиях in vitro: эффективность стерилизации, обеспечивающая наибольший выход стериль-ного материала при наименьшей его гибели, влияние типа экспланта и комбинаций регуляторов роста на каллусогенез, пролиферацию и регенерацию растений. Эффективность каллусогенеза составила от 65 до 100 % на всех экспериментальн… Show more

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“…After drying in air flow laminar box, the explants were transferred onto filter paper, placed on a solid surface of MS medium supplemented with 1.0 mg•L −1 2,4-D in Petri dishes, and co-cultivated in light conditions at a temperature of 21 • C for 72 h. After co-cultivation period, the explants were washed with liquid MS medium, with a lack organic components but supplemented with 300 mg•L −1 Tm, and then transferred to the medium for explants cultivation and elimination of Agrobacterium (MS medium containing 1.0 mg•L −1 2,4-D and 150 mg•L −1 tmimentine (Tm) with the addition of 100 mg•L −1 kanamycin sulfate (Km)). Two weeks later, the explants were transferred to regeneration medium-MS medium supplemented with 4.0 mg•L −1 N 6 -benzyladenine, mg•L −1 Zeatin, 5.0 mg•L −1 AgNO 3 [47], and 150 mg•L −1 Tm and 100 mg•L −1 Km. Every 2 weeks, explants were transferred to fresh media.…”
Section: Tissue Culture Agrobacterium-mediated Transformation and Obtaining Generation Tmentioning
confidence: 99%
“…After drying in air flow laminar box, the explants were transferred onto filter paper, placed on a solid surface of MS medium supplemented with 1.0 mg•L −1 2,4-D in Petri dishes, and co-cultivated in light conditions at a temperature of 21 • C for 72 h. After co-cultivation period, the explants were washed with liquid MS medium, with a lack organic components but supplemented with 300 mg•L −1 Tm, and then transferred to the medium for explants cultivation and elimination of Agrobacterium (MS medium containing 1.0 mg•L −1 2,4-D and 150 mg•L −1 tmimentine (Tm) with the addition of 100 mg•L −1 kanamycin sulfate (Km)). Two weeks later, the explants were transferred to regeneration medium-MS medium supplemented with 4.0 mg•L −1 N 6 -benzyladenine, mg•L −1 Zeatin, 5.0 mg•L −1 AgNO 3 [47], and 150 mg•L −1 Tm and 100 mg•L −1 Km. Every 2 weeks, explants were transferred to fresh media.…”
Section: Tissue Culture Agrobacterium-mediated Transformation and Obtaining Generation Tmentioning
confidence: 99%