2017
DOI: 10.15407/cryo27.02.110
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Hypothermic and Low-Temperature Storage of Garlic (Allium sativum L.) for in Vitro Collections

Abstract: Гіпотермічне та низькотемпературне зберігання рослин-регенерантів і меристем часнику (Allium sativum L.) для створення in vitro колекцій T.V. Ivchenko 2 , T.I. Vitsenya 2 , N.A. Shevchenko 1 *, N.O. Bashtan 2 , S.I. Kornienko 2 Hypothermic and Low-Temperature Storage of Garlic (Allium sativum L.) for In Vitro CollectionsРеферат: В Україні розроблюють способи створення колекцій генетичних ресурсів рослин. У роботі досліджували вплив різних умов зберігання на показники життєздатності колекційних зразків часнику… Show more

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Cited by 4 publications
(2 citation statements)
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“…The first group contained meristems dehydrated for 120 min with sterile airflow (AD), frozen by plunging into LN on a needle tip, and re-warmed in MS medium, enriched with 12%sucrose. Other groups consisted of meristems incubated for 60 min at 22 °C with the following cryoprotectant solutions: (i) PVS 2 (30% glycerol + 15% ethylene glycol + 15% dimethyl sulfoxide and 0.4 M sucrose [11]), (ii) 88% PVS 3 (44% glycerol + 44% sucrose [8]), (iii) modified PVS 1 (22% glycerol + 13% 1,2-propylene glycol + 13% ethylene glycol + 6% dimethyl sulfoxide and 0.4 M sucrose [14]) and (iv) PVS N (1 M sucrose + 15% glycerol + 14% ethylene glycol [4]). The meristems of all groups after PVSs treatment were cooling 1.8 mL cryovials («Corning», USA) or 50 µl hermetically sealed aluminum pans for differential scanning calorimetry (DSC) and were directly immersed into LN for 1 h. The specimens were re-warmed in water bath at 40 °C.…”
Section: Methodsmentioning
confidence: 99%
“…The first group contained meristems dehydrated for 120 min with sterile airflow (AD), frozen by plunging into LN on a needle tip, and re-warmed in MS medium, enriched with 12%sucrose. Other groups consisted of meristems incubated for 60 min at 22 °C with the following cryoprotectant solutions: (i) PVS 2 (30% glycerol + 15% ethylene glycol + 15% dimethyl sulfoxide and 0.4 M sucrose [11]), (ii) 88% PVS 3 (44% glycerol + 44% sucrose [8]), (iii) modified PVS 1 (22% glycerol + 13% 1,2-propylene glycol + 13% ethylene glycol + 6% dimethyl sulfoxide and 0.4 M sucrose [14]) and (iv) PVS N (1 M sucrose + 15% glycerol + 14% ethylene glycol [4]). The meristems of all groups after PVSs treatment were cooling 1.8 mL cryovials («Corning», USA) or 50 µl hermetically sealed aluminum pans for differential scanning calorimetry (DSC) and were directly immersed into LN for 1 h. The specimens were re-warmed in water bath at 40 °C.…”
Section: Methodsmentioning
confidence: 99%
“…To significantly reduce the intensity of metabolic processes (respiration, water loss, wilting, ethylene release) and to slow down the processes of physiological aging of cells in in vitro cultures, to prevent depletion of nutrient media, and to reduce chances of damage to plant material by bacterial infections, one can lower the storage temperature (Bamberg, J. B. et al, 2016, Ivchenko, T. et al, 2017. However, when explants are stored at low above-zero temperatures in temperaturedemanding cultures, excessive formation of reactive oxygen species is observed and they are able to lead to stress and induce mutations because of damage to DNA (Cassells, A.C. & Curry, R.F., 2001).…”
mentioning
confidence: 99%