2016
DOI: 10.17660/actahortic.2016.1113.40
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In vitro collection methods forMalusshoot cultures used for developing a cryogenic bank in Kazakhstan

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Cited by 11 publications
(11 citation statements)
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“…These recent cases emphasize the importance of explant disinfection and contamination, even though many disinfection protocols are already available. Romadanova et al (2016b) used 523 detection medium (Viss et al 1991) to detect fungal and bacterial contamination in the in vitro culture of apple cultivars, clonal rootstocks and wild M. sieversii (Ledeb. M.…”
Section: Explant Infection and Disinfection And Wounding-induced Bromentioning
confidence: 99%
See 1 more Smart Citation
“…These recent cases emphasize the importance of explant disinfection and contamination, even though many disinfection protocols are already available. Romadanova et al (2016b) used 523 detection medium (Viss et al 1991) to detect fungal and bacterial contamination in the in vitro culture of apple cultivars, clonal rootstocks and wild M. sieversii (Ledeb. M.…”
Section: Explant Infection and Disinfection And Wounding-induced Bromentioning
confidence: 99%
“…Shoot tip cryotherapy can be used to eradicate viruses from apple. In a study by Romadanova et al (2016b), shoot tips were excised from cold-hardened (22 °C for 8 h/day, then − 1 °C for 16 h/night, for 3 weeks) in vitro shoots and subjected to vitrification cryotherapy, as described by Reed and Yu (1995). Virus-free frequencies were 60-100% for ACLSV in six of the nine genotypes, 25-67% for ASPV in five of the six genotypes, 50% for ASGV in one genotype and 89% for ApMV in one genotype.…”
Section: Cryotherapymentioning
confidence: 99%
“…M. Roem. The collection was obtained in the period from 2002 to 2020 from field plants provided by the Kazakh Research Institute of Fruit Growing and Viticulture, "Liza" Farm, "Suzdaleva" Farm, "Integration-Turgen" LLP, wild forms were collected from the Main Botanical Garden (MBG) and from various areas of the Ile-Alatau National Park [13].…”
Section: Methodsmentioning
confidence: 99%
“…Plants were propagated in vitro on Murashige-Skoog (MS) medium [14] containing 30 g/L sucrose, 0.5 mg/L 6-benzylaminopurine (BAP), 0.01 mg/L indolylbutyric acid (IBA), 4.0 g/L Plant TC agar (Phytotechnology Laboratories®, Lenexa, KS), 1.25 g/L Gelrite™ (Phytotechnology Laboratories®), pH 5.7. All cultures were grown in glass culture vessels (237 mL) (Phytotechnology Laboratories®) in a growth room at 24°C±1°C with 16 h photoperiod of white fluorescent lights at 40 µM m -2 s -1 (standard growth room conditions) with two types of OPPLE tubular fluorescent lamps: YK 21RR 16/G 21W 6500K RGB and YK 21RL 16/G 21W 4000K RGB supplied by ElectroComplex in Corporation, Almaty, Republic of Kazakhstan (http://elcor.kz) [13]. Plants were subcultured in vitro every 3-4 weeks.…”
Section: Methodsmentioning
confidence: 99%
“…has been established and is constantly being updated. A list of cultures in the collection was included in the Botanic Gardens Conservation International (BGCI) database (Romadanova et al 2016a). Cryopreservation is not only used for the long-term preservation of the plant genetic diversity in Kazakhstan, but also for the recovery of crops from phytopathogens (Kushnarenko et al 2017;Romadanova et al 2016b).…”
Section: Conservation and Study Of Genetic Resources Of The Kazakhstamentioning
confidence: 99%