Cryopreservation of shoot apices and callus cultures of globe artichoke using vitrification method
Autor: | Alaa M. El-Minisy, Hattem M. El-Shabrawi, Valbona Sota, Shawky A. Bekheet |
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Rok vydání: | 2020 |
Předmět: |
0106 biological sciences
lcsh:QH426-470 Cryoprotectant lcsh:Biotechnology Biology Cell morphology 01 natural sciences Cryopreservation Globe artichoke 040501 horticulture Tissue culture lcsh:TP248.13-248.65 Genetics Vitrification Research fungi Fresh weight food and beverages 04 agricultural and veterinary sciences lcsh:Genetics Horticulture Callus Shoot 0405 other agricultural sciences 010606 plant biology & botany Biotechnology |
Zdroj: | Journal of Genetic Engineering & Biotechnology Journal of Genetic Engineering and Biotechnology, Vol 18, Iss 1, Pp 1-8 (2020) |
ISSN: | 2090-5920 |
DOI: | 10.1186/s43141-019-0016-1 |
Popis: | BackgroundCryogenic cooling became a crucial tool for the storage ofheterozygous plants such asglobe artichoke. This study was carried out to optimize a reliable method for in vitro cryopreservation of shoot apices and callus cultures of globe artichoke using dimethylsulfoxide (DMSO) and Plant Vitrification Solutions 2 (PVS2) as cryoprotectant solutions. Shoot apices were exposed to DMSO or PVS2 for 20, 40, 60, and 80 min prior to plunge in liquid nitrogen (LN).ResultsIt was found that using PVS2 as a cryoprotectant in cryopreservation of shoot apices of globe artichoke was more effective compared with using of DMSO alone. Among the exposure time tested, 60 min gave the best results of survival. The highest survival (60%), regeneration (56%), and proliferated shootlets (4.30) were obtained after cryoprotection with PVS2 for 60 min. Regarding callus cultures, the maximum values of fresh weights and subsequently growth value of recovered callus were registered with 40 min followed by 60 min exposure time. Related to the type of the tested cryoprotectants, the best survival and growth parameters of the cryopreserved callus cultures were obtained with PVS2 treatments. Treatment with PVS2 for 40 min registered the highest survival observations of cryopreserved callus. Also, the maximum values of fresh weight (1.30 g) and growth value (4.20) were obtained with 40 min exposure time. Microscopy analysis presented as cell morphology revealed that the treatment of PVS2 40% was the optimum for cell growth of cryopreserved callus of globe artichoke.ConclusionThe results demonstrated that using PVS2 as a cryoprotectant in cryopreservation of shoot apices and callus cultures of globe artichoke was more effective compared with DMSO. |
Databáze: | OpenAIRE |
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