Cryopreservation: A tool to conserve date palm in Saudi Arabia
The cryostoring of embryogenic tissue of the date palm (Phoenix dactylifera L. cv. Sagai) was examined through dehydrated-encapsulation, vitrification, and vitrification-encapsulation. The most extreme regeneration rate (53.33%) of epitomized, cryostored liquid nitrogen (+LN) treated embryos was obs...
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doaj-1471e266154642848cf3e3030d66077f2020-11-25T02:07:51ZengElsevierSaudi Journal of Biological Sciences1319-562X2019-11-0126718961902Cryopreservation: A tool to conserve date palm in Saudi ArabiaSaleh Alansi0Fahad Al-Qurainy1Mohammad Nadeem2Salim Khan3Mohamed Tarroum4Aref Alshameri5Abdel-Rhman Z. Gaafar6Department of Botany and Microbiology, College of Science, King Saud University, Riyadh 11451, Saudi ArabiaDepartment of Botany and Microbiology, College of Science, King Saud University, Riyadh 11451, Saudi ArabiaCorresponding author.; Department of Botany and Microbiology, College of Science, King Saud University, Riyadh 11451, Saudi ArabiaDepartment of Botany and Microbiology, College of Science, King Saud University, Riyadh 11451, Saudi ArabiaDepartment of Botany and Microbiology, College of Science, King Saud University, Riyadh 11451, Saudi ArabiaDepartment of Botany and Microbiology, College of Science, King Saud University, Riyadh 11451, Saudi ArabiaDepartment of Botany and Microbiology, College of Science, King Saud University, Riyadh 11451, Saudi ArabiaThe cryostoring of embryogenic tissue of the date palm (Phoenix dactylifera L. cv. Sagai) was examined through dehydrated-encapsulation, vitrification, and vitrification-encapsulation. The most extreme regeneration rate (53.33%) of epitomized, cryostored liquid nitrogen (+LN) treated embryos was observed when pre-embryonic masses were hatched with 0.5 M sucrose for 48 h pursued by 6 h air drying out. The most noteworthy survival rate (80.0%) of epitomized, cryopreserved embryonic cluster came about when calli were hatched with 0.3 or 0.7 M sucrose for 48 h pursued by four hours of lack of hydration, or with 0.5 M sucrose for 48 h without air drying out or with 2 h of air drying out. Following cryopreservation utilizing the embodiment vitrification convention, the most astounding survival (86.7%) as well as the greatest growth (46.7%) was accomplished when the typified vitrified, cryopreserved calli were treated with Vitrification Solution 2 for plants (PVS2) for 60 min at 25 °C. Cryopreservation utilizing the vitrification convention brought about the most extreme recuperation of 53.3%, when vitrified-cryopreserved calli were subjected to PVS2 solution for 30 min at 25 °C. Most extreme (40%) regeneration of vitrified, cryopreserved embryonic calli was seen when these calli were treated with PVS2 solution for 60 min at 25 °C. The outcome got amid this investigation of regrowth after cryopreservation of the cv. Sagai was over the base suitable for a cryo-germplasm bank. Recovery and regrowth were above 30% for all the techniques developed for the cv. Sagai. Keywords: Cryopreservation, Date palm, Embryogenesis, Vitrification, Encapsulation, Dehydrationhttp://www.sciencedirect.com/science/article/pii/S1319562X19300191 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Saleh Alansi Fahad Al-Qurainy Mohammad Nadeem Salim Khan Mohamed Tarroum Aref Alshameri Abdel-Rhman Z. Gaafar |
spellingShingle |
Saleh Alansi Fahad Al-Qurainy Mohammad Nadeem Salim Khan Mohamed Tarroum Aref Alshameri Abdel-Rhman Z. Gaafar Cryopreservation: A tool to conserve date palm in Saudi Arabia Saudi Journal of Biological Sciences |
author_facet |
Saleh Alansi Fahad Al-Qurainy Mohammad Nadeem Salim Khan Mohamed Tarroum Aref Alshameri Abdel-Rhman Z. Gaafar |
author_sort |
Saleh Alansi |
title |
Cryopreservation: A tool to conserve date palm in Saudi Arabia |
title_short |
Cryopreservation: A tool to conserve date palm in Saudi Arabia |
title_full |
Cryopreservation: A tool to conserve date palm in Saudi Arabia |
title_fullStr |
Cryopreservation: A tool to conserve date palm in Saudi Arabia |
title_full_unstemmed |
Cryopreservation: A tool to conserve date palm in Saudi Arabia |
title_sort |
cryopreservation: a tool to conserve date palm in saudi arabia |
publisher |
Elsevier |
series |
Saudi Journal of Biological Sciences |
issn |
1319-562X |
publishDate |
2019-11-01 |
description |
The cryostoring of embryogenic tissue of the date palm (Phoenix dactylifera L. cv. Sagai) was examined through dehydrated-encapsulation, vitrification, and vitrification-encapsulation. The most extreme regeneration rate (53.33%) of epitomized, cryostored liquid nitrogen (+LN) treated embryos was observed when pre-embryonic masses were hatched with 0.5 M sucrose for 48 h pursued by 6 h air drying out. The most noteworthy survival rate (80.0%) of epitomized, cryopreserved embryonic cluster came about when calli were hatched with 0.3 or 0.7 M sucrose for 48 h pursued by four hours of lack of hydration, or with 0.5 M sucrose for 48 h without air drying out or with 2 h of air drying out. Following cryopreservation utilizing the embodiment vitrification convention, the most astounding survival (86.7%) as well as the greatest growth (46.7%) was accomplished when the typified vitrified, cryopreserved calli were treated with Vitrification Solution 2 for plants (PVS2) for 60 min at 25 °C. Cryopreservation utilizing the vitrification convention brought about the most extreme recuperation of 53.3%, when vitrified-cryopreserved calli were subjected to PVS2 solution for 30 min at 25 °C. Most extreme (40%) regeneration of vitrified, cryopreserved embryonic calli was seen when these calli were treated with PVS2 solution for 60 min at 25 °C. The outcome got amid this investigation of regrowth after cryopreservation of the cv. Sagai was over the base suitable for a cryo-germplasm bank. Recovery and regrowth were above 30% for all the techniques developed for the cv. Sagai. Keywords: Cryopreservation, Date palm, Embryogenesis, Vitrification, Encapsulation, Dehydration |
url |
http://www.sciencedirect.com/science/article/pii/S1319562X19300191 |
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