Al-Balqa Applied University, Faculty of Agricultural Technology, Department of Biotechnology, Al-Salt, Jordan.
The University of Jordan, Hamdi Mango Center for Scientific Research (HMCSR), Amman, Jordan; The University of Jordan, Faculty of Agriculture, Department of Horticulture and Crop Sciences, Amman, Jordan.
Braz J Biol. 2024 Aug 12;84:e284231. doi: 10.1590/1519-6984.284231. eCollection 2024.
Date palm (Phoenix dactylifera( cv. Medjool is a significant plant, grown in Jordan. In vitro propagation gives operative resources for the significant propagation of date palms. Maximum callus induction was achieved from MS media supplemented with benzyl amino purine (BA) and naphthalene acetic acid (NAA). The highest plant regeneration was recorded on MS medium supplemented with dichlorophenoxyacetic acid (2,4-D) at 3.0 mg/L, and BA at 2.0 mg/L. A significant positive impact on shoot formation was recorded on MS medium supplemented with 1.0 mg/L BA with 0.5 to 1.5 mg/L NAA in both liquid and solid MS medium. To maintain survival and regrowth capacity, sucrose could be used for medium-term conservation at lower concentrations (0.1 - 0.2 M). In addition, sorbitol might be used at 0.1 M to maintain the quality of explants. The vitrification technique for long-term preservation was experimented. Embryogenic callus was used as explants for conservation. The survival as well as regrowth percentages of non-cryopreserved and cryopreserved tissue cultures were affected by their duration of treatment with the vitrification solution plant vitrification solution 2 (PVS2) and modified plant vitrification solution 2 (MPVS2). Results showed that using PVS2 for 60 minutes for cryopreserved calli was more effective than other treatments. After storage in liquid nitrogen, the highest survival rate (65%) and regrowth rate (40%) were achieved.
海枣(Phoenix dactylifera cv. Medjool)是一种重要的植物,在约旦种植。离体繁殖为海枣的重要繁殖提供了操作资源。最大的愈伤组织诱导是在添加苯氨基嘌呤(BA)和萘乙酸(NAA)的 MS 培养基上实现的。在补充有二氯苯氧乙酸(2,4-D)3.0mg/L 和 BA 2.0mg/L 的 MS 培养基上记录到最高的植物再生。在添加 1.0mg/L BA 和 0.5-1.5mg/L NAA 的 MS 培养基上,无论是在液体还是固体 MS 培养基中,对芽形成都有显著的正向影响。为了保持生存和再生能力,可以在较低浓度(0.1-0.2M)下使用蔗糖进行中期保存。此外,山梨醇可以在 0.1M 下使用以保持外植体的质量。还进行了长期保存的玻璃化技术实验。胚胎发生愈伤组织用作保存的外植体。未冷冻和冷冻组织培养物的存活率和再生率受到其用玻璃化溶液植物玻璃化溶液 2(PVS2)和改良植物玻璃化溶液 2(MPVS2)处理时间的影响。结果表明,对于冷冻愈伤组织,使用 PVS2 处理 60 分钟比其他处理更有效。在液氮中储存后,达到了最高的存活率(65%)和再生率(40%)。