Simão Mariela J, Collin Myriam, Garcia Renata O, Mansur Elisabeth, Pacheco Georgia, Engelmann Florent
Núcleo de Biotecnologia Vegetal, Instituto de Biologia Roberto Alcantara Gomes, Universidade do Estado do Rio de Janeiro, Rua São Francisco Xavier no. 524 PHLC Sala 505, Maracanã, Rio de Janeiro, CEP: 20550-013, Brazil.
DIADE, IRD, CIRAD, CNRS, Université de Montpellier, Montpellier, France.
Protoplasma. 2018 May;255(3):741-750. doi: 10.1007/s00709-017-1182-0. Epub 2017 Nov 12.
Cryopreservation stands out as the main strategy to ensure safe and cost efficient long-term conservation of plant germplasm, especially for biotechnological materials. However, the injuries associated with the procedure may result in structural damage and low recovery rates after cooling. Histological analysis provides useful information on the effects of osmotic dehydration, LN exposure, and recovery conditions on cellular integrity and tissue organization, allowing the determination of the critical steps of the cryopreservation protocol and, thus, the use of optimized treatments. Passiflora pohlii Mast. (Passifloraceae) is a native species from Brazil with potential agronomic interest. Recent studies showed the presence of saponins in its roots, which presented antioxidant activity. The goal of this work was to develop a cryopreservation technique for root tips of in vitro-derived plants of P. pohlii using the V-Cryo-plate technique and to characterize the anatomical alterations that occurred during the successive steps of the protocol. Root tips were excised from in vitro plants and precultured before adhesion to cryo-plates and then treated for different periods with the plant vitrification solutions PVS2 or PVS3. Treatment with PVS2 for 45 min resulted in higher recovery (79%) when compared with PVS3 (43%). The greatest number of adventitious roots per cryopreserved explant was also observed after a 45-min exposure to PVS2. Plasmolysis levels were higher in cortical cells of cryopreserved explants treated with PVS2, while pericycle and central cylinder cells were not damaged after this treatment. Thirty days after rewarming, no plasmolysis could be detected, regardless of the experimental conditions.
冷冻保存是确保植物种质安全且经济高效长期保存的主要策略,尤其是对于生物技术材料而言。然而,与该程序相关的损伤可能会导致冷却后结构破坏和恢复率低。组织学分析提供了关于渗透脱水、液氮暴露和恢复条件对细胞完整性和组织结构影响的有用信息,有助于确定冷冻保存方案的关键步骤,从而采用优化处理。多花西番莲(Passiflora pohlii Mast.,西番莲科)是一种来自巴西的本土物种,具有潜在的农艺价值。最近的研究表明其根部含有皂苷,并具有抗氧化活性。本研究的目的是利用V型冷冻板技术开发一种针对多花西番莲离体植株根尖的冷冻保存技术,并对该方案连续步骤中发生的解剖学变化进行表征。从离体植株上切取根尖,在粘附到冷冻板之前进行预培养,然后用植物玻璃化溶液PVS2或PVS3处理不同时间。与PVS3(43%)相比,用PVS2处理45分钟后的恢复率更高(79%)。在用PVS2处理45分钟后观察到每个冷冻保存外植体上不定根的数量最多。用PVS2处理的冷冻保存外植体的皮层细胞质壁分离程度更高,而在此处理后中柱鞘和中柱细胞未受损。复温30天后,无论实验条件如何,均未检测到质壁分离。