Salaj Terézia, Klubicová Katarína, Matusova Radoslava, Salaj Ján
Institute of Plant Genetics and Biotechnology, Plant Science and Biodiversity Center, Slovak Academy of Sciences, Nitra, Slovakia.
Front Plant Sci. 2019 Jan 29;10:13. doi: 10.3389/fpls.2019.00013. eCollection 2019.
Somatic embryogenesis was achieved in the conifers Arn. and in the hybrids × and ×. For initiation of embryogenic tissue in , immature zygotic embryos enclosed in megagametophytes were used. The initiated embryogenic cultures were maintained and proliferated on solid culture medium DCR supplemented with 9 μM 2,4-D and 2.2 μM BA. Microscopic investigations revealed the presence of bipolar early somatic embryos in proliferating tissue. Suspension cultures have also been established by resuspending the embryogenic tissue in liquid culture medium. Experimentation with abscisic acid concentration resulted in successful somatic embryo maturation. Besides abscisic acid, the carbohydrate content or higher concentration of gelling agent in maturation medium were also important requirements for somatic embryo maturation. Germination of cotyledonary somatic embryos occurred on hormone-free medium and terminated in somatic seedlings regeneration. The regenerated somatic seedlings were transferred to soil and were capable of successful development. For initiation of embryogenic tissue in hybrids juvenile explants as immature or mature zygotic embryos as well as cotyledons were used and 4.4 μM BA as sole plant growth regulator was sufficient. Medium of the same composition was also suitable for their long-term maintenance. Maturation of somatic embryos was achieved on solid DCR medium supplemented with 38 μM abscisic acid, polyethylene glycol (0, 5, 7.5, and 10% PEG-4000) and different carbohydrates such as maltose, sucrose and glucose (each 3%). PEG-4000 stimulated somatic embryo development depending on the carbohydrate source used. Cotyledonary somatic embryos germinated after desiccation treatment and the regenerated somatic seedlings were transferred to soil. Cryopreservation of embryogenic tissue could be an alternative method for long-term maintenance. For cryopreservation the slow-freezing method was used with success. Tissue regeneration in the post thaw period was relatively high and the regenerated tissue produced mature somatic embryos and subsequent plantlets. The embryogenic tissue was also used in experiments focused on genetic transformation either by biolistic () or -mediated ( hybrids) methods. A proteomic study was performed to gain a deeper insight into the early stages of somatic embryogenesis.
在针叶树Arn.以及杂交种×和×中实现了体细胞胚胎发生。对于×中胚性组织的诱导,使用了包裹在大配子体中的未成熟合子胚。诱导出的胚性培养物在添加了9 μM 2,4 - D和2.2 μM BA的固体培养基DCR上进行维持和增殖。显微镜观察显示在增殖组织中存在双极早期体细胞胚。通过将胚性组织重悬于液体培养基中也建立了悬浮培养物。对脱落酸浓度的实验导致体细胞胚成功成熟。除了脱落酸外,成熟培养基中的碳水化合物含量或更高浓度的胶凝剂也是体细胞胚成熟的重要条件。子叶体细胞胚在无激素培养基上萌发,并最终再生出体细胞幼苗。再生的体细胞幼苗被转移到土壤中并能够成功发育。对于×杂交种中胚性组织的诱导,使用了未成熟或成熟的合子胚以及子叶等幼嫩外植体,并且仅使用4.4 μM BA作为植物生长调节剂就足够了。相同成分的培养基也适合它们的长期维持。体细胞胚的成熟在添加了38 μM脱落酸、聚乙二醇(0、5、7.5和10% PEG - 4000)以及不同碳水化合物如麦芽糖、蔗糖和葡萄糖(各3%)的固体DCR培养基上实现。PEG - 4000根据所使用的碳水化合物来源刺激体细胞胚的发育。子叶体细胞胚在干燥处理后萌发,再生的体细胞幼苗被转移到土壤中。胚性组织的冷冻保存可能是一种长期保存的替代方法。对于冷冻保存,成功使用了慢速冷冻法。解冻后时期的组织再生率相对较高,再生组织产生成熟的体细胞胚和随后的植株。胚性组织还被用于通过生物枪法(×)或农杆菌介导(×杂交种)方法进行遗传转化的实验。进行了一项蛋白质组学研究以更深入地了解×体细胞胚胎发生的早期阶段。