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首页> 外文期刊>Frontiers in Plant Science >Somatic Embryogenesis in Selected Conifer Trees Pinus nigra Arn. and Abies Hybrids
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Somatic Embryogenesis in Selected Conifer Trees Pinus nigra Arn. and Abies Hybrids

机译:精选针叶树 Pinus nigra Arn的体细胞胚发生。和 Abies 杂种

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Somatic embryogenesis was achieved in the conifers Pinus nigra Arn. and in the hybrids Abies alba × A. cephalonica and Abies alba × A. numidica . For initiation of embryogenic tissue in P. nigra , 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 Abies 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 ( P. nigra ) or Agrobacterium -mediated ( Abies hybrids) methods. A proteomic study was performed to gain a deeper insight into the early stages of P. nigra somatic embryogenesis.
机译:针叶树Pinus nigra Arn实现了体细胞胚胎发生。杂种冷杉(Abies alba×A. cephalonica)和冷杉(Abies alba×A. numidica)的杂种。为了在黑假单胞菌中启动胚发生组织,使用了封闭在大型配子体中的未成熟合子胚。起始的胚发生培养物在补充有9μM2,4-D和2.2μMBA的固体培养基DCR上维持和增殖。显微镜下的调查显示,增生组织中存在双极早期体细胞胚。通过将胚发生组织重悬在液体培养基中也建立了悬浮培养物。脱落酸浓度的实验导致成功的体细胞胚成熟。除脱落酸外,成熟培养基中碳水化合物的含量或更高浓度的胶凝剂也是体细胞胚成熟的重要要求。子叶体细胞胚的发芽发生在无激素的培养基上,并终止于体细胞幼苗的再生。将再生的体细胞幼苗转移到土壤中并能够成功发育。为了在Abies杂种中启动胚发生组织,使用了未成熟或成熟的合子胚以及子叶的幼小外植体,而4.4μMBA作为唯一的植物生长调节剂就足够了。相同组成的培养基也适合于长期维护。在补充有38μM脱落酸,聚乙二醇(0、5、7.5和10%PEG-4000)和不同碳水化合物(例如麦芽糖,蔗糖和葡萄糖)(每种为3%)的固体DCR培养基上,体细胞胚成熟。 PEG-4000刺激体细胞胚发育,具体取决于所使用的碳水化合物来源。子叶体细胞胚经过干燥处理后发芽,并将再生的体细胞幼苗转移到土壤中。冷冻保存胚胎发生组织可能是长期维持的另一种方法。对于冷冻保存,成功使用了慢速冷冻方法。解冻后的组织再生较高,并且再生的组织产生成熟的体细胞胚和随后的小植株。胚发生组织还用于通过生物弹(P. nigra)或农杆菌介导的(Abies hybrids)方法进行遗传转化的实验中。进行了蛋白质组学研究,以更深入地了解黑假单胞菌体细胞胚发生的早期阶段。

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