首页> 外文期刊>Propagation of Ornamental Plants >Callus development in tree peonies (Paeonia sect. Moutan): influence of genotype, explant developmental stage and position, and plant growth regulators.
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Callus development in tree peonies (Paeonia sect. Moutan): influence of genotype, explant developmental stage and position, and plant growth regulators.

机译:树牡丹(<药属)中的愈伤组织发育:基因型,外植体发育阶段和位置以及植物生长调节剂的影响。

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Tree peonies (Paeonia sect. Moutan) are important ornamental plants, but their industrial exploitation is limited by the low yield of conventional propagation methods. In the present study, callus formation and development were successfully achieved through the selection of genotypes, developmental stage and position of explants, and plant growth regulators. Petiole layers collected during flowering as explants from seven different tree peony cultivars were cultured on Schenk and Hildebrandt (SH) medium supplemented with 0-2 mg l-1 2,4-D and subcultured on the same basal medium supplemented with 0.2-0.5 mg l-1 2,4-D and 2-6 mg l-1 BA. The best performing cultivar was 'Golden Era', which produced a nodular structure within 90 days, while small calluses with low frequency were observed in 'Luo Yang Hong'. Explants taken from the basal or top petioles between flowering and 1 week after blossom fall showed negligible browning. In contrast, considerable browning was observed in middle petiole explants or those collected later than 1 week after blossom fall. The optimum medium for callus induction was SH medium containing 1 mg l-1 2,4-D. Callus proliferated into nodule structures on SH medium containing 0.2 mg l-1 2,4-D and 6 mg l-1 BA for 'Golden Era' and 'Bartzella' and 0.5 mg l-1 2,4-D and 2 mg l-1 BA for 'High Noon'. Nodules continued to proliferate under dark conditions. When the nodules of 'Golden Era' were transferred onto SH medium supplemented with combination of 0.25 mg l-1 NAA and 0.5 mg l-1 thidiazuron, and under continuous light condition shoot-buds differentiated from them. Histological studies suggested that callus derived from cambium and cortex parenchyma cells and then differentiated into nodular callus. Increased division of the epidermal and subepidermal cells of nodular callus led to shoot-bud regeneration.
机译:牡丹(牡丹)是重要的观赏植物,但由于常规繁殖方法产量低而限制了其工业开发。在本研究中,通过选择基因型,外植体的发育阶段和位置以及植物生长调节剂,成功地实现了愈伤组织的形成和发育。在开花期间从七个不同的牡丹品种的外植体上收集的叶柄层在补充了0-2 mg l -1 2,4-D的Schenk和Hildebrandt(SH)培养基上培养,并在同一基础上继代培养培养基中添加了0.2-0.5 mg l -1 2,4-D和2-6 mg l -1 BA。表现最好的品种是“黄金时代”,在90天内产生了结节状的结构,而在“罗阳红”中观察到了频率较低的老茧。开花至开花后1周之间从基部或顶部叶柄提取的植株显示出可忽略的褐变。相反,在叶柄中部外植体或开花落下后1周后收集到的外植体中出现了明显的褐变。愈伤组织诱导的最佳培养基是含有1 mg l -1 2,4-D的SH培养基。愈伤组织在含有0.2 mg l -1 2,4-D和6 mg l -1 BA的SH培养基上增殖成根瘤结构,“黄金时代”和“ Bartzella”以及0.5 mg l -1 2,4-D和2 mg l -1 BA用于“正午”。结节在黑暗条件下继续扩散。将“金时代”的根瘤转移至补充有0.25 mg l -1 NAA和0.5mg l -1 噻唑隆的SH培养基上并在连续光照条件下芽预算与他们不同。组织学研究表明,愈伤组织来源于形成层和皮质薄壁细胞,然后分化为结节性愈伤组织。结节性愈伤组织的表皮和表皮下细胞分裂增加导致芽芽再生。

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