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Propagation through alginate encapsulation of axillary buds of Cannabis sativa L. — an important medicinal plant

机译:重要藻类植物大麻大麻腋芽的藻酸盐包封法繁殖

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摘要

Cannabis sativa L. (Cannabaceae) is an important medicinal plant well known for its pharmacologic and therapeutic potency. Because of allogamous nature of this species, it is difficult to maintain its potency and efficacy if grown from the seeds. Therefore, chemical profile-based screening, selection of high yielding elite clones and their propagation using biotechnological tools is the most suitable way to maintain their genetic lines. In this regard, we report a simple and efficient method for the in vitro propagation of a screened and selected high yielding drug type variety of Cannabis sativa, MX-1 using synthetic seed technology. Axillary buds of Cannabis sativa isolated from aseptic multiple shoot cultures were successfully encapsulated in calcium alginate beads. The best gel complexation was achieved using 5 % sodium alginate with 50 mM CaCl2.2H2O. Regrowth and conversion after encapsulation was evaluated both under in vitro and in vivo conditions on different planting substrates. The addition of antimicrobial substance — Plant Preservative Mixture (PPM) had a positive effect on overall plantlet development. Encapsulated explants exhibited the best regrowth and conversion frequency on Murashige and Skoog medium supplemented with thidiazuron (TDZ 0.5 μM) and PPM (0.075 %) under in vitro conditions. Under in vivo conditions, 100 % conversion of encapsulated explants was obtained on 1:1 potting mix- fertilome with coco natural growth medium, moistened with full strength MS medium without TDZ, supplemented with 3 % sucrose and 0.5 % PPM. Plantlets regenerated from the encapsulated explants were hardened off and successfully transferred to the soil. These plants are selected to be used in mass cultivation for the production of biomass as a starting material for the isolation of THC as a bulk active pharmaceutical.
机译:大麻(Cannabaceae)是一种重要的药用植物,以其药理和治疗功效而闻名。由于该物种的同种异性,如果从种子中生长出来,很难保持其效力和功效。因此,基于化学概况的筛选,高产优良克隆的选择以及使用生物技术工具的繁殖是维持其遗传系的最合适方法。在这方面,我们报告了一种简单有效的方法,用于使用合成种子技术体外筛选和选择的高产大麻品种MX-1的筛选和选择的高产药物类型品种。从无菌多次芽培养物中分离出的大麻的腋芽已成功地封装在藻酸钙珠粒中。使用5%海藻酸钠和50 mM CaCl2.2H2O可以达到最佳的凝胶配合效果。在体外和体内条件下,在不同种植基质上评估了包封后的再生和转化。添加抗微生物物质-植物防腐剂混合物(PPM)对植物的总体发育有积极影响。封装的外植体在体外条件下,在补充了噻唑隆(TDZ 0.5μM)和PPM(0.075%)的Murashige和Skoog培养基上表现出最佳的再生和转化频率。在体内条件下,在含有可可天然生长培养基的1:1盆栽混合受精剂上,用不含TDZ的全强度MS培养基润湿,并补充3%蔗糖和0.5%PPM,可以实现封装外植体100%的转化。从封装的外植体中再生出的小植株被硬化并成功转移到土壤中。选择这些植物用于大规模栽培,以生产生物质,作为分离THC的原料,作为原料药。

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