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In vitro mass multiplication of screw pines (Pandanus spp.) - an important costal bio- resource

机译:螺旋松(Pandanus spp。)的体外大量繁殖-一种重要的沿海生物资源

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An efficient in vitro mass multiplication protocol was developed for selected species of screw pine (Pandanus fascicularis Lam., P. furcatus Roxb.). The protocol could be successfully used for large scale production of planting materials leading to cultivation and making bio-fences or green belts in coastal areas, wetlands for protection and preventing soil erosion. This will facilitate the replenishment of the bio resource and also provide good breeding space for various fauna associated with it. For developing the tissue culture protocol, shoot tips and tillers from the mature plants were used as the explants. Surface sterilization with 0.1 % mercuric chloride for 1 min. Yielded good fraction (65 %) of contamination free explants. Explants inoculated in MS solid medium supplemented with 6-benzylaminopurine (BAP, 2.5 mg/l) and indole-3-acetic acid (IAA, 0.5 mg/l), induced 2-3 shoot buds in 5 weeks. These buds either individually or along with the explant portion, sub-cultured to fresh media containing the same hormonal combinations, resulted induction of 5-6 shoot buds in 4 weeks. Repeated subcultures of shoot buds in the same medium produced 8-10 shoot buds in every 4 weeks. Shoot elongation was achieved (similar to 3 cm) by transferring the shoot clusters or individual shoots to basal medium, and the elongated shoots were rooted in vitro or ex vitro. Root induction in shoots (87.4 %) was achieved in MS medium supplemented with 0.1 mg/l indole-3-butyric acid (IBA). Rooted shoots were established in paper/polythene cups filled with fine sand, which subsequently recorded 85 % establishment under the shade-net house with proper irrigation. Plants grown in poly-bags were later successfully established in different field conditions and recorded 100 % survival.
机译:针对选定的螺旋松树种(Pandanus fascicularis Lam。,P. furcatus Roxb。)开发了一种有效的体外大量繁殖方案。该方案可成功用于大规模生产种植材料,从而在沿海地区,湿地进行保护和防止水土流失的耕作并制作生物围栏或绿化带。这将促进生物资源的补充,并为与其相关的各种动物提供良好的繁殖空间。为了制定组织培养方案,将成熟植物的芽尖和分till用作外植体。用0.1%氯化汞进行表面灭菌1分钟。产生良好的分数(65%)的无污染外植体。在补充有6-苄基氨基嘌呤(BAP,2.5 mg / l)和吲哚-3-乙酸(IAA,0.5 mg / l)的MS固体培养基中接种的植株在5周内诱导了2-3个芽。将这些芽单独或与外植体部分一起继代培养至含有相同激素组合的新鲜培养基中,可在4周内诱导5-6个芽。在相同培养基中重复进行芽的继代培养,每4周产生8-10个芽。通过将枝条簇或单个枝条转移到基础培养基中,可以达到枝条伸长(大约3 cm),并且伸长的枝条可以在体外或离体生根。在补充有0.1 mg / l吲哚-3-丁酸(IBA)的MS培养基中,芽中的根诱导(87.4%)得以实现。在充满细砂的纸/聚乙烯杯中建立有根的芽,随后在适当灌溉的情况下,将其定植在荫网屋下85%。后来在不同的田间条件下成功建立了在塑料袋中生长的植物,并记录了100%的存活率。

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