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An efficient in vitro propagation methodology for Annatto (Bixa orellana L.)

机译:安纳托(Bixa orellana L.)的一种有效的体外繁殖方法

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摘要

Efficient methods were developed for both in vitro seed germination and micropropagation of an economically important dye yielding multipurpose tree, Bixa orellana L. Mature seeds were inoculated onto Murashige and Skoog (MS) medium supplemented with different concentrations of gibberellic acid (GA3). Highest frequency of germination (93.3 %) was recorded on medium supplemented with 3 μM GA3 against 13.33 % in control. Nodal explants cultured on MS medium fortified with 5 μM isopentanyl adenine (2-iP) produced maximum explants response (93.3 %) and highest number of shoots (35.71). Addition of relatively higher concentration (15 μM) of benzyl adenine (BA) resulted in the production of significantly (P < 0.05) reduced number of shoots (12.66). Sucrose at 87.6 mM was found to be the best carbohydrate source for multiple shoot induction compared to glucose and fructose. Regenerated shoots (3–4 cm) were rooted (95.5 %) on agar gelled MS medium supplemented with 10 μM indole-3-butyric acid (IBA). In vitro developed plantlets with well-developed roots were potted and acclimatized initially in the growth chamber and then moved to a green house with 83.3 % survival. The present protocol avoids the use of auxins in shoot multiplication medium, which will lower the cost, avoid callus formation and thus reduces the possibility of somaclonal variation in the regenerated plants. The method is efficient to produce over 32,000 hardened plants within a 10-month culture period starting from a single nodal explant.
机译:已开发出一种有效的方法,用于对具有重要经济意义的多用途树Bixa orellana L的重要树种进行体外种子萌发和微繁。将成熟种子接种到补充了不同浓度赤霉素(GA3)的Murashige和Skoog(MS)培养基上。在添加3μMGA3的培养基上记录的最高发芽率(93.3%),而对照中则为13.33%。在用5μM异戊烷腺嘌呤(2-iP)强化的MS培养基上培养的结节外植体产生最大的外植体反应(93.3%)和最高的芽数(35.71)。加入相对较高浓度(15μM)的苄腺嘌呤(BA)导致芽数显着减少(P <0.05)(12.66)。与葡萄糖和果糖相比,以87.6mM的蔗糖被发现是多次芽诱导的最佳碳水化合物来源。再生芽(3-4 cm)在琼脂胶凝MS培养基上生根(95.5%),补充10μg吲哚-3-丁酸(IBA)。将具有发达根部的体外发育小植株盆栽并使其最初在生长室中适应环境,然后移至存活率为83.3%的温室中。本方案避免了在枝条繁殖培养基中使用生长素,这将降低成本,避免愈伤组织形成,从而减少了再生植物体细胞克隆性变异的可能性。从单个节点外植体开始,在10个月的培养期内,该方法可有效生产32,000多株硬化植物。

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