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首页> 外文期刊>Plant Cell, Tissue and Organ Culture >Factors promoting efficient in vitro regeneration from de-embryonated cotyledon explants of Arachis hypogaea L.
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Factors promoting efficient in vitro regeneration from de-embryonated cotyledon explants of Arachis hypogaea L.

机译:促进花生无子叶子叶外植体高效再生的因素

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摘要

Highly efficient (>90%) protocols were developed for in vitro regeneration from de-embryonated cotyledon explants of peanut (Arachis hypogaea L.). Phytohormone combinations and concentrations, explant source and orientation, period of incubation and the response of genotypes were examined for optimization of the regeneration efficiency. Adventitious shoot primordia could be induced from de-embryonated cotyledon explants when (1) the proximal end of the explant was kept in contact with the shoot induction medium-I supplemented with 5 mg l−1 BAP + 2 mg l−1 2,4-D for 4 weeks, or (2) the distal end was kept in contact with shoot induction medium-II supplemented with only BAP at 20 mg l−1 for the first 2 weeks, followed by subculture in the same medium containing 15 mg l−1 BAP for the next 2 weeks. Orientation of placing the explant on the above media was critical for in vitro regeneration. The factors affecting the morphogenic responses like, repetitive organogenesis, shoot elongation, in vitro flowering and rhizogenesis were examined. Shoot bud formation was genotype independent. Histological studies showed multicellular origin of adventitious shoot primordia. The protocols gave healthy and fertile plants within 4 months.
机译:开发了一种高效(> 90%)的方案,用于从脱胚的花生子叶外植体(Arachis hypogaea L.)中进行体外再生。检查植物激素组合和浓度,外植体来源和方向,孵育时间和基因型反应,以优化再生效率。当(1)外植体的近端与补充有5 mg l −1 BAP + 2的芽诱导培养基I接触时,可以从去胚子叶外植体诱导不定芽原基。 mg l -1 2,4-D持续4周,或(2)远端与仅添加BAP且浓度为20 mg l -1的芽诱导培养基II保持接触前2周,然后在接下来的2周中在含有15 mg l -1 BAP的相同培养基中传代培养。将外植体放在上述培养基上的方向对于体外再生至关重要。研究了影响形态发生反应的因素,例如重复的器官发生,枝条伸长,体外开花和发根。芽的形成与基因型无关。组织学研究表明不定芽原基的多细胞起源。该方案在4个月内提供了健康,肥沃的植物。

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