首页> 外文期刊>HortScience >An efficient procedure for regeneration from leaf-derived calluses of Lonicera macranthoides 'Jincuilei', an important medicinal plant.
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An efficient procedure for regeneration from leaf-derived calluses of Lonicera macranthoides 'Jincuilei', an important medicinal plant.

机译:一种从重要的药用植物金银花'金银花'的叶状愈伤组织中再生的有效方法。

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'Jincuilei' is a mutant selected from Lonicera macranthoides Hand.-Mazz. It produces abundant flowers that never open with a chlorogenic acid (CGA) content up to 6.0%. Propagation through rooting or grafting has only a 30% survival rate. This study was undertaken to establish an efficient protocol for rapidly regenerating this mutant. Leaf explants were inoculated on Gamborg's B5 medium supplemented with different concentrations of 6-benzyladenine (BA) and 2,4-dichlorophenozyacetic acid (2,4-D). The optimal combination for callus induction was 4.4 micro M BA with 2.26 micro M 2,4-D, which resulted in 86.7% of leaf explants producing calluses in 4 weeks. Calluses produced from this optimal medium were cultured on B5 medium containing different concentrations of kinetin (KT) and alpha -naphthalene acetic acid (NAA). The best formulation for shoot induction was B5 medium containing 0.9 micro M KT and 5.4 micro M NAA in which 73.4% of cultured calluses produced shoots in 8 weeks, and shoot numbers ranged from three to six per callus piece (1 cm3). Adventitious shoots were cut and rooted in half-strength Murashige and Skoog medium supplemented with 14.8 micro M 3-indolebutyric acid. Roots initiated 10 d after culture, and rooting percentages ranged from 98% to 100%. Plantlets grown in a container substrate in a shaded greenhouse had over a 95% survival rate. During the last 6 years, over four million plantlets were regenerated using this established procedure, and there was no somaclonal variation. Fresh and dry weights of 1000 flowers, CGA contents, and dry flower yields of the regenerated plants were not significantly different from those of the stock 'Jincuilei' propagated by cutting, indicating that plants regenerated from this established procedure were stable. This established in vitro culture method has led to rapid commercial production of this medicinal plant on more than 1500 ha of production field.
机译:“金翠蕾”是选自 Lonicera macranthoides Hand.-Mazz的突变体。它会产生丰富的花朵,且从未打开,而其绿原酸(CGA)含量高达6.0%。通过生根或嫁接繁殖的存活率仅为30%。进行该研究以建立用于快速再生该突变体的有效方案。将叶片外植体接种在Gamborg's B 5 培养基上,该培养基添加了不同浓度的6-苄基腺嘌呤(BA)和2,4-二氯苯氧乙酸(2,4-D)。愈伤组织诱导的最佳组合是4.4 micro M BA和2.26 micro M 2,4-D,这导致4周内有86.7%的叶子外植体产生愈伤组织。从这种最佳培养基产生的愈伤组织在含有不同浓度的激动素(KT)和α-萘乙酸(NAA)的B 5 培养基中培养。诱导芽的最佳配方是B 5 培养基,其中含有0.9 micro M KT和5.4 micro M NAA,其中73.4%的已培养愈伤组织在8周内产生了芽,每个愈伤组织的芽数范围为3至6件(1 cm 3 )。切割不定芽,并在半强度Murashige和Skoog培养基中生根,补充14.8 micro M 3-吲哚丁酸。培养后10 d开始生根,生根百分比范围从98%到100%。在阴凉的温室中在容器基质中生长的小植株成活率超过95%。在过去的六年中,使用这种既定程序再生了超过四百万株小苗,并且没有体细胞克隆变异。再生植物的1000朵鲜花的新鲜和干燥重量,CGA含量和干燥花产量与通过切割繁殖的“金翠蕾”原种的那些没有显着差异,表明通过此既定程序再生的植物是稳定的。这种成熟的体外培养方法已导致该药用植物在超过1500公顷的生产场地上快速商业化生产。

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