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首页> 外文期刊>Journal of Plant Physiology >Somatic embryogenesis and plant regeneration from cotyledon explants of a timber-yielding leguminous tree, Dalbergia sissoo Roxb.
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Somatic embryogenesis and plant regeneration from cotyledon explants of a timber-yielding leguminous tree, Dalbergia sissoo Roxb.

机译:产木材的豆科树种黄檀(Dalbergia sissoo Roxb)的子叶外植体的体细胞胚发生和植物再生。

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摘要

Efficient plant regeneration through somatic embryogenesis was achieved from callus cultures derived from semi-mature cotyledon explants of Dalbergia sissoo Roxb., a timber-yielding leguminous tree. Somatic embryos developed over the surface of embryogenic callus and occasionally, directly from cotyledon explants without intervening callus phase. Callus cultures were initiated from cotyledon pieces of D. sissoo on Murashige and Skoog (1962) medium supplemented with 4.52, 9.04, 13.57, and 18.09 mumol/L 2,4-dichlorophenoxyacetic acid and 0.46 mumol/L Kinetin. Maximum percentage response for callus formation was 89 % on MS medium supplemented with 9.04 mumol/L 2,4-D and 0.46 mumol/L Kn. Somatic embryogenesis was achieved after transfer of embryogenic callus clumps to 1/2-MS medium without plant growth regulators (1/2-MS0). Average numbers of somatic embryos per callus clump was 26.5 on 1/2-MS0 medium after 15 weeks of culture. Addition of 0.68 mmol/L L-glutamine to 1/2-MS0 medium enhanced somatic embryogenesis frequency from 55 % to 66% and the number of somatic embryos per callus clump from 26.5 to 31.1. Histological studies were carried out to observe various developmental stages of somatic embryos. About 50 % of somatic embryos converted into plantlets on 1/2-MS0 medium containing 2 % sucrose, after 20 days of culture. Transfer of somatic embryos to 1/2-MS0 medium containing 10% sucrose for 15 days prior to transfer on 1/2-MS medium with 2 % sucrose enhanced the conversion of somatic embryos into plantlets from 50 to 75 %. The plantlets with shoots and roots were transferred to 1/2 and 1/4-liquid MS medium, each for 10 days, and then to plastic pots containing autoclaved peat moss and compost mixture (1 :1). 70% of the plantlets survived after 10 weeks of transfer to pots. 120 regenerated plantlets out of 150 were successfully acclimatised. After successful acclimatisation, plants were transferred to earthen pots.
机译:通过体细胞胚发生的有效植物再生,是通过采自半熟的子叶黄豆(Dalbergia sissoo Roxb。)的半成熟子叶外植体的愈伤组织培养物实现的。体细胞胚在胚性愈伤组织的表面上发育,偶尔,直接从子叶外植体发育而没有介入愈伤组织阶段。愈伤组织培养是在补充了4.52、9.04、13.57和18.09摩尔/升的2,4-二氯苯氧基乙酸和0.46摩尔/升Kinetin的Murashige和Skoog(1962)培养基上从D. sissoo的子叶碎片开始的。在补充了9.04摩尔/升的2,4-D和0.46摩尔/升的Kn的MS培养基上,愈伤组织形成的最大百分比响应为89%。在将胚性愈伤组织块转移至没有植物生长调节剂(1 / 2-MS0)的1 / 2-MS培养基中之后,实现了体细胞胚发生。培养15周后,在1 / 2-MS0培养基上每个愈伤组织团的体细胞胚的平均数目为26.5。在1 / 2-MS0培养基中添加0.68 mmol / L L-谷氨酰胺可使体细胞胚发生频率从55%增至66%,每个愈伤组织块的体细胞胚数从26.5增至31.1。进行组织学研究以观察体细胞胚的各个发育阶段。培养20天后,约50%的体细胞胚在含有2%蔗糖的1 / 2-MS0培养基上转化为小植株。将体细胞胚转移到含有10%蔗糖的1 / 2-MS0培养基中15天,然后再转移到具有2%蔗糖的1 / 2-MS培养基中,使体细胞胚转化为小植株的转化率从50%提高到75%。将具有芽和根的小植株分别转移至1/2和1/4液体MS培养基中10天,然后转移至装有高压灭菌的泥炭藓和堆肥混合物(1:1)的塑料盆中。移入盆栽10周后,有70%的小植株存活。已成功使150株中的120株再生小植株适应环境。成功适应环境后,将植物转移到土盆中。

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