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从产材豆科树木印度黄檀(Dalbergia sissoo Roxb.)的子叶外植体进行体细胞胚胎发生和植株再生

Somatic embryogenesis and plant regeneration from cotyledon explants of a timber-yielding leguminous tree, Dalbergia sissoo Roxb.

作者信息

Singh Ajay Kumar, Chand Suresh

机构信息

Plant Tissue Culture and Genetics Research Group, School of Life Sciences, Devi Ahilya University, Khandwa Road, Indore-452 017, India.

出版信息

J Plant Physiol. 2003 Apr;160(4):415-21. doi: 10.1078/0176-1617-00523.

Abstract

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-MSO). Average numbers of somatic embryos per callus clump was 26.5 on 1/2-MSO medium after 15 weeks of culture. Addition of 0.68 mmol/L L-glutamine to 1/2-MSO 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-MSO medium containing 2% sucrose, after 20 days of culture. Transfer of somatic embryos to 1/29-MSO 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 plantiets 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.

摘要

通过体细胞胚胎发生实现了高效的植物再生,所用愈伤组织培养物源自印度黄檀(Dalbergia sissoo Roxb.)半成熟子叶外植体,印度黄檀是一种产木材的豆科树木。体细胞胚在胚性愈伤组织表面发育,偶尔也直接从子叶外植体发育而来,不经过中间的愈伤组织阶段。在添加了4.52、9.04、13.57和18.09 μmol/L 2,4-二氯苯氧乙酸以及0.46 μmol/L激动素的Murashige和Skoog(1962)培养基上,从印度黄檀的子叶切块诱导出愈伤组织培养物。在添加9.04 μmol/L 2,4-D和0.46 μmol/L激动素的MS培养基上,愈伤组织形成的最大响应率为89%。将胚性愈伤组织团转移到不含植物生长调节剂的1/2-MS培养基(1/2-MSO)上后实现了体细胞胚胎发生。培养15周后,1/2-MSO培养基上每个愈伤组织团的体细胞胚平均数量为26.5个。向1/2-MSO培养基中添加0.68 mmol/L L-谷氨酰胺可将体细胞胚胎发生频率从55%提高到66%,每个愈伤组织团的体细胞胚数量从26.5个增加到31.1个。进行了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-MSO培养基上转化为小植株。在转移到含有2%蔗糖的1/2-MS培养基之前,将体细胞胚转移到含有10%蔗糖的1/2-MSO培养基上培养15天,可将体细胞胚转化为小植株的比例从50%提高到75%。将带有茎和根的小植株转移到1/2和1/4液体MS培养基中,各培养十天,然后转移到装有经高压灭菌的泥炭藓和堆肥混合物(1:1)的塑料盆中。转移到盆中10周后,70%的小植株存活。150株再生小植株中有120株成功驯化。成功驯化后,将植株转移到陶土盆中。

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