Department of Botany , Lady Keane College , Shillong, Meghalaya 793 001 , India.
AoB Plants. 2012;2012:pls032. doi: 10.1093/aobpla/pls032. Epub 2012 Nov 5.
Dendrobium longicornu, commonly known as the 'Long-horned Dendrobium', is an endangered and medicinally important epiphytic orchid. Over-exploitation and habitat destruction seriously threaten this orchid in Northeast India. Our objective was to develop an efficient protocol for the mass propagation of D. longicornu using axillary bud segments.
Axillary buds cultured in Murashige and Skoog semi-solid medium supplemented with α-naphthalene acetic acid (NAA), 2,4-dichlorophenoxy acetic acid (2,4-D) and 6-benzylaminopurine (BAP) readily developed into plantlets. These formed either directly from shoot buds or from intermediary protocorm-like bodies (PLBs). The maximum explant response (86.6 %) was obtained in medium supplemented with NAA at 30 µM, while the maximum number of shoots (4.42) and maximum bud-forming capacity (3.51) were observed in medium containing 15 µM BAP and 5 µM NAA in combination. Protocorm-like bodies were obtained when the medium contained 2,4-D. The maximum number of explants forming PLBs (41.48 %) was obtained in medium containing 15 µM BAP and 15 µM 2,4-D. Well-developed plantlets obtained after 20-25 weeks of culture were acclimatized and eventually transferred to the greenhouse. Over 60 % of these survived to form plants ∼3-4 cm tall after 90 days in glasshouse conditions using a substrate of crushed brick and charcoal, shredded bark and moss.
The method described can readily be used for the rapid and large-scale regeneration of D. longicornu. Its commercial adoption would reduce the collection of this medicinally important and increasingly rare orchid from the wild.
长角石斛,俗称“长角兰”,是一种濒危且具有药用价值的附生兰科植物。在印度东北部,过度开发和生境破坏严重威胁到这种兰花。我们的目的是利用腋芽段为长角石斛建立一个高效的大规模繁殖方法。
在添加α-萘乙酸(NAA)、2,4-二氯苯氧乙酸(2,4-D)和 6-苄基氨基嘌呤(BAP)的 Murashige 和 Skoog 半固体培养基中培养的腋芽很容易发育成小植株。这些小植株直接从芽点发育而来,或从中间原球茎状结构(PLB)发育而来。在添加 30 μM NAA 的培养基中,外植体的最大响应(86.6%),而在含有 15 μM BAP 和 5 μM NAA 的培养基中观察到最大的芽数(4.42)和最大的芽形成能力(3.51)。当培养基中含有 2,4-D 时,可获得原球茎状结构。在含有 15 μM BAP 和 15 μM 2,4-D 的培养基中,获得最大数量的形成 PLB 的外植体(41.48%)。经过 20-25 周的培养,获得发育良好的小植株,然后在温室中进行驯化,最终转移到温室中。在温室条件下,使用碎砖和木炭、碎树皮和苔藓作为基质,经过 90 天后,有超过 60%的小植株存活下来,形成了约 3-4 厘米高的植物。
本文描述的方法可用于长角石斛的快速和大规模繁殖。其商业应用将减少对这种药用价值高且日益稀缺的兰花的野外采集。