Januka Pathak, Seerjana Maharjan, Ganga Rijal, Aashi Maharjan, Madhu Shudan Thapa Magar
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Among eleven different combinations of plant growth regulators (BAP, á-Naphthalene acetic acid (NAA), Adenine sulphate, Kinetin and coconut water) treated for shoot multiplication, maximum number of shoots were obtained in 0.5 mg/L BAP + 0.5 mg/L NAA (5.8 ± 0.53 SE shoots per explant). Longest shoot length was recorded in MS medium with Adenine sulphate (1 mg/L) (2.54 ± 0.03 cm SE). Root induction was carried out by using MS medium with different concentrations (0.5, 1, 1.5, 2.0 mg/L) of Indole butyric acid (IBA) and NAA. The highest numbers of roots and longest root length, both were observed at 2 mg/L IBA (4.63 ± 0.56 SE and 2.09 ± 0.25 cm SE respectively). 2 mg/L NAA showed poor response for root number (0.94 ± 0.21 SE) and root length (0.43 ± 0.07 cm SE). Successful acclimatization of in-vitro grown plantlets was done by wrapping the plantlet with moss kept on fine pine bark and the survival rate of plantlet was about 80% after 30 days. 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引用次数: 0
摘要
金石斛是一种濒危的附生和石生兰花,具有药用和观赏价值。本研究的目的是建立菊花的微繁技术。以金菊未成熟种子为外植体进行微繁。原球茎在不含植物生长调节剂的Murashige和Skoog (MS)培养基中发育90天。原球茎在添加2mg /L苄基氨基嘌呤(BAP)、1mg /L动素和10%椰子水的MS培养基上转移30天后分化为微芽。在11种不同的植物生长调节剂(BAP、á-Naphthalene乙酸(NAA)、硫酸腺嘌呤(Adenine sulfate)、Kinetin和椰子水)组合中,0.5 mg/L BAP + 0.5 mg/L NAA处理的芽数最多(5.8±0.53 SE /外植体)。在含有硫酸腺嘌呤(1 mg/L)的MS培养基中,茎长最长(2.54±0.03 cm SE)。采用不同浓度(0.5、1、1.5、2.0 mg/L)吲哚丁酸(IBA)和NAA的MS培养基诱导生根。2 mg/L IBA处理的根数最多,根长最长(分别为4.63±0.56 SE和2.09±0.25 cm SE)。2 mg/L NAA对根数(0.94±0.21 SE)和根长(0.43±0.07 cm SE)的响应较差。用细松皮上保存的青苔包裹植株,成功地驯化了离体苗,30 d后成活率约为80%。该方案可为金菊的有效大规模繁殖和迁地保护提供依据。
Dendrobium chryseum is an endangered epiphytic and lithophytic orchid species having medicinal and ornamental value. The objective of the present study is to develop micropropagation protocol for D. chryseum. The immature seeds of D. chryseum were used as an explant for the micropropagation. Protocorms were developed within 90 days in Murashige and Skoog (MS) medium without plant growth regulators. Protocorms were differentiated into micro shoots after 30 days of transfer to MS medium supplemented with 2 mg/L Benzyl amino purine (BAP), 1 mg/L kinetin and 10% coconut water. Among eleven different combinations of plant growth regulators (BAP, á-Naphthalene acetic acid (NAA), Adenine sulphate, Kinetin and coconut water) treated for shoot multiplication, maximum number of shoots were obtained in 0.5 mg/L BAP + 0.5 mg/L NAA (5.8 ± 0.53 SE shoots per explant). Longest shoot length was recorded in MS medium with Adenine sulphate (1 mg/L) (2.54 ± 0.03 cm SE). Root induction was carried out by using MS medium with different concentrations (0.5, 1, 1.5, 2.0 mg/L) of Indole butyric acid (IBA) and NAA. The highest numbers of roots and longest root length, both were observed at 2 mg/L IBA (4.63 ± 0.56 SE and 2.09 ± 0.25 cm SE respectively). 2 mg/L NAA showed poor response for root number (0.94 ± 0.21 SE) and root length (0.43 ± 0.07 cm SE). Successful acclimatization of in-vitro grown plantlets was done by wrapping the plantlet with moss kept on fine pine bark and the survival rate of plantlet was about 80% after 30 days. This protocol could be helpful for the effective mass propagation and ex situ conservation of D. chryseum.