Cost-Effective in vitro Multiplication and Phenolic Profile of an Important Medicinal Orchid, Satyrium nepalense D. Don

IF 0.9 Q4 CHEMISTRY, MEDICINAL Journal of Biologically Active Products from Nature Pub Date : 2021-03-04 DOI:10.1080/22311866.2021.1911681
Deepak Singh, B. Mir, S. Babbar, S. Babbar
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引用次数: 1

Abstract

Abstract In this study we report a cost-effective and reproducible protocol for large-scale multiplication of an important medicinal orchid, Satyrium nepalense through a four-step protocol, involving asymbiotic seed germination, multiplication of protocorm-like bodies (PLBs), development and multiplication of shoots, and finally in vitro rooting of the developed shoots. Out of various media tested for seed germination, Mitra’s medium supplemented with 0.1 % peptone (BM) supported the highest (79.19 %) seed germination. Eight-weekold protocorms were sub-cultured on BM alone and supplemented with different concentrations (1-8 μM) of BAP, KN, or TDZ. The highest number of shoots was developed on the medium containing 4 μM KN. Here we also observed that the highest number of shoots were produced from protocorms cultured on a 2 % isubgol gelled medium out of the seven different low-cost gelling agents used. Further, optimal elongation of shoots was observed on BM alone and 2 % guar gum, among the tested gelling agents. Elongated shoots were transferred for rooting on BM containing 0-2 μM of IAA, IBA, or NAA. The best rhizogenic response was observed on BM fortified with 0.5 μM IBA and isubgol (3 %). The rooted plantlets showed a 76 % survival rate on acclimatization after transfer to the potting mixture of sand and vermiculite (1:1). HPLC analysis of therapeutically important phenolic acids of leaves and tubers of in vitro regenerated and in vivo plants revealed the presence of higher levels of selected phenolic acids in in vitro tissues than those from their native habitat. This protocol could facilitate the conservation and propagation of this important medicinal orchid.
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重要药用兰花油桐的成本效益体外繁殖及酚类物质特性
摘要在本研究中,我们报道了一种具有成本效益和可重复性的方案,通过四步方案对一种重要的药用兰花尼泊尔莎草进行大规模繁殖,包括无共生种子发芽、原球茎(PLBs)繁殖、芽的发育和繁殖,以及最终对发育的芽进行体外生根。在测试种子发芽的各种培养基中,添加0.1%蛋白胨(BM)的Mitra培养基支持最高的种子发芽率(79.19%)。8周龄的原球茎在单独的BM上亚培养,并补充不同浓度(1-8μM)的BAP、KN或TDZ。在含有4μM KN的培养基上产生了最高数量的芽。在这里,我们还观察到,在使用的七种不同的低成本胶凝剂中,在2%的isubgol凝胶培养基上培养的原球茎产生了最高的芽数。此外,在测试的胶凝剂中,在单独的BM和2%的瓜尔胶上观察到芽的最佳伸长率。将伸长的芽转移到含有0-2μM IAA、IBA或NAA的BM上生根。在添加0.5μM IBA和3%异丁醇的BM上观察到最佳的生根反应。将生根的植株转移到沙子和蛭石(1:1)的盆栽混合物中后,驯化后的成活率为76%。对体外再生和体内植物的叶子和块茎的治疗重要酚酸的HPLC分析显示,体外组织中所选酚酸的水平高于其原生栖息地的酚酸。该协议可以促进这种重要药用兰花的保护和繁殖。
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来源期刊
Journal of Biologically Active Products from Nature
Journal of Biologically Active Products from Nature Agricultural and Biological Sciences-Agricultural and Biological Sciences (miscellaneous)
CiteScore
2.10
自引率
0.00%
发文量
21
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