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A micropropagation protocol for mass multiplication of Terminalia arjuna - a valuable medicinal tree

机译:榄仁大量繁殖的微繁殖方案-一种有价值的药用树

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A reliable and efficient micropropagation protocol was developed through axillary shoot proliferation from nodal explants of mature Terminalia arjuna . Season of explants collection and maturity of explants showed direct influence on bud-break. Nodal stem segments collected during the months of April and May gave best response. Nodal segments of fresh sprouts originated from lopped tree of T. arjuna were used as explants for establishment of in vitro culture . Surface sterilized explants produced optimum number of shoots through activation of axillary buds - on modified Murashige and Skoog’s (M-MS) medium. Maximum (100%) in vitro shoot proliferation was obtained on M-MS medium supplemented with 8.86 μM BAP + additives (100 mg L -1 of ascorbic acid, 50 mg L -1 of citric acid, 50 mg L -1 of adenine sulphate and 25 mg L -1 PVP). Modified M-MS medium supplemented with 4.44 μM BAP + 0.54 μM NAA + additives was found to be best for 11.38±0.26 shoot multiplication. After four week of culturing the in vitro regenerated shoots were rooted when pulse treated with 984 μM IBA for 10 min and transferred on hormone free half strength MS medium containing 100 mg L -1 activated charcoal. In vitro regenerated plants were transferred to field after gradual hardening and acclimatization procedure. Present method can be used for large scale commercial production of this medicinally important tree.
机译:通过从成熟榄仁结节外植体的腋生芽增殖,建立了一种可靠和高效的微繁殖方案。外植体的采集季节和外植体的成熟度对芽的断裂有直接影响。在4月和5月的几个月中收集到的节茎节段响应最佳。将源自阿氏的倒立树的新鲜芽的节节段用作建立体外培养的外植体。经过表面灭菌的外植体通过在改良的Murashige和Skoog(M-MS)培养基上活化腋芽来产生最佳芽数。在补充了8.86μMBAP +添加剂(100 mg L -1的抗坏血酸,50 mg L -1的柠檬酸,50 mg L -1的腺嘌呤硫酸盐)的M-MS培养基上获得最大(100%)的体外芽增殖和25 mg L -1 PVP)。发现改良的M-MS培养基补充有4.44μMBAP + 0.54μMNAA +添加剂,最适合11.38±0.26枝条繁殖。培养四周后,当用984μMIBA脉冲处理10分钟时,将再生的再生芽生根,并转移到含有100 mg L -1活性炭的无激素半强度MS培养基上。经过逐步硬化和适应过程后,将体外再生的植物转移到田间。本方法可用于这种重要药用树的大规模商业生产。

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