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In vitro propagation of Rivina humilis L. through proliferation of axillary shoots and shoot tips of mature plants

机译:Rivina humilis L.通过腋生芽和成熟植物芽尖的体外繁殖

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In vitro propagation of Rivina humilis L. was attempted through proliferation of axillary shoots and shoot tips obtained from mature plants. The shoot tips and nodal shoot segments exhibited 70 and 80% shoot initiation when cultured on Murashige and Skoog (MS) basal medium supplemented with 4.44 mu M 6-benzylaminopurine (BAP)+2.85 indole-3-acetic acid (IAA) and 8.88 mu M BAP+2.68 mu M naphthalene acetic acid (NAA), respectively. Shoots (2 to 3) were obtained from both shoot tip and nodal explants on MS medium supplemented with BAP (2.22 mu M), IAA (2.85 mu M) and silver nitrate (4 mu M AgNO3). Multiplication was maximum on MS medium supplemented with BAP (8.88 mu M), IAA (2.85 mu M) and AgNO3 (4 mu M) wherein 3-4 shoots per nodal explant were obtained. Microshoot elongation was achieved on MS medium containing BAP (2.22 mu M) and gibberellic acid (2.89 mu M GA(3)). Shoots (3-4 cm) exhibited 100% rooting within 4 wk in medium containing half MS with IAA (2.85-5.71 mu M) or IBA (2.45-4.90 mu M) alone or in combination with BAP (2.22 mu M), resulting in simultaneous rooting and shoot growth. About 70% of micropropagated plants were established successfully in micropots and transferred to the field after 3 months.
机译:通过从成熟植物获得的腋生芽和芽梢的增殖尝试了Rivina humilis L.的体外繁殖。在Murashige和Skoog(MS)基础培养基上分别添加4.44μM 6-苄氨基嘌呤(BAP)+2.85吲哚-3-乙酸(IAA)和8.88 mu M BAP + 2.68μM萘乙酸(NAA)。在补充了BAP(2.22μM),IAA(2.85μM)和硝酸银(4μMAgNO3)的MS培养基上,从茎尖和节外植体中均获得芽(2至3个)。在补充了BAP(8.88μM),IAA(2.85μM)和AgNO3(4μM)的MS培养基上最大繁殖,其中每个结外植体获得3-4个芽。在含有BAP(2.22μM)和赤霉素(2.89μMGA(3))的MS培养基上实现了微芽伸长。幼芽(3-4厘米)在含有半MS的培养基中4周内表现出100%生根,其中MS单独或与IAP(2.25-4.90μM)或与BAP(2.22μM)结合使用,IBA(2.45-4.90μM)同时生根和芽生长。大约70%的微繁植物已在微盆中成功建立,并在3个月后转移到田间。

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