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Improving multiple shoot proliferation in bamboo mosaic virus-free Bambusa oldhamii Munro propagation by liquid culture

机译:通过液体培养改善无竹花叶病毒Bambusa oldhamii Munro繁殖中的多芽增殖

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摘要

An in vitro method for obtaining bamboo mosaic virus (BaMV)-free plantlets of Bambusa oldhamii Munro was developed. BaMV-free meristems were incubated on MS basal medium supplemented with 0.45 micro M thidiazuron (TDZ) to induce the development of multiple shoots. Multiple shoot proliferation was higher in stationary liquid culture than on semisolid medium. Cytokinin was the key component for inducing proliferation, and TDZ was the stable and effective cytokinin for proliferation in long-term subcultures. Multiple shoots rooted after 1 month in MS basal medium containing 10.74 to 26.85 micro M alpha -naphthaleneacetic acid with a rooting efficiency of 83%. Healthy, well-developed plantlets were transferred to soil in pots and raised in a greenhouse. Those plants derived from tissue culture were more vigorous than the ones derived from the traditional in vivo vegetative propagation method, air layering. The tissue culture-derived plants could produce the culms after 15 months. Fifteen of 38 plants flowered 2 years after being transplanted to the field..
机译:开发了一种体外获得无竹花叶Bambusa oldhamii Munro苗的方法。将不含BaMV的分生组织在补充有0.45 micro M噻唑隆(TDZ)的MS基础培养基上孵育,以诱导多个芽的发育。固定液体培养中的多芽增殖高于半固体培养基。细胞分裂素是诱导增殖的关键成分,而TDZ是长期传代培养中稳定有效的细胞分裂素。 1个月后,多芽在含有10.74至26.85微Mα-萘乙酸的MS基础培养基中生根,生根效率为83%。将健康,发育良好的小苗转移到盆中的土壤中,并在温室中饲养。那些来自组织培养的植物比来自传统的体内无性繁殖方法空气分层的植物更有活力。组织培养来源的植物可在15个月后产生茎秆。移植到田间两年后,38种植物中有15种开花。

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