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Establishment of Adventitious Bud Regeneration System from Bulb of Muscari Botryoides Mill

机译:穆斯卡里葡萄球菌鳞茎不定芽再生系统的建立

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The bulblets of Muscari botryoides Mill were selected as explants to develop the system of incubation in vitro on MS medium. Different sterilizing duration, various hormone as well as sucrose concentrations were designed for observing changes of the explants. The results show that the suitable sterilizing method of explants is to sterilize the scales for 8 minutes with 0.1 % HgCl2 solution generating that the contamination rate is only 4 %. The optimum combination for callus induction is MS medium with the addition of 2 mg/L 6-BA, 0.5 mg/L NAA and 5 % sucrose. Dark condition is conducive to callus induction. The optimal proliferation medium for adventitious buds is MS supplemented with 2.0 mg/L 6BA, 0.1 mg/L NAA and 3 % sucrose. The appropriate rooting medium is MS in combination with 0.3 mg/L NAA and 3.0 % sucrose. The survival rate of transplant is 95 % when the seedlings are transplanted into the matrix containing peat, vermiculite and soil with volume ratio 2:1:1:2.
机译:选择Muscari botryoides Mill的小球作为外植体,以开发在MS培养基上进行体外培养的系统。设计了不同的灭菌时间,各种激素以及蔗糖浓度以观察外植体的变化。结果表明,合适的外植体消毒方法是用0.1%的HgCl2溶液对鱼鳞进行8分钟的消毒,产生的污染率仅为4%。愈伤组织诱导的最佳组合是MS培养基,添加2 mg / L的6-BA,0.5 mg / L的NAA和5%的蔗糖。黑暗条件有利于愈伤组织的诱导。不定芽的最佳增殖培养基是MS,辅以2.0 mg / L 6BA,0.1 mg / L NAA和3%蔗糖。合适的生根培养基是MS与0.3 mg / L NAA和3.0%蔗糖的组合。将幼苗移植到泥炭,ver石和土壤体积比为2:1:1:2的基质中时,移植的成活率为95%。

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