首页> 外文期刊>Horticulture,Environment,and Biotechnology >Callus Induction and Plant Regeneration in Tanacetum cinerariaefolium (Trevir.) Schultz-Bip: an Important Medicinal Plant
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Callus Induction and Plant Regeneration in Tanacetum cinerariaefolium (Trevir.) Schultz-Bip: an Important Medicinal Plant

机译:鞣质醋柳(Trevir。)Schultz-Bip中的愈伤组织诱导和植物再生:重要的药用植物

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摘要

Pyrethrum is an important medicinal perennial herb belonging to the family Asteraceae. A method for rapid micropropagation of pyrethrum through plant regeneration from leaf and petiole explant derived calli has been developed. The petiole and leaf segments were cultured oil MS, SH and B5 media supplemented with the combination of auxins and BA for callus induction. All petiole explants on SH medium containing 2 mg.L-1 NAA and 0.2 mg.L-1 BA produced callus. The highest rate of callus growth was observed with the MS medium supplemented with 0.6 mg.L-1 BA and 4 mg.L-1 NAA. Shoot regeneration was obtained successfully by using step-by-step method. Firstly, callus was subcultured on MS medium containing 0.2 mg.L-1 2,4-D and then, the calli were transferred to MS medium containing 4 mg-L-1 BA, 1 mg.L-1 NAA and 0.5 mg.L-1 folic acid. In the latter step, some protuberances appeared on compact calli. These protuberances produced shoots oil MS media containing 1 mg.L-1 BA and 1 mg.L-1 NAA or 1 mg.L-1 BA and 2 mg.L-1 NAA and 0.4 mg.L-1 GA(3) The optimal rooting response was observed on B5 medium supplemented with 2 mg.L-1 NAA, on which 100% of the regenerated shoots developed roots with an average of 16 roots per shoot within 3 weeks. The plantlets were acclimatized and transferred to the greenhouse with 80% survival. This in vitro propagation protocol should be useful for conservation as well as mass propagation of this medicinal plant.
机译:除虫菊是菊科菊科多年生重要的重要药用植物。已经开发了通过从叶和叶柄外植体衍生的愈伤组织中再生植物来快速除虫菊的微繁殖的方法。将叶柄和叶段培养在MS,SH和B5油培养基中,辅以生长素和BA的组合,以诱导愈伤组织。在含有2 mg.L-1 NAA和0.2 mg.L-1 BA的SH培养基上的所有叶柄外植体均产生愈伤组织。补充0.6 mg.L-1 BA和4 mg.L-1 NAA的MS培养基观察到愈伤组织的生长速率最高。通过逐步方法成功地获得了芽再生。首先,将愈伤组织在含有0.2 mg.L-1 2,4-D的MS培养基上继代培养,然后将愈伤组织转移至含有4 mg-L-1 BA,1 mg.L-1 NAA和0.5 mg的MS培养基。 L-1叶酸。在后面的步骤中,紧凑的愈伤组织上出现了一些突起。这些突起产生的芽油MS培养基含有1 mg.L-1 BA和1mg.L-1 NAA或1mg.L-1 BA和2mg.L-1 NAA和0.4mg.L-1 GA(3)在补充有2 mg.L-1 NAA的B5培养基上观察到最佳的生根响应,其上再生芽的100%形成了根,在3周内平均每根芽有16个根。使小苗适应环境并转移到具有80%存活率的温室中。该体外繁殖方案对于该药用植物的保存以及大规模繁殖应该是有用的。

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