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红三叶组织培养及再生植株 被引量:12

Tissue Culture in vitro and Plant Regeneration from Callus as well as Explant of Red Clover(Trifolium pratense L.)
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摘要 本文采用MS,B5和PC一L2作为基本培养基,在不同激素组合条件下对红三叶(Trifoliumpratense)子叶及下胚轴进行组织培养。在MS,B5和PC一L2附加2mg/L2,4-D和0.5mg/LBA的培养基上,子叶及下胚轴愈伤组织诱导率均在89%以上。愈伤组织继代在B5无机盐十三倍MS有机成分+3%蔗糖+0.5mg/L2,4-D+0.5mg/L6BA0.2mg/LNAA,+10mg/LVc的培养基上生长良好。愈伤组织在B5附加0.1mg/L6BA+0.2mg/LIBA的培养基上再生植株。下胚轴在MS附加2mg/L6BA+1mg/LNAA的培养基上直接分化形成丛生苗,转入无激素NS培养基上再生根。实验表明VE,Vc,PVP和活性碳对愈伤组织褐化有抑制作用,10mg/LVc抗褐化作用最好。 Cotyledon and hypocotyl of Red Clover( Trifolium pratense L.) were placed respectively on MS,B5,PC- L2 medium containing various combinations of auxins and cytokinins to induce callus forma-tion。 Frequency of callus inducing was over 89%mthe media containing 2mg/L 2,4-D and 0.5 mg/L6BA。 The plant callus when transfering for generations in 3-week time duration to medium Bs containing thr-eefold organic components of MS+ 3%sucrose+0.5 mg/L2,4D+ 0.5mg/L 6BA+0. 2 mg/L NAA+10 mg/L Vc.was growing well.Callus tissue could obtain regenerated plan ts and Shoots after subculturewas placed onto medium containing 0. 1 mg/L 6BA+0. 2 mg/L ABA in B5 basal medium, Moreover,clus-tered shoots were obtained directly from hypocotyl segments on MS medium con tainin g 2 mg/ L 6日A一1mg/LNAA ,and then regenerated shoots were induced on a hormone free MS medium。 In the experiment,itwas indicated that VE.,Vc,PVP and activated charcoal would have some in hibition of browning reaction tocallus,among them,10 mg/LVc was shown to have the most effecti ve action to browning reaction in thisrespect。
机构地区 兰州大学生物系
出处 《草业学报》 CSCD 1994年第2期51-54,共4页 Acta Prataculturae Sinica
关键词 红三叶 组织培养 再生植株 Red Clover,Tissue culture,Plant regeneration,Inhibition to browning reaction
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