Tissue Culture and Rapid Propagation of Big Chili Phalaenopsis
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摘要: 采用蝴蝶兰品种“大辣椒”幼嫩花梗作为试验材料,通过正交试验设计研究基本培养基、植物生长调节剂成分及含量对花梗不定芽的诱导、增殖、分化、生根的影响。结果表明,不定芽诱导的最佳培养基为:花宝一号+NAA 0.3mg·L-1+6-BA 5mg·L-1;不定芽增殖和分化的最佳培养基为:花宝一号+NAA 0.2mg·L-1+6-BA6mg·L-1,增殖系数最高达到5.53倍;最佳的壮苗和生根培养基为1/2MS+NAA 0.2mg·L-1,生根率为96%,椰子汁、苹果汁、土豆汁作为复合添加物对生根较为有利;组培生根苗移栽成活率在91.5%以上。Abstract: The young,tender flower stalks of the Big Chili Phalaenopsis were used for this study on the tissue culture and rapid propagation of the orchid.Using an orthogonal design experiment,the effects of the basic culture medium as well as hormone application and concentration on the pedicelinduction,proliferation and differentiation of the adventitious buds and the seedling development and rooting of the plant were investigated.The results showed that(a)the best medium for inducing the adventitious buds was Hyponex No.1+NAA(0.3mg·L-1)+6-BA(5mg·L-1);(b)the best medium for the proliferation and differentiation of the adventitious buds was Hyponex No.1+NAA(0.2mg·L-1)+6-BA(6mg·L-1),which resulted in a multiplication factor up to 5.53times;(c)the best medium forseedling development and rooting was 1/2MS+NAA(0.2mg·L-1),which yielded a rooting rate of 96%,and coconut milk,apple juice,potato juice as parts of the composite additives were found to be advantageous for rooting;and(d)the survival rate of the transplanted tissue culture was greater than 91.5%.
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Key words:
- Phalaenopsis /
- orthogonal experiment /
- tissue culture
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[1] 王俊,杨书才,杨录军,等.郑州市蝴蝶兰产业现状、存在问题及发展建议[J].河南农业科学,2011,40(12):17-19. [2] 张永柏,曾俊弼.我国蝴蝶兰发展趋势和存在问题[J],中国花卉盆景,2001,(12):8-9. [3] YOUNG P S,MURTHY H N,YOEUP P K,et al.Mass multiplication of protocorm-like bodies using bioreactor system and subsequent plant regeneration in phalaenopsis[J].Plant Cell′fissure and Organ Culture,2000,63(1):67-72. [4] HUANG XIANG-NAN,ZANG XIN,LV XIA-HUI,et al..Rapid Propagation of Phalaenopsis Orchid by Tissue Culture[J].Journal of Henan Agricultural Sciences,2008,1:91-93. [5] 黄象男,藏新,吕晓辉,等.蝴蝶兰组培快繁技术研究[J].河南农业科学,2008,(1):91-93. [6] 张彦妮,边红琳,陈立新.蝴蝶兰幼嫩花梗组织培养和快速繁殖[J].草业科学,2011,28(4):590-595. [7] 曾碧玉,许传俊,张文惠,等.蝴蝶兰花梗初代培养研究[J].福建农业学报,2013,28(2):124-128. [8] 谭鹏鹏,彭方仁,江荣翠,等.蝴蝶兰丛生芽快繁体系的建立[J].林业科技开发,2013,27(4):80-84. [9] 林宗铿,黄德贵.应用正交设计方法探讨蝴蝶兰丛生芽生根壮苗的条件[J].福建热作科技,2012,27(1):4-5,11. [10] 李成慧,蔡斌,单丽丽,等.应用正交设计法探讨蝴蝶兰叶片类原球茎的诱导[J].扬州大学学报:农业与生命科学版,2014,25(2):76-78. [11] 王冬云,汪建亚,蔡桁,等.蝴蝶兰组培不定芽增殖条件的优化[J].华中农业大学学报,2007,26(6):856-858. [12] 何荆洲,卜朝阳,闭志强,等.蝴蝶兰离体培养花梗表面消毒试验初报[J].农业研究与应用,2011,132(1):1-4. [13] 尤海龙,司亮.蝴蝶兰组织培养过程中减轻外植体褐化的方法研究[J].中国林副特产,2009,101(4):19-21. [14] 唐德华、崔宝禄.蝴蝶兰外植体褐化控制的研究.安徽农业科学,2012,40(3):1294-1295. [15] 张伟,乔保建,李冰冰,等.蝴蝶兰高效组培快繁及温室移栽技术,江苏农业科学,2015,(9):83-86. [16] 叶秀仙,黄敏玲,樊荣辉,等.蝴蝶兰离体保存及其遗传稳定性研究.福建农业学报,2014,(10):976-981.
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