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文心兰规模化组培育苗关键技术研究     被引量:8

Key Technology Study on Oncidium Industrial Propagation by Tissue Culture

文献类型:期刊文献

中文题名:文心兰规模化组培育苗关键技术研究

英文题名:Key Technology Study on Oncidium Industrial Propagation by Tissue Culture

作者:欧阳彤[1] 陈胜[1] 汪凤珍[1]

第一作者:欧阳彤

机构:[1]中国林业科学研究院亚热带林业研究所

年份:2006

卷号:19

期号:5

起止页码:606-611

中文期刊名:林业科学研究

外文期刊名:Forest Research

收录:CSTPCD;;Scopus;北大核心:【北大核心2004】;CSCD:【CSCD2011_2012】;

基金:中国林科院亚热带林业研究所创新基金(2004-C-02)

语种:中文

中文关键词:文心兰;组织培养;规模化育苗;关键技术

外文关键词:Oncidium ; tissue cuhure ; industrial propagation ; key technology

分类号:S722.3

摘要:通过基本培养基(改良MS、改良KC、V&W及自制ZW系列)、植物激素(6-BA、KT、NAA、IBA)、培养条件(香蕉泥、蛋白胨、酵母提取物、糖、活性炭)等关键因子对文心兰组培各阶段影响的试验,探索了文心兰规模化组培育苗的关键技术。结果表明:(1)当6-BA0.1~2mg·L^-1,NAA0.1~1.0mg·L^-1时,可诱导拟原球茎形成与增殖;6-BA0.05~0.1mg·L^-1或附加NAA0.1mg·L^-1就可满足拟原球茎的分化;6-BA0.01mg·L^-1协同NAA或IBA0.1mg·L^-1处理,诱导生根快而粗壮;(2)添加活性炭1000mg·L^-1和维生素C30mg·L^-1对减轻外植体褐化是必要的;添加500~1000mg·L^-1蛋白胨或酵母提取物可促进诱导拟原球茎;香蕉泥100g·L^-1有助于拟原球茎分化和瓶苗健化;(3)MS高盐类培养基在每个培养阶段都有较高的致畸率,自制中盐ZW培养基,N:P:K为3:1:2.9,文心兰在其中生长健壮;(4)文心兰在无糖培养基中自养生长基本正常。
The key technology of Oncidium' s industrial propagation were studied by in situ investigating the effects of the key factors such as minimal medium (improved MS, improved KC, V&W and self-prepared ZW series,etc. ), phytohormone (6-BA, NAA, IBA, KT), additive (vitamin C, peptone, mashed banana, active carbon,sugar, etc. ), on the mass b that : ( 1 ) The protocorm like reeding in every stage during Oncidium's industrial body (PLB) could be induce and increase as long propagation. The results revealed as the concentration of 6-BA between 0.1- 2 mg·L^-1 and NAA 0.1 - 1.0 mg·L^-1. At the revulsive initial stage a concentration of 6-BA 2 mg·L^-1 and with NAA 0.2 mg·L^-1 was helpful to increase the propagation basic number of protocorm like body. The multiply and differentiation of PLB could take place as long as 6-BA 0.05 - 0.1 mg· L^-1 or addition of NAA 0.1 mg·L^- 1 .The root emerging could be accelerated and the roots become stronger cooperation of addition of low concentration 6-BA (0.01 -0.1 mg·L^-1 ) together with NAA or IBA(0.1 mg·L^-1 ). (2)The low concentration of auxin (0.01 - 0.1 mg·L^-1 ) and the sort of low concentration of mineral medium ( such as V&W, KC, etc. ) seemed to benefit the decrease of the malformation during PLB differentiation and seedling growth. (3)In order to reduce the explant browning addition of active carbon 1 000 mg·L^-1 and vitamin C 30 mg·L^-1 was necessary. Adding peptone 500 -1 000 mg·L^-1 or drawn substance of yeast seemed to promote the induction of PLB. Mashed banana 100 g ·L^-1 might benefit the PLB differentiation and improve the quality of test-tube plantlet. (4) Minimal mediums had notable effects on every stage of Oncidium tissue culture. The self-prepared ZW mediums with middle concentration of salt were more suitable to Oncidium propagation by tissue culture. (5)Oncidium was autotrophic without sugar in the medium.

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