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蔓花生组织培养和植株再生的条件优化
引用本文:张振霞,郑玉忠.蔓花生组织培养和植株再生的条件优化[J].广西植物,2009,29(1):83-86.
作者姓名:张振霞  郑玉忠
作者单位:韩山师范学院,生物系,广东,潮州,521041
基金项目:国家星火计划,韩山师范学院青年基金 
摘    要:应用MS为基本培养基,通过各种培养条件和不同激素配比,探讨蔓花生组织培养及其植株再生条件的优化。结果显示:幼叶为最佳的外植体,在幼叶愈伤诱导过程中,不超过12h光照,光照强度在21.6μmol.m-2.s-1均可;诱导愈伤组织的适宜培养基为MS+0.5mg/L6-BA+0.2mg/L2,4-D或MS+0.5mg/L6-BA+2mg/LNAA;最适的分化培养基为MS+1mg/LTDZ+2mg/L6-BA+0.5mg/LNAA;最适的生根培养基1/2MS+1mg/LNAA+1mg/LPP333。

关 键 词:蔓花生  组织培养  愈伤组织

Condition optimization for tissue culture of Arachis duranensis
ZHANG Zhen-Xi,ZHENG Yu-Zhong.Condition optimization for tissue culture of Arachis duranensis[J].Guihaia,2009,29(1):83-86.
Authors:ZHANG Zhen-Xi  ZHENG Yu-Zhong
Institution:Department of Biology, Hanshan Teachers College, Chaozhou 521041, China
Abstract:Condition optimization for tissue culture and regeneration of Arachis duranensis was studied.The results showed that the leaflet was the best experimental explant;the optimized medium for callus was MS+0.5 mg/L6-BA+0.2 mg/L2,4-D or MS+0.5 mg/L6-BA+0.2 mg/LNAA with illumination of 12h/d;the optimized medium for differentiation was MS+1 mg/LTDZ+2 mg/L6-BA+0.5 mg/LNAA;the optimized medium for root induction was 1/2MS+1 mg/LNAA+1 mg/LPP333.
Keywords:Arachis duranensis  tissue culture  callus
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