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番荔枝组织培养初步研究
引用本文:张振霞,郑玉忠.番荔枝组织培养初步研究[J].安徽农业科学,2007,35(14):4110-4111.
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;韩山师范学院生物系,广东潮州,521041
基金项目:国家星火计划项目(2005EA780080).
摘    要:对番荔枝的组织培养技术进行了研究.结果表明:以幼叶为外植体,采用NB+2,4-D 1 mg/L+6-BA 0.5 mg/L作为愈伤诱导培养基以及12 h光照处理,出愈率可达到87.50%;最佳分化培养基为NB+TDZ1 mg/L+6-BA 2mg/L+NAA 0.5mg/L,分化率为28.89%.

关 键 词:番荔枝  组织培养  愈伤组织
文章编号:0517-6611(2007)14-04110-02
收稿时间:2007-02-06
修稿时间:2007-02-06

Preliminary Study on Tissue Culture ofAnnona squamosa L.
ZHANG Zhen-xia et al.Preliminary Study on Tissue Culture ofAnnona squamosa L.[J].Journal of Anhui Agricultural Sciences,2007,35(14):4110-4111.
Authors:ZHANG Zhen-xia
Institution:Department of Biology, Hanshan Normal University, Chaozhou, Guangdong 521041
Abstract:Tissue culture technology of Annona squamosa L.was studied.Results showed that burgeon of Annona squamosa L.was good explants and the optimal medium for callus inducement was NB 2,4-D 1 mg/L 6-BA 0.5 mg/L with 12 h light.And the callus induction rate was up to 87.50 %.The optimal differentiation medium was NB TDZ 1 mg/L 6-BA 2 mg/L NAA 0.5 mg/L and the differentiation rate was 28.89 %.
Keywords:Annona squamosa L    Tissue culture  Callus
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