期刊文献+

攀西西南山茶幼叶愈伤组织诱导研究 被引量:5

Research on Callus Inducement of Camellia pitardii Young Leaves in Panxi Area
在线阅读 下载PDF
导出
摘要 [目的]探讨不同植物激素对西南山茶幼叶愈伤组织诱导的影响。[方法]以西南山茶幼叶为外植体,MS培养基为基本培养基,添加3种植物激素NAA、6-BA和2,4-D,浓度分别为0.5、1.0、2.0和4.0 mg/L,研究在不同浓度植物激素配比条件下西南山茶幼叶愈伤组织诱导率及生长状态。[结果]单因子诱导西南山茶幼叶愈伤组织形成时,适当浓度的NAA、6-BA和2,4-D均能起到显著的诱导效应,以0.5 mg/L浓度的2,4-D的效果最好,所形成的愈伤组织黄绿色,疏松,生长状态最好,利于培养,但随2,4-D浓度增高会导致愈伤组织的褐化现象严重。组合因子诱导时,以NAA 1.0 mg/L+6-BA 1.0 mg/L的诱导率最高,2,4-D 0.5 mg/L+6-BA 1.0 mg/L诱导愈伤组织的生长状态最好,利于培养。[结论]该研究为将植物组织培养技术应用于攀西西南山茶的快速繁殖提供了科学依据。 [ Objective] The study aimed to explore the effect of different plant hormone on callus inducement of young leaves of Camellia pitardii. [ Method] With C. pitardii young leaves as explant and MS medium as basic medium, three kinds of plant hormones of NAA, 6-BA and 2,4-D with conen. of 0.5, 1.0, 2.0 and 4.0 mg/L resp. were added into the medium to study the callus induction rate and growth state of C. pitardii young leaves under conditions of matching of plant hormone with different concn. [ Result ] When the forming of eaUus of C. pitardii young leaves induced by single factor, the NAA, 6-BA and 2,4-D with proper conen, could all has significant inductive effect, and the 2,4-D with 0.5 mg/L concn, was in the best result, in which the callus formed was yellowish green, loosened with optimal growth state, and favorable to be cultivated, but the browning of callus would be serious, which caused by the 2,4-D concn, rising up. When induced by combinatorial factors, the induction rate of NAA. 1.0 mg/L+ 6-BA 1.0 mg/L was highest, the 2, 4-D 0.5 mg/L + 6-BA 1.0 mg/L for induced callus was in the best growth state, and favorable to be cultured. [ Conclusion] The research provided scientific basis for the application of technology of plant tissue culture in the rapid propagation of C. pitardii in Panxi area.
作者 袁颖
机构地区 西昌学院农学系
出处 《安徽农业科学》 CAS 北大核心 2009年第17期7866-7867,共2页 Journal of Anhui Agricultural Sciences
基金 四川省教育厅青年基金项目
关键词 西南山茶 组织培养 愈伤组织 激素 Camellia pitardii Tissue culture Callus Hormone
  • 相关文献

参考文献6

二级参考文献43

共引文献42

同被引文献54

引证文献5

二级引证文献22

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部