首页 | 本学科首页   官方微博 | 高级检索  
     检索      

黄花矶松组织培养及培养基筛选研究
引用本文:王方琳,崔建国,尉秋实,张莹花,柴成武.黄花矶松组织培养及培养基筛选研究[J].中国农学通报,2014,30(13):45-50.
作者姓名:王方琳  崔建国  尉秋实  张莹花  柴成武
作者单位:1. 甘肃省治沙研究所2. 3. 甘肃民勤荒漠草地生态系统国家野外科学观测研究站/甘肃省治沙研究所4. 甘肃省荒漠化与风沙灾害防治重点实验室-省部共建国家重点实验室培育基地&甘肃省治沙研究所5. 甘肃省荒漠化防治与风沙灾害国家重点试验室/甘肃省治沙研究所
基金项目:国家科技计划(2012)“祁连山水源涵养林生态系统保育技术试验示范”(BAD16B00); 国家自然科学基金“沙区粘土质夹层土壤水分分布与植物的生态响应”(31100519)
摘    要:试验选用种子培养的黄花矶松无菌苗的子叶、茎段、下胚轴作为外植体材料,研究不同外植体的离体培养技术及其适宜的培养基。结果表明,生长素2,4-D对不定芽诱导具有明显的促进作用,在其浓度为1.5 mg/L时诱导率最高,子叶是诱导不定芽的良好外植体,最适培养基为MS+2,4-D 1.5 mg/L+6-BA 2.0 mg/L+NAA 1.0 mg/L。黄花矶松的最适增殖培养基为MS+6-BA 1.0 mg/L+NAA 1.0 mg/L,而且是以丛生芽的方式进行增殖的;最适生根培养基是1/2 MS+KT 1.0 mg/L+IBA1.0 mg/L。

关 键 词:黄花矶松  组织培养  培养基  愈伤组织
收稿时间:2013/11/10 0:00:00
修稿时间:2014/1/10 0:00:00

Research on Tissue Culture and Medium of Limoniumau-reum
Wang Fanglin,Cui Jianguo,Yu Qiushi,Zhang Yinghua,Chai Chengwu.Research on Tissue Culture and Medium of Limoniumau-reum[J].Chinese Agricultural Science Bulletin,2014,30(13):45-50.
Authors:Wang Fanglin  Cui Jianguo  Yu Qiushi  Zhang Yinghua  Chai Chengwu
Institution:(The State Key Laboratory of Desertification Combating Prevention and Sandstorm Disaster of Gansu Province/ Gansu Desert Control Research Institute, Wuwei Gansu 733000)
Abstract:Abstract: Experiment chooses seed development Limoniumau-reum no vaccine hypocotyl cotyledon stem section as explant materials ,study the culture of different explant technique, the results show that: the suitable medium auxin 2, 4-d on adventitious bud induction has an obvious role in promoting, when its concentration is 1.5 mg/L induction rate is highest, cotyledon is good explant of adventitious bud induction, the optimal culture medium for MS+ 2,4-D 1.5 mg/L+ 6-BA 2.0 mg/L+ NAA 1.0 mg/L Limoniumau-reum optimal proliferation medium was MS+6-BA 1.0 mg/L+ NAA 1.0 mg/L, and took the form of multiple shoot clumps proliferation; The optimum rooting medium was 1/2 MS+ KT 1.0 mg/L+ IBA 1.0 mg/L.
Keywords:callus tissue
本文献已被 CNKI 维普 等数据库收录!
点击此处可从《中国农学通报》浏览原始摘要信息
点击此处可从《中国农学通报》下载免费的PDF全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号