[1]王金玲,杜凤国.金钟连翘组织培养与快速繁殖[J].北方园艺,2012,36(08):138-139.
　WANG Jin-ling,DU Feng-guo.Study on the Tissue Culture and Rapid Propagation of Forsythia viridissima[J].Northern Horticulture,2012,36(08):138-139.

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金钟连翘组织培养与快速繁殖

《北方园艺》[ISSN:1001-0009/CN:23-1247/S] 卷: 第36卷期数: 2012年08期页码: 138-139 栏目: 出版日期: 2012-08-16

Title:: Study on the Tissue Culture and Rapid Propagation of Forsythia viridissima

文章编号:: 1001-0009（2012）08-0138-02

作者:: 王金玲¹; 杜凤国¹; 2; 1.北华大学林学院，吉林吉林132013；
2.吉林省林业与生态环境重点实验室，吉林吉林132013

Author(s):: WANG Jin-ling¹; DU Feng-guo¹; 2; 1.College of Forestry，Beihua University，Jilin，Jilin 132013;
2.Provincial Key Lab of Forestry and Ecological Environment,Jilin，Jilin 132013

关键词:: 金钟连翘; 组织培养; 快速繁殖

Keywords:: Forsythia viridissima; tissue culture; rapid propagation

分类号:: S 685.24

文献标志码:: A

摘要:: 以金钟连翘带芽茎段为外植体，基于MS培养基，添加不同浓度的 6-BA和 IBA进行离体培养。初代培养的最佳培养基为MS+6-BA 0.5 mg/L+NAA 0.1 mg/L。增殖和生根的最适培养基为MS+6-BA 1.0 mg/L+NAA 0.1 mg/L。

Abstract:: With shoot segments containing auxiliary buds of Forsythia viridissima as explants，MS was used as the basic medium with different concentration of 6-BA and IBA.The results showed that the initial medium was MS+6-BA 0.5 mg /L+NAA 0.1 mg /L，and the proliferation medium and the rooting medium was MS+6-BA 1.0 mg/L+NAA 0.1 mg/L，which established the tissue culture and rapid propagation system of Forsythia viridissima.

参考文献/References:

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[2]武翼,刘晓霞,冯家祺,等.变异连翘的组织培养及快速繁殖的研究[J].山东林业科技，2009(3):41-43.

[3]张红梅,肖小琴,及华,等.花叶连翘的组织培养和快速繁殖[J].植物生理学通讯，2002,38(5):453.

[4]汤行春,刘幼琪.连翘组织培养:I愈伤组织的诱导和培养条件的优化[J].湖北大学学报,2000,22(2):185.

[5]刘计权.连翘的组织培养研究[J].科技情报开发与经济,2007,17(9):185-186.

[6]丁桂琴,王凤英.金缘连翘的组织培养技术研究[J].农业科技咨询导报，2007(14)：253.

[7]李会宁,安育,杨欣.贯叶连翘的试管快繁研究[J].中国植物野生资源,2002,21(4)：61-63.

[8]王晶,赵爽,唐存莲,等.金边连翘工厂化组培育苗技术研究[J].河北林果研究,2010,25(3):289-291.

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备注/Memo

第一作者简介：王金玲（1985-），女，硕士，研究方向为野生动植物保护与利用。E-mail:15043240409@126.com。

责任作者：杜凤国（1960-），男，博士，教授，现主要从事濒危植物保育生物学与分子系统学及野生植物资源保护与开发利用方面工作。

收稿日期：2012-02-01

更新日期/Last Update: 2014-08-31