• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

[朱砂根的组织培养与植株再生]

[Tissue culture and plant regeneration of Ardisia crenata].

作者信息

Ma Mingdong, Liu Junli, Pu Shangrao

机构信息

School of Forest and Horticulture, Sichuan University of Agriculture, Ya'an 625014, China.

出版信息

Zhongguo Zhong Yao Za Zhi. 2009 Aug;34(16):2043-6.

PMID:19938541
Abstract

OBJECTIVE

Our research studied the fast-breeding technology of Ardisia crenata sims by using tissue culture and provided the scientific foundation for industry production.

METHOD

The effects of axillary buds and plant regeneration of different basic medium, hormones and additives on induction and multiplication were studied.

RESULT

The best culture medium for the induction of axillary buds, which took the stems of A. crenate were as explants, was MS + 6-BA 0.5 mg x L(-1) + NAA 0.1 mg x L(-1), and the best medium for multiplication was MS + 6-BA 2.0 mg x L(-1) + NAA 0.1 mg x L(-1) + KT 0.5 mg x L(-1), the best medium for roots generation was 1/2MS + IBA 0.2 mg x L(-1). We also found that the roots'generation, roots rate and mean number of roots can be promoted by adding 0.2% Ac, and the most suitable ground substance was river sand-perlite-vermiculite (1:1:1) or perlite-vermiculite (1:1). With axillary buds and plant regeneration methode, more than 80% A. crenata sims could be regenerated integratedly.

CONCLUSION

A. crenata sims can be regenerated integratedly and breeded fast by using axillary bud proliferation technology.

摘要

目的

本研究采用组织培养技术对朱砂根快繁技术进行研究,为其工业化生产提供科学依据。

方法

研究不同基本培养基、激素及添加剂对朱砂根腋芽诱导和增殖及植株再生的影响。

结果

以朱砂根茎段为外植体诱导腋芽的最佳培养基为MS + 6-BA 0.5 mg·L⁻¹ + NAA 0.1 mg·L⁻¹,增殖最佳培养基为MS + 6-BA 2.0 mg·L⁻¹ + NAA 0.1 mg·L⁻¹ + KT 0.5 mg·L⁻¹,生根最佳培养基为1/2MS + IBA 0.2 mg·L⁻¹。添加0.2%活性炭可促进生根、提高生根率和平均生根数,最适宜的基质为河沙-珍珠岩-蛭石(1:1:1)或珍珠岩-蛭石(1:1)。采用腋芽增殖和植株再生方法,朱砂根的再生完整率可达80%以上。

结论

利用腋芽增殖技术可实现朱砂根的完整再生和快速繁殖。

相似文献

1
[Tissue culture and plant regeneration of Ardisia crenata].[朱砂根的组织培养与植株再生]
Zhongguo Zhong Yao Za Zhi. 2009 Aug;34(16):2043-6.
2
[Studies on plantlet regeneration from the mature leaves of Dioscorea zingiberensis].[盾叶薯蓣成熟叶片植株再生研究]
Zhongguo Zhong Yao Za Zhi. 2004 Feb;29(2):129-32.
3
[Tissue culture and plantlet regeneration from embryo of Saussurea involucrate].[雪兔子胚胎的组织培养与植株再生]
Zhongguo Zhong Yao Za Zhi. 2005 Jun;30(11):814-6.
4
[Tissue culture and plant regeneration of Ixeridium sonchifolium].[苦苣菜的组织培养与植株再生]
Zhongguo Zhong Yao Za Zhi. 2008 Feb;33(4):368-71.
5
[Studies on plantlet regeneration and propagation of Gentiana stramines].[麻花艽组培苗再生与增殖研究]
Zhongguo Zhong Yao Za Zhi. 2006 May;31(10):797-800.
6
[Study on tissue culture and plant regeneration of the stem-tips and buds of Periploca forrestii].[大理白前茎尖和芽的组织培养与植株再生研究]
Zhong Yao Cai. 2011 Nov;34(11):1656-60.
7
[Study on tissue culture and rapid propagation of Atractylodes macrocephala].白术组织培养与快速繁殖研究
Zhong Yao Cai. 2006 Mar;29(3):212-3.
8
[Culture in vitro and plant regeneration of Panax japonicus].[人参的离体培养与植株再生]
Zhong Yao Cai. 2011 Dec;34(12):1818-23.
9
[Tissue culture and plant regeneration of Bolbostemma paniculatum].[土贝母的组织培养与植株再生]
Zhong Yao Cai. 2006 Mar;29(3):209-11.
10
[Study on tissue culture of pasqueflower].[白头翁组织培养研究]
Zhongguo Zhong Yao Za Zhi. 2004 Mar;29(3):215-8.