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  • CN 62-1070/P
  • ISSN 1000-694X
  • 双月刊 创刊于1981年
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生物与土壤

珍稀泌盐植物长叶红砂(Reaumuria trigyna)愈伤组织诱导及增殖

  • 党振华 ,
  • 秦晓春 ,
  • 王迎春
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  • 1. 内蒙古大学 生命科学学院 牧草与特色作物生物技术重点实验室, 内蒙古 呼和浩特 010021;
    2. 包头市园林科技研究所, 内蒙古 包头 014010
党振华(1982-),男,内蒙古包头人,博士,讲师,主要从事植物抗逆分子生物学及分子生态学研究。Email: zhdang_1982@aliyun.com

收稿日期: 2015-05-14

  修回日期: 2015-07-02

  网络出版日期: 2015-09-20

基金资助

国家自然科学基金项目(31360063);内蒙古自治区高等学校创新研究团队发展计划项目(NMGIRT1401)

Callus Induction and Proliferation in the Endemic Recretohalophyte Reaumuria trigyna

  • Dang Zhenhua ,
  • Qin Xiaochun ,
  • Wang Yingchun
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  • 1. Key Laboratory of Herbage & Endemic Crop Biotechnology in Inner Mongolia, College of Life Science, Inner Mongolia University, Hohhot 010021, China;
    2. Baotou Landscape Research Institute,Baotou 014010, Inner Mongolia, China

Received date: 2015-05-14

  Revised date: 2015-07-02

  Online published: 2015-09-20

摘要

以珍稀泌盐植物长叶红砂(Reaumuria trigyna)成熟种子和不同发育阶段幼苗的不同部位为外植体,对其愈伤组织诱导和增殖进行了系统研究。结果表明:在添加3.0 mg·L-12,4-D、1.0 mg·L-1NAA、0.5 mg·L-1 6-BA、30 g·L-1蔗糖和6.0 g·L-1琼脂,pH为5.8的MSO培养基中,出愈率达70%以上,生长量高于其他培养基,是该植物愈伤组织诱导的最佳培养体系;7 d下胚轴和25 d的幼苗较适合愈伤组织诱导,可形成淡黄色疏松愈伤组织,且褐化程度相对较低;适宜的继代周期为30~40 d,随着传代次数增加,愈伤组织颜色变淡,生长速度加快;NaCl浓度为50 mmol·L-1和100 mmol·L-1时促进愈伤组织生长,盐浓度过高则导致其生长受抑,甚至死亡。

本文引用格式

党振华 , 秦晓春 , 王迎春 . 珍稀泌盐植物长叶红砂(Reaumuria trigyna)愈伤组织诱导及增殖[J]. 中国沙漠, 2015 , 35(5) : 1262 -1267 . DOI: 10.7522/j.issn.1000-694X.2015.00099

Abstract

The aim of this study was to evaluate callus induction and proliferation in the endangered recretohalophyte Reaumuria trigyna. Mature seeds and seedlings at different development stages were used as the ex-plant materials. The best medium for callus formation and proliferation was improved MSO (pH 5.8) supplemented with 3.0 mg·L-1 2,4-dichlorophenoxyacetic acid, 1.0 mg·L-1 naphthaleneacetic acid, 0.5 mg·L-1 6-benzylaminopurine, 30 g·L-1 sucrose, 0.5 g·L-1 casein hydrolysate, and 6.0 g·L-1 agar. On this medium, the callus induction rate was greater than 70%, and the growth rate was higher than those of ex-plants on other media. The optimal ex-plants for callus induction were hypocotyls from 7-day-old and 25-day-old seedlings. The calli that formed from these ex-plants were loose, light yellow, and showed a lower browning rate, compared with calli that grew from other ex-plants. The optimum duration of the subculture cycle was 30-40 days. With longer passage times, the callus grew faster and was a lighter color. When calli were cultured on media with different NaCl concentrations, their growth was accelerated on media containing 50 and 100 mmol·L-1 NaCl, but higher concentrations of NaCl inhibited callus growth or resulted in callus death.

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