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细枝木麻黄离体培养过程中愈伤组织和再生芽的细胞组织学观察
引用本文:姜清彬,仲崇禄,陈羽,刘芬,张勇,陈珍.细枝木麻黄离体培养过程中愈伤组织和再生芽的细胞组织学观察[J].热带亚热带植物学报,2015,23(1):37-42.
作者姓名:姜清彬  仲崇禄  陈羽  刘芬  张勇  陈珍
作者单位:1. 中国林业科学研究院热带林业研究所,广州,510520
2. 中国林业科学研究院热带林业研究所,广州 510520; 中南林业科技大学生命科学与技术学院,长沙 410004
基金项目:中央公益性科研院所基金项目(RITFYWZX201203);“十二五”林业科技支撑计划项目(2012BAD01B0603)资助
摘    要:为探讨细枝木麻黄(Casuarina cunninghamianaMiq.)愈伤组织分化过程的细胞组织学,对离体培养条件下的愈伤组织进行扫描电子显微镜和石蜡切片观察,分析愈伤组织的细胞分裂、分化以及芽再生的发生过程。结果表明,新鲜外植体培养于愈伤组织诱导培养基上,伤口处的薄壁细胞开始脱分化,培养1周后形成明显的愈伤组织;继续培养2周后,胚性愈伤组织形成,且表层细胞启动分化形成芽原基;培养4周,可肉眼观察到胚性芽原基,数量增多并逐渐分化形成不定芽;培养至第6周,生成不定芽,并大量增殖和分化。因此,细枝木麻黄是通过愈伤组织分化形成胚状体的途径进行植株再生的,为建立细枝木麻黄组织培养高效再生体系提供了理论依据。

关 键 词:细枝木麻黄  离体培养  愈伤组织
收稿时间:7/1/2014 12:00:00 AM
修稿时间:2014/9/13 0:00:00

Cytohistological Observation of Callus and Adventitious Buds of Casuarina cunninghamiana Miq. in vitro
JIANG Qing-bin,ZHONG Chong-lu,CHEN Yu,LIU Fen,ZHANG Yong and CHEN Zhen.Cytohistological Observation of Callus and Adventitious Buds of Casuarina cunninghamiana Miq. in vitro[J].Journal of Tropical and Subtropical Botany,2015,23(1):37-42.
Authors:JIANG Qing-bin  ZHONG Chong-lu  CHEN Yu  LIU Fen  ZHANG Yong and CHEN Zhen
Institution:Research Institute of Tropical Forestry, Chinese Academy of Forestry, Guangzhou 510520, China,Research Institute of Tropical Forestry, Chinese Academy of Forestry, Guangzhou 510520, China,Research Institute of Tropical Forestry, Chinese Academy of Forestry, Guangzhou 510520, China,1. Research Institute of Tropical Forestry, Chinese Academy of Forestry, Guangzhou 510520, China;2. College of Life Science and Technology, Central South University of Forestry and Technology, Changsha 410004, China,Research Institute of Tropical Forestry, Chinese Academy of Forestry, Guangzhou 510520, China and Research Institute of Tropical Forestry, Chinese Academy of Forestry, Guangzhou 510520, China
Abstract:In order to understand the cytohistology of Casuarina cunninghamiana callus, cell division, callus differentiation and adventitious bud regeneration were studied under scanning electron microscope and paraffin sections. The results showed that parenchyma cells in the wound started dedifferentiation in the callus induction medium. After cultured for one week, callus were induced at the explant wound, and embryonic callus was formed. Bud primordium was induced from surface cells after two weeks. After culturing for a further four weeks, embryonic bud primordium became more increasely visible, and gradually differentiated to become adventitious bud. After another six weeks, most of the adventitious buds have proliferated and differentiated, and some developed to shoots. It was confirmed that the regeneration of C. cunninghamiana could be achieved through embryoid callus differentiation, it would provide basis for establishment of efficient regeneration system in C. cunninghamina.
Keywords:Casuarina cunninghamiana Miq    in vitro culture  Callus
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