In vitro and Ex vitro Propagations of Astilboides tabularis (Hemsl.) Engl. as a Rare and Endangered Species

U. Shin, Romika Ch, Ra, Hoduck Kang
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引用次数: 1

Abstract

This study was conducted to establish in vitro and ex vitro propagation systems and to secure the genetic resource for ex-situ conservation of Astilboides tabularis (Hemsl.) Engl. as a rare and endangered species. Plant materials were collected and prepared for various treatments for in vitro propagation by plant tissue culture and ex vitro propagation by root cuttings. For callus induction, leaf explants cultured on MS medium with BA 0.1 mg L-1 showed the highest rate at 24%, whereas the petioles supplemented with BA 0.5 mg L-1 exhibited the highest rate at 14%. Root explants treated with BA alone did not induce callus formation whereas a combination of BA and NAA showed 100% callus induction at concentrations of BA 0.1 + NAA 0.1 mg L1 and BA 1.0 + NAA 1.0 mgL-1. Shoots were produced at 50% from leaf explants treated with BA 0.1 mg L-1 concentration, whereas no shoots were observed even with the treatments from root segments. Rooting experiments supplemented with NAA 0.01 mgL-1 had the highest rate up to 86% with 15 small roots and 1.3 cm length. In order to increase the efficiency of in vitro potential regeneration of A. tabularis, additional studies would be needed for higher rooting rates from callus and induced shoot. Ex vitro propagation by root cuttings with large diameter and 7 cm length grew well above ground, whereas medium diameter and 7 cm length showed good rooting system in the first year. During the second year, small shoots grew well for medium diameter, whereas there were no significant differences among other treatments. Thus, the size and length of the cuttings were for the plants in the first year, which did not affect growth in the second year. Based on this work, A. tabularis root cutting for mass propagation would be possible by small size cutting system.
黄芪的离体和离体繁殖心血管病。珍稀濒危物种
本研究旨在建立黄芪离体和离体繁殖体系,为黄芪移地保护提供遗传资源保障。心血管病。作为稀有濒危物种。收集植物材料,通过组织培养和扦插法进行离体繁殖。叶片外植体在BA浓度为0.1 mg L-1的MS培养基上愈伤组织诱导率最高,为24%,叶柄在BA浓度为0.5 mg L-1的MS培养基上愈伤组织诱导率最高,为14%。BA单独处理的根外植体不诱导愈伤组织形成,而BA和NAA联合处理的根外植体在BA 0.1 + NAA 0.1 mg L1和BA 1.0 + NAA 1.0 mg l -1浓度下诱导愈伤组织形成率为100%。BA浓度为0.1 mg L-1时,叶片外植体的萌发率为50%,而根段处理也未萌发。NAA添加量为0.01 mg -1的生根试验,生根率最高,达86%,根长1.3 cm,小根15根。为了提高油油树的体外再生效率,还需要进一步研究如何提高愈伤组织和诱导苗的生根率。大直径和长7 cm的插条离体繁殖第一年在地上生长良好,而中直径和长7 cm的插条离体繁殖第一年生根良好。第二年,中径小芽生长良好,其他处理间差异不显著。因此,插条的大小和长度对第一年的植株是有利的,对第二年的生长没有影响。在此基础上,采用小尺寸扦插系统进行油桐根茎扦插是可行的。
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