首页> 外文OA文献 >Perbanyakan Tanaman Buah Naga Berdaging Buah Merah {Hylocereus Costaricensis) Melalui Teknik Kultur Jaringan*[micropropagation of Red Dragon Fruit (Hylocereus Costaricensis) Through in Vitro Culture]
【2h】

Perbanyakan Tanaman Buah Naga Berdaging Buah Merah {Hylocereus Costaricensis) Melalui Teknik Kultur Jaringan*[micropropagation of Red Dragon Fruit (Hylocereus Costaricensis) Through in Vitro Culture]

机译:通过组织培养技术繁殖红色激素果树(Hylocereus Costaricensis)* [通过体外培养进行红色火龙果(Hylocereus Costaricensis)的微繁殖]

摘要

Hylocereus costaricensis is new important fruit in Indonesia. One of constrain in its development is limitation of planting material.The aim of the research is to study the regeneration H. costaricensis through micro shoot induction of node explants. The experiments were carried out in the Tissue Culture Laboratory of Indonesian Coffee and Cocoa Research Institute. Experiment on microshoots proliferation stage was arranged in a Factorial Completely Randomized Design, with three replications.The first factor was Kinetin concentration consisted of five treatments i.e.: 0, 2.5, 5.0, 7.5 and 10.0 mg/1.The second factor was Indole acetic acid (IAA) concentration consisted of five levels i.e.: 0, 0.25, 0.5, 0.75 and 1 mg/1. Microshoots multiplication stage was arranged in a Factorial Completely Randomized Design,with three replications. The first factor was polyvinyl pyrrolidone (PVP) concentration consisted of six treatments i.e.: 0, 0.25, 0.5, 0.75, 1.0 and 1.25 %. The second factor was Cystein concentration consisted of four treatments i.e.: 0, 25, 50 and 75 mg/1. The microshoots rooting stage the results experiment was laid in a Factorial Completely Randomized Design, with three replications. The first factor was Giberalic acid (GA3) consisted of five treatments i.e.:0, 0.25, 0.5, 0.75 and 1 mg/1. The second factor was Boric acid concentration consisted of four levels i.e.: 0, 50, 100 and 150 mg/1. In the microshoots proliferation stage the results showed that there was interaction between IAA and Kinetin concentration on the microshoots proliferation and the number of shoot per explnat. The best results were obtained from the treatment 0.75 mg/1 IAA + 7.5 mg/1 Kinetin, whereas in this treatment the rate of microshoots proliferation and the number of microshoots perexplant was 50 % and 3.9, respectively. In the microshoots multiplication stage, the results showed that there was interaction between PVP and Cystein concentration. The best results were obtained from the treatment 0.75% PVP + 75 mg/1 Cystein, whereas in this treatment the rate of microshoots multiplication and the number of microshoots per explant was 95% and 6.3, respectively. In the rooting stage, the results showed that there was interaction between GA and Boric acid concentration. The experiment indicated that 0.5 mg/1 GA3 + 100 mg/1 Boric acid showed the best result to stimulate root induction of the in vitro microshoots propagation, whereas in this treatment the percentage of rooted microshoots and the hight of plantlet were 95% and 5.7 Cm, respectively.
机译:Hylocereus costaricensis是印度尼西亚的新重要水果。其发展的制约因素之一是种植材料的局限性。本研究的目的是通过结节外植体的微芽诱导研究木薯的再生。实验是在印尼咖啡和可可研究所的组织培养实验室中进行的。微芽增殖阶段的实验安排在因子完全随机设计中,重复三遍。第一个因子是Kinetin浓度,由五种处理组成:0、2.5、5.0、7.5和10.0 mg / 1,第二个因子是吲哚乙酸。 (IAA)浓度由五个水平组成,即:0、0.25、0.5、0.75和1 mg / 1。 Microshoots繁殖阶段安排在阶乘完全随机设计中,进行三次重复。第一个因素是聚乙烯吡咯烷酮(PVP)浓度由六种处理组成,即:0%,0.25%,0.5%,0.75%,1.0%和1.25%。第二个因素是半胱氨酸浓度由四种处理组成,即:0、25、50和75 mg / 1。在结果实验的微芽生根阶段,将其放置在因子完全随机设计中,重复三遍。第一个因素是吉百利酸(GA3),它由五种处理组成,即:0、0.25、0.5、0.75和1 mg / 1。第二个因素是硼酸浓度由四个水平组成:0、50、100和150 mg / 1。在微芽增殖阶段,结果表明,IAA和Kinetin浓度之间存在相互作用,从而影响微芽增殖和每单位芽的芽数。从0.75 mg / 1 IAA + 7.5 mg / 1 Kinetin处理可获得最佳结果,而在该处理中,微枝的增殖率和植株微枝的数量分别为50%和3.9。在微芽繁殖阶段,结果表明PVP和半胱氨酸浓度之间存在相互作用。从0.75%PVP + 75 mg / 1半胱氨酸的处理获得最佳结果,而在这种处理中,微枝的繁殖率和每个外植体的微枝数量分别为95%和6.3。在生根阶段,结果表明GA和硼酸浓度之间存在相互作用。实验表明,0.5 mg / 1 GA3 + 100 mg / 1硼酸刺激体外微枝繁殖的根诱导效果最好,而在这种处理中,生根微枝的百分比和苗高分别为95%和5.7厘米,分别。

著录项

  • 作者

    Priyono, Priyono;

  • 作者单位
  • 年度 2005
  • 总页数
  • 原文格式 PDF
  • 正文语种 ID
  • 中图分类

相似文献

  • 外文文献
  • 中文文献

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号