首页> 外文期刊>Journal of food, agriculture & environment >Induction of embryogenic callus and plant regeneration from nodes of greenhouse grown plants of Alstroemeria cv. Fuego
【24h】

Induction of embryogenic callus and plant regeneration from nodes of greenhouse grown plants of Alstroemeria cv. Fuego

机译:血清统计植物植物节点诱导胚胎愈伤组织植物再生。 Fuego

获取原文
获取原文并翻译 | 示例
           

摘要

Plant regeneration ability of callus was studied in the ornamental monocot Alstroemeria cv. Fuego. High frequency (23%) of compact callus induction was obtained on a Schenk and Hildebrant (SH) medium supplemented with 2 mg/l picloram from nodal segments excised from plants grown in the greenhouse. After three months of culture, compact embryogenic calluses (CECs) were transferred to the modified Murashige and Skoog (MS) medium supplemented with 5 mg/l picloram for further proliferation of CECs. Somatic embryos and subsequently plantlets were formed after transfer of the CEC to regeneration medium supplemented with various concentrations of BAR The highest plantlet formation was observed on MS medium supplemented with 0.5 mg/l BAR The total time needed to regenerate complete plants from the initiation of nodal segment culture was approximately 8 months.
机译:在观赏单极管德尔什罗罗形核糖体CV中研究了愈伤组织的再生能力。 Fuego。 在Schenk和Hildebrant(Sh)培养基上获得高频(23%)紧凑型愈伤组织诱导,该培养基(Sch)培养基中含有2mg / L菠菜的核心区段,从温室生长的植物中切除。 在三个月的培养后,将紧凑的胚胎愈伤组织(CEC)转移到补充有5mg / L氨基氯蛋白的改性Murashige和Skoog(MS)培养基中,用于进一步增殖CEC。 在将CEC转移到补充有各种浓度的浆料后,在补充有0.5mg / L棒的MS培养基中,在补充有0.5mg / L的MS培养基中,在补充有0.5mg / L的MS培养基中,从Nodal再生完整植物所需的总时间来观察到最高植物的再生培养基 分部文化大约是8个月。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

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