湖北农业科学 ›› 2021, Vol. 60 ›› Issue (13): 143-145.doi: 10.14088/j.cnki.issn0439-8114.2021.13.029

• 生物工程 • 上一篇    下一篇

麻城油茶体细胞胚胎发生及植株再生

庞芳芹, 张靖怡, 柳倩, 汤欣欣, 胡孝明, 朱华国   

  1. 黄冈师范学院生物与农业资源学院/经济林种质改良与资源综合利用湖北省重点实验室,湖北 黄冈 438000
  • 收稿日期:2020-11-13 出版日期:2021-07-10 发布日期:2021-07-26
  • 通讯作者: 朱华国(1979-),男,湖北黄冈人,教授,博士,主要从事植物遗传改良与生物技术利用,(电话)15926761181(电子信箱)57530422@qq.com。
  • 作者简介:庞芳芹(1977-),女,甘肃秦安人,实验师,主要从事植物生物技术研究,(电话)15926779793(电子信箱)17872080@qq.com。
  • 基金资助:
    经济林种质改良及资源综合利用湖北省重点实验室及大别山特色资源开发湖北省协同创新中心开放基金项目(201931403); 黄冈师范学院博士基金项目

Somatic embryogenesis and plant regeneration of Camellia oleifera in Macheng

PANG Fang-qin, ZHANG Jing-yi, LIU Qian, TANG Xin-xin, HU Xiao-ming, ZHU Hua-guo   

  1. College of Biology and Agricultural Sources,Huanggang Normal University/Hubei Key Laboratory of Economic Forest Germplasm Improvement and Resources Comprehensive Utilization,Huanggang 438000,Hubei,China
  • Received:2020-11-13 Online:2021-07-10 Published:2021-07-26

摘要: 为建立油茶通过体细胞胚胎发生方式获得再生植株的技术体系,以湖北麻城油茶7月中旬幼胚为试验材料,消毒后切块接种于分别附加了2.0 mg/L 2,4-D+1.0 mg/L KT和5.0 mg/L NAA+1.0 mg/L KT的MS培养基,进行愈伤组织诱导培养。1个月后统计出愈率,两种处理的愈伤组织诱导率分别为83.23%和45.34%;挑选状态良好的愈伤组织继代于附加了1.0 mg/L NAA+1.0 mg/L KT的MS培养基,培养2个月后可见明显的胚状体形成,统计胚状体平均发生率为15.25%;随后将胚状体继代于附加了1.0 mg/L NAA+3.0 mg/L 6-BA的MS培养基上进行胚状体发育和植株再生培养,获得具备完整子叶的胚状体后,转移至含有3.0 mg/L 6-BA的1/2MS培养基中进行生根培养,获得完整再生植株后驯化移栽至营养钵中继续生长。本研究建立了麻城油茶6个月内获得体细胞胚胎发生及植株再生的技术体系,为建立油茶农杆菌介导的遗传转化技术体系奠定了基础。

关键词: 油茶, 体细胞胚胎发生, 植株再生

Abstract: To establish a technical system for regeneration of Camellia oleifera by somatic embryogenesis. The immature embryos of Hubei Macheng Camellia oleifera in the middle of July were used as experimental materials. After sterilization, immature embryos were cut into pieces and inoculated on MS medium supplemented with 2.0 mg/L 2,4-D+1.0 mg/L KT and 5.0 mg/L NAA+1.0 mg/L KT, respectively. One month later, the callus induction rates of the two treatments were 83.23% and 45.34%, respectively. The callus was selected to be subculture on MS medium with 1.0 mg/L NAA+1.0 mg/L KT. After two months, obvious somatic embryos were observed, and the average induction rate of embryoid was 15.25%; the embryoids were then subcultured on MS medium supplemented with 1.0 mg/L NAA+3.0 mg/L 6-BA for embryoid development and plantlet regeneration. And then embryoids were transferred to 1/2MS medium containing 3.0 mg/L 6-BA for rooting culture. Complete regenerated plants can be obtained, and then domesticated and transplanted to the bowl for further growth. The technology system of somatic embryogenesis and plant regeneration in Macheng Camellia oleiferawas established in this study, which laid a foundation for the establishment of Agrobacterium mediated transformation technology system of Camellia oleifera.

Key words: Camellia oleifera, somatic embryogenesis, plant regeneration

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