农业工程2024,Vol.14Issue(12) :45-49.DOI:10.19998/j.cnki.2095-1795.202412307

破布叶组培快繁技术

Tissue culture and rapid propagation technology of Microcos paniculata L.

蔡清梅 陈冬怡 陈国华 胡国弟 周宏英
农业工程2024,Vol.14Issue(12) :45-49.DOI:10.19998/j.cnki.2095-1795.202412307

破布叶组培快繁技术

Tissue culture and rapid propagation technology of Microcos paniculata L.

蔡清梅 1陈冬怡 2陈国华 2胡国弟 1周宏英3
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作者信息

  • 1. 广东慧达康制药有限公司,广东 佛山 528244
  • 2. 中国科学院华南植物园,广东 广州 510650
  • 3. 广东良田农林科技有限公司,广东 清远 511800
  • 折叠

摘要

以破布叶茎段为外植体,通过植物组培快繁技术,培养成完整的脱毒植株.试验结果表明,外植体灭菌处理成功率 94%,诱导不定芽的最适培养基 1/4MS+0.5 mg/L 6-BA;不定芽继代增殖的最适培养基 1/4MS+0.5 mg/L 6-BA+0.1 mg/L NAA+0.1 mg/L GA3,增殖系数 3.3;最适出根培养基 1/4MS+1.0 mg/L IBA+0.1 mg/L NAA,出根率 93.1%;组培苗移栽成活率98%,为破布叶种苗提供了一种新型快速的繁殖方式,将促进岭南特色中药材破布叶高效新型产业化的形成和发展.

Abstract

Using stems of Microcos paniculata L.seedlings as explants,complete and virus-free plants were obtained by tissue culture and rapid propagation technology.Results showed that explants sterilization success rate was as high as 94%.Optimal medium for ad-ventitious buds induction was 1/4MS+0.5 mg/L 6-BA.Optimal medium for subculture multiplication was 1/4MS+0.5 mg/L 6-BA+0.1 mg/L NAA+0.1 mg/L GA3,and subculture multiplication factor was up to 3.3.Optimal medium for root was 1/4MS+1.0 mg/L IBA+0.1 mg/L NAA,while rooting rate was 93.1%.Transplanting survival rate was averaged at 98%.It could provide an effect way for rapid propagation of virus-free seedlings,which would promote formation and development of high efficiency and new industrialization of Microcos paniculata L.,a characteristic Lingnan medicinal plant.

关键词

破布叶/组培快繁/种苗/中药材

Key words

Microcos paniculata L./tissue culture and rapid propagation/seed seedlings/Chinese medicinal herbs

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出版年

2024
农业工程
北京卓众出版有限公司

农业工程

CSTPCD
影响因子:0.422
ISSN:2095-1795
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