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培养基主成分优化提高大花金挖耳胞内黄酮产量

李玉平 龚宁

李玉平, 龚宁. 培养基主成分优化提高大花金挖耳胞内黄酮产量[J]. 福建农业学报, 2019, 34(6): 652-659. doi: 10.19303/j.issn.1008-0384.2019.06.005
引用本文: 李玉平, 龚宁. 培养基主成分优化提高大花金挖耳胞内黄酮产量[J]. 福建农业学报, 2019, 34(6): 652-659. doi: 10.19303/j.issn.1008-0384.2019.06.005
LI Yu-ping, GONG Ning. Optimizing Medium for Flavonoid-producing Carpesium Macrocephalum Culture[J]. Fujian Journal of Agricultural Sciences, 2019, 34(6): 652-659. doi: 10.19303/j.issn.1008-0384.2019.06.005
Citation: LI Yu-ping, GONG Ning. Optimizing Medium for Flavonoid-producing Carpesium Macrocephalum Culture[J]. Fujian Journal of Agricultural Sciences, 2019, 34(6): 652-659. doi: 10.19303/j.issn.1008-0384.2019.06.005

培养基主成分优化提高大花金挖耳胞内黄酮产量

doi: 10.19303/j.issn.1008-0384.2019.06.005
基金项目: 

国家公益性行业(农业)科研专项 200903052

国家重点研发计划项目 2016YFC0402904

详细信息
    作者简介:

    李玉平(1970-), 男, 博士, 副教授, 主要从事植物资源保护与利用的教学与研究(E-mail:liyuping1970@nwafu.edu.cn)

    通讯作者:

    龚宁(1970-), 女, 博士, 副教授, 主要从事环境与食品安全研究(E-mail:Gongningcn@163.com)

  • 中图分类号: Q813.1

Optimizing Medium for Flavonoid-producing Carpesium Macrocephalum Culture

  • 摘要:   目的  优化组合培养基中大量、微量元素及附加激素等培养条件,筛选出大花金挖耳细胞培养黄酮的生产培养基。  方法  以NT+1.0 mg·L-1 NAA+0.2 mg·L-1 6-BA为基本培养基,先优化组合其大量元素NH4+、NO3-、K+,再优化组合微量元素MoO42-、Zn2+、BO33-、Co2+、Cu2+、I-、Mn2+,最后分别附加2,4-D、KT、GA3,测定大花金挖耳悬浮培养细胞生长、黄酮含量及产量。  结果  大量元素优化、微量元素优化及附加激素KT、GA3,大花金挖耳细胞培养物中黄酮产量均得到了显著提升(P < 0.05),添加2,4-D降低了黄酮产量。本研究筛选得到大花金挖耳细胞培养生产黄酮类化合物的最佳NT培养基为:大量元素NH4+、NO3-、K+分别为15.46 mmol·L-1、14.10 mmol·L-1、19.10 mmol·L-1,微量元素MoO42-、Zn2+、BO33-、Co2+、Cu2+、I-、Mn2+分别为3.0 μmol·L-1、0.06 mmol·L-1、0.4 mmol·L-1、0.2 μmol·L-1、0.4 μmol·L-1、10 μmol·L-1、0.2 mmol·L-1,附加KT 0.2 mg·L-1。在此培养条件下,大花金挖耳细胞培养物中黄酮含量达到2.05%,是基本培养基的1.68倍;黄酮产量为517.87 mg·L-1,是基本培养基的1.80倍。  结论  在前期研究的基础上,通过培养基主成分优化,提高了大花金挖耳细胞培养生产黄酮的产量,初步得到了黄酮生产培养基。
  • 图  1  大量元素优化组合对悬浮培养细胞生长、黄酮含量和产量的影响

    注:图中不同字母表示不同处理方法在0.05水平存在显著差异(P < 0.05),图 3~5同。

    Figure  1.  Effects of macro-elements on cell growth, flavonoids content and yield in culture suspension

    Note:Different lowercase letters within column indicate significant difference between different treatment methods at the 0.05 level; the same below.The same as Fig. 3-5.

    图  2  基本培养基NT0和生产培养基NT1中的悬浮培养细胞(7 d)

    Figure  2.  Cells in suspension culture with basic medium NT0 or production medium NT1 (7 d)

    图  3  微量元素优化组合对悬浮培养细胞生长、黄酮含量和产量的影响

    Figure  3.  Effects of micro-elements on cell growth, flavonoids content and yield in culture suspension

    图  4  2, 4-D对悬浮培养细胞生长、黄酮含量和产量的影响

    Figure  4.  Effects of 2, 4-D in varied concentrations on cell growth, flavonoids content and yield in culture suspension

    图  5  KT对悬浮培养细胞生长、黄酮含量和产量的影响

    Figure  5.  Effects of KT in varied concentrations on cell growth, flavonoids content and yield in culture suspension

    图  6  GA3对悬浮培养细胞生长、黄酮含量和产量的影响

    Figure  6.  Effects of GA3 in varied concentrations on cell growth, flavonoids content and yield in culture suspension

    表  1  大量元素氮、钾优化组合对大花金挖耳细胞培养生产黄酮类化合物试验

    Table  1.   Medium optimization on nitrogen and potassium for flavonoids-producing C. macrocephalum culture

    试验组
    Treatments
    大量元素Macroelements/(mmol·L-1)
    NH4+ NO3- K+
    CK 10.31 9.40 14.40
    15.46 9.40 14.40
    15.46 14.10 19.10
    15.46 18.79 23.79
    20.61 9.40 14.40
    20.61 14.10 19.10
    20.61 18.79 23.79
    下载: 导出CSV

    表  2  微量元素钼、锌优化组合对大花金挖耳培养细胞生产黄酮类化合物试验

    Table  2.   Medium optimization on molybdenum and zinc for flavonoids-producing C. macrocephalum culture

    试验组
    Treatments
    微量元素Microelements
    MoO42-/(μmol·L-1) Zn2+/(mmol·L-1)
    CK 1.0 0.03
    A 3.0 0.06
    B 3.0 0.09
    C 2.0 0.06
    D 2.0 0.09
    下载: 导出CSV
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