| Peer-Reviewed

Effects of Concentrations of IBA, NAA and 6-BA on the Proliferation and Rooting Culture of Chamomile

Received: 7 January 2020    Accepted: 9 June 2020    Published: 28 July 2020
Views:       Downloads:
Abstract

Objective: To select the best culture medium for proliferation and root culture. Method: Using aseptic buds obtained from the first generation of culture as the experimental material, different concentrations of auxin (IBA, NAA) and cytokinin 6-BA were combined to conduct proliferation culture and rooting culture of Chamomile. Result: The results showed that the aseptic buds of primary culture were transferred to MS +1.3 mg/L6-BA +0.2 mg LIBA +6.2 g/L agarose +30 g/L sucrose + 0.1 g/L activated carbon culture medium after initial screening. After 40 days of culture, the proliferation effect is the best, the proliferation coefficient is 6.2, the average plant height is 3.4 cm, and the plant grows strongly; The aseptic buds obtained from the initial culture were transferred to the 1/2 MS + 0.4 mg/LIBA + 0.1 mg/L NAA +6.2 g/L agar + 30 g/L sucrose Rhizome medium, and after 30 days of culture, the root rate reached 96 , The number of roots per plant reached 8.2, the average root length was 3.6 cm, and the root growth was the best.

Published in Asia-Pacific Journal of Biology (Volume 3, Issue 1)
Page(s) 1-6
Creative Commons

This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited.

Copyright

Copyright © The Author(s), 2024. Published by Science Publishing Group

Keywords

African Chrysanthemum, Proliferative Culture, Rooting Culture, 6-BA Concentration

References
[1] 高绍良, 周寒松, 张素芳. 非洲菊组织培养基筛选研究[J]. 中国农学通报, 2010,26 (7):210-213.
[2] 李娜,王平,吴志刚,张玉静.非洲菊组织培养研究进展[J].北方园艺,2011(21):178-181.
[3] 赵雁鸣,王羽飞,许昌慧等.非洲菊茎尖离体培养技术研究[J].安徽农学通报, 2015,21(5):12-14.
[4] Pierik R L M. Gerbera plantlets from in vitro cultivated capitulum erplant.Scientia Horticulturae,1973,1(1):117-120.
[5] 陈开陆,库文益,王向东.非洲菊组织培养和快速繁殖研究.西昌农业高等专科学校学报,2004,3(1):64-65.
[6] Murashige T. Clonal multiplication of Gerbera through tissue culture.Hort Sci. 1974, 9(3): 175-180.
[7] 黄衡宇,李鹂,杨胜辉.非洲菊的组织培养[J].吉首大学学报(自然科学版),2001,22(1).
[8] 鲁雪华,林勇,郭文杰.非洲菊小花托的离体培养.亚热带植物通讯,1996,25(2):21-24.
[9] 张平.非洲菊组织培养研究进展[J]. 宁德师范学院学报(自然科学版), 2004, 16(1):69-73.
[10] 鲁雪华等.几种因素对非洲菊离体培养再生植株的影响.植物生理学通讯.199,35(5):372-374.
[11] 郑秀芳等.非洲菊花托培养和植株再生.西南农业大学学报.2001,23(2):171-173.
[12] 李高燕,王海云,牛佳佳等.非洲菊组织培养研究进展[J].中国农学通报, 2009, 25(10):72-76.
[13] 席梦利,王节萍,章静娟等.多效唑在非洲菊组织培养中的应用[J].江苏农业科学, 2000,4(3):55-56.
[14] 陈海霞,李茂娟.非洲菊不同发育时期的花托诱导愈伤组织的研究[J].南方农业学报, 2008, 39(1):1-5.
[15] Guohua Ma,Jinfeng Lu,Jaime A, et al. Shoot organogenesis and somatic embryogenesis from leaf and shoot explants of Ochna integerrima (Lour) [J]. Plant Cell Tiss Organ Cult,2011,104(2):157-162.
[16] 刘丽荣,苏荣德,李忠利等.非洲菊组织培养繁殖的试验研究[J].辽宁农业职业技术学院学报, 2002, 4(3):13-15.
[17] 张子学,丁为群,褚锦彩等.非洲菊快速繁殖技术研究[J].种子,2006, 25(1):88-90.
[18] 张希太.非洲菊组织培养与快速繁殖试验研究[J].现代农业科技, 2011, (6):210-210.
[19] 成晟, 罗福来, 钟定业等.切花非洲菊组织培养及快速繁殖研究[J].分子植物育种, 2016,14(3):693-698.
[20] 刘晓燕.非洲菊离体组织培养与快速繁殖[J].耕作与栽培, 2001,11(3):22-22.
Cite This Article
  • APA Style

    Bai Yanrong, Wang Jinying. (2020). Effects of Concentrations of IBA, NAA and 6-BA on the Proliferation and Rooting Culture of Chamomile. Asia-Pacific Journal of Biology, 3(1), 1-6.

    Copy | Download

    ACS Style

    Bai Yanrong; Wang Jinying. Effects of Concentrations of IBA, NAA and 6-BA on the Proliferation and Rooting Culture of Chamomile. Asia-Pac. J. Biol. 2020, 3(1), 1-6.

    Copy | Download

    AMA Style

    Bai Yanrong, Wang Jinying. Effects of Concentrations of IBA, NAA and 6-BA on the Proliferation and Rooting Culture of Chamomile. Asia-Pac J Biol. 2020;3(1):1-6.

    Copy | Download

  • @article{10046032,
      author = {Bai Yanrong and Wang Jinying},
      title = {Effects of Concentrations of IBA, NAA and 6-BA on the Proliferation and Rooting Culture of Chamomile},
      journal = {Asia-Pacific Journal of Biology},
      volume = {3},
      number = {1},
      pages = {1-6},
      url = {https://www.sciencepublishinggroup.com/article/10046032},
      abstract = {Objective: To select the best culture medium for proliferation and root culture. Method: Using aseptic buds obtained from the first generation of culture as the experimental material, different concentrations of auxin (IBA, NAA) and cytokinin 6-BA were combined to conduct proliferation culture and rooting culture of Chamomile. Result: The results showed that the aseptic buds of primary culture were transferred to MS +1.3 mg/L6-BA +0.2 mg LIBA +6.2 g/L agarose +30 g/L sucrose + 0.1 g/L activated carbon culture medium after initial screening. After 40 days of culture, the proliferation effect is the best, the proliferation coefficient is 6.2, the average plant height is 3.4 cm, and the plant grows strongly; The aseptic buds obtained from the initial culture were transferred to the 1/2 MS + 0.4 mg/LIBA + 0.1 mg/L NAA +6.2 g/L agar + 30 g/L sucrose Rhizome medium, and after 30 days of culture, the root rate reached 96 , The number of roots per plant reached 8.2, the average root length was 3.6 cm, and the root growth was the best.},
     year = {2020}
    }
    

    Copy | Download

  • TY  - JOUR
    T1  - Effects of Concentrations of IBA, NAA and 6-BA on the Proliferation and Rooting Culture of Chamomile
    AU  - Bai Yanrong
    AU  - Wang Jinying
    Y1  - 2020/07/28
    PY  - 2020
    T2  - Asia-Pacific Journal of Biology
    JF  - Asia-Pacific Journal of Biology
    JO  - Asia-Pacific Journal of Biology
    SP  - 1
    EP  - 6
    PB  - Science Publishing Group
    UR  - http://www.sciencepg.com/article/10046032
    AB  - Objective: To select the best culture medium for proliferation and root culture. Method: Using aseptic buds obtained from the first generation of culture as the experimental material, different concentrations of auxin (IBA, NAA) and cytokinin 6-BA were combined to conduct proliferation culture and rooting culture of Chamomile. Result: The results showed that the aseptic buds of primary culture were transferred to MS +1.3 mg/L6-BA +0.2 mg LIBA +6.2 g/L agarose +30 g/L sucrose + 0.1 g/L activated carbon culture medium after initial screening. After 40 days of culture, the proliferation effect is the best, the proliferation coefficient is 6.2, the average plant height is 3.4 cm, and the plant grows strongly; The aseptic buds obtained from the initial culture were transferred to the 1/2 MS + 0.4 mg/LIBA + 0.1 mg/L NAA +6.2 g/L agar + 30 g/L sucrose Rhizome medium, and after 30 days of culture, the root rate reached 96 , The number of roots per plant reached 8.2, the average root length was 3.6 cm, and the root growth was the best.
    VL  - 3
    IS  - 1
    ER  - 

    Copy | Download

Author Information
  • College of Agronomy and Life Sciences, Kunming University, Kun Ming, China

  • School of Architectural Engineering and Management, Kunming University, Kunming, China

  • Sections