高级检索+

‘正午’牡丹微繁殖体系的建立

文书生, 成仿云, 钟原, 王新, 李刘泽木, 黄弄璋

文书生, 成仿云, 钟原, 王新, 李刘泽木, 黄弄璋. ‘正午’牡丹微繁殖体系的建立[J]. 植物科学学报, 2016, 34(1): 143-150. DOI: 10.11913/PSJ.2095-0837.2016.10143
引用本文: 文书生, 成仿云, 钟原, 王新, 李刘泽木, 黄弄璋. ‘正午’牡丹微繁殖体系的建立[J]. 植物科学学报, 2016, 34(1): 143-150. DOI: 10.11913/PSJ.2095-0837.2016.10143
WEN Shu-Sheng, CHENG Fang-Yun, ZHONG Yuan, WANG Xin, LI Liu-Zemu, HUANG Nong-Zhang. Protocol for the Micropropagation of Tree Peony (Paeonia × lemoinei ‘High Noon’)[J]. Plant Science Journal, 2016, 34(1): 143-150. DOI: 10.11913/PSJ.2095-0837.2016.10143
Citation: WEN Shu-Sheng, CHENG Fang-Yun, ZHONG Yuan, WANG Xin, LI Liu-Zemu, HUANG Nong-Zhang. Protocol for the Micropropagation of Tree Peony (Paeonia × lemoinei ‘High Noon’)[J]. Plant Science Journal, 2016, 34(1): 143-150. DOI: 10.11913/PSJ.2095-0837.2016.10143
文书生, 成仿云, 钟原, 王新, 李刘泽木, 黄弄璋. ‘正午’牡丹微繁殖体系的建立[J]. 植物科学学报, 2016, 34(1): 143-150. CSTR: 32231.14.PSJ.2095-0837.2016.10143
引用本文: 文书生, 成仿云, 钟原, 王新, 李刘泽木, 黄弄璋. ‘正午’牡丹微繁殖体系的建立[J]. 植物科学学报, 2016, 34(1): 143-150. CSTR: 32231.14.PSJ.2095-0837.2016.10143
WEN Shu-Sheng, CHENG Fang-Yun, ZHONG Yuan, WANG Xin, LI Liu-Zemu, HUANG Nong-Zhang. Protocol for the Micropropagation of Tree Peony (Paeonia × lemoinei ‘High Noon’)[J]. Plant Science Journal, 2016, 34(1): 143-150. CSTR: 32231.14.PSJ.2095-0837.2016.10143
Citation: WEN Shu-Sheng, CHENG Fang-Yun, ZHONG Yuan, WANG Xin, LI Liu-Zemu, HUANG Nong-Zhang. Protocol for the Micropropagation of Tree Peony (Paeonia × lemoinei ‘High Noon’)[J]. Plant Science Journal, 2016, 34(1): 143-150. CSTR: 32231.14.PSJ.2095-0837.2016.10143

‘正午’牡丹微繁殖体系的建立

基金项目: 

"十二五"农村领域国家科技计划课题(2012BAD01B0704).

详细信息
    作者简介:

    文书生(1988-),女,博士研究生,研究方向为花卉生物技术(E-mail:shusheng0507@126.com).

    通讯作者:

    成仿云,E-mail:chengfy8@263.net

  • 中图分类号: Q943.1;S685.11

Protocol for the Micropropagation of Tree Peony (Paeonia × lemoinei ‘High Noon’)

Funds: 

This work was supported by a grant from the National Science and Technology Support Program of China (2012BAD01B0704).

  • 摘要: 本研究以‘正午’牡丹腋芽为外植体,建立了高效的牡丹微繁殖体系.腋芽的初始培养基为WPM+ 0.5 mg/L BA+ 0.2 mg/L GA3,培养50 d 后,一个丛生芽平均可切分为13个繁殖体用于增殖培养;增殖培养基为WPM[1668 mg/L Ca(NO3)2·4 H2O]+ 0.5 mg/L BA+ 0.2 mg/L GA3,以35 d为一个继代培养周期,增殖率为3.0,共继代培养7次;生根培养时,先将无根苗在复壮培养基[1/2 MS (296 mg/L CaCl2)+ 0.5 g/L 活性炭]上培养20 d,再转入根诱导培养基[1/2 MS (296 mg/L CaCl2)+ 1.0 mg/L腐胺+ 1.0 mg/L IBA]培养30 d,最后转入根形成培养基[1/2 MS (296 mg/L CaCl2)+ 4.0 g/L 活性炭]培养20 d,其生根率达77.2%;驯化与移栽基质为珍珠岩:蛭石:草炭土 = 1:1:1,组培苗移栽成活率高达92.1%.这表明以‘正午’牡丹腋芽建立的微繁殖体系具备规模化商业生产的价值.
    Abstract: An efficient micropropagation protocol was developed for Paeonia × lemoinei ‘High Noon’ using axillary buds as explants. During initiation, 13 propagules were obtained after 50 d of culture with WPM + 0.5 mg/L BA + 0.2 mg/L GA3. During proliferation, three shoots were obtained after 35 d of culture with WPM[1668 mg/L Ca(NO3)2·4 H2O] + 0.5 mg/L BA + 0.2 mg/L GA3, and seven subcultures were carried out. For optimal rooting, the shoots were cultured with 1/2 MS (296 mg/L CaCl2) + 0.5 g/L activated charcoal for 20 d, then 1/2 MS (296 mg/L CaCl2) + 1.0 mg/L putrescine + 1.0 mg/L IBA for 30 d for root induction, and finally 1/2 MS (296 mg/L CaCl2) + 4.0 g/L activated charcoal for 20 d for root development. The rooting percentage of the shoots was 77.2%. During acclimatization, the rooted plantlets were transferred to pots containing a mix of vermiculite/peat/perlite (1:1:1 V/V/V) substrate, and the survival rate was 92.1%. The micropropagation protocol for Paeonia × lemoinei ‘High Noon’ established in this study is valuable for commercial use.
  • [1]

    Li SS,Yuan RY,Chen LG,Wang LS,Hao XH,Wang LJ,Zheng XC,Du H. Systematic qualitative and quantitative assessment of fatty acids in the seeds of 60 tree peony(Paeonia section Moutan)cultivars by GC-MS[J]. Food Chem,2015,173(15):133-140.

    [2]

    Cheng FY. Advances in the breeding of tree peonies and a cultivar system for the cultivar group[J]. Int J Plant Breed,2007,1(2):89-104.

    [3]

    George E,Hall M,Klerk G. Micropropagation:uses and methods[M]//George E,Hall M,Klerk G,eds. Plant Propagation by Tissue Culture. Berlin:Springer Publi-shers,2008:29-64.

    [4] 李玉龙,吴德玉,潘淑龙,徐少丽,卫志明,许智宏,李晓娟. 牡丹试管苗繁殖技术的研究[J]. 科学通报,1984,8(5):500-502.

    Li YL,Wu DY,Pan SL,Xu SL,Wei ZM,Xu ZH,Li XJ. In vitro propagation of Paeonia suffruticosa[J]. Chinese Science Bulletin,1984,8(5):500-502.

    [5]

    Harris RA,Mantell S. Effects of stage Ⅱ subculture durations on the multiplication rate and rooting capacity of micropropagated shoots of tree peony(Paeonia suffruticosa Andr.)[J]. J Hortic Sci,1991,66(1):95-102.

    [6]

    Bouza L,Jacques M,Miginiac E. In vitro propagation of Paeonia suffruticosa Andr. cv.'Mme de Vatry':Develo-pmental effects of exogenous hormones during the multiplication phase[J]. Sci Hortic,1994,57(3):241-251.

    [7] 孔祥生,张妙霞. 牡丹离体快繁技术研究[J]. 北方园艺,1998,3(4):87-89.
    [8]

    Beruto M,Lanteri L,Portogallo C. Micropropagation of tree peony (Paeonia suffruticosa)[J]. Plant Cell Tiss Organ Cult,2004,79(2):249-255.

    [9] Beruto M,Curir P. In vitro culture of tree peony through axillary budding[M]/李萍. 牡丹组织培养的研究[D]. 北京:北京林业大学,2007.

    Li P. Studies on the micropropagation of tree peonies[D]. Beijing:Beijing Forestry University,2007.

    [13] 张颖星. 牡丹离体快繁及多胺对组培苗生根影响的研究[D]. 北京:北京林业大学,2008.

    Zhang YX. Study on the micropropagation of tree peony and the effect of polyamines on in vitro rooting[D]. Beijing:Beijing Forestry University,2008.

    [14] 邱金梅. 牡丹离体快繁技术的研究[D]. 北京:北京林业大学,2010.

    Qiu JM. Study on the in vitro micropropagation of tree peony[D]. Beijing:Beijing Forestry University,2010.

    [15]

    Wang HY,He SL,Tanaka M,Van PT,Da Silva JAT. Effect of IBA concentration, carbon source, substrate, and light source on root induction ability of tree peony (Paeonia suffruticosa Andr.) plantlets in vitro[J]. Eur J Hortic Sci,2012, 77(3):122-128.

    [16]

    Qin L,Cheng FY,Zhong Y. Advances in the in vitro culture and micropropagation of tree peonies during the past half century[J]. Acta Hortic,2012,977(3):39-51.

    [17]

    Kessenich G,APS Nomenclature Committee. A. P. Saunders hybrid peonies (Lutea hybrid tree peonies)[M]//Peonies:the History of the Peonies and Their Originations. Washington: American Horticultural Society,1976:146-152.

    [18]

    Bouza L,Sotta B,Bonnet M,Jacques M,Arnaud Y. Hormone content and meristematic activity of Paeonia suffruticosa Andr. cv.'Madame de Vatry' vitroplants during in vitro rooting[J]. Acta Hortic,1992, 320(29):213-216.

    [19]

    Bouza L,Jacques M,Sotta B,Miginiac E. The reactivation of tree peony (Paeonia suffruticosa Andr.) vitroplants by chilling is correlated with modifications of abscisic acid, auxin and cytokinin levels[J]. Plant Sci,1994,97(2):153-160.

    [20]

    Rogers A. Peonies[M]. 5th ed. Oregon:Timber Press,1995:91-105.

    [21]

    Murashige T. Plant propagation through tissue cultures[J]. Ann Rev Plant Physiol,1974,25(1):135-166.

    [22]

    Lloyd G,McCown B. Commercially-feasible micropropagation of mountain laurel, Kalmia latifolia, by use of shoot-tip culture[J]. Comb Proc Intl Plant Prop Soc,1980,30:421-427.

    [23]

    Machado MP,da Silva ALL,Biasi LA,Deschamps C,Bespalhok Filho JC,Zanette F. Influence of calcium content of tissue on hyperhydricity and shoot-tip necrosis of in vitro regenerated shoots of Lavandula angustifolia Mill.[J]. Braz Arch Biol Technol,2014,57(5):636-643.

    [24]

    Li P,Cheng FY. Basal medium with modified calcium source and other factors influence on shoots culture of tree peony[J]. Acta Hortic,2008,766:383-389.

    [25]

    Bouza L,Jacques M,Miginiac E. Requirements for in vitro rooting of Paeonia suffruticosa Andr. cv. 'Mme de Vatry'[J]. Sci Hortic,1994,58(3):223-233.

    [26] 高建明,代真真,杨峰,张世清,陈河龙,郑金龙,易克贤. 抗茎枯病芦笋品种离体培养的研究[J]. 植物科学学报,2013,31(2):158-163.

    Gao JM, Dai ZZ, Yang F, Zhang SQ, Chen, HL, Zheng JL, Yi KX. Regeneration system establishment of disease-resistant asparagus variety[J]. Plant Science Journal, 2013, 31(2):158-163.

    [27] 秦敏,吴平平,姚明镜. 紫苏不同外植体的培养及再生[J]. 植物科学学报,2013,31(2): 151-157.

    Qin M,Wu PP,Yao MJ. Plant Regeneration from different explants of Perilla frutescens L. Britton[J]. Plant Science Journal, 2013, 31(2):151-157.

    [28] 姚平,孙书伟. 蓝莓组织培养瓶内复壮瓶外生根快繁技术[J]. 北方园艺,2009(4):161-162.
    [29] 吴建华,王锦秀. 枸杞新品系0502组织培养快繁技术研究[J]. 宁夏农林科技,2010(3):10-11.
    [30] 刘敏,苏乔,刘纪文. ‘欧美杨107'组培苗瓶外生根[J]. 植物生理学报,2010(10):1050-1054.

    Liu M, Su Q, Liu JW. Ex vitro rooting of Populus × euramericana cv. Neva microshoots[J]. Plant Physiology Communications, 2010, 46(10) :1050-1054.

    [31]

    Kaur A,Sandhu JS. High throughput in vitro micropropagation of sugarcane (Saccharum officinarum L.) from spi-ndle leaf roll segments: Cost analysis for agri-business industry[J]. Plant Cell Tiss Organ Cult,2015,120(1):339-350.

  • 期刊类型引用(0)

    其他类型引用(1)

计量
  • 文章访问数:  1109
  • HTML全文浏览量:  4
  • PDF下载量:  1087
  • 被引次数: 1
出版历程
  • 收稿日期:  2015-08-20
  • 网络出版日期:  2022-10-31
  • 发布日期:  2016-02-27

目录

    /

    返回文章
    返回