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Optim iza tion of Tissue Culture Conditions and Establishmentof Regenera tion System for Popu lus ×eu ram e ricana cl.‘J2’

  • Received Date: 2006-09-07
  • The key factors affecting the growth of Populus ×euram ericana cl. ‘J2’in vitro and the op timal tissueculture conditions for it were ascertained. The high frequency regeneration system for P. ×euram ericana cl. ‘J2’was also established in this study. The op timum basic culture medium wasMS; the op timal subculture medium androot inducement culture medium for shootwere 1 /2MS + NAA 0. 08 mg·L-1 + IBA 0. 08·mg L-1 ; active carbon disadvantaged the growth of P. ×euram ericana cl. ‘J2’; photoperiod had little effect on P. ×eu ram ericana cl.‘J2’, while light intensity and the pH value of subculture medium had great effect on it, the op timal light intensitywas 2 500 lx and the op timal pH value was 6. 5; the op timal shoot inducement culture medium for leaf2exp lantwasMS + BA1. 0 mg·L-1 + NAA0. 1 mg·L-1 and for leafstalk-exp lantwasMS + BA 1. 0 mg·L-1 + NAA 0. 2 mg·L-1.
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  • [1]

    Coleman G D, Erst S G. In vitro shoot regeneration of Populus deltiodes: effect of cytokinin and genotype [J]. Plant Cell Rep, 1989,8: 459~462
    [2]

    ConfalonieriM, Balestrazzi A, Cella R. Genetic transformation ofPopulus deltoides and P. ×euram ericana clones using Agrobacterium[J]. Plant Cell Tissue and Organ Culture, 1997, 48 (1) : 53~61
    [3]

    Chaturvedi H C, Sharma A K, Agha B Q, et al. Production of clonedtrees of Populus deltoides through in vitro regeneration of shoots fromleaf, stem and root exp lants and their field cultivation[J]. Indian JBiotech, 2004, 3: 203~208
    [4] 陈颖,韩一凡,李铃,等. 苏云金杆菌杀虫晶体蛋白基因转化美洲黑杨的研究[J]. 林业科学, 1995, 31 (2) : 97~103

    [5] 李红,王关林,李洪艳,等. 美洲黑杨的组织培养和快繁[J]. 植物生理学通讯, 2004, 40 (6) : 708

    [6] 康薇,郑进,刘凯于,等. 美洲黑杨(中嘉8号)离体叶片再生研究[J]. 武汉植物学研究, 2006, 24 (1) : 83~86

    [7] 易丽娟,曾幼玲,吕艳,等. 中林美荷杨叶柄的组织培养及植株再生[J]. 植物生理学通讯, 2004, 40 (5) : 576

    [8] 孙宇飞,高秀华,赵彦修,等. 欧美107杨组织培养再生系统的建立[J]. 山东师范大学学报(自然科学版) , 2004, 19 ( 2 ) : 85~87

    [9]

    MorisawaM, Steinhardt R A. Affecting factors of the differentiate ofslime fangus[J]. Exp Cell Res, 1982, 140: 341~351
    [10] 曹新祥,韩小云. 植物组织培养中的pH值[J]. 杭州师范学院学报(自然科学版) , 2003, 2 (1) : 60~63

    [11]

    Johansson L B, Calleberg E, Gedin A. Correlations between activated charcoal, Fe-EDTA and other organic media ingredients in cultured anthers ofAnem one canadensis[J]. Physiol Plant, 1990, 80:243~249
    [12] 胡蕙露,杨景华,杨荻荣,等. 银杏茎段试管培养条件筛选研究[J]. 林业科学, 2002, 38 (3) : 52~56

    [13] 詹祥灿. 植物体细胞胚状体与器官发生的激素调节[J]. 植物生理学报, 1983, 9 (3) : 317~323

    [14]

    Skoog F, Miller C O. Chemical regulation of growth and organ formation in p lant tissue cultured in vitro [J]. Biological Action ofGrowth Substances, 1957 (11) : 118~131
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Optim iza tion of Tissue Culture Conditions and Establishmentof Regenera tion System for Popu lus ×eu ram e ricana cl.‘J2’

  • 1. Forestry College, Shenyang Agriculture University, Shenyang 110161,Liaoning, China
  • 2. Research Institute of Forestry, CAF

Abstract: The key factors affecting the growth of Populus ×euram ericana cl. ‘J2’in vitro and the op timal tissueculture conditions for it were ascertained. The high frequency regeneration system for P. ×euram ericana cl. ‘J2’was also established in this study. The op timum basic culture medium wasMS; the op timal subculture medium androot inducement culture medium for shootwere 1 /2MS + NAA 0. 08 mg·L-1 + IBA 0. 08·mg L-1 ; active carbon disadvantaged the growth of P. ×euram ericana cl. ‘J2’; photoperiod had little effect on P. ×eu ram ericana cl.‘J2’, while light intensity and the pH value of subculture medium had great effect on it, the op timal light intensitywas 2 500 lx and the op timal pH value was 6. 5; the op timal shoot inducement culture medium for leaf2exp lantwasMS + BA1. 0 mg·L-1 + NAA0. 1 mg·L-1 and for leafstalk-exp lantwasMS + BA 1. 0 mg·L-1 + NAA 0. 2 mg·L-1.

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