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Citation:

In vitro Culture and Plant Regenera tion of Pa rthenoc issus qu inquefolia

  • Received Date: 2007-06-10
  • Adventitious shootswere successfully regenerated from cotyledon petioles, hypocotyl exp lants and leaf ex2p lants of in vitro cultures of Parthenocissus quinquefolia. They were cultured on half strengthMurashine and Skoog(MS) , B5 and Heller basalmedium supp lemented with various p lant growth regulators. Auxins, α2naphthaleneace2tic acid (NAA) and in combination with three cytokinins, benzylaminopurine (BA) , kinetin (KT) and thidiazuron( TDZ) were tried. The study showed that the highest regeneration rate were obtained by cotyledon petioles segmentsnear to the hypocotyl under dark time of 30 days cultured on half strengthMS basalmedium supp lemented with 0. 3mg·L -1BA (64. 67%) , hypocotyl exp lants cultured on half strengthMS basalmedium supp lemented with 2. 0 mg·L - 1 KT and 0. 05 mg·L -1NAA and Heller basalmedium supp lemented with 0. 5 mg·L -1BA and 0. 1 mg·L -1NAA ( both about 24% ). Leaf exp lants cultured on B5 basal medium supp lemented with 0. 5 mg·L -1 TDZ and0105 mg·L -1 NAA, the differentiation rate of adventitious budswas as high as 17. 7%. Using half strengthMS asthe multip lication medium for buds supp lemented with 0. 5 mg·L -1 62BA and 0. 1 mg·L -1 NAA, the multip lica2tion coefficient was 3 - 5. Half strengthMS and 0. 5 mg·L -1 IBA and 500 mg·L -1 activated carbon was suitablefor the rooting of regenerated p lantlets, and nearly 100% of these p lantlets survived after transp lanted.
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  • [1] 冯大领,李 云,孙振元. 爬山虎体细胞胚的发生及组织学研究[J]. 北京林业大学学报, 2004, 26 (4) : 97 - 99

    [2] 李正红,孙振元,刘秀贤,等. 地锦体细胞胚胎发生研究[J]. 林业科学研究, 2005, 18 (1) : 36 - 40

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    Martineli L , Gribaudo I. Somatic Embryogenesis in Grapevine [M].Nertherland Kluwer ,Academic PublishersMolecularBiology and Bi2otechnology of Grapevine, 2001: 327 - 351
    [4] 王关林, 方宏筠, 那 杰. 高活性细胞激动素TDZ在植物组织培养中的应用[J]. 植物学通报, 1997, 14 (3) : 47 - 53

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    Nagori R , Purohit S D . In vitro p lantlet regeneration in Annonasquam osa through direct shoot bud differentiation on hypocotyl seg2ments[J]. Scientia Horticulturae, 2004, 99: 89 - 98
    [6] 尚爱芹,蔡 汉,闫晓洁,等. 北海道黄杨下胚轴的离体培养及植株再生[J]. 中国农业科学, 2005, 38 (12) : 2502 - 2507

    [7] 张 松,温孚江,魏毓棠. 外植体处理及接种方式对大白菜植株再生的影响[J]. 山东农业大学学报(自然科学版) , 2001 , 32(1) : 78 - 80

    [8] 田志宏,王 涛,严 寒,等. 不同外植体对愈伤组织诱导及分化的影响[J]. 草业科学, 2004, 21 (5) : 71 - 76

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    沈阳化工大学材料科学与工程学院 沈阳 110142

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In vitro Culture and Plant Regenera tion of Pa rthenoc issus qu inquefolia

  • 1. Research Institute of Ornamental Horticulture and Landscape Architecture, China Agricultural University, Beijing 100094, China
  • 2. Research Institute of Forestry, CAF, Beijing 100091, China

Abstract: Adventitious shootswere successfully regenerated from cotyledon petioles, hypocotyl exp lants and leaf ex2p lants of in vitro cultures of Parthenocissus quinquefolia. They were cultured on half strengthMurashine and Skoog(MS) , B5 and Heller basalmedium supp lemented with various p lant growth regulators. Auxins, α2naphthaleneace2tic acid (NAA) and in combination with three cytokinins, benzylaminopurine (BA) , kinetin (KT) and thidiazuron( TDZ) were tried. The study showed that the highest regeneration rate were obtained by cotyledon petioles segmentsnear to the hypocotyl under dark time of 30 days cultured on half strengthMS basalmedium supp lemented with 0. 3mg·L -1BA (64. 67%) , hypocotyl exp lants cultured on half strengthMS basalmedium supp lemented with 2. 0 mg·L - 1 KT and 0. 05 mg·L -1NAA and Heller basalmedium supp lemented with 0. 5 mg·L -1BA and 0. 1 mg·L -1NAA ( both about 24% ). Leaf exp lants cultured on B5 basal medium supp lemented with 0. 5 mg·L -1 TDZ and0105 mg·L -1 NAA, the differentiation rate of adventitious budswas as high as 17. 7%. Using half strengthMS asthe multip lication medium for buds supp lemented with 0. 5 mg·L -1 62BA and 0. 1 mg·L -1 NAA, the multip lica2tion coefficient was 3 - 5. Half strengthMS and 0. 5 mg·L -1 IBA and 500 mg·L -1 activated carbon was suitablefor the rooting of regenerated p lantlets, and nearly 100% of these p lantlets survived after transp lanted.

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