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Preliminary Study on Shoots Regeneration from Tender Stems of\n Malus komarovii (Sarg.) Rehd. and Germplasm Reservation in vitro

  • The tender stems of Malus komarovii were used as explant and the suitable medium compositions were screened through uniform design experiments. The results showed that tissue culture of M. komarovii required different kinds of culture medium in different phases. SH+TDZ 2.45 mg·L-1+NAA 0.06 mg·L-1 for shoots regeneration immediately at base of tender stem, the rate of induction was 98.8%; 1/4 SH+KT 0.35 mg·L-1+NAA 0.05 mg·L-1 for rooting, the rate of rooting was more than 97%; 1/8 SH+ABA 2.05 mg·L-1+KT 0.50 mg·L-1 for germplasm preservation in vitro, the rate of dormancy was 95.5%. These plant materials could be maintained for 39 months by the methods of promoting dormancy and low nutrients at normal temperature.
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  • [1] 汪 松,解 焱. 中国物种红色名录(第一卷)[M]. 北京:高等教育出版社,2004:304-464

    [2] 顾地周,何晓燕,朱俊义,等. 细叶杜香的组织培养和快速繁殖[J]. 植物生理学通讯, 2007,43 (5):898

    [3] 曹孜义,刘国民. 实用植物组织培养技术教程[M].兰州:甘肃科学技术出版社,2002

    [4] 顾地周,朱俊义,姜云天,等. 东北刺人参组培快繁培养基的筛选[J]. 林业科学研究,2008,21(6):867-870

    [5] 顾地周,高捍东,顾美影,等. 笃斯越桔离体培养及植株再生体系的建立[J]. 林业科学研究,2009,22(2):226-229

    [6] 顾地周,丛小力,姜云天,等. 色木槭的组织培养与快速繁殖[J]. 植物生理学通讯,2008,44(2):432

    [7] 顾地周,丛小力,宋利丽,等. 木通马兜铃的组织培养和快速繁殖[J]. 植物生理学通讯,2008,44(1):136

    [8] 顾地周,高捍东,姜云天. 刺楸组培快繁及试管苗保存培养基的筛选[J]. 浙江大学学报:农业与生命科学版,2009,35(3):245-251

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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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Preliminary Study on Shoots Regeneration from Tender Stems of\n Malus komarovii (Sarg.) Rehd. and Germplasm Reservation in vitro

Abstract: The tender stems of Malus komarovii were used as explant and the suitable medium compositions were screened through uniform design experiments. The results showed that tissue culture of M. komarovii required different kinds of culture medium in different phases. SH+TDZ 2.45 mg·L-1+NAA 0.06 mg·L-1 for shoots regeneration immediately at base of tender stem, the rate of induction was 98.8%; 1/4 SH+KT 0.35 mg·L-1+NAA 0.05 mg·L-1 for rooting, the rate of rooting was more than 97%; 1/8 SH+ABA 2.05 mg·L-1+KT 0.50 mg·L-1 for germplasm preservation in vitro, the rate of dormancy was 95.5%. These plant materials could be maintained for 39 months by the methods of promoting dormancy and low nutrients at normal temperature.

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