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논문 기본 정보

자료유형
학술저널
저자정보
Yang Linlin (Henan University of Chinese Medicine) Chao Liqin (Henan University of Chinese Medicine) Su Xiuhong (Henan University of Chinese Medicine) Wang Chunyan (Henan University of Chinese Medicine) Dong Chengming (Henan University of Chinese Medicine) Chen Suiqing (Henan University of Chinese Medicine)
저널정보
한국식물생명공학회 Plant Biotechnology Reports Plant Biotechnology Reports 제15권 제4호
발행연도
2021.8
수록면
435 - 446 (12page)
DOI
10.1007/s11816-021-00690-5

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Lilium davidii var. unicolour Salisb is an important edible and medicinal plant. In?vitro plantlet regeneration in L. davidii var. unicolour Salisb and identification of genetic stability are the premises of large-scale cultivation, and also a way to meet the increasing global demand. The purpose of this study is to establish an efficient, rapid plant propagation process for L. davidii var. unicolour Salisb, and to define the genetic stability of its regenerants in?vitro under optimised conditions. The effects of different concentrations of 6-benzyladenine (6-BA) and thidiazuron (TDZ) on shoot multiplication and growth of L. davidii var. unicolour Salisb were investigated individually, or in combination with α-naphthalene acetic acid (NAA), using Murashige and Skoog (MS) solid or liquid medium. Inter-sample sequence repeat markers were used to assess genetic fidelity among plantlets. The results were that we achieved efficient and reliable regeneration, using scales as explants for shoot induction. The highest mean number (16.8) of shoots was differentiated de novo from the lower portion of the outer scales. After 4?weeks of incubation, superior multiplication rates (9.8%), mean shoot number (3.38), and length (5.46?cm) were achieved using MS liquid medium supplemented with TDZ. Auxins, such as indole butyric acid (IBA) and NAA, were employed for in?vitro root induction, and the maximum rooting rate (100%) was observed when samples were cultured on half-strength MS medium supplemented with NAA. In?vitro rooted plantlets of L. davidii var. unicolour Salisb were accli- matised in a greenhouse and plants grew well with a 90% survival rate. Inter-sample sequence repeat markers were used to assess genetic fidelity among plantlets, the best ISSR primer UBC 808 had the highest number of reproducible bands and produced 15 distinct bands and all micropropagated plants and the mother plant could be grouped in a single cluster with a 94% similarity level, indicating a low level of genetic polymorphism in micropropagated plants. The developed protocol described herein is simple and reliable for large-scale production of L. davidii var. unicolour Salisb, which provides a good technical support for large-scale cultivation of L. davidii var. unicolour Salisb.

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