Callus induction and in vitro mass culture of adventitious roots from leaf segment explants of Dendropanax morbifera Lev.

2nd International Conference on Natural Resources and Life Sciences

生态环境科学

Sukweenadhi, J.^1 ; Choi, J.Y.^2 ; Kim, Y.J.^2 ; Kaliraj, L.^3 ; Abid, S.^3 ; Ahn, J.C.^3 ; Yang, D.C.^2^3

Department of Plant Biotechnology, Faculty of Biotechnology, University of Surabaya, Jl. Raya Kali Rungkut, Surabaya

60293, Indonesia^1

Department of Oriental Medicinal Biotechnology, College of Life Science, Kyung Hee University, Yongin-si, Gyeonggi-do

130-701, Korea, Republic of^2

Graduate School of Biotechnology and Ginseng Bank, College of Life Science, Kyung Hee University, Yongin-si, Gyeonggi-do

130-701, Korea, Republic of^3

关键词: Adventitious root;    Adventitious root formation;    Bioreactor system;    Callus induction;    gingseng tree;    In-vitro;    Mass production;    Tissue culture systems;   

Others  :  https://iopscience.iop.org/article/10.1088/1755-1315/293/1/012024/pdf
DOI  :  10.1088/1755-1315/293/1/012024

学科分类：环境科学（综合）

来源: IOP

【 摘 要 】

Dendropanax morbifera Lev. is a unique species and natively found in Korea and distributed in the South regions, such as Jeju, Goheung, and Wando. In this study, tissue culture system for native D. morbifera was developed. The callus from native D. morbifera leaves was cultured on Woody Plant Media (WPM) supplemented with 30 g L-1 of sucrose, with addition of 2.4-D and bA [(0.5, 1.0, 2.0) mg L-1], separately and mixed. After 5 wk of culture, the highest induction of callus was obtained from 0.5 mg L-1 of 2.4-D mixed with 2.0 mg L1 of BA. Adventitious root formation on different media (MS, WPM, B5) with various auxins (IBA, IAA, and NAA) and different concentration [(0, 1, 3, 5) mg L-1] were tested. After 8 wk of culture, WPM showed better induction of adventitious root. The highest induction of adventitious root was obtained on 3.0 mg L-1 IBA. Root growth was best in WPM liquid medium with 3.0 mg L-1 of IBA and 30 g L-1 of sucrose. The same formulation with modified 1/2 WPM was successfully established in vitro adventitious roots culture in 18-L bioreactor system. This study also proposed as the mass production technique of adventitious roots from native D. morbifera.