Abstract
Broussonetia papyrifera is an important ecological and economic tree species. The sexual reproduction of B. papyrifera not only has a low germination rate, but also requires high environmental conditions. Therefore, asexual propagation using tissue culture can effectively improve the propagation efficiency of B. papyrifera. In this study, the leaves and budded shoots of B. papyrifera were used as explants, and different concentrations of plant growth regulators were added to Murashige and Skoog medium (MS) to establish a suitable system for explant callus formation, adventitious buds differentiation and rooting. The results showed that MS + 0.50 mg/L naphthaleneacetic acid (NAA) + 0.25 mg/L 6-benzyladenine(6-BA) and MS + 0.25 mg/L NAA + 0.50 mg/L 6-BA were the best mediums for rapid callus induction from leaf explants and shoot explants, respectively. The best medium combination for shoot differentiation and proliferation was MS + 0.05 mg/L NAA + 0.50 mg/L 6-BA, and the high propagation coefficient could also promote adventitious bud growth. The best rooting medium in the establishment of B. papyrifera tissue culture was MS + 0.25 mg/L NAA. Under this condition, the average rooting numbers of leaf explants and shoot explants were 1.71 and 13.86, respectively. In addition, the best transplanting substrate was a mixture of soil:perlite:vermiculite (20:1:1), and the survival rate was 91.1%. This study established a propagation system in vitro culture of B. papyrifera, and provided a reference for tissue culture of other woody plants.
Funder
Key Projects of National Forestry and Grassland Bureau
Natural Science Foundation of Hunan Province
Cited by
9 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献