2021ForestsOpen access

Effects of Plant Growth Regulators on the Rapid Propagation System of Broussonetia papyrifera L. Vent Explants

Jiakang Zhou, Yang Liu, Liang Wu, Yunlin Zhao, Wan Zhang, Guiyan Yang, Zhenggang Xu

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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.

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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.

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Available 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.

Key concepts: Explant culture, Broussonetia, Shoot, Botany, Biology, Callus, Perlite, Tissue culture

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