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春兰的植株再生

Plant Regeneration of Chun.

作者信息

Yu-Qing Zhou, Meng-Jie Zhang, Deng Zhang, Jun-Jie Zhang, Jing-Jian Li, Xiao-Yang Chen

机构信息

State Key Laboratory for Conservation and Utilization of Subtropical Agro-bioresources (South China Agricultural University), Guangzhou 510642, China.

Guangdong Key Laboratory for Innovative Development and Utilization of Forest Plant Germplasm, Guangzhou 510642, China.

出版信息

Open Life Sci. 2018 Apr 6;13:34-41. doi: 10.1515/biol-2018-0005. eCollection 2018 Jan.

Abstract

Chun is a large, fast-growing deciduous tree. In this study, we successfully developed a reliable and efficient protocol for the regeneration of fertile plants via callus induction from leaf segments of young Z. insignis seedlings. The best results were obtained with a medium containing 11.00 μM 6-benzyladenine (6-BA), 1.20 μM indole-3-butytric acid (IBA), and 0.45 μM 2,4-dichlorophenoxyacetic acid (2,4-D), which yielded morphogenic callus within 2 weeks at a frequency of 62.23%. We tested the effect of IBA alone and in combination with 6-BA on the bud differentiation response of Z. insignis callus. Shoots differentiated normally when cultured on differentiation medium containing 6.00 μM 6-BA and 1.20 μM IBA. Regenerated buds elongated successfully in medium containing 1.20 μM gibberellic acid (GA3). The elongated shoots were then transferred to Murashige and Skoog basal medium supplemented with various combinations of naphthalene acetic acid (NAA) for root induction; well-developed roots were achieved on MS basal medium supplemented with 0.01 μM NAA at a rooting rate of 89.23%. Rooted plantlets were successfully acclimatised to a greenhouse at a survival rate exceeding 90.00%.

摘要

香椿是一种大型的、生长迅速的落叶乔木。在本研究中,我们成功开发了一种可靠且高效的方案,通过从幼龄香椿幼苗的叶片切段诱导愈伤组织来再生可育植株。在含有11.00 μM 6-苄基腺嘌呤(6-BA)、1.20 μM吲哚-3-丁酸(IBA)和0.45 μM 2,4-二氯苯氧乙酸(2,4-D)的培养基上获得了最佳结果,该培养基在2周内以62.23%的频率产生了形态发生愈伤组织。我们测试了单独使用IBA以及IBA与6-BA组合对香椿愈伤组织芽分化反应的影响。当在含有6.00 μM 6-BA和1.20 μM IBA的分化培养基上培养时,芽正常分化。再生芽在含有1.20 μM赤霉素(GA3)的培养基中成功伸长。然后将伸长的芽转移到添加了不同萘乙酸(NAA)组合的Murashige和Skoog基本培养基上进行生根诱导;在添加了0.01 μM NAA的MS基本培养基上实现了发育良好的根系,生根率为89.23%。生根的植株成功适应了温室环境,成活率超过90.00%。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8328/7874715/28820e5ba68a/biol-13-034-g001.jpg

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