匍匐蒿组织培养与快速繁殖体系的建立

Q3 Pharmacology, Toxicology and Pharmaceutics
Chu Wang, Ya Xu, Yang Xu, Ye Wang, Na-Na Chang, Lu-Qi Huang, Hui Li
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引用次数: 0

摘要

匍匐茎蒿作为一种优质艾灸材料,具有很高的经济价值和研究前景。但由于种子发芽困难,其野生种质资源在中国分布较少。本研究以当年生长的嫩茎段为材料,研究外植体灭菌、不同植物生长调节剂组合及浓度对匍匐茎不定芽增殖和生根的影响,旨在构建匍匐茎离体快速繁殖技术体系。结果表明:自来水冲洗30 min, 75%乙醇浸泡30 s,然后用0.1%的HgCl_2处理5 min,用8%的NaClO处理10 min,用0.6%的植物苯胺处理10 min,对茎段进行灭菌,污染率最低,为25.83%。茎段未发生褐变,成功地对匍匐茎段进行了表面灭菌。在诱导培养阶段,当激动素(KT)浓度为0.05 mg·L~(-1), 6-苄基氨基丁二醇(6-BA)浓度为0.05 mg·L~(-1)时,不定根增殖系数为2.02,有效促进了匍匐茎的增殖和生长。在生根培养阶段,0.1 mg·L~(-1) 1-萘乙酸(NAA)能在短时间内有效诱导匍匐茎试管苗生根,生根率可达100%。添加少量活性炭也能促进生根,增强幼苗生长。移栽到90%营养土+ 10%珍珠岩的基质中,匍匐茎幼苗成活率为100%。本研究建立了一套高效的匍匐茎离体快速繁殖体系,克服了匍匐茎种子萌发困难,缩短了育种周期,降低了生产和种植成本。为匍匐茎的引种驯化、苗种繁殖、种质保护和产业化发展提供技术支持。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Establishment of tissue culture and rapid propagation system of Artemisia stolonifera].

As a high-quality moxibustion material, Artemisia stolonifera has high economic value and research prospects. However, due to difficulties in seed germination, its wild germplasm resources are sparsely distributed in China. This study used young stem segments grown in the current year to investigate the effects of explant sterilization, different combinations and concentrations of plant growth regulators on the proliferation and rooting of adventitious shoots, with the aim of constructing an in vitro rapid propagation technology system for A. stolonifera. The results showed that the lowest contamination rate of 25.83% was achieved when sterilizing the stem segments by rinsing with running water for 30 min, soaking in 75% ethanol for 30 s, followed by a 5 min treatment with 0.1% HgCl_2, 10 min with 8% NaClO, and 10 min with 0.6% phytosaniline. There was no browning of the stem segments, and surface sterilization of the A. stolonifera stem segments was successfully achieved. In the induction culture phase, when the concentration of kinetin(KT) was 0.05 mg·L~(-1) and 6-benzylaminopurine(6-BA) was 0.05 mg·L~(-1), the adventitious shoot proliferation coefficient was 2.02, effectively promoting the proliferation and growth of A. stolonifera. In the rooting culture phase, 0.1 mg·L~(-1) 1-naphthaleneacetic acid(NAA) effectively induced A. stolonifera test-tube seedlings to root within a short period, achieving a rooting rate of 100%. The addition of a small amount of activated charcoal also promoted rooting and strengthened seedling growth. The survival rate of A. stolonifera seedlings transplanted into a substrate consisting of 90% nutrient soil and 10% perlite was 100%. This study established an efficient in vitro rapid propagation system for A. stolonifera, overcoming difficulties with seed germination, shortening the breeding cycle, and reducing production and planting costs. It provides technical support for the introduction, domestication, seedling propagation, germplasm conservation, and industrial development of A. stolonifera.

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来源期刊
Zhongguo Zhongyao Zazhi
Zhongguo Zhongyao Zazhi Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (all)
CiteScore
1.50
自引率
0.00%
发文量
581
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