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小叶栀子再生体系的建立研究

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小叶栀子(Gardenia jasminoides Ellis.var.radicans)是优良的园林绿化景观植物,应用前景广阔.研究以小叶栀子的无菌叶片、顶芽为外植体,通过添加不同种类和质量浓度的植物生长调节剂进行愈伤组织的诱导、分化和生根培养,以期建立小叶栀子的再生体系.结果表明:外植体启动培养阶段,抑制杂菌污染的最佳抗生素组合为50 mg/L氨苄西林钠+50 mg/L硫酸链霉素的1∶1混合溶液,污染率为25%,优于200 mg/L头孢霉素溶液和对照组;愈伤组织诱导阶段,两种外植体(无菌叶片和无菌顶芽)最早出伤时间分别为接种后10d和18 d,最佳方案皆为MS培养基+2.0 mg/L 2,4-D+0.5 mg/L 6-BA,诱导率分别达到90%和93.3%;愈伤组织分化阶段,在MS培养基中添加0.05 mg/L的NAA和1.5~1.8 mg/L 6-BA,愈伤组织分化率普遍较高,其最佳植物生长调节剂配比为0.05 mg/L NAA+1.8 mg/L6-BA,分化率达到 96.7%;生根培养阶段,1/2 MS 培养基+0.1 mg/L NAA+0.5 mg/L IBA为最佳方案,生根率达26.67%.研究成功建立了一套高效的小叶栀子再生体系,为大规模扩繁小叶栀子幼苗提供了相应的技术支持,也为其广泛的推广应用创造了有利条件.
Study on the regeneration system of Gardenia jasminoides Ellis.var.radicans
Gardenia jasminoides Ellis.var.radicans is a fine landscape greening plant which has high research value and broad application prospect.Therefore,it is an important issue to establish the regeneration system of Gardenia jasminoides Ellis.var.radicans by plant tissue culture,which could set a system for the large-scale expanding propagation and production.Sterile leaves and terminal buds were selected as explants,the induction,differentiation of callus and rooting culture were carried out by adding different kinds and concentrations of plant growth regulators to screen out the best culture scheme.During initial culture of explant,the best combination of antibiotics to inhibit the contamination of bacteria was 50 mg/L ampicillin sodium+50 mg/L streptomycin sulfate(1:1)mixed solution with 25%pollution rate,better than that of the 200 mg/L cefotaxime solution and control group.During callus tissue induction,the first appeared time of callus for two kinds of explants(sterile leaves and sterile terminal buds)was 10 d and 18 d.The best combination plant growth regulators for callus tissue induction was MS medium+2.0 mg/L 2,4-D+0.5 mg/L 6-BA,and the induction rates were 90%(sterile leaves)and 93.3%(sterile terminal buds)respectively.During callus tissue differentiation,callus tissue differentiation rate was higher under moderate concentrations of NAA and higher concentration of 6-BA,and the best combination of plant growth regulators for callus differentiation was MS medium+0.05 mg/L NAA+1.8 mg/L 6-BA,and the differentiation rate reached 96.7%.During rooting-stage the best combination of plant growth regulators for rooting culture was 1/2 MS medium+0.1 mg/L NAA+0.5 mg/L IBA with 26.67%rooting rate.This study established a set of efficient regeneration system of Gardenia jasminoides Ellis.var.radicans,which would provide technical support for the large-scale expanding propagation,production and also create favorable conditions for its extensive popularization and application.

Gardenia jasminoides Ellis.var.radicansantibioticplant growth regulatortissue cultureplant regeneration

刘海涛、刘玲、吕沙妹

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淮南师范学院生物工程学院,安徽淮南 232038

资源与环境生物技术安徽普通高校重点实验室,安徽淮南 232038

小叶栀子 抗生素 植物生长调节剂 组织培养 植株再生

国家自然科学基金青年项目安徽省高校科学研究重点项目

31800256KJ2020A0649

2024

河南科技学院学报(自然科学版)
河南科技学院

河南科技学院学报(自然科学版)

影响因子:0.557
ISSN:1673-6060
年,卷(期):2024.52(1)
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