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发根农杆菌介导龙葵遗传转化体系优化OA

Optimization of Agrobacterium rhizogenes-Mediated Genetic Transformation System of Solanum nigrum

中文摘要英文摘要

该研究旨在通过建立发根农杆菌(Agrobacterium rhizogenes)介导的龙葵(Solanum nigrum)遗传转化体系,提高遗传转化效率及总黄酮含量.研究以龙葵叶片为外植体,探究菌株类型、菌液浓度等因素对龙葵毛状根诱导率的影响.基于该体系,构建重组质粒PBI121-6flag-SnCHI,通过农杆菌介导,诱导转SnCHI基因的毛状根,考察龙葵毛状根转SnCHI基因后的总黄酮含量变化.研究结果表明:菌株Ar.1193在OD600 为1.0、侵染25 min、共培养24 h条件下,龙葵毛状根诱导率可达88.49%.对转SnCHI基因毛状根进行qRT-PCR检测,发现其基因表达水平是空白组的28.81倍;测定转SnCHI基因毛状根的总黄酮含量,发现转SnCHI基因毛状根的总黄酮含量最高达空白组的4.14倍.成功建立龙葵遗传转化体系,对SnCHI基因的功能进行研究,为同属植物的组织培养和遗传转化研究提供参考.

The aim of this study was to establish an Agrobacterium rhizogenes-mediated genetic transformation system for Solanum nigrum(black nightshade)with the goal of enhancing transformation efficiency and increasing its total flavonoid content.Based on this system,the recombinant plasmid PBI121-6flag-SnCHI was constructed,the hairy roots of SnCHI gene transformation were induced by Agrobacterium-mediated pathway,and the content of total flavonoids in the hairy roots of S.nigrum after SnCHI gene transformation was investigated.The results showed that the induction rate of hairy roots of S.nigrum could reach 88.49%under the conditions of OD600 value of 1.0,infection for 25 min and co-culture for 24 h.The qRT-PCR detection of transgenic SnCHI hairy roots showed that the gene expression level was 28.81 times that of the blank group.The total flavonoid content of SnCHI transgenic hairy roots was determined,and it was found that the total flavonoid content of SnCHI transgenic hairy roots was up to 4.14 times that of the blank group.The genetic transformation system of S.nigrum was successfully established,and the function of SnCHI gene was studied,which provided a reference for tissue culture and genetic transformation of the same genus.

张静静;骆海霞;洪艳苹;赵世成

哈尔滨商业大学药学院,哈尔滨 150076哈尔滨商业大学药学院,哈尔滨 150076哈尔滨商业大学药学院,哈尔滨 150076哈尔滨商业大学药学院,哈尔滨 150076

农业科技

龙葵毛状根发根农杆菌遗传转化体系黄酮类化合物

Solanum nigrumhairy rootAgrobacterium rhizogenesgenetic transformation systemflavonoids

《植物研究》 2026 (1)

111-119,9

林木遗传育种国家重点实验室开放基金项目(K2017204).

10.7525/j.issn.1673-5102.2026.01.010

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