文献类型： 外文期刊

作者： Li, Danqing ¹ ; Ji, Chenxi ² ; Shao, Lingmei ³ ; Xu, Tong ² ; Chen, Xiaoxuan ² ; Wang, Xiaobin ⁴ ; Zhang, Runlong ² ; Cui, Yunqing ¹ ; Zhang, Jiaping ² ; Xia, Yiping ² ;

作者机构： 1.Zhejiang Sci Tech Univ, Dept Landscape Architecture, Hangzhou 310018, Peoples R China

2.Zhejiang Univ, Coll Agr & Biotechnol, Genom & Genet Engn Lab Ornamental Plants, Hangzhou 310058, Peoples R China

3.Shanghai Acad Agr Sci, Forestry & Pomol Res Inst, Shanghai Key Lab Protected Hort Technol, Shanghai 201403, Peoples R China

4.Jiangxi Agr Univ, Coll Agron, Jiangxi Prov Key Lab Postharvest Storage & Preserv, Nanchang 330045, Peoples R China

关键词： Iris spp.; Herbaceous flower; Embryogenic callus; In vitro regeneration; Flow cytometry techniques

期刊名称：JOURNAL OF PLANT GROWTH REGULATION （ 影响因子：4.4； 五年影响因子：4.9 ）

ISSN： 0721-7595

年卷期： 2025 年 44 卷 8 期

页码：

收录情况： SCI

摘要： Yellow flag (Iris pseudacorus L.), belonging to the genus of Iris, is a herbaceous flower with significant ornamental, ecological, and economic values. Nevertheless, its limitations include single flower color, short ornamental duration, and long breeding cycles, which impede its widespread landscape use and the development of new cultivars. In this study, an efficient and environmentally friendly strategy for embryogenic callus induction and plant regeneration of yellow flag was constructed. The results demonstrate the importance of utilizing tender embryos as explants to establish this environmentally friendly in vitro regeneration system. Notably, we achieved a contamination rate of 0% and a survival rate of 100% by employing 30 s alcohol disinfection. The optimal medium for callus induction was Murashige and Skoog (MS) medium supplemented with 2.0 mg/L 2,4-dichlorophenoxyacetic acid (2,4-D), and 0.20 mg/L kinetin (KT). Different concentrations of cytokinins, including 6-benzylaminopurine (6-BA), KT, and thidiazuron (TDZ), significantly influenced the regeneration rate of embryogenic callus regeneration, with 0.20 mg/L KT achieved the best embryogenic callus regeneration effect. Finally, the genetic stability of regenerated plants was verified by flow cytometry techniques. Consequently, we propose a protocol that optimizes embryogenic callus induction, leading to high rates of regeneration and minimal contamination. This protocol not only lays a foundation for the genetic improvement of irises through transgenic or gene-editing methods but also facilitates plant resource conservation and commercial rapid propagation.