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Somatic Embryogenesis and Plant Regeneration from Stem Explants of Pomegranate

文献类型： 外文期刊

作者： Wang, Jingting 1 ; Xia, Xinhui 2 ; Qin, Gaihua 3 ; Tang, Jingwen 1 ; Wang, Jun 1 ; Zhu, Wenhao 1 ; Qian, Ming 1 ; Li, Jiyu 3 ; Cui, Guangrong 1 ; Yang, Yuchen 2 ; Qian, Jingjing 1 ;

作者机构： 1.Anhui Sci & Technol Univ, Coll Agr, Fengyang 233100, Peoples R China

2.Sun Yat Sen Univ, Sch Ecol, State Key Lab Biocontrol, Shenzhen 518107, Peoples R China

3.Anhui Acad Agr Sci, Inst Hort, Key Lab Hort Crop Germplasm Innovat & Utilizat Coc, Hefei 230031, Peoples R China

4.Anhui Acad Agr Sci, Inst Hort Res, Key Lab Hort Crop Genet Improvement & Ecophysiol A, Hefei 230001, Peoples R China

关键词： in vitro culture; fruit tree; callus induction; plant growth regulators; optimal culture condition

期刊名称：HORTICULTURAE （ 影响因子：3.1； 五年影响因子：3.4 ）

ISSN：

年卷期： 2023 年 9 卷 9 期

页码：

收录情况： SCI

摘要： Plant regeneration through somatic embryogenesis provides a solution for maintaining and genetically improving crop or fruit varieties with desirable agronomic traits. For the fruit tree pomegranate (Punica granatum L.), despite some successful applications, the existing somatic embryogenesis protocols are limited by low availability of explants and susceptibility to browning. To address these problems, in this study, we developed an effective system for induction of high-vigor pomegranate somatic embryos derived from stem explants. The usage of stem explants breaks through the difficulty in obtaining material, thus making our system suitable for widespread commercial production. To enhance the performance of our system, we identified the optimal explants, subculture cycles and combination of basal media and plant growth regulators for each step. The results showed that inoculating stem explants onto a Murashige and Skoog (MS) medium supplemented with 1.0 mg/L 6-benzylaminopurine (6-BA) and 1.0 mg/L 1-naphthaleneacetic acid (NAA) achieved the best induction rate and growth status of pomegranate calli (induction rate = similar to 72%), and MS medium containing 0.5 mg/L 6-BA and 1.0 mg/L NAA was the optimal condition for the induction of embryogenic calli and somatic embryos (induction rate = similar to 74% and 79%, respectively). The optimal subculture period for embryogenic calli was found to be 30-35 days. Strong roots were then induced in the developed somatic embryo seedlings, which survived and grew well after transplantation to the natural environment, indicating the good vitality of the induced pomegranate somatic embryos. Together, our system provides a solution to mass somatic embryo induction and plant regeneration of pomegranate and lays a foundation for future genetic transformation and bioengineering improvement of pomegranate with favorable agronomic traits.

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