Identification and micropropagation of Homalomena pendula, an endangered medicinal plant

IF 2.3 3区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Plant Cell, Tissue and Organ Culture Pub Date : 2024-08-12 DOI:10.1007/s11240-024-02835-0
Le Nguyen Thoi Trung, Nguyen Hoang An, Phan Thi Thao Nguyen, Ho Nhat Quang, Hoang Tan Quang, Ton Nu Minh Thi, Hoang Xuan Thao, Tran Nam Thang, Truong Thi Bich Phuong
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Abstract

The large-leaved Homalomena (LLH, Homalomena pendula) represents an endangered medicinal plant species within Vietnam, primarily attributed to its recognized tonic properties. Despite its imminent threat of extinction within Vietnamese ecosystems, the development of a robust protocol for molecular species identification and large-scale propagation of LLH remains absent. Consequently, we present the first conservation endeavor for LLH based on plant micropropagation techniques, with plant materials validated through anatomical observations and DNA barcoding (rbcL). Our investigation yielded five rbcL sequences specific to LLH, serving as the current best barcode for LLH identification and thereby facilitating forthcoming taxonomic endeavors. Optimization of in vitro culture conditions revealed that the Murashige and Skoog (MS) medium supplemented with 2 mg/L 6-benzylaminopurine, 0.5 mg/L α-naphthaleneacetic acid, and 60 g/L mashed potato, alongside the incorporation of 0.5 mg/L indole-3-butyric acid to the basal MS medium, yielded optimal outcomes for shoot proliferation and root development, respectively. After successful micropropagation, acclimatization of rooted plantlets to a substrate comprising soil, coconut coir, and rice husk (in a 1:1:1 ratio) culminated in a 100% survival rate among the plants.

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濒危药用植物 Homalomena pendula 的鉴定和微繁殖
大叶何首乌(LLH,Homalomena pendula)是越南的一种濒危药用植物物种,主要归因于其公认的滋补特性。尽管 LLH 在越南生态系统中濒临灭绝,但目前仍未制定出一套强有力的方案来进行 LLH 的分子物种鉴定和大规模繁殖。因此,我们首次提出了基于植物微繁殖技术的 LLH 保护方法,并通过解剖观察和 DNA 条形码(rbcL)对植物材料进行了验证。我们的调查获得了五条 LLH 的特异性 rbcL 序列,这是目前识别 LLH 的最佳条形码,从而为今后的分类工作提供了便利。体外培养条件的优化表明,在 Murashige 和 Skoog(MS)培养基中添加 2 mg/L 6-苄基氨基嘌呤、0.5 mg/L α-萘乙酸和 60 g/L 马铃薯泥,并在基础 MS 培养基中添加 0.5 mg/L 吲哚-3-丁酸,可分别获得芽增殖和根发育的最佳结果。微繁殖成功后,将生根的小植株移入由土壤、椰糠和稻壳(比例为 1:1:1)组成的基质中,植株的存活率达到 100%。
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来源期刊
Plant Cell, Tissue and Organ Culture
Plant Cell, Tissue and Organ Culture 生物-生物工程与应用微生物
CiteScore
5.40
自引率
13.30%
发文量
203
审稿时长
3.3 months
期刊介绍: This journal highlights the myriad breakthrough technologies and discoveries in plant biology and biotechnology. Plant Cell, Tissue and Organ Culture (PCTOC: Journal of Plant Biotechnology) details high-throughput analysis of gene function and expression, gene silencing and overexpression analyses, RNAi, siRNA, and miRNA studies, and much more. It examines the transcriptional and/or translational events involved in gene regulation as well as those molecular controls involved in morphogenesis of plant cells and tissues. The journal also covers practical and applied plant biotechnology, including regeneration, organogenesis and somatic embryogenesis, gene transfer, gene flow, secondary metabolites, metabolic engineering, and impact of transgene(s) dissemination into managed and unmanaged plant systems.
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