- 1Jiangxi Key Laboratory for Sustainable Utilization of Chinese Materia Medica Resources, Lushan Botanical Garden, Jiangxi Province and Chinese Academy of Sciences, Jiujiang, China
- 2School of Pharmaceutical Sciences, State Key Laboratory of Antiviral Drugs, Pingyuan Laboratory, Zhengzhou University, Zhengzhou, China
- 3BioInnovation Institute, Copenhagen, Denmark
- 4State Key Laboratory of Phytochemistry and Natural Medicines in West China, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming, China
Editorial on the Research Topic
Plant natural products: biosynthesis, regulation, and function
Plant natural products, also referred to as plant specialized metabolites, are small molecules synthesized by plants. Throughout history, human have harnessed these compounds for diverse applications, including development of medicines, food supplements, and dyes. In their host organisms, these molecules perform diverse functions, such as mediating pollinators and mycorrhizal fungi interactions, defensing against biotic stresses like herbivores and pathogens, and protecting against abiotic stresses like UV-B radiation, frost, and drought (Dixon and Paiva, 1995).
Traditional phytochemical approaches, which typically involve isolating individual metabolites followed by targeted bioassays, have long provided foundational insights into the functions of these compounds. However, given the immense chemical diversity of plant natural products, estimated to exceed one million distinct structures (Afendi et al., 2012), these conventional methods are ill-suited for exploring the full metabolic landscape. The emergence of metabolomics has transformed this paradigm by enabling comprehensive, high-throughput analysis of hundreds to thousands of metabolites simultaneously, thereby offering unprecedented capacity to decipher metabolic functions. Moreover, these compounds are often minute quantities in planta, elucidating the biosynthetic pathways and regulatory networks that govern specialized metabolites is critical. Such understanding facilitates the development of synthetic biology strategies for heterologous production of these compounds in engineered organisms.
This Research Topic, entitled “Plant Natural Products: Biosynthesis, Regulation, and Function,” features 14 original research articles, one review, and one opinion piece from authors worldwide. Collectively, these contributions highlight cutting-edge discoveries across all aspects of plant specialized metabolism, from molecular mechanisms to ecological significance.
Metabolomics has emerged as a powerful tool for deciphering the dynamic chemical diversity of plants, offering insights into species-specific metabolites, developmental stage variations, and environmental responses. This approach is crucial due to the high specificity and contextual variability of plant natural products, necessitating comprehensive analyses across diverse species, ontogenetic stages, and environmental conditions. Pannequin et al. performed a comparative metabolome study of a large collection of bryophyte plants including 60 species, 15 orders, and 41 families, which provides a comprehensive overview of bryophyte chemodiversity and in-depth chemical feature of certain species. Liu et al. combined widely targeted metabolomics with biological activities assay, and sensory flavor analyses, revealing that the buds of Lonicera japonica Thunb. var. chinensis had great exploitation potentials in pharmaceuticals, beverages, and nutraceuticals. Yang et al. identified 154 common differential metabolites across diverse ripening stages of Baccaurea ramiflora Lour. fruit based on non-targeted metabolomics analysis, with L-sorbose and 5-hydroxyindole-3-acetic acid as taste biomarkers. Environmental stimuli frequently trigger plant natural products biosynthesis. Wang et al. investigated the effects of geography, soil and climatic factors on the two main secondary metabolites contents in the roots of Rubia cordifolia L. Their findings revealed that annual precipitation negatively correlated with the contents of purpurin and mollugin.
Notably, metabolomics combined with other omics approaches can provide an unbiased view of biological processes, thus facilitating the elucidation of underlying molecular mechanism. By integrated analyses of transcriptomic and metabolomic data from plant samples across various developmental stages and distinct locations, Chen et al. and Tian et al. uncovered the seasonal and spatial dynamics, as well as molecular regulation of flavonoid biosynthesis in Cyclocarya paliurus and Epimedium sagittatum, respectively. In another study, Yan et al., employed proteomic and metabolome analyses to reveal the reconfiguration of energy metabolism and terpenoid biosynthesis in cigar tobacco under low-light conditions, identifying 254 significantly differentially expressed metabolites and 780 significantly differentially expressed proteins.
Despite the rapid development of metabolomic technology, traditional phytochemical method remains playing a critical role in elucidating the functions of novel natural products. Liu et al. isolated six eudesmane-type sesquiterpenoids from Laggera pterodonta, and these compounds exhibited varying degrees of inhibitory effects against six plant pathogenic fungi, including Phytophthora nicotianae, Fusarium oxysporum, Alternaria alternata, Gloeosporium frucrigenum Berk, Colletotrichum fructicola, and Botrytis cinerea. Ruan et al. characterized nine new ent-atisane-type diterpenoids from Euphorbia fischeriana Steud, one of which exhibited significant antiviral activity against COVID-19 by directly binding to the virus’s RNA-dependent RNA polymerase. Additionally, Neel et al. reported that two major metabolites, gymnemic acid IV and gymnestrogenin from the leaves of Gymnema sylvestre were effective against Penicillium digitatum 6952, Penicillium expansum 2995, and Aspergillus flavus 6678.
In recent years, with the maturity of high-throughput sequencing technology and advancements in bioinformatics analysis methods, researches on the biosynthesis and regulation of natural products have expanded from model plants to medicinal plants. Wu et al. compared the function and sequences of key oil biosynthetic genes across different cultivars of Perilla frutescens, discovering crucial amino acid residues responsible for the catalytic activity of Δ12 fatty acid desaturases. Zeng et al. unveiled that the influence of sugar metabolism on oil synthesis varies throughout distinct fruit development stages in oil plant Symplocos paniculata. Senevirathne et al. summarized the mechanism of oxylipin signaling molecules to regulate phytocannabinoids production in Cannabis sativa. MYB transcription factors (TFs) are a class of important TFs that regulate the synthesis of various plant secondary metabolites. Wang et al. conducted a genome-wide analysis of MYB TFs in four Rheum L. plants, identifying 1054 MYB genes, with 12 characterizing a key role in anthraquinones biosynthesis. Virus-induced gene silencing (VIGS) is a powerful tool to detect gene functions in vivo, particularly in non-model plants. Yu et al. developed an easy and effective VIGS approach, which could facilitate endogenous gene studies in two Nepeta species. Finally, considering the complexity of plant secondary metabolism biosynthesis, Yin and Yang discussed an alternative chemoproteomic approach that uses affinity probes to identify active enzymes to elucidate biosynthetic pathway.
To date, our knowledge of the biosynthesis and regulation of specialized metabolites across various plant species remains limited. This Research Topic significantly advances the knowledge framework for integrated approach to understand the production and functions of plant natural products. We hope this Research Topic can serve as a landmark reference for future research in the field.
Author contributions
ZY: Writing – original draft. YW: Writing – review & editing. BJ: Writing – review & editing. XF: Writing – original draft.
Funding
The author(s) declare that financial support was received for the research and/or publication of this article. We thank the funding from the National Natural Science Foundation of China (No. 32360111 and 32371485), Yunnan Revitalization Talent Support Program “Top Team” Project (202305AT350001), Science Fund for Distinguished Young Scholars of Jiangxi Province (No. 20224ACB215004), Double Thousand Plan of Jiangxi Province (No. jxsq2023101106), Key Research and Development Program of Jiangxi Province (No. 20243BBI91010), Henan Province Outstanding Youth Foundation (No. 242300421097), and the Program for Scientific and Technological Innovation Talents in Universities of Henan Provincial Education Department (25HASTIT057).
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
The author(s) declared that they were an editorial board member of Frontiers, at the time of submission. This had no impact on the peer review process and the final decision.
Generative AI statement
The author(s) declare that no Generative AI was used in the creation of this manuscript.
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References
Afendi, F. M., Okada, T., Yamazaki, M., Hirai-Morita, A., Nakamura, Y., Nakamura, K., et al. (2012). KNApSAcK family databases: integrated metabolite-plant species databases for multifaceted plant research. Plant Cell Physiol. 53, e1. doi: 10.1093/pcp/pcr165
Keywords: plant specialized metabolites, biosynthesis, metabolomics, medicinal plants, phytochemistry
Citation: Yu Z, Wei Y, Ji B and Fang X (2025) Editorial: Plant natural products: biosynthesis, regulation, and function. Front. Plant Sci. 16:1661170. doi: 10.3389/fpls.2025.1661170
Received: 07 July 2025; Accepted: 20 July 2025;
Published: 31 July 2025.
Edited and Reviewed by:
Laigeng Li, Chinese Academy of Sciences (CAS), ChinaCopyright © 2025 Yu, Wei, Ji and Fang. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Xin Fang, eGluZmFuZ0BtYWlsLmtpYi5hYy5jbg==