Yan Luo , Lu Zhang , Chenliang Zhao , Yaxin Yang , Jianghai Ye , Kang He , Chunhua Lai , Juan Zou
{"title":"凤蝶的植物化学研究","authors":"Yan Luo , Lu Zhang , Chenliang Zhao , Yaxin Yang , Jianghai Ye , Kang He , Chunhua Lai , Juan Zou","doi":"10.1016/j.bse.2025.105072","DOIUrl":null,"url":null,"abstract":"<div><div><em>Pteris fauriei</em> Hieron., a terrestrial fern species belonging to the Pteridaceae family, is typically found in shaded understories of forests at elevations ranging from 300 to 800 m. This species preferentially colonizes acidic soils, particularly in moist environments adjacent to drainage ditches or other similar habitats. The phytochemical investigation of <em>P. fauriei</em> collected from Guizhou province was carried out and seven secondary metabolites were identified. They were characterized as: <em>ent</em>-11<em>α</em>-hydroxy-15-oxo-kaur-16-en-19-oic acid-<em>O</em>-<em>β</em>-<em>D</em>-glucoside (<strong>1</strong>), 16<em>β</em>-hydroxy-15-oxo-<em>ent</em>-kaur-19-oly-glucoside (<strong>2</strong>), 11<em>β</em>-hydroxy-15-oxo-<em>ent</em>-kaur-16-en-19-oic acid (<strong>3</strong>), <em>ent</em>-11<em>α</em>-hydroxy-15-oxo-kaur-19-oic acid (<strong>4</strong>), apigenin-7-<em>O</em>-<em>β</em>-D-glucoside (<strong>5</strong>), luteolin-7-<em>O</em>-<em>β</em>-D-glucoside (<strong>6</strong>), <em>β</em>-sitosterol (<strong>7</strong>). The structures of the obtained monomeric compounds were established based on their physicochemical properties, analysis of their NMR data and by comparing their spectroscopic data with those reported in the literature. Notably, compounds (<strong>1</strong>–<strong>5</strong>) were firstly isolated from this species and represented novel chemical records for <em>P. fauriei</em>, expanding the documented phytochemical profile of this species and offering a scientific foundation for the development and utilization of <em>P. fauriei</em>. The chemotaxonomic implications of these findings are discussed, particularly regarding the biosynthetic relationship between <em>ent</em>-kaurane diterpenoids and their ecological roles in Pteridaceae.</div></div>","PeriodicalId":8799,"journal":{"name":"Biochemical Systematics and Ecology","volume":"123 ","pages":"Article 105072"},"PeriodicalIF":1.4000,"publicationDate":"2025-06-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Phytochemical investigation of Pteris fauriei Hieron\",\"authors\":\"Yan Luo , Lu Zhang , Chenliang Zhao , Yaxin Yang , Jianghai Ye , Kang He , Chunhua Lai , Juan Zou\",\"doi\":\"10.1016/j.bse.2025.105072\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div><em>Pteris fauriei</em> Hieron., a terrestrial fern species belonging to the Pteridaceae family, is typically found in shaded understories of forests at elevations ranging from 300 to 800 m. This species preferentially colonizes acidic soils, particularly in moist environments adjacent to drainage ditches or other similar habitats. The phytochemical investigation of <em>P. fauriei</em> collected from Guizhou province was carried out and seven secondary metabolites were identified. They were characterized as: <em>ent</em>-11<em>α</em>-hydroxy-15-oxo-kaur-16-en-19-oic acid-<em>O</em>-<em>β</em>-<em>D</em>-glucoside (<strong>1</strong>), 16<em>β</em>-hydroxy-15-oxo-<em>ent</em>-kaur-19-oly-glucoside (<strong>2</strong>), 11<em>β</em>-hydroxy-15-oxo-<em>ent</em>-kaur-16-en-19-oic acid (<strong>3</strong>), <em>ent</em>-11<em>α</em>-hydroxy-15-oxo-kaur-19-oic acid (<strong>4</strong>), apigenin-7-<em>O</em>-<em>β</em>-D-glucoside (<strong>5</strong>), luteolin-7-<em>O</em>-<em>β</em>-D-glucoside (<strong>6</strong>), <em>β</em>-sitosterol (<strong>7</strong>). The structures of the obtained monomeric compounds were established based on their physicochemical properties, analysis of their NMR data and by comparing their spectroscopic data with those reported in the literature. Notably, compounds (<strong>1</strong>–<strong>5</strong>) were firstly isolated from this species and represented novel chemical records for <em>P. fauriei</em>, expanding the documented phytochemical profile of this species and offering a scientific foundation for the development and utilization of <em>P. fauriei</em>. The chemotaxonomic implications of these findings are discussed, particularly regarding the biosynthetic relationship between <em>ent</em>-kaurane diterpenoids and their ecological roles in Pteridaceae.</div></div>\",\"PeriodicalId\":8799,\"journal\":{\"name\":\"Biochemical Systematics and Ecology\",\"volume\":\"123 \",\"pages\":\"Article 105072\"},\"PeriodicalIF\":1.4000,\"publicationDate\":\"2025-06-24\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Biochemical Systematics and Ecology\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0305197825001218\",\"RegionNum\":4,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biochemical Systematics and Ecology","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0305197825001218","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
Phytochemical investigation of Pteris fauriei Hieron
Pteris fauriei Hieron., a terrestrial fern species belonging to the Pteridaceae family, is typically found in shaded understories of forests at elevations ranging from 300 to 800 m. This species preferentially colonizes acidic soils, particularly in moist environments adjacent to drainage ditches or other similar habitats. The phytochemical investigation of P. fauriei collected from Guizhou province was carried out and seven secondary metabolites were identified. They were characterized as: ent-11α-hydroxy-15-oxo-kaur-16-en-19-oic acid-O-β-D-glucoside (1), 16β-hydroxy-15-oxo-ent-kaur-19-oly-glucoside (2), 11β-hydroxy-15-oxo-ent-kaur-16-en-19-oic acid (3), ent-11α-hydroxy-15-oxo-kaur-19-oic acid (4), apigenin-7-O-β-D-glucoside (5), luteolin-7-O-β-D-glucoside (6), β-sitosterol (7). The structures of the obtained monomeric compounds were established based on their physicochemical properties, analysis of their NMR data and by comparing their spectroscopic data with those reported in the literature. Notably, compounds (1–5) were firstly isolated from this species and represented novel chemical records for P. fauriei, expanding the documented phytochemical profile of this species and offering a scientific foundation for the development and utilization of P. fauriei. The chemotaxonomic implications of these findings are discussed, particularly regarding the biosynthetic relationship between ent-kaurane diterpenoids and their ecological roles in Pteridaceae.
期刊介绍:
Biochemical Systematics and Ecology is devoted to the publication of original papers and reviews, both submitted and invited, in two subject areas: I) the application of biochemistry to problems relating to systematic biology of organisms (biochemical systematics); II) the role of biochemistry in interactions between organisms or between an organism and its environment (biochemical ecology).
In the Biochemical Systematics subject area, comparative studies of the distribution of (secondary) metabolites within a wider taxon (e.g. genus or family) are welcome. Comparative studies, encompassing multiple accessions of each of the taxa within their distribution are particularly encouraged. Welcome are also studies combining classical chemosystematic studies (such as comparative HPLC-MS or GC-MS investigations) with (macro-) molecular phylogenetic studies. Studies that involve the comparative use of compounds to help differentiate among species such as adulterants or substitutes that illustrate the applied use of chemosystematics are welcome. In contrast, studies solely employing macromolecular phylogenetic techniques (gene sequences, RAPD studies etc.) will be considered out of scope. Discouraged are manuscripts that report known or new compounds from a single source taxon without addressing a systematic hypothesis. Also considered out of scope are studies using outdated and hard to reproduce macromolecular techniques such as RAPDs in combination with standard chemosystematic techniques such as GC-FID and GC-MS.