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Despite their relatively poorly investigated phytochemistry, species of the genus Chuquiraga are widely commercialized. The present study reports the use of a high-resolution liquid chromatography-mass spectrometry-based metabolomics approach coupled with exploratory and supervised multivariate statistical analyses for species classification and chemical marker identification of four species of Chuquiraga (C. jussieui, C. weberbaueri, C. spinosa, and Chuquiraga sp.) from Ecuador and Peru. Based on these analyses, a high percentage of correct classifications (87% to 100%) allowed the prediction of the taxonomic identity of Chuquiraga species. Through the metabolite selection process, several key constituents with the potential to be chemical markers were identified. Samples of C. jussieui displayed alkyl glycosides and triterpenoid glycosides as discriminating metabolites, while Chuquiraga sp. displayed high concentrations of p-hydroxyacetophenone, p-hydroxyacetophenone 4-O-glucoside, p-hydroxyacetophenone 4-O-(6-O-apiosyl)-glucoside, and quinic acid ester derivatives as the main metabolites. Caffeic acid was characteristic for C. weberbaueri samples, whereas C. spinosa displayed higher concentrations of the following new phenylpropanoid ester derivatives: 2-O-caffeoyl-4-hydroxypentanedioic acid (24), 2-O-p-coumaroyl-4-hydroxypentanedioic acid (34), 2-O-feruloyl-4-hydroxypentanedioic acid (46), 2,4-O-dicaffeoylpentanedioic acid (71), and 2-O-caffeoyl-4-O-feruloylpentanedioic acid (77).
Assuntos
Asteraceae , Flavonoides/análise , Glicosídeos/análise , Espectrometria de Massas , Glucosídeos , Cromatografia Líquida , Cromatografia Líquida de Alta Pressão , MetabolômicaRESUMO
The Andean mountains are 'center stage' to some of the most spectacular examples of plant diversifications, where geographic isolation and past climatic fluctuations have played a major role. However, the influence of Andean geography and climate as drivers of metabolic variation in Andean plants is poorly elucidated. Here, we studied the influence of those factors on the metabolome of the subtribe Espeletiinae (Asteraceae) using liquid chromatography coupled to high-resolution mass spectrometry data of over two hundred samples from multiple locations. Our results demonstrate that metabolic profiles can discriminate Espeletiinae taxa at different geographic scales, revealing inter- and intraspecific metabolic variations: at the country level, segregation between Colombian and Venezuelan taxa was observed; regionally, between páramo massifs; and locally, between páramo complexes. Metabolic differences in Espeletiinae were mainly explained by geographic isolation, although differences in taxonomic genera, temperature, and elevation, were also important. Furthermore, we found that different species inhabiting the same páramo complex showed stronger chemical similarities than the same species at different locations, corroborating that geographic isolation represents the main driver of metabolic change in Espeletiinae. The current study serves as a starting point to fill in the gaps in how Andean geography and climate have shaped the metabolism of its vegetation and reveal the potential of untargeted metabolomics to study the environmental physiology of plants.
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Smallanthus sonchifolius, also known as yacón, is an Andean crop species commercialized for its nutraceutical and medicinal properties. The tuberous roots of yacón accumulate a diverse array of probiotic and bioactive metabolites including fructooligosaccharides and caffeic acid esters. However, the metabolic diversity of yacón remains unexplored, including the site of biosynthesis and accumulation of key metabolite classes. We report herein a multidisciplinary approach involving metabolomics, gene expression and scanning electron microscopy, to provide a comprehensive analysis of the diversity, distribution and spatial regulation of the specialized metabolism in yacón. Our results demonstrate that different metabolic fingerprints and gene expression patterns characterize specific tissues, organs and cultivars of yacón. Manual inspection of mass spectrometry data and molecular networking allowed the tentative identification of 71 metabolites, including undescribed structural analogues of known bioactive compounds. Imaging by scanning electron microscopy revealed the presence of a new type of glandular trichome in yacón bracts, with a distinctive metabolite profile. Furthermore, the high concentration of sesquiterpene lactones in capitate glandular trichomes and the restricted presence of certain flavonoids and caffeic acid esters in underground organs and internal tissues suggests that these metabolites could be involved in protective and ecological functions. This study demonstrates that individual organs and tissues make specific contributions to the highly diverse and specialized metabolome of yacón, which is proving to be a reservoir of previously undescribed molecules of potential significance in human health.
Assuntos
Asteraceae/metabolismo , Suplementos Nutricionais/análise , Regulação da Expressão Gênica de Plantas , Metaboloma , Compostos Fitoquímicos/metabolismo , Extratos Vegetais/metabolismo , Proteínas de Plantas/metabolismo , Asteraceae/genética , Asteraceae/crescimento & desenvolvimento , Folhas de Planta/genética , Folhas de Planta/crescimento & desenvolvimento , Folhas de Planta/metabolismo , Proteínas de Plantas/genética , Raízes de Plantas/genética , Raízes de Plantas/crescimento & desenvolvimento , Raízes de Plantas/metabolismoRESUMO
Acting as chemical defense or signaling compounds, secondary metabolites (SMs) play an essential role in the evolutionary success of many angiosperm plant families. However, the adaptive advantages that SMs confer, and the influence of environmental and developmental factors on SMs expression, remains poorly understood. A study of taxa endemic to the variable Andean climate, using a metabolomics approach, may provide further insight. By analyzing gene expression patterns and metabolic fingerprints, we report herein the developmental and environmental regulation of the secondary metabolism of Smallanthus sonchifolius (yacón), a medicinal Andean plant. Our results demonstrate a clear developmental stage dependent regulation of the secondary metabolism of yacón leaves wherein the metabolic diversity increases with plant age. However, environmental factors seem to regulate biosynthetic pathways, creating differences in the expression of chemical classes, pointing to an association between transcription levels of relevant genes and the relative amounts of more than 40 different metabolites. This study suggests that the secondary metabolism of yacón is regulated by a complex interplay between environmental factors and developmental stage and provides insight into the regulatory factors and adaptive roles of SMs in Andean taxa.
Assuntos
Asteraceae/genética , Asteraceae/metabolismo , Meio Ambiente , Perfilação da Expressão Gênica/métodos , Metabolômica/métodos , Metabolismo Secundário/genética , Asteraceae/crescimento & desenvolvimento , Clima , Análise por Conglomerados , Regulação da Expressão Gênica no Desenvolvimento , Regulação da Expressão Gênica de Plantas , Umidade , Luz , Folhas de Planta/genética , Folhas de Planta/crescimento & desenvolvimento , Folhas de Planta/metabolismo , Chuva , TemperaturaRESUMO
The present study is focused on the characterization of yacon [Smallanthus sonchifolius (Poepp. et Endl.) H. Robinson] accessions from different geographic origins (Bolivia, Ecuador, and Peru) by iPBS markers and metabolomic fingerprinting. The results showed that the number of amplified polymorphic fragment levels ranged from 20 up to 27 with a level of polymorphism ranging from 80 to 100%. Five of the iPBS primers used in this study provided no specific banding pattern able to discriminate between the different yacon accessions. However, two iPBS primer pairs were able to separate Peru accessions from those of Ecuador and Bolivia. The UPLC-HRMS/MS-based metabolomic fingerprinting showed highly similar metabolomic fingerprints characterized by the accumulation of high quantities of sesquiterpene lactones and diterpenes, but no apparent geographic clustering. The present study demonstrates that yacon accessions from different geographical origins maintained ex situ (in the Czech Republic) present a rather low chemical and genetic diversity.
Assuntos
Antioxidantes/química , Asteraceae/química , Diterpenos/química , Lactonas/química , Extratos Vegetais/química , Sesquiterpenos/química , Asteraceae/genética , Bolívia , Análise por Conglomerados , República Tcheca , Equador , Variação Genética , Geografia , Glicosilação , Espectrometria de Massas , Metabolômica , Análise Multivariada , Mapeamento de Peptídeos , Peru , Raízes de Plantas/química , RetroelementosRESUMO
The páramo ecosystem has the highest rate of diversification across plant lineages on earth, of which the genus Espeletia (Asteraceae) is a prime example. The current distribution and molecular phylogeny of Espeletia suggest the influence of Andean geography and past climatic fluctuations on the diversification of this genus. However, molecular markers have failed to reveal subtle biogeographical trends in Espeletia diversification, and metabolomic evidence for allopatric segregation in plants has never been reported. Here, we present for the first time a metabolomics approach based on liquid chromatography-mass spectrometry for revealing subtle biogeographical trends in Espeletia diversification. We demonstrate that Espeletia lineages can be distinguished by means of different metabolic fingerprints correlated to the country of origin on a global scale and to the páramo massif on a regional scale. Distinctive patterns in the accumulation of secondary metabolites according to the main diversification centers of Espeletia are also identified and a comprehensive phytochemical characterization is reported. These findings demonstrate that a variation in the metabolic fingerprints of Espeletia lineages followed the biogeography of this genus, suggesting that our untargeted metabolomics approach can be potentially used as a model to understand the biogeographic history of additional plant groups in the páramo ecosystem.
Assuntos
Asteraceae/metabolismo , Metaboloma , Metabolômica , Compostos Fitoquímicos/metabolismo , Adaptação Biológica , Asteraceae/química , Cromatografia Líquida de Alta Pressão , Cromatografia Líquida , Meio Ambiente , Geografia , Metabolômica/métodos , Compostos Fitoquímicos/química , Luz Solar , Espectrometria de Massas em TandemRESUMO
ABSTRACT In this study, a comprehensive phytochemical characterization of two morphologically related species from the genus Espeletia Mutis ex Bonpl., namely, Espeletia grandiflora Humb. & Bonpl. and Espeletia killipii Cuatrec., Asteraceae, has been performed by gas chromatography coupled to flame ionization detection, gas chromatography coupled to mass spectrometry and ultra-high performance liquid chromatography coupled to ultraviolet and high-resolution mass spectrometry. Analysis of ethanol extracts (70%, v/v) from leaves and concomitant compound dereplication allowed the identification of major peaks, most of them new reports for the genus Espeletia or the subtribe Espeletiinae. Chemical characterization of resins essential oils indicated several similarities and differences between both species and from other members of the subtribe. Chemometric analysis (hierarchical clustering analysis and orthogonal partial least-squares discriminant analysis) applied to the essential oil composition of 31 species from Espeletiinae furthermore allowed the identification of three primary clusters correlated with the taxonomy. Hence, this study underscored qualitative and semiquantitative differences between the chemical composition of leaves and resins of E. grandiflora and E. killipii, provided information on chemotaxonomy and described the presence of different trends in the essential oil composition from species of Espeletiinae.
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Introducción: Siparuna sessiliflora Kunth A. DC. es una especie vegetal comúnmente conocida en Colombia como limoncillo, utilizada por parte de varias comunidades indígenas para tratar diferentes problemas de salud. A pesar de contar con diversos registros de usos etnobotánicos, esta especie ha sido poco estudiada desde el punto de vista fitoquímico o de su actividad biológica. Objetivos: evaluar la actividad antibacteriana de los extractos y las fracciones obtenidos a partir de las hojas de Siparuna sessiliflora sobre Bacillus subtilis, Staphylococcus aureus, Escherichia coli y Pseudomonas aeruginosa. Métodos: el material vegetal fue extraído por maceración en frío con éter de petróleo y etanol 96 por ciento; estos extractos se fraccionaron por métodos cromatográficos y partición líquido/líquido; su actividad antibacteriana se evaluó por el método de difusión en gel por perforación en placa. Posteriormente, se identificaron los principales compuestos responsables de la bioactividad por medio de cromatografía de gases acolada a espectrometría de masas. Resultados: se encontró que las fracciones de alcaloides Alk 1 y Alk 2 presentaron actividad frente a B. subtilis, S. aureus y E. coli. Adicionalmente, la subfracción Alk 2A fue la más activa frente a B. subtilis. Se identificaron sobre todo alcaloides isoquinolínicos y un derivado del ácido cinámico como posibles compuestos responsables de la bioactividad. Conclusiones: se reportó la actividad antibacteriana de S. sessiliflora frente a bacterias grampositivas y gramnegativas, y se generó nuevo conocimiento sobre su fitoquímica que corrobora su uso tradicional en la cura de cuadros infecciosos.
Introduction: Siparuna sessiliflora Kunth A. DC. is a plant species popularly known in Colombia as «limoncillo¼ and used by several indigenous communities for treating different health disorders. Despite the many records of its ethnobotanical uses, this species has been poorly studied from a phytochemical or biological standpoint. Objectives: to evaluate the antibacterial activity of the extracts and fractions obtained from Siparuna sessiliflora´s leaves against Bacillus subtilis, Staphylococcus aureus, Escherichia coli and Pseudomonas aeruginosa. Methods: the plant material was extracted by cold maceration with petroleum ether and 96 percent ethanol. Those extracts were fractionated by chromatographic methods and liquid-liquid partitioning; additionally, its antibacterial activity was assessed by gel diffusion. Subsequently, there were identified the main bioactive compounds by gas chromatography-mass spectrometry. Results: it was found that the alkaloidal fractions Alk 1 and Alk 2 were active against B. subtilis, S. aureus and E. coli. Additionally, the subfraction Alk 2A was the most active against B. subtilis. Isoquinoline alkaloids and a cinnamic acid derivative were identified as possible compounds responsible for bioactivity. Conclusions: the antibacterial activity of S. sessiliflora against Gram positive and Gram negative bacteria was reported, so the new knowledge about its phytochemistry endorses its traditional use in the treatment of infections.