Abstract

BackgroundPlants have been used as an important source of indispensable bioactive compounds in various cosmetics, foods, and medicines. However, the subsequent functional annotation of these compounds seems arduous because of the largely uncharacterized, vast metabolic repertoire of plant species with known biological phenotypes. Hence, a rapid multi-parallel screening and characterization approach is needed for plant functional metabolites.ResultsFifty-one species representing three plant families, namely Asteraceae, Fabaceae, and Rosaceae, were subjected to metabolite profiling using gas chromatography time-of-flight mass spectrometry (GC-TOF-MS) and ultrahigh-performance liquid chromatography quadrupole orbitrap ion trap tandem mass spectrometry (UHPLC-Q-orbitrap-MS/MS) as well as multivariate analyses. Partial least squares discriminant analysis (PLS-DA) of the metabolite profiling datasets indicated a distinct clustered pattern for 51 species depending on plant parts (leaves and stems) and relative phylogeny. Examination of their relative metabolite contents showed that the extracts from Fabaceae plants were abundant in amino acids, fatty acids, and genistein compounds. However, the extracts from Rosaceae had higher levels of catechin and ellagic acid derivatives, whereas those from Asteraceae were higher in kaempferol derivatives and organic acids. Regardless of the different families, aromatic amino acids, branch chain amino acids, chlorogenic acid, flavonoids, and phenylpropanoids related to the shikimate pathway were abundant in leaves. Alternatively, certain amino acids (proline, lysine, and arginine) as well as fatty acids levels were higher in stem extracts. Further, we investigated the associated phenotypes, i.e., antioxidant activities, affected by the observed spatial (leaves and stem) and intra-family metabolomic disparity in the plant extracts. Pearson’s correlation analysis indicated that ellagic acid, mannitol, catechin, epicatechin, and quercetin derivatives were positively correlated with antioxidant phenotypes, whereas eriodictyol was positively correlated with tyrosinase inhibition activity.ConclusionsThis work suggests that metabolite profiling, including multi-parallel approaches and integrated bioassays, may help the expeditious characterization of plant-derived metabolites while simultaneously unraveling their chemodiversity.

Highlights

  • Plants have been used as an important source of indispensable bioactive compounds in various cosmetics, foods, and medicines

  • Metabolite profiling across spatial components and families (Asteraceae, Fabaceae, and Rosaceae) we examined the 2-D metabolomic profiles across the spatial components of 51 plant species belonging to three different families (Asteraceae, Fabaceae, and Rosaceae) that are widespread on the Korean peninsula

  • The principal components analysis (PCA) score plot based on the GCTOF-mass spectrometry (MS) data displayed a clustered pattern for the 51 samples, segregating them into three distinct groups according to the corresponding plant families across PC 1 (8.2%) and PC 2 (4.7%), while their spatial metabolic disparity was evident along PC 2 (Fig. 1a)

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Summary

Introduction

Plants have been used as an important source of indispensable bioactive compounds in various cosmetics, foods, and medicines. Plants have traditionally been used as an important source of pharmacologically active compounds that maintain human health. Plants have been a major source of numerous antioxidant compounds essential in medicines, cosmetics, and the food industry [1]. Tyrosinase inhibitory compounds from plants are used as anti-melanogenic agents [4]. It catalyzes the hydroxylation of tyrosine to LDOPA (L-3,4-dihydroxyphenylalanine), which is subsequently oxidized to L-dopaquinone. This is autopolymerized to form melanin pigments [5]. Natural inhibitors of tyrosinase are considered vital for treating dermatological hyper-pigmentation caused by overproduction of melanin [6, 7]

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