Peanuts (Arachis hypogaea) are among the most widely consumed legumes worldwide due to their nutritional value, taste, and affordability. The quality of peanuts is typically assessed based on their appearance, texture, flavor, and health benefits. Defining a quality standard for the peanut production chain is complex and requires understanding their chemical composition, stability, and sensory properties. This study aims to investigate a germination defect known as splitting, where the two cotyledons of the peanut separate. Splitting is associated with early germination, leading to premature metabolic activation, which can negatively affect peanut quality by causing dull flavors or increasing the risk of over-roasting. To comprehensively map the chemical composition of peanuts and assess the impact of germination defects on roasted product quality, the study employs omics approaches. Various peanut fractions were analyzed to understand the impact of germination defects. The study examined primary metabolites (i.e., free amino acids, organic acids, and sugars) after defatting, extraction, derivatization, and subsequent comprehensive two-dimensional gas chromatography-time of flight mass spectrometry (GC×GC-TOF MS) profiling [1]. The lipid fraction was analyzed for the presence of esterified and free fatty acids by dedicated lipid extraction, transesterification of the esterified fatty acid fraction, Fisher esterification for the free fatty acid fraction, and GC-FID analysis [2]. Lastly, the volatile fraction was explored using headspace solid-phase microextraction (HS-SPME) followed by GC×GC-TOFMS analysis. Results indicate that metabolic activation in split seeds leads to higher concentrations of monosaccharides such as mannitol and glucitol, while aroma precursors like valine, threonine, and sucrose are present in lower amounts compared to whole peanuts. Additionally, meaningful differences were also evident in the amount and distribution of lipids depending on the kernel state (whole vs. split). The volatilome confirmed further differentiation between kernel states, with compounds such as 2-pentyl furan and dihydro-3-methyl 2(3H)-furanone showing higher responses in split peanuts. In summary, this study highlights the significant impact of germination defects on peanut quality, providing valuable insights for defining high-quality peanuts based on chemical and sensory characteristics.

FOOD METABOLOMICS SUPPORTS INDUSTRIAL QUALITY RESEARCH: UNREVEALING COMPOSITIONAL CHANGES IN GERMINATED PEANUTS BY MULTIDIMENSIONAL GAS CHROMATOGRAPHY PLATFORMS

Angelica Fina;Andrea Caratti;Fulvia Trapani;Erica Liberto;Cristina Casetta;Carlo Bicchi;Chiara Cordero
2024-01-01

Abstract

Peanuts (Arachis hypogaea) are among the most widely consumed legumes worldwide due to their nutritional value, taste, and affordability. The quality of peanuts is typically assessed based on their appearance, texture, flavor, and health benefits. Defining a quality standard for the peanut production chain is complex and requires understanding their chemical composition, stability, and sensory properties. This study aims to investigate a germination defect known as splitting, where the two cotyledons of the peanut separate. Splitting is associated with early germination, leading to premature metabolic activation, which can negatively affect peanut quality by causing dull flavors or increasing the risk of over-roasting. To comprehensively map the chemical composition of peanuts and assess the impact of germination defects on roasted product quality, the study employs omics approaches. Various peanut fractions were analyzed to understand the impact of germination defects. The study examined primary metabolites (i.e., free amino acids, organic acids, and sugars) after defatting, extraction, derivatization, and subsequent comprehensive two-dimensional gas chromatography-time of flight mass spectrometry (GC×GC-TOF MS) profiling [1]. The lipid fraction was analyzed for the presence of esterified and free fatty acids by dedicated lipid extraction, transesterification of the esterified fatty acid fraction, Fisher esterification for the free fatty acid fraction, and GC-FID analysis [2]. Lastly, the volatile fraction was explored using headspace solid-phase microextraction (HS-SPME) followed by GC×GC-TOFMS analysis. Results indicate that metabolic activation in split seeds leads to higher concentrations of monosaccharides such as mannitol and glucitol, while aroma precursors like valine, threonine, and sucrose are present in lower amounts compared to whole peanuts. Additionally, meaningful differences were also evident in the amount and distribution of lipids depending on the kernel state (whole vs. split). The volatilome confirmed further differentiation between kernel states, with compounds such as 2-pentyl furan and dihydro-3-methyl 2(3H)-furanone showing higher responses in split peanuts. In summary, this study highlights the significant impact of germination defects on peanut quality, providing valuable insights for defining high-quality peanuts based on chemical and sensory characteristics.
2024
11th International Symposium on RECENT ADVANCES IN FOOD ANALYSIS - RAFA 2024
Prague, Czech Republic
November 5–8, 2024
BOOK OF ABSTRACTS 11th International Symposium on RECENT ADVANCES IN FOOD ANALYSIS
University of Chemistry and Technology, Prague
530
530
978-80-7592-268-7
food metabolomics, high quality peanuts, comprehensive two-dimensional gas chromatography
Angelica Fina, Andrea Caratti, Fulvia Trapani, Erica Liberto, Irene Cincera, Giuseppe Genova, Cristina Casetta, Carlo Bicchi, Chiara Cordero
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2318/2031907
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