Effects of the waxy genotype and storage temperature of pearled barley on the volatile compounds after cooking

Headspace solid-phase microextraction coupled with gas chromatography-mass spectrometry was utilized to analyze the volatile compounds in cooked barley. A total of 56 compounds were identified, including 18 aldehydes, 13 ketones, 6 alcohols, 6 furans, 5 acids, 2 furfurals, and 6 others. The grains o...

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Published inFOOD SCIENCE AND TECHNOLOGY RESEARCH Vol. 30; no. 2; pp. 223 - 230
Main Authors Kohyama, Noriko, Yanagisawa, Takashi
Format Journal Article
LanguageEnglish
Published Tsukuba Japanese Society for Food Science and Technology 2024
The Japanese Society for Food Science and Technology
Japan Science and Technology Agency
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Abstract Headspace solid-phase microextraction coupled with gas chromatography-mass spectrometry was utilized to analyze the volatile compounds in cooked barley. A total of 56 compounds were identified, including 18 aldehydes, 13 ketones, 6 alcohols, 6 furans, 5 acids, 2 furfurals, and 6 others. The grains of waxy and nonwaxy barley were pearled and stored at either 5 °C or 40 °C for 5 months prior to cooking. The waxy genotypes exhibited higher levels of key odorants in cooked barley, such as hexanal, 2-octenal, 2,4-nonadienal (E, E), and 2,4-decadienal (E, E), compared to the nonwaxy genotypes. Elevated storage temperatures (40 °C) led to an increase in 42 volatile compounds, particularly 2-butyl-2-octenal in cooked barley. Principal component analysis revealed distinguishable profiles of volatile compounds among the nonwaxy 40 °C storage group, the waxy hull-less 40 °C storage group, the waxy hulled 40 °C storage group, and the 5 °C storage group.
AbstractList Headspace solid-phase microextraction coupled with gas chromatography-mass spectrometry was utilized to analyze the volatile compounds in cooked barley. A total of 56 compounds were identified, including 18 aldehydes, 13 ketones, 6 alcohols, 6 furans, 5 acids, 2 furfurals, and 6 others. The grains of waxy and nonwaxy barley were pearled and stored at either 5 °C or 40 °C for 5 months prior to cooking. The waxy genotypes exhibited higher levels of key odorants in cooked barley, such as hexanal, 2-octenal, 2,4-nonadienal (E, E), and 2,4-decadienal (E, E), compared to the nonwaxy genotypes. Elevated storage temperatures (40 °C) led to an increase in 42 volatile compounds, particularly 2-butyl-2-octenal in cooked barley. Principal component analysis revealed distinguishable profiles of volatile compounds among the nonwaxy 40 °C storage group, the waxy hull-less 40 °C storage group, the waxy hulled 40 °C storage group, and the 5 °C storage group.
Headspace solid-phase microextraction coupled with gas chromatography-mass spectrometry was utilized to analyze the volatile compounds in cooked barley. A total of 56 compounds were identified, including 18 aldehydes, 13 ketones, 6 alcohols, 6 furans, 5 acids, 2 furfurals, and 6 others. The grains of waxy and nonwaxy barley were pearled and stored at either 5℃ or 40℃ for 5 months prior to cooking. The waxy genotypes exhibited higher levels of key odorants in cooked barley, such as hexanal, 2-octenal, 2,4-nonadienal (E, E), and 2,4-decadienal (E, E), compared to the nonwaxy genotypes. Elevated storage temperatures (40℃) led to an increase in 42 volatile compounds, particularly 2-butyl-2-octenal in cooked barley. Principal component analysis revealed distinguishable profiles of volatile compounds among the nonwaxy 40℃ storage group, the waxy hull-less 40℃ storage group, the waxy hulled 40℃ storage group, and the 5℃ storage group.
ArticleNumber FSTR-D-23-00120
Author Kohyama, Noriko
Yanagisawa, Takashi
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SubjectTerms Alcohols
Aldehydes
Barley
cooked barley
Cooking
Furans
Gas chromatography
Genotypes
Headspace
Hexanal
Ketones
Mass spectrometry
Mass spectroscopy
odor
Pesticides
Principal components analysis
Solid phase methods
Solid phases
storage
Storage temperature
volatile compound
Volatile compounds
waxy
Title Effects of the waxy genotype and storage temperature of pearled barley on the volatile compounds after cooking
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