• Applied Biological Chemistry
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• 제37권4호
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• pp.310-314
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• 1994

솔잎으로부터 프리 라디칼 소거 작용이 있는 물질을 분리하고, 여러 기기 분석 결과에 근거하여 4-hydroxy-5-methyl-3[2H]-furanone으로 동정하였다. 아울러 xylose와 glycine의 Maillard 반응을 통하여 이 물질을 합성하였다. 이 물질은 1,1-diphenyl-2-picrylhydrazyl(DPPH) 프리 라디칼에 대해 소거 작용을 보였으며(100 M의 DPPH의 50%를 환원 시키는데 필요한 농도, 즉 $SC_{50}=26\;{\mu}M$) 이는 구조적으로 유사한 공지의 항산화 물질인 $4-hydroxy-2,5-dimethyl-3[2H]-furanone(SC_{50}=53\;{\mu}M)$과 $3-hydroxy-2-methyl-{\gamma}-pyrone(SC_{50}=4.0\;mM)$에 비해 강력한 것이다. 4-Hydroxy-5-methyl-3[2H]-furanone은 3,4-dihydroxyphenylalanine과 linolenic acid의 자동 산화에 대해서 억제 작용을 나타내었다.

• 한국식품과학회지
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• 제20권2호
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• pp.157-163
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• 1988

Propylene glycol 용매계에서 0.5M DL-alanine(${\alpha}-amino-propionic acid$) 와 0.5M D-glucose 를 $100^{\circ}C,\;120^{\circ}C$ 및 $140^{\circ}C$에서 각각 20분, 2시간 반응시켜 생성되는 휘발성 화합물을 분석하고 반응온도와 시간이 갈색화반응 및 휘발성 화합물생성에 미치는 영향을 조사하였다. 갈색화반응 및 휘발성 화합물생성에 미치는 영향을 조사하였다. 갈색화반응은 반응온도와 시간이 증가함에 따라 급격히 증가 하였다. 휘발성 화합물은 7종의 alkylpyrazine, 4종의 pyrrole, 3종의 furan, 1종의 furanone 그리고 기타성분으로 2-hydroxy-3-methyl-2-cyclopenten-1-one을 포함하여 11종이 확인되었으며 pyrazine, pyrrole 및 furan화합물의 생성량은 반응온도가 높아지고 반응시간이 길어짐에 따라 급격히 증가하였다. 또한 alanine과 glucose의 마이야르 반응에 의해 생성되는 구수한 카라멜냄새 및 설탕 탄냄새(burnt sugar-like)는 주로 2-hydroxy-3-methyl-2-cyclopenten-1-one, 2, 5-dimethyl-4-hydroxy-3(2H)-furanone과 같은 함 산소화합물과 pyrazine, pyrrole과 같은 함 질소화합물에 의해 생성되는 것으로 추정되었다.

• 대한화장품학회지
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• 제22권2호
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• pp.70-75
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• 1996

DMHF (2.5-dimethyl-4-hydroxy-3[2H]-furanone), an antioxidative compound from the reaction of L-cysteine/D-glucose scavenged efficiently 1,1-diphenyl-2-picryl hydrazyl free radicals. It exhibited an inhibitory effect on the autoxidation of linolenic acid, and the protective effect against UV cytotoxicity in cultured human fibroblast. In addition, DMHF appeared to prevent the cellular melanogenesis in the cultured murine melanoma cells more effectively than kojic acid, a well known inhibitor of melanogenesis, while the former was not so effective as the latter for the inhibition of the tyrosinase. Considering that cellular melanogenesis is a metabolic process triggered by oxidative stress, it ovas tentatively deduced that the antioxidative property of DMHF might afford the effect against cellular pigmentation by alleviating the causative stress. In toxicological tests such as irritation and sensitization, this compound turned out to be safe. The results of this study suggest that DMHF may be a novel inhibitor of melanogenesis, and that night be useful for application in cosmetics.

• 한국연초학회지
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• 제19권2호
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• pp.151-158
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• 1997

Burley leaf tobacco extracts has been heated at loot for 2 hours and changes in non-volatile fructosazines and volatile components were investigated. Major changes for the heat treatment with corn syrup of burley leaf tobacco extracts were as follows, increases in the contents of 2,5-deoxyfructosazine and 2,5-fructosazine that is produce for the heating reaction of sugar and ammonia, production of pyraEine compounds, such as 2,6-dimethyl pyrazine,2,4-dimethyl pyrazine, ethrnyl pyrazine, methylethyl pyraxine, trimethyl pyrazine, 2-ethenyl-5-methyl pyrazine, 2-acetyl parazine and 2-acetyl-3-methyl pyrazine, increases in the content of furfuryl alcohol derived from sugar degrad ation, production of 2,5-dimethyl-4-hydroxy-3(2H)-furanone and 2,3-dihydro-3,5-dihydroxy-6-methyl-4H-pyran-4-one derived from thermal degradation of Amadori compounds.

• 한국식품영양과학회지
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• 제45권12호
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• pp.1755-1761
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• 2016

간장박 및 그 산가수분해물의 휘발성 향기성분을 SPME/GC/MSD 분석법으로 분석한 결과 총 79종의 화합물이 간장박(66종)과 산가수분해물(60종)에서 동정되었다. 에스테르 및 알코올류가 각각 15종으로 가장 많았고, 알데히드류 11종, 산류 9종, 방향족 화합물류 8종, 퓨란류 8종, 케톤류 7종 및 기타 화합물류 6종이었다. 함량 면에서는 간장박에서 알코올 함량(433.37 ng/g)이 가장 많았으며, 다음으로 알데히드류(273.01 ng/g), 에스테르류(236.80 ng/g) 및 방향족 화합물류(180.66 ng/g) 순이었다. 산가수분해물에서는 퓨란류가 249.27 ng/g으로 가장 많았으며(P<0.05), 알코올을 제외한 나머지 화합물류는 15 ng/g 미만이었다. 간장박에서는 4종의 에스테르류, 3-methylbutyl acetate(바나나/배향), ethyl 3-methyl butanoate(익은 과일향), ethylbenzene acetate(와인향), ethyl 3-methyl butanoate(사과향), 3종의 알코올류, 3-methyl-1-butanol(과일/위스키향), 2-phenylethanol(꽃/달콤한향), 1-octen-3-ol(버섯향), 4종의 알데히드류, (E)-2-phenyl-2-butenal(초코렛향), benzaldehyde(알몬드향), 3-methylbutanal(엿기름향), 2-phenylacetaldehyde(꽃향), 4종의 방향족 화합물류, 4-ethyl-2-methoxyphenol(연기향/간장향), 4-ethylphenol(약품향), 4-vinyl-2-methoxyphenol(나무향), phenol(나무향) 및 2종의 퓨란류, fufural(알몬드향), 4-hydroxy-2,5-dimethyl-3(2H)-furanone(카라멜향)이 지배적이었다. 반면에 산가수분해물에서는 furfural, 5-methylfurfural(알몬드향), 3-methyl-1-butanol, 2-phenylethanol, 4-ethyl-2-methoxyphenol, 3-methylbutanal, benzaldehyde 등의 화합물이 지배적이었다.

• Preventive Nutrition and Food Science
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• 제14권1호
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• pp.76-85
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• 2009

This study determined the effect of refrigerated and thermal storage on the volatile profile of commercial aseptic soymilk. Volatile components in commercial aseptic soymilk stored either under refrigerated ($4^{\circ}C$) or thermal ($55^{\circ}C$) conditions for 30 days were periodically analyzed by combined solvent-assisted flavor evaporation-gas chromatography-mass spectrometry (SAFE-GC-MS). The concentrations of most of the volatile components, including aldehydes, ketones, alcohols, acids, nitrogen- and sulfur-containing compounds, alkylfurans, furan derivatives and phenolic compounds, were affected to a greater extent by thermal storage compared with refrigerated storage. Profound increases in some volatile compounds with low odor detection thresholds, such as hexanal, octanal, (E)-2-octenal, (E,E)-2,4-decadienal, 1-octen-3-ol, 3-ethyl-2,5-dimethylpyrazine, 2,3-diethyl-5-methylpyrazine, 2-pentylfuran, 4-hydroxy-2,5-dimethyl-3(2H)-furanone, dimethyl trisulfide, guaiacol, 4-vinylguaiacol and 4-vinylphenol, were observed in thermal stored soymilk. The volatile profile changes caused by thermal storage may influence the aroma quality of thermal-stored aseptic soymilk.

• 한국식품과학회지
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• 제49권6호
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• pp.617-624
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• 2017

본 연구는 다크 초콜릿을 복합 유산균 스타터인 ABT-5를 이용하여 발효시켰을 때, 항산화 성분과 활성 그리고 향기 성분의 변화를 발효 전 다크 초콜릿과 비교하였다. 발효 시간에 따른 pH의 감소와 적정 산도의 증가 및 가스 크로마토그래피 분석에 의한 lactic acid 성분비의 증가를 측정함으로써 다크 초콜릿의 발효가 진행되었음을 확인하였다. 6, 12, 그리고 24시간 발효한 다크 초콜릿의 총 폴리페놀과 플라보노이드 함량 및 DPPH와 ABTS 라디칼 소거능 활성이 발효 전 대조구 대비 유사한 수준으로 유지되었다. 한편, 6, 12시간 발효한 다크 초콜릿은 대조구에 대비하여 산화스트레스에 의한 ROS 발생 및 세포 독성으로부터 세포를 유의적으로 보호하였다. 가스 크로마토그래피에서 검출된 4-hydroxy-2,5-dimethyl-3(2H)-furanone와 헤드스페이스 가스 크로마토그래피를 통해 검출된 2-furanmethanol은 중요한 향미 성분으로 확인되었으며, 해당 성분들은 발효 다크 초콜릿의 풍미를 증진시킬 것으로 예상되었다. 본 연구에서는 복합유산균을 이용해 다크 초콜릿을 발효했으며, 발효 시간에 따른 항산화 활성의 변화를 분석하였으며, 발효에 의한 다크 초콜릿의 향미 성분의 증가를 측정함으로써 고부가가치 다크 초콜릿 개발 가능성을 제시한다.

• 한국식품과학회지
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• 제32권3호
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• pp.507-512
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• 2000

고품질 둥굴레차의 제조를 위한 기반연구로서 solid-phase microextraction(SPME)을 이용한 headspace 방법에 의해 볶음 전 중자(steaming) 여부에 따른 둥굴레차의 향기성분 특성을 비교하였다. SPME fiber에 대한 향기성분의 흡착조건은 $60^{\circ}C$에서 30분이 적합하였고, 무중자 및 중자(120분)된 시료를 $130^{\circ}C$에서 15분간 볶음 처리하여 분석 GC chromatogram에서는 40여 종의 peak가 분리되었고, 전반적인 pattern은 유사하였으나 서로 상이한 peak특성이 관찰되었다. 분리된 성분들을 GC-MS와 retention time 비교에 의해 25종을 동정하였으며, 무중자 볶음처리 둥굴레는 2,3-dihydro-3,5-dihydroxy-6-methyl-4H-pyran-4-one, 2,5-di-methyl-4-hydroxy-3(2H)-furanone, 2-acetyl-1-pyrroline 등의 pyrazine류 함량이 중자 후 볶음 둥굴레보다 높게 나타나 둥굴레의 고유한 향과 맛에 큰 영향을 미칠 것으로 추정되었다. 특히 중자 후 볶음 처리한 둥굴레의 경우에는 acetic acid(8.17%)와 hexanoic acid(5.43%)의 함량이 무중자 시료(2.40%와 2.00%)보다 높게 나타났다.

• Preventive Nutrition and Food Science
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• 제13권1호
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• pp.54-59
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• 2008

This study was conducted to investigate the effect of pH on the formation of furfural compounds from glucose and fructose reacting with amino acid enantiomers in the Maillard reaction. Hydroxymethylfurfural (HMF) content was highest at pH 4.0, and decreased with increasing pH. HMF was significantly higher in glucose-based systems than fructose-based systems. Furfuryl alcohol (FFA) and 5-methyl-2-furaldehyde (MF) were not increased with increasing pH, and only small amounts were formed. In addition, 2-furaldehyde (F) was found to increase in the systems, as pH increased. However, the content was small and variable. 2,5-Dimethyl-4-hydroxy-3(2H)-furanone (DMHF) was only found in Glc/D-Asn, Glc/L-Lys and Fru/D-Lys system, but the content was not increased with increasing pH. 2-acetylfuran (AF) was higher in Glc (or Fru)/L-Lys and Glc (or Fru)/D-Lys systems at pH 7.0. However, at pH 4.0, the content of AF was higher in the Glc (or Fru)/Gly and Glc (or Fru)/L-Asn systems. Therefore, this study aimed to observe the effect of pH, sugars and amino acid enantiomers on the production of furfural and related compounds by the Maillard reaction. A clear tendency was observed for some classes of compounds to be more easily formed at higher or lower pH. HMF was more readily formed at lower pH, while FFA, F, DMHF and MF were inhibited by acidic conditions. Particularly, compounds like FFA, F and MF were not affected by pH changes. In addition, DMHF and MF were only formed in L-Lys and D-Lys system.

• Journal of Microbiology and Biotechnology
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• 제16권3호
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• pp.349-354
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• 2006

Furaneol, a key aroma compound found in strawberry, pineapple, and processed foodstuffs, has been known to possess various biological activities on animal models. In this study, the antimicrobial effects of furaneol against human pathogenic microorganisms were investigated. The results indicated that furaneol displayed a broad spectrum of antimicrobial activities against Gram-positive and Gram-negative bacteria and fungi without hemolytic activity on human erythrocyte cells. To confirm the antifungal activity of furaneol, we examined the accumulation of intracellular trehalose as a stress response marker on toxic agents and its effect on dimorphic transition of Candida albicans. The results demonstrated that furaneol induced significant accumulation of intracellular trehalose and exerted its antifungal effect by disrupting serum-induced mycelial forms. These results suggest that furaneol could be a therapeutic agent having a broad spectrum of antimicrobial activity on human pathogenic microorganisms.