• 제목/요약/키워드: Maillard

검색결과 233건 처리시간 0.029초

Effects of Searing Cooking on Sensory and Physicochemical Properties of Beef Steak

  • Yoo, Ji Hyun;Kim, Ji Won;Yong, Hae In;Baek, Ki Ho;Lee, Hyun Jung;Jo, Cheorun
    • 한국축산식품학회지
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    • 제40권1호
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    • pp.44-54
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    • 2020
  • The purpose of the present study was to evaluate the sensory and instrumental quality of thawed beef steak prepared by searing and oven cooking. Beef purchased in the local market was divided into two groups; one group was cooked in a 180℃ oven until the internal temperature reached 60℃, and the other group was oven cooked until 35℃, then cooked in a 250℃ pan until the internal temperature reached 60℃. Despite a noticeable change in appearance due to the high temperature of the searing, there was no significant difference in juiciness, water content, and cooking loss between the searing-cooked and the oven-cooked steaks. However, in searing cooking, both scores of overall flavor and roast meat flavor were significantly higher than those of oven cooking. In the searing-cooked steak, the reducing sugar, which is a reactant of the Maillard reaction, was lower and Maillard-reaction products were higher than oven-cooked steak. From our results, it can be concluded that searing does not improve juiciness of the steak, but improves the flavor of beef steak due to higher levels of Maillard reaction products.

The Effect of pH on the Formation of Furfural Compounds in the Glucose and Fructose with Amino Acid Enantiomers in Maillard Reaction

  • Kim, Ji-Sang;Lee, Young-Soon
    • 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.

Chemical and Free Radical-scavenging Activity Changes of Ginsenoside Re by Maillard Reaction and Its Possible Use as a Renoprotective Agent

  • Yamabe, Noriko;Song, Kyung-Il;Lee, Woo-Jung;Han, Im-Ho;Lee, Ji-Hwan;Ham, Jung-Yeob;Kim, Su-Nam;Park, Jeong-Hill;Kang, Ki-Sung
    • Journal of Ginseng Research
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    • 제36권3호
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    • pp.256-262
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    • 2012
  • Reactive oxygen species play critical role in kidney damage. Free radical-scavenging activities of Panax ginseng are known to be increased by heat-processing. The structural change of ginsenoside and the generation of Maillard reaction products (MRPs) are closely related to the increased free radical-scavenging activities. In the present study, we have demonstrated the Maillard reaction model experiment using ginsenoside Re and glycine mixture to identify the renoprotective effect of MRPs from ginseng or ginsenosides. Ginsenoside Re was transformed into less-polar ginsenosides, namely Rg2, Rg6 and F4 by heat-processing. The free radical-scavenging activity of ginsenoside Re-glycine mixture was increased in a temperature-dependant manner by heatprocessing. The improved free radical-scavenging activity by heat-processing was mediated by the generation of antioxidant MRPs which led to the protection of LLC-PK1 renal epithelial cells from oxidative stress. Although the free radical scavenging activities of less-polar ginsenosides were weak, they could protect LLC-PK1 cells from oxidative stress. Therefore, MRPs and less-polar ginsenosides contributed to the combined renoprotective effects against oxidative renal damage.

Reaction Flavoring에 의한 진주조개 (Pinctada fucata) 추출물의 풍미개선 (Enhancing the Flavor of Pearl Oyster (Pinctada fucata) Extract Using Reaction Flavoring)

  • 강정구;남기호;강진영;황석민;김정균;오광수
    • 한국수산과학회지
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    • 제40권6호
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    • pp.350-355
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    • 2007
  • The optimal substrates and reaction flavoring conditions were examined to develop pearl oyster extract (POE) flavor using the Maillard reaction under a model system. The sugar for the Maillard reaction was glucose, and the amino acid was cysteine, with glycine as the reaction substrate. A three-dimensional response surface method was used to monitor the dynamic changes of the substrates during the Maillard reaction. To enhance the flavor of POE, a two-step enzymatic hydrolysate (Brix $20^{\circ}$) was reacted with the precursors (1:1, v/v). A 2:1:1 mixture of 0.4 M glucose:0.4 M glycine:0.4 M cysteine (v/v) was selected as a suitable reaction system for the reappearance of baked potato odor and boiled meat odor, and masking the shellfish odor. The two-step enzymatic hydrolysate and selected precursors were reacted in a high-pressure reactor to optimize the reaction parameters. The optimum conditions were 150 minutes at $120\;^{\circ}C$ and pH 7.0. The pH was the most critical factor for the response of the baked potato odor and masking the shellfish odor, while the reaction time affected the reappearance of the boiled meat odor.

Maillard 반응에서 유래되는 저분자 Carbonyl 화합물의 DNA손상작용에 대한 활성산소종의 역할 (Role of Active Oxygens on DNA Damage by Low Molecular Carbonyl Compounds Derived from Maillard Reaction)

  • 김선봉;박성준;강진훈;변한석;박영호
    • 한국식품영양과학회지
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    • 제19권6호
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    • pp.565-570
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    • 1990
  • Plasmid pBR322 DNA와 Maillard 반응생성물중 카르보닐화합물인 glyoxal, methyl glyoxal, dihydroxyacetone, diacetyl, glyceraldehyde, glycolaldehyde 및 furfural 등과 각각 37$^{\circ}C$에서 반응시켰을때 나타나는 DNA 손상능과 활성산소소거제에 의한 DNA손상억제 작용을 agarose gel 전기영동을 통하여 살펴보았다. 카르보닐화합물을 37$^{\circ}C$에서 6시간 동안 반응시켰을 경우, furfural을 제외한 모든 카르보닐화합물에 DNA 손상능이 나타났는데, 그 중에서도 glyoxal, methyl glyoxal 및 dihyd-roxyacetone 이 diacetyl, glyceraldehyde 및 glyco-laldehyde보다 BNA의 손상능이 크게 나타났다. 또한 plasmid DNA와 카르보닐화합물의 반응계에 각종 활성산소소거제의 첨가를 통하여 이들 카르보닐화합물에 대한 DNA의 손상을 검토한 결과 일중항산소, 과산화수소, superoxide anion 등이 주요원인물질로 밝혀졌으며, hydroxyl radical은 그 작용이 미약하거나 거의 영향을 나타내지 않는 것으로 나타났다.

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초음파 처리 키토산과 메일라드 반응액 혼합물에 의한 tyrosinase 억제 활성 및 항균력 분석 (Tyrosinase inhibitory activity and antimicrobial activity by mixtures of ultrasonicated chitosan and Maillard reaction products)

  • 김경자;양용준
    • 한국산학기술학회논문지
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    • 제11권7호
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    • pp.2522-2527
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    • 2010
  • 본 연구의 목적은 초음파 처리 키토산과 메일라드 반응액 혼합물에 의한 tyrosinase 억제 활성과 항균력을 조사하고자 하였다. 감자로부터 tyrosinase를 분리하여 SDS-PAGE후 일반 단백질 염색과 tyrosinase 활성 염색을 행하여 tyrosinase를 확인하였다. 여러 가지 당 (glucose, fructose, galactose, xylose, arabinose or ribose)과 cystein과의 반응으로 생성된 메일라드 반응 산물의 tyrosinase 억제 활성을 비교한 결과, glucose과 cystein 반응으로 생성된 메일라드 반응 산물의 tyrosinase 억제 활성이 가장 높은 것으로 나타났다. 0.5% 아세트산에 녹인 1% 키토산을 시간별로 초음파 처리한 후 항균력을 조사한 결과 1 시간 이상 초음파 처리한 경우 E. coli 균주 와 S. aureus 균주에서 억제 활성을 보였다. 갈변 억제 활성과 항균력을 가진 혼합물 제조를 위하여 초음파 처리 키토산과 메일라드 반응액을 혼합비를 달리하여 조사한 결과 부피 비로 1 : 1 로 혼합한 경우가 tyrosinase 억제 활성과 항균력이 가장 효과가 높은 것으로 조사되었다.

FT-IR and X-Ray Diffraction Characterization of Melanoidins Formed from Glucose and Fructose with Amino Acid Enantiomers in the Maillard Reaction

  • Kim, Ji-Sang;Lee, Young-Soon
    • Food Science and Biotechnology
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    • 제18권2호
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    • pp.546-551
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    • 2009
  • The objective of this study was to investigate Fourier transform infrared (FT-IR) spectrometry and the X-ray diffraction (XRD) characterization of melanoidins formed from glucose and fructose with amino acid enantiomers in the Maillard reaction. Before dialysis, FT-IR spectroscopy of all the samples showed that the characteristic absorption intensities appeared as a broad and intense band of the stretching vibration of the -OH group at 3,400/cm for a high pH. The absorption bands of the melanoidins sharply decreased in intensity after dialysis as compared to those before dialysis. In particular, the absorption bands at 992 and 575/cm disappeared. The XRD confirmed that the crystal structure of the melanoidins disappeared after dialysis and a new crystal structure was formed at 9 and $28^{\circ}$ ($2{\theta}$. In particular, broad diffraction peaks were formed in the $10-21^{\circ}$ ($2{\theta}$) range for a high pH, while other sharp diffraction peaks disappeared.

Development of Grilled-type Shrimp Flavor by Maillard Reaction and Sensory Evaluation

  • Kim, Myung-Chan;Oh, Jung-Hwan;Kim, Bong-Yeon;Cho, Sueng-Mock;Lee, Da-Sun;Nam, Min-Hee;Kim, Seon-Bong;Lee, Yang-Bong
    • Preventive Nutrition and Food Science
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    • 제15권4호
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    • pp.309-315
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    • 2010
  • A grilled-type shrimp flavor was developed through the Maillard reaction to reduce or mask fish odor or off-flavor in seafood. Model systems were created by using enzymatic hydrolysate of shrimp and adding precursors to increase flavor quality and stability. Amino acid precursors such as cysteine and methionine, sugar precursors such as glucose, xylose, ribose, and sucrose, and one particular compound of glucosamine were tried and their flavor qualities were tested by sensory evaluation. Also, the optimum reaction condition was investigated using the pH values of pH 5, 6, 7, and 8 with reaction times of 1 hr, 2 hr and 3 hr after the best precursors were determined. The best condition of the precursors for grilled-type shrimp flavor was the mixtures of methionine, threonine, xylose, and glucosamine. The optimum reaction condition was at pH 8.0 and 2 hr reaction time.