• 한국식품조리과학회지
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• 제9권1호
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• pp.43-51
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• 1993

Buckwheat protein isolate was tested for the effects of pH, addition of sodium chloride and heat treatment on solubility, emulsion capacities, emulsion stability, surface hydrophobicity, foam capacities and foam stability. The solubility of buckwheat protein isolate was affected by pH and showed the lowest value at pH 4.5, the isoelectric point of buckwheat protein isolate. The solubility significantly as the pH value reached closer to either ends of the pH, i.e., pH 1.0 and 11.0. The effects of NaCl concentration on solubility were as follows; at pH 2.0, the solubility significantly decreased when NaCl was added; at pH 4.5, it increased above 0.6 M; at pH 7.0 it increased; and at pH 9.0 it decreased. The solubility increased above $80^{\circ}C$, at all pH ranges. The emulsion capacity was the lowest at pH 4.5. It significantly increased as the pH approached higher acidic or alkalic regions. At pH 2.0, when NaCl was added, the emulsion capacity decreased, but it increased at pH 4.5 and showed the maximum value at pH 7.0 and 9.0 with 0.6 M and 0.8 M NaCl concentrations. Upon heating, the emulsion capacity decreased at acidic pH's but was maximised at pH 7.0 and 9.0 on $60^{\circ}C$ heat treatment. The emulsion stability was the lowest at pH 4.5 but increased with heat treatment. At acidic pH, the emulsion stability increased with the increase in NaCl concentration but decreased at pH 7.0 and 9.0. Generally, at other pH ranges, the emulsion stability was decreased with increased heating temperature. The surface hydrophobicity showed the highest value at pH 2.0 and the lowest value at pH 11.0. As NaCl concentrationed, the surface hydrophobicity decreased at acidic pH. The NaCl concentration had no significant effects on surface hydrophobicity at pH 7.0, 9.0 except for the highest value observed at 0.8 M and 0.4 M. At all pH ranges, the surface hydrophobicity was increased, when the temperature increased. The foam capacity decreased, with increased in pH value. At acidic pH, the foam capacity was decreased with the increased in NaCl concentration. The highest value was observed upon adding 0.2 M or 0.4 M NaCl at pH 7.0 and 9.0. Heat treatments of $60^{\circ}C$ and $40^{\circ}C$ showed the highest foam capacity values at pH 2.0 and 4.5, respectively. At pH 7.0 and 9.0, the foam capacity decreased with the increased in temperature. The foam stability was not significantly related to different pH values. The addition of 0.4 M NaCl at pH 2.0, 7.0 and 9.0 showed the highest stability and the addition of 1.0 M at pH 4.5 showed the lowest. The higher the heating temperature, the lower the foam stability at pH 2.0 and 9.0. However, the foam stability increased at pH 4.5 and 7.0 before reaching $80^{\circ}C$.

• 한국식품영양과학회지
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• 제35권2호
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• pp.212-218
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• 2006

독화된 진주담치 (blue mussel, Mylilus edulis)를 pH 처리, 온도별 저장 그리고 가열에 의한 마비성 패류독의 독성과 독조성 특성 변화는 다음과 같다. pH 3으로 조절한 시료가 14.1 MU/g$(100\%)$으로 가장 높은 독성이 검출되었고, pH 5는 12.9 MU/g$(92.1\%)$, pH 7은 9.0 MU/g$(63.8\%)$으로 검출되었으나, 마비성 패류독은 독성이 불안정한 알칼리 조건인 pH 9에서는 3.6 Mu/g$(25.5\%)$, pH 10은 0.8 Mu/g$(5.7\%)$으로 독성 이 검출되었다. 저장기간 동안의 독성은 pH(3, 5, 7, 9) 그리고 온도(30, -5, $20^{\circ}C$)에서 5일$(19.9\~65.3\%)$까지 현저하게 감소하였으나, 5일 후부터 30일까지는 약간의 독성이 감소하였다. 그리고 더 높은 온도에서 저장에서는 독성이 더 빨리 감소하였다. 대부분의 성분인 C군(C1, C2)과 GTX1,2,3,4, STX 그리고 dcSTX으로 8개의 성분이 검출되었고, 8개의 독성분 중에서 GTX1,4, STX 그리고 dcSTX는 모든 가공 조건에서 독성이 감소함에 따라 제일 먼저 감소하였다. 독성이 기준 독성치(4 MU/g)보다 3배 이상이더라도 마쇄된 패류 육에 pH를 알칼리 (pH 7이상)로 처리하고, 10분의 가열에 의해 독성을 완전히 제거할 수 있었다.

• 한국수정란이식학회지
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• 제18권2호
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• pp.85-90
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• 2003

본 연구는 개 난소의 수송온도가 난자의 생존률에 미치는 영향과 체외성숙 배양시 성숙률에 미치는 영향에 대하여 검토하였다. 1. 개 난소를 4$^{\circ}C$와 38$^{\circ}C$에 저장 후 5시간 내로 연구실로 운반한 난소에서 채취한 난자를 체외배양 하여 생존율을 조사한 결과 체외배양 24시간째 13.2%(15/114), 77.8%(105/135)의 생존율을 보였으며, 48시간째는 0% (0/129), 72.9% (129/177) 의 생존율을 나타내어 38$^{\circ}C$에 수송한 난소에서 채취한 난자가 4$^{\circ}C$에 수송한 난소에서 채취한 난자보다 유의적으로 높은 생존율을 보였다. 2. 체외성숙 배양 24, 48, 96 시간 체외배양하여 핵 성숙율을 확인한 결과 MI∼MII까지의 성숙율이 8.3% (6/72), 8.9% (9/101), 9.5% (8/84)로 체외배양 시간을 96시간까지 연장하여도 성숙률이 증가하지 않았다.

• 대한화학회지
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• 제37권7호
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• pp.662-671
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• 1993

isonitrosomethylacetoacetate(H-IMAA)의 이민유도체를 리간드로하는 새로운 Ni(II) 및 Pd(II)착물, Ni(IMAA-NH)(IMAA-NH'), Ni(IMAA-NH)(IMAA-NR),$ Pd(IMAA-NH)_2$, 및 $Pd(IMAA-NR)_2(R=CH_3,\;n-C_3H_7,\;n-C_4H_9$, 또는 $CH_2C_6H_5)$을 합성하고, 이들 착물의 구조를 원소분석, 전자흡수분광법, 적외선흡수분광법, $^1H$ 및 $^{13}C$ 핵자기공명분광법으로 조사하였다. 여기서 H-IMAA-MH 및 H-IMAA-NR은 각각 isonitrosomethylacetoacetate imine 및 N-alkylisonitrosomethylacetoacetate imine 유도체를 나타낸다.

• 대한한의학회지
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• 제26권1호
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• pp.174-186
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• 2005

Objectives : The water extract of Samul-tang (SMT) has traditionally been used for treatment of ischemic heart and brain damage in oriental medicine. However, little is known about the mechanism by which the water extract of SMT rescues cells from these damages. Methods: This study was designed to investigate the protective mechanisms of SMT on oxidative stress-induced toxicity in H9c2 cardiomyoblast cells. Treatment with $H_2O_2$ markedly induced death of H9c2 cardiomyoblast cells in a dose-dependent manner. Results: The characteristics of H20z-induced death of H9c2 showed apparent apoptotic features such as DNA fragmentation and morphological change. However, SMT significantly reduced both H202-induced cell death and morphological change. The decrease of Bc-2 expression by High were inhibited by SMT. In addition, the increase of Bax expression was also inhibited by SMT. The cotreatment of SMT and $H_2O_2$ in H9c2 cells also induced the phosphorylation of ERK in a time-dependent manner. Moreover, PD98059, a specific inhibitor of ERK1/2 attenuated the protective effects of SMT on $H_2O_2-induced$ toxicity in H9c2 cardiomyoblast cells. These results suggest that both ERK1/2 signaling pathways play important roles in the protective effects of SMT on $H_2O_2-induced$ apoptotic death of H9c2 cells. Also, the expression profile of proteins in $H_2O_2$ cardiomyoblast cells were screened by using two-dimensional (2-D) gel electrophoresis. Among 300 spots resolved in 2-D gels, the comparison of control versus apoptosis cells revealed that signal intensity of 17 spots increased and 11 spots decreased. Conclusions: Taken together, this study suggests that the protectiw effects of the water extract of SMT against oxidative damages may be mediated by the modulation of Bc1-2 and Bax expression via the regulation of the ERK signaling pathway.

• The Korean Journal of Physiology and Pharmacology
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• 제26권5호
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• pp.325-333
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• 2022

Heart failure (HF) has become one of the severe public health problems. The detailed role of mitochondrial function in HF was still unclear. Benzoylaconine (BAC) is a traditional Chinese medicine, but its role in HF still needs to be explored. In this study, oxygen-glucose deprivation and reperfusion (OGD/R) was executed to mimic the injury of H9C2 cells in HF. The viability of H9C2 cells was assessed via MTT assay. OGD/R treatment markedly decreased the viability of H9C2 cells, but BAC treatment evidently increased the viability of OGD/R-treated H9C2 cells. The apoptosis of H9C2 was enhanced by OGD/R treatment but suppressed by BAC treatment. The mitochondrial membrane potential was evaluated via JC-1 assay. BAC improved the mitochondrial function and suppressed oxidative stress in OGD/R-treated H9C2 cells. Moreover, Western blot analysis revealed that the protein expression of p-AMPK and PGC-1α were reduced in OGD/R-treated H9C2 cells, which was reversed by BAC. Rescue assays indicated that AMPK attenuation reversed the BAC-mediated protective effect on OGD/R-treated cardiomyocytes. Moreover, BAC alleviated myocardial injury in vivo. In a word, BAC modulated the mitochondrial function in OGD/R-induced cardiomyocyte injury by activation of the AMPK/PGC-1 axis. The findings might provide support for the application of BAC in the treatment of HF.

• 대한화학회지
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• 제15권5호
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• pp.228-235
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• 1971

니트로벤젠 및 1,2,4-트리클로로벤젠에서의 n-브롬화부틸의 溶解度를 $19^{\circ},\;25^{\circ},\;40^{\circ}C$에서 브롬화갈륨이 있을때와 없을때에 각각 測定하여 보았다. 브롬화갈륨이 存在하지 않을때에 니트로벤젠에서의 n-브롬화부틸의 溶解度가 1,2,4-트리클로로벤젠 보다 더 큰점은 n-브롬화부틸과 니트로벤젠과의 相互作用이 1,2,4-트리클로로벤젠 보다 더 강하다는 것을 나타낸다. 브롬화갈륨이 存在할 때에는 溶液內에서 n-브롬화부틸과 브롬화갈륨의 1:1 complex, $n-C_4H_9Br{\cdot}GaBr_3$가 형성된다. 이 complex의 instability constant K를 計算하였다. $n-C_4H_9Br{\cdot}GaBr_3{\\rightleftharpoons}n-C_4H_9Br+\frac{1}{2}Ga_2Br_6$ 또한 이 complex의 解離에 대한 엔탈피, 자유에너지 및 엔트로피도 산출하였다.

• 한국식품과학회지
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• 제23권3호
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• pp.355-359
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• 1991

글루타민산 나트륨(MSG)의 열안정성을 조사하기 위하여 가열온도 및 pH를 변화시키면서 가열 중 MSG의 분해정도를 비교하였다. 가열온도와 pH의 범위는 각각 $100{\sim}120^{\circ},\;4{\sim}9C$로 하였고, MSG는 2% 용액으로 만들었으며 가열 중 잔류 MSG 농도를 HPLC로 측정하였다. 그 결과 pH 4와 $120^{\circ}C$의 3시간 가열로 약 73% MSG가 감소한 반면, $100^{\circ}C$에서의 3시간 가열은 12% 정도만이 감소함을 보였다. 가열온도와 pH에 따른 초기 MSG의 분해속도와 분해 속도상수{(%MSG/log(hrs)}를 비교한 결과 $110^{\circ}C$와 $120^{\circ}C$에서의 초기 분해속도는 pH 4가 가장 빨랐으며 분해 속도상수도 상당히 높은 값을 보였다. 분해가 가장 적었던 pH 범위는 $pH6{\sim}8$ 범위였다. 또한 가열온도에 영향을 가장 많이 받았던 pH 4와 pH 5의 MSG 열분해 속도상수와 1/T의 관계에서 계산된 활성화에너지는 각각 18.3 kcal/mole과 9.2 kcal/mole이었다.

• 한국결정학회지
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• 제11권1호
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• pp.46-51
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• 2000

The molecular structures of 2-SC₄H₃CH=NN(H)C/sub 6/H/sub 5/(C/sub 11/H/sub 10/N₂S) and (GaMe₂)₂(2-SC₄H₃CH=NNC/sub 6/H/sub 5/)₂(C/sub 26/H/sub 30/Ga₂N₄S₂) have been determined by X-ray diffraction. Crystallographic data for 2-SC₄H₃CH=NN(H)C/sub 6/H/sub 5/:orthorhombic space group P2₁2₁2₁, a=6.108(1)Å, b=7.593(1)Å, c=22.356(2)Å, V=1037.1(3)ų, Z=4, R=0.0613. Crystallographic data for (GaMe₂)₂(2-SC₄H₃CH=NNC/sub 6/H/sub 5/)₂:monoclinic space group P2₁/n, a=15.996(2) Å, c=9.879(3)Å, β=100.07.(2)°, V=2764.599)ų, Z=4, R=0.0503.

• 약학회지
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• 제45권2호
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• pp.180-189
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• 2001

We have reported that water-extracted Korean mistletoe (KM-110) had various biological activities such as antitumor and immunomodulatory activity, and the pectin fraction (KML-C) of the extract was one of major factors related to its biological functions. In this paper, we produced murine monoclonal antibody (mAb) against KML-C. The cAbs obtained were largely classified into two groups according to specificity to KML-C and ML-I, a pectin from European mistletoe. One group mAbs (9H7-D10 and 3C2-lH4) strongly reacted with KML-C, but not ML-I. In contrast, another group cAbs (8Bll-2C5, BE12-3E9 and 5E10-Fl) reacted with both KML-C and ML-1. The subisotypes of these mobs were shown to be IgGl (9H7-lD10, 3C2-lH4 and 8Bll-2C5) or IgM (8E12-3E9 and 5E10-Fl). To develop an assay system for determination of the amount of KML-C, we established the sandwich ELISA (enzyme-linked immunosorbent assay) method using these mAbs and horse radish peroxidase (HRP)-labelled cAbs. In various combinations of the cAbs for coated antibody and detection antibody, the sandwich ELISA quantitatively detected KML-C, showing the detection limit ranging from 7-5,000 ng/ml. Especially reproducibility (C.V) of the sandwich ELISA, in which 8E12-3E9 was used for coating antibody and 8Bll-2C5-HRP for detection antibody, was 4.59-5.83 in intra assay, and 3.9-9.4 in inter assay.