• Journal of Nutrition and Health
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• 제33권6호
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• pp.613-618
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• 2000

This study was to investigate the effect of dietary protein and fiber on the antioxidant enzyme activities of brain in acute or chronic ethanol-treated rats. Male Sprague-Dawley rats were fed on diets containing two levels of protein(7%, 20%) with two levels of fiber (5%, 10%) Rats were administered 40%(v/v) ethanol(5g/kg body weight)orally 90min before decaptiation in acute ethanol-treated groups and 25%(v/v) ethanol(5g/kg body weight) once a day for 5 weeks in chronic ethanol treated-groups. The rats were sacrificed after 5 weeks of feeding periods. Superoxide dismutase and gluthathione S-transferase activities were lower in chronic ethanol-treated groups than acute ethanol-treated groups whereas catalase and glutathuone peroxidase activities were significantly increased by chronic ethanol treatment. Low protein supplement accelerated to change of their activities however dietary fiber levels did not affect antioxidant enzyme activities. Chronic ethanol treatment and/or low protein supplement results in increasing the brain lipid peroxide content but in lowering glutathione level. (Korean J Nutrition 33(6) ; 613~618, 2000)

• Applied Biological Chemistry
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• 제42권2호
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• pp.162-165
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• 1999

Spraque-Dawley계 수컷랫트에 단풍취로부터 분리한 화합물을 경구투여하고 혈청 ethanol농도와 간의 ADH 활성에 미치는 효과를 검토한 결과 알코올대사를 촉진시키는 성분은 apigenin $7-O-{\beta}-D-glucoside$로 확인되었다.

• 한국식품과학회지
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• 제37권5호
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• pp.833-837
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• 2005

송화분, 참나무화분 및 백합화분에 대한 항산화 효능을 DPPH radical 소거능 및 동물조직의 지질산화 억제효능을 이용하여 평가하였다. 각 화분을 ethanol, 50% ethanol 및 물을 이용하여 추출물을 조제한 후 이들에 대한 DPPH radical 소거능을 분석한 결과 50% 소거능을 나타내는 $EC_{50}$ 값은, 송화분의 경우 50% ethanol 추출물(40.0mg/mL)이 가장 낮게 나타났으며 물 추출물(46.8mg/mL), 100% ethanol 추출물(131.2mg/mL) 순 이었다. 참나무화분에서는 50% ethanol 추출물(3.2mg/mL), 100%, ethanol 추출물(4.5mg/mL), 물 추출물(8.3mg/mL) 순이었고 백합화분에서는 100% ethanol 추출물의 $EC_{50}$값이 14.0mg/mL로, 50% ethanol 추출물(24.0mg/mL) 및 물 추출물(18.8mg/mL)에 비해 가장 낮았다. 3 종의 화분에서는 참나무 화분의 DPPH radical 소거능이 우수한 것으로 나타났다. 한편 $ascorbate-Fe^{3+}-EDTA$에 의해 유도되는 뇌조직에서의 지질산화도는 송화분, 참나무화분, 백합화분 추출물에 의해 모두 농도 의존적으로 억제되었으며 신장에서의 지질산화도 억제되었다. 그리고 이 중에서 송화분보다는 참나무와 백합화분의 효능이 우수한 것으로 나타났다. 화분 추출물에 대한 총 polyphenol의 함량을 분석한 결과 참나무화분$(32.5{\pm}2.9{\mu}g/mg\;pollen)$이 백합화분$(25.9{\pm}1.4{\mu}g/mg\;pollen)$이나 송화분$(9.3{\pm}0.7{\mu}g/mg\;pollen)$보다 높게 나타났다.

• KSBB Journal
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• 제4권1호
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• pp.11-14
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• 1989

Tower fermentor를 이용한 연속 알콜발효에서 cell re-cycle과 aeration에 대한 영향을 검토하였다. 균주는 floc-culationg 효모인 Saccharomyces cerecisiae TS4를 를 사용하였다. 15% glucose를 사용한 cell recycle system의 연속 알콜발효에서 cell 농도는 50%/1였고, ethanol productiv는 26.4g EtOH/l-hr로서 cell농도가 가장 높은 값을 나타내었으며, aeration rate는 3.8$\times$ $10^-^3$ VVM이상부터는 ethanol pro-ductivity가 감소하였다.

• 한국미생물·생명공학회지
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• 제19권4호
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• pp.398-404
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• 1991

효모를 Na-alginate에 고정화한 후 연속반응기를 이용한 glucose 발효로 에탄올을 생산하였다. 그 결과 고정화 효모의 활성화 시간은 20~25시간이었다. 연속발효에서 고정화효모의 온도안정성은 30~$37^{\circ}C$였으며 pH 안정성은 pH 4.0~pH 8.0, 최적 희석속도는 $0.2h^[-1}$ 이었고 에탄올생산 최적 당농도는 15%였다. 최적조건에서 에탄올수율은 0.23, 생산된 에탄올 농도는 33.90g/l 그리고 에탄올 생산성은 7.12g/$l\cdot h$로 각각 나타났다.

• 약학회지
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• 제51권5호
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• pp.343-349
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• 2007

To investigate the effect of ethanol extract of Saxifraga stolonifera MEERBURGH on skin care, we measured anti-oxidant and anti-aging activity. S. stolonifera ethanol extract itself had anti-oxidant activity in a dose-dependent manner in DPPH radical scavenging. Silica dose-dependently increased the intracellular ROS generation in RAW 264.7 cells. S. stolonifera ethanol extract inhibited silica-induced intracellular superoxide anion generation, $H_2O_2$ and hydroperoxide generation in RAW 264.7 cells. S. stolonifera ethanol extract significantly inhibited both hyaluronidase and elastase activity, also significantly inhibited MMP-1(collagenase) activity as well. In NIH 3T3 fibroblast cells, S. stolonifera ethanol extract significantly increased collagen-like polymer synthesis, which suggesting the S. stolonifera ethanol extract might be used as hydration and anti-wrinkle agents. From the above results, it is suggested that the main ingredients of S. stolonifera ethanol extract play an important role in anti-oxidant and anti-aging activity.

• 신재생에너지
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• 제7권4호
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• pp.3-9
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• 2011

Optimization of initial total sugar concentration of sweet sorghum juice, aeration time and aeration rate on ethanol production was performed by response surface methodology (RSM). The optimum conditions for ethanol production from concentrated sweet sorghum juice were determined as follows: initial total sugar concentration, 21.2 Brix; aeration time, 7.66h; aeration rate, 1.22 vvm. At the optimum conditions, the maximum ethanol yield was predicted to be 91.65% by model prediction. Similarly, 92.98% of ethanol yield was obtained by verification experiment using optimum conditions after 48 h of fermentation. This result was in agreement with the model prediction.

• Journal of Microbiology and Biotechnology
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• 제7권1호
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• pp.62-67
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• 1997

To enhance the hyperproductive and low energy-consuming ethanol fermentation rate, the thermotolerant yeast S. cerevisiae RA-74-2 cells were immobilized. An efficient immobilization condition was proved to be $1.5{\%}$ (w/v) alginate solution, neutral pH and 20 h activation of beads. The fermentation characteristics and stability at various temperatures were examined as compared with free S. cerevisiae RA-74-2 cells. The immobilized cells had excellent fermentation rate at the range of pH 3-7 at 30-$42^{\circ}C$ in 15-$20{\%}$ glucose media. When the seed volume was adjusted to 0.12 (v/v) (6ml bead/50 ml medium), $11{\%}$ (w/v) ethanol was produced during the first 34 hand $12.15{\%}$ (w/v) ethanol [$95{\%}$ (w/v) of theoretical yield] during the first 60 h in $25{\%}$ glucose medium. In repetitive fermentation using a 2 litre fermentor, 5.79-$7.27{\%}$ (w/v) ethanol [76-$95{\%}$ (w/v) of theoretical yield] was produced during the 40-55 h in $15{\%}$ glucose media. These data suggested the fact that alginate beads of thermotolerant S. cerevisiae RA-74-2 cells would contribute to economic and hyperproductive ethanol fermentation at high temperature.

• International Journal of Advanced Culture Technology
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• 제7권3호
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• pp.10-24
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• 2019

This study aimed to investigate the effects and epidermis penetration system with polymer micelle of Red Pinus densiflora extract. In the antioxidant test, the total concentration of polyphenol compounds was determined to be $137.5163{\pm}7.70mg/g$ in ethanol extract, $133.956{\pm}1.57mg/g$ in hydrothermal extract. The DPPH radical scavenging effects were $95.29{\pm}0.15%$ in ethanol extract at 1,000 mg/L. Elastase inhibition rates were $100.00{\pm}2.85%$ in ethanol extract at 2,000 mg/L. The antimicrobial effect of the ethanol extraction was higher than that of hydrothermal extractions. In the epidermal permeability experiment, it was confirmed that the permeation of the polymer micelle containing the Red Pinus densiflora's ethanol extract and cell penetrating peptides was remarkable. Here, we confirmed that ethanol extract of Red Pinus densiflora displayed excellent the effects in antioxidant test and epidermis penetration system with polymer micelle. As a result, Red Pinus densiflora extract has potential to be used as a safe and natural cosmetic material in the future.

• Journal of Nutrition and Health
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• 제29권7호
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• pp.721-728
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• 1996

The level of oxidative tissue damage caused by free radicals generated from ethanol oxidation was determined in the myocardium of chronic ethanol fed-rats and the protective action of various radical scavenging enzymes was monitored, also. Adult male Sprague-Dawley rats were given ethanol in an amount of 36% of total calories via Lieber-DeCarli liquid diet for 6 weeks. Control group was pair-fed with the diet containing isocaloric amount of dextrin-maltose instead of ethanol. Chronic ethanol administration resulted in the increased amount of myocardial thiobarbituric acid reactive substance(TBARS), th parameter of lipid peroxidation, under our experimental condition. Chronic ethanol ingestion did not cause any change in activities of either glutathione peroxidase or glutathione reductase and glucose-6-phosphate dehydrogenase were decreased after ethanol treatment. Therefore, chronic ethanol administration seemed to cause considerble changes in cellular defense function against oxidative tissue damage in rat myocardium through glutathione utilizing system and radical generation system. However the ultimate net result of chronic ethanol inestion on the myocardium of rat was the oxidative tissue damage revealed by increased TBARS content.