• 제목/요약/키워드: Ethanol1

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Pichia stipitis에 의한 Xylose 발효의 최적조건 결정 (Determination of Optimum Conditions for Xylose Fermentation by Pichia stipitis)

  • 권순효;유연우서진호
    • KSBB Journal
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    • 제8권5호
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    • pp.452-456
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    • 1993
  • Pichia stipitis CBS 5776에 의한 xylose의 최적 알코올 발효조건에 대한 연구를 수행하였다. 최적 세포성장 및 최대 ethanol 생성은 초가 pH가 5.0인 100 g/l 의 xylose배지를 이용하여 $30^{\circ}C$에서 0.05VVM으로 통기하고 300rpm으로 교반하는 발효 조건에셔 얻을 수 있었다. 이러한 최적 발효조건 서의 최대 비성장속도와 최대 세포농도는 각각 $0.14hr^{-1}$$1.3\times109$ cells/ml이였다. 또한 최대 etha­n nol 농도는 72시간 발효시에 100 g/l 의 xylose 중 에셔 96%을 이용하여 40.2 g/l 을 얻었으며, 이때 의 단위부피당 ethanol 생산성은 0.56 g/l-hr이고 ethanol 수율은 0.42g-ethanol/g-xylose로서 이론수율의 82%였다.

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쑥추출물이 혈중 에탄올 농도와 간기능에 미치는 효과 (The Effects of Extracts from Mugwort on the Blood Ethanol Concentration and Liver Function)

  • 김민준;이치호
    • 한국축산식품학회지
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    • 제18권4호
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    • pp.348-357
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    • 1998
  • This study was conducted to investigate the effects of mugwort extracts on the blood ethanol concentration and liver function in rats. Sprague-Dawley rats were used, the rats administered with 25% ethanol (5g/kg$.$B.W.) were devided into three groups (CON-E ; 25% ethanol administered to the CON-E) according to the administered ethanol concentration and the levels of administered mugwonts. Mugwont roots extracts were administered via the caudal vein. Ethanol concentration was measured at the time of 0, 1, 2 and 3hr by gas chromatography. GOT(Glutamic Oxaloacetic Transaminase) and GPT(Glutamic Pyruvic Transaminase) were measured at the time of 0 and 5hr. Components of each extracts were analyzed by using high performance liquid chromatography. Cell number, GOT and GPT were investigated by using rat hepatocyte culture. Megwort extracts were added at the levels of 1% or 2%. Hepatocyte culture were into five groups according to the addition levels. The results were summarized as follows ; 1. Catechin contents of 8∼10mg/100g and the contents of (-)-epigallocatechin was high in the water extracts. 2. Ethanol degradation efficiency declines in the following order : MDW-E>MOH-E>CON-E. 3. The numbers of rat hepatocytes declines in the following order : 2% MDW-L>1%MDW-L>1%MOH-L>CON-L>2%MOH-L. These results suggest that crude catechin of mugwort extracts may play important roles to degrade ethanol and recover liver function in rats.

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물김치 서식 미생물, Lactobacillus plantarum, Leuconostoc mesenteroides, Kluyveromyces marxianus 생육에 Ethanol과 유기산이 미치는 영향 (Effect of Ethanol and/or Organic Acids on the Growth of Lactobacillus plantarum, Leuconostoc mesenteroides, Kluyveromyces marxianus Identified from Mul-kimchi)

  • 한영숙
    • 동아시아식생활학회지
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    • 제13권5호
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    • pp.425-432
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    • 2003
  • 본 연구에서는 ethanol 과 일부 유기산(adipic acid, citric acid, acetic acid)을 첨가하였을 때 물김치 발효에 관여하는 미생물 생육의 변화를 측정하였으며 그 결과를 요약하면 다음과 같다. Ethanol 및 유기산의 첨가가 물김치 서식 미생물에 미치는 영향을 직접적으로 살펴보기 위하여 pH 4.3 의 buffer 용액에 ethanol 과 유기산을 농도별로 첨가하고 Lactobacillus plantarum, Leuconostoc mesenteroides, Kluyveromyces marxianus을 접종하여 균의 생육에 미치는 영향을 살펴 본 결과 L. plantarum 와 Leu. mesenteroides에서는 ethanol 농도가 높을수록 그리고 유기산 종류에서는 adipic acid를 첨가했을 때 성장 억제 효과가 가장 크게 나타났다. 비교 균주에서는 L. plantarum이 Leu. mesenteroides보다 유기산과 에탄올에 영향을 받아 생육이 더욱 억제되었다. Ethanol에 대해서는 L. plantarum이 Leu. mesenteroides보다 숙성 72 시간째에 40.0% 정도 생육이 억제되었으나 유기산의 경우에는 종류에 따라 생육억제 정도가 달랐다. Acetic acid의 경우 L. plantarumol 약 40.0% 정도, citric acid의 경우는 L. plantarum이 약 15.0% 정도 생육이 억제되었지만 adipic acid의 경우는 L. plantarum 와 Leu. mesenteroides 모두에게 억제 효과가 있어 무첨가군에 비해 50.0∼60.0% 정도 생육이 감소되었다. K. marxianus에서도 ethanol 농도가 높을수록 성장 억제에 효과적이나 유기산에 대해서는 차이를 보이지 않았다. Ethanol 및 유기산이 각 균에 어떠한 영향을 주었는가을 알기 위해 균체내 물질의 누출을 260nm에서의 흡광도를 측정하여 관찰한 결과 L. plantarum 에서는 ethanol 2.0% 첨가 에서와 adipic acid 0.1 를 첨가한 실험군에서 24 시간 후의 흡광도가 가장 많이 증가되었다. Leu. mesenteroides에서는 ethanol 첨가시 유의적인 차이가 보이지 않았고 유기산 중 adipic acid 첨가시 흡광도가 많이 증가되었다. K. marxianus 에서는 ethanol 농도가 높을수록 흡광도가 증가되었고 유기산 중 citric acid 에서 많이 증가되었다.

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Effects of feeding ethanol on growth performances, carcass characteristics, and lipid metabolism of finishing Korean cattle (Hanwoo) steers

  • Choi, Chang Bon;Kwon, Hana;Hwang, Kyung Hyun;Lee, Hyun-Jeong;Kim, Jong Yeon
    • Asian-Australasian Journal of Animal Sciences
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    • 제32권3호
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    • pp.366-374
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    • 2019
  • Objective: The purpose of this study was to determine the effects of feeding ethanol on growth performances, carcass characteristics, and lipid metabolism of finishing Korean cattle (Hanwoo) steers. Methods: Thirty (30) Hanwoo steers (average 25.1 months of age, body weight 660.1 kg) were assigned to three treatments: control (0% ethanol), E-3 (1.44% ethanol for 3 months), or E-5 (0.72% ethanol for 2 months followed by 1.44% ethanol for 3 months). The animals were allotted by treatment group into six pens and fed concentrate and perennial ryegrass. Ethanol (30%, v/v) was supplemented into drinking water twice a day to meet final concentrations based on average water consumption of finishing Hanwoo steers. Results: There were no statistical differences among the groups in final body weight, average daily gain, or carcass yield grade indices such as cold carcass weight, fat thickness, and loin area. The marbling score tended (p = 0.228) to increase with the highest score (6.7) in the E-5 group followed by 6.3 and 6.0 in E-3 and control groups, respectively. The appearance frequencies of quality grades of $1^{{+}{+}}$ (the best), $1^{+}$, 1, and 2, were; 30%, 50%, 0%, and 20% for control, 10%, 80%, 10%, and 0% for E-3, and 10%, 80%, 0%, and 10% for E-5 groups, respectively, indicating improvements of quality grades by feeding ethanol. Concentrations of serum glucose tended to decrease whereas those of insulin and non-esterified fatty acid to increase by feeding ethanol (E-3 and E-5; p>0.05). Conclusion: Feeding ethanol directly into drinking water of finishing Hanwoo steers stimulated lipogenesis in intramuscular adipose tissue (marbling) and thereby improved carcass quality grade. The serum metabolites results supported the hypothesis of lipolysis of existing adipose tissue, such as abdominal fats, and lipogenesis in intramuscular adipocytes.

상기생이 ethanol을 장기 투여한 흰쥐의 골 대사에 미치는 영향 (Effects of Taxilli Ramulus Extract on Bone Metabolism of Ethanol Treated Rats)

  • 정주화;정지천
    • 대한한의학회지
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    • 제22권4호
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    • pp.1-9
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    • 2001
  • Objectives : To investigate the effect of Taxilli Ramulus (TR) extract on bone metabolism of ethanol-treated animal model. Methods : The changes of serum calcium, calcitonin, estrogen level, a1ka1ine phosphatase activity, osteocalcin, parathyroid hormone content and urine calcium level were observed with ethanol treatment for 60 days. The results were compared with an ethanol- TR extract double treatment group. Results : We observed increment of serum osteocalcin, parathyroid hormone content, alkaline phosphatase activity and urine calcium level by chronic ethanol feed and they were recovered to near normal level with Taxilli Ramulus extract treatment. Weight gain, serum calcium level, calcitonin and estrogen content were remarkably reduced with ethanol treatment and their levels were normalized by Taxilli Ramulus extract. Conclusions : These results showed that Taxilli Ramulus extract have the ability to recover to normal in the body an abnormal calcium metabolism process due to external factors. These results suggested that Taxilli Ramulus extract have preventive effects on calcium concentration loss and osteoporosis.

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Ethanol-induced Activiationof Transcription Factor NF-$\kappa$B and AP-1 in C6 Glial Cells

  • Park, Jae -Won;Shim, Young-Sup
    • Preventive Nutrition and Food Science
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    • 제4권3호
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    • pp.209-214
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    • 1999
  • In this study, the effectof ethanol and acetaldehyde on DNA binding activities of NF-$textsc{k}$B and AP-1 were evaluated in C6 rat glial cells. Both NF-$textsc{k}$B and AP-1 are important transcription factors for the expression of various cytokines in glial cells. Our data showed that neither ethanol nor acetaldehyde induced conspicuous cell death of C6 cells at clinically realistic concentrations. When the DNA binding activities of nuclear NF-$textsc{k}$B and AP-1 were estimated using electrophoretic mobility shift assay (EMSA), ethanol(0.3%) or acetaldehyde(1mM) induced transient activation of these transcription factors, which attained peak levels at 4~8 hours and declined to basal levels at 12 hours after treatement . The supershift analysis showed that the increased activities of NF-$textsc{k}$B in ethanol/acetaldehyde-treated C6 cells were due to the preferential induction of p65/p50 heterodimer complex. The DNA binding activities of these transcriptional factors decreased below basal levels when cells were cultured with either ethanol or acetaldehyde for 24 hours, and showed the inhibitory effect of chronic ehtanol /acetaldehyde treatment on the activities of these transsriptional factors. Our data indicate that either ethanol or acetaldehyde can induce functional changes of glial cells throught bi-directional modulation of NF-$textsc{k}$B and AP-1 DNA binding activities.

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Protective Effect of Isoliquiritigenin against Ethanol-Induced Hepatic Steatosis by Regulating the SIRT1-AMPK Pathway

  • Na, Ann-Yae;Yang, Eun-Ju;Jeon, Ju Mi;Ki, Sung Hwan;Song, Kyung-Sik;Lee, Sangkyu
    • Toxicological Research
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    • 제34권1호
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    • pp.23-29
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    • 2018
  • Ethanol-induced fat accumulation, the earliest and most common response of the liver to ethanol exposure, may be involved in the pathogenesis of liver diseases. Isoliquiritigenin (ISL), an important constituent of Glycyrrhizae Radix, is a chalcone derivative that exhibits antioxidant, anti-inflammatory, and phytoestrogenic activities. However, the effect of ISL treatment on lipid accumulation in hepatocytes and alcoholic hepatitis remains unclear. Therefore, we evaluated the effect and underlying mechanism of ISL on ethanol-induced hepatic steatosis by treating AML-12 cells with 200 mM ethanol and/or ISL ($0{\sim}50{\mu}M$) for 72 hr. Lipid accumulation was assayed by oil red O staining, and the expression of sirtuin1 (SIRT1), sterol regulatory element-binding protein-1c (SREBP-1c), AMP-activated protein kinase (AMPK), and peroxisome proliferator-activated receptor alpha ($PPAR{\alpha}$) was studied by western blotting. Our results indicated that ISL treatment upregulated SIRT1 expression and downregulated SREBP-1c expression in ethanol-treated cells. Similarly, oil red O staining revealed a decrease in ethanol-induced fat accumulation upon co-treatment of ethanol-treated cells with 10, 20, and $50{\mu}M$ of ISL. These findings suggest that ISL can reduce ethanol induced-hepatic lipogenesis by activating the SIRT1-AMPK pathway and thus improve lipid metabolism in alcoholic fatty livers.

마우스에 있어서 Diethylstilbestrol의 면역독성에 미치는 홍삼 Ethanol 유출물의 영향 (The Effect of Red Ginseng Ethanol Extract on the Immunotoxicity of Diethylstilbestrol in ICR Mice)

  • 이덕행;안영근
    • Environmental Analysis Health and Toxicology
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    • 제6권1_2호
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    • pp.39-57
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    • 1991
  • The effect of red ginseng ethanol extract on the immunotoxicity of diethylstilbestrol (DES) was studied in ICR mice. ICR male mice were divided into S groups (10 mice/group), and red ginseng ethanol extract (50, 100 and 200 mg/kg body wt., respectively) and DES (1 mg/kg body wt.) were injected intraperitoneally (i.p.) to ICR mice once a day for 2 weeks. Mice were sensitized and challenged with sheep red blood cells (S-RBC). Immune response were evaluated by humoral immunity, cell-mediated immunity, non-specific immunity, and circulating leukocyte counts. The results of this study were summarized as followings: 1. The DES-treated control group as compared with normal group showed the tendency to decrease body weight rate and relative liver weight, decreased both humoral and cellular immune responses, phagocyte activity, and circulating leukocyte counts, but increased the natural killer (NK) cell activity. 2. Compared with the DES-treated control group, DES plus red ginseng ethanol extract-treated groups significantly decreased the body weight rate (P<0.01). Relative liver weight was significantly decreased in DES plus red ginseng ethanol extract (50mg/kg)-treated group (P<0.01), but significantly increased in DES plus red ginseng ethanol extract (100mg/kg)-treated group (P<0.01). Relative spleen and thymus weights were significantly enhanced in DES plus red ginseng ethanol extract (100 mg/kg)-treated group (P<0.01), but significantly decreased in DES plus red ginseng ethanol extract (200 mg/kg)-treated group (P<0.01). 3. Both humoral and cellular immune responses were significantly decreased in DES plus red ginseng ethanol extract-treated groups rather than in the DES-treated control group (P<0.01). Especially, it weakened the decrease in DES plus red ginseng ethanol extract (100 mg/kg)-treated group. 4. Phagocyte activity and circulating leukocyte counts were significantly decreased in DES plus red ginseng ethanol extract-treated groups rather than in the DES-treated control group (P<0.01). Especially, it weakened the decrease in DES plus red ginseng ethanol extract (100 mg/kg)-treated group. NK cell activity was significantly enhanced in DES plus red ginseng ethanol extract (100 mg/kg)-treated group (P<0.01), but significantly decreased in DES plus red ginseng ethanol extract (50 and 200 mg/kg)-treated groups (P<0.01).

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HepG2 세포에서 Ethanol, Glycerol, 4-Methylpyrazole 및 Isoniazid에 의한 Human CYP2E1 활성변화 (Differential Role of Ethanol, Glycerol, 4-Methylpyrazole and Isoniazid on Human CYP2E1 Activity in Intact HepG2 Cells)

  • 최달웅
    • Toxicological Research
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    • 제19권3호
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    • pp.235-240
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    • 2003
  • The modification of CYP2E1 activity is of considerable interest because of its role in the metabolic activation of a variety of toxic chemicals. In the present studies, the time-course of changes in human CYP2E1 activities was determined after treatment with ethanol, glycerol, 4-methylpyrazole or isoniazid using intact HepG2 cells transfected by human CYP2E1. Hydroxylation of chlorzoxazone was chosen for the measurement of CYP2E1 activity. CYP2E1 protein levels were increased upon cultivation of cells in the presence of ethanol, glycerol, 4-methylpyrazole or isoniazid for 24 hr. After 24 hr cultivation, ethanol or glycerol increased CYP2E1 activities, whereas 4-methylpyrazole or isoniazid inhibited. This different effect of the chemical inducers on CYP2E1 activi-ties persisted to subsequent 24 hr. Competitive inhibition study suggested that 4-methylpyrazole or isoniazid has stronger binding affinity to CYP2E1 than ethanol or glycerol. These results demonstrate that different binding affinity of the chemical inducers to the active site of CYP2E1 plays important role in determining real CYP2E1 activity in intact cells after treatment with the chemical inducers. Present study would be helpful in precise understanding of human CYP2E1-mediated toxicity.

폐압축보드를 이용한 바이오에탄올 생산 (Bioethanol Production by using Wasted MDF)

  • 강양래;황진식;배기한;조훈호;이은정;조영손;남기두
    • KSBB Journal
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    • 제31권1호
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    • pp.73-78
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    • 2016
  • The aim of this study attempted to verify the possibility of bioethanol production using wasted medium density fiberboard (wMDF). In order to produce bioethanol from wood cellulosic materials must be carried out the process of pretreatment, saccharification, fermentation and distillation. First, the wMDF was pretreated using sodium chlorite and pretreated wMDF was prepared to 8% slurry and then slurry was saccharified with the commercial enzyme (Cellic CTec3). The fermentable sugar and pH of saccharified substrate were about 5.5% glucose and 4.4, respectively. Herein we compared the results of ethanol yield according to the nutrients added or without addition to increase ethanol yield. Ethanol fermentation was finished in about 24 hours, but it was delayed in experimental group without nutrients. Ethanol content and fermentation ratio of the final fermented mash prepared by utilizing jar fermenter was 25.40 g/L and 86.64%, respectively. At this time, the maximum ethanol productivity was confirmed as 1.78 g/Lh (ethanol content 21.38 g/L, 12 h), and the overall ethanol productivity was 1.05 g/Lh (ethanol content 25.27 g/L, 24 h). Using fermented liquid we could produced bioethanol 95.37% by continuous distillator packed with copper element in laboratory scale. These results show that wMDF has a potential valuable for bioethanol production.