• Title/Summary/Keyword: S-transferase

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The Effect of Ginseng on the Hepatic Glutathione S-Transferase Activity (인삼이 간 Glutathione S-Transferase 활성에 미치는 효과)

  • 김낙두;김승희;김신근
    • YAKHAK HOEJI
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    • v.25 no.4
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    • pp.153-160
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    • 1981
  • The investigation aimed to study the effect of ginseng on the hepatic glutathion S-transferase activity. The ginseng methanol extract was administered to rats and mice for 10 days and their hepatic gluthatione S-transferase activities were measured by the method of Habig et al. Glutathione S-transferase activities in the rat treated with 100 and 500mg/kg ginseng methanol extract were increased by 13.4% and 17.10%, respectively and their increases were statistically significant. Similar results were also found in the mouse treated with ginseng 100mg/kg methanol extract. To investigate components of the extract which induce the enzyme, the methanol extract was fractionated into ether and butanol fraction and their effect on the enzyme was compared. Glutathione S-transferase activities in the rat treated with ether fraction were increased by 13.1%, similar to that obtained with ginseng methanol extract, whereas, butanol fraction did not show any increase in the enzyme activities. In the rats treated with maltol, one of the components in ether fraction, 5mg/kg for 10 days, activity of glutathione S-transferase was increased by 7.89%, but its increase was not significantly different from control group. Therefore, it may be concluded that ginseng methanol extract and its ether soluble fraction had effect on the elevation of glutathione S-transferase activities, whereas, butanol fraction of ginseng methanol extract had no effect on the enzyme.

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Effect of Garlic on the Hepatic Glutathione S-Transferase and Glutathione Peroxidase Activity in Rat - garlic effect on the glutathione S- transferase and glutathione peroxidase

  • Huh, Keun;Park, Jong-Min;Lee, Sang-Il
    • Archives of Pharmacal Research
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    • v.8 no.4
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    • pp.197-203
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    • 1985
  • It was attempted to observe the effect of garlic on the hepatic glutathione s-transferase and glutathione peroxidase activity in this study. Glutathione s-transferase (EC 2.5.1.18) are thought to play a physiological role in initiating the detoxication of potential alkylating agents, inclnding pharmacologically active compounds. Glutathione peroxidase (EC 1. 11. 1. 9) might play an important role in the protection of cellular structures against oxidative challenge. The activities of glutathione s-transferase and glutathione peroxidase in rat liver were increased by the treatment of garlic juice. Allicin fraction, heat-treated allicin fraction and garlic butanol fraction markedly inhibited glutathione s-transferase activity in vitro, whereas glutathione peroxidase activity was significantly increased in heat-treated allicin fraction and garlic butanol fraction.

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Effect of Diallyl Disulfide on the Hepatic Glutathione S-Transferase Activity in Rat : Diallyl Disulfide Effect on the Glutathione S-Transferase

  • Huh, Keun;Lee, Sang-Il;Park, Jong-Min;Kim, Seok-Hwan
    • Archives of Pharmacal Research
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    • v.9 no.4
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    • pp.205-209
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    • 1986
  • Glutathione s-transferase in thought to play a key role in initiating the detoxication of potential alkylating agents, including pharmacologically active compounds. It is widely accepted that garlic contained allin which is converted to allicin by allinase. Allicin is easily degraded to diallyl disulfide and other components. This report attempted to observe the effect of diallyl disulfide on some biological activities. It was observed that the activity of serum transaminase was not changed by the treatment of diallyl disulfide. The liver cytosolic glutathione s-transferase was significantly increased. where as the microsomal glutathione s-transferase was not increased.

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Serum Ornithine Carbamyl Transferase Activity in Korean (한국인(韓國人) 혈청(血淸) Ornithine Carbamyl Transferase 활성(活性)에 관(關)한 연구(硏究))

  • Tchai, B.S.
    • Journal of Nutrition and Health
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    • v.8 no.2
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    • pp.15-18
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    • 1975
  • In man, ornithine carbamyl transferase is localized mainly in the liver and to a lesser extent in the smll intestine. Because of these findings, one might expect damage only to the liver or perhaps the small intestine to cause elevated ornithine carbamyl transferase activity in serum $(_S-OCT)$. Serum ornithine carbamyl transferase activity was determined in thirty normal subjects, and fifteen patients with viral hepatitis and fifteen patients with liver cirrhosis. The correlation of $_S-OCT$ with $_S-GPT$ and $_S-GOT$ was studied. The mean $_S-OCT$ activity in thirty normal Korean subjects was $0.094{\pm}0.043$I.U./L of serum. Elevated $_S-OCT$ activity was observed in patients with liver disease. The correlation coefficient was 0.18 for $_S-OCT$ and $_S-GPT$, ana 0.40 for $_S-OCT$ and $_S-GOT$.

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Catalase, Glutathione S-Transferase and Thioltransferase Respond Differently to Oxidative Stress in Schizosaccharomyces pombe

  • Cho, Young-Wook;Park, Eun-Hee;Lim, Chang-Jin
    • BMB Reports
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    • v.33 no.4
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    • pp.344-348
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    • 2000
  • The logarithmically growing Schizosaccharomyces pombe cells were subjected to high heat ($40^{\circ}C$), hydrogen peroxide, and heavy metals such as mercuric chloride and cadmium chloride. Then, the stress responses of catalase, glutathione S-transferase and thioltransferase were investigated. The high heat and cadmium chloride enhanced the catalase activity. The glutathione S-transferase activity of S. pombe cells was increased after treatments with heavy metals. The thioltransferase activity of S. pombe cells was completely abolished by mercuric chloride. Hydrogen peroxide caused no effect on the activities of glutathione S-transferase and thioltransferase. These results suggest that the response of S. pombe cells against oxidative stress is very complicated.

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Isolation of Gglutatihone S-Ttransferase(ClGST) Gene from Codonopsis lanceolata (더덕에서 Glutathione S-transferase (ClGST) 유전자의 분리)

  • Kim Jin-Ju;Yang Deok-Chun
    • Korean Journal of Plant Resources
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    • v.18 no.2
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    • pp.240-245
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    • 2005
  • A cDNA clone homologous to glutathione S-transferase gene was isolated and characterized from Codonopsis lanceolata(ClGST). The ClGST is 761 nucleotides long and has an open reading frame of 522 bp with a deduced amino acid sequence of 173 residues. The ClGST shows meaning homology to A. thaliana(AAC63629) $71\%$, C. chinense(CAI51314) $73\%$, E. esula(AAE65767) $75\%$, H. muticus(CAA55039) $70\%$, N. plumbaginifolia(CAA96431) $77\%$, S. commersonii(AAB65163).

Effect of Erythritol on Glucosyl Transferase and Fructosyl Transferase Gene Expression in Streptococcus mutans (Streptococcus mutans의 Glucosyl Transferase와 Fructosyl Transferase 유전자 발현에 대한 Erythritol의 효과)

  • Young-Nam PARK;Jae-Ki RYU
    • Korean Journal of Clinical Laboratory Science
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    • v.55 no.3
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    • pp.151-158
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    • 2023
  • Erythritol is a sweetener produced by yeast from glucose and a natural sugar found in fermented foods such as mushrooms, wine, fruits, rice wine, and soy sauce. Correct information and basic data when producing or using products for preventing dental caries by checking the gene expression patterns of glucosyl transferase (GTF) and fructosyl transferase (FTF) of Streptococcus mutans in erythritol and other sweeteners it was implemented to provide. Erythritol inhibited the growth of Streptococcus mutans, which is involved in dental caries. When used as a sweetener to replace sucrose, erythritol had an excellent caries-preventative effect. In particular, erythritol reduced the expressions of gtfB, gtfC, gtfD, and FTF, which are related to the synthesis of extracellular polysaccharides, and thereby reduced the formation of dental plaque and the attachment rate of bacteria to tooth surfaces. The study shows erythritol has potential use as an anticariogenic sweetener that inhibits the mechanism underlying caries caused by Streptococci.

Effect of Sophorae Flos Aqua-acupuncture Solution on the Quinone Reductase and Glutathione S-transferase Activities of Hepa 1c1c7 Cells (괴화약침액이 간세포의 Quinone redutase 와 Glutathione S-transferase 활성에 미치는 영향)

  • Lee Ki-Taek;Lim Jong-Kook
    • Korean Journal of Acupuncture
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    • v.20 no.1
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    • pp.39-43
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    • 2003
  • Sophorae Flos aqua-acupuncture solution(SFAS) was prepared and tested for the induction of quinone reductase and glutathione S-transferase activities and glutathione. SFAS significantly induced QR activity at the concentrations of $0.5{\times},\;1{\times}\;and\;3{\times}$ in cell culture. However, GST activity in murine Hepa 1c1c7 cells was slightly increased with SFAS. SFAS increased GSH levels.

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Activity of Glutathione S-transferase and Effect of Alcohol Decomposition on the Fruit of Hovenia dulcis Thunb (지구자의 Glutathione S-transferase 활성과 알코올 분해효과)

  • Cha, Bae-Cheon;Lee, Eun-Hee;Lee, Eun;Park, Hang-Ho
    • YAKHAK HOEJI
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    • v.48 no.3
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    • pp.213-217
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    • 2004
  • For the determination of glutathione S-transferase activity, a new method was established by using HPLC system. Moreover, amount of enzyme for a optimum reaction was determined by a comparative study with a variety concentration of enzyme. Using a established method, activity of glutathione S-transferase that is alcohol metabolizing enzyme was investigated on the fruit of Hovenia dulcis Thunb. As the result of experiment, EtOH and $H_2O$ extracts of the fruit of Hovenia dulcis Thunb showed visible a synergistic effect of glutathione S-transferase activity. On a continuous experiment, EtOH and $H_2O$ extracts of the fruit of Hovenia dulcis Thunb showed alcohol decomposition activity on the in vivo test using rat. These results suggest that the fruit of Hovenia dulcis Thunb may be useful in the prevention of hangover.

Nucleotide Sequence and Homology Analysis of phnC Gene Encoding Glutathione S-transferase from Pseudomonas sp.DJ77 (Pseudomonas sp. DJ77에서 Glutathione S-transferase를 암호하는 phnC 유전자의 염기서열과 상동성 분석)

  • 우희종;신명수;김성재;정용제;정안식;박광균;김영창
    • Korean Journal of Microbiology
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    • v.33 no.2
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    • pp.86-91
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    • 1997
  • Pseudomonas sp. DJ77로부터 클로닝된 glutathione S-transferase 유전자(phnC)의 염기서열을 결정하였다. 603bp의 open reading frame(ORF)이 존재하였고 개시코돈 앞에서 Shine-Dalgarno sequence를, 종결코돈 뒤에서는 terminator sequence를 발견하였다. phnC 유전자에서 만들어지는 phnC 단백질은 21,416 Da으로 SDS-polyacrylamide gel 전기영동 결과와 일치하였다. PhnC는 Bulkholderia cepacia LB400, Cycloclasticus oligotrophus RB1의 GST와 각각 53.7%, 49%의 높은 상동성을 나타냈다. 아미노산 서열의 상동성과 필수잔기들의 존재유무로 판단할 때 PhnC GST는 theta class GSTs와 진화적으로 유연관계가 높았지만 alpha, mu, pi, sigma class GSTs에서 구조적, 기능적으로 중요하다고 알려진 아미노산 잔기들이 PhnC GST에도 보존되어 있었다. 또한, phnC 유전자의 위치가 C. oligotrophus RB1, B. cepacia LB400 등의 GST 유전자 위치와 유사하다는 점에서 PhnC 효소는 난분해성 방향족 탄화수소의 분해에 관여하는 것으로 생각된다.

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