• 제목/요약/키워드: Sulfhydryl Group

검색결과 76건 처리시간 0.029초

토끼 적혈구막의 NaK ATPase의 활성도에 대한 aconite의 작용 (Action of Aconite on Sodium-Potassium Activated ATPase in Rabbit Red Cell Membrane)

  • 고일섭
    • The Korean Journal of Physiology
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    • 제10권1호
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    • pp.15-24
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    • 1976
  • The action of aconite on the sodium plus potassium activated ATPase activity in the rabbit red cell membrane has been investigated and the experiments were also designed to determine the mechanism of action of aconite on the ATPase activity. The following results were observed. 1. The activity of the NaK ATPase from red cell membrane is stimulated by aconite, and the concentration of aconite for maximal activity is about 80 mg%. The pH optimum for the aconite sensitive component is 8.0. 2. The activating effect of aconite on the ATPase, with a given concentration of sodium in the medium, is increased by raising the potassium concentration but activity ratio is decreased. 3. The activating effect of aconite on the ATPase, with a given concentration of potassium in the medium, is increased by raising the sodium concentration but activity ratio is decreased. 4. The action of aconite on the ATPase activity is inhibited by calcium ions and the effect of inhibition is increased by small amounts of calcium but decreased by larger amounts. 5. The activating effect of aconite on the ATPase was not related to the sulfhydryl group of cysteine, the amino group of lysine, the hydroxyl group of threonine or the imidazole group of histidine. 6. The action of aconite on the ATPase activity is due to carboxyl group of the enzyme of NaK ATPase.

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Saponin이 토끼 적혈구막의 $Na^{+}-K^{+}-ATPase$의 활성도에 미치는 영향 (Effect of Saponin on Sodium-Potassium activated ATPase in Rabbit Red Cell Membrane)

  • 강병남;고일섭
    • The Korean Journal of Physiology
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    • 제8권1호
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    • pp.67-76
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    • 1974
  • The effect of saponin on the sodium plus potassium activated ATPase activity was studied in the rabbit red cell ghosts and the experiments were also designed to determine the mechanism of action of saponin on the APTase activity. The following results were observed. 1. The ATPase activity of rabbit red cell ghosts is inhibited by low concentration of saponin but increased by high concentration. The activating effect of saponin on the $Na^{+}-K^{+}-ATPase$ activity is inhibited by ouabain but the stimulation of the $Mg^{++}-ATPase$ by high concentration of saponin is not inhibited by ouabain. 2. The activity ratio of $Na^{+}-K^{+}-ATPase$ by high concentration of saponin is decreased by raising the potassium concentration, and is increased by raising the sodium concentration. 3. The ATPase activity is increased by small amounts of calcium but inhibited by larger amounts. The activity ratio of the enzyme by saponin is decreased by raising the calcium concertration 4. The action on the ATPase activity was not related to the amino group of lysine, the hydroxyl group of threonine, the imidazole group of histidine, or the carboxyl group of aspartic acid. 5. The action of saponin on the ATPase activity is due to sulfhydryl group of the enzyme of $Na^{+}-K^{+}-ATPase$.

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Theobromine이 적혈구막의 NaK ATPase의 활성도에 대한 작용 (Action of Theobromine on Sodium-Potassium activated ATPase in Red Cell Membrane)

  • 고일섭
    • The Korean Journal of Physiology
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    • 제12권1_2호
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    • pp.25-34
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    • 1978
  • The action of theobromine on the sodium plus potassium activated ATPase activity In the rabbit red cell membrane has teen investigated and the experiments were also designed to determine the mechanism of action of theobromine on the ATPase activity. The following results were observed. 1. The activity of the NaK ATPase from red fell membrane is stimulated by theobromine, and the concentration of theobromine for maximal activity is about 3mM. 2. The activating effect of theobromine on the ATPase, with a given concentration of potassium in the medium, is increased by raising the sodium concentration but activity ratio is decreased. 3. The activating effect of theobromine on the ATPase, with a given concentration of sodium in the medium. is increased by the raising the potassium concentration but activity ratio is decreased. 4. The NaK ATPase activity is increased by small amounts of calcium but decreased by larger amounts. The activity of the enzyme by theobromine is increased by small amounts of calcium but decreased by larger amounts. 5. The activating effect of theobromine on the ATPase was not related to the hydroxyl group of threonine and imidazole group of histicline. 6. The activating effect of theobromine on the ATPase is due to sulfhydryl group, amino group and carboxyl group of the enzyme of NaK ATPase.

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Pilocarpine이 토끼 적혈구막의 NaK ATPase의 활성도에 대한 작용 (Action of Pilocarpine on Sodium-Potassium activated ATPase in Rabbit Red Cell Membrane)

  • 고일섭
    • The Korean Journal of Physiology
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    • 제11권1호
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    • pp.11-20
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    • 1977
  • The action of pilocarpine on the sodium plus potassium activated ATPase activity in the rabbit red cell membrane has been investigated and the experiments were also designed to determine the mechanism of action of pilocarpine on the ATPase activity. The following results were observed. 1. The activity of the NaK ATPase from red cell membrane is stimulated by pilocarpine, and the concentration of pilocarpine for maximal activity is about 3 mM. The pH optimum for the pilocarpine sensitive component is 8.0. 2. The activating effect of pilocarpine on the ATPase, with a given concentration of sodium .in the medium, is increased by raising the potassium concentration but activity ratio is decreased 3. The activating effect of pilocarpine on the ATPase, with a given concentration of Potassium in the medium, is increased by raising the sodium concentration but activity ratio is decreased 4. The NaK ATPase activity is increased by small amounts of calcium but decreased by 'larger amounts. The activity ratio of the enzyme by pilocarpine is decreased by small amounts .of calcium but decreased by larger amounts. 5. The activating effect of pilocarpine on the ATPase was not related to the sulfhydryl group of cysteine, the hydroxyl group of threonine or the imidazole group of histidine. 6. The activating effect of pilocarpine on the ATPase is due to amino group and carboxyl group of the enzyme of NaK ATPase

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Anthraquinone이 토끼 적혈주막의 NaK ATPase웨 활성도에 대한 작용 (Action of Anthraquinone on Sodium-Potassium activated -ATPase in Rabbit Red Cell Membrane-)

  • 고일섭
    • The Korean Journal of Physiology
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    • 제11권1호
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    • pp.1-9
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    • 1977
  • Action of anthraquinone on the sodium plus potassium activated ATPase activity in the rabbit red cell membrane has been investigated and the experiments were also designed to determine the mechanism of action of anthraquinone on the ATPase activity. The following results were obtained 1. The activity of the NaK ATPase from red cell membrane is inhibited by anthraquinone and the concentration of anthraquinone for maximal inhibition is about 5mM. 2. The ratio of inhibition of NaK ATPase by anthraquinone, with a giving concentration of sodium in the medium, is increased by raising the potassium concentration. 3. The ratio of inhibition of NaK ATPase by anthraquinone, with a given concentration of potassium in the medium, is increased by raising the sodium concentration. 4. The action of anthraquinone on the NaK ATPase activity is inhibited by calcium ions and the ratio of inhibition is increased by small amounts of calcium but almost constant by larger amounts. 5. The inhibitory action of anthraquinone on the NaK ATPase activity was not related to the amino group of lysine, the hydroxyl group of threonine or the imidazole group of histidine. 6. The inhibitory action of anthraquinone on the ATPase activity is due to sulfhydryl group or the carboxyl group of the enzyme of NaK ATPase.

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적혈구막의 NaK ATPase의 활성도에 대한 ascorbic acid의 작용 (Action of Ascorbic acid on Sodium-Potassium activated ATPase in Red Cell Membrane)

  • 고일섭
    • The Korean Journal of Physiology
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    • 제12권1_2호
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    • pp.15-23
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    • 1978
  • The action of ascorbic acid on the sodium Plus potassium activated ATPase activity in the rabbit red cell membrane has been investigated and the experiments were also designed to determine the mechanism of action if ascorbic acid on the ATPase activity The following results were observed. 1. The activity of the NaK ATPase from red cell membrane is stimulated by ascorbic acid and the concentration of ascorbic acid for maximal activity is about 8 mM. 2. The activating effect of ascorbic acid on the ATPase activaty, with a given concentration of sodium in the medium, is increased by raisins the potassium concentration but activity ratio is decreased. 3. The activating effect of ascorbic acid on the ATPase activity, with a given concentration of potassium in the medium, is increased by raising the sodium concentration but activity ratio is decreased. 4. The action of ascorbic acid on the ATPase activity is stimulated by calcium ions and activity ratio is increased by raising the calcium concentration. 5. The activating effect of ascorbic acid on the ATPase activity was not related to the sulfhydryl group of cysteine or the hydroxyl group of threonine. 6. The activating effect of ascorbic acid on the ATPase activity is due to amino group and carboxyl group of the enzyme of NaK ATPase.

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Mesna의 쥐 고환에 대한 방사선 보호 효과 (Radioprotective Effect of Mesna on Mouse Testis)

  • 류삼열;김재철;김상보;박인규
    • Radiation Oncology Journal
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    • 제8권2호
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    • pp.145-150
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    • 1990
  • 고환암에서 mesna는 ifosfamide와 병용 투여하면 요관 계통의 부작용을 방지할 수 있으며, adriamycin과 같이 사용하는 경우 항암제의 세포증식 억제능을 감소시키지 않으면서 부작용을 경감 시킨다. 방사선 보호제의 sulfhydryl가 방사선에 의하여 발생하는 hydroxyl 유리기와 반응하여 조직을 보호할 수 있고, 역시 체내에서 유리기를 발생하는 adriamycin의 독작용을 musua가 감소시키는 사실에 근거하여, 쥐에 mesna와 방사선을 투여하여 mesna의 방사선보호 작용을 관찰하였다. 본 연구에서는 방사선 단독 처치군과 mesna와 방사선 처치군에서 고환의 수정관 내의 배아세포의 수와 형태적 변화를 현미경 하에서 매주 비교하고 재생 능력의 차이를 확인하였다. 양쪽 군에서 공히 초기에 세포 수가 감소하고 후기에 다시 세포가 증식 하였으며, 가장 세포 수가 적게 관찰된 시기는 방사선 조사 후 3주 째였다. 모든 관찰 기간에서 mesna 처치군의 평균 배아 세포수가 방사선 단독 처치군보다 통계적으로 유의하게 많이 관찰되었고(p<0.05), 또한 mesna 처치군에서 더 유효한 세포 재생 능력이 있음이 관찰되었다. 이는 mesna가 방사선 상해로부터 고환의 수정관 내 배아세포를 보호하고 있음을 입증하는 것으로 사료된다. Mesna가 고환 이외의 다른 조직을 방사선으로부터 보호할 수 있는지의 여부와 종양의 관해율을 저해하지 않을지에 대하여는 더 이상의 연구가 필요할 것으로 생각된다.

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Saccharomyces cerevisiae에서 얻은 Purine Nucleoside Phosphorylase의 반응기작과 효소에 대한 Sulfhydryl Reagent의 영향 (Reaction Mechanism of Purine Nucleoside Phosphorylase and Effects of Reactive Agents for SH Group on the Enzyme in Saccharomyces cerevisiae)

  • 최혜선
    • 미생물학회지
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    • 제32권3호
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    • pp.222-231
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    • 1994
  • Saccharomyces cerevisiae에서 얻은 purine nucleoside phosphorylase (PNP)의 반응 기작을 밝히기 위해 반응속도론적 분석이 수행되어졌다. 반응기작에 PNP${\cdot}$phosphate와 PNP${\cdot}$ribose 1-phosphate의 binary complex가 형성되는 것으로 추정되어진다. Initial velocity와 product inhibition study의 결과는 반응이 ordered bi, bi reaction으로 일어난다는 것과 일치하고 있다. 두 개의 기질중 무기인산이 효소에 먼저 붙고, 그 다음에 nucleoside, 그리고 base가 효소를 떠나는 첫 번째 생성물이고 마지막으로 ribose 1-phosphate가 생성되고 효소는 원래의 상태로 돌아간다. 반응속도론적 분석에 이해 제안된 작용기작은 sulfhydryl reagents인 p-chloromercuribenzoate(PCMB) and 5,5'-dithiobisnitrobenzoate (DTNB)에 의한 효소의 불활성화에 대한 기질으 보호작용의 결과와 일치하고 있다. PNP는 ribose 1-phosphate와 phosphate에 의해 보호되지만 nucleoside나 base에 의해서는 아무런 효과과 없다는 사실은 반응 순서가 효소에 무기인산이 먼저 붙는 ordered bi, bi 기작이라는 것을 지지하고 있다. PCMB 나 DTNB에 의해 불활성화된 PNP는 dithiothreitol(DTT)에 의해서는 활성이 완전히 회복되고 2-mercaptoethanol에 의해서는 77%의 활성이 회복된다는 사실은 효소의 불활성화가 가역적이라는 것을 시사하고 있다. PCMB에 의해 불활성화된 효소는 inosine이 변화하는 기질일때 정상효소보다 높은 $K_m$과 낮은 $V_m$ 값을 보여주고 이런 현상은 DTT 처리시 원래의 상태로 돌아온다. DTNB에 의해 불활성화된 효소는 PCMB 처리시와 비슷하게 정상효소보다 높은 $V_m$ 값을 보이지만 $V_m$ 값은 큰 변화가 없다. S. cerevisiae PNP에서 발견되는 높은 무기인산의 농도에서의 하위단위체간의 음성적 협동성이 PCMB나 DTNB를 처리한 PNP에서는 보이지 않았다.

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미강 저장 중 지방의 산패에 따라 생성된 산화 지질이 단백질의 기능기에 미치는 영향에 관한 연구 (Changes in Functional Groups of Protein by Lipid Deterioration in the Biological System of Rice Bran)

  • 송영옥;최홍식
    • 한국식품과학회지
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    • 제22권5호
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    • pp.596-601
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    • 1990
  • 미강의 산소 농도를 제한하고 상대습도 65% 온도 $35^{\circ}C$의 저장 조건하에서 함유 지방질의 가수분해를 최대한 유도한 시료와 온도 $25-30^{\circ}C$, 상대습도 70-80%인 공기중에 방치하여 함유 지방질의 가수분해와 지방질의 산화를 동시에 유도한 미강을 시료로 하여 지방의 산화양상에 따른 단백질의 물리 화학적인 변화 즉, sulfhydryl과 disulfide group, 단백질의 용해도, 유효성 lysine, protease의 활성변화 등을 실험하였다. 산소 농도를 제한한 system에서는 지방질의 가수분해는 급격히 일어난 반면 산화는 서서히 진행되었고, 공기 중에 방치한 system에서는 지방질의 가수분해와 자동산화가 현저하게 진행되었다. 이때 각종 단백질 기능기의 함량의 감소현상은 저장기간보다 지방의 산패 정도와 더 깊은 상관성을 보였다. 지방질의 산패와 주요 단백질 기능기함량과의 상관계수는 두 system 모두에서 -0.8 이상으로서, 지방질의 산패는 단백질의 이화학적인 변화에 중요한 영향을 미침이 관찰되었다(p<0.05).

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Long-term Supplementation of Epimedium koreanum Nakai in Rats and Its Effects on In Vivo Antioxidant Status with Age

  • Lim, Heung-Bin;Lee, Dong-Wook
    • Food Science and Biotechnology
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    • 제16권3호
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    • pp.404-408
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    • 2007
  • In this study, we investigated the effects by age of long-tenn supplementation of Epimedium koreanum Nakai (EKN)-containing water on the in vivo antioxidant capacities of rats. All rats were reared in a conventional system, and none of the rats showed any signs of aversion to the EKN solution. Neither the mean nor maximum life spans of the rats were extended by long-tenn administration of the solution. The EKN extract caused decreases in the levels of serum thiobarbituric acid reactive substances in the rats. The activities of superoxide dismutase, catalase, and glutathione (GSH) peroxidase within the liver cytosol decreased with age in both the control and EKN-supplemented groups. GSH peroxidase activity, however, was higher at old age in the EKN-supplemented group. The activities of GSH reductase and GSH-S-transferase, and the levels of free-sulfhydryl (SH) and total-SH group gradually decreased with age in both groups. However, there was some tendency for higher levels in the EKN supplemented group at a corresponding age. These results indicate that long-tenn supplementation of EKN water extracts alone does not exhibit discernible adverse effects in rats, and has some enhancing effects on the antioxidant capacities of the blood and liver, but it does not have life-prolonging effects.