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      KCI등재 SCOPUS SCIE

      Effect of Glucose, Its Analogs and Some Amino Acids on Pre-steady State Kinetics of ATP Hydrolysis by PM-ATPase of Pathogenic Yeast (Candida albicans)

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      https://www.riss.kr/link?id=A104261558

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      다국어 초록 (Multilingual Abstract)

      Fast kinetics of transient pH changes and difference spectrum formation have been investigated following mixing of ADP/ATP with partially purified plasma membrane PM-ATPase of the pathogenic yeast Candida albicans in the presence of five nutrients: gl...

      Fast kinetics of transient pH changes and difference spectrum formation have been investigated following mixing of ADP/ATP with partially purified plasma membrane PM-ATPase of the pathogenic yeast Candida albicans in the presence of five nutrients: glucose, glutamic acid, proline, lysine, and arginine and two analogs of glucose: 2-deoxy D-glucose and xylose. Average H+ - absorption to release ratio, indicative of population of ATPase undergoing complete hydrolytic cycle, was found to be 0.27 for control. This ratio varied between 0.25 (proline) to 0.36 (arginine) for all other compounds tested, except for glucose. In the presence of glucose, H+ - absorption to release ratio was exceptionally high (0.92). While no UV difference spectrum was observed with ADP, mixing of ATP with ATPase led to a large conformational change. Exposure to different nutrients restricted the magnitude of the conformational change; the analogs of glucose were found to be ineffective. This suppression was maximal in the case of glucose (80%); with other nutrients, the magnitude of suppression ranged from 40-50%. Rate of H+ - absorption, which is indicative of E~P complex dissociation, showed positive correlation with suppression of conformational change only in the case of glucose and no other nutrient/analog. Mode of interaction of glucose with plasma membrane H+-ATPase thus appears to be strikingly distinct compared to that of other nutrients/analogs tested. The results obtained lead us to propose a model for explaining glucose stimulation of plasma membrane H+ - ATPase activity.

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      참고문헌 (Reference)

      1 Gupta P, "purification and kinetic characterization of plasma membrane H+-ATPase of Candida albicans. Biochem Int 24" 907-915, 1991

      2 de la Fuente N, "Yeast gene YOR137c is involved in the activation of the yeast plasma membrane H+-ATPase by glucose." 420 : 17-19, 1997

      3 Auer M, "Three-dimensional map of the plasma membrane H+-ATPase in the open conformation." 392 : 840-843, 1998

      4 Tokiwa T, "The pre-steady state of myosin-adenosine triphosphate system. 2. Initial rapid absorption and liberation of hydrogen ion by a stopped flow method. J Biochem 57" 616-625. 1965

      5 Koretz JF, "Studies on mechanism of myosin and actomyosiATPase. Cold Spring Harbor Sym Quant Biol 37" 179-184, 1972

      6 Serrano R, "Structure and function of proton translocating ATPase in the plasma membranes of plants and fungi. Biochim Biophys Acta 947" 1-28. 1988

      7 Amin M, "Pre-steady state kinetic studies on H+-ATPase from Candida albicans" 126 : 776-780, 1999

      8 Eraso P, "Molecular mechanism of regulation of yeast plasma membrane H+-ATPase by glucose. Interaction between domains and identification of new regulatory sites. J Biol Chem 269" 10393-10399. 1994

      9 Venema K, "Metabolic modulation of transport coupling ratio in yeast plasma membrane H+-ATPase." 270 : 19659-.-19667, 1995

      10 Clarke DM, "Location of high affinity Ca2+ binding sites within the predicted transmembrane domain of the sarcoplasmic reticulum Ca2-ATPase. Nature 339" 476-478, 1989

      1 Gupta P, "purification and kinetic characterization of plasma membrane H+-ATPase of Candida albicans. Biochem Int 24" 907-915, 1991

      2 de la Fuente N, "Yeast gene YOR137c is involved in the activation of the yeast plasma membrane H+-ATPase by glucose." 420 : 17-19, 1997

      3 Auer M, "Three-dimensional map of the plasma membrane H+-ATPase in the open conformation." 392 : 840-843, 1998

      4 Tokiwa T, "The pre-steady state of myosin-adenosine triphosphate system. 2. Initial rapid absorption and liberation of hydrogen ion by a stopped flow method. J Biochem 57" 616-625. 1965

      5 Koretz JF, "Studies on mechanism of myosin and actomyosiATPase. Cold Spring Harbor Sym Quant Biol 37" 179-184, 1972

      6 Serrano R, "Structure and function of proton translocating ATPase in the plasma membranes of plants and fungi. Biochim Biophys Acta 947" 1-28. 1988

      7 Amin M, "Pre-steady state kinetic studies on H+-ATPase from Candida albicans" 126 : 776-780, 1999

      8 Eraso P, "Molecular mechanism of regulation of yeast plasma membrane H+-ATPase by glucose. Interaction between domains and identification of new regulatory sites. J Biol Chem 269" 10393-10399. 1994

      9 Venema K, "Metabolic modulation of transport coupling ratio in yeast plasma membrane H+-ATPase." 270 : 19659-.-19667, 1995

      10 Clarke DM, "Location of high affinity Ca2+ binding sites within the predicted transmembrane domain of the sarcoplasmic reticulum Ca2-ATPase. Nature 339" 476-478, 1989

      11 "Interaction of heavy meromyosin with substrate II. Rate of the formation of ATP-induced ultraviolet difference spectrum of heavy meromyosin measured by stopped-flow method. Biochim Biophys Acta 172" 319-327, 1969

      12 Serrano R, "In vivo glucose activation of the yeast plasma membrane ATPase. FEBS Lett 156" 11-14. 1983

      13 Portillo F, "Detection analysis of yeast plasma membrane H+-ATPase and identification of a regulatory domain at the carboxyl terminus. FEBS Lett 247" 381-385, 1989

      14 Serrano R, "Catalytic and regulatory sites of yeast plasma membrane H+-ATPase studied by directed mutagenesis. Biochim Biophys Acta 1018" 195-199. 1990

      15 Yeramian E, "Analysis of multiexponential functions without a hypothesis as to the number of components. Nature 326" 169-174. 1987

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      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2023 평가예정 해외DB학술지평가 신청대상 (해외등재 학술지 평가)
      2020-01-01 평가 등재학술지 유지 (해외등재 학술지 평가) KCI등재
      2010-02-02 학회명변경 한글명 : 한국동물학회 -> 한국통합생물학회
      영문명 : 미등록 -> The Korean Society for Integrative Biology
      KCI등재
      2010-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2008-02-26 학술지명변경 한글명 : Integrative Biosciences -> Animal Cells and Systems
      외국어명 : Integrative Biosciences -> Animal Cells and Systems
      KCI등재
      2008-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2006-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2005-04-15 학술지등록 한글명 : Integrative Biosciences
      외국어명 : Integrative Biosciences
      KCI등재
      2004-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2001-07-01 평가 등재학술지 선정 (등재후보2차) KCI등재
      1999-01-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      학술지 인용정보

      학술지 인용정보
      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 0.45 0.24 0.33
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.28 0.26 0.395 0.04
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