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Peroxynitrite chemistry: Formation, decomposition and possible deactivation mechanisms by thiols.

机译:过氧亚硝酸盐化学:硫醇的形成,分解和可能的失活机理。

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摘要

Kinetics of formation and decomposition of peroxynitrite was studied in acidic and buffer solutions. Peroxynitrous acid was formed in acidic media by the reaction of H2O2 with HNO2 and NO +. Bimolecular rate constant for reaction of H2O2 with HNO2 at 25°C was determined to be 3.7 x 10 3 M-1 s-1. Peroxynitrous acid formed is highly unstable with half life of approximately 1 second. Decomposition of peroxynitrite is highly pH-dependent. In acidic media, peroxynitrous acid decomposes to nitrate while at neutral to slightly basic media, products of decomposition is nitrite, oxygen and acidic protons. In strongly basic pH, the products of peroxynitrite decomposition were nitrite and oxygen in a 2:1 ratio.;Kinetics and mechanism of oxidation of cysteine (CYSH) and glutathione (GSH) by peroxynitrite, as radical deactivation agents were also studied. Peroxynitrite reacts with CYSH/GSH at acidic pH to produce corresponding S-nitrosothiol and disulfide. The reaction is first order in peroxynitrite, acid and thiol. Mass spectrometer technique confirms formation of nitrosothiol as product of oxidation. Mechanism of formation can be rationalized as occurring through acid catalyzed decomposition of PN through intermediacy of HNO2/ +N=O, which is capable of nitrosating thiol function.;In basic pH, peroxynitrite oxidizes CYSH/GSH through a two electron oxidation mechanism via sulfinic acid to corresponding disulfide. Mass spectrometer technique suggests that stable product of CYSH/GSH oxidation by peroxynitrite at pH 7.4 is disulfide of corresponding initial thiol. EPR studies on oxidation of CYSH/GSH by peroxynitrite at pH 7.4 suggest pathway of oxidation goes via formation of thiyl radicals. Bimolecular rate constants for oxidation of GSH by peroxynitrite at 25°C (pH 7.0) was determined to be 587 M-1 s-1, while the bimolecular rate constants for oxidation of CYSH by peroxynitrite at 25°C (pH 7.4) was determined to be 2.0 x 103 M-1 s-1.;Decomposition dynamics showed first order dependence with respect to pH. Rate constant of decomposition of peroxynitrite in absence of a substrate at pH 3.0 was determined to be 0.98 s-1 and 0.10 s-1 at pH 8.0. Data generated from EPR studies indicates generation of ·OH radical as a decomposition product of peroxynitrite.
机译:在酸性和缓冲溶液中研究了过氧亚硝酸盐形成和分解的动力学。过氧亚硝酸是在酸性介质中通过H2O2与HNO2和NO +的反应而形成的。在25℃下H 2 O 2与HNO 2反应的双分子速率常数确定为3.7×10 3 M-1 s-1。形成的过氧亚硝酸非常不稳定,半衰期约为1秒。过氧亚硝酸盐的分解高度依赖于pH。在酸性介质中,过氧亚硝酸分解为硝酸盐,而在中性至弱碱性介质中,分解产物为亚硝酸盐,氧气和酸性质子。在强碱性pH下,过氧亚硝酸盐的分解产物为亚硝酸盐和氧气,比例为2:1。研究了过氧亚硝酸盐作为自由基失活剂的半胱氨酸(CYSH)和谷胱甘肽(GSH)氧化的动力学和机理。过氧亚硝酸盐与CYSH / GSH在酸性pH下反应,生成相应的S-亚硝基硫醇和二硫化物。反应是过氧亚硝酸盐,酸和硫醇的一级反应。质谱技术证实了亚硝基硫醇是氧化产物。形成机理可以合理地解释为是通过HNO2 / + N = O介导的酸催化PN分解而实现的,能够亚硝化巯基的功能。酸生成相应的二硫化物。质谱技术表明,在pH 7.4时,过氧亚硝酸盐氧化CYSH / GSH的稳定产物是相应的初始硫醇的二硫键。 EPR研究在pH 7.4时过氧亚硝酸盐对CYSH / GSH的氧化作用,表明氧化途径是通过巯基的形成。测定过氧亚硝酸盐在25°C(pH 7.0)氧化GSH的双分子速率常数为587 M-1 s-1,而测定过氧亚硝酸盐在25°C(pH 7.4)氧化CYSH的双分子速率常数。为2.0 x 103 M-1 s-1 。;分解动力学显示出相对于pH的一阶依赖性。在pH 3.0下,在没有底物的情况下,过氧亚硝酸盐的分解速率常数确定为0.98 s-1和0.10 s-1。从EPR研究获得的数据表明,生成了-OH自由基作为过氧亚硝酸盐的分解产物。

著录项

  • 作者

    Olagunju, Olufunke.;

  • 作者单位

    Portland State University.;

  • 授予单位 Portland State University.;
  • 学科 Chemistry Physical.;Biophysics General.
  • 学位 Ph.D.
  • 年度 2008
  • 页码 180 p.
  • 总页数 180
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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