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作 者:储高升[1] 张淑娟[1] 姚思德[2] 窦大营[2] 张志成[1]
机构地区:[1]中国科学技术大学应用化学系,合肥230026 [2]中国科学院上海原子核所,信箱上海201800800204
出 处:《物理化学学报》2002年第9期812-816,共5页Acta Physico-Chimica Sinica
基 金:国家自然科学基金(39800036)资助项目~~
摘 要:研究了水-乙腈混合溶液中SO~●_4-自由基氧化酪氨酸的反应.实验结果表明,SO~●_4-自由基氧化酪氨酸的反应机制不因乙腈的加入而改变,但所产生的瞬态粒子的动力学行为受到较大影响.随介质中乙腈体积分数的增加,SO~●_4-的衰变速率减慢而酪氨酸中性自由基(TyrO●)的衰变速率加快.我们认为这两种自由基所呈现出来的相反的溶剂效应是由于其所带电荷的不同.随介质中乙腈体积分数的增加,SO~●_4-氧化酪氨酸的反应速率减慢.这一实验结果意味着,在有机溶剂存在的情况下TyrO●/TyrOH的氧化还原电势可能发生了变化,从而旁证了关于TyrO●/TyrOH的氧化还原电势因酪氨酸从游离状态变到肽或蛋白质中而发生变化的推测.This work presents the study on the oxidation of TyrOH by in water/ACN mixed media.Investigationsshow that the reaction mechanism between TyrOH and does not change by the addition of ACN,whereas the kinetic behavior of the transient species produced is significantly affected.The decay of decelerates with increasing volume fraction of ACN in mixed media whereas the decay of accelerates.We suggest that the contrary effects of the solvent on the decay of both and are due to their different charges.The deceleration of the oxidation of TyrOH by with the increase of ACN fraction may demonstrate that in the presence of organic solvents the redox potential of /TyrOH is altered,which provides support for the suggestion that the redox potential of / TyrOH might be altered with their inclusion into peptides and proteins.
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