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首页> 外文期刊>Mutation Research: International Journal on Mutagenesis, Chromosome Breakage and Related Subjects >Biphasic kinetics in the reaction between amino acids or glutathione and the chromium acetate cluster, (Cr3O(OAc)6)+.
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Biphasic kinetics in the reaction between amino acids or glutathione and the chromium acetate cluster, (Cr3O(OAc)6)+.

机译:氨基酸或谷胱甘肽与乙酸铬簇(Cr3O(OAc)6)+之间反应的双相动力学。

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Kinetics for the breakdown of the trinuclear chromium acetate cluster with a series of monoprotic and diprotic amino acid ligands and with glutathione in aqueous media have been investigated spectrophotometrically at pH 3.5-5.5 and in a temperature range of 45-60 degrees C. Under pseudo-first-order conditions, reactions with these ligands exhibited biphasic kinetic behavior that can be accounted for by a consecutive two-step reaction, A-->B-->C, where A is assumed to be a forced ion pair, B an intermediate and C is the product; experimental data fit to a biexponential equation for the transformation. Rates for k(short), k(long), and k(obs) were determined by manual extrapolation of absorbance data or curve-fitting routines; associated activation parameters for each step of the reaction were calculated using the Eyring equation. Rates for the first and second steps of the reaction are on the order of approximately 10(-4) and approximately 10(-5)s(-1), respectively. The large negative values of DeltaS++ and smaller DeltaH++ in the first step indicate an associative step, while high positive values of DeltaS(double dagger) in the second step indicate dissociation. To account for the results mechanistically, the results are interpreted to be a first step of ligand exchange with a pseudo-axial aqua ligand, followed by a dissociative step involving acetate or oxo ligand displacement. The dissociative step is the rate determining step, with k(obs) approximately k(long). The results demonstrate reaction pathways that are available to the Cr(III) metal centers that may be physiologically relevant in the ligand-rich environment of biological systems. Under general conditions Cr(III) clusters may be expected to be broken down, unless some unique biological environment stabilizes the cluster. The present study has application to the processes related to Cr(III) transport and excretion, to potential mechanisms of Cr(III) action in a biological setting, and to the pharmacokinetics of Cr(III) supplements for animal and human consumption.
机译:已在pH值为3.5-5.5且温度范围为45-60℃的条件下,用分光光度法研究了具有一系列单质子和双质子氨基酸配体以及谷胱甘肽的三核乙酸铬簇分解动力学。一阶条件下,与这些配体的反应表现出两相动力学行为,这可以通过连续的两步反应A-> B-> C来解释,其中A被认为是强制离子对,B被认为是中间离子C是乘积;实验数据适合用于转换的双指数方程式。 k(short),k(long)和k(obs)的比率由吸光度数据的手动外推法或曲线拟合程序确定;反应的每个步骤的相关活化参数均使用Eyring方程计算。反应的第一和第二步骤的速率分别为大约10(-4)和大约10(-5)s(-1)。第一步中较大的DeltaS ++负值表示较小的DeltaH ++,而第二步中的较高DeltaS(双匕首)表示正值表示离解。为了从机理上解释结果,将结果解释为与假轴水基配体交换配体的第一步,然后是涉及乙酸酯或氧代配体置换的解离步骤。分离步骤是速率确定步骤,其中k(obs)大约为k(long)。结果表明可用于Cr(III)金属中心的反应途径在生物系统的富含配体的环境中可能与生理相关。在一般条件下,除非某些独特的生物环境稳定了该簇,否则可能会分解Cr(III)簇。本研究已应用于有关Cr(III)的运输和排泄的过程,在生物环境中Cr(III)作用的潜在机制以及用于动物和人类食用的Cr(III)补充剂的药代动力学。

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