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过氧化物酶催化硫氰酸盐氧化过程中次硫氰酸盐生成的动力学

Kinetics of hypothiocyanite production during peroxidase-catalyzed oxidation of thiocyanate.

作者信息

Pruitt K M, Tenovuo J

出版信息

Biochim Biophys Acta. 1982 Jun 4;704(2):204-14. doi: 10.1016/0167-4838(82)90147-9.

Abstract

We report here a kinetic study of the generation of hypothiocyanite (OSCN-), a product of lactoperoxidase-catalyzed oxidation of thiocyanate ion. Previous studies have measured OSCN- by reactions involving the oxidation of sulfhydryl compounds. Our results show that a more suitable kinetic analysis of OSCN- can be based on absorbance changes measured at 235 nm. About 90% of the oxidation products of SCN- observed at 235 nm were reactive with sulfhydryls and could be reduced with 2-mercaptoethanol. Both thiocyanate and peroxide were rate-limiting and the formation of OSCN- was proportional to the initial concentration of H2O2 until an equimolar concentration of H2O2 and SCN- was reached. This equimolar concentration gave the maximum generation of OSCN-. High concentrations (greater than 100 micrograms/ml) of lactoperoxidase decreased OSCN- generation, but only if the SCN- was added to the enzyme prior to addition of H2O2. With lactoperoxidase concentrations exceeding 1 microgram/ml, the reaction velocity was rapid, but the decay of OSCN- was slow. Free H2O2 in the reaction mixture always resulted in rapid decay of OSCN-. Addition of varying concentrations of peroxide to solutions containing 1 microgram/ml of enzyme and [SCN-] = 5 mM gave a family of hyperbolic A235 vs. time curves. Both the initial slopes and the plateaus of these curves increased linearly with increasing initial peroxide concentrations up to [H2O2] = 0.4 mM, remained relatively constant in the range [H2O2] = 0.4 to 0.8 mM, and decreased rapidly above [H2O2] = 0.8 mM. These results are consistent with the following kinetic model: Hydrogen peroxide reacts rapidly with lactoperoxidase to produce compound I. This compound I oxidizes SCN- to OSCN- and also oxidizes OSCN- to O2SCN-. The OSCN- also reacts with SCN-. The formation of OSCN- is associated with the appearance of an absorbance peak at 225-235 nm. The oxidation of OSCN- by excess peroxide or its decomposition at high concentrations is associated with a decrease in A235 and the appearance of a peak at 245-255 nm. The extinction coefficient for OSCN- was determined to be 1.29 x 10(3) M-1 . cm-1. The second-order rate constant for the oxidation of thiocyanate by compound I was estimated to be 2 x 10(5) M-1 . s-1.

摘要

我们在此报告一项关于次硫氰酸盐(OSCN-)生成的动力学研究,次硫氰酸盐是硫氰酸根离子经乳过氧化物酶催化氧化的产物。以往的研究通过涉及巯基化合物氧化的反应来测定OSCN-。我们的结果表明,对OSCN-进行更合适的动力学分析可基于在235nm处测得的吸光度变化。在235nm处观察到的SCN-氧化产物中约90%可与巯基反应,并可用2-巯基乙醇还原。硫氰酸盐和过氧化物都是限速因素,在达到H2O2和SCN-等摩尔浓度之前,OSCN-的形成与H2O2的初始浓度成正比。这种等摩尔浓度产生了最大量的OSCN-。高浓度(大于100微克/毫升)的乳过氧化物酶会降低OSCN-的生成,但前提是在加入H2O2之前先将SCN-加入酶中。当乳过氧化物酶浓度超过1微克/毫升时,反应速度很快,但OSCN-的衰减很慢。反应混合物中的游离H2O2总是导致OSCN-迅速衰减。向含有1微克/毫升酶且[SCN-]=5mM的溶液中加入不同浓度的过氧化物,得到了一系列A235对时间的双曲线曲线。这些曲线的初始斜率和平稳期均随初始过氧化物浓度的增加呈线性增加,直至[H2O2]=0.4mM,在[H2O2]=0.4至0.8mM范围内保持相对恒定,而在[H2O2]>0.8mM时迅速下降。这些结果与以下动力学模型一致:过氧化氢与乳过氧化物酶迅速反应生成化合物I。该化合物I将SCN-氧化为OSCN-,同时也将OSCN-氧化为O2SCN-。OSCN-也与SCN-反应。OSCN-的形成与在225 - 235nm处出现吸光度峰相关。过量过氧化物对OSCN-的氧化或其在高浓度下的分解与A235的降低以及在245 - 255nm处出现峰相关。OSCN-的消光系数测定为1.29×10(3) M-1·cm-1。化合物I氧化硫氰酸盐的二级速率常数估计为2×10(5) M-1·s-1。

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