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半高铁血红素蛋白的电子顺磁共振光谱学

EPR spectroscopy of semi-methemerythrin.

作者信息

Muhoberac B B, Wharton D C, Babcock L M, Harrinton P C, Wilkins R G

出版信息

Biochim Biophys Acta. 1980 Dec 16;626(2):337-45. doi: 10.1016/0005-2795(80)90128-2.

Abstract

EPR spectra of semi-met forms of octameric hemerythrin from Themiste zostericola, prepared by one electron reduction of methemerythrin or by one electron oxidation of deoxyhemerythrin, have been visualized at liquid helium temperatures. The spectrum of that prepared by one electron reduction has principal g-values of 1.96 +/- 0.01, 1.88 +/- 0.01, and 1.67 +/- 0.02 while that obtained by one electron oxidation has g = 1.95 +/- 0.01, 1.72 +/- 0.01, and 1.68 +/- 0.02. The amplitude of either spectrum decreases with time on incubation at room temperature according to a first order rate with t 1/2 = 5-8 min, apparently because of an intramolecular disproportionation. Similar EPR spectra have been obtained with semi-metmyohemerythrin of T. zostericola and with the octameric semi-met form of Phascolopsis gouldii. However, these forms disproportionate to a much lesser degree. The azide adduct of the octameric semi-met form of T. zostericola has g-values of 1.94 +/- 0.01, 1.85 +/- 0.01, and 1.57 +/- 0.02. Its EPR spectrum differs somewhat from those of the azide adducts of the octamer of P. gouldii and the monomer of T. zostericola although all are resistant to disproportionation. Methemerythrin and deoxyhemerythrin have no EPR spectra even at liquid helium temperature.

摘要

通过高铁血红素的单电子还原或脱氧血红素的单电子氧化制备的来自多毛海蚯蚓(Themiste zostericola)的八聚体血红素半金属形式的电子顺磁共振(EPR)光谱,已在液氦温度下可视化。通过单电子还原制备的光谱的主要g值为1.96±0.01、1.88±0.01和1.67±0.02,而通过单电子氧化获得的光谱的g值为1.95±0.01、1.72±0.01和1.68±0.02。在室温下孵育时,任一光谱的幅度根据一级速率随时间降低,t1/2 = 5 - 8分钟,这显然是由于分子内歧化作用。用多毛海蚯蚓的半金属肌红蛋白和古氏潜铠虾(Phascolopsis gouldii)的八聚体半金属形式也获得了类似的EPR光谱。然而,这些形式的歧化程度要小得多。多毛海蚯蚓八聚体半金属形式的叠氮化物加合物的g值为1.94±0.01、1.85±0.01和1.57±0.02。其EPR光谱与古氏潜铠虾八聚体和多毛海蚯蚓单体的叠氮化物加合物的光谱有些不同,尽管它们都抗歧化。高铁血红素和脱氧血红素即使在液氦温度下也没有EPR光谱。

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