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通过荧光发射光谱法检测α-脲酶解离

Detection of alpha-urease dissociation by fluorescence emission spectroscopy.

作者信息

Omar S, Beauregard M

机构信息

Chemistry Department, University of Prince Edward Island, Charlottetown, Canada.

出版信息

Biochem Biophys Res Commun. 1994 Jun 30;201(3):1096-9. doi: 10.1006/bbrc.1994.1818.

Abstract

alpha-Urease (E.C. 3.5.1.5) is a hexameric enzyme that can dissociate into two active trimers and further into six monomers (Hirai M., Kawa-Hirai, R., Hirai T., Ueki T. (1993) Eur. J. Biochem. 215, 55-61). We have attempted to detect these dissociation products using fluorescence emission and polarization spectroscopy. Our data suggest that the hexamer, the trimer and denatured monomer have fluorescence emission maximum at 330nm, 332nm, and 346nm, respectively, under our experimental conditions. We have also found that the conformation of urease subunits is only slightly modified upon dissociation to trimer, but drastically changed upon further dissociation leading to monomer.

摘要

α-脲酶(E.C. 3.5.1.5)是一种六聚体酶,可解离成两个活性三聚体,进而解离成六个单体(平井M.、川平井R.、平井T.、植木T.(1993年)《欧洲生物化学杂志》215卷,55 - 61页)。我们尝试使用荧光发射和偏振光谱法检测这些解离产物。我们的数据表明,在我们的实验条件下,六聚体、三聚体和变性单体的荧光发射最大值分别在330nm、332nm和346nm处。我们还发现,脲酶亚基的构象在解离成三聚体时仅略有改变,但在进一步解离成单体时会发生剧烈变化。

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