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脂氧合酶的比较荧光特性

Comparative fluorescence properties of lipoxygenases.

作者信息

Macías P, Zamora R, Pinto M C, Gutiérrez-Merino C

机构信息

Departamento de Bioquímica y Biología Molecular y Genética. Facultad de Ciencias, Universidad de Extremadura, Badajoz, Spain.

出版信息

Comp Biochem Physiol B. 1988;89(3):531-7. doi: 10.1016/0305-0491(88)90170-8.

Abstract
  1. Lipoxygenases purified from tomato, rat liver and soybean show a fluorescence band centered at 648 nm, which is likely to derive from Tyr and Trp. 2. The intensity of this fluorescence range from 0.7 to 1.0% of the intensity of their major intrinsic fluorescence band (lambda max = 343 nm) in all these lipoxygenases. 3. At inhibitory concentrations, ditizone partly quenches the fluorescence of the lipoxygenases above 600 nm. 4. Saturating concentrations of linoleic acid produce 79% quenching of the fluorescence at 648 nm of soybean lipoxygenase inactivated by treatment with 1 mM dithiothreitol. From these data we have obtained an apparent Kd for linoleic acid-lipoxygenase complex dissociation of 34 +/- 3 microM. 5. It is suggested that the fluorescence above 600 nm reveals the presence of aromatic amino acids located near or at the catalytic center.
摘要
  1. 从番茄、大鼠肝脏和大豆中纯化得到的脂氧合酶显示出一条以648 nm为中心的荧光带,这可能源自酪氨酸(Tyr)和色氨酸(Trp)。2. 在所有这些脂氧合酶中,该荧光强度占其主要固有荧光带(λmax = 343 nm)强度的0.7%至1.0%。3. 在抑制浓度下,双硫腙会部分淬灭脂氧合酶在600 nm以上的荧光。4. 饱和浓度的亚油酸会使经1 mM二硫苏糖醇处理而失活的大豆脂氧合酶在648 nm处的荧光淬灭79%。根据这些数据,我们得出亚油酸 - 脂氧合酶复合物解离的表观解离常数(Kd)为34 ± 3 μM。5. 有人提出,600 nm以上的荧光揭示了位于催化中心附近或催化中心处的芳香族氨基酸的存在。

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