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13-Ls-氢过氧化亚油酸和亚油酸诱导的脂氧合酶-1的荧光和吸光度变化。

Changes in the fluorescence and absorbance of lipoxygenase-1 induced by 13-Ls-hydroperoxylinoleic acid and linoleic acid.

作者信息

Egmond M R, Finazzi-Agró A, Fasella P M, Veldink G A, Vliegenthart J F

出版信息

Biochim Biophys Acta. 1975 Jul 27;397(1):43-9. doi: 10.1016/0005-2744(75)90177-1.

Abstract
  1. The addition of 13-Ls-hydroperoxylinoleic acid to lipoxygenase-1 (linoleate: oxygen oxidoreductase EC 1.13.11.12) from soybeans at pH 9 and 25 degrees C causes a quenching of the fluorescence of the enzyme at 328 nm when exciited at 280 nm and gives rise to an increase of the absorbance of the enzyme in the 300 nm to 450 nm region. 2. In the absence of 02, addition of linoleic acid to enzyme treated with 13-Ls-hydroperoxylinoleic acid, causes an increase of the fluorescence at 328 nm and a decrease of the absorbance in the 300 nm to 450 nm region. 3. The fluorescence changes are suggested to be directly coupled to the absorbance changes via a non-radioactive energy transfer process. 4. It is proposed that the observed fluorescence and absorbance changes are related to changes in the formal change of iron in the protein.
摘要
  1. 在pH值为9、温度为25摄氏度的条件下,将13-Ls-氢过氧化亚油酸添加到来自大豆的脂氧合酶-1(亚油酸:氧氧化还原酶,EC 1.13.11.12)中,当在280纳米处激发时,会导致该酶在328纳米处的荧光猝灭,并使该酶在300纳米至450纳米区域的吸光度增加。2. 在没有氧气的情况下,将亚油酸添加到用13-Ls-氢过氧化亚油酸处理过的酶中,会导致328纳米处的荧光增加以及300纳米至450纳米区域的吸光度降低。3. 荧光变化被认为是通过非放射性能量转移过程直接与吸光度变化相关联的。4. 有人提出,观察到的荧光和吸光度变化与蛋白质中铁的形式变化有关。

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