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Photoenzymatic Repair of Ultraviolet Damage in DNA : II. Formation of an enzyme-substrate complex

机译:DNA中紫外线损伤的光酶修复:II.。酶-底物复合物的形成

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摘要

The photoenzyme from bakers' yeast which repairs ultraviolet-inactivated transforming DNA is mechanically bound to ultraviolet-irradiated DNA in the dark, but not to unirradiated DNA. In the bound condition it is stabilized against inactivation by heat and heavy metals. Both the mechanical binding and stabilization are eliminated by illumination. These observations are consistent with the reaction scheme suggested by kinetic studies, in which the enzyme combines with the ultraviolet lesions in DNA and the complex absorbs light, producing repair and subsequent liberation of the enzyme. The approximately exponential decrease of heat stabilization during illumination gives the first order rate constant for the light-dependent step at the corresponding light intensity. This quantity in turn sets limits on the possible magnitude of the molar absorption coefficient of the enzyme-substrate complex and on the quantum yield of the process.
机译:面包师酵母中修复紫外线灭活的转化DNA的光酶在黑暗中机械结合到紫外线照射的DNA,但未结合到未照射的DNA。在约束条件下,它被稳定以防热和重金属灭活。通过照明消除了机械结合和稳定性。这些观察结果与动力学研究提出的反应方案是一致的,在动力学研究中,酶与DNA中的紫外线损伤结合,复合物吸收光,产生修复作用,随后释放酶。照明过程中热稳定度的指数下降使光依赖步骤在相应的光强度下具有一阶速率常数。该量进而限制了酶-底物复合物的摩尔吸收系数的可能大小以及方法的量子产率。

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  • 作者

    Rupert, Claud S.;

  • 作者单位
  • 年度 1962
  • 总页数
  • 原文格式 PDF
  • 正文语种 {"code":"en","name":"English","id":9}
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