首页> 外文期刊>Bioorganic and medicinal chemistry >Understanding the radical mechanism of lipoxygenases using 31P NMR spin trapping.
【24h】

Understanding the radical mechanism of lipoxygenases using 31P NMR spin trapping.

机译:使用31P NMR自旋捕获了解脂氧合酶的自由基机理。

获取原文
获取原文并翻译 | 示例
       

摘要

In this paper, we use our quantitative (31)P NMR spin trapping methods, already developed for simple oxygen- and carbon-centered radicals, to understand the radical intermediates generated by enzymatic systems and more specifically lipoxygenases. Our methodology rests on the fact that free radicals react with the nitroxide phosphorus compound, 5-diisopropoxy-phosphoryl-5-methyl-1-pyrroline-N-oxide (DIPPMPO), to form stable radical adducts, which are suitably detected and accurately quantified using (31)P NMR in the presence of a phosphorus containing internal standard. This system was thus applied to better understand the mechanism of enzymatic oxidation of linoleic acid by soybean lipoxygenases-1 (LOX). The total amount of radicals trapped by DIPPMPO was detected by (31)P NMR at different experimental conditions. In particular the effect of dioxygen concentration on the amount of radicals being trapped was studied. At low dioxygen concentration, a huge increase of radicals trapped was observed with respect to the amount of radicals being trapped at normal dioxygen concentrations.
机译:在本文中,我们使用我们已经针对简单的以氧和碳为中心的自由基开发的定量(31)P NMR自旋捕集方法,来了解由酶促系统生成的自由基中间体,尤其是脂氧合酶。我们的方法基于以下事实:自由基与氮氧化物磷化合物,5-二异丙氧基-磷酰基-5-甲基-1-吡咯啉-N-氧化物(DIPPMPO)反应,形成稳定的自由基加合物,可对其进行适当检测和准确定量在含磷内标的存在下使用(31)P NMR。因此,该系统用于更好地理解大豆脂氧合酶-1(LOX)酶催化亚油酸氧化的机理。在不同的实验条件下,通过(31)P NMR检测DIPPMPO捕获的自由基总量。特别地,研究了双氧浓度对被捕获的自由基量的影响。在低的双氧浓度下,相对于在正常的双氧浓度下被俘获的自由基的数量,观察到捕获的自由基大量增加。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号