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Repurposing Nonheme Iron Hydroxylases To Enable Catalytic Nitrile Installation through an Azido Group Assistance

机译:重新利用非血红素铁羟化酶以通过叠氮基团协助实现催化腈的安装

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摘要

Three mononuclear nonheme iron and 2-oxoglutarate dependent enzymes, L-Ile 4-hydroxylase, L-Leu 5-hydroxylase and polyoxin dihydroxylase, are previously reported to catalyze the hydroxylation of L-isoleucine, L-leucine, and L-alpha-amino-delta-carbamoylhydroxyvaleric acid (ACV). In this study, we showed that these enzymes can accommodate leucine isomers and catalyze regiospecific hydroxylation. On the basis of these results, as a proof-of-concept, we demonstrated that the outcome of the reaction can be redirected by installation of an assisting group within the substrate. Specifically, instead of canonical hydroxylation, these enzymes can catalyze non-native nitrile group installation when an azido group is introduced. The reaction is likely to proceed through C-H bond activation by an Fe(IV)-oxo species, followed by azido-directed C N bond formation. These results offer a unique opportunity to investigate and expand the reaction repertoire of Fe/2OG enzymes.
机译:先前已报道了三种单核非血红素铁和2-氧戊二酸依赖性酶L-Ile 4-羟化酶,L-Leu 5-羟化酶和多氧合二羟化酶催化L-异亮氨酸,L-亮氨酸和L-α-氨基的羟化反应-δ-氨基甲酰基羟基戊酸(ACV)。在这项研究中,我们表明这些酶可以容纳亮氨酸异构体并催化区域特异性羟基化。基于这些结果,作为概念验证,我们证明了可以通过在底物内安装辅助基团来重定向反应的结果。具体而言,当引入叠氮基时,这些酶可以代替规范的羟基化反应,催化非天然腈基的形成。该反应很可能通过Fe(IV)-氧代物种的C-H键激活而进行,然后形成叠氮基指导的C N键。这些结果提供了一个独特的机会来研究和扩大Fe / 2OG酶的反应范围。

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  • 来源
    《Journal of the American Chemical Society》 |2019年第8期|3419-3423|共5页
  • 作者单位

    North Carolina State Univ, Dept Chem, Box 8204, Raleigh, NC 27695 USA;

    North Carolina State Univ, Dept Chem, Box 8204, Raleigh, NC 27695 USA;

    Carnegie Mellon Univ, Dept Chem, 4400 5th Ave, Pittsburgh, PA 15213 USA;

    Carnegie Mellon Univ, Dept Chem, 4400 5th Ave, Pittsburgh, PA 15213 USA;

    North Carolina State Univ, Dept Chem, Box 8204, Raleigh, NC 27695 USA;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
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