首页> 外文期刊>Science >Extending the Carbon Chain:Hydrocarbon Formation Catalyzed by Vanadium/Molybdenum Nitrogenases
【24h】

Extending the Carbon Chain:Hydrocarbon Formation Catalyzed by Vanadium/Molybdenum Nitrogenases

机译:延长碳链:钒/钼氮酶催化的烃形成

获取原文
获取原文并翻译 | 示例
       

摘要

In a small-scale reaction, vanadium-dependent nitrogenase has previously been shown to catalyze reductive catenation of carbon monoxide (CO) to ethylene, ethane, propylene, and propane. Here, we report the identification of additional hydrocarbon products [a-butylene, n-butane, and methane (CH_4)] in a scaled-up reaction featuring 20 milligrams of vanadium-iron protein, the catalytic component of vanadium nitrogenase. Additionally, we show that the more common molybdenum-dependent nitrogenase can generate the same hydrocarbons from CO, although CH_4 was not detected. The identification of CO as a substrate for both molybdenum- and vanadium-nitrogenases strengthens the hypothesis that CO reduction is an evolutionary relic of the function of the nitrogenase family. Moreover, the comparison between the CO-reducing capacities of the two nitrogenases suggests that the identity of heterometal at the active cofactor site affects the efficiency and product distribution of this reaction.
机译:在小规模的反应中,钒依赖的固氮酶先前已显示出催化一氧化碳(CO)还原连接到乙烯,乙烷,丙烯和丙烷的能力。在这里,我们报告了在以20毫克钒铁蛋白(钒氮酶的催化成分)为特征的放大反应中,鉴定了其他烃类产物[α-丁烯,正丁烷和甲烷(CH_4)]。此外,我们显示了更常见的钼依赖性固氮酶可以从CO中生成相同的碳氢化合物,尽管未检测到CH_4。将CO鉴定为钼和钒氮酶的底物,可以强化以下假设:CO还原是硝化酶家族功能的进化产物。此外,两种固氮酶的CO还原能力之间的比较表明,活性辅因子位点上的杂金属身份会影响该反应的效率和产物分布。

著录项

  • 来源
    《Science》 |2011年第6043期|p.753-755|共3页
  • 作者单位

    Department of Molecular Biology and Biochemistry, University of California, Irvine, CA 92697-3900, USA.;

    Department of Molecular Biology and Biochemistry, University of California, Irvine, CA 92697-3900, USA.;

    Department of Molecular Biology and Biochemistry, University of California, Irvine, CA 92697-3900, 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
  • 中图分类
  • 关键词

  • 入库时间 2022-08-18 02:54:05

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