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The biosynthetic pathway of coenzyme F430 in methanogenic and methanotrophic archaea

机译:辅酶F430在产甲烷和甲烷营养古细菌中的生物合成途径

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摘要

Methyl-coenzyme M reductase (MCR) is the key enzyme of methanogenesis and anaerobic methane oxidation. The activity of MCR is dependent on the unique nickel-containing tetrapyrrole known as coenzyme F430. We used comparative genomics to identify the coenzyme F430 biosynthesis (cfb) genes and characterized the encoded enzymes from Methanosarcina acetivorans C2A. The pathway involves nickelochelation by a nickel-specific chelatase, followed by amidation to form Ni-sirohydrochlorin a, c-diamide. Next, a primitive homolog of nitrogenase mediates a six-electron reduction and g-lactamization reaction before a Mur ligase homolog forms the six-membered carbocyclic ring in the final step of the pathway. These data show that coenzyme F430 can be synthesized from sirohydrochlorin using Cfb enzymes produced heterologously in a nonmethanogen host and identify several targets for inhibitors of biological methane formation.
机译:甲基辅酶M还原酶(MCR)是甲烷生成和厌氧甲烷氧化的关键酶。 MCR的活性取决于称为辅酶F430的独特含镍四吡咯。我们使用比较基因组学来鉴定辅酶F430生物合成(cfb)基因,并表征了乙草甲烷菌(Methanosarcina acetivorans C2A)编码的酶。该途径涉及通过镍特异性螯合酶进行镍螯合,然后酰胺化以形成Ni-西罗盐酸霉素a,c-二酰胺。接下来,在途径的最后一步中,Mur连接酶同源物形成六元碳环,然后氮酶的原始同源物介导六电子还原和g-内酰胺化反应。这些数据表明,可以使用在非甲烷源宿主中异源产生的Cfb酶,从西氯霉素合成辅酶F430,并确定了一些生物甲烷形成抑制剂的靶标。

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  • 来源
    《Science》 |2016年第6310期|339-342|共4页
  • 作者单位

    Auburn Univ, Dept Chem & Biochem, Auburn, AL 36849 USA;

    Auburn Univ, Dept Chem & Biochem, Auburn, AL 36849 USA;

    Auburn Univ, Dept Chem & Biochem, Auburn, AL 36849 USA;

    Auburn Univ, Dept Chem & Biochem, Auburn, AL 36849 USA|Zhengzhou Univ Light Ind, Sch Food & Biol Engn, Zhengzhou 450002, Peoples R China;

    Auburn Univ, Dept Chem & Biochem, Auburn, AL 36849 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);
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  • 正文语种 eng
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