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Heterologous Biosynthesis of Nodulisporic Acid F

机译:根瘤菌酸F的异源生物合成

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摘要

Nodulisporic acids comprise a group of valuable indole diterpenes that exhibit potent insecticidal activities. We report the identification of a gene cluster in the genome of the filamentous fungus Hypoxylon pulicicidum ( Nodulisporium sp.) that contains genes responsible for the biosynthesis of nodulisporic acids. Using Penicillium paxilli as a heterologous host, and through pathway reconstitution experiments, we identified the function of four genes involved in the biosynthesis of the nodulisporic acid core compound, nodulisporic acid F (NAF). Two of these genes ( nodM and nodW ) are especially significant as they encode enzymes with previously unreported functionality: nodM encodes a 3-geranylgeranylindole epoxidase capable of catalyzing only a single epoxidation step to prime formation of the distinctive ring structure of nodulisporic acids, and nodW encodes the first reported gene product capable of introducing a carboxylic acid moiety to an indole diterpene core structure that acts as a reactive handle for further modification. Here, we present the enzymatic basis for the biosynthetic branch point that gives rise to nodulisporic acids.
机译:根瘤菌酸包含一组有价值的吲哚二萜,它们具有有效的杀虫活性。我们报告了在丝状真菌Hypoxylon pulicicidum(Nodulisporium sp。)的基因组中的一个基因簇的鉴定,该基因簇包含负责根瘤菌酸的生物合成的基因。使用青霉青霉菌作为异源宿主,并通过途径重建实验,我们确定了参与结节孢子酸核心化合物结节孢子酸F(NAF)生物合成的四个基因的功能。这些基因中的两个(nodM和nodW)特别重要,因为它们编码的酶以前没有报告过的功能:nodM编码一个3-geranylgeranylindole环氧酶,该酶只能催化一个环氧化步骤,从而引发结节孢子酸独特的环结构的形成,而nodW编码第一个报告的基因产物,该产物能够将羧酸部分引入吲哚二萜核心结构,该结构充当进一步修饰的反应性手柄。在这里,我们介绍了引起结节孢子酸的生物合成分支点的酶促基础。

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  • 来源
    《Journal of the American Chemical Society》 |2018年第2期|582-585|共4页
  • 作者单位

    Ferrier Research Institute, Victoria University of Wellington, Wellington 6012, New Zealand,Biomolecular Interaction Centre, University of Canterbury, 20 Kirkwood Avenue, Christchurch 8041, New Zealand;

    Ferrier Research Institute, Victoria University of Wellington, Wellington 6012, New Zealand,Biomolecular Interaction Centre, University of Canterbury, 20 Kirkwood Avenue, Christchurch 8041, New Zealand;

    Ferrier Research Institute, Victoria University of Wellington, Wellington 6012, New Zealand,Biomolecular Interaction Centre, University of Canterbury, 20 Kirkwood Avenue, Christchurch 8041, New Zealand;

    Biomolecular Interaction Centre, University of Canterbury, 20 Kirkwood Avenue, Christchurch 8041, New Zealand;

    Institute of Fundamental Sciences, Massey University, Private Bag 11 222, Palmerston North 4442, New Zealand;

    Protein Science & Engineering, Callaghan Innovation, University of Canterbury, Private Bag 4800, Christchurch 8140, New Zealand;

    Institute of Fundamental Sciences, Massey University, Private Bag 11 222, Palmerston North 4442, New Zealand;

    Ferrier Research Institute, Victoria University of Wellington, Wellington 6012, New Zealand,Biomolecular Interaction Centre, University of Canterbury, 20 Kirkwood Avenue, Christchurch 8041, New Zealand;

  • 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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  • 入库时间 2022-08-18 03:07:16

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