Probst Corinna, Ringel Phillip, Boysen Verena, Wirsing Lisette, Alexander Mariko Matsuda, Mendel Ralf R, Kruse Tobias
Department of Plant Biology, Braunschweig University of Technology, 38106 Braunschweig, Germany.
Cellular Proteomics, Helmholtz Centre for Infection Research, 38124 Braunschweig, Germany.
Fungal Genet Biol. 2014 May;66:69-78. doi: 10.1016/j.fgb.2014.02.004. Epub 2014 Feb 23.
Molybdenum (Mo) is a trace element that is essential for important cellular processes. To gain biological activity, Mo must be complexed in the molybdenum cofactor (Moco), a pterin derivative of low molecular weight. Moco synthesis is a multi-step pathway that involves a variable number of genes in eukaryotes, which are assigned to four steps of eukaryotic Moco biosynthesis. Moco biosynthesis mutants lack any Moco-dependent enzymatic activities, including assimilation of nitrate (plants and fungi), detoxification of sulfite (humans and plants) and utilization of hypoxanthine as sole N-source (fungi). We report the first comprehensive genetic characterization of the Neurospora crassa (N. crassa) Moco biosynthesis pathway, annotating five genes which encode all pathway enzymes, and compare it with the characterized Aspergillus nidulans pathway. Biochemical characterization of the corresponding knock-out mutants confirms our annotation model, documenting the N. crassa/A. nidulans (fungal) Moco biosynthesis as unique, combining the organizational structure of both plant and human Moco biosynthesis genes.
钼(Mo)是一种对重要细胞过程必不可少的微量元素。为了获得生物活性,钼必须与钼辅因子(Moco)结合,Moco是一种低分子量的蝶呤衍生物。Moco合成是一条多步骤途径,在真核生物中涉及数量可变的基因,这些基因被分配到真核生物Moco生物合成的四个步骤中。Moco生物合成突变体缺乏任何依赖Moco的酶活性,包括硝酸盐同化(植物和真菌)、亚硫酸盐解毒(人类和植物)以及利用次黄嘌呤作为唯一氮源(真菌)。我们报告了粗糙脉孢菌(N. crassa)Moco生物合成途径的首次全面遗传特征分析,注释了五个编码所有途径酶的基因,并将其与已表征的构巢曲霉途径进行比较。相应敲除突变体的生化特征证实了我们的注释模型,证明了粗糙脉孢菌/构巢曲霉(真菌)的Moco生物合成是独特的,结合了植物和人类Moco生物合成基因的组织结构。