首页> 外文期刊>Pesticide Biochemistry and Physiology >A novel fungicide aminopyrifen inhibits GWT-1 protein in glycosylphosphatidylinositol-anchor biosynthesis in Neurospora crassa
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A novel fungicide aminopyrifen inhibits GWT-1 protein in glycosylphosphatidylinositol-anchor biosynthesis in Neurospora crassa

机译:新型杀菌剂氨基吡啶豆在神经孢子群中的糖基磷脂酰肌醇 - 锚锚生物合成中抑制GWT-1蛋白

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摘要

Aminopyrifen, 4-phenoxybenzyl 2-amino-6-methylnicotinate, strongly inhibited the mycelial growth of a wild type Neurospora crassa strain on Vogel's minimal medium containing 1.2% sucrose, with a 0.001 mg/L concentration required for 50% growth inhibition. Similar to micafungin, an inhibitor of beta-1, 3-glucan synthetase, aminopyrifen further inhibited the growth of N. crassa deletion mutants of MAP kinase cascade genes, such as mak-1 and mak-2, than the wild-type strain, suggesting that aminopyrifen perturbs cell wall-related processes. Furthermore, we found that three chitin synthase gene mutants (chs-1, chs-5, and chs-7) were highly sensitive to both chemicals; however, aminopyrifen, but not micafungin, induced a swollen germ tube from the conidia of chs-5 and chs-7 mutants on Vogel's medium containing 1.2% sucrose. To elucidate the target protein of aminopyrifen, we isolated mutants resistant to aminopyrifen after UV treatment of conidia of the wild-type strain or the chs-5 strain. The resistance mutations were localized to the gwt-1 gene that encodes an acyltransferase, GWT-1, which participates in the biosynthesis of the glycosylphosphatidylinositol (GPI) precursor, and were found to result in S180F and V178A alterations in the protein. These results strongly suggest that aminopyrifen works as an inhibitor targeting GWT-1, a protein involved in GPI-anchor biosynthesis.
机译:氨基吡啶,4-苯氧基苄基2-氨基-6-甲基甲酸酯强烈抑制伴随含有1.2%蔗糖的VoGel最小培养基的野生型神经孢子菌株的菌丝体生长,50%生长抑制所需的0.001mg / L浓度。类似于Micafungin,β-1,3-葡聚糖合成酶的抑制剂,氨基吡芬进一步抑制了Map激酶级联基因的N.Crassa缺失突变体的生长,如MAK-1和MAK-2,而不是野生型菌株,建议氨基吡啶蛋白渗透细胞壁相关过程。此外,我们发现三个几丁质合成酶基因突变体(CHS-1,CHS-5和CHS-7)对两种化学物质非常敏感;然而,氨基吡啶蛋白,但不是Micafungin,从CHS-5和CHS-7突变体的CHS-7突变体诱导含有1.2%蔗糖的vogel培养基的肿胀胚筒。为了阐明氨基吡啶的靶蛋白,我们在UV处理野生型菌株或CHS-5菌株的紫外线处理后抵抗氨基吡啶的突变体。将抗性突变定位于编码酰基转移酶的GWT-1基因,GWT-1,其参与糖基磷脂酰肌醇(GPI)前体的生物合成,并且发现导致蛋白质中的S180F和V178A改变。这些结果强烈表明,氨基吡啶薄荷作为靶向GWT-1的抑制剂,其参与GPI锚生物合成的蛋白质。

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