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首页> 外文期刊>Fungal biology and biotechnology. >Identification of the UDP-glucose-4-epimerase required for galactofuranose biosynthesis and galactose metabolism in A. niger
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Identification of the UDP-glucose-4-epimerase required for galactofuranose biosynthesis and galactose metabolism in A. niger

机译:鉴定黑曲霉生物合成和半乳糖代谢所需的UDP-葡萄糖-4-表异构酶

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Background Galactofuranose (Gal f )-containing glycoconjugates are important to secure the integrity of the cell wall of filamentous fungi. Mutations that prevent the biosynthesis of Gal f -containing molecules compromise cell wall integrity. In response to cell wall weakening, the cell wall integrity (CWI)-pathway is activated to reinforce the strength of the cell wall. Activation of CWI-pathway in Aspergillus niger is characterized by the specific induction of the agsA gene, which encodes a cell wall α-glucan synthase. Results In this study, we screened a collection of cell wall mutants with an induced expression of agsA for defects in Gal f biosynthesis using a with anti-Gal f antibody (L10). From this collection of mutants, we previously identified mutants in the UDP-galactopyranose mutase encoding gene ( ugmA ). Here, we have identified six additional UDP-galactopyranose mutase ( ugmA ) mutants and one mutant (named mutant #41) in an additional complementation group that displayed strongly reduced Gal f -levels in the cell wall. By using a whole genome sequencing approach, 21 SNPs in coding regions were identified between mutant #41 and its parental strain which changed the amino acid sequence of the encoded proteins. One of these mutations was in gene An14g03820, which codes for a putative UDP-glucose-4-epimerase (UgeA). The A to G mutation in this gene causes an amino acid change of Asn to Asp at position 191 in the UgeA protein. Targeted deletion of ugeA resulted in an even more severe reduction of Gal f in N-linked glucans, indicating that the UgeA protein in mutant #41 is partially active. The ugeA gene is also required for growth on galactose despite the presence of two UgeA homologs in the A. niger genome. Conclusion By using a classical mutant screen and whole genome sequencing of a new Gal f -deficient mutant, the UDP-glucose-4-epimerase gene ( ugeA ) has been identified. UgeA is required for the biosynthesis of Gal f as well as for galactose metabolism in Aspergillus niger .
机译:背景含半乳糖呋喃糖(Gal f)的糖结合物对于确保丝状真菌细胞壁的完整性很重要。阻止含有Gal f的分子生物合成的突变会损害细胞壁的完整性。响应于细胞壁减弱,细胞壁完整性(CWI)-途径被激活以增强细胞壁的强度。黑曲霉中CWI途径的活化以agsA基因的特异性诱导为特征,该基因编码细胞壁α-葡聚糖合酶。结果在这项研究中,我们使用抗Gal f抗体(L10)筛选了具有agsA诱导表达的细胞壁突变体集合,用于Gal f生物合成中的缺陷。从该突变体集合中,我们先前在UDP-吡喃半乳糖突变酶编码基因(ugmA)中确定了突变体。在这里,我们在另一个互补组中鉴定出了六个额外的UDP-半乳糖吡喃糖突变酶(ugmA)突变体和一个突变体(命名为突变体#41),该互补组在细胞壁中显示出大大降低的Gal f水平。通过使用全基因组测序方法,在突变体#41和其亲本菌株之间鉴定出编码区中的21个SNP,从而改变了编码蛋白的氨基酸序列。这些突变之一是在基因An14g03820中,该基因编码一个假定的UDP-葡萄糖-4-表异构酶(UgeA)。该基因中的A到G突变导致UgeA蛋白中第191位的Asn氨基酸变为Asp。 ugeA的靶向缺失导致N-连接的葡聚糖中Gal f的降低更为严重,表明突变体#41中的UgeA蛋白具有部分活性。尽管在黑曲霉基因组中存在两个UgeA同源物,但在半乳糖上生长也需要ugeA基因。结论通过经典的突变体筛选和新的Gal f缺陷突变体的全基因组测序,已鉴定出UDP-葡萄糖-4-表观异构酶基因(ugeA)。 UgeA是黑曲霉的Galf生物合成和半乳糖代谢所必需的。

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