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The Aspergillus fumigatus Protein GliK Protects against Oxidative Stress and Is Essential for Gliotoxin Biosynthesis

机译:烟曲霉蛋白GliK可以抵抗氧化应激,对胶质生物合成至关重要

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The function of a number of genes in the gliotoxin biosynthetic cluster (gli) in Aspergillus fumigatus remains unknown. Here, we demonstrate that gliK deletion from two strains of A. fumigatus completely abolished gliotoxin biosynthesis. Furthermore, exogenous H2O2 (1 mM), but not gliotoxin, significantly induced A. fumigatus gliK expression (P = 0.0101). While both mutants exhibited significant sensitivity to both exogenous gliotoxin (P < 0.001) and H2O2 (P < 0.01), unexpectedly, exogenous gliotoxin relieved H2O2-induced growth inhibition in a dose-dependent manner (0 to 10 μg/ml). Gliotoxin-containing organic extracts derived from A. fumigatus ATCC 26933 significantly inhibited (P < 0.05) the growth of the ΔgliK26933 deletion mutant. The A. fumigatus ΔgliK26933 mutant secreted metabolites, devoid of disulfide linkages or free thiols, that were detectable by reverse-phase high-performance liquid chromatography and liquid chromatography-mass spectrometry with m/z 394 to 396. These metabolites (m/z 394 to 396) were present at significantly higher levels in the culture supernatants of the A. fumigatus ΔgliK26933 mutant than in those of the wild type (P = 0.0024 [fold difference, 24] and P = 0.0003 [fold difference, 9.6], respectively) and were absent from A. fumigatus ΔgliG. Significantly elevated levels of ergothioneine were present in aqueous mycelial extracts of the A. fumigatus ΔgliK26933 mutant compared to the wild type (P < 0.001). Determination of the gliotoxin uptake rate revealed a significant difference (P = 0.0045) between that of A. fumigatus ATCC 46645 (9.3 pg/mg mycelium/min) and the ΔgliK46645 mutant (31.4 pg/mg mycelium/min), strongly suggesting that gliK absence and the presence of elevated ergothioneine levels impede exogenously added gliotoxin efflux. Our results confirm a role for gliK in gliotoxin biosynthesis and reveal new insights into gliotoxin functionality in A. fumigatus.
机译:烟曲霉中胶质毒素生物合成簇( gli )中许多基因的功能尚不清楚。在这里,我们证明从两个烟曲霉菌株中的 gliK 缺失完全消除了胶质毒素的生物合成。此外,外源H 2 O 2 (1 mM)而非胶质毒素显着诱导了 A。烟气gliK 表达( P = 0.0101)。尽管这两个突变体均对外源性胶质毒素( P <0.001)和H 2 O 2 P <0.01),出乎意料的是,外源性胶质毒素以剂量依赖的方式(0至10μg/ ml)缓解了H 2 O 2 诱导的生长抑制。烟曲霉ATCC 26933衍生的含胶体毒素的有机提取物显着抑制( P <0.05)Δ gliK 26933 缺失突变体的生长。烟曲霉Δ gliK 26933 突变体分泌的代谢产物无二硫键或游离硫醇,可通过反相高效液相色谱和液相色谱-质谱检测光谱法使用 m / z 394至396。这些代谢产物( m / z 394至396)在烟曲霉Δ< em> gliK 26933 突变体比野生型突变体( P = 0.0024 [倍数差异,24]和 P =烟曲霉Δ gliG 中没有0.0003 [倍数差异,分别为9.6]。与野生型相比,烟曲霉Δ gliK 26933 突变体的水菌丝体提取物中的麦角硫因水平显着升高( P <0.001 )。胶质毒素摄取率的测定表明,烟曲霉ATCC 46645(9.3 pg / mg菌丝/分钟)和Δ gliK 之间存在显着差异( P = 0.0045)。 46645 突变体(31.4 pg / mg菌丝体/分钟),强烈表明 gliK 的缺失和麦角硫因水平的升高阻碍了外源性胶质毒素外排。我们的结果证实了 gliK 在胶质毒素生物合成中的作用,并揭示了对烟曲霉胶质毒素功能的新见解。

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