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烟曲霉蛋白GliK可抵御氧化应激,且对Gliotoxin生物合成至关重要。

The Aspergillus fumigatus protein GliK protects against oxidative stress and is essential for gliotoxin biosynthesis.

作者信息

Gallagher Lorna, Owens Rebecca A, Dolan Stephen K, O'Keeffe Grainne, Schrettl Markus, Kavanagh Kevin, Jones Gary W, Doyle Sean

机构信息

Department of Biology and National Institute for Cellular Biotechnology, National University of Ireland Maynooth, Maynooth, County Kildare, Ireland.

出版信息

Eukaryot Cell. 2012 Oct;11(10):1226-38. doi: 10.1128/EC.00113-12. Epub 2012 Aug 17.

Abstract

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 H(2)O(2) (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 H(2)O(2) (P < 0.01), unexpectedly, exogenous gliotoxin relieved H(2)O(2)-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 ΔgliK(26933) deletion mutant. The A. fumigatus ΔgliK(26933) 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 ΔgliK(26933) 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 ΔgliK(26933) 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 ΔgliK(46645) 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.

摘要

烟曲霉中麦角硫因生物合成簇(gli)中多个基因的功能仍不清楚。在此,我们证明从两株烟曲霉中缺失gliK完全消除了麦角硫因的生物合成。此外,外源H₂O₂(1 mM)而非麦角硫因能显著诱导烟曲霉gliK表达(P = 0.0101)。虽然这两个突变体对外源麦角硫因(P < 0.001)和H₂O₂(P < 0.01)均表现出显著敏感性,但出乎意料的是,外源麦角硫因能以剂量依赖方式(0至10 μg/ml)缓解H₂O₂诱导的生长抑制。源自烟曲霉ATCC 26933的含麦角硫因有机提取物显著抑制(P < 0.05)ΔgliK(26933)缺失突变体的生长。烟曲霉ΔgliK(26933)突变体分泌的代谢产物缺乏二硫键或游离巯基,可通过反相高效液相色谱和液相色谱 - 质谱联用检测,其质荷比为394至396。这些代谢产物(质荷比394至396)在烟曲霉ΔgliK(26933)突变体的培养上清液中的含量显著高于野生型(分别为P = 0.0024 [倍数差异,24]和P = 0.0003 [倍数差异,9.6]),且在烟曲霉ΔgliG中不存在。与野生型相比,烟曲霉ΔgliK(26933)突变体的水性菌丝提取物中麦角硫因水平显著升高(P < 0.001)。麦角硫因摄取率的测定显示烟曲霉ATCC 46645(9.3 pg/mg菌丝体/分钟)与ΔgliK(46645)突变体(31.4 pg/mg菌丝体/分钟)之间存在显著差异(P = 0.0045),强烈表明缺失gliK和麦角硫因水平升高会阻碍外源添加的麦角硫因流出。我们的结果证实了gliK在麦角硫因生物合成中的作用,并揭示了烟曲霉中麦角硫因功能的新见解。

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