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Influence of the chloride channel of Fusarium oxysporum on extracellular laccase activity and virulence on tomato plants

机译:镰刀镰刀菌氯通道对番茄植物细胞外漆酶活性和毒力的影响

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CLC-type voltage-gated chloride channels are a family of proteins which mediate chloride transport across the plasma and intracellular membranes. A clc1 gene from the vascular wilt fungus Fusarium oxysporum was characterized and disrupted. The predicted Clc1 protein contained highly conserved transmembrane and CBS domains of this protein family and showed significant identities to the Saccharomyces cerevisiae GEF1 and the Cryptococcus neoformans CLC-A chloride channels. Inactivation of clc1 caused a deficiency in laccase activity which was more severe than that found in any of the structural laccase mutants previously described. The addition of copper sulphate to the growth medium resulted in total recovery of extracellular laccase activity in Δclc1 mutants, although it did not activate transcription of any laccase genes. The pleiotropic phenotype displayed by the Fusarium chloride channel-deficient mutants included a significant delay in the development of disease on tomato plants, with a higher sensitivity to oxidative stress compounds as well as a significant decrease in laccase activity, thus suggesting a possible connection between virulence and the two processes. Nevertheless, we cannot rule out that additional phenotypes present in the Δclc1 mutants could play an essential role in the full virulence of Fusarium.
机译:CLC型电压门控氯化物通道是蛋白质的一系列蛋白质,其在血浆和细胞内膜上介导氯化物输送。来自血管枯萎真菌镰刀菌的CLC1基因特征和破坏。预测的CLC1蛋白含有高度保守的跨膜和该蛋白质系列的CBS结构域,并且对酿酒酵母GEF1和密集的CLC-N氯化物通道显示出显着的身份。 CLC1的失活导致漆酶活性的缺乏,其比先前描述的任何结构漆酶突变体中发现更严重。硫酸铜向生长培养基中加入ΔClC1突变体中细胞外漆酶活性的总回收,尽管它没有激活任何漆酶基因的转录。镰状氯化物通道缺陷型突变体显示的磷酸化表型包括番茄植物疾病发展的显着延迟,对氧化应激化合物的敏感性较高,以及漆酶活性的显着降低,从而表明毒力之间可能的连接和两个过程。然而,我们不能排除ΔClC1突变体中存在的其他表型可以在镰刀菌的全部毒力中起重要作用。

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