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Fungicides and sterol-deficient mutants of Ustilago maydis: plasma membrane physico-chemical characteristics do not explain growth inhibition

机译:Ustilago maydis的杀菌剂和甾醇缺乏突变体:血浆膜的物理化学特性不解释生长抑制

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Plasma membrane vesicles from erg11 and erg2 sterol-deficient mutants and from wild-type Ustilago maydis sporidia treated with and without inhibitors of sterol 14α-demethylase or sterol Δ8-Δ7 isomerase (triadimenol and fenpropimorph fungicides, respectively) were purified by aqueous two-phase partitioning. Changes in plasma membrane lipid composition were mostly restricted to sterols and complex lipid-bound fatty acids (CLB fatty acids). There was a greater accumulation of abnormal sterols (14α-methyl- or Δ8-unsaturated sterols) in plasma membranes from sterol-deficient mutants than from those treated with their fungicide counterparts. However, greater growth inhibition was observed on fungicide-treated wild-type than on mutants. Changes in CLB fatty acids were restricted to alterations in the relative proportion of linoleic acid (18:2) with respect to oleic acid (18:1). The 18:2 to 18:1 ratio found in CLB fatty acids in plasma membranes could be correlated to rates of sporidial growth but not to accumulation of a particular abnormal sterol or to the extent of sterol replacement. Plasma membrane permeability to protons was increased moderately in the mutants only. No changes were observed in plasma membrane fluidity. Plasma membrane H+-ATPase activity was increased up to twofold in those cases with lower growth rate. It was concluded that fungicide-induced growth inhibition in U. maydis was not due to accumulation of abnormal sterols in plasma membranes but probably due to intracellular ATP depletion by the H+-ATPase and that changes in 18:2 to 18:1 ratio in CLB fatty acids were not directly dependent on the plasma membrane physical state or lipid composition but were possibly part of a stress adaptation mechanism.
机译:通过两相水溶液纯化来自ERG11和ERG2甾醇缺失突变体和用甾醇14α-脱甲基酶或甾醇δ8-Δ7异构酶(三元酚和芬太科尔和FENPROPIMORPH杀菌剂的野生型Ustilago MAYDIS孢子的血浆膜囊泡。分区。质膜脂肪组合物的变化主要限于甾醇和复合脂质结合的脂肪酸(CLB脂肪酸)。在甾醇缺陷型突变体中血浆膜中的异常甾醇(14α-甲基 - 或Δ8-不饱和甾甾型)的积累量大于用杀真菌剂对应物处理的那些。然而,在杀菌剂处理的野生型上观察到比突变体更大的生长抑制。 CLB脂肪酸的变化仅限于亚油酸(18:2)相对于油酸(18:1)的相对比例的改变。在血浆膜中CLB脂肪酸中发现的18:2至18:1可以与孢子液生长的速率相关,而不是对特定异常的甾醇的积累或甾醇替代的程度相关。质子膜渗透性仅在突变体中适度增加。在血浆膜流动性中没有观察到变化。在较低生长速率的情况下,血浆膜H + -ATPase活性增加至两倍。得出结论是,杀菌剂诱导的U. maydis诱导的生长抑制不是由于血浆膜中的异常甾醇的积累,但可能是由于H + -ATP酶的细胞内ATP耗竭,并且在CLB中的比例为18:2至18:1。脂肪酸不直接依赖于血浆膜的物理状态或脂质组合物,而是可能是应力适应机制的一部分。

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