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Antifungal activity of alkanols: inhibition of growth of spoilage yeasts

机译:链烷醇的抗真菌活性:抑制腐败酵母的生长

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Primary aliphatic alkanols from C6 to C_(13) were tested for their antifungal activity against Saccharomyces cerevisiae using a broth dilution method. Undecanol (C_(11)) was found to be the most potent fungicide against this yeast with the minimum fungicidal concentration (MFC) of 25 ug/ml (0.14 mM), followed by decanol (C_(10)) with the minimum inhibitory concentration (MIC) of 50 μg/ml (0.31 mM). The time-kill curve study showed that undecanol was fungicidal against S. cerevisiae at any growth stages. This fungicidal activity was not influenced by pH values. Dodecanol (C_(12)) was the most effective fungistatic but did not show any fungicidal activity up to 1600 μg/mL. Fungistatic dodecanol quickly reduced cell viability, but the cell viability recovered shortly after and then finally became no longer different from the control indicating that the effect of dodecanol on S. cerevisiae was classified as a sublethal damage. However, fungistatic dodecanol combined with sublethal amount of ane-thole showed a fungicidal activity against this yeast. Anethole completely restricted the recovery of cell viability. Therefore expression of the synergistic effect was probably due to the blockade of the recovering process from dodecanol induced-stress. The alkanols tested inhibited glucose-induced acidification by inhibiting the plasma membrane H~+-ATPase. Octanol (C8) increased plasma membrane fluidity in the spheroplast cells of S. cerevisiae. The same series of aliphatic primary alkanols was also tested against a food spoilage fungus Zygosacchar-omyces bailii and compared with their effects against S. cerevisiae. Decanol was found to be the most potent fungicide against Z bailii with an MFC of 50 μg/ml (0.31 mM), whereas undecanol was found to be the most potent fungistatic with an MIC of 25 μg/ml (0.14 mM). The time-kill curve study showed that decanol was fungicidal against Z. bailii at any growth stage.
机译:使用肉汤稀释方法对来自C6至C_(13)的初级脂族链烷醇从C6到C_(13)进行抗真菌活性,用于使用肉汤稀释方法对酿酒酵母进行抗真菌活性。发现未甲烷醇(C_(11))是对该酵母的最有效的杀菌剂,其最小杀菌剂浓度(MFC)为25ug / ml(0.14mm),其次是癸醇(C_(10)),最小抑制浓度(MIC)为50μg/ ml(0.31mm)。时间杀死曲线研究表明,未在任何生长阶段对酿酒酵母的杀菌剂是杀菌剂。这种杀真菌活性不受pH值的影响。十二烷醇(C_(12))是最有效的功能性,但没有显示出可杀菌活性高达1600μg/ ml。稳定性十二烷醇迅速降低细胞活力,但短暂后的细胞活力恢复,然后终于不再与对照不同,表明十二烷醇对酿酒酵母的影响被归类为核心损伤。然而,与止核量的Ane-kole相结合的杀菌十二烷醇表达了对该酵母的杀真菌活性。苯乙烯完全限制了细胞活力的恢复。因此,表达协同效应可能是由于十二烷醇诱导应激的回收过程的阻断。通过抑制血浆膜H〜+ -ATPase来测试链烷醇抑制葡萄糖诱导的酸化。辛醇(C8)增加了S.酿酒酵母的血球体细胞中的血浆膜流动性。同一系列脂肪族原代链醇也针对食物腐败的真菌Zygosacchar-Omyces Bailii进行了测试,并与其对酿酒酵母的影响进行比较。发现癸醇是针对Z Zailii的最有效的杀菌剂,MFC为50μg/ ml(0.31mm),而未甲烷醇被发现是最有效的稳定性,MIC为25μg/ ml(0.14mm)。时间杀死曲线研究表明,在任何生长阶段,癸醇对Z.Bailii进行了杀菌剂。

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