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Thiamine increases the resistance of baker's yeast Saccharomyces cerevisiae against oxidative, osmotic and thermal stress, through mechanisms partly independent of thiamine diphosphate-bound enzymes

机译:硫胺素通过部分独立于硫胺素二磷酸结合酶的机制提高了面包酵母啤酒酵母对氧化,渗透和热胁迫的抵抗力

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摘要

Numerous recent studies have established a hypothesis that thiamine (vitamin B-1) is involved in the responses of different organisms against stress, also suggesting that underlying mechanisms are not limited to the universal role of thiamine diphosphate (TDP) in the central cellular metabolism. The current work aimed at characterising the effect of exogenously added thiamine on the response of baker's yeast Saccharomyces cerevisiae to the oxidative (1 mM H2O2), osmotic (1 M sorbitol) and thermal (42 degrees C) stress. As compared to the yeast culture in thiamine-free medium, in the presence of 1.4 mu M external thiamine, (1) the relative mRNA levels of major TDP-dependent enzymes under stress conditions vs. unstressed control (the 'stress/control ratio') were moderately lower, (2) the stress/control ratio was strongly decreased for the transcript levels of several stress markers localised to the cytoplasm, peroxisomes, the cell wall and (with the strongest effect observed) the mitochondria (e.g. Mn-superoxide dismutase), (3) the production of reactive oxygen and nitrogen species under stress conditions was markedly decreased, with the significant alleviation of concomitant protein oxidation. The results obtained suggest the involvement of thiamine in the maintenance of redox balance in yeast cells under oxidative stress conditions, partly independent of the functions of TDP-dependent enzymes.
机译:最近的许多研究已经建立了这样的假设:硫胺素(维生素B-1)参与不同生物体对压力的反应,也表明潜在的机制不仅限于硫胺素二磷酸酯(TDP)在中央细胞代谢中的普遍作用。当前的工作旨在表征外源添加的硫胺素对面包酵母啤酒酵母对氧化应激(1 mM H2O2),渗透压(1 M山梨糖醇)和热应激(42摄氏度)的响应。与在无硫胺素的培养基中进行酵母培养相比,在存在1.4μM外部硫胺素的情况下,(1)应激条件下与不受胁迫的对照相比,主要TDP依赖性酶的相对mRNA水平(``胁迫/对照比'' )适度降低,(2)定位于细胞质,过氧化物酶体,细胞壁和线粒体(例如锰超氧化物歧化酶)的几种胁迫标记的转录水平,胁迫/控制比大大降低),(3)胁迫条件下活性氧和氮的产生明显减少,显着减轻了伴随的蛋白质氧化。获得的结果表明,硫胺素在氧化应激条件下参与酵母细胞氧化还原平衡的维持,部分独立于TDP依赖性酶的功能。

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