食品科学 ›› 2017, Vol. 38 ›› Issue (4): 26-31.doi: 10.7506/spkx1002-6630-201704005

• 生物工程 • 上一篇    下一篇

内源性氧化胁迫促进酿酒酵母合成谷胱甘肽的潜在机制分析

王立梅,任清华,郑丽雪,孙 姜,齐 斌,朱益波   

  1. 1.常熟理工学院生物与食品工程学院,江苏 常熟 215500;2.烟台啤酒青岛朝日有限公司,山东 烟台 264000; 3.中海海洋无锡海洋工程装备有限公司,江苏 无锡 214000
  • 出版日期:2017-02-25 发布日期:2017-02-28
  • 基金资助:
    国家自然科学基金面上项目(31171758)

Elucidation of the Underlying Mechanism by Which Endogenous Oxidative Stress Promotes Glutathione Synthesis of Saccharomyces cerevisiae

WANG Limei, REN Qinghua, ZHENG Lixue, SUN Jiang, QI Bin, ZHU Yibo   

  1. 1. College of Biological and Food Engineering, Changshu Institute of Technology, Changshu 215500, China; 2. Yantai Beer Tsingtao Asahi Co. Ltd., Yantai 264000, China; 3. Wuxi Ocean Engineering Equipment Co. Ltd. of Zhonghai Ocean, Wuxi 214000, China
  • Online:2017-02-25 Published:2017-02-28

摘要: 利用转录组学分析手段结合生理生化特性来研究酿酒酵母突变株高产谷胱甘肽的潜在机制。结果表明:突变株谷胱甘肽合成限速酶、抗氧化酶活力及其编码基因表达量、过氧化氢和还原型辅酶Ⅱ(nicotinamide adeninedinucleotide phosphate,NADPH)含量显著提高;丙酮酸激酶活力、丙酮酸、柠檬酸和琥珀酸含量显著降低;此外,三羧酸循环和磷酸戊糖途径的基因表达量分别显著下调和上调。因此,突变株可能在遭受内源性活性氧过氧化氢的胁迫下,通过调节谷胱甘肽合成限速酶活力加强了谷胱甘肽的合成,与抗氧化酶共同抵御氧化胁迫;丙酮酸激酶活力减弱降低了丙酮酸的合成,减少了三羧酸循环的通量,使得磷酸戊糖途径通量增加,从而提高了NADPH含量,为谷胱甘肽的合成提供了充足的还原力。

关键词: 谷胱甘肽, 氧化胁迫, 酿酒酵母, 还原型辅酶Ⅱ

Abstract: The potential mechanism for glutathione oversynthesis in the Saccharomyces cerevisiae mutant Y518 was researched using transcriptome analysis combined with physiological and biochemical characteristics. The results indicated that the rate-limiting enzyme of glutathione synthesis, antioxidant enzymes activities and the expression levels of their encoding genes, and the contents of hydrogen peroxide and nicotinamide adenine dinucleotide phosphate (NADPH) were significantly increased in the mutant whereas pyruvatekinase activity, the contents of pyruvate, citrate and succinate were markedly decreased. Besides, the expression levels of genes involved in the citrate cycle were significantly down-regulated while those involved in the pentose phosphate pathway were significantly up-regulated. Therefore, under endogenous oxidative stress, the mutant might strengthen the synthesis of glutathione by adjusting the activities of rate-limiting enzymes of glutathione synthesis to defend against oxidative stress together with the antioxidant enzymes. Meanwhile, weakened pyruvatekinase activity decreased pyruvate generation, which led to declined citrate cycle flux and increased NADPH production by the pentose phosphate pathway and consequently provided appropriate reducing power for glutathione biosynthesis.

Key words: glutathione, oxidative stress, Saccharomyces cerevisiae, NADPH

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