Samokhvalov V, Ignatov V, Kondrashova M
Department of Biochemistry, Saratov State University, Astarkhanskaya Street 83, Saratov 410026, Russia.
Biochimie. 2004 Jan;86(1):39-46. doi: 10.1016/j.biochi.2003.10.019.
We investigated oxidative processes in mitochondria of Saccharomyces cerevisiae grown on ethanol in the course of chronological aging. We elaborated a model of chronological aging that avoids the influence of exhaustion of medium, as well as the accumulation of toxic metabolites during aging. A decrease in total respiration of cells and, even more, of the contribution of respiration coupled with ATP-synthesis was observed during aging. Aging is also related with the decrease of the contribution of malonate-insensitive respiration. Activities of citrate-synthase (CS), alpha-ketoglutarate dehydrogenase (KGDH) and malate dehydrogenase (MDH) were threefold decreased. The activity of NADP-dependent isocitrate dehydrogenase (NADP-ICDH) decreased more significantly, while the activity of NAD-dependent isocitrate dehydrogenase (NAD-ICDH) fell even greater, being completely inactivated on the third week of aging. In contrast, succinate dehydrogenase (SDH), enzymes of glyoxylate cycle (GCL) (isocitrate lyase (ICL) and malate synthase (MLS)), and enzymes of ethanol oxidation (alcohol dehydrogenase (ADH) and acetaldehyde dehydrogenase (ACDH)), were activated by 50% or more. The behavior of oxidative enzymes and metabolic pathways are apparently inherent to a more viable, long-lived cells in population, selected in the course of chronological aging. This selection allows cells to reveal the mechanism of their higher viability as caused by shunting of complete Krebs cycle by glyoxylate cycle, with a concomitant increased rate of the most efficient energy source, namely succinate formation and oxidation. Thiobarbituric-reactive species (TAR species) increased during aging. We supposed that to be the immediate cause of damage of a part of yeast population. These data show that a greater succinate contribution to respiration in more active cells is a general property of yeast and animal tissues.
我们研究了在乙醇上生长的酿酒酵母线粒体在时序老化过程中的氧化过程。我们构建了一个时序老化模型,该模型避免了培养基耗尽以及老化过程中有毒代谢物积累的影响。在老化过程中,观察到细胞的总呼吸速率下降,尤其是与ATP合成偶联的呼吸作用的贡献下降。老化还与丙二酸不敏感呼吸作用的贡献降低有关。柠檬酸合酶(CS)、α-酮戊二酸脱氢酶(KGDH)和苹果酸脱氢酶(MDH)的活性降低了三倍。NADP依赖的异柠檬酸脱氢酶(NADP-ICDH)的活性下降更为显著,而NAD依赖的异柠檬酸脱氢酶(NAD-ICDH)的活性下降更大,在老化的第三周完全失活。相比之下,琥珀酸脱氢酶(SDH)、乙醛酸循环(GCL)的酶(异柠檬酸裂解酶(ICL)和苹果酸合酶(MLS))以及乙醇氧化的酶(乙醇脱氢酶(ADH)和乙醛脱氢酶(ACDH))被激活了50%或更多。氧化酶和代谢途径的行为显然是在时序老化过程中选择的更具活力、寿命更长的细胞群体所固有的。这种选择使细胞能够揭示其更高活力的机制,即通过乙醛酸循环分流完整的三羧酸循环,同时增加最有效的能量来源琥珀酸的形成和氧化速率。硫代巴比妥酸反应性物质(TAR物质)在老化过程中增加。我们认为这是一部分酵母群体受损的直接原因。这些数据表明,在更活跃的细胞中,琥珀酸对呼吸的贡献更大是酵母和动物组织的普遍特性。