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A small metabolic flux model to identify transient metabolic regulations in Saccharomyces cerevisiae

机译:一个小型代谢通量模型,用于识别酿酒酵母中的瞬时代谢调控

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摘要

The understanding of dynamic metabolic regulations is important for physiological studies and strain characterization tasks. The present study combined transient experiments with online metabolic flux analysis (MFA) in order to quantify metabolic regulations, namely carbon catabolite repression of respiration and transient acetic-acid production, in Saccharomyces cerevisiae during aerobic growth on glucose. The aim was to investigate which additional information can be gained from using a small metabolic flux model to study transient growth provoked by shift-up and shift-down experiments, compared to online monitoring alone. The MFA model allowed us to propose new correlations between pathways of the central metabolism. A linear correlation between glycolytic flux and respiratory capacity holds for shift-down and shift-up experiments. This confirmed that respiratory functions were subjected to carbon catabolite repression and suggested that respiratory capacity is controlled by the glycolytic flux rather than the glucose influx. Furthermore, the model showed that control of repression of respiration by the glycolytic flux was a dynamic phenomenon. Co-factor balancing within the MFA model showed that transient acetic-acid production indicated a transient limitation in another part of the central metabolism but not in oxidative phosphorylation. However, at super-critical growth rates and when coupling of anabolism and catabolism is resumed, the limitation shifts to oxidative phosphorylation, with the consequence that ethanol is formed. The online application of small metabolic flux models to transient experiments enhanced the physiological insight into transient growth and opens up the use of transient experiments as an efficient tool to understand dynamic metabolic regulations.
机译:动态代谢调节的理解对于生理学研究和菌株表征任务很重要。本研究将瞬时实验与在线代谢通量分析(MFA)相结合,以量化酿酒酵母在葡萄糖有氧生长过程中代谢规律,即碳分解代谢物对呼吸的抑制作用和瞬时乙酸的产生。目的是研究与单独的在线监测相比,使用小的代谢通量模型研究由上移和下移实验引起的瞬时生长,可以从中获得哪些其他信息。 MFA模型使我们能够提出中央代谢途径之间的新关联。糖酵解通量和呼吸能力之间的线性相关性适用于降档和升档实验。这证实呼吸功能受到碳分解代谢物的抑制,并表明呼吸能力是由糖酵解通量而不是葡萄糖流入控制的。此外,该模型表明,通过糖酵解通量控制呼吸抑制是一种动态现象。 MFA模型中的辅助因子平衡表明,短暂的乙酸产生表明在中央代谢的另一部分存在短暂的局限性,但在氧化磷酸化中却没有。但是,在超临界生长速率下,当恢复合成代谢和分解代谢的耦合时,限制将转移到氧化磷酸化,从而形成乙醇。小代谢通量模型在瞬态实验中的在线应用增强了对瞬态生长的生理洞察力,并开辟了使用瞬态实验作为了解动态代谢规律的有效工具的机会。

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