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首页> 外文期刊>Bioprocess and Biosystems Engineering >Quantitative metabolic flux analysis revealed uneconomical utilization of ATP and NADPH in Acremonium chrysogenum fed with soybean oil
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Quantitative metabolic flux analysis revealed uneconomical utilization of ATP and NADPH in Acremonium chrysogenum fed with soybean oil

机译:定量代谢通量分析显示,大豆油喂养的产黄曲霉中ATP和NADPH的利用不经济

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摘要

A metabolic network was constructed for the Acremonium chrysogenum cultivation fed with soybean oil. Metabolic flux analysis indicated that the shift from exponential growth to rapid cephalosporin C (CPC) formation was accompanied by 1.63- and 5-fold carbon flux enlargement in TCA cycle and glyoxylate by-pass, respectively. The flux via pentose phosphate pathway branch was little affected during the rapid CPC formation period; the contributory explanation was that 35.6% of NADPH was consumed in the dissimilation of fatty acids. Estimation of NADPH, ATP generation, and consumption demonstrated that, with soybean oil as carbon source in rapid CPC formation phase, the NADPH consumed in fatty acid catabolism was fourfold greater than that used in the CPC biosynthesis-relevant part; simultaneously, more than 90% energy spent was not directly related to the CPC formation. Therefore, the improvement of CPC production yield through optimization of the NADPH, ATP generation, and consumption was put forward.
机译:构建了一个大豆油饲育的产黄曲霉的代谢网络。代谢通量分析表明,从指数生长到快速头孢菌素C(CPC)形成的转变分别伴随着TCA循环和乙醛酸旁路的碳通量增加了1.63和5倍。在快速CPC形成期间,通过戊糖磷酸途径分支的通量几乎没有受到影响。造成这种现象的原因是,NADPH的35.6%被用于脂肪酸的异化。对NADPH,ATP产生和消耗的估算表明,以大豆油为快速CPC形成阶段的碳源,脂肪酸分解代谢中消耗的NADPH比CPC生物合成相关部分中消耗的NADPH大四倍。同时,超过90%的能源消耗与CPC的形成没有直接关系。因此,提出了通过优化NADPH,ATP产生和消耗来提高CPC产量的方法。

著录项

  • 来源
    《Bioprocess and Biosystems Engineering》 |2010年第9期|p.1119-1129|共11页
  • 作者单位

    State Key Laboratory of Bioreactor Engineering, East China University of Science and Technology, 130 Meilong Road, P.O. Box 329, Shanghai 200237, People's Republic of China;

    rnState Key Laboratory of Bioreactor Engineering, East China University of Science and Technology, 130 Meilong Road, P.O. Box 329, Shanghai 200237, People's Republic of China;

    rnState Key Laboratory of Bioreactor Engineering, East China University of Science and Technology, 130 Meilong Road, P.O. Box 329, Shanghai 200237, People's Republic of China;

    rnState Key Laboratory of Bioreactor Engineering, East China University of Science and Technology, 130 Meilong Road, P.O. Box 329, Shanghai 200237, People's Republic of China;

    rnState Key Laboratory of Bioreactor Engineering, East China University of Science and Technology, 130 Meilong Road, P.O. Box 329, Shanghai 200237, People's Republic of China;

    rnShanxi Weiqida Pharmaceutical Co. Ltd, Shanxi 037000, People's Republic of China;

    rnState Key Laboratory of Bioreactor Engineering, East China University of Science and Technology, 130 Meilong Road, P.O. Box 329, Shanghai 200237, People's Republic of China;

    rnState Key Laboratory of Bioreactor Engineering, East China University of Science and Technology, 130 Meilong Road, P.O. Box 329, Shanghai 200237, People's Republic of China;

    rnState Key Laboratory of Bioreactor Engineering, East China University of Science and Technology, 130 Meilong Road, P.O. Box 329, Shanghai 200237, People's Republic of China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    metabolic flux analysis; acremonium chrysogenum; fed-batch cultivation; cephalosporin C;

    机译:代谢通量分析;产黄顶孢分批补料栽培;头孢菌素C;

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