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Improved riboflavin production with Ashbya gossypii from vegetable oil based on C-13 metabolic network analysis with combined labeling analysis by GC/MS, LC/MS, 1D, and 2D NMR

机译:基于C-13代谢网络分析,通过GC / MS,LC / MS,1D和2D NMR组合标记分析,改善了植物油中的植物油植物油的生成植物油。

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摘要

The fungus Ashbya gossypii is an important industrial producer of riboflavin, i.e. vitamin B-2. In order to meet the constantly increasing demands for improved production processes, it appears essential to better understand the underlying metabolic pathways of the vitamin. Here, we used a highly sophisticated set-up of parallel C-13 tracer studies with labeling analysis by GC/MS, LC/MS, 1D, and 2D NMR to resolve carbon fluxes in the overproducing strain A. gossypii B2 during growth and subsequent riboflavin production from vegetable oil as carbon source, yeast extract, and supplemented glycine. The studies provided a detailed picture of the underlying metabolism. Glycine was exclusively used as carbon-two donor of the vitamin's pyrimidine ring, which is part of its iso-alloxazine ring structure, but did not contribute to the carbon-one metabolism due to the proven absence of a functional glycine cleavage system. The pools of serine and glycine were closely connected due to a highly reversible serine hydroxymethyltransferase. Transmembrane formate flux simulations revealed that the one-carbon metabolism displayed a severe bottleneck during initial riboflavin production, which was overcome in later phases of the cultivation by intrinsic formate accumulation. The transiently limiting carbon-one pool was successfully replenished by time-resolved feeding of small amounts of formate and serine, respectively. This increased the intracellular availability of glycine, serine, and formate and resulted in a final riboflavin titer increase of 45%.
机译:真菌ashbya gossypii是核黄素的重要工业生产商,即维生素B-2。为了满足改善生产过程的不断增加的需求,似乎是更好地理解维生素的潜在代谢途径。这里,我们使用了通过GC / MS,LC / MS,1D和2D NMR的标记分析的平行C-13示踪研究的高度复杂的并联分析,以在生长和随后的碳脂腺中解析碳通量A. Gossypii B2中的碳通量从植物油作为碳源,酵母提取物和补充甘氨酸的核黄素生产。研究提供了潜在的新陈代谢的详细情况。甘氨酸专门用作维生素的嘧啶环的碳两种供体,这是其异甲嗪环结构的一部分,但由于经过验证的甘氨酸切割系统的缺失,没有导致碳 - 一种代谢。由于高度可逆的丝氨酸羟甲基转移酶,丝氨酸和甘氨酸的池密密地连接。跨膜甲酸杂气杂气模拟显示,单碳代谢在初始核黄素产生期间呈现严重的瓶颈,这在后期甲酸覆盖物的培养阶段克服了克服。通过分辨含量的少量甲酸盐和丝氨酸成功补充瞬时限制的碳 - 一池。这增加了甘氨酸,丝氨酸和甲状腺素的细胞内可用性,并导致最终核黄素滴度增加45%。

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