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Metabolic Profiling of Geobacter sulfurreducens during Industrial Bioprocess Scale-Up

机译:工业生物工艺规模放大过程中,Geobacter sulfreducens的代谢谱分析

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摘要

During the industrial scale-up of bioprocesses it is important to establish that the biological system has not changed significantly when moving from small laboratory-scale shake flasks or culturing bottles to an industrially relevant production level. Therefore, during upscaling of biomass production for a range of metal transformations, including the production of biogenic magnetite nanoparticles by Geobacter sulfurreducens, from 100-ml bench-scale to 5-liter fermentors, we applied Fourier transform infrared (FTIR) spectroscopy as a metabolic fingerprinting approach followed by the analysis of bacterial cell extracts by gas chromatography-mass spectrometry (GC-MS) for metabolic profiling. FTIR results clearly differentiated between the phenotypic changes associated with different growth phases as well as the two culturing conditions. Furthermore, the clustering patterns displayed by multivariate analysis were in agreement with the turbidimetric measurements, which displayed an extended lag phase for cells grown in a 5-liter bioreactor (24 h) compared to those grown in 100-ml serum bottles (6 h). GC-MS analysis of the cell extracts demonstrated an overall accumulation of fumarate during the lag phase under both culturing conditions, coinciding with the detected concentrations of oxaloacetate, pyruvate, nicotinamide, and glycerol-3-phosphate being at their lowest levels compared to other growth phases. These metabolites were overlaid onto a metabolic network of G. sulfurreducens, and taking into account the levels of these metabolites throughout the fermentation process, the limited availability of oxaloacetate and nicotinamide would seem to be the main metabolic bottleneck resulting from this scale-up process. Additional metabolite-feeding experiments were carried out to validate the above hypothesis. Nicotinamide supplementation (1 mM) did not display any significant effects on the lag phase of G. sulfurreducens cells grown in the 100-ml serum bottles. However, it significantly improved the growth behavior of cells grown in the 5-liter bioreactor by reducing the lag phase from 24 h to 6 h, while providing higher yield than in the 100-ml serum bottles.
机译:在生物工艺的工业规模放大过程中,重要的是要确定从小型实验室规模的摇瓶或培养瓶发展到与工业相关的生产水平时,生物系统没有发生重大变化。因此,在从一系列生物转化的生物质生产的升级过程中,包括从减少细菌数量的100毫升台式发酵罐到5升发酵罐的Geobacter sulfreducens生产生物磁铁矿纳米颗粒,我们应用了傅里叶变换红外(FTIR)光谱作为代谢指纹分析法,然后通过气相色谱-质谱(GC-MS)分析细菌细胞提取物以进行代谢分析。 FTIR结果清楚地区分了与不同生长期相关的表型变化以及两种培养条件。此外,通过多变量分析显示的聚类模式与浊度测量结果相符,比浊测量显示,与在100 ml血清瓶中培养的细胞(6 h)相比,在5升生物反应器中培养的细胞(24 h)具有延长的滞后阶段。 。 GC-MS对细胞提取物的分析表明,在两种培养条件下,均处于滞后阶段,富马酸盐的总积累量与所检测到的草酰乙酸,丙酮酸,烟酰胺和3-磷酸甘油的浓度处于最低水平(与其他生长相比)相吻合。阶段。这些代谢物被覆盖在硫还原菌的代谢网络上,考虑到整个发酵过程中这些代谢物的水平,草酰乙酸和烟酰胺的有限供应似乎是这种扩大过程的主要代谢瓶颈。进行了其他代谢物喂养实验,以验证上述假设。补充烟酰胺(1 mM)对在100 ml血清瓶中生长的G.sulfreducens细胞的迟滞期没有显示任何显着影响。但是,通过将滞后阶段从24小时减少到6小时,它显着改善了在5升生物反应器中生长的细胞的生长行为,同时提供了比100毫升血清瓶更高的产量。

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