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首页> 外文期刊>BMC Microbiology >Scale-up of anaerobic 1,3-propanediol production by Clostridium butyricum DSP1 from crude glycerol
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Scale-up of anaerobic 1,3-propanediol production by Clostridium butyricum DSP1 from crude glycerol

机译:丁酸梭菌DSP1从粗甘油生产厌氧1,3-丙二醇的规模扩大

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Background As the production of biofuels from raw materials continuously increases, optimization of production processes is necessary. A very important issue is the development of wasteless methods of biodiesel production. One way of utilization of glycerol generated in biodiesel production is its microbial conversion to 1,3-PD (1,3-propanediol). Results The study investigated the scale-up of 1,3-PD synthesis from crude glycerol by Clostridium butyricum. Batch fermentations were carried out in 6.6?L, 42?L and 150?L bioreactors. It was observed that cultivation of C. butyricum on a pilot scale did not decrease the efficiency of 1,3-PD production. The highest concentrations of 1,3-PD, 37?g/L for batch fermentation and 71?g/L for fed-batch fermentation, were obtained in the 6.6?L bioreactor. The kinetic parameters of 1,3-PD synthesis from crude glycerol established for batch fermentation were similar regarding all three bioreactor capacities. During fed-batch fermentation, the concentration of 1,3-PD in the 150?L bioreactor was lower and the substrate was not completely utilized. That suggested the presence of multifunctional environmental stresses in the 150?L bioreactor, which was confirmed by protein analysis. Conclusion The values of effectivity parameters for 1,3-PD synthesis in batch fermentations carried out in 6.6?L, 42?L and 150?L bioreactors were similar. The parameters obtained during fed-batch fermentations in the 150?L bioreactor differed in the rate and percentage of substrate utilization. The analysis of cell proteins demonstrated that a number of multifunctional stresses occurred during fed-batch fermentations in the 150?L bioreactor, which suggests the possibility of identifying the key stages in the biochemical process where inhibition of 1,3-PD synthesis pathways can be observed.
机译:背景技术随着从原材料生产生物燃料的持续增长,必须优化生产工艺。一个非常重要的问题是生物柴油生产无浪费方法的发展。利用生物柴油生产中产生的甘油的一种方法是将其微生物转化为1,3-PD(1,3-丙二醇)。结果研究研究了丁酸梭菌从粗甘油中合成1,3-PD的规模。分批发酵在6.6?L,42?L和150?L生物反应器中进行。观察到在中试规模上种植丁酸梭菌不会降低1,3-PD的生产效率。在6.6?L生物反应器中获得最高浓度的1,3-PD,对于分批发酵为37?g / L,对于分批补料发酵为71?g / L。对于所有三个生物反应器容量,由用于间歇发酵建立的粗甘油合成1,3-PD的动力学参数相似。分批补料发酵过程中,150?L生物反应器中的1,3-PD浓度较低,底物没有被完全利用。这表明在150?L生物反应器中存在多功能环境胁迫,这一点已通过蛋白质分析得到了证实。结论在6.6?L,42?L和150?L生物反应器中进行分批发酵的1,3-PD合成的有效参数值相似。在150?L生物反应器中的分批补料发酵过程中获得的参数在底物利用率和百分比上有所不同。对细胞蛋白的分析表明,在150?L生物反应器的分批补料发酵过程中,发生了许多多功能应激反应,这表明有可能确定生化过程中关键阶段的可能,其中可能抑制1,3-PD合成途径。观测到的。

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