Department of Biotechnology and Food Microbiology, Poznań University of Life Sciences, Wojska Polskiego 48, Poznan, 60-527, Poland.
BMC Microbiol. 2014 Feb 20;14:45. doi: 10.1186/1471-2180-14-45.
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).
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.
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.
随着生物燃料原料产量的不断增加,有必要对生产工艺进行优化。一个非常重要的问题是开发无废生物柴油生产方法。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)。
本研究考察了利用丁酸梭菌从粗甘油合成 1,3-PD 的放大规模。在 6.6 L、42 L 和 150 L 生物反应器中进行分批发酵。结果表明,丁酸梭菌在中试规模下的培养并未降低 1,3-PD 生产的效率。在 6.6 L 生物反应器中,分批发酵获得的 1,3-PD 最高浓度为 37 g/L,补料分批发酵获得的 1,3-PD 最高浓度为 71 g/L。在三种生物反应器容量下,建立的从粗甘油合成 1,3-PD 的分批发酵动力学参数相似。在补料分批发酵过程中,150 L 生物反应器中 1,3-PD 的浓度较低,且底物未完全利用。这表明 150 L 生物反应器中存在多功能环境胁迫,这一推测通过蛋白质分析得到了证实。
在 6.6 L、42 L 和 150 L 生物反应器中进行的分批发酵中,1,3-PD 合成的有效性参数值相似。在 150 L 生物反应器中进行的补料分批发酵中的参数在底物利用率的速率和百分比上有所不同。细胞蛋白分析表明,在 150 L 生物反应器中进行补料分批发酵时发生了多种多功能应激,这表明有可能确定生化过程中的关键阶段,在这些阶段可以观察到 1,3-PD 合成途径的抑制。