Nolasco-Hipolito Cirilo, Matsunaka Toshiyuki, Kobayashi Genta, Sonomoto Kenji, Ishizaki Ayaaki
Laboratory of Microbial Technology, Department of Bioscience and Biotechnology, Faculty of Agriculture, Graduate School, Kyushu University, 6-10-1 Hakozaki, Higashi-ku, Fukuoka 812-8581, Japan.
J Biosci Bioeng. 2002;93(3):281-7. doi: 10.1263/jbb.93.281.
An efficient bioreactor, termed a 'synchronized fresh cell bioreactor', was developed and consisted of a pH-dependent substrate feed system coupled with cross flow filtration and turbidity control. The effect of high dilution rate and high cell density coupled with high cell viability on the production of l-lactic acid in continuous culture by Lactococcus lactis IO-1 in enzyme-hydrolysed sago starch medium was investigated. For all changes in dilution rate, cells responded in a synchronized way to the addition of glucose by increasing the rate of biomass formation. Consequently, a glucose-free feed solution was required to maintain the cell concentration at a particular pre-set value. This set-up facilitated the maintenance of the cells in a permanent log phase. At a cell concentration of 15 gl(-1) and a feed glucose concentration of 53 gl(-1), volumetric LA productivities of 8.2, 19.3 and 33.1 gl(-1)h(-1) were obtained at dilution rates of 0.21, 0.50 and 1.1 h(-1), respectively. The respective residual glucose concentrations in the spent medium were 1.90, 0.24 and 3.80 gl(-1). By increasing the cell density, the volumetric productivity increased proportionally. At high cell density, higher dilution rates resulted in lower lactate concentrations in the culture medium resulting in higher productivity. This reactor facilitated efficient operation with high cell viability by maintaining the cells in continuous growth phase for long-term fermentation. Therefore, the growth rate (mu) was calculated according to the Monod equation. Using this system, high specific productivities can be obtained which guarantees high commercial productivity at economical cost with only a small investment for setting up the sago industry.
开发了一种高效生物反应器,称为“同步新鲜细胞生物反应器”,它由一个pH依赖的底物进料系统与错流过滤和浊度控制相结合组成。研究了高稀释率、高细胞密度以及高细胞活力对乳酸乳球菌IO-1在酶解西米淀粉培养基中连续培养生产L-乳酸的影响。对于稀释率的所有变化,细胞通过增加生物量形成速率以同步方式响应葡萄糖的添加。因此,需要无葡萄糖进料溶液将细胞浓度维持在特定预设值。这种设置有助于将细胞维持在永久对数期。在细胞浓度为15 g/L和进料葡萄糖浓度为53 g/L时,在稀释率分别为0.21、0.50和1.1 h⁻¹时,体积乳酸生产率分别为8.2、19.3和33.1 g/(L·h)。废培养基中各自的残余葡萄糖浓度分别为1.90、0.24和3.80 g/L。通过增加细胞密度,体积生产率成比例增加。在高细胞密度下,较高的稀释率导致培养基中乳酸浓度较低,从而提高了生产率。该反应器通过使细胞处于连续生长阶段以进行长期发酵,促进了具有高细胞活力的高效操作。因此,根据莫诺德方程计算生长速率(μ)。使用该系统,可以获得高比生产率,这保证了以经济成本实现高商业生产率,只需对西米产业进行少量投资。