Cell Factory Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Daejeon, 34141, Republic of Korea.
Department of Chemical and Biomolecular Engineering, KAIST, Daejeon, 34141, Republic of Korea.
J Microbiol. 2018 Jan;56(1):56-64. doi: 10.1007/s12275-018-7488-6. Epub 2018 Jan 4.
Increased lipid accumulation of algal cells as a response to environmental stress factors attracted much attention of researchers to incorporate this stress response into industrial algal cultivation process with the aim of enhancing algal lipid productivity. This study applies high-salinity stress condition to a two-phase process in which microalgal cells are initially grown in freshwater medium until late exponential phase and subsequently subjected to high-salinity condition that induces excessive lipid accumulation. Our initial experiment revealed that the concentrated culture of Chlorella sorokiniana HS1 exhibited the intense fluorescence of Nile red at the NaCl concentration of 60 g/L along with 1 g/L of supplemental bicarbonate after 48 h of induction period without significantly compromising cultural integrity. These conditions were further verified with the algal culture grown for 7 days in a 1 L bottle reactor that reached late exponential phase; a 12% increment in the lipid content of harvested biomass was observed upon inducing high lipid accumulation in the concentrated algal culture at the density of 5.0 g DW/L. Although an increase in the sum of carbohydrate and lipid contents of harvested biomass indicated that the external carbon source supplemented during the induction period increased overall carbon assimilation, a decrease in carbohydrate content suggested the potential reallocation of cellular carbon that promoted lipid droplet formation under high-salinity stress. These results thus emphasize that the two-phase process can be successfully implemented to enhance algal lipid productivity by incorporating high-salinity stress conditions into the pre-concentrated sedimentation ponds of industrial algal production system.
藻细胞对环境胁迫因子的脂质积累增加引起了研究人员的极大关注,他们希望将这种应激反应纳入工业藻类培养过程中,以提高藻类的脂质生产力。本研究将高盐度胁迫条件应用于两阶段过程中,即在淡水培养基中初始培养微藻细胞,直到指数生长期后期,然后再将其置于高盐度条件下,从而诱导过度的脂质积累。我们的初步实验表明,在诱导期 48 小时后,在 60g/L 的 NaCl 浓度下,HS1 小球藻浓缩培养物表现出尼罗红的强烈荧光,同时补充 1g/L 的碳酸氢盐,而不会显著损害培养物的完整性。在 1L 瓶式反应器中培养 7 天的藻类证实了这些条件,在 5.0gDW/L 的浓缩藻密度下诱导高脂质积累时,收获生物量的脂质含量增加了 12%。尽管收获生物量中碳水化合物和脂质含量的总和增加表明诱导期补充的外部碳源增加了整体碳同化,但碳水化合物含量的降低表明细胞碳的潜在再分配促进了高盐胁迫下的脂质滴形成。因此,这些结果强调了两阶段过程可以通过将高盐度胁迫条件纳入工业藻类生产系统的预浓缩沉降池中成功实施,以提高藻类的脂质生产力。