Koren Idan, Boussiba Sammy, Khozin-Goldberg Inna, Zarka Aliza
Microalgal Biotechnology Laboratory, French Associates Institute for Agriculture and Biotechnology of Drylands, The Jacob Blaustein Institutes for Desert Research, Ben-Gurion University of the Negev, Sede Boker Campus, Midreshet Ben-Gurion 8499000, Israel.
Biology (Basel). 2021 Feb 16;10(2):157. doi: 10.3390/biology10020157.
Several green algae can divide by multiple fission and spontaneously synchronize their cell cycle with the available light regime. The yields that can be obtained from a microalgal culture are directly affected by cell cycle events. is considered as one of the most promising microalgae for biotechnological applications due to its fast growth and the flexible trophic capabilities. It is intensively investigated in the context of bio-commodities production (carotenoids, storage lipids); however, the pattern of cell-cycle events under common cultivation strategies was not yet characterized for . In this study, we have employed fluorescence microscopy to characterize the basic cell-cycle dynamics under batch and continuous modes of phototrophic cultivation. Staining with SYBR green-applied in DMSO solution-enabled, for the first time, the clear and simple visualization of polynuclear stages in this microalga. Accordingly, we concluded that divides by a consecutive pattern of multiple fission, whereby it spontaneously synchronizes growth and cell division according to the available illumination regime. In high-light continuous culture or low-light batch culture, cell-cycle was completed within several light-dark (L/D) cycles (14 h/10 h); however, cell divisions were synchronized with the dark periods only in the high-light continuous culture. In both modes of cultivation, daughter cell release was mainly facilitated by division of 8 and 16-polynuclear cells. The results of this study are of both fundamental and applied science significance and are also important for the development of an efficient nuclear transformation system for
几种绿藻可通过多次分裂进行繁殖,并能使其细胞周期与可用光照模式自发同步。微藻培养的产量直接受细胞周期事件的影响。由于其生长迅速且营养能力灵活,被认为是生物技术应用中最有前景的微藻之一。在生物商品生产(类胡萝卜素、储存脂质)方面对其进行了深入研究;然而,在常见培养策略下的细胞周期事件模式尚未针对[具体藻类名称]进行表征。在本研究中,我们采用荧光显微镜来表征光合培养的分批和连续模式下的基本细胞周期动态。用SYBR绿(溶于二甲基亚砜溶液)染色首次实现了在这种微藻中清晰且简单地观察多核阶段。因此,我们得出结论,[具体藻类名称]通过连续的多次分裂模式进行繁殖,从而根据可用光照模式自发同步生长和细胞分裂。在高光连续培养或低光分批培养中,[具体藻类名称]细胞周期在几个明暗(L/D)周期(14小时/10小时)内完成;然而,仅在高光连续培养中细胞分裂与黑暗期同步。在两种培养模式下,子细胞释放主要由8核和16核细胞的分裂促进。本研究结果具有基础科学和应用科学意义,对于开发有效的[具体藻类名称]核转化系统也很重要