Key Laboratory of Biofuels, Shandong Provincial Key Laboratory of Energy Genetics, Qingdao Institute of Bioenergy and Bioprocess Technology, Chinese Academy of Sciences, No. 189 Songling Road, Qingdao 266101, China; University of Chinese Academy of Sciences, Beijing 100049, China.
Metab Eng. 2013 Sep;19:17-25. doi: 10.1016/j.ymben.2013.05.001. Epub 2013 May 28.
Because cyanobacteria are photosynthetic, fast-growing microorganisms that can accumulate sucrose under salt stress, they have a potential application as a sugar source for the biomass-derived production of renewable fuels and chemicals. In the present study, the production of sucrose by the cyanobacteria Synechocystis sp. PCC6803, Synechococcus elongatus PCC7942, and Anabaena sp. PCC7120 was examined. The three species displayed different growth curves and intracellular sucrose accumulation rates in response to NaCl. Synechocystis sp. PCC6803 was used to examine the impact of modifying the metabolic pathway on the levels of sucrose production. The co-overexpression of sps (slr0045), spp (slr0953), and ugp (slr0207) lead to a 2-fold increase in intracellular sucrose accumulation, whereas knockout of ggpS (sll1566) resulted in a 1.5-fold increase in the production of this sugar. When combined, these genetic modifications resulted in a fourfold increase in intracellular sucrose accumulation. To explore methods for optimizing the transport of the intracellular sucrose to the growth medium, the acid-wash technique and the CscB (sucrose permease)-dependent export method were evaluated using Synechocystis sp. PCC6803. Whereas the acid-wash technique proved to be effective, the CscB-dependent export method was not effective. Taken together, these results suggest that using genetic engineering, photosynthetic cyanobacteria can be optimized for efficient sucrose production.
由于蓝藻是能够在盐胁迫下积累蔗糖的光合、快速生长的微生物,因此它们有可能作为生物量衍生生产可再生燃料和化学品的糖源。在本研究中,研究了聚球藻 PCC6803、聚球藻 elongatus PCC7942 和鱼腥藻 PCC7120 这三种蓝藻产生蔗糖的情况。这三种蓝藻在 NaCl 胁迫下表现出不同的生长曲线和细胞内蔗糖积累率。聚球藻 PCC6803 被用来研究修饰代谢途径对蔗糖生产水平的影响。sps(slr0045)、spp(slr0953) 和 ugp(slr0207) 的共过表达导致细胞内蔗糖积累增加了 2 倍,而 ggpS(sll1566) 的敲除导致这种糖的产量增加了 1.5 倍。当这些遗传修饰结合使用时,细胞内蔗糖的积累增加了 4 倍。为了探索优化细胞内蔗糖向生长培养基中运输的方法,使用聚球藻 PCC6803 评估了酸洗技术和 CscB(蔗糖透性酶)依赖性出口方法。虽然酸洗技术被证明是有效的,但 CscB 依赖性出口方法并不有效。综上所述,这些结果表明,通过遗传工程,可以对光合蓝藻进行优化,以实现高效蔗糖生产。