Department of Biotechnology, Graduate School of Engineering, Tokyo University of Agriculture & Technology, 2-24-16 Naka-cho, Koganei, Tokyo 184-8588, Japan ; JST, CREST, 2-24-16 Naka-cho, Koganei, Tokyo 184-8588, Japan.
Biotechnol Biofuels. 2014 Apr 9;7:56. doi: 10.1186/1754-6834-7-56. eCollection 2014.
Cyanobacteria are an attractive candidate for the production of biofuel because of their ability to capture carbon dioxide by photosynthesis and grow on non-arable land. However, because huge quantities of water are required for cultivation, strict water management is one of the greatest issues in algae- and cyanobacteria-based biofuel production. In this study, we aim to construct a lytic cyanobacterium that can be regulated by a physical signal (green-light illumination) for future use in the recovery of biofuel related compounds.
We introduced T4 bacteriophage-derived lysis genes encoding holin and endolysin under the control of the green-light regulated cpcG2 promoter in Synechocystis sp. PCC 6803. When cells harboring the lysis genes were illuminated with both red and green light, we observed a considerable decrease in growth rate, a significant increase in cellular phycocyanin released in the medium, and a considerable fraction of dead cells. These effects were not observed when these cells were illuminated with only red light, or when cells not containing the lysis genes were grown under either red light or red and green light. These results indicate that our constructed green-light inducible lytic system was clearly induced by green-light illumination, resulting in lytic cells that released intracellular phycocyanin into the culture supernatant. This property suggests a future possibility to construct photosynthetic genetically modified organisms that are unable to survive under sunlight exposure. Expression of the self-lysis system with green-light illumination was also found to greatly increase the fragility of the cell membrane, as determined by subjecting the induced cells to detergent, osmotic-shock, and freeze-thaw treatments.
A green-light inducible lytic system was constructed in Synechocystis sp. PCC 6803. The engineered lytic cyanobacterial cells should be beneficial for the recovery of biofuels and related compounds from cells with minimal effort and energy, due to the fragile nature of the induced cells. Furthermore, the use of light-sensing two-component systems to regulate the expression of exogenous genes in cyanobacteria promises to replace conventional chemical inducers in many bioprocess applications, impacting the limiting water management issues.
蓝藻由于能够通过光合作用捕获二氧化碳并在非耕地生长,因此成为生物燃料生产的有吸引力的候选物。然而,由于培养需要大量的水,因此严格的水资源管理是藻类和蓝藻生物燃料生产中最大的问题之一。在这项研究中,我们旨在构建一种可通过物理信号(绿光照射)调控的裂解蓝藻,以便将来用于回收生物燃料相关化合物。
我们在聚球藻 PCC 6803 中引入了 T4 噬菌体衍生的裂解基因,这些基因编码的 holin 和内溶素受绿光调控的 cpcG2 启动子的调控。当携带裂解基因的细胞同时受到红光和绿光照射时,我们观察到生长速度显著下降,细胞中释放到培养基中的藻蓝蛋白显著增加,以及相当一部分细胞死亡。当这些细胞仅受到红光照射时,或者当不含有裂解基因的细胞在红光或红光和绿光下生长时,均未观察到这些效应。这些结果表明,我们构建的绿光诱导裂解系统确实可以被绿光照射诱导,导致裂解细胞将细胞内的藻蓝蛋白释放到培养上清液中。这一特性表明未来有可能构建在阳光照射下无法生存的光合作用基因修饰生物体。通过用去污剂、渗透压休克和冻融处理诱导细胞,发现用绿光诱导表达自我裂解系统也大大增加了细胞膜的脆弱性。
在聚球藻 PCC 6803 中构建了一种绿光诱导的裂解系统。由于诱导细胞的脆弱性,该工程裂解蓝藻细胞应该有助于从细胞中以最小的努力和能量回收生物燃料和相关化合物。此外,使用光感应双组分系统来调控蓝藻中外源基因的表达有望取代许多生物过程应用中的传统化学诱导剂,从而影响到限制水管理的问题。