Department of Biochemistry, Faculty of Science, Chulalongkorn University, Bangkok, 10330, Thailand.
Research Unit on Sustainable Algal Cultivation and Applications, Chulalongkorn University, Bangkok, 10330, Thailand.
Sci Rep. 2024 Apr 26;14(1):9640. doi: 10.1038/s41598-024-60016-7.
Photoautotrophic cyanobacteria assimilate the greenhouse gas carbon dioxide as their sole carbon source for producing useful bioproducts. However, harvesting the cells from their liquid media is a major bottleneck in the process. Thus, an easy-to-harvest method, such as auto-flocculation, is desirable. Here, we found that cyanobacterium Synechocystis sp. PCC 6803 co-flocculated with a natural fungal contamination in the presence of the antibiotic erythromycin (EM) but not without EM. The fungi in the co-flocculated biomass were isolated and found to consist of five species with the filamentous Purpureocillium lilacinum and Aspergillus protuberus making up 71% of the overall fungal population. The optimal co-cultivation for flocculation was an initial 5 mg (fresh weight) of fungi, an initial cell density of Synechocystis of 0.2 OD, 10 µM EM, and 14 days of cultivation in 100 mL of BG11 medium with no organic compound. This yielded 248 ± 28 mg/L of the Synechocystis-fungi flocculated biomass from 560 ± 35 mg/L of total biomass, a 44 ± 2% biomass flocculation efficiency. Furthermore, the EM treated Synechocystis cells in the Synechocystis-fungi flocculate had a normal cell color and morphology, while those in the axenic suspension exhibited strong chlorosis. Thus, the occurrence of the Synechocystis-fungi flocculation was mediated by EM, and the co-flocculation with the fungi protected Synechocystis against the development of chlorosis. Transcriptomic analysis suggested that the EM-mediated co-flocculation was a result of down-regulation of the minor pilin genes and up-regulation of several genes including the chaperone gene for pilin regulation, the S-layer protein genes, the exopolysaccharide-polymerization gene, and the genes for signaling proteins involved in cell attachment and abiotic-stress responses. The CuSO stress can also mediate Synechocystis-fungi flocculation but at a lower flocculation efficiency than that caused by EM. The EM treatment may be applied in the co-culture between other cyanobacteria and fungi to mediate cell bio-flocculation.
光自养蓝藻将温室气体二氧化碳作为其唯一的碳源来生产有用的生物制品。然而,从液体培养基中收获细胞是该过程中的主要瓶颈。因此,需要一种易于收获的方法,例如自絮凝。在这里,我们发现,在抗生素红霉素(EM)存在的情况下,蓝藻集胞藻 PCC 6803 与天然真菌污染物共同絮凝,但在没有 EM 的情况下则不会。共絮凝生物量中的真菌被分离出来,并发现由五个物种组成,丝状紫青霉和粗糙青霉构成了整个真菌种群的 71%。絮凝的最佳共培养条件是初始真菌量为 5mg(湿重)、集胞藻初始细胞密度为 0.2 OD、EM 初始浓度为 10µM,以及在无有机化合物的 100mL BG11 培养基中培养 14 天。从 560±35mg/L 的总生物量中,得到了 248±28mg/L 的集胞藻-真菌絮凝生物量,生物量絮凝效率为 44±2%。此外,在 EM 处理的集胞藻细胞中,集胞藻-真菌絮体中的细胞颜色和形态正常,而在无菌悬浮液中的细胞表现出强烈的黄化。因此,集胞藻-真菌絮凝的发生是由 EM 介导的,与真菌的共絮凝保护集胞藻免受黄化的发展。转录组分析表明,EM 介导的共絮凝是由于次要菌毛基因的下调和包括菌毛调节伴侣基因、S 层蛋白基因、胞外多糖聚合基因以及参与细胞附着和非生物胁迫反应的信号蛋白基因在内的几个基因的上调所致。CuSO 胁迫也可以介导集胞藻-真菌絮凝,但絮凝效率低于 EM 引起的絮凝效率。EM 处理可应用于其他蓝藻和真菌的共培养中,以介导细胞生物絮凝。