Engineering a Photoautotrophic Microbial Coculture toward Enhanced Biohydrogen ProductionShow others and affiliations
2024 (English)In: Environmental Science and Technology, ISSN 0013-936X, E-ISSN 1520-5851, Vol. 59, no 1, p. 337-348Article in journal (Refereed) Published
Abstract [en]
The application of synthetic phototrophic microbial consortia holds promise for sustainable bioenergy production. Nevertheless, strategies for the efficient construction and regulation of such consortia remain challenging. Applying tools of genetic engineering, this study successfully constructed a synthetic community of phototrophs using Rhodopseudomonas palustris (R. palustris) and an engineered strain of Synechocystis sp PCC6803 for acetate production (Synechocystis_acs), enabling the production of biohydrogen and fatty acids during nitrogen and carbon dioxide fixation. Elemental balance confirmed carbon capture and nitrogen fixation into the consortium. The strategy of circadian illumination effectively limited oxygen levels in the system, ensuring the activity of the nitrogenase in R. palustris, despite oxygenic photosynthesis happening in Synechocystis. When infrared light was introduced into the circadian illumination, the production of H2 (9.70 μmol mg–1) and fatty acids (especially C16 and C18) was significantly enhanced. Proteomic analysis indicated acetate exchange and light-dependent regulation of metabolic activities. Infrared illumination significantly stimulated the expression of proteins coding for nitrogen fixation, carbohydrate metabolism, and transporters in R. palustris, while constant white light led to the most upregulation of photosynthesis-related proteins in Synechocystis_acs. This study demonstrated the successful construction and light regulation of a phototrophic community, enabling H2 and fatty acid production through carbon and nitrogen fixation.
Place, publisher, year, edition, pages
American Chemical Society (ACS), 2024. Vol. 59, no 1, p. 337-348
Keywords [en]
phototrophic community, H2 production, proteomics, metabolite exchange
National Category
Molecular Biology Microbiology
Identifiers
URN: urn:nbn:se:uu:diva-555159DOI: 10.1021/acs.est.4c08629ISI: 001378934800001PubMedID: 39668362Scopus ID: 2-s2.0-85214979749OAI: oai:DiVA.org:uu-555159DiVA, id: diva2:1954336
Funder
EU, Horizon 2020, 1010007332025-04-242025-04-242025-04-24Bibliographically approved