Overproduction of the Flv3B flavodiiron, enhances the photobiological hydrogen production by the nitrogen-fixing cyanobacterium Nostoc PCC 7120

• Published in: Microbial cell factories Vol. 19; no. 1; p. 65
• Main Authors: Roumezi, Baptiste, Avilan, Luisana, Risoul, Véronique, Brugna, Myriam, Rabouille, Sophie, Latifi, Amel
• Format: Journal Article
• Language: English
• Published: England BioMed Central Ltd 10-03-2020; BioMed Central; BMC
• Subjects: Alternative energy sources; Bacterial proteins; Biochemistry; Biochemistry, Molecular Biology; Biotechnology; Chemical properties; Cyanobacteria; Enzymes; Flavodiiron; Gene expression; Genes; Genetic research; Heterocyte; Hydrogen; Hydrogen production; Hydrogenase; Hypotheses; Immunoglobulins; Life Sciences; Metabolic engineering; Methods; Microbiological research; Microorganisms; Neomycin; Nitrogen; Nitrogen fixation; Nitrogenation; Nostoc; Photosynthesis; Photosynthetic bacteria; Physiological aspects; Plant biochemistry; Protein synthesis; Proteins; Renewable energy; Transcription (Genetics); France; Hydrogenase; Heterocyte; Hydrogen; Cyanobacteria; Flavodiiron
• ISSN: 1475-2859; 1475-2859
• DOI: 10.1186/s12934-020-01320-5

The ability of some photosynthetic microorganisms, particularly cyanobacteria and microalgae, to produce hydrogen (H
) is a promising alternative for renewable, clean-energy production. However, the most recent, related studies point out that much improvement is needed for sustainable cyanobacterial-based H
production to become economically viable. In this study, we investigated the impact of induced O
-consumption on H
photoproduction yields in the heterocyte-forming, N
-fixing cyanobacterium Nostoc PCC7120.
The flv3B gene, encoding a flavodiiron protein naturally expressed in Nostoc heterocytes, was overexpressed. Under aerobic and phototrophic growth conditions, the recombinant strain displayed a significantly higher H
production than the wild type. Nitrogenase activity assays indicated that flv3B overexpression did not enhance the nitrogen fixation rates. Interestingly, the transcription of the hox genes, encoding the NiFe Hox hydrogenase, was significantly elevated, as shown by the quantitative RT-PCR analyses.
We conclude that the overproduced Flv3B protein might have enhanced O
-consumption, thus creating conditions inducing hox genes and facilitating H
production. The present study clearly demonstrates the potential to use metabolic engineered cyanobacteria for photosynthesis driven H
production.