Deletion of Flv3A facilitates long-term H2 photoproduction in diazotrophic Anabaena sp. PCC 7120.

IF 5.4 2区 生物学 Q1 PLANT SCIENCES Physiologia plantarum Pub Date : 2025-01-01 DOI:10.1111/ppl.70087
Meilin He, Anita Santana-Sánchez, Gábor Szilveszter Tóth, Maria Ermakova, Darius Collard, Sergey Kosourov, Yagut Allahverdiyeva
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Abstract

Molecular hydrogen (H2) is a promising energy carrier, and its production by photosynthetic microorganisms holds substantial potential for advancing renewable energy generation. The nitrogenase-mediated H2 production using heterocyst-forming cyanobacteria represents a promising approach, as the process utilizes light energy and photosynthetic reductants while being naturally protected from O2-rich environments by its restriction to microoxic heterocyst cells. We investigated the impact of deleting the vegetative cell-specific flavodiiron protein, Flv3A, on the long-term H2 photoproduction of the model heterocyst-forming cyanobacterium Anabaena sp. PCC 7120. The H2 photoproduction response was evaluated under varying atmospheric conditions, with or without N2 and O2, and compared to the ∆hupL mutant, which is deficient in the large subunit of uptake hydrogenase, and the ∆hupL/flv3A double mutant. Unlike the ΔhupL mutant, H2 photoproduction in Δflv3A is not enhanced by increased nitrogenase activity or high accumulation of sugars in cells. Our results suggest that the absence of the vegetative cell-localized Flv3A positively affects H2 photoproduction in heterocysts by simultaneously downregulating hupL expression and enhancing the O2 tolerance of nitrogenase via a yet unexplored mechanism. These findings advance our understanding of nitrogenase-driven H2 production and provide a new strategy to address key limitations in long-term photobiological H2 production.

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来源期刊
Physiologia plantarum
Physiologia plantarum 生物-植物科学
CiteScore
11.00
自引率
3.10%
发文量
224
审稿时长
3.9 months
期刊介绍: Physiologia Plantarum is an international journal committed to publishing the best full-length original research papers that advance our understanding of primary mechanisms of plant development, growth and productivity as well as plant interactions with the biotic and abiotic environment. All organisational levels of experimental plant biology – from molecular and cell biology, biochemistry and biophysics to ecophysiology and global change biology – fall within the scope of the journal. The content is distributed between 5 main subject areas supervised by Subject Editors specialised in the respective domain: (1) biochemistry and metabolism, (2) ecophysiology, stress and adaptation, (3) uptake, transport and assimilation, (4) development, growth and differentiation, (5) photobiology and photosynthesis.
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