98%
921
2 minutes
20
Autotrophic nitrate-reducing Fe(II)-oxidizing (NRFeOx) microorganisms fix CO and oxidize Fe(II) coupled to denitrification, influencing carbon, iron, and nitrogen cycles in pH-neutral, anoxic environments. However, the distribution of electrons from Fe(II) oxidation to either biomass production (CO fixation) or energy generation (nitrate reduction) in autotrophic NRFeOx microorganisms has not been quantified. We therefore cultivated the autotrophic NRFeOx culture KS at different initial Fe/N ratios, followed geochemical parameters, identified minerals, analyzed N isotopes, and applied numerical modeling. We found that at all initial Fe/N ratios, the ratios of Fe(II) to nitrate were slightly higher (5.11 to 5.94 at Fe/N ratios of 10:1 and 10:0.5) or lower (4.27 to 4.59 at Fe/N ratios of 10:4, 10:2, 5:2, and 5:1) than the theoretical ratio for 100% Fe(II) oxidation being coupled to nitrate reduction (5:1). The main N denitrification product was NO (71.88 to 96.29% at Fe/N ratios of 10:4 and 5:1; 43.13 to 66.26% at an Fe/N ratio of 10:1), implying that denitrification during NRFeOx was incomplete in culture KS. Based on the reaction model, on average 12% of electrons from Fe(II) oxidation were used for CO fixation while 88% of electrons were used for reduction of NO to NO at Fe/N ratios of 10:4, 10:2, 5:2, and 5:1. With 10 mM Fe(II) (and 4, 2, 1, or 0.5 mM nitrate), most cells were closely associated with and partially encrusted by the Fe(III) (oxyhydr)oxide minerals, whereas at 5 mM Fe(II), most cells were free of cell surface mineral precipitates. The genus (>80%) dominated culture KS regardless of the initial Fe/N ratios. Our results showed that Fe/N ratios play a key role in regulating NO emissions, for distributing electrons between nitrate reduction and CO fixation, and for the degree of cell-mineral interactions in the autotrophic NRFeOx culture KS. Autotrophic NRFeOx microorganisms that oxidize Fe(II), reduce nitrate, and produce biomass play a key role in carbon, iron, and nitrogen cycles in pH-neutral, anoxic environments. Electrons from Fe(II) oxidation are used for the reduction of both carbon dioxide and nitrate. However, the question is how many electrons go into biomass production versus energy generation during autotrophic growth. Here, we demonstrated that in the autotrophic NRFeOx culture KS cultivated at Fe/N ratios of 10:4, 10:2, 5:2, and 5:1, ca. 12% of electrons went into biomass formation, while 88% of electrons were used for reduction of NO to NO. Isotope analysis also showed that denitrification during NRFeOx was incomplete in culture KS and the main N denitrification product was NO. Therefore, most electrons stemming from Fe(II) oxidation seemed to be used for NO formation in culture KS. This is environmentally important for the greenhouse gas budget.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10057050 | PMC |
http://dx.doi.org/10.1128/aem.00196-23 | DOI Listing |
Environ Sci Process Impacts
August 2025
State Key Laboratory of Geomicrobiology and Environmental Changes, School of Environmental Studies, China University of Geosciences, Wuhan 430074, Hubei, China.
The bacterium strain HJ-2 has been reported as a nitrate-dependent iron-oxidizing bacterium, surprisingly with Fe(III) reduction ability. The control of iron redox cycling by the strain HJ-2 in the Fe(II)-Fe(III) co-existing system is mysterious and worthy of exploration. The present study demonstrates that HJ-2 utilizes nitrate as an electron acceptor to rapidly oxidize Fe(II), with negligible Fe(III) reduction, under neutral pH and anaerobic conditions in a co-existing Fe and ferrihydrite system.
View Article and Find Full Text PDFLangmuir
August 2025
School of Chemistry and Chemical Engineering, Yangzhou University, Yangzhou 225002, China.
Fe-based single-atom catalysts display extraordinary activity in the Fenton-like reaction, but low Fe atom densities limit their overall catalytic performance. In addition, high-valent iron (as Fe═O) plays a pivotal role due to the selective degradation of contaminants in water. However, it is rarely reported for Fe═O generation in the HO-based Fenton-like process.
View Article and Find Full Text PDFNanomaterials (Basel)
July 2025
National Institute of Advanced Industrial Science and Technology, 4-205, Sakurazaka, Moriyama, Nagoya 463-8560, Japan.
TbCu-type Sm-based compounds can be produced in bulk and potentially surpass NdFeB as permanent magnets. However, as the processes to prepare anisotropic magnetic particles are limited, the full potential of TbCu-type Sm-based compounds cannot be exploited. In this study, metastable TbCu-type phases of anisotropic Sm-Fe-N ultrafine particles were prepared using the low-oxygen induction thermal plasma (LO-ITP) process.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
August 2025
Key Laboratory for Advanced Ceramics and Machining Technology of Ministry of Education, Tianjin Key Laboratory of Composite and Functional Materials, School of Materials Science and Engineering, Tianjin University, Tianjin, 300072, China.
Fe-N-C catalyst is the most promising non-noble metal oxygen reduction catalyst for proton-exchange membrane fuel cells (PEMFCs); however, their practical applications are still limited by unsatisfactory long-term stability. This is because the N atoms of the active FeN moiety are easy to protonate, leading to the leaching of Fe atoms, and the HO generated during oxygen reduction reaction (ORR) process triggers the Fenton reaction, further accelerating the dissolution of Fe. To address these critical stability challenge, we developed a general strategy to transform FeN single-atom sites to FeN dual-atom sites in Fe-N-C catalysts with various carbon substrates.
View Article and Find Full Text PDFACS Nano
July 2025
Beijing Key Laboratory of Construction Tailorable Advanced Functional Materials and Green Applications, Experimental Center of Advanced Materials, School of Materials Science and Engineering, Beijing Institute of Technology, Beijing 100081, China.
Breaking the known activity-stability trade-off is essential for the broad implementation of Fe-N-C catalysts in fuel cells. Here, we report the development of an atomically dispersed Fe-N-C catalyst with highly active FeN sites on carbon support with dispersed graphitic microdomains (FeN-Gmd), which were generated during the FeC-catalyzed graphitization. The introduction of graphitic microdomain makes the FeN-Gmd exhibit outstanding oxygen reduction reaction activity when used as a cathode catalyst in practical fuel cells, with impressive peak power densities of 1.
View Article and Find Full Text PDF