Towards understanding nitrate-reducing Fe(II) oxidation in Ferrigenium straubiae: spotlight on old and new key protein candidates
Stefanie BeckeriD, Daniel StraubiD, James HempiD, Andreas A. KappleriD
Abstract
3.Autotrophic Fe(II) oxidation is a key microbial process linking iron cycling to global carbon and nitrogen turnover in anoxic and low-oxygen environments. While Fe(II) oxidation, and electron utilization by canonical denitrification or oxygen-reducing pathways have been proposed, the whole electron transport chain via the periplasm is unknown. To address this gap, we compared the transcriptome of Ferrigenium straubiae strain KS (= KCTC 25982; = DSM 118991) cultivated under autotrophic conditions using Fe(II) as the electron donor and either nitrate or oxygen as the terminal electron acceptor. Additionally, we reanalyzed the genome using bioinformatic tools (FeGenie, MHCScan, Foldseek, AlphaFold, COFACTOR, and InterProScan) to classify known, putative, and previously uncharacterized proteins. Using these analyses, we (i) identified a form II RubisCO-mediated, sedoheptulose-7-phosphate-forming transaldolase variant of the Calvin-Benson-Bassham cycle, (ii) revealed the metabolic possibility of a reversed oxidative TCA cycle and an alternative CO2 fixation route via 10-formyl-tetrahydrofolate, (iii) found novel structural features of the proposed Fe(II) oxidases (Cyc2 and MtoA/B: {beta}-barrel outer membrane cytochromes), (iv) uncovered a nitric oxide reductase (eNOR-family) and two redox complexes specifically upregulated under nitrate-reducing Fe(II)-oxidizing conditions, including one comprising a sphaeroides heme protein homolog, and (v) reveal a cytochrome c rich gene area encoding ten heme proteins and (iv) proposed a conserved nonaheme cytochrome c to link Fe(II) oxidation to quinone reduction. 2. RepositoriesGenBank whole genome sequence of strain KS: JAGRPI00000000 IMG Taxon ID of strain KS: 2878407288 NCBI BioProject ID of RNA-Seq data: PRJNA1399691 Strain availability: KCTC 25982 and DSM 118991 Normalized transcripts and Log2FoldChanges (Excel file), and supplementary information are available with the online version of this article.
02 /Specification & Classification
Click any tag to browse matching papers- Citations
- 1
- Organism
- Assay
- Research Focus
- Approach
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Unraveling Fe(II)-oxidizing mechanisms in a facultative Fe(II) oxidizer Sideroxydans lithotrophicus ES-1 via culturing, transcriptomics, and RT-qPCR
N. Zhou, J. L. Keffer, … C. S. Chan·bioRxiv·Aug 18, 2021
- Iron oxidation is regulated by the two-component system, RegSR, and plays a role in photolithoheterotrophic growth in Rhodopseudomonas palustris
N. W. Haas, A. Jain, … K. R. Fixen·bioRxiv·Aug 19, 2021
- "Candidatus Siderophilus nitratireducens": a psychrophilic, nap-dependent nitrate-reducing iron oxidizer within the new order Siderophiliales
F. Corbera-Rubio, G. R. Stouten, … M. Laureni·bioRxiv·Sep 4, 2023
- Evidence for quinol oxidase activity of ImoA, a novel NapC/NirT family protein from the neutrophilic Fe(II) oxidizing bacterium Sideroxydans lithotrophicus ES-1
A. Jain, A. Coelho, … C. M. Paquete·bioRxiv·Jan 10, 2022
- Iron oxidation by a fused cytochrome-porin common to diverse iron-oxidizing bacteria
J. L. Keffer, S. M. McAllister, … C. Chan·bioRxiv·Apr 17, 2021
- Structural model of Cyc2, the primary electron acceptor of Acidithiobacillus ferrooxidans’ respiratory chain, as a modular cytochrome - β-barrel fusion protein, and mechanistic proposals based on this model
Luciano A. Abriata·bioRxiv·Feb 12, 2018