# Kinetic and Potentiometric Characteristics of Ferredoxin: NADP+ Oxidoreductase from Chlorobaculum tepidum

**Authors:** Dominykas Laibakojis, Daisuke Seo, Narimantas Čėnas, Mindaugas Lesanavičius

PMC · DOI: 10.3390/ijms27010481 · International Journal of Molecular Sciences · 2026-01-02

## TL;DR

This study investigates the redox properties and reaction mechanisms of a key enzyme in Chlorobaculum tepidum, revealing insights into its electron transfer behavior and potential applications in bioelectrochemical systems.

## Contribution

The study provides new insights into the reoxidation mechanism of FAD in CtFNR and its electron transfer properties using various oxidants.

## Key findings

- The reoxidation of FAD semiquinone is the rate-limiting step in CtFNR reactions.
- The two-electron reduction midpoint potential of FAD at pH 7.0 is −0.282 V.
- Electron transfer distances in reactions with Q and ArNO2 range from 2.6–3.4 Å.

## Abstract

Chlorobaculum tepidum ferredoxin: NADP+ oxidoreductase (CtFNR) is a dimeric thioredoxin reductase (TrxR)-type FNR, whose mechanism and redox properties are poorly characterized. In this work, we focused on the reoxidation mechanisms of its flavin adenine dinucleotide (FAD) cofactor using quinones (Q), nitroaromatics (ArNO2), and other nonphysiological oxidants with different single-electron reduction midpoint potentials (E71) and electrostatic charge. Like in other FNRs, the rate-limiting step of the reaction is the reoxidation of FAD semiquinone (FADH•). However, only one FAD per dimer functions in CtFNR due to some nonequivalence of the NADP(H) binding domains in separate subunits. The reactivity of Q increases with increasing E71, while ArNO2 form another analogous series of lower reactivity. The compounds are reduced in a dominant single-electron way. These data are consistent with an “outer sphere” electron transfer mechanism. On the basis of reactions with 3-acetylpyridine adenine dinucleotide phosphate, the two-electron reduction midpoint potential of FAD at pH 7.0 is −0.282 V. In CtFNR, 11% FADH• was stabilized at equilibrium. Calculated electron transfer distances in reactions with Q and ArNO2 were in the range of 2.6–3.4 Å. Taken together with previous studies of Rhodopseudomonas palustris and Bacillus subtilis FNRs, this work allows us to generalize the information on the catalytic ant thermodynamic properties of TrxR-type FNRs. In addition, our data may be valuable from an applied perspective, e.g., the use of redox mediators in photobioelectrochemical systems or microbial cells based on anoxygenic phototrophic bacteria.

## Linked entities

- **Proteins:** trxR (F420-dependent thioredoxin reductase), BRCA2 (BRCA2 DNA repair associated)
- **Chemicals:** 3-acetylpyridine adenine dinucleotide phosphate (PubChem CID 3036915)
- **Species:** Chlorobaculum tepidum (taxon 1097), Rhodopseudomonas palustris (taxon 1076), Bacillus subtilis (taxon 1423)

## Full-text entities

- **Chemicals:** quinones (MESH:D011809), 3-acetylpyridine adenine dinucleotide phosphate (MESH:C048483), Q (MESH:D005973), NADP(H) (MESH:D009249), FAD (MESH:D005182), ArNO2 (-)
- **Species:** Bacillus subtilis (species) [taxon 1423], Chlorobaculum tepidum (species) [taxon 1097], Rhodopseudomonas palustris (species) [taxon 1076]

## Full text

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## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12786658/full.md

## References

62 references — full list in the complete paper: https://tomesphere.com/paper/PMC12786658/full.md

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Source: https://tomesphere.com/paper/PMC12786658