| Title: |
Spectroscopic insights into the mechanism of anammox hydrazine synthase |
| Authors: |
Versantvoort, Wouter; Hienerwadel, Rainer; Ferousi, Christina; van der Velden, Pieter; Berthomieu, Catherine; van Niftrik, Laura; Baymann, Frauke |
| Contributors: |
Radboud University Nijmegen; Luminy Génétique et Biophysique des Plantes (LGBP); Institut de Biosciences et Biotechnologies d'Aix-Marseille (ex-IBEB) (BIAM); Aix Marseille Université (AMU)-Centre National de la Recherche Scientifique (CNRS)-Direction de Recherche Fondamentale (CEA) (DRF (CEA)); Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Aix Marseille Université (AMU)-Centre National de la Recherche Scientifique (CNRS)-Direction de Recherche Fondamentale (CEA) (DRF (CEA)); Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA); Interactions Protéine Métal (IPM); Bioénergétique et Ingénierie des Protéines (BIP); Aix Marseille Université (AMU)-Centre National de la Recherche Scientifique (CNRS) |
| Source: |
https://hal.science/hal-03960395 ; 2023. |
| Publisher Information: |
CCSD |
| Publication Year: |
2023 |
| Collection: |
Aix-Marseille Université: HAL |
| Subject Terms: |
[SDV]Life Sciences [q-bio]; [SDV.BBM.BC]Life Sciences [q-bio]/Biochemistry; Molecular Biology/Biochemistry [q-bio.BM]; [SDV.BBM.BP]Life Sciences [q-bio]/Biochemistry; Molecular Biology/Biophysics |
| Description: |
Anaerobic ammonium oxidizing bacteria make a living oxidizing ammonium with nitrite as electron acceptor, intermediates nitric oxide and hydrazine, and end product dinitrogen gas. Hydrazine is a biologically unique free intermediate in this metabolism, and is produced by the enzyme hydrazine synthase. Crystallization of ‘ Candidatus Kuenenia stuttgartiensis’ hydrazine synthase allowed for an initial hypothesis of its reaction mechanism. In this hypothesis, nitric oxide is first reduced to hydroxylamine after which hydroxylamine is condensed with ammonium to form hydrazine. Hydrazine synthase is a tetraheme cytochrome c , containing two proposed active site hemes (γI & αI) in the γ- and α-subunit, respectively, connected by an intra-enzymatic tunnel. Here we combined the data from electrochemistry-induced Fourier transform infrared (FTIR) spectroscopy, EPR and optical spectroscopy to shed light on the redox properties and protein dynamics of hydrazine synthase in the context of its reaction mechanism. Redox titrations revealed two low potential low spin hemes with midpoint potentials of ∼-360 mV and ∼-310 mV for heme αII and γII, respectively. Heme γI showed redox transitions in the range of 0 mV, consisting of both low spin and high spin characteristics in optical and EPR spectroscopy. Electrochemistry-induced FTIR spectroscopy indicated an aspartic acid ligating a OH$^-$ /H$_ 2$O at the heme γI axial site as a possible candidate for involvement in this mixed spin characteristic. Furthermore, EPR spectroscopy confirmed the ability of heme γI to bind NO in the reduced state. Heme αI exhibited a rhombic high spin signal, in line with its ligation by a proximal tyrosine observed in the crystal structure. Redox titrations down to −610 mV nor addition of dithionite resulted in the reduction of heme αI, indicating a very low midpoint potential for this heme. In vivo chemistry at this heme αI, the candidate for the comproportionation of hydroxylamine and ammonium, is thus likely to be initiated solely on the ... |
| Document Type: |
report |
| Language: |
English |
| Relation: |
BIORXIV: 2023.01.22.525020 |
| DOI: |
10.1101/2023.01.22.525020 |
| Availability: |
https://hal.science/hal-03960395; https://hal.science/hal-03960395v1/document; https://hal.science/hal-03960395v1/file/Versantvoort%20et%20al%202023.pdf; https://doi.org/10.1101/2023.01.22.525020 |
| Rights: |
https://about.hal.science/hal-authorisation-v1/ ; info:eu-repo/semantics/OpenAccess |
| Accession Number: |
edsbas.3FDF9858 |
| Database: |
BASE |