Content area

Abstract

Soil microbes play a crucial role in reducing nitrogen loss from agricultural systems by converting nitrate to ammonium through the dissimilatory nitrate reduction to ammonium (DNRA) pathway. Central to this important pathway in the global nitrogen cycle is the pentaheme enzyme cytochrome c nitrite reductase (NrfA). NrfA is a soluble, periplasmic enzyme that catalyzes the six-electron, eight-proton reduction of nitrite to ammonium at a single active site. This reaction is facilitated by its redox partners, quinol oxidases. In Chapter 1, I review current knowledge on the regulation, homology, and maturation of NrfA. In Chapter 2, I summarize the latest progress in elucidating the reaction mechanism of ammonia production. Building on this mechanistic understanding, I next investigated the functional roles of two key hemes within the NrfA architecture. In Chapter 3, my goal was to determine the influence of heme 1’s proximal ligand on active site tuning and catalytic efficiency. We replaced the coordinating lysine with a histidine to create an all-His variant that is found natively in some DNRA organisms. As expected, this variant demonstrated greatly reduced substrate affinity and catalytic efficiency but maintained roughly half of wild-type activity levels. The catalytic changes emphasize the importance of first- and second-sphere residues on active site tuning and catalysis. In Chapter 4, I investigated the role of heme 5 which sits at the NrfA homo-dimer interface and is hypothesized to mediate electron sharing and/or electron storage. We introduced a site-directed H290M mutation, replacing the native heme 5 histidine ligand with methionine to create a functional knockout. Surprisingly, spectroscopic and electrochemical analyses revealed that this mutation significantly altered the redox potentials and reduction sequence of the hemes. These findings suggest that heme 5 may play a broader role in maintaining redox cooperativity across the hemes. Finally, in chapter 5, I characterized NrfA’s redox partner and quinol oxidase, NrfH. Although still in early stages, our work on NrfH lays a foundation for future studies aimed at harnessing its electron-donating capabilities. Together, these findings advance our understanding of DNRA enzymology and may inform strategies to enhance nitrogen retention in agricultural soils.

Details

1010268
Title
Investigating Structure-Function Relationships in Cytochrome c Nitrite Reductase: Tuning Catalysis and Redox Cooperativity
Number of pages
153
Publication year
2025
Degree date
2025
School code
0128
Source
DAI-B 87/5(E), Dissertation Abstracts International
ISBN
9798297981171
Committee member
Hamberger, Bjoern; TerAvest, Michaela; Hu, Jian; Hausinger, Robert
University/institution
Michigan State University
Department
Biochemistry and Molecular Biology - Doctor of Philosophy
University location
United States -- Michigan
Degree
Ph.D.
Source type
Dissertation or Thesis
Language
English
Document type
Dissertation/Thesis
Dissertation/thesis number
32280250
ProQuest document ID
3268298941
Document URL
https://www.proquest.com/dissertations-theses/investigating-structure-function-relationships/docview/3268298941/se-2?accountid=208611
Copyright
Database copyright ProQuest LLC; ProQuest does not claim copyright in the individual underlying works.
Database
ProQuest One Academic