Stability of the tyrosyl radical in the beta subunit of Arcobacter bivalviorum ribonucleotide reductase

Arcobacter spp., such as Arcobacter bivalviorum (A. bivalviorum), are free-living organisms found in diverse environments and associated with animals. They are considered emerging enteropathogens and potential zoonotic agents. Ribonucleotide reductase (RNR) is the key enzyme that is used to convert...

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Main Author: Alqurashi, Abdulmajeed
Format: Article
Language:English
Published: Penerbit Universiti Kebangsaan Malaysia 2024
Online Access:http://journalarticle.ukm.my/24739/
http://journalarticle.ukm.my/24739/1/MAT%2011.pdf
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author Alqurashi, Abdulmajeed
author_facet Alqurashi, Abdulmajeed
author_sort Alqurashi, Abdulmajeed
building UKM Institutional Repository
collection Online Access
description Arcobacter spp., such as Arcobacter bivalviorum (A. bivalviorum), are free-living organisms found in diverse environments and associated with animals. They are considered emerging enteropathogens and potential zoonotic agents. Ribonucleotide reductase (RNR) is the key enzyme that is used to convert ribonucleotides into deoxyribonucleoside triphosphates (dNTPs). This process utilises radical-based chemistry and is crucial for DNA biosynthesis and repair. There are three RNR classes, with class I RNR the most studied, present in A. bivalviorum, eukaryotes, and many prokaryotes. Class I RNRs are further divided into three subclasses: Ia, Ib, and Ic. Class Ib RNRs use a dimanganese-oxo centre, unlike class Ia RNRs, which use a diiron-oxo centre. A. bivalviorum possesses a class Ia enzyme that requires a diferric tyrosyl radical cofactor located within its beta (β) subunit. Indeed, both the efficiency and fidelity of DNA synthesis are influenced by the stability of the tyrosyl radical (Y•) in the RNR, which is a critical aspect of its enzymatic function. This study investigates the stability of the Y-radical (Y•) site within the RNR β subunit of A. bivalviorum and the nature of the neighbouring amino acid residues. To achieve these goals, we developed a model of the RNR β subunit of A. bivalviorum, using the RNR β subunit of Aquifex aeolicus as a reference template (7aik.1. A PDB). The results provide some important details about the radical site and its surrounding residues, highlighting the influence of the protein structure on the stability of the radical. These findings may guide the development of novel inhibitors targeting this enzyme in A. bivalviorum.
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spelling oai:generic.eprints.org:247392025-01-17T07:44:59Z http://journalarticle.ukm.my/24739/ Stability of the tyrosyl radical in the beta subunit of Arcobacter bivalviorum ribonucleotide reductase Alqurashi, Abdulmajeed Arcobacter spp., such as Arcobacter bivalviorum (A. bivalviorum), are free-living organisms found in diverse environments and associated with animals. They are considered emerging enteropathogens and potential zoonotic agents. Ribonucleotide reductase (RNR) is the key enzyme that is used to convert ribonucleotides into deoxyribonucleoside triphosphates (dNTPs). This process utilises radical-based chemistry and is crucial for DNA biosynthesis and repair. There are three RNR classes, with class I RNR the most studied, present in A. bivalviorum, eukaryotes, and many prokaryotes. Class I RNRs are further divided into three subclasses: Ia, Ib, and Ic. Class Ib RNRs use a dimanganese-oxo centre, unlike class Ia RNRs, which use a diiron-oxo centre. A. bivalviorum possesses a class Ia enzyme that requires a diferric tyrosyl radical cofactor located within its beta (β) subunit. Indeed, both the efficiency and fidelity of DNA synthesis are influenced by the stability of the tyrosyl radical (Y•) in the RNR, which is a critical aspect of its enzymatic function. This study investigates the stability of the Y-radical (Y•) site within the RNR β subunit of A. bivalviorum and the nature of the neighbouring amino acid residues. To achieve these goals, we developed a model of the RNR β subunit of A. bivalviorum, using the RNR β subunit of Aquifex aeolicus as a reference template (7aik.1. A PDB). The results provide some important details about the radical site and its surrounding residues, highlighting the influence of the protein structure on the stability of the radical. These findings may guide the development of novel inhibitors targeting this enzyme in A. bivalviorum. Penerbit Universiti Kebangsaan Malaysia 2024 Article PeerReviewed application/pdf en http://journalarticle.ukm.my/24739/1/MAT%2011.pdf Alqurashi, Abdulmajeed (2024) Stability of the tyrosyl radical in the beta subunit of Arcobacter bivalviorum ribonucleotide reductase. Malaysian Applied Biology, 53 (3). pp. 117-124. ISSN 0126-8643 https://jms.mabjournal.com/index.php/mab/issue/view/60
spellingShingle Alqurashi, Abdulmajeed
Stability of the tyrosyl radical in the beta subunit of Arcobacter bivalviorum ribonucleotide reductase
title Stability of the tyrosyl radical in the beta subunit of Arcobacter bivalviorum ribonucleotide reductase
title_full Stability of the tyrosyl radical in the beta subunit of Arcobacter bivalviorum ribonucleotide reductase
title_fullStr Stability of the tyrosyl radical in the beta subunit of Arcobacter bivalviorum ribonucleotide reductase
title_full_unstemmed Stability of the tyrosyl radical in the beta subunit of Arcobacter bivalviorum ribonucleotide reductase
title_short Stability of the tyrosyl radical in the beta subunit of Arcobacter bivalviorum ribonucleotide reductase
title_sort stability of the tyrosyl radical in the beta subunit of arcobacter bivalviorum ribonucleotide reductase
url http://journalarticle.ukm.my/24739/
http://journalarticle.ukm.my/24739/
http://journalarticle.ukm.my/24739/1/MAT%2011.pdf