Metal-free ribonucleotide reduction powered by a DOPA radical in Mycoplasma pathogens

Vivek Srinivas, Hugo Lebrette, Daniel Lundin, Yuri Kutin, Margareta Sahlin, Michael Lerche, Jürgen Eirich, Rui M. M. Branca, Nicholas Cox, Britt-Marie Sjöberg and Martin Högbom ()
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Vivek Srinivas: Stockholm University, Arrhenius Laboratories for Natural Sciences
Hugo Lebrette: Stockholm University, Arrhenius Laboratories for Natural Sciences
Daniel Lundin: Stockholm University, Arrhenius Laboratories for Natural Sciences
Yuri Kutin: Max Planck Institute for Chemical Energy Conversion, Mülheim an der Ruhr
Margareta Sahlin: Stockholm University, Arrhenius Laboratories for Natural Sciences
Michael Lerche: Stockholm University, Arrhenius Laboratories for Natural Sciences
Jürgen Eirich: Science for Life Laboratory, Karolinska Institutet
Rui M. M. Branca: Science for Life Laboratory, Karolinska Institutet
Nicholas Cox: Australian National University
Britt-Marie Sjöberg: Stockholm University, Arrhenius Laboratories for Natural Sciences
Martin Högbom: Stockholm University, Arrhenius Laboratories for Natural Sciences

Nature, 2018, vol. 563, issue 7731, 416-420

Abstract: Abstract Ribonucleotide reductase (RNR) catalyses the only known de novo pathway for the production of all four deoxyribonucleotides that are required for DNA synthesis1,2. It is essential for all organisms that use DNA as their genetic material and is a current drug target3,4. Since the discovery that iron is required for function in the aerobic, class I RNR found in all eukaryotes and many bacteria, a dinuclear metal site has been viewed as necessary to generate and stabilize the catalytic radical that is essential for RNR activity5–7. Here we describe a group of RNR proteins in Mollicutes—including Mycoplasma pathogens—that possess a metal-independent stable radical residing on a modified tyrosyl residue. Structural, biochemical and spectroscopic characterization reveal a stable 3,4-dihydroxyphenylalanine (DOPA) radical species that directly supports ribonucleotide reduction in vitro and in vivo. This observation overturns the presumed requirement for a dinuclear metal site in aerobic ribonucleotide reductase. The metal-independent radical requires new mechanisms for radical generation and stabilization, processes that are targeted by RNR inhibitors. It is possible that this RNR variant provides an advantage under metal starvation induced by the immune system. Organisms that encode this type of RNR—some of which are developing resistance to antibiotics—are involved in diseases of the respiratory, urinary and genital tracts. Further characterization of this RNR family and its mechanism of cofactor generation will provide insight into new enzymatic chemistry and be of value in devising strategies to combat the pathogens that utilize it. We propose that this RNR subclass is denoted class Ie.

Keywords: Ribonucleotide Reduction; Dopa Group; Dinuclear Metal Site; Presumed Requirement; Total Reflection X-ray Fluorescence (TXRF) (search for similar items in EconPapers)
Date: 2018
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DOI: 10.1038/s41586-018-0653-6

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