The Role of the MntABC Transporter System in the Oxidative Stress Resistance of Deinococcus radiodurans

TL;DR

This study identifies the MntABC transporter system as crucial for manganese accumulation and oxidative stress resistance in Deinococcus radiodurans.

Contribution

The study reveals the MntABC system's role in Mn ion homeostasis and oxidative stress resistance in D. radiodurans.

Findings

Mutation of MntABC proteins reduces intracellular Mn accumulation and oxidative stress resistance.

Fluorescence labeling confirms the MntABC system's cellular membrane localization.

Structure modeling and docking reveal key active sites and interactions of MntABC proteins.

Abstract

The accumulation of high levels of manganese ions complexed with small molecules has been proposed as a pivotal factor contributing to the extraordinary radiation resistance of Deinococcus radiodurans. However, the molecular mechanisms governing the manganese ion homeostasis remain elusive. In this study, we characterize the role of the MntABC transporter system for Mn ion accumulation in D. radiodurans. Its cellular membrane localization is unequivocally demonstrated through fluorescence labeling techniques. Mutation of the protein components of the MntABC led to a significant decrease in intracellular Mn ion accumulation, concomitant with impaired cellular growth, decreased resistance against hydrogen peroxide, and gamma-ray irradiation-induced oxidative stresses, indicating that the MntABC system plays an indispensable role in resistance of D. radiodurans to oxidative stresses. Protein structure modeling and molecular docking are employed to analyze the key active sites of the MntABC proteins and their intermolecular interactions. The results demonstrate that the MntABC system is essential for maintaining Mn ion homeostasis and the oxidative stress resistance of D. radiodurans.

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