Abstract

ABSTRACTShewanella oneidensis MR-1 is a metal-reducing bacterium with the ability to utilize many different terminal electron acceptors, including oxygen and solid-metal oxides. Both metal oxide reduction and aerobic respiration have been studied extensively in this organism. However, electron transport chain processes upstream of the terminal oxidoreductases have been relatively understudied in this organism, especially electron transfer from NADH to respiratory quinones. Genome annotation indicates that S. oneidensis MR-1 encodes four NADH dehydrogenases, a proton-translocating dehydrogenase (Nuo), two sodium ion-translocating dehydrogenases (Nqr1 and Nqr2), and an “uncoupling” dehydrogenase (Ndh), but none of these complexes have been studied. Therefore, we conducted a study specifically focused on the effects of individual NADH dehydrogenase knockouts in S. oneidensis MR-1. We observed that two of the single-mutant strains, the ΔnuoN and ΔnqrF1 mutants, exhibited significant growth defects compared with the wild type. However, the defects were minor and only apparent under certain growth conditions. Further testing of the ΔnuoN ΔnqrF1 double-mutant strain yielded no growth in minimal medium under oxic conditions, indicating that Nuo and Nqr1 have overlapping functions, but at least one is necessary for aerobic growth. Coutilization of proton- and sodium ion-dependent energetics has important implications for the growth of this organism in environments with varied pH and salinity, including microbial electrochemical systems.IMPORTANCE Bacteria utilize a wide variety of metabolic pathways that allow them to take advantage of different energy sources, and to do so with varied efficiency. The efficiency of a metabolic process determines the growth yield of an organism, or the amount of biomass it produces per amount of substrate consumed. This parameter has important implications in biotechnology and wastewater treatment, where low growth yields are often preferred to minimize the production of microbial biomass. In this study, we investigated respiratory pathways containing NADH dehydrogenases with varied efficiency (i.e., the number of ions translocated per NADH oxidized) in the metal-reducing bacterium Shewanella oneidensis MR-1. We observed that two different respiratory pathways are used concurrently, and at least one pathway must be functional for growth under oxic conditions.

Highlights

  • Shewanella oneidensis MR-1 is a metal-reducing bacterium with the ability to utilize many different terminal electron acceptors, including oxygen and solidmetal oxides

  • We analyzed an existing whole-genome fitness profiling data set from a study by Deutschbauer et al [31] to gain initial insights into environmental conditions that influence the function of each NADH dehydrogenase encoded in the S. oneidensis MR-1 genome

  • All fitness defects were weak under anoxic conditions, which may be due to the lack of significant tricarboxylic acid (TCA) cycle activity in S. oneidensis MR-1 when oxygen is absent [32], resulting in less NADH generation from most substrates

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Summary

Introduction

Shewanella oneidensis MR-1 is a metal-reducing bacterium with the ability to utilize many different terminal electron acceptors, including oxygen and solidmetal oxides. Both metal oxide reduction and aerobic respiration have been studied extensively in this organism. Genome annotation indicates that S. oneidensis MR-1 encodes four NADH dehydrogenases, a protontranslocating dehydrogenase (Nuo), two sodium ion-translocating dehydrogenases (Nqr and Nqr2), and an “uncoupling” dehydrogenase (Ndh), but none of these complexes have been studied. We investigated respiratory pathways containing NADH dehydrogenases with varied efficiency (i.e., the number of ions translocated per NADH oxidized) in the metal-reducing bacterium Shewanella oneidensis MR-1. While the Mtr pathway and other terminal oxidoreductases are well studied, upstream processes that transfer electrons into the respiratory quinol pool are less well understood. We note that the Nqr and Nqr labels are not used consistently across studies and genome databases, but we refer to them here as shown above

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