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      Origin and Evolution of the Sodium -Pumping NADH: Ubiquinone Oxidoreductase

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      PLoS ONE
      Public Library of Science

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          Abstract

          The sodium -pumping NADH: ubiquinone oxidoreductase (Na +-NQR) is the main ion pump and the primary entry site for electrons into the respiratory chain of many different types of pathogenic bacteria. This enzymatic complex creates a transmembrane gradient of sodium that is used by the cell to sustain ionic homeostasis, nutrient transport, ATP synthesis, flagellum rotation and other essential processes. Comparative genomics data demonstrate that the nqr operon, which encodes all Na +-NQR subunits, is found in a large variety of bacterial lineages with different habitats and metabolic strategies. Here we studied the distribution, origin and evolution of this enzymatic complex. The molecular phylogenetic analyses and the organizations of the nqr operon indicate that Na +-NQR evolved within the Chlorobi/Bacteroidetes group, after the duplication and subsequent neofunctionalization of the operon that encodes the homolog RNF complex. Subsequently, the nqr operon dispersed through multiple horizontal transfer events to other bacterial lineages such as Chlamydiae, Planctomyces and α, β, γ and δ -proteobacteria. Considering the biochemical properties of the Na +-NQR complex and its physiological role in different bacteria, we propose a detailed scenario to explain the molecular mechanisms that gave rise to its novel redox- dependent sodium -pumping activity. Our model postulates that the evolution of the Na +-NQR complex involved a functional divergence from its RNF homolog, following the duplication of the rnf operon, the loss of the rnfB gene and the recruitment of the reductase subunit of an aromatic monooxygenase.

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          Most cited references59

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          Bacterial iron homeostasis.

          Iron is essential to virtually all organisms, but poses problems of toxicity and poor solubility. Bacteria have evolved various mechanisms to counter the problems imposed by their iron dependence, allowing them to achieve effective iron homeostasis under a range of iron regimes. Highly efficient iron acquisition systems are used to scavenge iron from the environment under iron-restricted conditions. In many cases, this involves the secretion and internalisation of extracellular ferric chelators called siderophores. Ferrous iron can also be directly imported by the G protein-like transporter, FeoB. For pathogens, host-iron complexes (transferrin, lactoferrin, haem, haemoglobin) are directly used as iron sources. Bacterial iron storage proteins (ferritin, bacterioferritin) provide intracellular iron reserves for use when external supplies are restricted, and iron detoxification proteins (Dps) are employed to protect the chromosome from iron-induced free radical damage. There is evidence that bacteria control their iron requirements in response to iron availability by down-regulating the expression of iron proteins during iron-restricted growth. And finally, the expression of the iron homeostatic machinery is subject to iron-dependent global control ensuring that iron acquisition, storage and consumption are geared to iron availability and that intracellular levels of free iron do not reach toxic levels.
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            Iron-sulfur clusters: nature's modular, multipurpose structures.

            Iron-sulfur proteins are found in all life forms. Most frequently, they contain Fe2S2, Fe3S4, and Fe4S4 clusters. These modular clusters undergo oxidation-reduction reactions, may be inserted or removed from proteins, can influence protein structure by preferential side chain ligation, and can be interconverted. In addition to their electron transfer function, iron-sulfur clusters act as catalytic centers and sensors of iron and oxygen. Their most common oxidation states are paramagnetic and present significant challenges for understanding the magnetic properties of mixed valence systems. Iron-sulfur clusters now rank with such biological prosthetic groups as hemes and flavins in pervasive occurrence and multiplicity of function.
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              Iron and microbial infection.

              The use of iron as a cofactor in basic metabolic pathways is essential to both pathogenic microorganisms and their hosts. It is also a pivotal component of the innate immune response through its role in the generation of toxic oxygen and nitrogen intermediates. During evolution, the shared requirement of micro- and macroorganisms for this important nutrient has shaped the pathogen-host relationship. Here, we discuss how pathogens compete with the host for iron, and also how the host uses iron to counteract this threat.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS One
                PLoS ONE
                plos
                plosone
                PLoS ONE
                Public Library of Science (San Francisco, USA )
                1932-6203
                2014
                8 May 2014
                : 9
                : 5
                : e96696
                Affiliations
                [1 ]Canadian Institute for Advanced Research and Biology Department, University of New Brunswick, Fredericton, NB, Canada
                [2 ]Biology Department, Rensselaer Polytechnic Institute, Troy, New York, United States of America
                University of Lausanne, Switzerland
                Author notes

                Competing Interests: The authors have declared that no competing interests exist.

                Conceived and designed the experiments: ARP OJ. Performed the experiments: ARP OJ. Analyzed the data: ARP OJ. Contributed reagents/materials/analysis tools: ARP OJ BB. Wrote the paper: ARP BB OJ.

                Article
                PONE-D-14-00803
                10.1371/journal.pone.0096696
                4014512
                24809444
                423177b8-5998-46d6-a3c4-6969c76b01f1
                Copyright @ 2014

                This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

                History
                : 7 January 2014
                : 11 April 2014
                Page count
                Pages: 14
                Funding
                This work was partially supported by NSF Grant MCB 1052234 (OJ and BB), and NSERC Discovery 402421-2011 CFI-LOF 28276 and NBIF RIF2012-006 (ARP). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
                Categories
                Research Article
                Biology and Life Sciences
                Biochemistry
                Enzymology
                Enzyme Chemistry
                Cofactors (Biochemistry)
                Enzymes
                Bioenergetics
                Metabolism
                Computational Biology
                Genome Evolution
                Evolutionary Biology
                Evolutionary Systematics
                Phylogenetics
                Organismal Evolution
                Microbial Evolution
                Bacterial Evolution
                Microbiology
                Bacteriology
                Bacterial Biochemistry
                Bacterial Physiology
                Medical Microbiology
                Microbial Pathogens
                Bacterial Pathogens
                Microbial Physiology
                Microbial Metabolism

                Uncategorized
                Uncategorized

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