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      The structure of the bacterial iron–catecholate transporter Fiu suggests that it imports substrates via a two-step mechanism

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          Abstract

          The ferric iron uptake (Fiu) transporter from Escherichia coli functions in the transport of iron–catecholate complexes across the bacterial outer membrane, providing the bacterium with iron, which is essential for growth. Recently it has become clear that Fiu also represents a liability for E. coli because its activity allows import of antimicrobial compounds that mimic catecholate. This inadvertent import suggests the potential utility of antimicrobial catechol siderophore mimetics in managing bacterial infections. However, to fully exploit these compounds, a detailed understanding of the mechanism of transport through Fiu and related transporters is required. To address this question, we determined the crystal structure of Fiu at 2.1–2.9 Å and analyzed its function in E. coli. Through analysis of the Fiuo crystal structure, in combination with in silico docking and mutagenesis, we provide insight into how Fiu and related transporters bind catecholate in a surface-exposed cavity. Moreover, through determination of the structure of Fiu in multiple crystal states, we revealed the presence of a large, selectively gated cavity in the interior of this transporter. This chamber is large enough to accommodate the Fiu substrate and may allow import of substrates via a two-step mechanism. This would avoid channel formation through the transporter and inadvertent import of toxic molecules. As Fiu and its homologs are the targets of substrate-mimicking antibiotics, these results may assist in the development of these compounds.

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          Most cited references56

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          Outer membrane permeability and antibiotic resistance.

          To date most antibiotics are targeted at intracellular processes, and must be able to penetrate the bacterial cell envelope. In particular, the outer membrane of gram-negative bacteria provides a formidable barrier that must be overcome. There are essentially two pathways that antibiotics can take through the outer membrane: a lipid-mediated pathway for hydrophobic antibiotics, and general diffusion porins for hydrophilic antibiotics. The lipid and protein compositions of the outer membrane have a strong impact on the sensitivity of bacteria to many types of antibiotics, and drug resistance involving modifications of these macromolecules is common. This review will describe the molecular mechanisms for permeation of antibiotics through the outer membrane, and the strategies that bacteria have deployed to resist antibiotics by modifications of these pathways.
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            CASTp: computed atlas of surface topography of proteins with structural and topographical mapping of functionally annotated residues

            Cavities on a proteins surface as well as specific amino acid positioning within it create the physicochemical properties needed for a protein to perform its function. CASTp () is an online tool that locates and measures pockets and voids on 3D protein structures. This new version of CASTp includes annotated functional information of specific residues on the protein structure. The annotations are derived from the Protein Data Bank (PDB), Swiss-Prot, as well as Online Mendelian Inheritance in Man (OMIM), the latter contains information on the variant single nucleotide polymorphisms (SNPs) that are known to cause disease. These annotated residues are mapped to surface pockets, interior voids or other regions of the PDB structures. We use a semi-global pair-wise sequence alignment method to obtain sequence mapping between entries in Swiss-Prot, OMIM and entries in PDB. The updated CASTp web server can be used to study surface features, functional regions and specific roles of key residues of proteins.
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              Colicin biology.

              Colicins are proteins produced by and toxic for some strains of Escherichia coli. They are produced by strains of E. coli carrying a colicinogenic plasmid that bears the genetic determinants for colicin synthesis, immunity, and release. Insights gained into each fundamental aspect of their biology are presented: their synthesis, which is under SOS regulation; their release into the extracellular medium, which involves the colicin lysis protein; and their uptake mechanisms and modes of action. Colicins are organized into three domains, each one involved in a different step of the process of killing sensitive bacteria. The structures of some colicins are known at the atomic level and are discussed. Colicins exert their lethal action by first binding to specific receptors, which are outer membrane proteins used for the entry of specific nutrients. They are then translocated through the outer membrane and transit through the periplasm by either the Tol or the TonB system. The components of each system are known, and their implication in the functioning of the system is described. Colicins then reach their lethal target and act either by forming a voltage-dependent channel into the inner membrane or by using their endonuclease activity on DNA, rRNA, or tRNA. The mechanisms of inhibition by specific and cognate immunity proteins are presented. Finally, the use of colicins as laboratory or biotechnological tools and their mode of evolution are discussed.
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                Author and article information

                Journal
                J Biol Chem
                J. Biol. Chem
                jbc
                jbc
                JBC
                The Journal of Biological Chemistry
                American Society for Biochemistry and Molecular Biology (11200 Rockville Pike, Suite 302, Rockville, MD 20852-3110, U.S.A. )
                0021-9258
                1083-351X
                20 December 2019
                11 November 2019
                11 November 2019
                : 294
                : 51
                : 19523-19534
                Affiliations
                []School of Biological Sciences, Monash University, Clayton, 3800 Victoria, Australia
                [§ ]Infection and Immunity Program, Biomedicine Discovery Institute and Department of Microbiology, Monash University, Clayton, 3800 Victoria, Australia
                Author notes
                [1 ] Supported by Sir Henry Wellcome Fellowship Award 106077/Z/14/Z. To whom correspondence should be addressed. E-mail: rhys.grinter@ 123456monash.edu .
                [2]

                An Australian Research Council Australian Laureate Fellow (FL130100038).

                Edited by Ursula Jakob

                Author information
                https://orcid.org/0000-0002-8195-5348
                Article
                RA119.011018
                10.1074/jbc.RA119.011018
                6926462
                31712312
                3a9e2c38-224b-4516-96cc-52d921f07550
                © 2019 Grinter and Lithgow.

                Author's Choice—Final version open access under the terms of the Creative Commons CC-BY license.

                History
                : 10 September 2019
                : 6 November 2019
                Funding
                Funded by: Wellcome Trust (Wellcome) , open-funder-registry 10.13039/100004440;
                Award ID: 106077/Z/14/Z
                Award Recipient :
                Funded by: Australian Research Council
                Award ID: FL130100038
                Award Recipient :
                Funded by: Department of Health | National Health and Medical Research Council (NHMRC) , open-funder-registry 10.13039/501100000925;
                Award ID: 1092262
                Award Recipient :
                Categories
                Protein Structure and Folding

                Biochemistry
                membrane transport,x-ray crystallography,escherichia coli (e. coli),protein structure,outer membrane,siderophore,bacterial outer membrane,ferric iron uptake (fiu),iron acquisition,solute uptake,tonb-dependent transporter

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