Nature Communications · 2021 · 63 citations · 54 references
Life SciencesBiochemistryMolecular BiologyEnzyme MechanismEnzymologyStructural BiologyActive Site ArchitectureCatalytic MechanismsEnzyme Active SitesEnzyme FunctionProtein StructureRedox EnzymesCryo-electron Microscopy ReconstructionCytochrome OxidasesEscherichia ColiHeme CofactorsProtein Redox StatesRedox PotentialSubunit AssemblyTerminal Oxidases
Abstract Cytochrome bd quinol:O 2 oxidoreductases are respiratory terminal oxidases so far only identified in prokaryotes, including several pathogenic bacteria. Escherichia coli contains two bd oxidases of which only the bd -I type is structurally characterized. Here, we report the structure of the Escherichia coli cytochrome bd -II type oxidase with the bound inhibitor aurachin D as obtained by electron cryo-microscopy at 3 Å resolution. The oxidase consists of subunits AppB, C and X that show an architecture similar to that of bd -I. The three heme cofactors are found in AppC, while AppB is stabilized by a structural ubiquinone-8 at the homologous positions. A fourth subunit present in bd -I is lacking in bd -II. Accordingly, heme b 595 is exposed to the membrane but heme d embedded within the protein and showing an unexpectedly high redox potential is the catalytically active centre. The structure of the Q-loop is fully resolved, revealing the specific aurachin binding.
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