| Literature DB >> 33568648 |
Stefan Steimle1, Trevor van Eeuwen2, Yavuz Ozturk1,3, Hee Jong Kim2, Merav Braitbard4, Nur Selamoglu1, Benjamin A Garcia5, Dina Schneidman-Duhovny4, Kenji Murakami6, Fevzi Daldal7.
Abstract
Respiratory electron transport complexes are organized as individual entities or combined as large supercomplexes (SC). Gram-negative bacteria deploy a mitochondrial-like cytochrome (cyt) bc1 (Complex III, CIII2), and may have specific cbb3-type cyt c oxidases (Complex IV, CIV) instead of the canonical aa3-type CIV. Electron transfer between these complexes is mediated by soluble (c2) and membrane-anchored (cy) cyts. Here, we report the structure of an engineered bc1-cbb3 type SC (CIII2CIV, 5.2 Å resolution) and three conformers of native CIII2 (3.3 Å resolution). The SC is active in vivo and in vitro, contains all catalytic subunits and cofactors, and two extra transmembrane helices attributed to cyt cy and the assembly factor CcoH. The cyt cy is integral to SC, its cyt domain is mobile and it conveys electrons to CIV differently than cyt c2. The successful production of a native-like functional SC and determination of its structure illustrate the characteristics of membrane-confined and membrane-external respiratory electron transport pathways in Gram-negative bacteria.Entities:
Year: 2021 PMID: 33568648 PMCID: PMC7876108 DOI: 10.1038/s41467-021-21051-4
Source DB: PubMed Journal: Nat Commun ISSN: 2041-1723 Impact factor: 14.919