Identification and characterization of the novel subunit CcoM in the cbb₃-Cytochrome c oxidase from Pseudomonas stutzeri ZoBell

Cytochrome c oxidases (CcOs), members of the heme-copper containing oxidase (HCO) superfamily, are the terminal enzymes of aerobic respiratory chains. The cbb3-type cytochrome c oxidases (cbb3-CcO) form the C-family and 
Cytochrome c oxidases (CcOs), members of the heme-copper containing oxidase (HCO) superfamily, are the terminal enzymes of aerobic respiratory chains. The cbb3-type cytochrome c oxidases (cbb3-CcO) form the C-family and have only the central catalytic subunit in common with the A- and B-family HCOs. In Pseudomonas stutzeri, two cbb3 operons are organized in a tandem repeat. The atomic structure of the first cbb3 isoform (Cbb3-1) was determined at 3.2 Å resolution in 2010 (S. Buschmann, E. Warkentin, H. Xie, J. D. Langer, U. Ermler, and H. Michel, Science 329:327-330, 2010, http://dx.doi.org/10.1126/science.1187303). Unexpectedly, the electron density map of Cbb3-1 revealed the presence of an additional transmembrane helix (TMH) which could not be assigned to any known protein. We now identified this TMH as the previously uncharacterized protein PstZoBell_05036, using a customized matrix-assisted laser desorption ionization (MALDI)-tandem mass spectrometry setup. The amino acid sequence matches the electron density of the unassigned TMH. Consequently, the protein was renamed CcoM. In order to identify the function of this new subunit in the cbb3 complex, we generated and analyzed a CcoM knockout strain. The results of the biochemical and biophysical characterization indicate that CcoM may be involved in CcO complex assembly or stabilization. In addition, we found that CcoM plays a role in anaerobic respiration, as the ΔCcoM strain displayed altered growth rates under anaerobic denitrifying conditions.om Pseudomonas stutzeri, a bacterium closely related to the human pathogen Pseudomonas aeruginosa.
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Metadaten
Author:Martin Kohlstädt, Sabine Buschmann, Hao Xie, Anja Resemann, Eberhard Warkentin, Julian David Langer, Hartmut Michel
URN:urn:nbn:de:hebis:30:3-415333
DOI:http://dx.doi.org/10.1128/mBio.01921-15
ISSN:2150-7511
ISSN:2161-2129
Pubmed Id:http://www.ncbi.nlm.nih.gov/pubmed?term=26814183
Parent Title (English):mBio
Publisher:American Society for Microbiology
Place of publication:Washington, DC
Document Type:Article
Language:English
Date of Publication (online):2016/01/26
Date of first Publication:2016/01/26
Publishing Institution:Universitätsbibliothek Johann Christian Senckenberg
Release Date:2016/10/17
Volume:7
Issue:1, Nr. e01921-15
Pagenumber:9
First Page:1
Last Page:9
Note:
Copyright © 2016 Kohlstaedt et al. This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-ShareAlike 3.0 Unported license, which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original author and source are credited.
HeBIS PPN:425323609
Institutes:Biochemie und Chemie
MPI für Biophysik
Dewey Decimal Classification:570 Biowissenschaften; Biologie
Sammlungen:Universitätspublikationen
Licence (German):License LogoCreative Commons - Namensnennung-Keine kommerzielle Nutzung-Weitergabe unter gleichen Bedingungen

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