Literature DB >> 11456494

Site-directed mutation of the highly conserved region near the Q-loop of the cytochrome bd quinol oxidase from Escherichia coli specifically perturbs heme b595.

J Zhang1, P Hellwig, J P Osborne, H W Huang , P Moënne-Loccoz, A A Konstantinov, R B Gennis.   

Abstract

Cytochrome bd is one of the two quinol oxidases in the respiratory chain of Escherichia coli. The enzyme contains three heme prosthetic groups. The dioxygen binding site is heme d, which is thought to be part of the heme-heme binuclear center along with heme b(595), which is a high-spin heme whose function is not known. Protein sequence alignments [Osborne, J. P., and Gennis, R. B. (1999) Biochim. Biophys Acta 1410, 32--50] of cytochrome bd quinol oxidase sequences from different microorganisms have revealed a highly conserved sequence (GWXXXEXGRQPW; bold letters indicate strictly conserved residues) predicted to be on the periplasmic side of the membrane between transmembrane helices 8 and 9 in subunit I. The functional importance of this region is investigated in the current work by site-directed mutagenesis. Several mutations in this region (W441A, E445A/Q, R448A, Q449A, and W451A) resulted in a catalytically inactive enzyme with abnormal UV--vis spectra. E445A was selected for detailed analysis because of the absence of the absorption bands from heme b(595). Detailed spectroscopic and chemical analyses, indeed, show that one of the three heme prosthetic groups in the enzyme, heme b(595), is specifically perturbed and mostly missing from this mutant. Surprisingly, heme d, while known to interact with heme b(595), appears relatively unperturbed, whereas the low-spin heme b(558) shows some modification. This is the first report of a mutation that specifically affects the binding site of heme b(595).

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Year:  2001        PMID: 11456494     DOI: 10.1021/bi010469m

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  11 in total

1.  Heme-heme and heme-ligand interactions in the di-heme oxygen-reducing site of cytochrome bd from Escherichia coli revealed by nanosecond absorption spectroscopy.

Authors:  Fabrice Rappaport; Jie Zhang; Marten H Vos; Robert B Gennis; Vitaliy B Borisov
Journal:  Biochim Biophys Acta       Date:  2010-05-28

2.  Oxoferryl-porphyrin radical catalytic intermediate in cytochrome bd oxidases protects cells from formation of reactive oxygen species.

Authors:  Angela Paulus; Sebastiaan Gijsbertus Hendrik Rossius; Madelon Dijk; Simon de Vries
Journal:  J Biol Chem       Date:  2012-01-27       Impact factor: 5.157

3.  Pressure-regulated biosynthesis of cytochrome bd in piezo- and psychrophilic deep-sea bacterium Shewanella violacea DSS12.

Authors:  Hideyuki Tamegai; Hiroaki Kawano; Akihiro Ishii; Sayaka Chikuma; Kaoru Nakasone; Chiaki Kato
Journal:  Extremophiles       Date:  2005-04-21       Impact factor: 2.395

4.  Time-resolved electrometric and optical studies on cytochrome bd suggest a mechanism of electron-proton coupling in the di-heme active site.

Authors:  Ilya Belevich; Vitaliy B Borisov; Jie Zhang; Ke Yang; Alexander A Konstantinov; Robert B Gennis; Michael I Verkhovsky
Journal:  Proc Natl Acad Sci U S A       Date:  2005-02-22       Impact factor: 11.205

5.  Cytochrome bd oxidase, oxidative stress, and dioxygen tolerance of the strictly anaerobic bacterium Moorella thermoacetica.

Authors:  Amaresh Das; Radu Silaghi-Dumitrescu; Lars G Ljungdahl; Donald M Kurtz
Journal:  J Bacteriol       Date:  2005-03       Impact factor: 3.490

6.  The fully oxidized form of the cytochrome bd quinol oxidase from E. coli does not participate in the catalytic cycle: direct evidence from rapid kinetics studies.

Authors:  Ke Yang; Vitaliy B Borisov; Alexander A Konstantinov; Robert B Gennis
Journal:  FEBS Lett       Date:  2008-09-26       Impact factor: 4.124

7.  Characterization and expression analysis of the cytochrome bd oxidase operon from Desulfovibrio gigas.

Authors:  Patrícia Machado; Rute Félix; Rute Rodrigues; Solange Oliveira; Claudina Rodrigues-Pousada
Journal:  Curr Microbiol       Date:  2006-03-18       Impact factor: 2.188

8.  Functional importance of Glutamate-445 and Glutamate-99 in proton-coupled electron transfer during oxygen reduction by cytochrome bd from Escherichia coli.

Authors:  Ranjani Murali; Robert B Gennis
Journal:  Biochim Biophys Acta Bioenerg       Date:  2018-04-30       Impact factor: 3.991

9.  Development of a machine learning method to predict membrane protein-ligand binding residues using basic sequence information.

Authors:  M Xavier Suresh; M Michael Gromiha; Makiko Suwa
Journal:  Adv Bioinformatics       Date:  2015-01-31

10.  Homologous bd oxidases share the same architecture but differ in mechanism.

Authors:  Alexander Theßeling; Tim Rasmussen; Sabrina Burschel; Daniel Wohlwend; Jan Kägi; Rolf Müller; Bettina Böttcher; Thorsten Friedrich
Journal:  Nat Commun       Date:  2019-11-13       Impact factor: 14.919

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