Back to Search
Start Over
The carboxy-terminal insert in the Q-loop is needed for functionality of Escherichia coli cytochrome bd-I.
- Source :
-
Biochimica et biophysica acta. Bioenergetics [Biochim Biophys Acta Bioenerg] 2020 Jun 01; Vol. 1861 (5-6), pp. 148175. Date of Electronic Publication: 2020 Feb 12. - Publication Year :
- 2020
-
Abstract
- Cytochrome bd, a component of the prokaryotic respiratory chain, is important under physiological stress and during pathogenicity. Electrons from quinol substrates are passed on via heme groups in the CydA subunit and used to reduce molecular oxygen. Close to the quinol binding site, CydA displays a periplasmic hydrophilic loop called Q-loop that is essential for quinol oxidation. In the carboxy-terminal part of this loop, CydA from Escherichia coli and other proteobacteria harbors an insert of ~60 residues with unknown function. In the current work, we demonstrate that growth of the multiple-deletion strain E. coli MB43∆cydA (∆cydA∆cydB∆appB∆cyoB∆nuoB) can be enhanced by transformation with E. coli cytochrome bd-I and we utilize this system for assessment of Q-loop mutants. Deletion of the cytochrome bd-I Q-loop insert abolished MB43∆cydA growth recovery. Swapping the cytochrome bd-I Q-loop for the Q-loop from Geobacillus thermodenitrificans or Mycobacterium tuberculosis CydA, which lack the insert, did not enhance the growth of MB43∆cydA, whereas swapping for the Q-loop from E. coli cytochrome bd-II recovered growth. Alanine scanning experiments identified the cytochrome bd-I Q-loop insert regions Ile <superscript>318</superscript> -Met <superscript>322</superscript> , Gln <superscript>338</superscript> -Asp <superscript>342</superscript> , Tyr <superscript>353</superscript> -Leu <superscript>357</superscript> , and Thr <superscript>368</superscript> -Ile <superscript>372</superscript> as important for enzyme functionality. Those mutants that completely failed to recover growth of MB43∆cydA also lacked oxygen consumption activity and heme absorption peaks. Moreover, we were not able to isolate cytochrome bd-I from these inactive mutants. The results indicate that the cytochrome bd Q-loop exhibits low plasticity and that the Q-loop insert in E. coli is needed for complete, stable, assembly of cytochrome bd-I.<br />Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.<br /> (Copyright © 2020. Published by Elsevier B.V.)
- Subjects :
- Alanine genetics
Amino Acid Sequence
Cell Membrane metabolism
Cytochrome b Group isolation & purification
Electron Transport Chain Complex Proteins isolation & purification
Escherichia coli growth & development
Escherichia coli Proteins isolation & purification
Heme metabolism
Mutagenesis genetics
Mutant Proteins chemistry
Mutant Proteins isolation & purification
Mutant Proteins metabolism
Oxidoreductases isolation & purification
Oxygen Consumption
Protein Structure, Secondary
Structure-Activity Relationship
Cytochrome b Group chemistry
Cytochrome b Group metabolism
Electron Transport Chain Complex Proteins chemistry
Electron Transport Chain Complex Proteins metabolism
Escherichia coli metabolism
Escherichia coli Proteins chemistry
Escherichia coli Proteins metabolism
Oxidoreductases chemistry
Oxidoreductases metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1879-2650
- Volume :
- 1861
- Issue :
- 5-6
- Database :
- MEDLINE
- Journal :
- Biochimica et biophysica acta. Bioenergetics
- Publication Type :
- Academic Journal
- Accession number :
- 32061652
- Full Text :
- https://doi.org/10.1016/j.bbabio.2020.148175