Cytochrome bd in Mycobacterium tuberculosis: A respiratory chain protein involved in the defense against antibacterials

被引:39
作者
Mascolo, Ludovica [1 ]
Bald, Dirk [1 ]
机构
[1] Vrije Univ Amsterdam, Fac Sci, Amsterdam Inst Mol Med & Syst, Dept Mol Cell Biol, De Boelelaan 1108, NL-1081 HZ Amsterdam, Netherlands
基金
欧盟地平线“2020”;
关键词
Cytochrome bd; Mycobacterium tuberculosis; Respiratory chain; Antibacterials; ESCHERICHIA-COLI; ENERGY-METABOLISM; QUINOL OXIDASE; ATP SYNTHASE; IN-VITRO; OXYGEN; PURIFICATION; COMPLEX; DIARYLQUINOLINES; FLEXIBILITY;
D O I
10.1016/j.pbiomolbio.2019.11.002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The branched respiratory chain of Mycobacterium tuberculosis has attracted attention as a highly promising target for next-generation antibacterials. This system includes two terminal oxidases of which the exclusively bacterial cytochrome bd represents the less energy-efficient one. Albeit dispensable for growth under standard laboratory conditions, cytochrome bd is important during environmental stress. In this review, we discuss the role of cytochrome bd during infection of the mammalian host and in the defense against antibacterials. Deeper insight into the biochemistry of mycobacterial cytochrome bd is needed to understand the physiological role of this bacteria-specific defense factor. Conversely, cytochrome bd may be utilized to gain information on mycobacterial physiology in vitro and during host infection. Knowledge-based manipulation of cytochrome bd function may assist in designing the next-generation tuberculosis combination chemotherapy. (C) 2019 The Authors. Published by Elsevier Ltd.
引用
收藏
页码:55 / 63
页数:9
相关论文
共 103 条
[41]   Activation of type II NADH dehydrogenase by quinolinequinones mediates antitubercular cell death [J].
Heikal, Adam ;
Hards, Kiel ;
Cheung, Chen-Yi ;
Menorca, Ayana ;
Timmer, Mattie S. M. ;
Stocker, Bridget L. ;
Cook, Gregory M. .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2016, 71 (10) :2840-2847
[42]   Subunit CydX of Escherichia coli cytochrome bd ubiquinol oxidase is essential for assembly and stability of the di-heme active site [J].
Hoeser, Jo ;
Hong, Sangjin ;
Gehmann, Gerfried ;
Gennis, Robert B. ;
Friedrich, Thorsten .
FEBS LETTERS, 2014, 588 (09) :1537-1541
[43]   Meropenem-Clavulanate Is Effective Against Extensively Drug-Resistant Mycobacterium tuberculosis [J].
Hugonnet, Jean-Emmanuel ;
Tremblay, Lee W. ;
Boshoff, Helena I. ;
Barry, Clifton E., III ;
Blanchard, John S. .
SCIENCE, 2009, 323 (5918) :1215-1218
[44]   Bioenergetics of Mycobacterium: An Emerging Landscape for Drug Discovery [J].
Iqbal, Iram Khan ;
Bajeli, Sapna ;
Akela, Ajit Kumar ;
Kumar, Ashwani .
PATHOGENS, 2018, 7 (01)
[45]   Electrogenic reactions of cytochrome bd [J].
Jasaitis, A ;
Borisov, VB ;
Belevich, NP ;
Morgan, JE ;
Konstantinov, AA ;
Verkhovsky, MI .
BIOCHEMISTRY, 2000, 39 (45) :13800-13809
[46]   Roles of Alanine Dehydrogenase and Induction of Its Gene in Mycobacterium smegmatis under Respiration-Inhibitory Conditions [J].
Jeong, Ji-A ;
Park, Sae Woong ;
Yoon, Dahae ;
Kim, Suhkmann ;
Kang, Ho-Young ;
Oh, Jeong-Il .
JOURNAL OF BACTERIOLOGY, 2018, 200 (14)
[47]   Respiration of Escherichia coli in the mouse intestine [J].
Jones, Shari A. ;
Chowdhury, Fatema Z. ;
Fabich, Andrew J. ;
Anderson, April ;
Schreiner, Darrel M. ;
House, Anetra L. ;
Autieri, Steven M. ;
Leatham, Mary P. ;
Lins, Jeremy J. ;
Jorgensen, Mathias ;
Cohen, Paul S. ;
Conway, Tyrrell .
INFECTION AND IMMUNITY, 2007, 75 (10) :4891-4899
[48]   Cytochrome bd-Dependent Bioenergetics and Antinitrosative Defenses in Salmonella Pathogenesis [J].
Jones-Carson, Jessica ;
Husain, Maroof ;
Liu, Lin ;
Orlicky, David J. ;
Vazquez-Torres, Andres .
MBIO, 2016, 7 (06)
[49]   CYTOCHROME BD OXIDASE FROM AZOTOBACTER-VINELANDII - PURIFICATION AND QUANTITATION OF LIGAND-BINDING TO THE OXYGEN REDUCTION SITE [J].
JUNEMANN, S ;
WRIGGLESWORTH, JM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (27) :16213-16220
[50]   Exploiting the synthetic lethality between terminal respiratory oxidases to kill Mycobacterium tuberculosis and clear host infection [J].
Kalia, Nitin P. ;
Hasenoehrl, Erik J. ;
Ab Rahman, Nurlilah B. ;
Koh, Vanessa H. ;
Ang, Michelle L. T. ;
Sajorda, Dannah R. ;
Hards, Kiel ;
Gruber, Gerhard ;
Alonso, Sylvie ;
Cook, Gregory M. ;
Berney, Michael ;
Pethe, Kevin .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2017, 114 (28) :7426-7431