Bacterial Enzymes and Antibiotic Resistance

被引:118
作者
Egorov, A. M. [1 ]
Ulyashova, M. M. [1 ]
Rubtsova, M. Yu. [1 ]
机构
[1] Moscow MV Lomonosov State Univ, Chem Fac, Leninskie Gori 1,Bldg 3, Moscow 119991, Russia
基金
俄罗斯科学基金会;
关键词
antibiotic resistance; enzymes; mutant forms; antibiotics; AMINOGLYCOSIDE RESISTANCE; STAPHYLOCOCCUS-AUREUS; QUINOLONE ACTION; MECHANISMS; BINDING; DETERMINANT; INHIBITORS; EMERGENCE; EVOLUTION; PROTEIN;
D O I
10.32607/20758251-2018-10-4-33-48
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 resistance of microorganisms to antibiotics has been developing for more than 2 billion years and is widely distributed among various representatives of the microbiological world. Bacterial enzymes play a key role in the emergence of resistance. Classification of these enzymes is based on their participation in various biochemical mechanisms: modification of the enzymes that act as antibiotic targets, enzymatic modification of intracellular targets, enzymatic transformation of antibiotics, and the implementation of cellular metabolism reactions. The main mechanisms of resistance development are associated with the evolution of superfamilies of bacterial enzymes due to the variability of the genes encoding them. The collection of all antibiotic resistance genes is known as the resistome. Tens of thousands of enzymes and their mutants that implement various mechanisms of resistance form a new community that is called "the enzystome." Analysis of the structure and functional characteristics of enzymes, which are the targets for different classes of antibiotics, will allow us to develop new strategies for overcoming the resistance.
引用
收藏
页码:33 / 48
页数:16
相关论文
共 95 条
[1]   Mechanism of Quinolone Action and Resistance [J].
Aldred, Katie J. ;
Kerns, Robert J. ;
Osheroff, Neil .
BIOCHEMISTRY, 2014, 53 (10) :1565-1574
[2]  
[Anonymous], 2016, PERSPECT MED, DOI [10.1101/cshperspect.a025395, DOI 10.1101/CSHPERSPECT.A025395]
[3]  
[Anonymous], 2014, ABSTR APPL ANAL, DOI DOI 10.1155/2014/502756
[4]  
[Anonymous], 2014, Antimicrobial Resistance: Global Report on Surveillance.
[5]   Synthesis and Evaluation of Hetero- and Homodimers of Ribosome-Targeting Antibiotics: Antimicrobial Activity, in Vitro Inhibition of Translation, and Drug Resistance [J].
Berkov-Zrihen, Yifat ;
Green, Keith D. ;
Labby, Kristin J. ;
Feldman, Mark ;
Garneau-Tsodikova, Sylvie ;
Fridman, Micha .
JOURNAL OF MEDICINAL CHEMISTRY, 2013, 56 (13) :5613-5625
[6]   Domain - Domain interactions in the aminoglycoside antibiotic resistance enzyme AAC(6')-APH(2") [J].
Boehr, DD ;
Daigle, DM ;
Wright, GD .
BIOCHEMISTRY, 2004, 43 (30) :9846-9855
[7]   Broad-spectrum peptide inhibitors of aminoglycoside antibotic resistance enzymes [J].
Boehr, DD ;
Draker, KA ;
Koteva, K ;
Bains, M ;
Hancock, RE ;
Wright, GD .
CHEMISTRY & BIOLOGY, 2003, 10 (02) :189-196
[8]   β-Lactamases: A Focus on Current Challenges [J].
Bonomo, Robert A. .
COLD SPRING HARBOR PERSPECTIVES IN MEDICINE, 2017, 7 (01)
[9]   Multiple Global Suppressors of Protein Stability Defects Facilitate the Evolution of Extended-Spectrum TEM β-Lactamases [J].
Brown, Nicholas G. ;
Pennington, Jeanine M. ;
Huang, Wanzhi ;
Ayvaz, Tulin ;
Palzkill, Timothy .
JOURNAL OF MOLECULAR BIOLOGY, 2010, 404 (05) :832-846
[10]   β-Lactams and β-Lactamase Inhibitors: An Overview [J].
Bush, Karen ;
Bradford, Patricia A. .
COLD SPRING HARBOR PERSPECTIVES IN MEDICINE, 2016, 6 (08)