Tetracycline-modifying enzyme SmTetX from Stenotrophomonas maltophilia

被引:2
|
作者
Maly, Martin [1 ,2 ]
Kolenko, Petr [1 ,2 ]
Stransky, Jan [1 ]
Svecova, Leona [1 ]
Duskova, Jarmila [1 ]
Koval', Tomas [1 ]
Skalova, Tereza [1 ]
Trundova, Maria [1 ]
Adamkova, Kristyna [1 ]
Cerny, Jiri [1 ]
Bozikova, Paulina [1 ]
Dohnalek, Jan [1 ]
机构
[1] Czech Acad Sci, Inst Biotechnol, Vvi, BIOCEV, Prumyslova 595, Vestec 25250, Czech Republic
[2] Czech Tech Univ, Fac Nucl Sci & Phys Engn, Brehova 7, Prague 11519 1, Czech Republic
关键词
FAD-dependent monooxygenases; tetracycline; antibiotic resistance; P-HYDROXYBENZOATE HYDROXYLASE; STRUCTURAL BASIS; DEGRADING MONOOXYGENASE; MOLECULAR-BIOLOGY; WEB SERVER; OMIT MAPS; RESISTANCE; TIGECYCLINE; FAD; ANTIBIOTICS;
D O I
10.1107/S2053230X23005381
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The resistance of the emerging human pathogen Stenotrophomonas maltophilia to tetracycline antibiotics mainly depends on multidrug efflux pumps and ribosomal protection enzymes. However, the genomes of several strains of this Gram-negative bacterium code for a FAD-dependent monooxygenase (SmTetX) homologous to tetracycline destructases. This protein was recombinantly produced and its structure and function were investigated. Activity assays using SmTetX showed its ability to modify oxytetracycline with a catalytic rate comparable to those of other destructases. SmTetX shares its fold with the tetracycline destructase TetX from Bacteroides thetaiotaomicron; however, its active site possesses an aromatic region that is unique in this enzyme family. A docking study confirmed tetracycline and its analogues to be the preferred binders amongst various classes of antibiotics.
引用
收藏
页码:180 / 192
页数:13
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