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Biochemical Characteristics of New Delhi Metallo-β-Lactamase-1 Show Unexpected Difference to Other MBLs
被引:23
作者:
Li, Tao
[1
]
Wang, Qin
[1
]
Chen, Fanghong
[1
]
Li, Xiang
[1
]
Luo, Sen
[1
]
Fang, Huali
[1
]
Wang, Dehui
[1
]
Li, Zhan
[1
]
Hou, Xiaojun
[1
]
Wang, Hui
[1
]
机构:
[1] Beijing Inst Microbiol & Epidemiol, State Key Lab Pathogens & Biosecur, Beijing, Peoples R China
来源:
PLOS ONE
|
2013年
/
8卷
/
04期
基金:
中国国家自然科学基金;
关键词:
METALLO-BETA-LACTAMASE;
PSEUDOMONAS-AERUGINOSA;
ANTIBIOTIC-RESISTANCE;
CHELATION-THERAPY;
CRYSTAL-STRUCTURE;
MECHANISM;
NDM-1;
INHIBITION;
REVEALS;
D O I:
10.1371/journal.pone.0061914
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
New Delhi metallo-beta-lactamase (NDM-1) is a new metallo-beta-lactamase (MBL) that has recently emerged as a global threat because it confers bacteria with resistance to almost all clinically used beta-lactam antibiotics. To determine the molecular basis of this threat, NDM-1 was purified from Escherichia coli TransB (DE3) carrying cloned blaNDM-1 gene by an anion-exchange chromatography step followed by a gel permeation chromatography step. The purified enzyme was stable even in extremely alkaline buffer (pH 11) and reached its highest activity at a low temperature (15 degrees C), which was different from other MBLs. The 50% inhibition concentration of EDTA against NDM-1 was 412 nM, which showed that NDM-1 was more susceptible to EDTA than other MBLs. The effects of zinc on NDM-1 differed between cephem and carbapenem complexes, but inhibition at high Zn2+ concentration was observed for all of tested beta-lactam compounds.
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