期刊
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY
卷 52, 期 8, 页码 2905-2908出版社
AMER SOC MICROBIOLOGY
DOI: 10.1128/AAC.00166-08
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Purified recombinant VIM-7 possesses efficient penicillinase and carbapenemase activities comparable to those of VIM-2. Cephalosporinase activity was variable and generally lower than those of VIM-1 and VIM-2. A homology model suggests that the VIM-7 Tyr-218 Phe substitution may be responsible for the reduced catalytic efficiency against certain cephalosporins, including ceftazidime and cefepime.
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