TEM-89 (CMT-3) is the first complex mutant β-lactamase produced by a clinical strain of Proteus mirabilis (strain Pm 631). This new enzyme, which has a pI of 6.28, is derived from TEM-3 and has a single amino acid substitution also encountered in TEM-59 (inhibitor-resistant TEM β-lactamase IRT-17): Ser-130 to Gly. TEM-89 hydrolyzed penicillins to the same extent that TEM-3 did but lost almost all hydrolytic activity for cephalosporins and, like TEM-59, was highly resistant to inhibitors.
CITATION STYLE
Neuwirth, C., Madec, S., Siebor, E., Pechinot, A., Duez, J. M., Pruneaux, M., … Labia, R. (2001). TEM-89 β-lactamase produced by a Proteus mirabilis clinical isolate: New complex mutant (CMT 3) with mutations in both TEM-59 (IRT-17) and TEM-3. Antimicrobial Agents and Chemotherapy, 45(12), 3591–3594. https://doi.org/10.1128/AAC.45.12.3591-3594.2001
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