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Antimicrobial Agents and Chemotherapy, April 2005, p. 1564-1566, Vol. 49, No. 4
0066-4804/05/$08.00+0 doi:10.1128/AAC.49.4.1564-1566.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.
Dipartimento di Scienze e Tecnologie Biomediche, Università di L'Aquila, L'Aquila,1 Dipartimento di Biologia Molecolare, Università di Siena, Siena,2 Ospedale di Circolo di Varese, Varese,3 Dipartimento di Scienze Microbiologiche e Ginecologiche, Sez. di Microbiologia, Università di Catania, Catania, Italy4
Received 19 July 2004/ Returned for modification 16 September 2004/ Accepted 28 November 2004
A new natural TEM derivative with extended-spectrum ß-lactamase activity, TEM-134, was identified in a ceftazidime-resistant clinical isolate of Citrobacter koseri. Compared to TEM-1, TEM-134 contains the following mutations: Q39K, E104K, R164H, and G238S. The blaTEM-134 gene was not transferable by conjugation and, apparently, was chromosomally encoded. Expression studies with Escherichia coli revealed efficient cefotaximase and ceftazidimase activity for TEM-134.
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