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Antimicrobial Agents and Chemotherapy, July 2009, p. 2902-2907, Vol. 53, No. 7
0066-4804/09/$08.00+0 doi:10.1128/AAC.01513-08
Copyright © 2009, American Society for Microbiology. All Rights Reserved.

Department of Medical Laboratory Science and Biotechnology, China Medical University, Taichung 404, Taiwan,1 Department of Biotechnology, Asia University, Taichung 413, Taiwan2
Received 12 November 2008/ Returned for modification 6 January 2009/ Accepted 25 April 2009
Two ampD homologues, ampDI and ampDII, of Stenotrophomonas maltophilia have been cloned and analyzed. Comparative genomic analysis revealed that the genomic context of the ampDII genes is quite different, whereas that of the ampDI genes is more conserved in S. maltophilia strains. The ampD system of S. maltophilia is distinct from that of the Enterobacteriaceae and Pseudomonas aeruginosa in three respects. (i) AmpDI of S. maltophilia is not encoded in an ampDE operon, in contrast to what happens in the Enterobacteriaceae and P. aeruginosa. (ii) The AmpD systems of the Enterobacteriaceae and P. aeruginosa are generally involved in the regulation of ampR-linked ampC gene expression, while AmpDI of S. maltophilia is responsible for the regulation of two intrinsic β-lactamase genes, of which the L2 gene, but not the L1 gene, is linked to ampR. (iii) S. maltophilia exhibits a one-step L1 and L2 gene derepression model involving ampDI, distinct from the two- or three-step derepression of the Enterobacteriaceae and P. aeruginosa. Moreover, the ampDI and ampDII genes are constitutively expressed and not regulated by the inducer and AmpR protein, and the expression of ampDII is weaker than that of ampDI. Finally, AmpDII is not associated with the derepression of β-lactamases, and its role in S. maltophilia remains unclear.
Published ahead of print on 4 May 2009.
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