4.7 Article

ACI-1 from Acidaminococcus fermentans:: Characterization of the first β-lactamase in anaerobic cocci

Journal

ANTIMICROBIAL AGENTS AND CHEMOTHERAPY
Volume 44, Issue 11, Pages 3144-3149

Publisher

AMER SOC MICROBIOLOGY
DOI: 10.1128/AAC.44.11.3144-3149.2000

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Acidaminococcus fermentans belongs to the group of strictly anaerobic gram-negative cocci. All previously described Acidaminococcus strains are susceptible to beta -lactam antibiotics. An A. fermentans strain (RYC-MR95) resistant to penicillin and expanded-spectrum cephalosporin (amoxicillin and cefotaxime MICs, 64 mug/ml) was isolated from a human perianal abscess. A fragment encoding a beta -lactamase from genomic DNA was cloned in Escherichia coli K-12 strain HB101, and the recombinant strain expressed resistance to amoxicillin (MIC, 1,024 mug/ml) and cefotaxime (MIC, 4 mug/ml). Clavulanic acid decreased the MICs to 8 and 0.03 mug/ml, respectively. Analysis of the nucleotide sequence revealed a new class A beta -lactamase, ACI-1. In accordance with its biochemical properties, we propose to assign ACI-1 to functional group 2be, The ACI-1 enzyme (estimated pi 4.3) had <50% amino acid identity with any other class A -lactamases, the closest being ROB-1 from Haemophilus influenzae (44%). ACI-1 was closer to class A beta -lactamases from some gram-positive organisms (41 to 44% amino acid identity with Bacillus beta -lactamases) than to most class A enzymes from gram-negative organisms (TEM-1, 24.6%). The aci1 gene had a G+C content of 42.1%, in contrast with 56% G+C content for genomic DNA from A. fermentans, thus suggesting that aci1 may have been obtained by horizontal gene transfer.

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