The Legionella (Fluoribacter) gormanii metallo-beta-lactamase: a new member of the highly divergent lineage of molecular-subclass B3 beta-lactamases. 2000

L Boschi, and P S Mercuri, and M L Riccio, and G Amicosante, and M Galleni, and J M Frère, and G M Rossolini
Dipartimento di Biologia Molecolare, Sezione di Microbiologia, Università di Siena, I-53100 Siena, Italy.

A metallo-beta-lactamase determinant was cloned from a genomic library of Legionella (Fluoribacter) gormanii ATCC 33297(T) constructed in the plasmid vector pACYC184 and transformed into Escherichia coli DH5alpha, by screening for clones showing a reduced susceptibility to imipenem. The product of the cloned determinant, named FEZ-1, contains a 30-kDa polypeptide and exhibits an isoelectric pH of 7.6. Sequencing revealed that FEZ-1 is a molecular-class B beta-lactamase which shares the closest structural similarity (29.7% of identical residues) with the L1 enzyme of Stenotrophomonas maltophilia, being a new member of the highly divergent subclass B3 lineage. All the residues that in L1 are known to be directly or indirectly involved in coordination of the zinc ions were found to be conserved also in FEZ-1, suggesting that the geometry of zinc coordination in the active site of the latter enzyme is identical to that of L1. Unlike L1, however, FEZ-1 appeared to be monomeric in gel permeation chromatography experiments and exhibited a distinctive substrate specificity with a marked preference for cephalosporins and meropenem. The properties of FEZ-1 overall resembled those of a beta-lactamase previously purified from the same strain of L. gormanii (T. Fujii, K. Sato, K. Miyata, M. Inoue, and S. Mitsuhashi, Antimicrob. Agents Chemother. 29:925-926, 1986) and are as yet unique among class B enzymes, reinforcing the notion that considerable functional heterogeneity can be encountered among members of this class. A system for overexpression of the bla(FEZ-1) gene in E. coli, based on the T7 phage promoter, was also developed.

UI MeSH Term Description Entries
D007875 Legionella Gram-negative aerobic rods, isolated from surface water or thermally polluted lakes or streams. Member are pathogenic for man. Legionella pneumophila is the causative agent for LEGIONNAIRES' DISEASE.
D008969 Molecular Sequence Data Descriptions of specific amino acid, carbohydrate, or nucleotide sequences which have appeared in the published literature and/or are deposited in and maintained by databanks such as GENBANK, European Molecular Biology Laboratory (EMBL), National Biomedical Research Foundation (NBRF), or other sequence repositories. Sequence Data, Molecular,Molecular Sequencing Data,Data, Molecular Sequence,Data, Molecular Sequencing,Sequencing Data, Molecular
D003001 Cloning, Molecular The insertion of recombinant DNA molecules from prokaryotic and/or eukaryotic sources into a replicating vehicle, such as a plasmid or virus vector, and the introduction of the resultant hybrid molecules into recipient cells without altering the viability of those cells. Molecular Cloning
D005798 Genes, Bacterial The functional hereditary units of BACTERIA. Bacterial Gene,Bacterial Genes,Gene, Bacterial
D000595 Amino Acid Sequence The order of amino acids as they occur in a polypeptide chain. This is referred to as the primary structure of proteins. It is of fundamental importance in determining PROTEIN CONFORMATION. Protein Structure, Primary,Amino Acid Sequences,Sequence, Amino Acid,Sequences, Amino Acid,Primary Protein Structure,Primary Protein Structures,Protein Structures, Primary,Structure, Primary Protein,Structures, Primary Protein
D001483 Base Sequence The sequence of PURINES and PYRIMIDINES in nucleic acids and polynucleotides. It is also called nucleotide sequence. DNA Sequence,Nucleotide Sequence,RNA Sequence,DNA Sequences,Base Sequences,Nucleotide Sequences,RNA Sequences,Sequence, Base,Sequence, DNA,Sequence, Nucleotide,Sequence, RNA,Sequences, Base,Sequences, DNA,Sequences, Nucleotide,Sequences, RNA
D001618 beta-Lactamases Enzymes found in many bacteria which catalyze the hydrolysis of the amide bond in the beta-lactam ring. Well known antibiotics destroyed by these enzymes are penicillins and cephalosporins. beta-Lactamase,beta Lactamase,beta Lactamases
D016415 Sequence Alignment The arrangement of two or more amino acid or base sequences from an organism or organisms in such a way as to align areas of the sequences sharing common properties. The degree of relatedness or homology between the sequences is predicted computationally or statistically based on weights assigned to the elements aligned between the sequences. This in turn can serve as a potential indicator of the genetic relatedness between the organisms. Sequence Homology Determination,Determination, Sequence Homology,Alignment, Sequence,Alignments, Sequence,Determinations, Sequence Homology,Sequence Alignments,Sequence Homology Determinations

Related Publications

L Boschi, and P S Mercuri, and M L Riccio, and G Amicosante, and M Galleni, and J M Frère, and G M Rossolini
January 2003, Journal of molecular biology,
L Boschi, and P S Mercuri, and M L Riccio, and G Amicosante, and M Galleni, and J M Frère, and G M Rossolini
December 2001, Antimicrobial agents and chemotherapy,
L Boschi, and P S Mercuri, and M L Riccio, and G Amicosante, and M Galleni, and J M Frère, and G M Rossolini
December 2004, Antimicrobial agents and chemotherapy,
L Boschi, and P S Mercuri, and M L Riccio, and G Amicosante, and M Galleni, and J M Frère, and G M Rossolini
May 2014, The Journal of antimicrobial chemotherapy,
L Boschi, and P S Mercuri, and M L Riccio, and G Amicosante, and M Galleni, and J M Frère, and G M Rossolini
May 1986, Antimicrobial agents and chemotherapy,
L Boschi, and P S Mercuri, and M L Riccio, and G Amicosante, and M Galleni, and J M Frère, and G M Rossolini
August 2004, The Journal of biological chemistry,
L Boschi, and P S Mercuri, and M L Riccio, and G Amicosante, and M Galleni, and J M Frère, and G M Rossolini
August 2008, Antimicrobial agents and chemotherapy,
L Boschi, and P S Mercuri, and M L Riccio, and G Amicosante, and M Galleni, and J M Frère, and G M Rossolini
January 2019, Emerging microbes & infections,
L Boschi, and P S Mercuri, and M L Riccio, and G Amicosante, and M Galleni, and J M Frère, and G M Rossolini
September 2022, Antimicrobial agents and chemotherapy,
L Boschi, and P S Mercuri, and M L Riccio, and G Amicosante, and M Galleni, and J M Frère, and G M Rossolini
September 2018, Journal of global antimicrobial resistance,
Copied contents to your clipboard!