Literature DB >> 8759860

Structure of the low-affinity penicillin-binding protein 5 PBP5fm in wild-type and highly penicillin-resistant strains of Enterococcus faecium.

W Zorzi1, X Y Zhou, O Dardenne, J Lamotte, D Raze, J Pierre, L Gutmann, J Coyette.   

Abstract

Among its penicillin-binding proteins (PBPs), Enterococcus faecium possesses a low-affinity PBP5, PBP5fm, which is the main target involved in beta-lactam resistance. A 7.7-kb EcoRI chromosomal fragment of E. faecium D63r containing the pbp5fm gene was cloned and sequenced. Two open reading frames (ORFs) were found. A 2,037-bp ORF encoded the deduced 73.8-kDa PBP5fm, the amino acid sequences of which were, respectively, 99.8, 78.5, and 62% homologous to those of the low-affinity plasmid-encoded PBP3r of Enterococcus hirae S185r and the chromosome-encoded PBP5 of E. hirae R40 and Enterococcus faecalis 56R. A second 597-bp ORF, designated psrfm, was found 2.3 kb upstream of pbp5fm. It appeared to be 285 bp shorter than and 74% homologous with the regulatory gene psr of E. hirae ATCC 9790. Different clinical isolates of E. faecium, for which a wide range of benzylpenicillin MICs were observed, showed that the increases in MICs were related to two mechanisms. For some strains of intermediate resistance (MICs of 16 to 64 micrograms/ml), the increased level of resistance could be explained by the presence of larger quantities of PBP5fm which had an affinity for benzylpenicillin (second-order rate constant of protein acylation [k+2/K] values of 17 to 25 M(-1) s(-1)) that remained unchanged. For the two most highly resistant strains, EFM-1 (MIC, 90 micrograms/ml) and H80721 (MIC, 512 micrograms/ml), the resistance was related to different amino acid substitutions yielding very-low-affinity PBP5fm variants (k+2/K < or = 1.5 M(-1) s(-1)) which were synthesized in small quantities. More specifically, it appeared, with a three-dimensional model of the C-terminal domain of PBP5fm, that the substitutions of Met-485, located in the third position after the conserved SDN triad, by Thr in EFM-1 and by Ala in H80721 were the most likely cause of the decreasing affinity of PBP5fm observed in these strains.

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Year:  1996        PMID: 8759860      PMCID: PMC178279          DOI: 10.1128/jb.178.16.4948-4957.1996

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  42 in total

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Authors:  O Herzberg; J Moult
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Authors:  J M Ghuysen; J M Frère; M Leyh-Bouille; M Nguyen-Distèche; J Coyette
Journal:  Biochem J       Date:  1986-04-01       Impact factor: 3.857

3.  One or two low affinity penicillin-binding proteins may be responsible for the range of susceptibility of Enterococcus faecium to benzylpenicillin.

Authors:  R Williamson; C le Bouguénec; L Gutmann; T Horaud
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4.  Characterization of translational initiation sites in E. coli.

Authors:  G D Stormo; T D Schneider; L M Gold
Journal:  Nucleic Acids Res       Date:  1982-05-11       Impact factor: 16.971

5.  Engineering a novel beta-lactamase by a single point mutation.

Authors:  F Jacob; B Joris; O Dideberg; J Dusart; J M Ghuysen; J M Frère
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6.  Nucleotide sequence of the pbpA gene and characteristics of the deduced amino acid sequence of penicillin-binding protein 2 of Escherichia coli K12.

Authors:  S Asoh; H Matsuzawa; F Ishino; J L Strominger; M Matsuhashi; T Ohta
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7.  Identification of a streptococcal penicillin-binding protein that reacts very slowly with penicillin.

Authors:  R Fontana; R Cerini; P Longoni; A Grossato; P Canepari
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Authors:  J M Frère; J M Ghuysen; H R Perkins; M Nieto
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9.  Streptomyces K15 DD-peptidase-catalysed reactions with suicide beta-lactam carbonyl donors.

Authors:  M Leyh-Bouille; M Nguyen-Distèche; S Pirlot; A Veithen; C Bourguignon; J M Ghuysen
Journal:  Biochem J       Date:  1986-04-01       Impact factor: 3.857

10.  The penicillin-binding proteins in Streptococcus faecalis ATCC 9790.

Authors:  J Coyette; J M Ghuysen; R Fontana
Journal:  Eur J Biochem       Date:  1980-09
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  43 in total

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Review 2.  Biochemistry and comparative genomics of SxxK superfamily acyltransferases offer a clue to the mycobacterial paradox: presence of penicillin-susceptible target proteins versus lack of efficiency of penicillin as therapeutic agent.

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4.  Contribution of penicillin-binding protein homologs to antibiotic resistance, cell morphology, and virulence of Listeria monocytogenes EGDe.

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5.  Enterococci: on the back burner but still simmering.

Authors:  George M Eliopoulos
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6.  PBP5 complementation of a PBP3 deficiency in Enterococcus hirae.

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7.  The GTPase CpgA is implicated in the deposition of the peptidoglycan sacculus in Bacillus subtilis.

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8.  Genetic linkage and cotransfer of a novel, vanB-containing transposon (Tn5382) and a low-affinity penicillin-binding protein 5 gene in a clinical vancomycin-resistant Enterococcus faecium isolate.

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10.  Reaction of soluble penicillin-binding protein 2a of methicillin-resistant Staphylococcus aureus with beta-lactams and acyclic substrates: kinetics in homogeneous solution.

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