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

被引:99
作者
Zorzi, W
Ziou, XY
Dardenne, O
Lamotte, J
Raze, D
Pierre, J
Gutmann, L
Coyette, J
机构
[1] UNIV LIEGE, INST CHIM, CTR INGN PROT, B-4000 Sart Tilman Par Liege, BELGIUM
[2] UNIV PARIS 06, LAB RECH MOL ANTIBIOT, F-75270 PARIS 06, FRANCE
关键词
D O I
10.1128/jb.178.16.4948-4957.1996
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
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 he 285 bp shorter than and 74% homologous with the regulatory gene pst 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 mu g/ml), the increased level of resistance could he 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 mu g/ml) and H80721 (MIG, 512 mu g/ml), the resistance was related to different amino acid substitutions yielding very-low-affinity PBP5fm variants (k(+2)/k less than or equal to 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.
引用
收藏
页码:4948 / 4957
页数:10
相关论文
共 52 条
  • [1] MODIFICATION OF PENICILLIN-BINDING PROTEINS OF PENICILLIN-RESISTANT MUTANTS OF DIFFERENT SPECIES OF ENTEROCOCCI
    ALOBEID, S
    GUTMANN, L
    WILLIAMSON, R
    [J]. JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1990, 26 (05) : 613 - 618
  • [2] AUTOMATED DNA SEQUENCING - ULTRASENSITIVE DETECTION OF FLUORESCENT BANDS DURING ELECTROPHORESIS
    ANSORGE, W
    SPROAT, B
    STEGEMANN, J
    SCHWAGER, C
    ZENKE, M
    [J]. NUCLEIC ACIDS RESEARCH, 1987, 15 (11) : 4593 - 4602
  • [3] NUCLEOTIDE-SEQUENCE OF THE PBPA GENE AND CHARACTERISTICS OF THE DEDUCED AMINO-ACID-SEQUENCE OF PENICILLIN-BINDING PROTEIN-2 OF ESCHERICHIA-COLI-K12
    ASOH, S
    MATSUZAWA, H
    ISHINO, F
    STROMINGER, JL
    MATSUHASHI, M
    OHTA, T
    [J]. EUROPEAN JOURNAL OF BIOCHEMISTRY, 1986, 160 (02): : 231 - 238
  • [4] 18TH KREBS,HANS LECTURE - KNOWLEDGE-BASED PROTEIN MODELING AND DESIGN
    BLUNDELL, T
    CARNEY, D
    GARDNER, S
    HAYES, F
    HOWLIN, B
    HUBBARD, T
    OVERINGTON, J
    SINGH, DA
    SIBANDA, BL
    SUTCLIFFE, M
    [J]. EUROPEAN JOURNAL OF BIOCHEMISTRY, 1988, 172 (03): : 513 - 520
  • [5] THE 3-D STRUCTURE OF HIV-1 PROTEINASE AND THE DESIGN OF ANTIVIRAL AGENTS FOR THE TREATMENT OF AIDS
    BLUNDELL, TL
    LAPATTO, R
    WILDERSPIN, AF
    HEMMINGS, AM
    HOBART, PM
    DANLEY, DE
    WHITTLE, PJ
    [J]. TRENDS IN BIOCHEMICAL SCIENCES, 1990, 15 (11) : 425 - 430
  • [6] INSERTION OF AN EXTRA AMINO-ACID IS THE MAIN CAUSE OF THE LOW AFFINITY OF PENICILLIN-BINDING PROTEIN-2 IN PENICILLIN-RESISTANT STRAINS OF NEISSERIA-GONORRHOEAE
    BRANNIGAN, JA
    TIRODIMOS, IA
    ZHANG, QY
    DOWSON, CG
    SPRATT, BG
    [J]. MOLECULAR MICROBIOLOGY, 1990, 4 (06) : 913 - 919
  • [7] SOLUBILIZATION AND ISOLATION OF MEMBRANE-BOUND DD-CARBOXYPEPTIDASE OF STREPTOCOCCUS-FAECALIS ATCC-9790 - PROPERTIES OF PURIFIED ENZYME
    COYETTE, J
    GHUYSEN, JM
    FONTANA, R
    [J]. EUROPEAN JOURNAL OF BIOCHEMISTRY, 1978, 88 (01): : 297 - 305
  • [8] THE PENICILLIN-BINDING PROTEINS IN STREPTOCOCCUS-FAECALIS ATCC-9790
    COYETTE, J
    GHUYSEN, JM
    FONTANA, R
    [J]. EUROPEAN JOURNAL OF BIOCHEMISTRY, 1980, 110 (02): : 445 - 456
  • [9] DARDENNE O, UNPUB
  • [10] EVOLUTION OF PENICILLIN RESISTANCE IN STREPTOCOCCUS-PNEUMONIAE - THE ROLE OF STREPTOCOCCUS-MITIS IN THE FORMATION OF A LOW-AFFINITY PBP2B IN STREPTOCOCCUS-PNEUMONIAE
    DOWSON, CG
    COFFEY, TJ
    KELL, C
    WHILEY, RA
    [J]. MOLECULAR MICROBIOLOGY, 1993, 9 (03) : 635 - 643