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PMID: 6312873 Published · ppublish English Journal Article

Kinetic studies on inactivation of Citrobacter freundii cephalosporinase by sulbactam.

Antimicrobial agents and chemotherapy ·Vol. 24 ·No. 1 ·1983-07-00 ·Pages 23-30

Yamaguchi A, Hirata T, Sawai T

Abstract

The inactivation kinetics for inhibition by sulbactam (CP45,899) of Citrobacter freundii GN346 cephalosporinase were studied in detail and compared with those of type Ib penicillinase or TEM-2 beta-lactamase mediated by R plasmid RGN823. The rate constant for progressive inactivation of the cephalosporinase was significantly larger than that measured with the penicillinase. The number of sulbactam molecules required to cause complete inactivation of one cephalosporinase molecule (turnover number) was 80. The turnover number for the penicillinase was 5,200. The powerful inhibition by sulbactam of this cephalosporinase is similar to clavulanic acid inhibition of the penicillinase (turnover number, 115; reported by others). The affinity of sulbactam for the cephalosporinase, expressed as Ki, was 500 microM; this value was much higher than that for the penicillinase, which was estimated to be 0.5 microM. These results indicated that sulbactam is an effective progressive inactivator but a poor competitive inhibitor for the cephalosporinase. Our study also revealed that the cephalosporinase and sulbactam formed a long-lived inhibitor-enzyme complex which we termed the pseudo-irreversible complex. The half-life of the complex was 550 min at pH 7.0 and 30 degrees C.

MeSH Terms
Binding, Competitive Cephalosporinase/metabolism Chromatography, Gel Citrobacter/drug effects,enzymology Kinetics Penicillanic Acid/metabolism,pharmacology Sulbactam beta-Lactamase Inhibitors
Chemicals
beta-Lactamase Inhibitors Penicillanic Acid Cephalosporinase Sulbactam
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Yamaguchi A
Hirata T
Sawai T
References (16)
16 references, click to expand
  1. Kinetic studies on the inactivation of Escherichia coli RTEM beta-lactamase by clavulanic acid.
    Biochemistry. 1978 May 30;17(11):2180-4 PMID: 352394
  2. Iodometric assay method for beta-lactamase with various beta-lactam antibiotics as substrates.
    Antimicrob Agents Chemother. 1978 Jun;13(6):910-3 PMID: 677858
  3. 6-beta-bromopenicillanic acid, a potent beta-lactamase inhibitor.
    Proc Natl Acad Sci U S A. 1978 Sep;75(9):4145-9 PMID: 212736
  4. CP-45,899, a beta-lactamase inhibitor that extends the antibacterial spectrum of beta-lactams: initial bacteriological characterization.
    Antimicrob Agents Chemother. 1978 Sep;14(3):414-9 PMID: 309306
  5. [Kinetics of beta-lactamase inhibition by clavulanic acid].
    Biochim Biophys Acta. 1978 Oct 12;526(2):572-9 PMID: 363163
  6. Comparative inhibition beta-lactamases by novel beta-lactam compounds.
    Antimicrob Agents Chemother. 1979 Feb;15(2):171-6 PMID: 311616
  7. The inhibition of staphylococcal beta-lactamase by clavulanic acid.
    Biochem J. 1979 Apr 1;179(1):67-76 PMID: 38773
  8. Inhibition kinetics of three R-factor-mediated beta-lactamases by a new beta-lactam sulfone (CP 45899).
    Biochim Biophys Acta. 1980 Feb 14;611(2):351-7 PMID: 6243991
  9. Inactivation of the RTEM beta-lactamase from Escherichia coli. Interaction of penam sulfones with enzyme.
    Biochemistry. 1981 May 12;20(10):2726-31 PMID: 7018564
  10. Penicillanic acid sulfone: an unexpected isotope effect in the interaction of 6 alpha- and 6 beta-monodeuterio and of 6,6-dideuterio derivatives with RTEM beta-lactamase from Escherichia coli.
    Biochemistry. 1981 Jun 23;20(13):3680-7 PMID: 6268140
  11. Penicillanic acid sulfone: interaction with RTEM beta-lactamase from Escherichia coli at different pH values.
    Biochemistry. 1981 Jun 23;20(13):3688-95 PMID: 6268141
  12. The inhibition of beta-lactamases from gram-negative bacteria by clavulanic acid.
    Biochem J. 1981 Dec 1;199(3):779-87 PMID: 7041890
  13. Characterization of eight beta-lactamases of Gram-negative bacteria.
    J Bacteriol. 1982 Nov;152(2):567-71 PMID: 6752115
  14. Interaction of azthreonam and related monobactams with beta-lactamases from gram-negative bacteria.
    Antimicrob Agents Chemother. 1982 Sep;22(3):414-20 PMID: 6982680
  15. Cefoxitin, N-formimidoyl thienamycin, clavulanic acid, and penicillanic acid sulfone as suicide inhibitors for different types of beta-lactamases produced by gram-negative bacteria.
    J Antibiot (Tokyo). 1982 Nov;35(11):1594-602 PMID: 6298169
  16. Micro-iodometric assay for penicillinase.
    Biochem J. 1962 May;83:236-40 PMID: 14480578
Article Info
Journal
Antimicrobial agents and chemotherapy
Abbr.
Antimicrob Agents Chemother
ISSN
0066-4804
Published
1983-07-00
Pages
23-30
Language
English
Region
United States
NLM ID
0315061
PMCID
PMC185099
Subset
IM
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