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Mechanism of irreversible inactivation of phosphomannose isomerases by silver ions and flamazine.
Wells, T N; Scully, P; Paravicini, G; Proudfoot, A E; Payton, M A.
Afiliación
  • Wells TN; Glaxo Institute for Molecular Biology, Geneva, Switzerland.
Biochemistry ; 34(24): 7896-903, 1995 Jun 20.
Article en En | MEDLINE | ID: mdl-7794901
Silver ions and silver-containing compounds have been used as topical antimicrobial agents in a variety of clinical situations. We have previously shown that the enzyme phosphomannose isomerase (PMI) is essential for the biosynthesis of Candida albicans cell walls. In this study, we find that PMI can be inhibited by silver ions. This process is shown to be irreversible, and is a two-step process, involving an intermediate complex with a dissociation constant, Ki, of 59 +/- 8 microM, and a maximum rate of inactivation of 0.25 +/- 0.04 min-1 in 50 mM Hepes buffer, pH 8.0 at 37 degrees C. The enzyme can be protected against this inactivation by the substrate mannose 6-phosphate, with a dissociation constant of 0.31 +/- 0.04 mM, close to its Km value. Flamazine (silver sulfadiazine) is a silver-containing antibiotic which is used clinically as a topical antimicrobial and antifungal agent. We compared the ability of silver sulfadiazine and two other silver-containing compounds to irreversibly inactivate C. albicans PMI. The addition of the organic moiety increased the affinity of the compounds, with silver sulfadiazine showing a Ki of 190 +/- 30 nM. In all cases, the maximum inhibition rate was similar, implying a similar rate-determining step. Silver sulfadiazine does not inhibit Escherichia coli PMI, and this suggests a role of the only free cysteine, Cys-150, in the inactivation process. To confirm this, we mutated this residue to alanine in C. albicans PMI. The resultant Cys150 --> Ala mutant protein showed similar Vm and Km values to the wild-type enzyme.(ABSTRACT TRUNCATED AT 250 WORDS)
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Compuestos Organometálicos / Plata / Sulfadiazina de Plata / Candida albicans / Manosa-6-Fosfato Isomerasa Idioma: En Revista: Biochemistry Año: 1995 Tipo del documento: Article País de afiliación: Suiza Pais de publicación: Estados Unidos
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Compuestos Organometálicos / Plata / Sulfadiazina de Plata / Candida albicans / Manosa-6-Fosfato Isomerasa Idioma: En Revista: Biochemistry Año: 1995 Tipo del documento: Article País de afiliación: Suiza Pais de publicación: Estados Unidos