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1.
Rev. argent. microbiol ; 32(3): 157-160, jul.-sept. 2000.
Artículo en Español | LILACS | ID: lil-332520

RESUMEN

Severe mycotic infections are a source of concern in immunocompromised patients or in those who receive chemotherapy for hematological malignant diseases. One of the causes is referred to the appearance of antimycotic resistant microorganisms. Fluconazole is one of the antimycotic used for invasive mycoses treatment. Therefore it is necessary to evaluate the factors that originate this resistance. In the present report the yeast Saccharomyces cerevisiae S288c was used as a model system. In resistant strains the accumulation of the lipophilic cation Rhodamine 6G, L-leucine uptake and growth inhibition by crystal violet dye were determined. The results presented herein demonstrate the correlation between the membrane potential and the resistance to fluconazole presented by S. cerevisiae strain S288c.


Asunto(s)
Antifúngicos/farmacología , Fluconazol , Potenciales de la Membrana , Farmacorresistencia Microbiana , Rodaminas , Saccharomyces cerevisiae , Antifúngicos/metabolismo , Medios de Cultivo , Esteroles/metabolismo , Fluconazol , Violeta de Genciana , Leucina , Lípidos de la Membrana/metabolismo , Prolina , Saccharomyces cerevisiae
2.
Rev. argent. microbiol ; 22(1): 7-16, 1990.
Artículo en Español | LILACS-Express | LILACS, BINACIS | ID: biblio-1171555

RESUMEN

L-leucine entrance into Saccharomyces cerevisiae is mediated by the general amino acid permease, GAP and two transport systems, S1 and S2, kinetically characterized. S1 is a high-affinity, low-velocity transport system, operating at lower L-leucine external concentration (0.05-0.1 mM), while S2 is a low-affinity, high-velocity transport system, operating at higher L-leucine external concentration (1.0 mM). In cells grown in minimal medium containing ammonium as sole nitrogen source the values of L-leucine entrance and uptake are smaller than those in cells grown in L-proline containing medium. When GAP is repressed by ammonium, L-leucine entrance is mediate by systems S1 and S2. Both systems are inhibited by ammonium. When GAP is derepressed, in cells grown in L-proline medium, L-leucine is transported by systems S1 and GAP (lower L-leucine external concentration), and mainly by S2 (higher L-leucine external concentration). GAP is the largest system inhibited by ammonium.

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