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Characterisation of glucose transport in Saccharomyces cerevisiae with plasma membrane vesicles (countertransport) and intact cells (initial uptake) with single Hxt1, Hxt2, Hxt3, Hxt4, Hxt6, Hxt7 or Gal2 transporters

2002; Oxford University Press; Volume: 2; Issue: 4 Linguagem: Inglês

10.1111/j.1567-1364.2002.tb00121.x

1567-1364

Andreas Maier, Bernhard Völker, Eckhard Boles, Gà ⁄ nter Fred Fuhrmann,

DNA Repair Mechanisms

The yeast glucose transporters Hxt1, Hxt2, Hxt3, Hxt4, Hxt6, Hxt7 and Gal2, individually expressed in an hxt1-7 null mutant strain, demonstrate the phenomenon of countertransport. Thus, these transporters, which are the most important glucose transporters in Saccharomyces cerevisiae, are facilitated diffusion transporters. Apparent Km-values from high to low affinity, determined from countertransport and initial-uptake experiments, respectively, are: Hxt6 0.9±0.2 and 1.4±0.1 mM, Hxt7 1.3±0.3 and 1.9±0.1 mM, Gal2 1.5 and 1.6±0.1 mM, Hxt2 2.9±0.3 and 4.6±0.3 mM, Hxt4 6.2±0.5 and 6.2±0.3 mM, Hxt3 28.6±6.8 and 34.2±3.2 mM, and Hxt1 107±49 and 129±9 mM. From both independent methods, countertransport and initial uptake, the same range of apparent Km-values was obtained for each transporter. In contrast to that in human erythrocytes, the facilitated diffusion transport mechanism of glucose in yeast was symmetric. Besides facilitated diffusion there existed in all single glucose transport mutants, except for the HXT1 strain, significant first-order behaviour.