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Journal of Bacteriology, April 2000, p. 2153-2162, Vol. 182, No. 8
0021-9193/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.

Multiple Hexose Transporters of Schizosaccharomyces pombe

Sylvia Heiland,1 Nada Radovanovic,1 Milan Höfer,1 Joris Winderickx,2 and Hella Lichtenberg1,*

Botanisches Institut, Universität Bonn, 53115 Bonn, Germany,1 and Laboratorium voor Moleculaire Celbiologie, Katholieke Universiteit Leuven, B-3001 Leuven-Heverlee, Belgium2

Received 30 September 1999/Accepted 19 January 2000

We have identified a family of six hexose transporter genes (Ght1 to Ght6) in the fission yeast Schizosaccharomyces pombe. Sequence homology to Saccharomyces cerevisiae and mammalian hexose transporters (Hxtp and GLUTp, respectively) and secondary-structure predictions of 12 transmembrane domains for each of the Ght proteins place them into the sugar porter subfamily within the major facilitator superfamily. Interestingly, among this sugar porter family, the emerging S. pombe hexose transporter family clusters are separate from monosaccharide transporters of other yeasts (S. cerevisiae, Kluyveromyces lactis, and Candida albicans) and of humans, suggesting that these proteins form a distinct structural family of hexose transporters. Expression of the Ght1, Ght2, Ght5, and Ght6 genes in the S. cerevisiae mutant RE700A may functionally complement its D-glucose uptake-deficient phenotype. Northern blot analysis and reverse transcription-PCR showed that among all Ght's of S. pombe, Ght5 is the most prominently expressed hexose transporter. Ght1p, Ght2p, and Ght5p displayed significantly higher specificities for D-glucose than for D-fructose. Analysis of the previously described S. pombe D-glucose transport-deficient mutant YGS-5 revealed that this strain is defective in the Ght1, Ght5, and Ght6 genes. Based on an analysis of three S. pombe strains bearing single or double mutations in Ght3 and Ght4, we conclude that the Ght3p function is required for D-gluconate transport in S. pombe. The function of Ght4p remains to be clarified. Ght6p exhibited a slightly higher affinity to D-fructose than to D-glucose, and among the Ght's it is the transporter with the highest specificity for D-fructose.


* Corresponding author. Mailing address: Botanisches Institut, Universität Bonn, Kirschallee 1, 53115 Bonn, Germany. Phone: 49 228 73 55 18. Fax: 49 228 73 55 04. E-mail: H.Lichtenberg{at}uni-bonn.de.


Journal of Bacteriology, April 2000, p. 2153-2162, Vol. 182, No. 8
0021-9193/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.



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