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Transmembrane segments 1, 5, 7 and 8 are required for high-affinity glucose transport by Saccharomyces cerevisiae Hxt2 transporter.
- Source :
-
The Biochemical journal [Biochem J] 2003 May 15; Vol. 372 (Pt 1), pp. 247-52. - Publication Year :
- 2003
-
Abstract
- Hxt2 is a high-affinity facilitative glucose transporter of Saccharomyces cerevisiae and belongs to the major facilitator superfamily. Hxt1 shares approximately 70% amino acid identity with Hxt2 in its transmembrane segments (TMs) and inter-TM loops, but transports D-glucose with an affinity about one-tenth of that of Hxt2. To determine which TMs of Hxt2 are important for high-affinity glucose transport, we constructed chimaeras of Hxt2 and Hxt1 by randomly replacing each of the 12 TMs of Hxt2 with the corresponding segment of Hxt1, for a total of 4096 different transporters. Among > 20000 yeast transformants screened, 39 different clones were selected by plate assays of high-affinity glucose-transport activity and sequenced. With only two exceptions, the selected chimaeras contained Hxt2 TMs 1, 5, 7 and 8. We then constructed chimaeras corresponding to all 16 possible combinations of Hxt2 TMs 1, 5, 7 and 8. Only one chimaera, namely that containing all four Hxt2 TMs, exhibited transport activity comparable with that of Hxt2. The K (m) and V (max) values for D-glucose transport, and the substrate specificity of this chimaera were almost identical with those of Hxt2. These results indicate that TMs 1, 5, 7 and 8 are necessary for exhibiting high-affinity glucose-transport activity of Hxt2.
- Subjects :
- DNA Shuffling
Glucose Transport Proteins, Facilitative
Membrane Proteins genetics
Monosaccharide Transport Proteins genetics
Protein Structure, Tertiary physiology
Recombinant Fusion Proteins genetics
Recombinant Fusion Proteins metabolism
Substrate Specificity
Glucose metabolism
Membrane Proteins metabolism
Monosaccharide Transport Proteins metabolism
Saccharomyces cerevisiae metabolism
Saccharomyces cerevisiae Proteins
Subjects
Details
- Language :
- English
- ISSN :
- 0264-6021
- Volume :
- 372
- Issue :
- Pt 1
- Database :
- MEDLINE
- Journal :
- The Biochemical journal
- Publication Type :
- Academic Journal
- Accession number :
- 12603199
- Full Text :
- https://doi.org/10.1042/BJ20030044