Composition and functional analysis of the Saccharomyces cerevisiae trehalose synthase complex

Citation
W. Bell et al., Composition and functional analysis of the Saccharomyces cerevisiae trehalose synthase complex, J BIOL CHEM, 273(50), 1998, pp. 33311-33319
Citations number
33
Categorie Soggetti
Biochemistry & Biophysics
Journal title
JOURNAL OF BIOLOGICAL CHEMISTRY
ISSN journal
00219258 → ACNP
Volume
273
Issue
50
Year of publication
1998
Pages
33311 - 33319
Database
ISI
SICI code
0021-9258(199812)273:50<33311:CAFAOT>2.0.ZU;2-H
Abstract
In the yeast Saccharomyces cerevisiae, trehalose-6-phosphate synthase (TPS) and trehalose-6-phosphate phosphatase (TPP), which convert glucose 6-phosp hate plus UDP-glucose to trehalose, are part of the trehalose synthase comp lex. In addition to the TPS1 (previously also called GGS1, CIF1, BYP1, FDP1 , GLC6, and TSS1) and TPS2 (also described as HOG2 and PFK3) gene products, this complex also contains a regulatory subunit encoded by TSL1. We have c onstructed a set of isogenic strains carrying all possible combinations of deletions of these three genes and of TPS3, a homologue of TSL1 identified by systematic sequencing, Deletion of TPS1 totally abolished TPS activity a nd measurable trehalose, whereas deletion of any of the other genes in most cases reduced both. Similarly, deletion of TPS2 completely abolished TPP a ctivity, and deletion of any of the other genes resulted in a reduction of this activity. Therefore, it appears that all subunits are required for opt imal enzymatic activity. Since we observed measurable trehalose in strains lacking all but the TPS1 gene, some phosphatase activity in addition to Tps 2 can hydrolyze trehalose 6-phosphate, Deletion of TPS3, in particular in a tsl1 Delta background, reduced both TPS and TPP activities and trehalose c ontent, Deletion of TPS2, TSL1, or TPS3 and, in particular, of TSL1 plus TP S3 destabilized the trehalose synthase complex. We conclude that Tps3 is a fourth subunit of the complex with functions partially redundant to those o f Tsl1. Among the four genes studied, TPS1 is necessary and sufficient for growth on glucose and fructose. Even when overproduced, none of the other s ubunits could take over this function of Tps1 despite the homology shared b y all four proteins. A portion of Tps1 appears to occur in a form not bound by the complex. Whereas TPS activity in the complex is inhibited by P-i, P -i stimulates the monomeric form of Tps1, We discuss the possible role of d ifferentially regulated Tps1 in a complex-bound or monomeric form in light of the requirement of Tps1 for trehalose production and for growth on. gluc ose and fructose.