W. Bell et al., Composition and functional analysis of the Saccharomyces cerevisiae trehalose synthase complex, J BIOL CHEM, 273(50), 1998, pp. 33311-33319
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.