The Saccharomyces cerevisiae YDL219w (DTD1) gene, which codes for an amino
acid sequence sharing 34% identity with the Escherichia coli D-Tyr-tRNA(Tyr
) deacylase, was cloned, and its product was functionally characterized. Ov
erexpression in the yeast of the DTD1 gene from a multicopy plasmid increas
ed D-Tyr-tRNA(Tyr) deacylase activity in crude extracts by two orders of ma
gnitude. Upon disruption of the chromosomal gene, deacylase activity was de
creased by more than 90%, and the sensitivity to D-tyrosine of the growth o
f S. cerevisiae was exacerbated. The toxicity of D-tyrosine was also enhanc
ed under conditions of nitrogen starvation, which stimulate the uptake of D
-amino acids. In relation with these behaviors, the capacity of purified S.
cerevisiae tyrosyl-tRNA synthetase to produce D-Tyr-tRNA(Tyr) could be sho
wn. Finally, the phylogenetic distribution of genes homologous to DTD1 was
examined in connection with L-tyrosine prototrophy or auxotrophy. In the au
xotrophs, DTD1-like genes are systematically absent. In the prototrophs, th
e putative occurrence of a deacylase is variable. It possibly depends on th
e L-tyrosine anabolic pathway adopted by the cell.