A strategy to alter the flocculation properties of nonflocculent yeast in s
uch a way that flocculation occurred toward the end of fermentation was dev
eloped. In a double cross-over event, the wild-type FLO1 promoter of the ha
ploid, nonflocculent S. cerevisiae FY23 strain was replaced by a construct
consisting of the SMRI-410 marker gene and the HSP30 promoter. In this way,
the genomic copy of the wild-type FLO1 open reading frame was brought unde
r transcriptional control of the HSP30 promoter. The transformants showed s
trong flocculation toward the end of fermentation, resulting in a distinctl
y clearer beer than the beer obtained with wild-type cells. The other prope
rties of the wild-type strain were conserved. Moreover, it was shown that t
he transformants were extremely stable and that flocculation could be induc
ed earlier during fermentation by a heat-shock treatment or the addition of
ethanol to the medium. These results suggest that the flocculation propert
ies of weakly flocculent brewer's yeast strains can be improved using contr
olled expression of the FLO1 gene.