In this study, we attempted to isolate yeast by an enriched culture method from 124 flower samples collected from various regions of Japan. Forty-seven isolates which vigorously fermented and did not form a film on the YM medium containing 10% glucose were obtained. On the basis of the analyses of filtrates of
sake mashes which were products of froth forming tests, only 3 isolates--TP1, DR3, and KM8-3 strains--produced good aromas although 30 isolates produced alcohol equivalent to
sake yeast
kyokai No. 9. The small-scale
sake brewing tests with TP1, DR3, and KM8-3 strains revealed that TP1 had equivalent fermentation ability to
sake yeast
kyokai No. 9. On the basis of molecular evolutionary analyses based on DNA sequences of 26S rDNA-D1/D2 and ITS regions, TP1 was identified as
Saccharomyces cerevisiae. The
sake produced by TP1 showed particular compositions of aroma compounds and organic acids. Especially, high ethyl caproate concentration, high citric acid concentration, low succinic acid concentration, high isoamyl alcohol/ isobutyl alcohol ratio, and high malic acid/ succinic acid ratio were shown. The TP1 strain was deemed a useful yeast for
sake production because it did not form foam on
sake mash and was able to reduce TTC. It is expected that the TP1 will be used for
sake production as a useful yeast which is able to produce a unique flavor.
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