Methods which can produce highly concentrated γ-lactones in
shochu mash by lactic acid bacteria (LAB) in collaboration with
shochu yeast were studied. Three strains (26-a, 26-d and 41-d) of LAB having a high hydration ability of unsaturated fatty acids were selected from 48 "
doburoku" in Japan. Two strains (26-a and 26-d) were identified with
Lactobacillus brevis by their homogeny of 16SrDNA, while the other (41-d) was not identified.
In
shochu brewing, unpolished rice was preferable in the supply of unsaturated fatty acids to polished rice such as
koji (polishing rate 90% of rice) as raw materials. Furthermore, for β-oxidation and esterification of hydrated fatty acid,
shochu yeast (SH4 or AW101) was superior to the
sake yeast (K701). When LAB was added to the
shochu mash, the first day of the secondary addition was preferable. Regarding the number of additional cell bodies of LAB, 1x10
6 cfu/ml was preferable to 1x10
5cfu/ml and 1x10
4cfu/ml. As the result of brewing rice
shochu under these conditions, γ-dodecalactone (0.16-0.35ppm) and γ-nonalactone (0.07-0.15ppm) were produced by three strains of LAB in collaboration with two
shochu yeast respectively, and γ-decalactone (0.09-0.12ppm) was produced only by LAB (26-d) in collaboration with each
shochu yeast.
Results of sensory tests showed that the flavor of the
shochu brewed using LAB was evaluated more highly than the control (LAB was not used). For taste and total evaluation,
shochu brewed using LAB of 26-d and of 41-d was judged considerably better than the control.
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