Takahashi Toshinari, Furukawa Akihisa, Hara Shodo, Mizoguchi Haruhiko
General Research Laboratory, Kiku-Masamune Sake Brewing Co. Ltd., 1-8-6 Uozaki-nishimachi, Higashinada-ku, Kobe 658-0026, Japan.
J Biosci Bioeng. 2004;97(6):412-8. doi: 10.1016/S1389-1723(04)70228-5.
Sake yeasts take up gamma-aminobutyric acid (GABA) derived from rice-koji in the primary stage of sake brewing. The GABA content in sake brewed with the UGA1 disruptant, which lacked GABA transaminase, was higher than that brewed with the wild-type strain K701. The UGA1 disruptant derived from sake yeast could not grow on a medium with GABA as the sole nitrogen source. We have isolated the sake yeast mutants of K701 that were unable to grow on a medium containing GABA as the sole nitrogen source. The growth defect of GAB7-1 and GAB7-2 mutants on GABA plates was complemented by UGA1, which encodes GABA transaminase, and UGA2, which encodes succinic semialdehyde dehydrogenase (SSADH), respectively. DNA sequence analysis revealed that GAB7-1 had a homozygous nonsense mutation in UGA1 and GAB7-2 had a heterozygous mutation (G247D) in UGA2. The GABA transaminase activity of GAB7-1 and the SSADH activity of GAB7-2 were markedly lower than those of K701. These GAB mutants displayed a higher intracellular GABA content. The GABA contents in sake brewed with the mutants GAB7-1 and GAB7-2 were 2.0 and 2.1 times higher, respectively, than that brewed with the wild-type strain K701. These results suggest that the reduced function of the GABA utilization pathway increases the GABA content in sake.
清酒酵母在清酒酿造的初级阶段会摄取源自米曲的γ-氨基丁酸(GABA)。用缺乏GABA转氨酶的UGA1破坏菌株酿造的清酒中的GABA含量高于用野生型菌株K701酿造的清酒。源自清酒酵母的UGA1破坏菌株无法在以GABA作为唯一氮源的培养基上生长。我们分离出了K701的清酒酵母突变体,这些突变体无法在含有GABA作为唯一氮源的培养基上生长。GAB7 - 1和GAB7 - 2突变体在GABA平板上的生长缺陷分别由编码GABA转氨酶的UGA1和编码琥珀酸半醛脱氢酶(SSADH)的UGA2互补。DNA序列分析表明,GAB7 - 1在UGA1中存在纯合无义突变,GAB7 - 2在UGA2中存在杂合突变(G247D)。GAB7 - 1的GABA转氨酶活性和GAB7 - 2的SSADH活性明显低于K701。这些GAB突变体表现出较高的细胞内GABA含量。用突变体GAB7 - 1和GAB7 - 2酿造的清酒中的GABA含量分别比用野生型菌株K701酿造的清酒高2.0倍和2.1倍。这些结果表明,GABA利用途径功能的降低会增加清酒中的GABA含量。