National Research Institute of Brewing, 3-7-1 Kagamiyama, Higashihiroshima, Hiroshima 739-0046, Japan.
National Research Institute of Brewing, 3-7-1 Kagamiyama, Higashihiroshima, Hiroshima 739-0046, Japan; Graduate School of Biosphere Sciences, Hiroshima University, 1-3-2 Kagamiyama, Higashihiroshima, Hiroshima 739-8511, Japan.
J Biosci Bioeng. 2014 Jul;118(1):50-5. doi: 10.1016/j.jbiosc.2013.12.017. Epub 2014 Feb 4.
Among industrial yeasts used for alcoholic beverage production, most wine and weizen beer yeasts decarboxylate ferulic acid to 4-vinylguaiacol, which has a smoke-like flavor, whereas sake, shochu, top-fermenting, and bottom-fermenting yeast strains lack this ability. However, the factors underlying this difference among industrial yeasts are not clear. We previously confirmed that both PAD1 (phenylacrylic acid decarboxylase gene, YDR538W) and FDC1 (ferulic acid decarboxylase gene, YDR539W) are essential for the decarboxylation of phenylacrylic acids in Saccharomyces cerevisiae. In the present study, single nucleotide polymorphisms (SNPs) of PAD1 and FDC1 in sake, shochu, wine, weizen, top-fermenting, bottom-fermenting, and laboratory yeast strains were examined to clarify the differences in ferulic acid decarboxylation ability between these types of yeast. For PAD1, a nonsense mutation was observed in the gene sequence of standard top-fermenting yeast. Gene sequence analysis of FDC1 revealed that sake, shochu, and standard top-fermenting yeasts contained a nonsense mutation, whereas a frameshift mutation was identified in the FDC1 gene of bottom-fermenting yeast. No nonsense or frameshift mutations were detected in laboratory, wine, or weizen beer yeast strains. When FDC1 was introduced into sake and shochu yeast strains, the transformants exhibited ferulic acid decarboxylation activity. Our findings indicate that a positive relationship exists between SNPs in PAD1 and FDC1 genes and the ferulic acid decarboxylation ability of industrial yeast strains.
在用于酒精饮料生产的工业酵母中,大多数葡萄酒和小麦啤酒酵母将阿魏酸脱羧生成 4-乙烯基愈创木酚,具有烟熏味,而清酒、烧酒、上面发酵和下面发酵酵母菌株则缺乏这种能力。然而,工业酵母之间存在这种差异的原因尚不清楚。我们之前已经证实,PAD1(苯丙烯酸脱羧酶基因,YDR538W)和 FDC1(阿魏酸脱羧酶基因,YDR539W)对于酿酒酵母中苯丙烯酸的脱羧作用都是必需的。在本研究中,检查了清酒、烧酒、葡萄酒、小麦啤酒、上面发酵、下面发酵和实验室酵母菌株中 PAD1 和 FDC1 的单核苷酸多态性(SNP),以阐明这些类型酵母之间阿魏酸脱羧能力的差异。对于 PAD1,在标准上面发酵酵母的基因序列中观察到无义突变。FDC1 的基因序列分析表明,清酒、烧酒和标准上面发酵酵母含有无义突变,而下面发酵酵母的 FDC1 基因则存在移码突变。在实验室、葡萄酒或小麦啤酒酵母菌株中未检测到无义或移码突变。当 FDC1 被引入清酒和烧酒酵母菌株中时,转化体表现出阿魏酸脱羧活性。我们的研究结果表明,PAD1 和 FDC1 基因中的 SNP 与工业酵母菌株的阿魏酸脱羧能力之间存在正相关关系。