Department of Environmental Sciences, Saga University, Saga, Japan.
Annu Rev Food Sci Technol. 2013;4:215-35. doi: 10.1146/annurev-food-030212-182545.
Sake is an alcoholic beverage of Japan, with a tradition lasting more than 1,300 years; it is produced from rice and water by fermenting with the koji mold Aspergillus oryzae and sake yeast Saccharomyces cerevisiae. Breeding research on sake yeasts was originally developed in Japan by incorporating microbiological and genetic research methodologies adopted in other scientific areas. Since the advent of a genetic paradigm, isolation of yeast mutants has been a dominant approach for the breeding of favorable sake yeasts. These sake yeasts include (a) those that do not form foams (produced by isolating a mutant that does not stick to foams, thus decreasing the cost of sake production); (b) those that do not produce urea, which leads to the formation of ethyl carbamate, a possible carcinogen (isolated by positive selection in a canavanine-, arginine-, and ornithine-containing medium); (c) those that produce an increased amount of ethyl caproate, an apple-like flavor (produced by isolating a mutant resistant to cerulenin, an inhibitor of fatty-acid synthesis); and (d) those that produce a decreased amount of pyruvate (produced by isolating a mutant resistant to an inhibitor of mitochondrial transport, thus decreasing the amount of diacetyl). Given that sake yeasts perform sexual reproduction, sporulation and mating are potent approaches for their breeding. Recently, the genome sequences of sake yeasts have been determined and made publicly accessible. By utilizing this information, the quantitative trait loci (QTLs) for the brewing characteristics of sake yeasts have been identified, which paves a way to DNA marker-assisted selection of the mated strains. Genetic engineering technologies for experimental yeast strains have recently been established by academic groups, and these technologies have also been applied to the breeding of sake yeasts. Sake yeasts whose genomes have been modified with these technologies correspond to genetically modified organisms (GMOs). However, technologies that enable the elimination of extraneous DNA sequences from the genome of sake yeast have been developed. Sake yeasts genetically modified with these technologies are called self-cloning yeasts and do not contain extraneous DNA sequences. These yeasts were exempted from the Japanese government's guidelines for genetically modified food. Protoplast fusion has also been utilized to breed favorable sake yeasts. Future directions for the breeding of sake yeasts are also proposed in this review. The reviewed research provides perspectives for the breeding of brewery yeasts in other fermentation industries.
清酒是一种日本的酒精饮料,拥有超过 1300 年的悠久历史,它是由大米和水通过发酵米曲霉和酿酒酵母制成的。清酒酵母的选育研究最初是在日本发展起来的,采用了其他科学领域的微生物学和遗传学研究方法。自遗传模式出现以来,酵母突变体的分离一直是选育优良清酒酵母的主要方法。这些清酒酵母包括:(a)不产生泡沫的酵母(通过分离不附着于泡沫的突变体来生产,从而降低清酒的生产成本);(b)不产生尿素的酵母,尿素会导致形成可能致癌的氨基甲酸乙酯(通过在含有瓜氨酸、精氨酸和鸟氨酸的培养基中进行正选择来分离);(c)产生更多己酸乙酯的酵母,具有苹果味(通过分离对脂肪酸合成抑制剂萎锈灵具有抗性的突变体来生产);以及(d)产生较少丙酮酸的酵母(通过分离对线粒体转运抑制剂具有抗性的突变体来生产,从而减少双乙酰的含量)。由于清酒酵母进行有性繁殖,因此孢子形成和交配是其选育的有效方法。最近,清酒酵母的基因组序列已经被确定并公开。利用这些信息,已经确定了与清酒酵母酿造特性相关的数量性状位点(QTL),为交配菌株的 DNA 标记辅助选择铺平了道路。学术团体最近建立了用于实验酵母菌株的遗传工程技术,这些技术也已应用于清酒酵母的选育。经过这些技术修饰基因组的清酒酵母属于基因修饰生物(GMO)。但是,已经开发出能够从清酒酵母基因组中消除外源 DNA 序列的技术。经过这些技术修饰的清酒酵母称为自克隆酵母,不含有外源 DNA 序列。这些酵母被日本政府的基因改造食品指南豁免。原生质体融合也被用于选育优良的清酒酵母。本文还提出了清酒酵母选育的未来方向。综述中的研究为其他发酵工业中啤酒酵母的选育提供了参考。