Research Laboratories for Alcoholic Beverage Technologies, Kirin Holdings Company, Ltd., 1-17-1 Namamugi, Tsurumi-ku, Yokohama, Kanagawa 230-8628, Japan.
Food Safety and Quality Assurance Center, Kirin Holdings Company, Ltd., 1-17-1 Namamugi, Tsurumi-ku, Yokohama, Kanagawa 230-8628, Japan.
J Biosci Bioeng. 2021 Jan;131(1):61-67. doi: 10.1016/j.jbiosc.2020.08.009. Epub 2020 Oct 21.
The genetic diversity of bottom-fermenting yeast classified as Saccharomyces pastorianus is poor because strains are restricted to a few genetically distinct groups. Crossbreeding is an effective approach to construct novel yeast strains, but it is difficult because of inefficiency to obtain mating-competent cells (MCCs) of bottom-fermenting yeast. By using mating pheromone-supersensitive mutants, we previously isolated several mating-competent meiotic segregants from two bottom-fermenting yeast strains: high isoamyl acetate-producing KY1247, and low diacetyl-producing KY2645. Here, we constructed novel non-GM hybrids carrying preferable characteristics from both parents by crossbreeding these bottom-fermenting strains for the first time. Sixteen a/a-type meiotic segregants from KY2645 and 12 α/α-type meiotic segregants from KY1247 were mixed, and cells resembling zygotes were isolated via micromanipulation. In total, 149 hybrids were obtained and verified by examining known single-nucleotide polymorphisms (SNPs) between the parental strains. A sporulation test showed that some of the hybrids were able to sporulate. Moreover, fermentation tests on a test-tube and pilot-plant scale identified two hybrids with production levels of isoamyl acetate and diacetyl that were almost the same as KY1247 and KY2645, respectively. Both of these hybrids produced satisfactory beer in terms of taste, flavor, and overall quality, comparable to that produced by the parental strains. Collectively, our results suggest that crossbreeding between bottom-fermenting yeast strains has the potential to increase the diversity of yeast strains available for brewing, and our method of isolating MCCs provides a huge advance for crossbreeding of bottom-fermenting yeast without using DNA recombination techniques.
发酵底层酵母中归为酿酒酵母(Saccharomyces pastorianus)的遗传多样性较差,因为这些菌株仅限于少数遗传上明显不同的群体。杂交是构建新型酵母菌株的有效方法,但由于难以获得具有交配能力的细胞(MCCs),因此难以实现。通过使用交配信息素超敏突变体,我们之前从两种发酵底层酵母菌株中分离到了几个具有交配能力的减数分裂分离子:高异戊酸乙酯产生菌株 KY1247 和低双乙酰产生菌株 KY2645。在这里,我们首次通过杂交这两种发酵底层酵母菌株,构建了携带双亲优点的新型非转基因杂交体。从 KY2645 中获得了 16 个 a/a 型减数分裂分离子,从 KY1247 中获得了 12 个α/α型减数分裂分离子,通过微操作将类似于合子的细胞分离出来。总共获得了 149 个杂交体,并通过检查亲本菌株之间已知的单核苷酸多态性(SNP)进行了验证。孢子形成测试表明,一些杂交体能够进行孢子形成。此外,在试管和中试工厂规模的发酵试验中,鉴定出两种具有与 KY1247 和 KY2645 分别相似的异戊酸乙酯和双乙酰产量水平的杂交体。这两种杂交体在口感、风味和整体质量方面都生产出了令人满意的啤酒,可与亲本菌株相媲美。总的来说,我们的研究结果表明,底层发酵酵母菌株之间的杂交具有增加可用于酿造的酵母菌株多样性的潜力,而我们分离 MCCs 的方法为不使用 DNA 重组技术进行底层发酵酵母的杂交提供了巨大的进步。