Renaissance BioScience Corporation, Vancouver, British Columbia, Canada
Renaissance BioScience Corporation, Vancouver, British Columbia, Canada.
Appl Environ Microbiol. 2021 Jan 15;87(3). doi: 10.1128/AEM.02434-20.
Lager beer is produced by , which is a natural allopolyploid hybrid between and Lager strains are classified into two major groups based largely on genomic composition: group I and group II. Group I strains are allotriploid, whereas group II strains are allotetraploid. A lack of phenotypic diversity in commercial lager strains has led to substantial interest in the reconstitution of allotetraploid lager strains by hybridization of and strains. Such strategies rely on the hybridization of wild isolates, which carry unacceptable traits for commercial lager beer such as phenolic off flavors and incomplete utilization of carbohydrates. Using an alternative breeding strategy, we have created lager hybrids containing the domesticated subgenome from an industrial strain by hybridizing diploid meiotic segregants of this strain to a variety of ale strains. Five hybrids were isolated which had fermentation characteristics similar to those of prototypical commercial lager strains but with unique phenotypic variation due to the contributions of the parents. Genomic analysis of these lager hybrids identified novel allotetraploid genomes carrying three copies of the genome and one copy of the genome. Most importantly, these hybrids do not possess the negative traits which result from breeding wild The lager strains produced using industrial in this study are immediately suitable for industrial lager beer production. All lager beer is produced using two related lager yeast types: group I and group II, which are highly similar, resulting in a lack of strain diversity for lager beer production. To date, approaches for generating new lager yeasts have generated strains possessing undesirable brewing characteristics which render them commercially inviable. We have used an alternative approach that circumvents this issue and created new lager strains that are directly suitable for lager beer production. These novel lager strains also possess a unique genomic architecture, which may lead to a better understanding of industrial yeast hybrids. We propose that strains created using our approach be classified as a third group of lager strains (group III). We anticipate that these novel lager strains will be of great industrial relevance and that this technique will be applicable to the creation of additional novel lager strains that will help broaden the diversity in commercial lager beer strains.
拉格啤酒是由啤酒酵母产生的,啤酒酵母是 和 之间的天然异源多倍体杂种。根据基因组组成,拉格菌株主要分为两大类:I 组和 II 组。I 组菌株是异源三倍体,而 II 组菌株是异源四倍体。商业拉格菌株缺乏表型多样性,这导致人们对通过 和 菌株杂交来重建 异源四倍体拉格菌株产生了浓厚的兴趣。这种策略依赖于野生 菌株的杂交,而野生 菌株携带酚类异味和不完全利用碳水化合物等不可接受的商业拉格啤酒特征。我们采用了一种替代的育种策略,通过将该菌株的二倍体减数分裂分离物与各种 艾尔菌株杂交,创造出含有驯化的 亚基因组的 拉格杂种。杂交了五种 拉格杂种,它们的发酵特性与典型的商业拉格菌株相似,但由于 亲本的贡献,具有独特的表型变异。对这些 拉格杂种的基因组分析确定了新型异源四倍体基因组,这些基因组携带 基因组的三个拷贝和 基因组的一个拷贝。最重要的是,这些杂种没有由于对野生 菌株进行选育而产生的负面特征。本研究中使用工业 菌株生产的 拉格菌株立即适用于工业拉格啤酒生产。所有的拉格啤酒都是使用两种相关的拉格酵母类型生产的:I 组和 II 组,它们非常相似,导致拉格啤酒生产的菌株多样性缺乏。迄今为止,产生新的拉格酵母的方法产生了具有不可接受酿造特性的菌株,使其在商业上不可行。我们采用了一种替代方法来规避这个问题,并创造了直接适用于拉格啤酒生产的新拉格菌株。这些新型拉格菌株还具有独特的基因组结构,这可能有助于更好地理解工业酵母杂种。我们建议使用我们的方法创建的菌株被归类为第三组拉格菌株(第三组)。我们预计这些新型拉格菌株将具有重要的工业意义,并且该技术将适用于创建更多的新型拉格菌株,这将有助于扩大商业拉格啤酒菌株的多样性。