VTT Technical Research Centre of Finland, Tietotie 2, P.O. Box 1000, 02044 VTT, Espoo, Finland.
Escarpment Laboratories, Guelph, ON, Canada.
Appl Microbiol Biotechnol. 2021 Nov;105(21-22):8359-8376. doi: 10.1007/s00253-021-11626-y. Epub 2021 Oct 13.
Yeast breeding is a powerful tool for developing and improving brewing yeast in a number of industry-relevant respects. However, breeding of industrial brewing yeast can be challenging, as strains are typically sterile and have large complex genomes. To facilitate breeding, we used the CRISPR/Cas9 system to generate double-stranded breaks in the MAT locus, generating transformants with a single specified mating type. The single mating type remained stable even after loss of the Cas9 plasmid, despite the strains being homothallic, and these strains could be readily mated with other brewing yeast transformants of opposite mating type. As a proof of concept, we applied this technology to generate yeast hybrids with an aim to increase β-lyase activity for fermentation of beer with enhanced hop flavour. First, a genetic and phenotypic pre-screening of 38 strains was carried out in order to identify potential parent strains with high β-lyase activity. Mating-competent transformants of eight parent strains were generated, and these were used to generate over 60 hybrids that were screened for β-lyase activity. Selected phenolic off-flavour positive (POF +) hybrids were further sporulated to generate meiotic segregants with high β-lyase activity, efficient wort fermentation, and lack of POF, all traits that are desirable in strains for the fermentation of modern hop-forward beers. Our study demonstrates the power of combining the CRISPR/Cas9 system with classic yeast breeding to facilitate development and diversification of brewing yeast. KEY POINTS: • CRISPR/Cas9-based mating-type switching was applied to industrial yeast strains. • Transformed strains could be readily mated to form intraspecific hybrids. • Hybrids exhibited heterosis for a number of brewing-relevant traits.
酵母育种是在许多与工业相关的方面开发和改进酿造酵母的有力工具。然而,工业酿造酵母的育种可能具有挑战性,因为菌株通常是无菌的,并且具有大型复杂基因组。为了便于育种,我们使用 CRISPR/Cas9 系统在 MAT 基因座产生双链断裂,产生具有单一指定交配型的转化体。尽管菌株是同型接合的,但在失去 Cas9 质粒后,单一交配型仍然保持稳定,这些菌株可以与其他具有相反交配型的酿造酵母转化体轻松交配。作为概念验证,我们应用这项技术生成酵母杂种,旨在提高 β-裂合酶活性,用于发酵具有增强的啤酒花风味的啤酒。首先,对 38 株进行了遗传和表型预筛选,以鉴定具有高β-裂合酶活性的潜在亲本菌株。生成了八个亲本菌株的有性繁殖能力转化体,并使用这些转化体生成了超过 60 个杂种,对其β-裂合酶活性进行了筛选。选择酚类异味阳性(POF+)杂种进一步进行减数分裂,生成具有高β-裂合酶活性、高效麦汁发酵和缺乏 POF 的减数分裂分离子,所有这些性状都是现代高酒花啤酒发酵菌株所需要的。我们的研究表明,将 CRISPR/Cas9 系统与经典酵母育种相结合,有助于开发和多样化酿造酵母的强大功能。 关键点: • 基于 CRISPR/Cas9 的交配型转换应用于工业酵母菌株。 • 转化菌株可以轻松交配形成种内杂种。 • 杂种表现出许多与酿造相关的性状杂种优势。