Department of Integrated Biosciences, Graduate School of Frontier Sciences, The University of Tokyo, Chiba 277-8562, Japan.
National Research Institute of Brewing, Higashi-Hiroshima, Hiroshima 739-0046, Japan.
Cells. 2021 May 24;10(6):1299. doi: 10.3390/cells10061299.
Sake yeast is mostly diploid, so the introduction of recessive mutations to improve brewing characteristics requires considerable effort. To construct sake yeast with multiple excellent brewing characteristics, we used an evidence-based approach that exploits genome editing technology. Our breeding targeted the , , , and genes. We introduced eight mutations into standard sake yeast to construct a non-foam-forming strain that makes sake without producing carcinogens or an unpleasant odor, while producing a sweet aroma. Small-scale fermentation tests showed that the desired sake could be brewed with our genome-edited strains. The existence of a few unexpected genetic perturbations introduced during breeding proved that genome editing technology is extremely effective for the serial breeding of sake yeast.
清酒酵母大多为二倍体,因此要引入隐性突变来改善酿造特性需要付出相当大的努力。为了构建具有多种优良酿造特性的清酒酵母,我们采用了一种基于证据的方法,利用基因组编辑技术。我们的育种目标是 、 、 、 基因。我们向标准清酒酵母中引入了 8 个突变,构建了一种不产生泡沫的菌株,该菌株在不产生致癌物或异味的情况下酿造清酒,同时产生甜美的香气。小规模发酵试验表明,我们经过基因组编辑的菌株可以酿造出所需的清酒。在育种过程中引入的一些意想不到的遗传干扰的存在证明了基因组编辑技术对于清酒酵母的连续育种非常有效。