Kotaka Atsushi, Sahara Hiroshi, Kondo Akihiko, Ueda Mitsuyoshi, Hata Yoji
Research Institute, Gekkeikan Sake Co. Ltd., 101 Shimotoba-koyanagi-cho, Fushimi-ku, Kyoto 612-8385, Japan.
Appl Microbiol Biotechnol. 2009 Feb;82(2):387-95. doi: 10.1007/s00253-008-1833-3. Epub 2009 Jan 10.
Sake yeast, a diploid Saccharomyces cerevisiae strain, is useful for industry but difficult to genetically engineer because it hardly sporulates. Until now, only a few recessive mutants of sake yeast have been obtained. To solve this problem, we developed the high-efficiency loss of heterozygosity (HELOH) method, which applies a two-step gene disruption. First, a heterozygous disruptant was constructed by gene replacement with URA3, followed by marker recycling on medium containing 5-fluoroorotic acid (5-FOA). Subsequently, spontaneous loss of heterozygosity (LOH) yielding a homozygous disruptant was selected for in a second round of gene integration. During this step, the wild-type allele of the heterozygous disruptant was marked by URA3 integration, and the resulting transformants were cultivated in non-selective medium to induce recombination and then grown on medium with 5-FOA to enrich for mutants that had undergone LOH. Although the frequency with which LOH occurs is extremely low, many homozygous disruptants were obtained with the HELOH method. Thus, we were able to efficiently construct homozygous disruptants of diploid sake yeast without sporulation, and sake yeast strains with multiple auxotrophies and a protease deficiency could be constructed. The HELOH method, therefore, facilitated the utilization of diploid sake yeast for genetic engineering purposes.
清酒酵母是一种二倍体酿酒酵母菌株,在工业上很有用,但由于其几乎不产孢,因此难以进行基因工程改造。到目前为止,仅获得了少数清酒酵母的隐性突变体。为了解决这个问题,我们开发了高效杂合性缺失(HELOH)方法,该方法采用两步基因破坏。首先,通过用URA3进行基因替换构建杂合破坏体,然后在含有5-氟乳清酸(5-FOA)的培养基上进行标记回收。随后,在第二轮基因整合中选择产生纯合破坏体的自发杂合性缺失(LOH)。在这一步骤中,杂合破坏体的野生型等位基因通过URA3整合进行标记,将所得转化体在非选择性培养基中培养以诱导重组,然后在含有5-FOA的培养基上生长以富集发生LOH的突变体。尽管LOH发生的频率极低,但通过HELOH方法获得了许多纯合破坏体。因此,我们能够在不产孢的情况下高效构建二倍体清酒酵母的纯合破坏体,并且可以构建具有多种营养缺陷型和蛋白酶缺陷的清酒酵母菌株。因此,HELOH方法促进了二倍体清酒酵母在基因工程中的应用。