Skip to main content
Log in

Efficient generation of recessive traits in diploid sake yeast by targeted gene disruption and loss of heterozygosity

  • Methods
  • Published:
Applied Microbiology and Biotechnology Aims and scope Submit manuscript

Abstract

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.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4

Similar content being viewed by others

References

  • Akada R, Kitagawa T, Kaneko S, Toyonaga D, Ito S, Kakihara Y, Hoshida H, Morimura S, Kondo A, Kida K (2006) PCR-mediated seamless gene deletion and marker recycling in Saccharomyces cerevisiae. Yeast 23:399–405

    Article  CAS  PubMed  Google Scholar 

  • Alani E, Cao L, Kleckner N (1987) A method for gene disruption that allows repeated use of URA3 selection in the construction of multiply disrupted yeast strains. Genetics 116:541–545

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Amberg DC, Botstein D, Beasley EM (1995) Precise gene disruption in Saccharomyces cerevisiae by double fusion polymerase chain reaction. Yeast 11:1275–1280

    Article  CAS  PubMed  Google Scholar 

  • Boeke JD, LaCroute F, Fink GR (1984) A positive selection for mutants lacking orotidine-5′-phosphate decarboxylase activity in yeast: 5-fluoro-orotic acid resistance. Mol Gen Genet 197:345–346

    Article  CAS  PubMed  Google Scholar 

  • Brachmann CB, Davies A, Cost GJ, Caputo E, Li J, Hieter P, Boeke JD (1998) Designer deletion strains derived from Saccharomyces cerevisiae S288C: a useful set of strains and plasmids for PCR-mediated gene disruption and other applications. Yeast 14:115–132

    Article  CAS  PubMed  Google Scholar 

  • Daigaku Y, Endo K, Watanabe E, Ono T, Yamamoto K (2004) Loss of heterozygosity and DNA damage repair in Saccharomyces cerevisiae. Mutat Res 556:183–191

    Article  CAS  PubMed  Google Scholar 

  • Fukuda K, Yamamoto N, Kiyokawa Y, Yanagiuchi T, Wakai Y, Kitamoto K, Inoue Y, Kimura A (1998) Brewing properties of sake yeast whose EST2 gene encoding isoamyl acetate-hydrolyzing esterase was disrupted. J Ferment Bioeng 85:101–106

    Article  CAS  Google Scholar 

  • Hashimoto S, Ogura M, Aritomi K, Hoshida H, Nishizawa Y, Akada R (2005) Isolation of auxotrophic mutants of diploid industrial yeast strains after UV mutagenesis. Appl Environ Microbiol 71:312–319

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Hiraoka M, Watanabe K, Umezu K, Maki H (2000) Spontaneous loss of heterozygosity in diploid Saccharomyces cerevisiae cells. Genetics 156:1531–1548

    CAS  PubMed  PubMed Central  Google Scholar 

  • Ito H, Fukuda Y, Murata K, Kimura A (1983) Transformation of intact yeast cells treated with alkali cations. J Bacteriol 153:163–168

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Jones EW (1991) Tackling the protease problem in Saccharomyces cerevisiae. Methods Enzymol 194:428–453

    Article  CAS  PubMed  Google Scholar 

  • Kaya M, Ito J, Kotaka A, Matsumura K, Bando H, Sahara H, Ogino C, Shibasaki S, Kuroda K, Ueda M, Kondo A, Hata Y (2008) Isoflavone aglycones production from isoflavone glycosides by display of β-glucosidase from Aspergillus oryzae on yeast cell surface. Appl Microbiol Biotechnol 79:51–60

    Article  CAS  PubMed  Google Scholar 

  • Kitamoto K, Oda K, Gomi K, Takahashi K (1990) Construction of uracil and tryptophan auxotrophic mutants from sake yeasts by disruption of URA3 and TRP1 genes. Agric Biol Chem 54:2979–2987

    CAS  Google Scholar 

  • Kotaka A, Bando H, Kaya M, Kato-Murai M, Kuroda K, Sahara H, Hata Y, Kondo A, Ueda M (2008a) Direct ethanol production from barley β-glucan by sake yeast displaying Aspergillus oryzae β-glucosidase and endoglucanase. J Biosci Bioeng 105:622–627

    Article  CAS  PubMed  Google Scholar 

  • Kotaka A, Sahara H, Hata Y, Abe Y, Kondo A, Kato-Murai M, Kuroda K, Ueda M (2008b) Efficient and direct fermentation of starch to ethanol by sake yeast strains displaying fungal glucoamylases. Biosci Biotechnol Biochem 72:1376–1379

    Article  CAS  PubMed  Google Scholar 

  • Kuwayama H, Obara S, Morio T, Katoh M, Urushihara H, Tanaka Y (2002) PCR-mediated generation of a gene disruption construct without the use of DNA ligase and plasmid vectors. Nucleic Acids Res 30:E2

    Article  PubMed  PubMed Central  Google Scholar 

  • Ramírez M, Vinagre A, Ambrona J, Molina F, Maqueda M, Rebollo JE (2004) Genetic instability of heterozygous, hybrid, natural wine yeasts. Appl Environ Microbiol 70:4686–4691

    Article  PubMed  PubMed Central  Google Scholar 

  • Saito S, Mieno Y, Nagashima T, Kumagai C, Kitamoto K (1996) Breeding of a new type of baker's yeast by δ-integration for overproduction of glucoamylase using a homothallic yeast. J Ferment Bioeng 81:98–103

    Article  CAS  Google Scholar 

  • Takagi Y, Akada R, Kumagai H, Yamamoto K, Tamaki H (2008) Loss of heterozygosity is induced in Candida albicans by ultraviolet irradiation. Appl Microbiol Biotechnol 77:1073–1082

    Article  CAS  PubMed  Google Scholar 

  • Wang ZY, He XP, Zhang BR (2007) Over-expression of GSH1 gene and disruption of PEP4 gene in self-cloning industrial brewer's yeast. Int J Food Microbiol 119:192–199

    Article  CAS  PubMed  Google Scholar 

  • Zaret KS, Sherman F (1985) α-Aminoadipate as a primary nitrogen source for Saccharomyces cerevisiae mutants. J Bacteriol 162:579–583

    Article  CAS  PubMed  PubMed Central  Google Scholar 

Download references

Acknowledgments

This work was partially supported by the Research and Development Program for New Bio-industry Initiatives of the Bio-oriented Technology Research Advancement Institution.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Atsushi Kotaka.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Kotaka, A., Sahara, H., Kondo, A. et al. Efficient generation of recessive traits in diploid sake yeast by targeted gene disruption and loss of heterozygosity. Appl Microbiol Biotechnol 82, 387–395 (2009). https://doi.org/10.1007/s00253-008-1833-3

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00253-008-1833-3

Keywords

Navigation