Conditions for protoplast formation and fusion of the killer yeast

Killer 효모의 원형질체 형성 및 융합조건

  • 정기택 (경북대학교 농과대학 식품공학과) ;
  • 방광웅 (경북대학교 농과대학 식품공학과) ;
  • 송형익 (대구공업전문대학 식품공업과) ;
  • 김재근 (계명실업전문대학 식품공학과) ;
  • 정용진 (경북대학교 농과대학 식품공학과)
  • Published : 1989.12.01

Abstract

Auxotrophic mutant were isolated from wild types by the treatment with NTG as a mutagen, and the conditions of protoplast formation for them were established. The protoplasts of killer yeast Saccharomyces cerevisiae K52 were formed to the level of above 70% when cells grown for 20 hr in PM medium were treated with 200 unit/ml Lyticase 50,000 at $30^{\circ}C$ for 60 min after pretreatment of 50 mM 2-mercaptoethanol in 10mM potassium phosphate buffer (pH 7.5) containing EDTA and 0.6 M sorbitol for 15 min. Also, the protoplast of the recipient S. cerevisiae S 29 were formed to the level of above 85% as it was cultured to the log phase of 24 hr in PM medium under the same conditions. The fusion frequency between the protoplast of killer yeast S. cerevisiae K 52 and the protoplast of recipient S. cerevisiae S 29 was reached to $8.2\times 10^{-6}$ when the hypertonic regeneration medium embeded with the fused protoplasts after mixing the parental protoplasts to 10$^{8}$ cells/ml in SP buffer containing 20 mM $CaCl_{2}$ and 30% PEG 6,000 for 15 min at $30^{\circ}C$ were incubated.

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