Summary
A method has been developed for the transfer of genes from other yeast strains and species to industrial yeast strains, using a haploid, kar1-1 mutant strain of Saccharomyces cerevisiae as a vector. The sta2 gene, conferring the ability to metabolize starch was transferred from an autotrophic haploid strain of S. cerevisiae (S. diastaticus) and the melibiose-metabolism (mel) gene(s), from S. kluyveri, to the kar1-1 mutant [K5-5A; (α ade2 his4 can1 gal) by normal mating and protoplast fusion. From this strain, the genes were transferred to baker's yeast and brewing yeast strains, which did not utilize starch, and to baker's yeast strains, which did not utilize melibiose, by protoplast fusion, spore-cell pairing, or rare-mating. Strains that utilized starch or melibiose were obtained by all three methods. Pulsed-field gel electrophoresis preparations showed little change in the mobility of the chromosomes of the hybrids. The most probable explanation for the results obtained is that single chromosomes were transferred, first, from the donor strains to the kar1-1 haploid mutant strain, and then from the kar1-1 vector to the recipient industrial strain of S. cerevisiae. The transfer of the genes is probably accomplished through formation of disomic strains and the, in the case of the hybrids that metabolize starch, by integration of the sta2 gene into the genome of the industrial yeast strains.
Similar content being viewed by others
Explore related subjects
Discover the latest articles and news from researchers in related subjects, suggested using machine learning.References
Bignell GR, Evans IH (1990) Localization of glucoamylase genes of Saccharomyces cerevisiae by pulsed field gel electrophoresis. Antonie Van Leeuwenhoek 58:49–55
Casey GP, Xiao W, Rank GH (1988) Construction of alpha-galactosidase-positive strains of industrial baker's yeast. Am Assoc Brew Chem 46:67–71
Conde J, Fink GR (1976) A mutant of Saccharomyces cerevisiae defective for nuclear fusion. Proc Natl Acad Sci USA 73:3651–3655
Dutcher SK (1981) Internuclear transfer of genetic information in kar1/KAR heterokaryons in Saccharomyces cerevisiae. Mol Cell Biol 1:245–253
Johnston JR, Mortimer RK (1959) Use of snail digestive juice in the isolation of yeast spore tetrads. J Bacteriol 78:292
Johnson JR, Contopoulou CR, Mortimer RK (1988) Karyotyping of yeast strains of several genera by field inversion gel electrophoresis. Yeast 4:191–198
Naumov G, Turakainen H, Naumova E, Aho S, Korhola M (1990) A new family of polymorphic genes in Saccharomyces cerevisiae: alpha-galactosidase genes MEL1-MEL7. Mol Gen Genet 224:119–128
Nilsson-Tillgren T, Petersen JGL, Holmberg S, Kielland-Brandt MC (1980) Transfer of chromosome III during kar1-mediated cytoduction in yeast. Carlsberg Res Commun 45:113–117
Patel D, Evans IH, Bevan EA (1990) A genetic analysis of glyco-amylase activity in the diastatic yeast Saccharomyces diastaticus NCYC 625. Curr Genet 17:281–288
Spencer JFT, Spencer DM, Bruce IJ (1989a) Yeast genetics, a manual of methods. Springer, Berlin Heidelberg New York
Spencer JFT, Spencer DM, Schiappacasse MC, Heluane H, Reynolds N, Figueroa LI de (1989b) Two new methods for recovery and genetic analysis of hybrids after fusion of yeast protoplasts. Curr Microbiol 18:285–287
Streiblova E (1988) Cytological methods. In: Campbell I, Duffus JH (eds) Yeast, a practical approach. IRL Press, Oxford, pp 9–49
Vaughan Martini A, Martini A (1987) Three newly delimited species of Saccharomyces sensu stricto. Antonie Van Leeuwenhoek 53:77–84
Vezinhet F, Blondin B, Barre P (1991) Mapping of the FLO5 gene of Saccharomyces cerevisiae by transfer of a chromosome during cytoduction. Biotechnol Lett 13:47–52
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Spencer, J.F.T., Spencer, D.M., de Figueroa, L. et al. Transfer of genes for utilization of starch (sta2) and melibiose (mel) to industrial strains of Saccharomyces cerevisiae by single-chromosome transfer, using a kar1 mutant as vector. Appl Microbiol Biotechnol 37, 230–234 (1992). https://doi.org/10.1007/BF00178176
Received:
Accepted:
Issue Date:
DOI: https://doi.org/10.1007/BF00178176


