In Saccharomyces spp. the ability to use melibiose depends on the pres
ence of a MEL gene encoding alpha-galactosidase. We used two cloned ME
L genes as probes to characterize the physical structure and chromosom
al location of the MEL genes in several industrial and natural Mel+ st
rains of Saccharomyces cerevisiae, Saccharomyces pastorianus, and Sacc
haromyces bayanus. Electrokaryotyping showed that all of the S. pastor
ianus strains and most of the S. bayanus strains studied had one MEL l
ocus. The MEL gene in S. bayanus strains was similar but not identical
to the S. pastorianus MEL gene. Mel+ S. cerevisiae strains had one to
seven loci containing MEL sequences. The MEL genes of these strains c
ould be divided into two categories on the basis of hybridization to M
EL1, one group exhibiting strong hybridization to MEL1 and the other g
roup exhibiting weak hybridization to MEL1. In S. pastorianus and S. b
ayanus strains, the MEL gene was expressed as a single 1.5-kb transcri
pt, and the expression was galactose inducible. In some S. cerevisiae
strains, the MEL genes were expressed even without induction at fairly
high levels. Expression was usually further induced by galactose. In
two strains, CBS 5378 and CBS 4903, expression of the MEL genes was at
the same level without induction as it was in most other strains with
induction. In all S. cerevisiae strains, irrespective of the number o
f MEL genes, mRNA of only one size (1.6 kb) was observed.