Ca. Fewson et al., RELATIONSHIPS AMONGST SOME BACTERIAL AND YEAST LACTATE AND MANDELATE DEHYDROGENASES, Journal of General Microbiology, 139, 1993, pp. 1345-1352
Five yeast strains were isolated by enrichment culture on the basis of
their ability to grow on mandelate and two of these strains were iden
tified as Rhodotorula glutinis. In addition, a range of yeasts from cu
lture collections was screened for growth on mandelate. The results su
ggest that mandelate utilization is a widespread but not universal cha
racteristic within the genus Rhodotorula. Several of the yeasts contai
ned an inducible NAD-dependent D(-)-mandelate dehydrogenase and an ind
ucible dye-linked (presumably flavoprotein) L(+)-mandelate dehydrogena
se. All the D(-)-mandelate dehydrogenases from the yeasts showed immun
ological cross-reactivity with each other (as judged by both immunoinh
ibition and immunoblotting), as did all the yeast L(+)-mandelate dehyd
rogenases that were tested. Determination of N-terminal amino acid seq
uences of several bacterial and yeast lactate and mandelate dehydrogen
ases, together with the evidence from the immunological studies, confi
rmed and extended previous proposals that there are several major grou
ps of such dehydrogenases: FMN-dependent, membrane-bound L(+)-lactate
and L(+)-mandelate dehydrogenases (M(r) = approx. 44000) in bacteria,
mitochondrial flavocytochrome b, L(+)-lactate and L(+)-mandelate dehyd
rogenases (M(r) = approx. 59000) in yeasts, FAD-dependent. membrane-bo
und D(-)-lactate and D(-)-mandelate dehydrogenases in bacteria, and so
luble NAD-dependent D(-)-mandelate dehydrogenases in both bacteria and
yeasts.