Chemostat cultivation enables investigations into the effects of indiv
idual environmental parameters on sugar transport in yeasts. Various m
eans are available to manipulate the specific rate of sugar uptake (q(
s)) in sugar-limited chemostat cultures. A straightforward way to mani
pulate q,is variation of the dilution rate, which, in substrate-limite
d chemostat cultures, is equal to the specific growth rate. Alternativ
ely, q(s) can be varied independently of the growth rate by mixed-subs
trate cultivation or by variation of the biomass yield on sugar. The l
atter can be achieved for example, by addition of nonmetabolizable wea
k acids to the growth medium or by variation of the oxygen supply. Suc
h controlled manipulation of metabolic fluxes cannot be achieved in ba
tch cultures, in which various parameters that ape essential for the k
inetics of sugar transport cannot be controlled. In sugar-limited chem
ostat cultures, yeasts adapt their sugar transport systems to cope wit
h the low residual sugar concentrations, which are often in the microm
olar range. Under these conditions, yeasts with high-affinity proton s
ymport carriers have a competitive advantage over yeasts that transpor
t sugars vip facilitated-diffusion carriers. Chemostat cultivation off
ers unique possibilities to study the energetic consequences of sugar
transport in growing cells. For example, anaerobic, sugar-limited chem
ostat cultivation has been used to quantify the energy requirement for
maltose-proton symport in Saccharomyces cerevisiae. Controlled variat
ion of growth conditions in chemostat cultures can be used to study th
e differential expression of genes involved in sugar transport and as
such can make an important contribution to the ongoing studies on the
molecular biology of sugar transport in yeasts.