C. Venturin et al., GLUCOSE-METABOLISM, ENZYMATIC ANALYSIS AND PRODUCT FORMATION IN CHEMOSTAT CULTURE OF HANSENIASPORA-UVARUM, Yeast, 11(4), 1995, pp. 327-336
The physiology of Hanseniaspora uvarum K-5 was studied in glucose-limi
ted chemostat cultures and upon glucose pulse. Up to a dilution rate o
f 0.28 h(-1), glucose was completely metabolized in biomass and CO2. A
bove this value, increase in the dilution rate was accompanied by sequ
ential production of metabolites (glycerol, acetate and ethanol) and d
ecrease in cell yield. Similar results were observed upon glucose puls
e. From the enzyme activities (pyruvate dehydrogenase, pyruvate decarb
oxylase, NAD and NADP-dependent acetaldehyde dehydrogenases, acetyl co
enzyme A synthetase and alcohol dehydrogenase) and substrate affinitie
s, the following conclusions were drawn with respect to product format
ion of cells: (1) pyruvate was preferentially metabolized via pyruvate
dehydrogenase, when biomass and CO2 were the only products formed; (2
) acetaldehyde formed by pyruvate decarboxylase was preferentially oxi
dized in acetate by NADP-dependent aldehyde dehydrogenase; acetate acc
umulation results from insufficient activity of acetyl-CoA synthetase
required for the complete oxidation of acetate; (3) acetaldehyde was o
xidized in ethanol by alcohol dehydrogenase, in addition to acetate pr
oduction.