TY - CHAP
T1 - Systems biology of yeast
T2 - International Specialised Symposium on Yeasts, ISSY 25
AU - Salusjärvi, Laura
AU - Pitkänen, Juha-Pekka
AU - Koivistoinen, Heini
AU - Ruohonen, Laura
AU - Penttilä, Merja
PY - 2006
Y1 - 2006
N2 - We are interested in broadening the substrate utilisation
range of the yeast Saccharomyces cerevisiae and in
connection to this to study nutritional responses and
signalling at a global level. S. cerevisiae does not
naturally utilise pentose sugars unlike most other fungi,
and recombinant S. cerevisiae strains have been
constructed that contain the xylose utilisation pathway
from other yeasts. The xylose reductase enzyme (XR)
prefers NADPH as a cofactor while the next step in the
pathway xylitol dehydrogenase (XDH), NAD+. This is
believed to create a redox cofactor imbalance in the
cells and limit xylose fermentation. Other suggested
rate-limiting steps in xylose utilisation and the use of
xylose as a fermentative carbon source include xylose
uptake and limitations in the pentose phosphate pathway
(PPP) reactions.
In order to understand redox and nutrient regulation in
general, and the physiology of xylose utilising S.
cerevisiae, we carried out chemostat cultures on xylose
as a carbon source, and compared those with glucose
cultures. Transcriptional profiling and proteomics were
carried out. The results are in good agreement. In
addition to the expected responses in cellular redox
metabolism and PPP, also new responses towards xylose as
a carbon source were discovered such as the up-regulation
of pathways for alternative carbon source utilisation and
responses for nutritional control and starvation. The
physiology of the recombinant yeast appears to be neither
fully repressed (fermentative) nor derepressed
(gluconeogenic).
AB - We are interested in broadening the substrate utilisation
range of the yeast Saccharomyces cerevisiae and in
connection to this to study nutritional responses and
signalling at a global level. S. cerevisiae does not
naturally utilise pentose sugars unlike most other fungi,
and recombinant S. cerevisiae strains have been
constructed that contain the xylose utilisation pathway
from other yeasts. The xylose reductase enzyme (XR)
prefers NADPH as a cofactor while the next step in the
pathway xylitol dehydrogenase (XDH), NAD+. This is
believed to create a redox cofactor imbalance in the
cells and limit xylose fermentation. Other suggested
rate-limiting steps in xylose utilisation and the use of
xylose as a fermentative carbon source include xylose
uptake and limitations in the pentose phosphate pathway
(PPP) reactions.
In order to understand redox and nutrient regulation in
general, and the physiology of xylose utilising S.
cerevisiae, we carried out chemostat cultures on xylose
as a carbon source, and compared those with glucose
cultures. Transcriptional profiling and proteomics were
carried out. The results are in good agreement. In
addition to the expected responses in cellular redox
metabolism and PPP, also new responses towards xylose as
a carbon source were discovered such as the up-regulation
of pathways for alternative carbon source utilisation and
responses for nutritional control and starvation. The
physiology of the recombinant yeast appears to be neither
fully repressed (fermentative) nor derepressed
(gluconeogenic).
M3 - Conference abstract in proceedings
SN - 951-38-6307-7
T3 - VTT Symposium
SP - 149
BT - International Specialised Symposium on Yeasts ISSY25
PB - VTT Technical Research Centre of Finland
CY - Espoo
Y2 - 18 June 2006 through 21 June 2006
ER -