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Book of Abstracts (PDF) - International Mycological Association

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IMC7 Thursday August 15th Lectures<br />

308, 1098 SM Amsterdam, The Netherlands. - E-mail:<br />

teixeira@science.uva.nl<br />

The metabolic network <strong>of</strong> the living cell is endowed with<br />

an amazing capacity to cope with different environmental<br />

conditions. This capacity is due to a variety <strong>of</strong> signal<br />

transducing and regulatory systems designed to tune the<br />

cell's metabolic machinery to prevailing physico-chemical<br />

conditions e.g. nutrient availability, temperature,<br />

osmolarity and the nature <strong>of</strong> the energy source. Although<br />

the mechanisms that underly various adaptive responses<br />

may differ in many respects, they seem to have in common<br />

that the energetic and redox state <strong>of</strong> the cell is crucial to<br />

their functioning on the one hand and that they affect<br />

energy and redox catabolism on the other. In this context, it<br />

will be shown that the extent to which exponentially<br />

growing cells can withstand a heat shock is related to the<br />

ATP pools and to their potential to adapt the internal<br />

trehalose and glycogen metabolism. Further, a quantitative<br />

flux analysis <strong>of</strong> strains modified in the levels <strong>of</strong> proteins<br />

(hap4p and hexokinase 2) that take part in general glucose<br />

repression regulatory pathways, will illustrate the role <strong>of</strong><br />

these pathways in the bioenergetics <strong>of</strong> yeast growth and<br />

maintenance. Finally, we will present an example <strong>of</strong> the<br />

transient transcriptional and physiological events which are<br />

invoked when steady state glucose-limited chemostat<br />

cultures are challenged with oleate as energy source. Here<br />

again, the initial adaptive response (prior to peroxisome<br />

biosynthesis) is gouverned by redox and energetic<br />

imbalance.<br />

342 - Uptake and catabolism <strong>of</strong> glucose<br />

M. Mattey<br />

University <strong>of</strong> Strathclyde, 204, George Street, Glasgow G1<br />

1XW, Scotland, U.K. - E-mail: m.mattey@strath.ac.uk<br />

Fungi are chemoheterotrophs found in a variety <strong>of</strong> habitats<br />

and their life cycles are similarly varied. Strategies adopted<br />

by fungi vary from typical 'r' strategists, with a high<br />

reproductive rate and a short life cycle, to 'K-'strategists<br />

which use resources efficiently and reproduce more slowly.<br />

Whatever their environmental niche most fungi can use<br />

glucose and do so with the same basic biochemistry. The<br />

uptake <strong>of</strong> glucose uses members <strong>of</strong> the major facilitator<br />

superfamily which mediate the thermodynamically<br />

downhill movement <strong>of</strong> glucose across the cell membrane.<br />

Free glucose within the cell is maintained at a low level by<br />

hexokinase, which also confines the subsequent<br />

metabolism to the cell by phosphorylation. Glycolysis is<br />

the most common pathway for the degradation <strong>of</strong> glucose.<br />

Although the basic biochemistry is the same in most cases,<br />

the regulation <strong>of</strong> the enzymes differs for different<br />

strategies. Faced with a surfeit <strong>of</strong> glucose, a situation that<br />

may occur naturally or in industrial processes, fungi grow<br />

rapidly, but this may not be enough to use all the glucose<br />

that enters the cell by simple diffusion. The rate <strong>of</strong><br />

diffusion can exceed the maximum uptake rate <strong>of</strong><br />

facilitated transport. When this happens facilitated<br />

transport appears to shut down by an unknown mechanism,<br />

and free internal glucose levels rise. In the opposite<br />

situation, with oligotrophic media, the problem becomes<br />

108<br />

<strong>Book</strong> <strong>of</strong> <strong>Abstracts</strong><br />

one <strong>of</strong> how to maintain internal metabolite levels when the<br />

entry rate is less than the flux.<br />

343 - Galactose metabolism in Trichoderma and<br />

Aspergillus: properties, regulation and identification <strong>of</strong><br />

a second, reductive pathway<br />

B. Seiboth 1 , L. Karaffa 2 & C.P. Kubicek 1*<br />

1 Section Microbial Biochemistry and Gene Technology,<br />

Institute <strong>of</strong> Chemical Engineering, TU Wien,<br />

Getreidemarkt 9/166, A-1060 Wien, Austria. - 2 Department<br />

<strong>of</strong> Microbiology and Biotechnology, Faculty <strong>of</strong> Sciences,<br />

University <strong>of</strong> Debrecen, H-4010, P.O.Box 63, Debrecen,<br />

Hungary. - E-mail: ckubicek@mail.zserv.tuwien.ac.at<br />

D-Galactose metabolism via the Leloir pathway is a<br />

ubiquitous trait in pro- and eukaryotic cells. Its metabolic<br />

regulation has been extensively studied in yeast<br />

(Saccharomyces, Kluyveromyces) but not in filamentous<br />

fungi. A more detailed knowledge on the latter would be<br />

worthwhile, as lactose (1,4-0-β-D-galactopyranosyl-Dglucose)<br />

arising from whey - represents a renewable carbon<br />

source for several fungal fermentations, notably cellulase<br />

production by Hypocrea jecorina (anamorph Trichoderma<br />

reesei), but an effective exploitation <strong>of</strong> lactose for the<br />

biotechnical utlization is still hampered by its slow<br />

metabolism and a lack <strong>of</strong> basic knowledge on its utilization<br />

in H. jecorina and filamentous fungi in general. We<br />

therefore have functionally characterized the genes for the<br />

Leloir pathway in H. jecorina. Here we will report that<br />

they differ from the yeast counterparts with respect to<br />

genomic organization, protein structure and genetic<br />

regulation. We will also provide evidence for the<br />

involvement <strong>of</strong> the Leloir pathway in cellulase induction<br />

by lactose. Further, we will provide evidence for the<br />

existence <strong>of</strong> a second, so far unknown pathway <strong>of</strong> Dgalactose<br />

breakdown in H. jecorina and Aspergillus<br />

nidulans which involves a NADPH-aldose reductase<br />

dependent reduction to D-dulcitol, and its subsequent<br />

oxidation by 2-arabinitol dehydrogenase to D-tagatose.

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