Book of Abstracts (PDF) - International Mycological Association
Book of Abstracts (PDF) - International Mycological Association
Book of Abstracts (PDF) - International Mycological Association
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IMC7 Main Congress Theme V: CELL BIOLOGY AND PHYSIOLOGY Posters<br />
mainly responsible for facilitating water uptake via fine<br />
roots <strong>of</strong> spruce, and that the down-regulation <strong>of</strong> gene<br />
expression is an adaptation to the improved water supply<br />
mediated by the symbiotic fungus.<br />
1144 - Characterisation <strong>of</strong> a phosphate transporter in<br />
Candida albicans<br />
P. Martineau * , T.-L. Tremblay & L. Giasson<br />
Laval University, School <strong>of</strong> Dentistry, GREB, Quebec, Qc,<br />
G1K 7P4, Canada. - E-mail:<br />
philippemartineau@videotron.ca<br />
The human pathogen Candida albicans is a dimorphic<br />
fungus that can reversibly alter its mode <strong>of</strong> growth from<br />
yeast-like cells to mycelial cells, depending upon its<br />
environment. As the mycelial form is usually associated<br />
with candidiasis, genes involved in the control <strong>of</strong><br />
dimorphism represent potential targets for the development<br />
<strong>of</strong> antifungal drugs. Using the differential display<br />
technique, we have identified a gene preferentially<br />
expressed in the mycelial cells. We have cloned and<br />
sequenced that gene. Sequence analysis revealed that this<br />
gene displays 70% homology with the Saccharomyces<br />
cerevisiae Pho89 gene, encoding a phosphate transporter.<br />
The C. albicans CaPho89 gene was cloned into a S.<br />
cerevisiae expression vector and transformed into a S.<br />
cerevisiae pho89 null mutant strain. Phosphate transport in<br />
the transformants was evaluated using [ 32 P]orthophosphate.<br />
The results obtained showed that CaPho89<br />
could complement the S. cerevisiae pho89 mutation,<br />
suggesting that CaPho89 encodes a functionnal phosphate<br />
transporter.<br />
1145 - Mitochondrial group-I intron in a higher<br />
basidiomycete, Pleurotus ostreatus, is mobile in sexual<br />
crosses<br />
T. Matsumoto * & Y. Fukumasa-Nakai<br />
Tottori <strong>Mycological</strong> Institute, Kokoge-211, Tottori-shi,<br />
Tottori, Japan. - E-mail: kin-matu@infosakyu.ne.jp<br />
Inter-parental recombination between mitochondrial (mt)<br />
genomes <strong>of</strong> Pleurotus ostreatus occurred at high frequency<br />
in sexual crosses. To reveal the process leading to this<br />
recombination, we estimated a certain recombination site in<br />
each parental mitochondrial genome contributing to the<br />
generation <strong>of</strong> the new restriction fragments which<br />
characterized a RFLP pattern <strong>of</strong> recombinant mtDNA, and<br />
determined their nucleotide sequences. It was found that<br />
the regions <strong>of</strong> recombination within parental mtDNAs<br />
possessed consensus sequences in common, which were<br />
divided by some regions <strong>of</strong> non-consensus sequences.<br />
Meanwhile, the nucleotide sequences in the new restriction<br />
fragments and their surrounding regions in recombinant<br />
mtDNA were harbored all consensus and non-consensus<br />
sequences recognized in both parental mtDNA, suggesting<br />
that this structure was caused by the integration <strong>of</strong> regions<br />
with non-consensus sequences that exist in only one<br />
parental mtDNA to the other. All non-consensus sequences<br />
were homologous to the sequences <strong>of</strong> the group I intron<br />
reported in fungi. They also included the ORF sequences<br />
that encode the LAGLIDADG motif, a characteristic <strong>of</strong><br />
endonuclease involved in intron mobility. These results<br />
indicate that the manner <strong>of</strong> recombination for generating<br />
the new restriction fragment is elucidated by gene<br />
conversion, achieved by the mobility <strong>of</strong> the introns. This<br />
suggests that, in P. ostreatus, intron mobility is playing a<br />
large role for the increase <strong>of</strong> diversity <strong>of</strong> mtDNA.<br />
1146 - Effect <strong>of</strong> carminic acid and other mediators on<br />
lignosulfonates degradation by extracellular enzymes <strong>of</strong><br />
Trametes versicolor<br />
A. Matuszewska * , G. Nowak & A. Leonowicz<br />
M. Curie-Sklodowska University, Departament <strong>of</strong><br />
Biochemistry, Pl. M. Curie-Sklodowskiej 3, 20-031 Lublin,<br />
Poland. - E-mail: amatusze@hermes.umcs.lublin.pl<br />
Many low-molecular mass compounds have been<br />
suggested as possibly mediating mobile factors during<br />
biodegradation <strong>of</strong> lignin. Degradation <strong>of</strong> lignosulfonates by<br />
ligninolytic enzymes produced by the white-rot fungus<br />
Trametes versicolor was studied. The 29,6 kDa fraction <strong>of</strong><br />
Peritan Na obtained by a gel filtration method using a<br />
Sephadex G-100 column was used as a substrate. The<br />
substrate was incubated with extracellular idiophasic<br />
enzymes <strong>of</strong> Trametes versicolor and with mediators. HBT<br />
(1-hydroxybenzotriazole), ABTS (2,2'azinobis-(3ethylbenzenthiazoline-6-sulfonic<br />
acid) and carminic acid<br />
were used as mediators. Following the incubation products<br />
were separated using gel filtration on a Sephadex G-50<br />
column and capillary electrophoresis. When the mediators<br />
were added to the incubation mixture, depolymerization<br />
was more extensive than in the experiment with no<br />
mediators. In the presence <strong>of</strong> carminic acid the<br />
depolymerization was the most extensive and as it's result a<br />
fraction <strong>of</strong> about 2 kDa appeared. Similar results were<br />
observed when HBT or ABTS were used. However,<br />
products <strong>of</strong> higher molecular weight besides the 2 kDa<br />
fraction were also obtained. Experiments with the reaction<br />
mixtures supplemented with H2O 2 were also performed.<br />
The above experiments revealed that only in the case <strong>of</strong><br />
HBT used as a mediator H 2O 2 addition resulted in the<br />
increased depolymerization <strong>of</strong> lignosulfonates. Supported<br />
by the EC Contract ICA 2-CT-2000-10050, and by KBN<br />
grant 139/E-SPUB-M-5PR-UE/DZ 280/2000.<br />
<strong>Book</strong> <strong>of</strong> <strong>Abstracts</strong> 347