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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

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