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 />
Cellobiose dehydrogenase(CDH)is an extracellular enzyme<br />
produced by wood-degrading and also other fungi. In this<br />
communication, CDH activity <strong>of</strong> 24 Cladosporium isolates<br />
was measured using a zymogram procedure for<br />
determining the possible role <strong>of</strong> the CDH in the fungal<br />
pathogenesis. 2,6-Dichlorophenolindophenol (DCPIP) was<br />
added into czapek agar medium containing Avicel (1%<br />
w/v) and cellobiose (20mM). The blue coloured agar plates<br />
were inoculated with fungal spores and incubated for 5<br />
days at 25C. Production <strong>of</strong> CDH was assessed by the<br />
measuring zones <strong>of</strong> clarification in the agar around the<br />
growing colonies. This clarification was higher for 10<br />
clinical Cladosporium isolates (5-6 mm) as compared with<br />
14 environmental ones (0.5-1.4 mm)(P3)-glucan, the major matrix wall component,<br />
was immuno-localized in all regions <strong>of</strong> elongating and nonelongating<br />
hyphae. A number <strong>of</strong> cytochemical,<br />
biochemical and physiological controls were performed to<br />
assure the reliability <strong>of</strong> these findings. We suggest that in<br />
elongating regions, the matrix is synthesized first and<br />
synthesis <strong>of</strong> micr<strong>of</strong>ibrilar component follows. Another<br />
explanation for our results is that localized apical cellulose<br />
hydrolysis by endoglucanase creates plastic wall regions<br />
consisting mainly <strong>of</strong> β-(1-3)-glucans, which expand under<br />
turgor and/or cytoskeleton pressure. Cellulose deposition<br />
quickly follows.<br />
1178 - Aspergillus nidulans polarity genes swoA, a<br />
protein mannosyl transferase, and swoF, an Nmyristoyl<br />
transferase<br />
B.D. Shaw * & M. Momany<br />
University <strong>of</strong> Georgia, Plant Biology, 2502 Plant Science,<br />
Athens, GA, 30602, U.S.A. - E-mail:<br />
bshaw@botany.uga.edu<br />
Hyphal growth in filamentous fungi requires first<br />
establishment and then maintenance <strong>of</strong> polarity and is<br />
necessary for disease in many fungal pathosystems.<br />
Germination <strong>of</strong> Aspergillus nidulans conidia involves<br />
isotropic (nonpolar) expansion <strong>of</strong> the cell through the first<br />
two nuclear divisions. Subsequent development is polar<br />
with production <strong>of</strong> a germ tube and establishment <strong>of</strong><br />
vegetative growth. The A. nidulans swo mutants are<br />
temperature sensitive mutants defective in one or both<br />
stages <strong>of</strong> polar growth during the process <strong>of</strong> spore<br />
germination. A. nidulans swoAp is a protein mannosyl<br />
transferase, a protein responsible for the first stage <strong>of</strong> Oglycosylation.<br />
A glycosylated substrate <strong>of</strong> swoAp may be a<br />
cell wall associated protein important for polar growth.<br />
swoFp is an N-myristoyl transferase, a protein responsible<br />
for the co-translational addition <strong>of</strong> a small fatty acid to the<br />
N-terminus <strong>of</strong> its substrate thereby giving it higher affinity<br />
for association with the membrane. In Saccharomyces<br />
cerevisiae N-myristoyl transferase substrates are<br />
commonly signaling proteins. The temperature-sensitive<br />
allele changes a conserved aspartic acid to a tyrosine. The<br />
wild type D appears to stabilize a Beta strand bend through<br />
two hydrogen bonds and an ionic interaction. A<br />
myristoylated substrate <strong>of</strong> swoFp may be a signaling<br />
molecule important for polar growth. A proteomics<br />
approach is being taken to characterize the substrates <strong>of</strong><br />
these proteins.<br />
1179 - Effect <strong>of</strong> bacteria on germination and mycelial<br />
growth <strong>of</strong> arbuscular mycorrizal fungi, in vitro<br />
S.A.G. Soares 1 , L.C. Maia 1 , R.L.R. Mariano 3 , U.M.T.<br />
Cavalcante 2 & G.A. Silva 1*<br />
1 Departamento de Micologia - UFPE, 50670-420 Recife -<br />
PE, Brazil. - 2 Departamento de Biologia - UFRPE, 52171-<br />
900 Recife - PE, Brazil. - 3 Departamento de Agronomia -<br />
UFRPE, 52171-900 Recife - PE, Brazil. - E-mail:<br />
gladstonesilva@yahoo.com<br />
The effect <strong>of</strong> plant growth promoted rhizobacteria (PGPR)<br />
on germination and mycelial growth <strong>of</strong> Gigaspora albida,<br />
Glomus etunicatum and Scutellospora heterogama was<br />
studied. Aqueos suspensions <strong>of</strong> Bacillus cereus (C210),<br />
Bacillus sp. (RAB9), B. thuringiensis subvar. kurstakii<br />
(ENF10) and Pseudomonas chlororaphis (GN1212) were<br />
<strong>Book</strong> <strong>of</strong> <strong>Abstracts</strong> 357