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1.
Braz. j. microbiol ; 41(1): 253-263, Jan.-Mar. 2010. ilus, graf
Article in English | LILACS | ID: lil-531759

ABSTRACT

Sclerotium rolfsii (Sacc.) is a serious plant pathogenic fungus and lacks perfect (basidial) stage in production. Protoplast fusion technology was employed to reconstruct fusants from this fungus. Two strains designated as A and R were used. Maximum protoplast yields of 3.8x10(5) /g mycelia and 2.8x10(5) /g mycelia were formed in strains A and R respectively. Osmotic stabilizer sucrose 1M gave maximum yield. Lysing enzyme at the rate of 15mg/ml was found best for yield. Fusion of protoplasts from strains A and R was carried out in fusion media containing PEG 4000 30 percent (w/v) with 0.2mM CaCl2. Four fusants F1, F2, F3 and F4 were recovered. Morphological, physiological and pathogenic characters of fusants were compared with parent strains on carrots, beans and tomato.


Subject(s)
Ascomycota/enzymology , Basidiomycota/genetics , Enzyme Stability , Gene Fusion , Protoplasts/enzymology , Food Samples , Methods , Methods , Virulence
2.
Genet. mol. res. (Online) ; 3(4): 449-455, 2004. ilus, tab
Article in English | LILACS | ID: lil-410889

ABSTRACT

Penicillium griseoroseum, a deuteromycete fungus producer of pectinolytic enzymes, was transformed with a gene encoding for green fluorescent protein (GFP). The selection of transformants was based on the homologous nitrate reductase gene (niaD). Protoplasts of a P. griseoroseum Nia mutant (PG63) were co-transformed with the plasmids pNPG1 and pAN52-1-GFP. The plasmid pNPG-1 carries the homologous niaD gene and pAN52-1-GFP carries the SGFP-TYG version of GFP. The highest transformation efficiency (102 transformants/µg of pNPG1) resulted from the utilization of equimolar amounts of transforming and co-transforming vectors. Analysis of pAN52-1-GFP insertions into the genomic DNA of the transformants revealed single and multiple copy integrations. The transformants possessing a single copy of the gfp gene showed a low level of fluorescence, whereas multicopy transformants displayed strong fluorescence under visualization with fluorescent light. The transformants showing high expression of the gfp gene had the normal mycelia pigmentation altered, displaying a bright green-yellowish color, visible with the naked eye on the plates, without the aid of any kind of fluorescent light or special filter set.


Subject(s)
DNA, Fungal/genetics , Genome, Fungal , Luminescent Proteins/genetics , Mutation , Penicillium/genetics , Transformation, Genetic/genetics , Luminescent Proteins/analysis , Microscopy, Fluorescence , Penicillium/enzymology , Plasmids/genetics , Polygalacturonase/genetics , Protoplasts/enzymology
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