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Green fluorescent protein (GFP) as a reporter gene for the plant pathogenic oomycete Phytophthora ramorum

Riedel, Marko;
Zugehörigkeit
Plants and Pathogens Group, Institute Earth Nature and Landscape, University of Applied Sciences of Western Switzerland, 150 Route de Presinge 1254 Jussy, Switzerland
Calmin, Gautier;
Zugehörigkeit
Plants and Pathogens Group, Institute Earth Nature and Landscape, University of Applied Sciences of Western Switzerland, 150 Route de Presinge 1254 Jussy, Switzerland
Belbahri, Lassaad;
Zugehörigkeit
Plants and Pathogens Group, Institute Earth Nature and Landscape, University of Applied Sciences of Western Switzerland, 150 Route de Presinge 1254 Jussy, Switzerland
Lefort, Francois;
GND
1182046916
Zugehörigkeit
Julius Kuehn-Institute (JKI), Federal Research Centre for Cultivated Plants, Institute for Biosafety of Genetically Modified Plants,
Götz, Monika;
GND
12395519X
Zugehörigkeit
Julius Kuehn-Institute (JKI), Federal Research Centre for Cultivated Plants, Institute for Plant Protection in Horticulture and Forests
Wagner, Stefan;
GND
1058984977
Zugehörigkeit
Julius Kuehn-Institute (JKI), Federal Research Centre for Cultivated Plants, Institute for Plant Protection in Horticulture and Forests
Werres, Sabine

Transgenic Phytophthora ramorum strains that produce green fluorescent protein (GFP) constitutively were obtained after stable DNA integration using a polyethylene glycol and CaCl2-based transformation protocol. Green fluorescent protein production was studied in developing colonies and in different propagules of the pathogen to evaluate its use in molecular and physiological studies. About 12% of the GFP transformants produced GFP to a level detectable by a confocal laser scanning microscope. Green fluorescent protein could be visualized in structures with vital protoplasm, such as hyphal tips and germinating cysts. In infection studies with Rhododendron, one of the GFP expressing strains showed aggressiveness equal to that of the corresponding non-labelled isolate. Thus, GFP could be used as a reporter gene in P. ramorum. Limitations of the technology are discussed.

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