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6 Wood Discoloration

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2.4 Identification 31<br />

In addition to the pairing of compatible monokaryons to insert genetic<br />

material in a fungus from another isolate, fusion of fungal protoplasts can be<br />

performed. Protoplast fusion can be used to make hybrids between cells of the<br />

same mating type, as well as of dikaryotic cells or even between species and genera.<br />

Spheroplasts (cell wall partially removed by lysing enzymes) or protoplasts<br />

(cell wall completely removed) fuse by electric influence or through osmotic<br />

active substances (polyethylene glycol) and some of them regenerate to new<br />

hyphae. Protoplast fusion is used for genetic studies as well as for isolate improvement.<br />

Experiments on wood fungi comprise, e.g., Auricularia polytricha,<br />

Gloeophyllum trabeum, Heterobasidion annosum, Lentinula edodes, Oligoporus<br />

placenta, Ophiostoma piceae, O. ulmi, Phanerochaete chrysosporium, Pleurotus<br />

ostreatus, Trametes versicolor, and Trichoderma spp. (Nutsubidze et al. 1990;<br />

Trojanowski and Hüttermann 1984; Royer et al. 1991; Sunagawa et al. 1992;<br />

Rui and Morrell 1993; Richards 1994; Tokimoto et al. 1998; Bartholomew et al.<br />

2001; Xiao and Morrell 2004). Interspecific fusions (Toyomasu and Mori 1989;<br />

Eguchi and Higaki 1992) and intergeneric fusions (Liang and Chang 1989) were<br />

reported. With increasing genetic distance of the fusion partners, however, the<br />

hybrids are instable, do no fruit, die, or the obtained fruit bodies correspond to<br />

one of the parents, that is, obviously one of the two nuclei has been eliminated<br />

before.<br />

Protoplasts have been produced from O. piceae with the aim of subsequently<br />

inserting genetic material capable of producing fluorescent proteins to allow visualization<br />

of hyphae of that species in wood by using fluorescence microscopy<br />

(Xiao and Morrell 2004).<br />

2.4<br />

Identification<br />

2.4.1<br />

Traditional Methods<br />

Determination keys and descriptions for Deuteromycetes are based on morphology,<br />

color, and development (conidiogenesis) of conidia and conidiogenous<br />

cells (Figs. 2.8–2.10) (Carmichael et al. 1980; Domsch et al. 1980; v. Arx<br />

1981; Wang 1990; Hoog and Guarro 1995; Schwantes 1996; Kiffer and Morelet<br />

2000; Samson et al. 2004).<br />

The fruit bodies of Ascomycetes and Basidiomycetes serve to identify species<br />

on the basis of macro- and microscopic characteristics using keys or illustrated<br />

books: Kreisel 1961; Domański 1972; Domański et al. 1973; Breitenbach and<br />

Kränzlin 1981, 1986, 1991, 1995; Moser 1983; Jülich 1984; Hanlin 1990; Jahn<br />

1990; Wang and Zabel 1990; Ryvarden and Gilbertson 1993, 1994; Huckfeldt<br />

and Schmidt 2005; yeasts: Barnett et al. 1990). There are identification kits<br />

www.taq.ir

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