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5 Diversity and Functions of Soil Microflora in Development of Plants 79<br />

deserticola. The greatest <strong>plant</strong> growth and AM colonization responses in sterilized<br />

and nonsterilized soils was observed with pea, G. deserticola and<br />

sodium alginate pellets as carrier for F. oxysporum inoculum.Application of F.<br />

oxysporum increased shoot dry matter, N and P concentrations of pea and<br />

sorghum <strong>plant</strong>s and the level of AM fungi colonization.<br />

Piriformospora indica, a newly described axenically cultivable phytopromotional<br />

endosymbiont, which mimics the capabilities of AM fungi, was<br />

recently described by Varma et al. (1999) and Singh et al. (2000). The fungus<br />

has a broad host spectrum and inoculation with the fungus and application<br />

of culture filtrate promotes <strong>plant</strong> growth and biomass production. It mobilizes<br />

the insoluble phosphate and translocates the phosphorus to the host in<br />

an energy-dependent process. As a biological hardening agent of micropropagated<br />

<strong>plant</strong>s, it renders more than 90 % survival rate for laboratory to<br />

field transferred <strong>plant</strong>lets. Regenerative protoplasts of P. indica have been<br />

successfully isolated, which opens up the possibility of improving symbiosis<br />

by transgenic manipulation of the fungal component in a symbiosis-specific<br />

manner.<br />

In the ectomycorrhizal (EM) symbiosis between fungi and trees, the fungus<br />

completely ensheaths the tree roots and takes over water and mineral nutrient<br />

supply, while the <strong>plant</strong> supplies photosynthate (Wiemken and Boller 2002). N<br />

and P are the main elements limiting <strong>plant</strong> growth in terrestrial ecosystems.<br />

One of the great assets of the ectomycorrhizal symbiosis is its capability to<br />

short-circuit nutrient uptake from organic material to the symbiotic partner.<br />

In addition to mobilizing mineral nutrients from organic sources, EM fungi<br />

may also link <strong>plant</strong>s to rock directly though secretion of organic acids and<br />

solubilizing nutrients from the mineral part of soil. Many EM fungi also retain<br />

considerable saprotrophic potential, for example, production of lignindegrading<br />

enzymes, a quality that benefits the symbionts in the acquisition of<br />

nutrients from lignin-rich organic material.<br />

Sulfur nutrition of <strong>plant</strong>s is largely determined by sulfate uptake of the<br />

roots, the allocation of sulfate to the sites of sulfate reduction and assimilation,<br />

the reduction of sulfate to sulfide and its assimilation into reduced sulfur-containing<br />

amino acids and peptides and the allocation of reduced sulfur<br />

to growing tissues (Rennenberg 1999). EM colonization of oak and beech tree<br />

roots can alter the response of sulfate uptake to sulfate availability in the soil<br />

and enhance xylem transport of sulfate to the leaves. Simultaneously, sulfate<br />

reduction in the roots seems to be stimulated by EM association. These interactions<br />

between EM association and the processes involved in sulfur nutrition<br />

are required to provide sufficient amounts of reduced sulfur for<br />

increased protein synthesis that is used to enhance tree growth.<br />

Information on the diversity of ericoid mycorrhizal endophytes in the Ericaeae<br />

and Epacridaceae has been compiled over the years by several authors<br />

(Varma and Bonfante 1994; Read 1996; Bergero et al. 2000; Berch 2001; Perotto<br />

et al. 2002). Hymenoscyphus ericae and Oidiodendron sp. appear to be the

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