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Host and Non-Host Impact on the Physiologyof the AM Symbiosis 143<br />

nificant rate of trehalose, a short-term fungal storage carbohydrate, was<br />

13 C-labelled when 13 CO2 was supplied to asymbiotic spores. However, after<br />

deciphering the metabolic pathways involved, these authors concluded<br />

that such 13 C incorporation occurred via dark fixation, a side part of gluconeogenesis<br />

which does not lead to net gain of C. Nevertheless, such dark<br />

fixation seems to have an important role in anaplerotic reactions, thus explaining<br />

the better pre-symbiotic AM fungal development shown in the<br />

presence of CO2.<br />

2.4<br />

Light<br />

In nature, the exposure of soil-borne AM fungi to light is an extremely<br />

unlikely event (see Chap. 6), as underground roots are the colonized plant<br />

organ. Surprisingly, light treatment affects the growth pattern of axenically<br />

growing hyphae. Light induced hyphal branching in developing germ<br />

tubes of Gi. gigantea, Gi. rosea and G. intraradices (Nagahashi et al. 2000).<br />

In a study with Gi. gigantea, wavelengthsinthebluetoUVrangewere<br />

identified as the responsive ones (Nagahashi and Douds 2003). Blue light<br />

has been found to regulate all known differentiation processes in Basidiomycetes<br />

(Kues et al. 1998). The biological relevance of these findings in<br />

nature still remains unclear, and it has been suggested that a general mechanism<br />

of stress response could be implicated (Kues et al. 1998); in any case,<br />

in vitro systems are ideal to further study such intriguing questions.<br />

3<br />

Pre-Symbiotic AM Fungal Growth<br />

More than 80% of all plant species are hosts for AM fungi. Depending on the<br />

host status, plant signals perceived by AM fungi differ. Whereas there are<br />

abundant data on the stimulatory effects of plant signals from host plants<br />

on AM fungal spore germination, hyphal growth and branching, there are<br />

contradictory reports on the effect of signals from non-host plants on AM<br />

fungi (Giovannetti and Sbrana 1998; Vierheilig et al. 1998; Giovannetti<br />

2000). To our knowledge, although AM fungi can grow to some extent in<br />

the presence of AM non-host plants, in general, they do not grow on their<br />

root surface and do not form appressoria on them. As the pre-symbiotic<br />

phase is characterized by the presence of both root and AM fungi, still in the<br />

absence of physical contact between them, it can be concluded that the nonhost<br />

status of plants to AM fungi is determined during the pre-symbiotic<br />

stage of the symbiosis.

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