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126<br />

Galdino Andrade<br />

significant quantities of bio-insecticide crystals in pollen, leaves and roots,<br />

their effect on the functional groups of soil microorganisms is little understood.<br />

The influence of the mineralogical composition of the soil on the stability<br />

of the bio-insecticide crystals has been reported by several authors. Tapp et al.<br />

(1995a) showed that the toxin is rapidly adsorbed or linked to clay minerals in<br />

the soil, remaining protected from degradation by soil microorganisms. In<br />

another study, Tapp et al. (1995b) showed that the toxin adsorbed by clay minerals<br />

becomes resistant to hydrolytic action of the enzymes produced by the<br />

soil microbiota. It has also been shown that soils with high levels of organic<br />

matter have a high protein crystal adsorption capacity (Palm et al. 1994). Sims<br />

et al. (1996) observed that B. thuringiensis var kurstaki Cry1Ab toxin present<br />

in Bt-transgenic maize tissues incorporated in the soil can be detected by<br />

bioassays with insects susceptible to the bio-insecticide action of the crystal.<br />

According to the results obtained by these authors, the bioassay allows the<br />

detection of smaller quantities of the protein (around 0.5 ng/ml in the diet)<br />

compared to the ELISA test (50.0 ng/g of soil). Sims et al. (1997), working with<br />

bioassays on B. thuringiensis var kurstaki transgenic cotton toxin inactivation<br />

in soils, observed that the toxin mean life in the soil ranges from 15 to 32 days,<br />

and less than 25 % of the initial activity remains after 120 days.<br />

6 Effect of Bacillus thuringiensis and Its Bio-insecticide<br />

Protein on Functional Soil Microorganism Assemblage<br />

Plant roots and their <strong>surface</strong>s constitute dynamic habitats densely colonised<br />

by soil-borne microbiota. The high microbial activity in these habitats is due<br />

to a flow of organic substances from the photosynthetic parts of the <strong>plant</strong>s to<br />

the roots (Olsson and Person 1999). This flow consists of low molecular<br />

weight organic substances (e.g. sugars, fatty acids and amino acids), as well as<br />

more complex substances (e.g. starch, cellulose and proteins). The chemical<br />

composition of this organic matter (the rhizodeposition) varies among <strong>plant</strong><br />

species and growth stages, and is affected by <strong>plant</strong> growth conditions (Curl<br />

and Truelove 1986). The functional groups of microorganisms of nitrogen,<br />

phosphorus and carbon cycling are important to the maintenance of nutrient<br />

turnover. These microorganisms interact with the <strong>plant</strong> roots, supply nutrients<br />

and participate actively in <strong>plant</strong> nutrition and growth (Andrade 1999).<br />

Mycorrhizal fungi are ubiquitous soil inhabitants and form a symbiotic<br />

relationship with the roots of most terrestrial <strong>plant</strong>s. When arbuscular mycorrhizae<br />

(AM) form, there are significant changes in the <strong>plant</strong> and root physiology.<br />

Photosynthetic rates increase and the nutritional status of the host tissues<br />

changes and thus, the quality and quantity of root exudates (Linderman<br />

1992). Altered exudation induces changes in the composition of microbial<br />

communities in the rhizosphere soil (Andrade et al. 1997) that may influence

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