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Influence of Microorganisms on Phosphorus Bioavailability in Soils 183<br />

surrounding the roots (Watt et al. 1993; Gregory and Hinsinger 1999). Amellal<br />

et al. (1999) found a significant aggregation and stabilization of rootadhering<br />

soil by bacterial extracellular polysaccharides combined with an<br />

increase in aggregate mean weight, diameter, aggregate macro-porosity,<br />

adhering soil: root mass ratio, water-stable > 200 µm aggregates and 0.1–<br />

2 µm elementary clayey microaggregates. Watt et al. (1993) reported a 10%<br />

higher soil binding capacity of bacterial mucilages in comparison to plant<br />

released materials.<br />

Phospholipides in root and bacterial mucilages are powerful surfactants<br />

that alter the interaction of soil solids with water and ions (Read et al.<br />

2003). The occupation of adsorption sites as well as influences on aggregate<br />

stability and water balance can facilitate phosphorus diffusion processes.<br />

3.4<br />

Release of Phosphorus from Organic Sources<br />

Between 20 and 85% of the total P in agricultural soils are present in<br />

the organic form, including inositol phosphate esters, phospholipids, nucleic<br />

acids, phosphate linked to sugars and derivatives of phosphoric acid<br />

(Tarafdar et al. 2001). Microorganisms mineralize organic materials like<br />

plant residues and organic manures and enable the nutrient cycling. Using<br />

an isotopic dilution technique, Oehl et al. (2001) found a daily mineralization<br />

of 1.7 mg P kg −1 in an organically fertilized loamy silt soil. This amount<br />

was approximately equivalent to soil solution P, indicating that mineralization<br />

is a significant process in delivering available P. Although soil solutions<br />

can include higher concentrations of organic than of inorganic phosphates,<br />

plants can acquire phosphorus only in inorganic form (Tarafdar et al. 2002).<br />

For this reason phosphatases which hydrolyse C–O–P ester bonds are very<br />

importantforPnutrition.DependingontheirpHoptimum,acidandalkaline<br />

phosphatases can be determined. Phosphodiesterase, which is able<br />

to degrade nucleic acids, has not been extensively studied in soils (Dodor<br />

and Ali Tabatabai 2003). Acid phosphatases are released by plant roots as<br />

well as by microorganisms (Seeling and Jungk 1996; Yadaf and Tarafdar<br />

2001), while alkaline phosphatases are probably mostly of microbial origin<br />

(Tarafdar and Claasen 1988). The largest portion of extracellular soil phosphatases<br />

is derived from the microbial population and strongly correlates<br />

with microbial biomass (Dodor and Ali Tabatabai 2003). Tarafdar et al.<br />

(2001) identified a better hydrolysis of lecithin and phytin by fungal acid<br />

phosphatases in comparison to those of plant origin. Glycerophosphate<br />

was equally hydrolyzed by both enzymes. Tarafdar et al. (2002) reported<br />

that different fungi released only 25% of their acid phosphatases extracellularly,<br />

but a 39 times higher extracellular phytase activity was noted in

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