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Page 2 Plant-Bacteria Interactions Edited by Iqbal Ahmad, John ...

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contrast to the in planta results, population enhancements were not observed<br />

when R. etli and P. polymyxa were cocultured in vitro using minimal media in<br />

the absence of the seedling. The addition of seed exudates to the growth media<br />

also failed to stimulate the population increases. Mutants of A. brasilense and<br />

R. leguminosarum altered in the production of extracellular polysaccharides.<br />

Binaciotto et al. [180] showed the involvement of these polysaccharides in the<br />

attachment of these bacteria to the structures of AM fungi. In soil, an extensive<br />

network of AM fungi develops and PGPR are usually associated with fungal<br />

surfaces [181]. Azotobacter chroococcum and Pseudomonas fluorescens were attracted<br />

toward tomato roots colonized <strong>by</strong> Glomus fasciculatum compared to nonvesiculararbuscular<br />

mycorrhizal tomato roots [182]. The presence of G. clarum decreased<br />

or did not significantly affect plant growth under the different culture conditions.<br />

The presence of AM fungi stimulated the nitrogen-fixing bacterial population of<br />

upland rice. <strong>Bacteria</strong>l species had different effects, under both culture conditions,<br />

and some genera of nitrogen-fixing bacteria increased root and shoot growth at<br />

different plant growth stages. The level of mycorrhiza colonization had no influence<br />

on plant growth [183].<br />

5.6<br />

Other Dimensions of <strong>Plant</strong> Growth Promoting Activities<br />

5.6.1<br />

ACC Deaminase Activity<br />

5.6 Other Dimensions of <strong>Plant</strong> Growth Promoting Activitiesj97<br />

Ethylene is the only gaseous hormone produced <strong>by</strong> plants. It is also known as the<br />

wounding hormone because its production in the plant can be induced <strong>by</strong> physical<br />

or chemical perturbation of plant tissues. Among its myriad effects on plant growth<br />

and development, ethylene production can inhibit root growth. In some cases, the<br />

growth promotion effects of ACC deaminase producing PGPR appear to be best<br />

expressed in stressful situations such as in heavy metal contaminated soils [184].<br />

The enzyme ACC deaminase plays a key role in degrading ACC. The products of<br />

this hydrolysis, ammonia and a-ketobutyrate, can be used <strong>by</strong> the bacterium as a<br />

source of nitrogen and carbon for growth [185]. In this way, the bacterium acts as a<br />

sink for ACC and as such is lowering the ethylene level in plants, preventing some<br />

of the potentially deleterious consequences of high ethylene concentrations. In<br />

nature, ACC deaminase has been commonly found in soil bacteria that colonize<br />

plant roots [186]. Many of these microorganisms were identified <strong>by</strong> their ability to<br />

grow on minimal media containing ACC as its sole nitrogen source. In this<br />

way, Azospirillum spp., Herbaspirillum spp., Azoarcus, Azorhizobium caulinodans,<br />

Gluconoacetobacter diazotrophicus, Burkholderia vietnamiensis, Azotobacter spp.,<br />

Azorhizophilus and Pseudomonas spp. were all found to be able to use ACC as the<br />

sole nitrogen source for growth. An example of such an ACC deaminase containing<br />

bacterium is the PGPR Pseudomonas putida GR12-2 [187] that stimulates<br />

root growth of a number of different plants (canola, lettuce and tomato) under

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