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

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still viable and showed inhibition of IR. IR can be mediated <strong>by</strong> polysaccharides such<br />

as xanthum gum or <strong>by</strong> AFPs that have been reported in few bacteria, for example,<br />

Antarctic Moraxella, [38] Arctic Rhizobacterium [39,40], cold-acclimated Micrococcus<br />

and Rhodococcus [41]. Therefore, it was hypothesized that IR activity can potentially<br />

contribute to overall viability of a microbial consortium under Chinook conditions.<br />

10.3<br />

Mechanism of <strong>Plant</strong> Growth Promotion at Low Temperature<br />

When deciding on the type of bacterial strains to be used with a plant for a given<br />

climatic condition, understanding of the mechanism of plant growth promotion is<br />

essential; for example, the overwintering ability of PGPR is fundamental when<br />

considering them to use in colder climates. There is evidence that Pseudomonas<br />

sp. are able to overwinter in sufficient quantities on roots of winter wheat [42,43].<br />

The principal mechanisms of plant growth promotion in colder regions include<br />

phytostimulation and frost injury protection.<br />

10.3.1<br />

Phytostimulation<br />

10.3 Mechanism of <strong>Plant</strong> Growth Promotion at Low Temperaturej201<br />

Phytostimulators are chemical compounds produced <strong>by</strong> a number of bacteria that<br />

directly enhance plant growth. Different genera of bacteria such as Proteus mirabilus,<br />

Pseudomonas vulgaris, Klebsiella pneumoniae, Bacillus cereus, Escherichia coli and so on<br />

produce auxin cytokinins, gibberellins and abscisic acid [30]. Quantitatively, auxins<br />

are the most abundant phytohormone secreted <strong>by</strong> PGPR strains such as Azospirullum<br />

and is the major factor that stimulates root generation and enhances root<br />

growth. ABA and ethylene have been shown to play an essential role in plant stress<br />

signaling [43]. A more direct correlation is evident between the level of ABA and the<br />

increasing freeze tolerance [44,45]. Exogenous application of ABA can increase<br />

freeze tolerance in both woody and herbaceous plants [46,47]. Several studies have<br />

convincingly demonstrated that exogenous application of ABA increases cold tolerance.<br />

Application of ABA at room temperature increased cold resistance in callus<br />

explants of tobacco, cucumber, winter wheat and alfalfa. Therefore, the PGPR strains<br />

capable of producing ABA can be used for protecting seedlings and plants from<br />

freeze injuries and hence can contribute to growth enhancement at low<br />

temperature.<br />

Another important factor in phytostimulation is lowering the plant ethylene level,<br />

which gets elevated during stress in plants. Higher concentrations of ethylene are<br />

inhibitive to plant growth. Any factor or stimulus that causes changes in endogenous<br />

levels of ethylene in plants leads to enhanced growth and development [43]. It has<br />

been discovered that certain microorganisms contain an enzyme, ACC deaminase,<br />

that hydrolyzes ACC into ammonia and a-ketobutyrate [48]. Hall et al. [49] reported<br />

that a soil isolate P. putida GR12-12 contains a gene for ACC deaminase, which<br />

hydrolyzes ACC, the immediate precursor of ethylene synthesized in plant tissues,

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