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extracellular enzymes and EPS, which are the virulence factors of this bacterium. In<br />

Xcc 8004, production of extracellular enzymes and EPS has been shown to be subject<br />

to regulation <strong>by</strong> the rpf (regulation of pathogenicity factor) cluster comprising some<br />

nine genes (rpfA-I). It has indicated that Xcc appears to have a unique system for<br />

cell-to-cell signaling; it shares similarities with the system employed <strong>by</strong> V. harveyi<br />

and R. solanacearum. Most evident is that all three species appears to contain<br />

specialized two-component regulators to integrate and/or sense their respective QS<br />

signals [49,118–121].<br />

7.4.4<br />

Other <strong>Bacteria</strong><br />

7.5 Quorum-Sensing Signal Molecules in Gram-Negative <strong>Bacteria</strong>j139<br />

More than 30 species of the genus Burkholderia are described, many of which are<br />

human pathogens [68]. It has been indicated that all Burkholderia sp. investigated so<br />

far employ QS systems that relay on AHL signal molecules to express certain<br />

phenotypic traits in a population density manner.<br />

The role of the quorum-sensing system in the expression of a variety of traits was<br />

found in Pseudomonas corrugate that produce short-chain AHL quorum-sensing<br />

signal molecules. The main AHL produced was N-hexanoyl-L-homoserine lactone<br />

(C 6-AHL). These bacteria also possess an AHL quorum-sensing system designated<br />

PcoI/PcoR [122].<br />

Pomianek and Semmelhack [123] have discovered effective modulators of the<br />

autoinducer-1 circuit for bacterial quorum sensing <strong>by</strong> the synthesis and evaluation of<br />

a small library of aryl-substituted acyl-homoserine lactone analogues. This series<br />

highlights the sensitivity to structure of the contrasting responses of agonism<br />

and antagonism of the natural signal and identifies an analogue that provokes the<br />

same response as the natural signal but at 10-fold lower concentration, a<br />

superagonist .<br />

AHL signal molecules are utilized <strong>by</strong> Gram-negative bacteria to regulate gene<br />

expression in a density-dependent manner, as for example, S. liquefaciens MG1 and<br />

P. putida IsoF colonize tomato roots, produce AHL in the rhizosphere and increase<br />

systemic resistance of tomato plants against the fungal leaf pathogen, Alternaria<br />

alternata. The AHL-negative mutant S. liquefaciens MG44 was less effective in reducing<br />

symptoms and A. alternata growth. Salicylic acid (SA) levels were increased<br />

in leaves when AHL-producing bacteria colonized the rhizosphere [131].<br />

7.5<br />

Quorum-Sensing Signal Molecules in Gram-Negative <strong>Bacteria</strong><br />

Three types of autoinducers are reported in literature (i) AHL, acyl-HSL or HSL)<br />

found in Gram-negative bacteria, autoinducer peptides (AIP) in Gram-positive<br />

bacteria and autoinducer-2 compounds (AI-2s), which are found in Gram-negative<br />

and Gram-positive bacteria. Some of the common signal molecules are listed in<br />

Table 7.2.

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