thaliana. Upon infection of cabbage plants it causes the black rot disease. In non-host plants like pepper (Capsicum annuum) and tobacco (Nicotiana tabacum), however, it induces an HR. For X. campestris pv. campestris, LPSs [26–29], as well as muropeptides [30], fragments of the bacterial cell wall material peptidoglycan, have been characterized as MAMPs. Non-host resistance of plants towards X. campestris pv. campestris seems to be a very complex situation, where multiple elicitors are
active in parallel [26, 31]. The genetic analyses performed during the last years identified several gene loci that are linked to the pathogenicity of X. campestris pv. campestris in host plants and to the induction of a resistance response in non-host plants. Protein secretion systems, in particular the type III secretion system, have an important role in the pathogenic interactions with plants [32–35]. Further virulence factors are exported by type II secretion systems [32, 36]. They BIBF1120 are involved in the secretion of extracellular selleckchem enzymes including plant cell wall degrading enzymes like selleck chemicals llc pectate lyases (EC 4.2.2.2), also known as polygalacturonate lyases [37–40], or polygalacturonases (EC 3.2.1.15) [40, 41]. Pectate lyases catalyze the cleavage of α1,4 glycosidic bonds between galacturonic acid residues of homogalacturonans. Likewise, polygalacturonases catalyze
the cleavage of the glycosidic bonds between adjacent galacturonic acid residues, but the hydrolysis of the glycosidic linkage results in the addition of a water molecule from the environment. Genome data which are now available for several strains have further added to our understanding of pathogenicity loci in X. campestris[42–47]. More information can be derived from closely related pathogens like Xylella fastidiosa, where a polygalacturonase has been characterized that is similar to the pglA2 gene product of X. campestris pv. campestris B100 [48]. Rapid progress is currently achieved in identifying and analyzing regulation in X. campestris[49–52]. Concerning signal transduction, there has been substantial advancement of science related to two complex systems of cell-cell communication that employ
a diffusible signal factor (DSF) [53] and a diffusible factor (DF) [54], respectively. In addition, more and more X. campestris Etoposide solubility dmso two-component systems signal-transduction systems are characterized experimentally [55–58]. In previous analyses, the X. campestris pv. campestris tonB gene cluster showed some very interesting characteristics. TonB systems of Gram-negative bacteria are multi-component transport systems that perform the specific active uptake of various compounds across the outer membrane [59]. These systems consist of the core components TonB, ExbB, and ExbD, which are located at or within the inner membrane, and variable so-called TonB-dependent receptors, which are located in the outer membrane, and which are specific for the imported substrate [60].