In addition selleckchem to GlxR, two additional transcriptional regulators, RamB and RamA, are also involved in regulating the expression of aceB and aceA (Gerstmeir et al., 2004; Cramer et al., 2006). However,

in contrast to RamB, which only represses aceB and aceA genes in the presence of glucose, GlxR repressed both genes, regardless of the carbon source. RamA is an activator of aceB and aceA in the presence of acetate (Arndt & Eikmanns, 2008). The involvement of the three regulators GlxR, RamA and RamB or even more regulator(s) in the same aceB–aceA intergenic region would appear to make the regulation of both genes more complex (Cramer et al., 2006). The crp gene from S. coelicolor successfully complemented check details the glxR mutant of C. glutamicum; thus, the growth defect phenotype was restored to that of the wild type. Derouaux et al. (2004b) suggested that the CRP homologues of the actinomycetes species, including S. coelicolor, C. glutamicum and mycobacterial strains, belong to the same CRP subgroup under the large CRP–FNR superfamily. Interestingly, Derouaux et al. (2004a) also reported that the CRP of S. coelicolor does not play any role in CCR, and yet modulates complex physiological processes such as germination

and morphological development, via a Cya– cAMP–CRP system. Based on the classification of both CRPs under the same CRP subfamily and successful complementation, there is a strong possibility of functional similarities between the two CRP homologues from C. glutamicum and S. coelicolor, even though C. glutamicum does not have any developmental processes, such as morphological differentiation. As in the case of S. coelicolor, the growth defect phenotype of the glxR mutant indicates that GlxR plays an important role in cell viability. Based on physiological and molecular genetic studies, and bioinformatic analyses of the whole genome sequence of C. glutamicum, it would appear that the molecular mechanism of global carbon regulation such as CCR is quite different from that in Gram-negative or low GC Gram-positive bacteria (Moon et al., 2007; Arndt & Eikmanns, 2008; Cha et al., 2010). The first report of CCR in C. glutamicum was related

to glutamate uptake (Krämer & Lambert, 1990; Kronemeyer et al., 1995). However, there is no in vivo experimental evidence that GlxR is involved in the catabolite Thiamet G repression of glutamate uptake. The derepression of pgluA-lacZ in the glxR mutant in the glucose medium suggests that the gluABCD operon is repressed by GlxR. In C. glutamicum, the enzymes involved in gluconate catabolism (gntP and gntK), phosphoenolpyruvate carboxykinase (pck) and alcohol dehydrogenase (adhA), are also subjected to CCR by glucose (Letek et al., 2006; Han et al., 2007; Kohl et al., 2008). The presence of potential GlxR-binding sites (TGTGA-N6-TCACA) in the promoter regions of the genes encoding these enzymes indicates that GlxR is a repressor of these genes.