For quantitative analysis, tridecanoic acid was used as an internal standard. All determinations were performed in triplicate experiments. The data were recorded as means and SDs. The polysaccharide was isolated from freeze-dried cells using the classical alkali treatment as has been reported previously

(Elbein & Mitchell, 1973; Gunja-Smith et al., 1977; Lillie & Pringle, 1980; Lou et al., 1997), and visualized using a TLC method (Seibold & Eikmanns, 2007). Total CYC202 concentration polysaccharide was determined using the phenol–sulfuric acid method (Dubois et al., 1956). For quantitative analysis, the extracted polysaccharide was digested with α-amylase (; 10 IU mg−1 of dried polysaccharide; Sigma) and amyloglucosidase (; 20 IU mg−1 of dried polysaccharide; Sigma) in 50 mM sodium acetate buffer (pH 5) at 55 °C for 3–4 h and with gentle vortexing. Commercial glycogen standard (1 mg mL−1) was used as a control

for enzymatic hydrolysis. The amount of glucose formed under these conditions was taken as a measure of glycogen in cells. Glucose was determined using a specific glucose oxidase method (Keston, 1956). All determinations were performed in triplicate experiments. The data were recorded Navitoclax chemical structure as means and SDs. Various genomic databases of Rhodococcus strains are now available for public research. Among them, the genome sequence of R. jostii strain RHA1 has been the first sequence publicly available for the screening and identification of genes and metabolic pathways (http://www.ncbi.nlm.nih.gov/genomes/lproks.cgi). Recently, we identified six putative genes (glgA, glgB, glgC, glgE, glgP and glgX) involved in glycogen biosynthesis and mobilization in a genome-wide bioinformatic study of the genomic database Montelukast Sodium of strain RHA1 (Hernández et al., 2008). Using these RHA1 sequences, we performed a genome-wide examination of key genes involved in glycogen metabolism in the available databases of R. opacus B4, Rhodococcus erythropolis PR4 and R. erythropolis SK121. The degree of identity of full protein sequences of these species is shown in Table 2. In all cases, a high identity between orthologous

proteins was observed. In general, we observed similar gene arrangements in all strains, with little differences. The glgB, glgE and glgP genes occurred in a cluster, whereas glgA and glgC were adjacent and clustered in the opposite orientation. Only in the R. erythropolis SK121 genome was a gene coding for a putative O-methyltransferase enzyme found between glgA and glgC. Finally, glgX was located in a separate cluster associated with another carbohydrate metabolism gene, which encodes a putative 1–4-α-d-glucan 1-α-d-glucosylmutase (also called maltooligosyl trehalose synthase) in the genome of all the strains studied. These results suggested that the different strains possess the genetic potential to synthesize and mobilize glycogen.