Orthologous proteins to Rv2135c, identified by reciprocal BLAST, are found widely in other mycobacteria as well as various taxa of bacteria, including Staphylococcus aureus and E. coli. Most of them are annotated as phosphoglycerate mutases or hypothetical proteins. It is possible that they are actually

phosphatases. Experimental characterization of a sufficiently large number of bacterial histidine https://www.selleckchem.com/products/bay-57-1293.html phosphatases will increase the accuracy of the automatic annotation systems towards a better understanding of this important group of enzymes. Methods Bacteria strains and culture conditions E. coli strain DH5α was used for the maintenance and cloning of plasmids. ICG-001 Plasmid pET23b (Novagen, USA) was used as expression vector. It contains an inbuilt optional C-terminal hexahistidine tag for ease of protein purification. E. coli BL21 (DE3) was used as recipient hosts for recombinant protein expression [61]. E. coli was grown in Luria-Bertani (LB) medium. M. tuberculosis H37Ra (ATCC 25177) was grown on Middlebrook 7H11 agar supplemented with 10% Middlebrook OADC [Oleic acid Albumin

Dextrose Catalase] Enrichment (Difco BBL, USA). M. tuberculosis genomic DNA was prepared as previously described [62]. Identification of histidine phosphatase motif in this website Rv2135c Using NCBI BLAST [35, 38], Rv2135c protein was found to be similar to proteins of histidine phosphatase superfamily. Some of the similar proteins were aligned with Rv2135c using ClustalX2 with the default parameters [37]. The similar proteins included in the alignment are some experimentally

characterized and predicted members of the superfamily. These are M. tuberculosis probable co-factor dependent phosphoglycerate mutase Rv0489 (GenBank accession number (GAN) CAE55288.1) [16], E. coli cofactor dependent phosphoglycerate mutase (E.colidpgM, Swissprot P62707), PhoE a broad specificity phosphatase from B. stearothermophilus (Protein data bank (PDB)1H2E_A) [63], Rv3214, (GAN CAE55568) a M. tuberculosis acid phosphatase [3], an acid phosphatase from Bacillus licheniformis (Bacillusap, GAN EID46354), SB-3CT newly characterized glucosyl-3-phosphoglycerate phosphatase of M. tuberculosis, Rv2419c [17] (Swissprot P71724), and Rv3837c (GAN CAB06204) an uncharacterized paralog of Rv2135c. Members of histidine phosphatase superfamily from eukaryotes, the cofactor dependent phosphoglycerate mutase of Saccharomyces arboricola (YDR051pgm) (GAN EJS44264) and phosphoglycerate mutase domain containing protein of Cryptosporidium parvum (Cryparpgm) (GAN CAD98474) were also included. Cloning of Rv2135c and Rv0489 The open reading frame of Rv2135c and Rv0489 in the virulent strain H37Rv of M. tuberculosis is completely identical to the non-virulent strain H37Ra.