7.1.19] Nitrosococcus oceani 78 402 2e-110 PD739884, PD015803, pfam00485, COG3954 ACK79243.1 ynbD Phosphosterase, PA-phosphatase Polaromonas naphthalenivorans 81 759 1e-81 PD589889, pfam 01569, COG0474, CD03386, CD00127 * The sequence and annotation of the complete A. ferrooxidans strain ATCC 23270 genome

is available at the Comprehensive Microbial Resource (CMR) (J. Craig Venter Institute, http://​www.​jcvi.​org) and in GenBank/EMBL/DDBJ accession number CP001219. a Proposed eFT508 research buy gene name. b Proposed enzyme activity with EC number if available c Organism with the best BlastP hit to the candidate gene. d Percentage of similarity (% Sim) of candidate gene to that found in the organism listed in row (c). e Score of BlastP match. f E value of BlastP match. g Motif and domains identified in the candidate

proteins: CD, Conserved Domains; COG, Clusters of Orthologous Groups of Proteins; Pfam, protein families; PD, Prodom (protein domains); PS, Prosite tat signal peptide Three additional gene clusters termed cbb2 (four genes), cbb3 (twelve Selleckchem CH5424802 genes) and cbb4 (five genes) were identified that are predicted to encode functions related to CO2 fixation and central carbon metabolism (Table 3). RT-PCR experiments revealed that gene clusters cbb2, cbb3 and cbb4 are transcribed as single units, respectively, and thus constitute operons (Figure 2B-D). cbb2 contains genes (cbbL2 and cbbS2) encoding additional copies of the large and small subunit of form IAq RubisCO and associated RubisCO activation genes (cbbQ2 and cbbO2) (Figure 2B). The deduced amino acid sequences of these genes are similar but not identical to the corresponding proteins encoded in the cbb1 operon; CbbL1 and CbbL2 exhibit 84% amino acid sequence identity, whereas CbbS1 and CbbS2 share 56% identity

and CbbQ1 and CbbO1 have 84% and 59% identity with CbbQ2 and CbbO2, respectively. Genes predicted to be encoded by operons cbb3 and cbb4 are listed in Table 3 and their organization within these operons is shown in Figure 2. The two enzymes that are unique to the CBB cycle are RubisCO (encoded by operons cbb1 and cbb2) and phosphoribulokinase (encoded by operon cbb4). RuBisCO selleck inhibitor catalyzes the Ureohydrolase first step of the cycle, the carboxylation of ribulose-1,5-bisphosphate (RuBP) with CO2. Phosphoribulokinase catalyzes the last step of the cycle which is the regeneration of the CO2 acceptor molecule, RuBP, by phosphorylation of ribulose 5-phosphate with ATP. Other steps of the cycle, encoded in operon cbb3, are catalyzed by enzymes common to glycolytic and gluconeogenic pathways in central carbon metabolism [8, 36]. Promoters of the σ70-type and rho-independent transcriptional stops were predicted for operons cbb1-4 (Figure 2). In addition, potential CbbR-binding sites were identified in the four operons based on the detection of conserved TNA-N7-TNA and T-N11-A motifs described above for operon cbb1 (Figure 2).