Because of the highly distinctive morphology of C. aureus and the precautions taken, the possibility of contamination is exceedingly low. Genomic DNA was extracted from the cells using MasterPure Complete DNA and RNA purification Kit (Epicentre, WI, USA).

The polymerase chain reaction (PCR) was performed using a total volume of 25 μl and the PuRe Taq Ready-To-Go PCR beads kit (GE Healthcare, Buckinghamshire, UK). Nearly the entire SSU rRNA gene was amplified from genomic DNA using eukaryotic universal primers (PF1: 5′-GCGCTACCTGGTTGATCCTGCCAGT-3′ and R4: 5′-GATCCTTCTGCAGGTTCACCTAC-3′). The PCR protocol had an initial denaturation stage at 95°C for 2 min; 35 cycles involving 94°C for 45 s (denaturation), 55°C for 45 s (annealing), and 72°C for 1.5 min (extension); selleck inhibitor and final extension at 72°C for 5 min. The amplified DNA fragments were purified from agarose gels

using UltraClean 15 DNA Purification Kit (MO Bio, CA, USA), and then cloned into the TOPO TA Cloning Kit (Invitrogen, CA, USA). The C. aureus sequence was deposited in DDBJ/EMBL/GenBank under the accession number EU753419. The SSU rRNA sequence of C. aureus was visually aligned with taxa representing all of the major groups of eukaryotes, forming (i) a 38-taxon alignment with ambiguously aligned regions excluded (988 unambiguously aligned positions). In order to more STI571 order comprehensively CH5183284 solubility dmso evaluate the phylogenetic position of C. aureus within the Euglenozoa, we analyzed three additional datasets: (ii) a 35-taxon alignment of euglenozoan sequences and ten relatively Morin Hydrate short environmental sequences (760 unambiguously aligned positions); (iii) a 29-taxon alignment of euglenozoan sequences including three fast-evolving euglenid sequences – namely Astasia torta (AF403152), Menoidium bibacillatum (AF247598) and Ploeotia costata (AF525486) – and excluding the short environmental

sequences (734 unambiguously aligned positions); and (iv) a 25-taxon alignment of euglenozoan sequences excluding both the short environmental sequences and the fastest-evolving euglenid sequences (1025 unambiguously aligned positions). The highly divergent sequences from phagotrophic euglenids produced a large number of ambiguously aligned regions in the 35-taxon and 29-taxon alignments; accordingly, these regions were excluded from our analyses. PhyML [16] was used to analyze all four datasets (one heuristic search per dataset) with maximum-likelihood (ML) using a general-time reversible (GTR) model of base substitutions [17] that incorporated invariable sites and a discrete gamma distribution (eight categories) (GTR + I + G model). The GTR model was selected using the program MrAIC 1.4.3 with PhyML http://​www.​abc.​se/​~007E;nylander/​mraic/​mraic.​html. Model parameters were estimated from each of the original datasets.