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Complete genome sequence of Rhodospirillum rubrum type strain (S1T)
Standards in Genomic Sciences volume 4, pages293–302 (2011)
Rhodospirillum rubrum (Esmarch 1887) Molisch 1907 is the type species of the genus Rhodospirillum, which is the type genus of the family Rhodospirillaceae in the class Alphaproteobacteria. The species is of special interest because it is an anoxygenic phototroph that produces extracellular elemental sulfur (instead of oxygen) while harvesting light. It contains one of the most simple photosynthetic systems currently known, lacking light harvesting complex 2. Strain S1T can grow on carbon monoxide as sole energy source. With currently over 1,750 PubMed entries, R. rubrum is one of the most intensively studied microbial species, in particular for physiological and genetic studies. Next to R. centenum strain SW, the genome sequence of strain S1T is only the second genome of a member of the genus Rhodospirillum to be published, but the first type strain genome from the genus. The 4,352,825 bp long chromosome and 53,732 bp plasmid with a total of 3,850 protein-coding and 83 RNA genes were sequenced as part of the DOE Joint Genome Institute Program DOEM 2002.
Strain S1T (= ATCC 11170 = DSM 467) is the neotype strain of the species Rhodospirillum rubrum, which is the type species of the genus Rhodospirillum. The genus name is derived from the ancient Greek term rhodon, meaning rose, and the Latin spira, meaning coil. Rubrum is Latin for red. Currently R. rubrum is one out of only four species with a validly described name in this genus. Strain S1T (van Niel) was designated as the neotype strain for R. rubrum by Pfennig and Trüper in 1971 , with the description of the strain in complete agreement with the species description given by van Niel in 1944  for the initial deposition at the American Type Culture Collection (ATCC). A comparative genomic analysis with the only other publicly available rhodospirillal genome was recently published by Lu et al. . Here we present a summary classification and a set of features for R. rubrum S1T, together with the description of the complete genomic sequencing and annotation.
Classification and features
Figure 1 shows the phylogenetic neighborhood of R. rubrum S1T in a 16S rRNA based tree. The sequences of the four 16S rRNA gene copies in the genome do not differ from each other, and do not differ from the previously published 16S rRNA sequence (X87278), which contains two ambiguous base calls.
A representative genomic 16S rRNA sequence of strain S1T was compared using NCBI BLAST under default settings (e.g., considering only the high-scoring segment pairs (HSPs) from the best 250 hits) with the most recent release of the Greengenes database  and the relative frequencies, weighted by BLAST scores, of taxa and keywords (reduced to their stem ) were determined. The five most frequent genera were Rhizobium (41.6%), Rhodospirillum (30.8%), Aquaspirillum (6.2%), Rhodocista (4.2%) and Novosphingobium (3.5%) (130 hits in total). Regarding the 16 hits to sequences from members of the species, the average identity within HSPs was 98.5%, whereas the average coverage by HSPs was 97.8%. Regarding the five hits to sequences from other members of the genus, the average identity within HSPs was 95.3%, whereas the average coverage by HSPs was 95.0%. Among all other species, the one yielding the highest score was Rhodospirillum photometricum, which corresponded to an identity of 96.0% and an HSP coverage of 96.9%. (Note that the Greengenes database uses the INSDC (= EMBL/NCBI/DDBJ) annotation, which is not an authoritative source for nomenclature or classification.) The highest-scoring environmental sequence was AM691104 (‘Rhodobacteraceae clone EG16’), which showed an identity of 91.7% and an HSP coverage of 97.2%. The five most frequent keywords within the labels of environmental samples which yielded hits were ‘ocean’ (2.5%), ‘microbi’ (2.4%), ‘soil’ (2.1%), ‘skin’ (1.8%) and ‘aquat/rank’ (1.8%) (120 hits in total). Environmental samples which yielded hits of a higher score than the highest scoring species were not found.
Cells of R. rubrum stain Gram-negative, are motile, vibrioid to short spiral-shaped with a size of 0.8–1 µm (Figure 2). Colonies are purple-colored because the cells contain a carotenoid pigment required to gather light energy for photosynthesis. R. rubrum does not produce oxygen, but elemental sulfur as a by-product of photosynthesis, using bacteriochlorophyll, which enables the absorbtion of light at wavelengths longer than those absorbed by plants. Strain S1T is a facultative anaerobe that uses alcoholic fermentation under low oxygen conditions, but respiration under aerobic conditions. Photosynthesis is genetically suppressed under aerobic conditions; R. rubrum is colorless under these conditions. The regulation of the photosynthetic machinery is still poorly understood, though the organism is phototactic . The RuBisCO (Ribulose-1,5-bisphosphate carboxylase oxygenase) of R. rubrum is highly unusual in its simplicity as a homodimer .
R. rubrum is a well-established model organism for studies on nitrogen fixation and the organism possesses two related but distinct nitrogenase systems that utilize distinct metals at the active site . The post-translational regulation of nitrogenase in R. rubrum is relatively unusual in that it utilizes a reversible ADP-ribosylation process [31–35]. The organism has also been used to study bacterial growth on carbon monoxide as an energy source , and its carbon monoxide sensor, termed CooA, has been the paradigm for such sensors . R. rubrum provides several potential biotechnological applications, e.g. the accumulation of PHB precursors for plastic production in the cell, as well as the production of hydrogen fuel.
The composition of the R. rubrum cell wall has previously been reported in various publications. The main fatty acids of strain S1T are unbranched, with unsaturated acids C16:1 w7c (34.1%), C18:1 w7c/12t/9t (32.8%) and C18:1 2OH (6.9%) dominating over a minority of saturated acids: C16:0 (11.6%) and C14:0 (4.0%) [analyzed with a culture of CCUG 17859, http://www.ccug.se].
Genome sequencing and annotation
Genome project history
This organism was selected for sequencing on the basis of the DOE Joint Genome Institute Program DOEM 2002. The genome project is deposited in the Genomes On Line Database  and the complete genome sequence is deposited in GenBank. Sequencing, finishing and annotation were performed by the DOE Joint Genome Institute (JGI). A summary of the project information is shown in Table 2.
The history of strain S1T starts with C. B. van Niel (strain ATH 1.1.1, probably 1941) → S.R. Elsden strain S1 → NCI(M)B 8255 → ATCC 11170, from which later on DSM 467, LMG 4362 and CCRC 16403 were derived.
Growth conditions and DNA isolation
The culture of strain S1T, ATCC 11170, used to prepare genomic DNA (gDNA) for sequencing was only 3 transfers away from the original deposit. The culture used to prepare genomic DNA (gDNA) for sequencing, was purified from the original deposit on rich SMN  plates, and then grown in SMN liquid medium aerobically. MasterPure Genomic DNA Purification Kit from Epicentre (Madison, WI) was used for total DNA isolation from R. rubrum, with a few minor modifications as described previously . One-half to 1 ml of cells was used for DNA isolation. After isopropanol precipitation, DNA was resuspended in 500 µl of 0.1 M sodium acetate and 0.05 M MOPS (pH 8.0), then reprecipitated with 2 volume of ethanol. This step was repeated twice and significantly improved the quality of DNA. The purity, quality and size of the bulk gDNA preparation were assessed by JGI according to DOE-JGI guidelines.
Genome sequencing and assembly
The genome was sequenced using the Sanger sequencing platform (3 kb and 40 kb DNA libraries). All general aspects of library construction and sequencing performed at the JGI can be found at . The Phred/Phrap/Consed  software package was used for sequence assembly and quality assessment. After the shotgun stage, reads were assembled with parallel phrap (High Performance Software, LLC). Possible mis-assemblies were corrected with Dupfinisher or transposon bombing of bridging clones (Epicentre Biotechnologies, Madison, WI) . Gaps between contigs were closed by editing in Consed, custom primer walk or PCR amplification. A total of 847 additional custom primer reactions were necessary to close gaps and to raise the quality of the finished sequence. The completed genome sequence contains 62,976 reads, achieving an average of 11-fold sequence coverage with an error rate of less than 1 in 50,000.
Genes were identified using two gene modeling programs, Glimmer  and Critica  as part of the Oak Ridge National Laboratory genome annotation pipeline. The two sets of gene calls were combined using Critica as the preferred start call for genes with the same stop codon. Genes with less than 80 amino acids which were predicted by only one of the gene callers and had no Blast hit in the KEGG database at 1e-05, were deleted. This was followed by a round of manual curation to eliminate obvious overlaps. The predicted CDSs were translated and used to search the National Center for Biotechnology Information (NCBI) nonredundant database, UniProt, TIGRFam, Pfam, PRIAM, KEGG, COG, and InterPro databases. These data sources were combined to assert a product description for each predicted protein. Non-coding genes and miscellaneous features were predicted using tRNAscan-SE , TMHMM , and signalP . Additional gene prediction analysis and manual functional annotation was performed within the Integrated Microbial Genomes (IMG) platform developed by the Joint Genome Institute, Walnut Creek, CA, USA .
The genome consists of a 4,352,825 bp long chromosome with a 65% G+C content and a 53,732 bp plasmid with 60% G+C content (Table 3 and Figure 3). Of the 3,933 genes predicted, 3,850 were protein-coding genes, and 83 RNAs; nine pseudogenes were also identified. The majority of the protein-coding genes (72.7%) were assigned a putative function while the remaining ones were annotated as hypothetical proteins. The distribution of genes into COGs functional categories is presented in Table 4.
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We would like to gratefully acknowledge the help of Brian J. Tindall and his team (DSMZ) for growing a R. rubrum culture for the EM image. The work conducted by the U.S. Department of Energy Joint Genome Institute was supported by the Office of Science of the U.S. Department of Energy under Contract No. DE-AC02-05CH11231, and was also supported by NIGMS grant GM65891 to G. P. R.