Complete genome sequence of Dyadobacter fermentans type strain (NS114T)

Dyadobacter fermentans (Chelius and Triplett, 2000) is the type species of the genus Dyadobacter. It is of phylogenetic interest because of its location in the Cytophagaceae, a very diverse family within the order ‘Sphingobacteriales’. D. fermentans has a mainly respiratory metabolism, stains Gram-negative, is non-motile and oxidase and catalase positive. It is characterized by the production of cell filaments in aging cultures, a flexirubin-like pigment and its ability to ferment glucose, which is almost unique in the aerobically living members of this taxonomically difficult family. Here we describe the features of this organism, together with the complete genome sequence, and its annotation. This is the first complete genome sequence of the sphingobacterial genus Dyadobacter, and this 6,967,790 bp long single replicon genome with its 5804 protein-coding and 50 RNA genes is part of the Genomic Encyclopedia of Bacteria and Archaea project.


Introduction
Strain NS114 T (= DSM 18053 = ATCC 700827 = CIP 107007) is the type strain of Dyadobacter fermentans, which is the type species of the genus Dyadobacter. D. fermentans was described by Chelius and Triplett in 2000 [1] as mainly aerobic, but also able to grow by fermentation of glucose, Gram negative and nonmotile. The organism is of significant interest for its position in the tree of life, because the genus Dyadobacter (currently seven species, Figure 1) is rather isolated within the family Cytophagaceae [6], as it has less than 88% similarity of the 16S rRNA gene sequence to any other bacteria with standing in nomenclature, with Persicitalea and Runella as closest neighboring genera. Here we present a summary classification and a set of features for D. fermentans, strain NS114 T together with the description of the complete genomic sequencing and annotation.

Classification and features
Strain NS114 T was isolated in a study on the endophytic community of maize plants, where bacteria were isolated from plants which had been grown using surface sterilized seeds in autoclaved synthetic soil in greenhouses [1]. Plant stems were surface sterilized and crushed prior to plating. The organism was found in stem tissues of plants which were cultivated on a nitrogen-free nutrient solution, but not in the nitrogen-fertilized counterparts. The type strain of Runella zeae (NS12 T ) was co-isolated from the same material, although no microscopic evidence has been presented to date that members of these species were living within the plant tissue [1]. Members of the species D. fermentans were regularly found in cysts of the soybean nematode Heterodera glycines [12]. D. fermentans was also isolated from contaminated soil as a result of its ability to grow on 7,8-benzoquinoline [9], a nitrogencontaining heterocyclic aromatic hydrocarbon (azaarene) widely distributed in products of incomplete combustion processes, with toxic and cancerogenic effects. Two isolates from a lime stone cavern in Arizona share significant 16S rRNA gene sequence similarity of 98% (DQ207364 and DQ207362). Only a few closely related phylotypes from environmental samples and global surveys are recorded to be highly related to D. fermentans, a fact suggesting that members of this taxon are not very abundant: three clones of uncultured bacteria of a deep sea sediment collected at the Western Tropical Pacific Warm Pool in the Pacific Ocean (AM085468, AM085473 and AM085489) and one of the activated sludge of a membrane bioreactor (EU283373) are recorded (as of May 2009). Intrageneric similarity within the genus Dyadobacter is rather low [13]. D. fermentans has been recognized by its flexirubin-like yellow pigment and by its growth as flocculent filaments of ovoid rods in old cultures Table  1 [1]. The rod-shaped cells of strain NS114 T occur polarly attached in groups of 2-4 cells during logarithmic growth, cells being frequently arranged at an angle to give V-formations. As the culture ages, irregular filaments or ovoid rods form ( Figure 2) which sediment as fluffs in liquid culture [1]. The cells are Gram negative, non-motile and nonsporulating, oxidase and catalase positive. Like many plant associated bacteria, strain NS114 T produces copious amounts of slime when grown on nitrogen-limited agar. The organism grows aerobically, however it is also reported to be able to ferment glucose and sucrose in the O/F-test in Hugh-Leifson medium [1,13], which according to our own observations might be an experimental artifact due to prolonged incubation. The colony color of strain NS114 T is yellow to orange [1,13]. The absorbance maximum of an ethanol extract of the cells is at 450 nm, and the absorbance peak broadens under alkaline conditions, which is a typical feature of flexirubin-like pigments [1]. This pigment was found in all six species of the genus Dyadobacter thus confirming that the presence of the pigment is a property of the genus [14][15][16][17][18]. Figure 1 shows the phylogenetic neighborhood of D. fermentans strain NS114 T in a 16S rRNA based tree. Analysis of the four 16S rRNA gene sequences in the genome of strain NS114 T indicated that three copies are almost identical, and one differs by seven nucleotides from these. The sequences of the three identical 16S rRNA genes differ by two nucleotides from the previously published 16S rRNA sequence generated from DSM 18053 (AF137029). The slight differences between the genome data and the reported 16S rRNA gene sequence are probably the result of sequencing errors in the previously reported sequence data.

Chemotaxonomy
The whole cell fatty acid pattern of strain NS114 T is dominated by unsaturated, and saturated isobranched, straight chain unsaturated and large amounts of iso-branched, hydroxylated species. Major components are iso-C15:0-2OH and/or C16:1ω7c (43.5%), C16:1 ω5c (17.5%) and iso-C15:0 (16.8). Considerable amounts of the 3hydroxylated fatty acids iso-C15:0-3OH, C16:0-3OH and iso-C17:0 -3OH are detected [1]. The quinone composition has not been investigated for strain NS114 T . The main component reported for the closely related type strains of D. ginsengisoli and D. alkalitolerans is menaquinone MK-7 [16,18]. Cells of strain NS114 T contain spermidine as the major cellular polyamine and putrescine, cadaverine and spermine as minor components. The latter compound was not detected in any of the three other strains studied to date of the family Cytophagaceae, representing Flexibacter flexilis, Microscilla marina, and D. beijingensis [19]. The polar lipid composition has not been investigated in either this strain or other members of the genus Dyadobacter.

Genome sequencing and annotation Genome project history
This organism was selected for sequencing on the basis of its phylogenetic position, and is part of the Genomic Encyclopedia of Bacteria and Archaea project. The genome project is deposited in the Genomes OnLine Database [5] and the complete genome sequence 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 Growth conditions and DNA isolation D. fermentans NS114 T , DSM18053, was grown in DSMZ medium 830 (R2A Medium) at 28°C [20]. DNA was isolated from 1-1.5 g of cell paste using Qiagen Genomic 500 DNA Kit (Qiagen, Hilden, Germany) with a modified protocol (FT) for cell lysis as described in Wu et al. [21]. Evidence codes -IDA: Inferred from Direct Assay (first time in publication); TAS: Traceable Author Statement (i.e., a direct report exists in the literature); NAS: Non-traceable Author Statement (i.e., not directly observed for the living, isolated sample, but based on a generally accepted property for the species, or anecdotal evidence). These evidence codes are from the Gene Ontology project [11]. If the evidence code is IDA the property was directly observed for a living isolate by one of the authors or an expert mentioned in the acknowledgements.

Genome sequencing and assembly
The genome was sequenced using a combination of 8 kb and fosmid DNA libraries. All general aspects of library construction and sequencing performed at the JGI can be found at the JGI website (http://www.jgi.doe.gov). Draft assemblies were based on 86,260 total reads. The Phred/-Phrap/Consed software package was used for sequence assembly and quality assessment [22][23][24]. After the shotgun stage, reads were assembled with parallel phrap. Possible mis-assemblies were corrected with Dupfinisher or transposon bombing of bridging clones [25]. Gaps between contigs were closed by editing in Consed, custom primer walk or PCR amplification. A total of 1,042 additional reactions were necessary to close gaps and to raise the quality of the finished sequence. The error rate of the completed genome sequence is less than 1 in 100,000. Together all libraries provided 10.6x coverage of the genome.

Genome annotation
Genes were identified using Prodigal [26] as part of the Oak Ridge National Laboratory genome an-notation pipeline , followed by a round of manual curation using the JGI GenePRIMP pipeline [27]. The predicted CDSs were translated and used to search the National Center for Biotechnology Information (NCBI) nonredundant database, Uni-Prot, TIGRFam, Pfam, PRIAM, KEGG, COG, and In-terPro databases. Additional gene prediction analysis and manual functional annotation was performed within the Integrated Microbial Genomes Expert Review (IMG-ER) platform [28].

Genome properties
The genome is 6,967,790 bp long and comprises one main circular chromosome with a 51.4% GC content (Table 3, Figure 3). Of the 5,854 genes predicted, 5,804 were protein coding genes, and 50 were RNAs. In addition, 85 pseudogenes were identified. The majority of the protein-coding genes (64.7%) were assigned with a putative function while those remaining were annotated as hypothetical proteins. The properties and the statistics of the genome are summarized in Table 3. The distribution of genes into COG functional categories is presented in Table 4.