Genome sequence of the ocean sediment bacterium Saccharomonospora marina type strain (XMU15T)

Saccharomonospora marina Liu et al. 2010 is a member of the genus Saccharomonospora, in the family Pseudonocardiaceae that is poorly characterized at the genome level thus far. Members of the genus Saccharomonospora are of interest because they originate from diverse habitats, such as leaf litter, manure, compost, surface of peat, moist, over-heated grain, and ocean sediment, where they might play a role in the primary degradation of plant material by attacking hemicellulose. Organisms belonging to the genus are usually Gram-positive staining, non-acid fast, and classify among the actinomycetes. Here we describe the features of this organism, together with the complete genome sequence (permanent draft status), and annotation. The 5,965,593 bp long chromosome with its 5,727 protein-coding and 57 RNA genes was sequenced as part of the DOE funded Community Sequencing Program (CSP) 2010 at the Joint Genome Institute (JGI).


Introduction
Strain XMU15 T (= DSM 45390 = KCTC 19701 = CCTCC AA 209048) is the type strain of the species Saccharomonospora marina [1], one of nine species currently in the genus Saccharomonospora [2]. The strain was originally isolated from an ocean sediment sample collected from Zhaoan Bay, East China Sea, in 2005 [1]. The genus name Saccharomonospora was derived from the Greek words for sakchâr, sugar, monos, single or solitary, and spore, a seed or spore, meaning the sugar (containing) single-spored (organism) [3]; the species epithet was derived from the Latin adjective marina, of the sea, referring to the origin of the strain [1]. S. marina and the other type strains of the genus Saccharomonospora were selected for genome sequencing in one of the DOE Community Sequencing Projects (CSP 312) at Joint Genome Institute (JGI), because members of the genus (which originate from diverse habitats, such as leaf litter, manure, compost, surface of peat, moist, over-heated grain and ocean sediment) might play a role in the primary degradation of plant material by attacking hemicellulose. This expectation was underpinned by the results of the analysis of the genome of S. viridis [4], one of the recently sequenced GEBA genomes [5]. The S. viridis genome, the first sequenced genome from the genus Saccharomonospora, contained an unusually large number (24 in total) genes for glycosyl hydrolases (GH) belonging to 14 GH families, which were identified in the Carbon Active Enzyme Database [6]. Hydrolysis of cellulose and starch were also reported for other members of the genus (that are included in CSP 312), including S. marina [1], S. halophila [7], S. saliphila [8], S. paurometabolica [9], and S. xinjiangensis [10]. Here we present a summary classification and a set of features for S. marina XMU15 T , together with the description of the genomic sequencing and annotation.

Classification and features
A representative genomic 16S rRNA sequence of S. marina XMU15 T was compared using NCBI BLAST [11,12] 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 [13] and the relative frequencies of taxa and keywords (reduced to their stem [14]) were determined, weighted by BLAST scores. The most frequently occurring genera were Gordonia (63.5%), Saccharomonospora (24.1%), Actinomycetospora (4.5%), Actinopolyspora (1.8%) and Pseudonocardia (1.4%) (195 hits in total). Regarding the single hit to sequences from members of the species, the average identity within HSPs was 99.7%, whereas the average coverage by HSPs was 100.1%. Regarding the 23 hits to sequences from other members of the genus, the average identity within HSPs was 96.1%, whereas the average coverage by HSPs was 98.3%. Among all other species, the one yielding the highest score was Saccharomonospora saliphila (HM368568), which corresponded to an identity of 99.9% and an HSP coverage of 92.1%. (Note that the Greengenes database uses the INSDC (= EMBL/NCBI/DDBJ) annotation, which is not an authoritative source for nomenclature or classification. For instance, the Gordonia hits are likely to be caused by misannotations in INSDC). The highest-scoring environmental sequence was FN667533 ('stages composting process pilot scale municipal drum compost clone PS3734'), which showed an identity of 96.0% and a HSP coverage of 97.9%. The most frequently occurring keywords within the labels of all environmental samples which yielded hits were 'skin' (6.3%), 'forearm' (2.8%), 'soil' (2.6%), 'fossa' (2.5%) and 'volar' (2.3%) (55 hits in total). These keywords do not fit to the known habitat of strain XMU15 T , because Saccharomonospora rarely occurs in environmental samples so that more distant relatives (here from human skin) distort the automatically generated list of keywords. Environmental samples which yielded hits of a higher score than the highest scoring species were not found. . Non-motile, smooth or wrinkled spores were observed on the aerial mycelium, occasionally in short spore chains [1]. The growth range of strain XMU15 T spans from 28-37°C, with an optimum at 28°C, and pH 7.0 on ISP 2 medium [1]. Strain XMU15 T grows well in up to 5% NaCl, with an optimum at 0-3% NaCl [1]. Substrates used by the strain are summarized in the strain description [1].

Genome sequencing and annotation Genome project history
This organism was selected for sequencing as part of the DOE Joint Genome Institute Community Sequencing Program (CSP) 2010, CSP 312, "Whole genome type strain sequences of the genus Saccharomonospora -a taxonomically troubled genus with bioenergetic potential". The genome project is deposited in the Genomes On Line Database [21] 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.  [15,16] of the 16S rRNA gene sequence under the maximum likelihood (ML) criterion [17]. Rooting was done initially using the midpoint method [18] and then checked for its agreement with the current classification ( Table 1). The branches are scaled in terms of the expected number of substitutions per site. Numbers adjacent to the branches are support values from 600 ML bootstrap replicates [19] (left) and from 1,000 maximum-parsimony bootstrap replicates [20] (right) if larger than 60%. Lineages with type strain genome sequencing projects registered in GOLD [21] are labeled with one asterisk, those also listed as 'Complete and Published' with two asterisks [4,22,23], with S. azurea missing second asterisk but published in this issue [24]. Actinopolyspora iraqiensis Ruan et al. 1994 [25] was ignored in the tree. The species was proposed to be a later heterotypic synonym of S. halophila [26], although the name A. iraqiensis would have had priority over S. halophila. This taxonomic problem will soon be resolved with regard to the genomes of A. iraqiensis and S. halophila, which were both part of CSP 312. Standards in Genomic Sciences  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. If the evidence code is IDA, then the property was directly observed for a living isolate by one of the authors or an expert mentioned in the acknowledgements [38]. [39] at 28°C. DNA was isolated from 0.5-1 g of cell paste using Jetflex Genomic DNA Purification Kit (GENOMED 600100) following the standard protocol as recommended by the manufacturer with the following modifications: extended cell lysis time (60 min.) with additional 30µl achromopeptidase, lysostaphin, mutanolysin; proteinase K was added at 6-fold the supplier recommended amount for 60 min. at 58°C. The purity, quality and size of the bulk gDNA preparation were assessed by JGI according to DOE-JGI guidelines. DNA is available through the DNA Bank Network [40].

Genome sequencing and assembly
The genome was sequenced using a combination of Illumina and 454 sequencing platforms. All general aspects of library construction and sequencing can be found at the JGI website [41]. Pyrosequencing reads were assembled using the Newbler assembler (Roche). The initial Newbler assembly consisting of 185 contigs in one scaffold was converted into a phrap [42] assembly by making fake reads from the consensus, to collect the read pairs in the 454 paired end library. Illumina GAii sequencing data (5,096.2 Mb) was assembled with Velvet [43] and the consensus sequences were shredded into 1.5 kb overlapped fake reads and assembled together with the 454 data. The 454 draft assembly was based on 95.6 Mb 454 draft data and all of the 454 paired end data. Newbler parameters are -consed -a 50 -l 350 -g -m -ml 20. The Phred/Phrap/Consed software package [42] was used for sequence assembly and quality assessment in the subsequent finishing process. After the shotgun stage, reads were assembled with parallel phrap (High Performance Software, LLC). Possible mis-assemblies were corrected with gapResolution [41], Dupfinisher [44], or sequencing cloned bridging PCR fragments with subcloning. Gaps between contigs were closed by editing in Consed, by PCR and by Bubble PCR primer walks (J.-F. Chang, unpublished). A total of 233 additional reactions were necessary to close gaps and to raise the quality of the finished sequence. Illumina reads were also used to correct potential base errors and increase consensus quality using a software Polisher developed at JGI [45].
The error rate of the completed genome sequence is less than 1 in 100,000. Together, the combination of the Illumina and 454 sequencing platforms provided 788.6 x coverage of the genome. The final assembly contained 397,729 pyrosequence and 61,582,867 Illumina reads.

Genome annotation
Genes were identified using Prodigal [46] as part of the Oak Ridge National Laboratory genome annotation pipeline, followed by a round of manual curation using the JGI GenePRIMP pipeline [47]. The predicted CDSs were translated and used to search the National Center for Biotechnology Information (NCBI) non-redundant 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 [48], RNAMMer [49], Rfam [50], TMHMM [51], and signalP [52].

Genome properties
The genome consists of a 5,965,593 bp long circular chromosome with a 68.9% G+C content (Table  3 and Figure 3). Of the 5,784 genes predicted, 5,727 were protein-coding genes, and 57 RNAs; 149 pseudogenes were also identified. The majority of the protein-coding genes (75.0%) 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.