Lawrence Berkeley National Laboratory Recent Work Title Draft genome sequence of Marinobacterium rhizophilum CL-YJ9T (DSM 18822T), isolated from the rhizosphere of the coastal tidal-flat plant Suaeda japonica. Permalink https://escholarship.org/uc/item/5bh6103g Journal Standards in genomic sciences, 12(1) ISSN 1944-3277 Authors Choi, Dong Han Jang, Gwang Ii Lapidus, Alla et al. Publication Date 2017 DOI 10.1186/s40793-017-0275-x Peer reviewed eScholarship.org Powered by the California Digital Library University of California Choi et al. Standards in Genomic Sciences (2017) 12:65 DOI 10.1186/s40793-017-0275-x SHORTGENOMEREPORT Open Access Draft genome sequence of Marinobacterium rhizophilum CL-YJ9T (DSM 18822T), isolated from the rhizosphere of the coastal tidal-flat plant Suaeda japonica Dong Han Choi1†, Gwang II Jang2†, Alla Lapidus3,4, Alex Copeland5, T. B. K. Reddy5, Supratim Mukherjee5, Marcel Huntemann5, Neha Varghese4, Natalia Ivanova5, Manoj Pillay6, Brian J. Tindall7, Markus Göker7, Tanja Woyke5, Hans-Peter Klenk8, Nikos C. Kyrpides5 and Byung Cheol Cho2* Abstract The genus Marinobacterium belongs to the family Alteromonadaceae within the class Gammaproteobacteria and was reported in 1997. Currently the genus Marinobacterium contains 16 species. Marinobacterium rhizophilum CL-YJ9T was isolated from sediment associated with the roots of a plant growing in a tidal flat of Youngjong Island, Korea. The genome of the strain CL-YJ9T was sequenced through the Genomic Encyclopedia of Type Strains, Phase I: KMG project. Here we report the main features of the draft genome of the strain. The 5,364,574 bp long draft genome consists of 58 scaffolds with 4762 protein-coding and 91 RNA genes. Based on the genomic analyses, the strain seems to adapt to osmotic changes by intracellular production as well as extracellular uptake of compatible solutes, such as ectoine and betaine. In addition, the strain has a number of genes to defense against oxygen stresses such as reactive oxygen species and hypoxia. Keywords: Genome, Marinobacterium rhizophilum, Suaeda Japonica,Rhizosphere,GEBA Introduction (M. jannaschii, M. litorale, M. rhizophilum, M. stanieri and The genus Marinobacterium within the family Alteromona- M. profundum) and one unidentified strain are found in the daceae was established in 1997 by González et al. [1]. GenBank database. Among them, genomic features of M. Currently the genus Marinobacterium contains 16 species rhizophilum CL-YJ9T (=DSM 18822=KCCM 42386T), iso- with validly published names (Fig. 1). All Marinobacterium lated from the rhizosphere of a plant Suaeda japonica inha- strains have been isolated from marine environments [1– biting a coastal tidal flat, Korea, will be presented here. 11] such as sea water, tidal flat, deep-sea sediment, and coral mucus. Interestingly, their habitats include tropical waters Organism information [12, 13], Arctic marine sediment [7], tidal flats [4, 11] as well Classification and features as deep sea sediment [10], indicating that the genus has well By phylogenetic analysis of the 16S rRNA gene se- adapted to diverse environments. In the GOLD database quence (Fig. 1), M. rhizophilum strain CL-YJ9T was [14], genome sequencing of 38 strains from 11 Marinobac- positioned within the genus Marinobacterium and terium species are identified to be finished or in progress. formed a distinct branch together with Marinobacter- In addition, six genome sequences from five species ium profundum PAMC 27536T and Marinobacterium nitratireducens CN44T (Fig. 1). Strain CL-YJ9T was * Correspondence: [email protected] most closely related to Marinobacterium profundum † T Equal contributors PAMC 27536 , which appeared as its sister species in 2 Microbial Oceanography Laboratory, School of Earth and Environmental the tree. Strain CL-YJ9T grows under strictly aerobic Sciences, and Research Institute of Oceanography, Seoul National University, Gwanak-ro, Gwanak-gu, Seoul 151-742, Republic of Korea conditions (Table 1). The optimal growth of strain T Full list of author information is available at the end of the article CL-YJ9 occurs at pH 7.0, with a growth range of © The Author(s). 2017 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. Choi et al. Standards in Genomic Sciences (2017) 12:65 Page 2 of 7 Fig. 1 Neighbour-joining phylogenetic tree, based on 16S rRNA gene sequences, showing the relationships between strain CL-YJ9T,membersofthe genus Marinobacterium and other related genera. Bootstrap percentages >60% (based on 1000 resamplings) are shown below or above the corresponding branches. Solid circles indicate that the corresponding nodes are also recovered in the maximum-likelihood and maximum-parsimony trees. Terasakiella pusillum IFO 13613T (AB006768) was used as an outgroup. Bar, 0.02 nucleotide substitutions per site pH 6.0–9.0. Growth occurs in the presence of 1.0– Growth conditions and genomic DNA preparation 5.0% (w/v)NaCl(optimum3.0%)andat5–30 °C M. rhizophilum strain CL-YJ9T was grown in DSMZ (optimum 25 °C) (Table 1). Cells of strain CL-YJ9T medium 514 (http://www.dsmz.de) at 28 °C and aerobe are rod-shaped, on average approximately 0.3–0.4 μm conditions. Genomic DNA was isolated using Jetflex wide and 0.6–0.8 μm long and motile by means of Genomic DNA Purification Kit (GENOMED 600100) monopolar flagella (Fig. 2). following the standard protocol provided by the manu- facturer but additionally applying 50 μl proteinase K and using a 60 min incubation time. DNA is available Genome sequencing information through the DNA Bank Network [23]. Genome project history The strain CL-YJ9T was chosen for genome sequencing by the phylogeny-based selection [15, 16] as a part of the Genome sequencing and assembly Genomic Encyclopedia of Type Strains, Phase I: the KMG Using the purified genomic DNA, the draft genome of project [17]. The KMG project, the first of the production M. rhizophilum CL-YJ9 T was generated at the DOE-JGI phases of the GEBA: sequencing a myriad of type strains using the Illumina technology [24]. An Illumina standard initiative [18, 19] and a Genomic Standards Consortium shotgun library was constructed and sequenced using project [20] was set up to increase the sequencing cover- the Illumina HiSeq 2000 platform which generated age of key reference microbial genomes and to generate a 7,253,734 reads totaling 1088.1 Mbp. All general aspects large genomic basis for the discovery of genes encoding of library construction and sequencing performed at the novel enzymes [21]. The genome sequencing, finishing JGI can be found at the JGI website. All raw Illumina and annotation were performed by the DOE-JGI using sequence data was passed through DUK, a filtering pro- state of the art sequencing technology [22]. A summary of gram developed at JGI, which removes known Illumina the project information is presented in Table 2. sequencing and library-preparation artifacts [25]. The Choi et al. Standards in Genomic Sciences (2017) 12:65 Page 3 of 7 Table 1 Classification and general features of M. rhizophilum CL-YJ9T [8, 9] MIGS ID Property Term Evidence codea Classification Domain Bacteria TAS [39] Phylum Proteobacteria TAS [40] Class Gammaproteobacteria TAS [41] Order Alteromonadales TAS [42] Family Alteromonadaceae TAS [43] Genus Marinobacterium TAS [1] Species Marinobacterium TAS [4] rhizophilum Type strain CL-YJ9T TAS [4] Gram stain Negative TAS [4] Cell shape Straight rods TAS [4] Motility Motile TAS [4] Sporulation Not reported NAS Temperature 5-30 °C TAS [4] Fig. 2 Transmission electron microscopy image of Marinobacterium range rhizophilum CL-YJ9T Optimum 25 °C TAS [4] temperature (version r41043) [27]. Parameters for assembly steps were pH range; 6.0-9.0; 7.0 TAS [4] exactly same as in Choi et al. [28]. The final draft assembly Optimum contained 68 contigs in 58 scaffolds. The total size of the Carbon Glucose, sucrose, mannose, TAS [4] source glycerol, glycine, mannitol genome is 5.4 Mbp and the final assembly is based on 638.1 Mbp of Illumina data, which provides an average MIGS-6 Habitat Sediment closely associated TAS [4] with the roots of a plant 119.1X coverage of the genome. (Suaeda japonica) MIGS-6.3 Salinity 1-5% (optimum: 3%) TAS [4] Genome annotation MIGS-22 Oxygen Strictly aerobic TAS [4] As described in Choi et al. [28], identification of genes was requirement performed using Prodigal [29] as part of the DOE-JGI MIGS-15 Biotic Microbiota of the rhizome of TAS [4] Annotation pipeline [30, 31]. After translation of the relationship Suaeda japonica MIGS-14 Pathogenicity Non-pathogenic NAS Table 2 Genome sequencing project information MIGS-4 Geographic Youngjong Island, Korea TAS [4] MIGS ID Property Term location MIGS-31 Finishing quality Level 1: Standard Draft MIGS-5 Sample November, 2005 TAS [4] collection MIGS-28 Libraries used Illumina Std shotgun library MIGS-4.1 Latitude 37.485o N TAS [4] MIGS-29 Sequencing platforms Illumina HiSeq 2000 MIGS-4.2 Longitude 126.516o E TAS [4] MIGS- Fold coverage 119.1X 31.2 MIGS-4.3 Depth Not reported NAS MIGS-30 Assemblers Velvet v. 1.1.04, ALLPATHS v. MIGS-4.4 Altitude Not reported NAS R37654 aEvidence codes - IDA inferred from direct assay, TAS traceable author MIGS-32 Gene calling method Prodigal v2.5 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 Locus Tag F451 based on a generally accepted property for the species, or anecdotal Genbank ID ARJM00000000 evidence).