Skip to main content
Genome Announcements logoLink to Genome Announcements
. 2016 Oct 13;4(5):e01155-16. doi: 10.1128/genomeA.01155-16

Draft Genome Sequence of Arenibacter sp. Strain C-21, an Iodine-Accumulating Bacterium Isolated from Surface Marine Sediment

Kohei Ito a, Nobuyoshi Nakajima b, Shigeki Yamamura b,c, Masaru Tomita a, Haruo Suzuki a,, Seigo Amachi d,
PMCID: PMC5064120  PMID: 27738047

Abstract

Arenibacter sp. strain C-21, isolated from surface marine sediment of Japan, accumulates iodine in the presence of glucose and iodide (I-). We report here the draft genome sequence of this strain to provide insight into the molecular mechanism underlying its iodine-accumulating ability.

GENOME ANNOUNCEMENT

Bacteria may play significant roles in the biogeochemical cycling of iodine through volatilization, oxidation, reduction, and accumulation of this element (1). Previously, we isolated Arenibacter sp. strain C-21 from surface marine sediment collected from Sagami Bay, Kanagawa, Japan (2). When strain C-21 was grown in the presence of 0.1 µM iodide ion (I-), it accumulated iodine with a maximum concentration factor of 5.5 × 103. Subsequent studies revealed that glucose, oxygen, and calcium ion were required for iodine uptake by this strain (3). However, glucose-independent uptake of iodine was observed if a hydrogen peroxide-generating system or iodide-oxidizing system was present. A possible mechanism of iodine uptake and accumulation by strain C-21 was proposed in which a membrane-bound glucose oxidase and haloperoxidase are involved (3).

Arenibacter sp. strain C-21 was grown in Marine broth 2216 (Difco), and DNA was extracted using a DNeasy blood and tissue kit (Qiagen, Hilden, Germany). Whole-genome sequencing was performed using paired-end sequencing on an Illumina MiSeq. The sequencer produced 300-bp paired-end reads that were obtained from 550-bp inserts. The quality of the reads was checked using PRINSEQ (4). De novo genome assembly was performed using Velvet 1.2.10 (5, 6). The resulting assembly contains 92 contigs consisting of 5,667,524 bp, with a G+C content of 39.7%. Genome annotation was performed using Prokka version 1.11, which is a pipeline comprising several bioinformatic tools (7). Briefly, Aragorn (8) detected 39 tRNA genes, Barrnap predicted four (one of 16S, one of 23S, and two of 5S) rRNA genes, and Prodigal (9) identified 4,766 protein-coding DNA sequences (CDSs), of which 438 contained signal peptides identified using SignalP (10). Of the 4,766 proteins, 1,578 were hypothetical proteins of unknown function, 2,140 proteins were annotated by UniProtKB (11), 761 proteins were annotated by Pfam (12), 343 proteins were annotated by NCBI’s Conserved Domain Database (CDD) (13), and 57 proteins were annotated by HAMAP (14). For example, of the annotated proteins, 39 were SusD family proteins (Pfam: PF07980), 35 were arylsulfatase (UniProtKB: P51691 and Q0TUK6), and 18 were vitamin B12 transporter BtuB (HAMAP: MF_01531). At least 28 genes coding for c-type cytochromes were identified in the genome. A BLASTp search (15, 16) revealed that the genome contained at least five genes annotated as PAP2 superfamily proteins (Pfam: PF01569) that are homologous to vanadium iodoperoxidase from Zobellia galactanivorans (PDB: 4USZ_A) (17). The draft genome sequence of Arenibacter sp. strain C-21 represents a valuable resource for future comparative functional genomic studies.

Accession number(s).

Arenibacter sp. strain C-21 whole-genome shotgun project has been deposited at DDBJ under the accession number BDGL00000000. The version described in this paper is the first version, BDGL01000000, which consists of sequences BDGL01000001 to BDGL01000092.

ACKNOWLEDGMENTS

This work was supported in part by research funding from Yamagata Prefecture and Tsuruoka City.

Footnotes

Citation Ito K, Nakajima N, Yamamura S, Tomita M, Suzuki H, Amachi S. 2016. Draft genome sequence of Arenibacter sp. strain C-21, an iodine-accumulating bacterium isolated from surface marine sediment. Genome Announc 4(5):e01155-16. doi:10.1128/genomeA.01155-16.

REFERENCES

  • 1.Amachi S. 2008. Microbial contribution to global iodine cycling: volatilization, accumulation, reduction, oxidation, and sorption of iodine. Microbes Environ 23:269–276. doi: 10.1264/jsme2.ME08548. [DOI] [PubMed] [Google Scholar]
  • 2.Amachi S, Mishima Y, Shinoyama H, Muramatsu Y, Fujii T. 2005. Active transport and accumulation of iodide by newly isolated marine bacteria. Appl Environ Microbiol 71:741–745. doi: 10.1128/AEM.71.2.741-745.2005. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Amachi S, Kimura K, Muramatsu Y, Shinoyama H, Fujii T. 2007. Hydrogen peroxide-dependent uptake of iodine by marine Flavobacteriaceae bacterium strain C-21. Appl Environ Microbiol 73:7536–7541. doi: 10.1128/AEM.01592-07. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Schmieder R, Edwards R. 2011. Quality control and preprocessing of metagenomic datasets. Bioinformatics 27:863–864. doi: 10.1093/bioinformatics/btr026. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Zerbino DR, Birney E. 2008. Velvet: algorithms for de novo short read assembly using de Bruijn graphs. Genome Res 18:821–829. doi: 10.1101/gr.074492.107. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Zerbino DR. 2010. Using the Velvet de novo assembler for short-read sequencing technologies. Curr Protoc Bioinformatics Chapter 11:Unit 11.5. doi: 10.1002/0471250953.bi1105s31. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Seemann T. 2014. Prokka: rapid prokaryotic genome annotation. Bioinformatics 30:2068–2069. doi: 10.1093/bioinformatics/btu153. [DOI] [PubMed] [Google Scholar]
  • 8.Laslett D, Canback B. 2004. ARAGORN, a program to detect tRNA genes and tmRNA genes in nucleotide sequences. Nucleic Acids Res 32:11–16. doi: 10.1093/nar/gkh152. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Hyatt D, Chen G-L, Locascio PF, Land ML, Larimer FW, Hauser LJ. 2010. Prodigal: prokaryotic gene recognition and translation initiation site identification. BMC Bioinformatics 11:119. doi: 10.1186/1471-2105-11-119. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Petersen TN, Brunak S, von Heijne G, Nielsen H. 2011. SignalP 4.0: discriminating signal peptides from transmembrane regions. Nat Methods 8:785–786. doi: 10.1038/nmeth.1701. [DOI] [PubMed] [Google Scholar]
  • 11.UniProt Consortium 2014. Activities at the universal protein resource (UniProt). Nucleic Acids Res 42:D191–D198. doi: 10.1093/nar/gkt1140. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Finn RD, Coggill P, Eberhardt RY, Eddy SR, Mistry J, Mitchell AL, Potter SC, Punta M, Qureshi M, Sangrador-Vegas A, Salazar GA, Tate J, Bateman A. 2016. The Pfam protein families database: towards a more sustainable future. Nucleic Acids Res 44:D279–D285. doi: 10.1093/nar/gkv1344. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Marchler-Bauer A, Derbyshire MK, Gonzales NR, Lu S, Chitsaz F, Geer LY, Geer RC, He J, Gwadz M, Hurwitz DI, Lanczycki CJ, Lu F, Marchler GH, Song JS, Thanki N, Wang Z, Yamashita RA, Zhang D, Zheng C, Bryant SH. 2015. CDD: NCBI’s conserved domain database. Nucleic Acids Res 43:D222–D226. doi: 10.1093/nar/gku1221. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Lima T, Auchincloss AH, Coudert E, Keller G, Michoud K, Rivoire C, Bulliard V, de Castro E, Lachaize C, Baratin D, Phan I, Bougueleret L, Bairoch A. 2009. Hamap: a database of completely sequenced microbial proteome sets and manually curated microbial protein families in UniProtKB/Swiss-Prot. Nucleic Acids Res 37:D471–D478. doi: 10.1093/nar/gkn661. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Altschul SF, Madden TL, Schäffer AA, Zhang J, Zhang Z, Miller W, Lipman DJ. 1997. Gapped BLAST and PSI-BLAST: a new generation of protein database search programs. Nucleic Acids Res 25:3389–3402. doi: 10.1093/nar/25.17.3389. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Altschul SF, Gish W, Miller W, Myers EW, Lipman DJ. 1990. Basic Local Alignment Search Tool. J Mol Biol 215:403–410. doi: 10.1016/S0022-2836(05)80360-2. [DOI] [PubMed] [Google Scholar]
  • 17.Fournier J-B, Rebuffet E, Delage L, Grijol R, Meslet-Cladière L, Rzonca J, Potin P, Michel G, Czjzek M, Leblanc C. 2014. The vanadium iodoperoxidase from the marine Flavobacteriaceae species Zobellia galactanivorans reveals novel molecular and evolutionary features of halide specificity in the vanadium haloperoxidase enzyme family. Appl Environ Microbiol 80:7561–7573. doi: 10.1128/AEM.02430-14. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Genome Announcements are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES