Skip to main content
Genome Announcements logoLink to Genome Announcements
. 2016 Jul 14;4(4):e00640-16. doi: 10.1128/genomeA.00640-16

Draft Whole-Genome Sequence of the Type Strain Bacillus aquimaris TF12T

Ismael L Hernández-González 1, Gabriela Olmedo-Álvarez 1,
PMCID: PMC4945792  PMID: 27417832

Abstract

Bacillus aquimaris TF12 is a Gram-positive bacteria isolated from a tidal flat of the Yellow Sea in South Korea. We report the draft whole-genome sequence of Bacillus aquimaris TF12, the type strain of a set of bacteria typically associated with marine habitats and with a potentially high biotechnology value.

GENOME ANNOUNCEMENT

In the past few decades, there has been an increasing interest in marine organisms as a possible source of bioactive compounds. Bacillus species have been isolated from a huge variety of environments, both terrestrial and aquatic. Bacillus aquimaris TF12 is the type strain of a set of bacteria typically associated with marine habitats. It is a moderately halophilic bacterium isolated from seawater of a tidal flat of the Yellow Sea in South Korea (1). Strains of B. aquimaris have been studied as a possible source of bioactive compounds, such as starch-degrading enzymes (2), proteases (3, 4), and organic solvent stable alkaline cellulases (5).

The type strain of B. aquimaris TF12 was obtained from DSMZ (Deutsche Sammlung von Mikroorganismen und Zellkulturen GmbH). Its genome was sequenced using a hybrid method. The raw reads were obtained using 454 GS-FLX and Illumina mate-pair sequencing. The 454 reads were processed using the Newbler software, while Illumina reads were trimmed and filtered by quality and length employing the FastX-toolkit (http://hannonlab.cshl.edu/fastx_toolkit/index.html). The de novo assembly was performed using MIRA3 (6) and Velvet (7). The final assembly resulted in 30 contigs (>1000 bp) that comprise 4,035,445 bases with a G+C content of 37.3%. Genome annotation was done employing RAST (Rapid Annotation using Subsystem Technology) (8). It contains 4,184 open reading frames (ORF) and 23 rRNA and 83 tRNA genes. Almost 21.2% of the ORFs were hypothetical proteins (1,013 ORFs). The phylogenetic reconstruction using the 16S rRNA gene showed that the closest strain to B. aquimaris TF12 was Bacillus coahuilensis m4-4 (9), with which it shares 25% of orthologs genes.

The annotation of the genome through RAST showed that B. aquimaris had numerous genes for amino acid and carbohydrate metabolism, followed by cofactors, vitamins, prosthetic groups, and pigments subsystems. Puspasari et al. (2012) (2) reported an α-amylase isolated from B. aquimaris MKSC 2.6 which together with the sequences of other Bacillus species defined a new sub-family of α-amylases (GH13) (2). To verify if B. aquimaris TF12 carried a homologous sequence to this α-amylase, we did a search in the genome of Bacillus aquimaris TF12 using the amino acids sequence of the BaqA gene (accession no. JN797599). Although the best hit showed 84% identity with the BaqA sequence, it exhibited the motif of two consecutive tryptophan residues that defines the proposed subfamily.

The search for possible proteases using the MEROPS BLAST server (MEROPS v9.13) (10) identified 172 proteins classified in 9 families. The families of proteolytic protein most represented are those comprising metallo peptidases (72), followed by the family of serine peptidases (61), cysteine peptidases (24), aspartic peptidases (4), peptidase inhibitors (4), peptidases of unknown catalytic type (3), asparagine peptidases (2), a threonine peptidase, and a mixed peptidase.

Furthermore, relevant to the importance of this species as a producer of compounds of biotechnological value, B. aquimaris and its relatives represent one new group inside the Bacillus genus. The knowledge obtained from the study of the genome of this organism would shed light on the evolution of the Bacillus genus.

Nucleotide sequence accession numbers.

This whole-genome shotgun project has been deposited in DDBJ/EMBL/GenBank under the accession no. LQXM00000000. The version described in this paper is the first version, LQXM01000000.

ACKNOWLEDGMENT

We acknowledge Africa Islas for technical assistance.

Funding Statement

I.L.H.-G. was supported by a fellowship from CONACYT.

Footnotes

Citation Hernández-González IL, Olmedo-Álvarez G. 2016. Draft whole-genome sequence of the type strain Bacillus aquimaris TF12T. Genome Announc 4(4):e00640-16. doi:10.1128/genomeA.00640-16.

REFERENCES

  • 1.Yoon JH, Kim IG, Kang KH, Oh TK, Park YH. 2003. Bacillus marisflavi sp. nov. and Bacillus aquimaris sp. nov., isolated from seawater of a tidal flat of the Yellow Sea in Korea. Int J Syst Evol Microbiol 53:1297–1303. doi: 10.1099/ijs.0.02365-0. [DOI] [PubMed] [Google Scholar]
  • 2.Puspasari F, Radjasa OK, Noer AS, Nurachman Z, Syah YM, van der Maarel M, Dijkhuizen L, Janeček S, Natalia D. 2013. Raw starch-degrading α-amylase from Bacillus aquimaris MKSC 6.2: isolation and expression of the gene, bioinformatics and biochemical characterization of the recombinant enzyme. J Appl Microbiol 114:108–120. doi: 10.1111/jam.12025. [DOI] [PubMed] [Google Scholar]
  • 3.Thaz CJ, Jayaraman G. 2014. Stability and detergent compatibility of a predominantly β-sheet serine protease from halotolerant B. aquimaris VITP4 strain. Appl Biochem Biotechnol 172:687–700. doi: 10.1007/s12010-013-0524-4. [DOI] [PubMed] [Google Scholar]
  • 4.Phelan RW, O’Halloran JA, Kennedy J, Morrissey JP, Dobson AD, O’Gara F, Barbosa TM. 2012. Diversity and bioactive potential of endospore-forming bacteria cultured from the marine sponge Haliclona simulans. J Appl Microbiol 112:65–78. doi: 10.1111/j.1365-2672.2011.05173.x. [DOI] [PubMed] [Google Scholar]
  • 5.Trivedi N, Gupta V, Kumar M, Kumari P, Reddy CR, Jha B. 2011. Solvent tolerant marine bacterium Bacillus aquimaris secreting organic solvent stable alkaline cellulase. Chemosphere 83:706–712. doi: 10.1016/j.chemosphere.2011.02.006. [DOI] [PubMed] [Google Scholar]
  • 6.Chevreux B, Wetter T, Suhai S. 1999. Genome sequence assembly using trace signals and additional sequence information, p. 45–56. In Computer science and biology. Proceedings of the German Conference on Bioinformatics, GCB 99. GCB, Hannover, Germany. [Google Scholar]
  • 7.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]
  • 8.Aziz RK, Bartels D, Best AA, DeJongh M, Disz T, Edwards RA, Formsma K, Gerdes S, Glass EM, Kubal M, Meyer F, Olsen GJ, Olson R, Osterman AL, Overbeek RA, McNeil LK, Paarmann D, Paczian T, Parrello B, Pusch GD, Reich C, Stevens R, Vassieva O, Vonstein V, Wilke A, Zagnitko O. 2008. The RAST server: Rapid Annotations using Subsystems Technology. BMC Genomics 9:75. doi: 10.1186/1471-2164-9-75. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Cerritos R, Vinuesa P, Eguiarte LE, Herrera-Estrella L, Alcaraz-Peraza LD, Arvizu-Gómez JL, Olmedo G, Ramirez E, Siefert JL, Souza V. 2008. Bacillus coahuilensis sp. nov., a moderately halophilic species from a desiccation lagoon in the Cuatro Ciénegas valley in Coahuila, Mexico. Int J Syst Evol Microbiol 58:919–923. doi: 10.1099/ijs.0.64959-0. [DOI] [PubMed] [Google Scholar]
  • 10.Rawlings ND, Barrett AJ, Bateman A. 2012. MEROPS: the database of proteolytic enzymes, their substrates and inhibitors. Nucleic Acids Res 40:D343–D350. doi: 10.1093/nar/gkr987. [DOI] [PMC free article] [PubMed] [Google Scholar]

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

RESOURCES