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Journal of Bacteriology logoLink to Journal of Bacteriology
. 2012 Nov;194(21):5961–5962. doi: 10.1128/JB.01332-12

Draft Genome Sequence of Staphylococcus vitulinus F1028, a Strain Isolated from a Block of Fermented Soybean

Young-Do Nam a,b, Won-Hyong Chung c, Myung-Ji Seo a,b, Seong-Il Lim a,
PMCID: PMC3486121  PMID: 23045483

Abstract

Staphylococcus vitulinus is a coagulase-negative staphylococcus in the family Staphylococcaceae. This report describes the draft genome sequence of S. vitulinus F1028, which was isolated from a traditional Korean soybean food (meju). This 2.56-Mbp genome sequence is the first S. vitulinus genome of a strain isolated from a fermented soybean product.

GENOME ANNOUNCEMENT

Staphylococcus is a group of Gram-positive bacteria that form grape-like clusters. It currently contains 47 species (http://www.bacterio.cict.fr/), which normally inhabit the skin and mucosal surfaces of humans and other animals (4). Most Staphylococcus strains are known to be harmless, but some strains of S. aureus, S. pseudintermedius, and S. epidermidis can cause severe infections (2). Therefore, most of the 573 available Staphylococcus genomes are focused on the pathogenic potential of these microorganisms (http://www.ncbi.nlm.nih.gov/genome/). Staphylococcus spp. are known to be major components of Korean soybean paste (8) and Japanese miso (5), while they are readily isolated from fermented sausages (3). Thus, there is a need for genomic data to understand the roles of nonpathogenic Staphylococcus spp. in fermentation processes. Staphylococcus vitulinus and S. pulvereri were first described as novel Staphylococcus spp. in 1994 (11) and 1995 (12), respectively, although S. pulvereri was identified as a junior synonym of S. vitulinus in 2004 (10). In this study, a new strain, S. vitulinus F1028, which shares 99.5% 16S rRNA gene sequence similarity with S. vitulinus ATCC 51145T, was isolated from a traditional Korean fermented soybean food product, meju. This report announces the first sequenced genome of a Staphylococcus strain that participates in soybean fermentation.

The genomic DNA of S. vitulinus F1028 was extracted using a G-spin bacterial genomic extraction kit (iNtRON Biotechnology, Republic of Korea). The draft genome sequence of S. vitulinus F1028 was determined using an Ion Torrent personal genome machine (PGM) with 316 100-Mb sequencing chips (150-bp library), according to the manufacturer's instructions (9). Approximately 2,723,000 reads were produced, with an average read length of 91 bases (total, 237 Mb). The reads were assembled into 223 contigs (>1 kb in size) with an approximately 93-fold coverage using the CLC Genomics Workbench 5.0.1 program (CLC Bio, Denmark) and the Newbler assembler (454 Life Sciences, Branford, CT). The draft genome of S. vitulinus F1028 measured 2,561,113 bp in length, with a G+C content of 32.4%. Gene prediction and annotation of the assembled contigs were performed by combining the outputs of the following analytical tools: RNAmmer 1.2 for rRNAs (6), tRNA scan-SE 1.23 for tRNAs (7), and RAST 4.0 (Rapid Annotation using Subsystem Technology) for proteins (1). The draft genome sequence contained a single copy of the 16S rRNA gene, a single copy of the 23S rRNA gene, and 26 copies of tRNA genes. Of the 2,539 predicted protein-coding genes, 97 genes were assigned putative functions, and 537 genes were assigned as hypothetical proteins based on the subsystem categorization. Using the functional annotation by the COG (Clusters of Orthologous Groups) database, 2,110 genes were classified into 21 COG classes and 1,453 COG families. No toxin-related genes that may be harmful to humans, such as enterotoxin proteins, were present in the genome. Further in-depth analysis will be necessary to elucidate fully the genomic differences between pathogenic and nonpathogenic Staphylococcus strains and to understand the roles of Staphylococcus in fermentation processes.

Nucleotide sequence accession numbers.

This Whole Genome Shotgun project has been deposited in DDBJ/EMBL/GenBank under accession no. AJTR00000000. The version described here is the first version, AJTR00000000.

ACKNOWLEDGMENT

This study was supported by a grant from the Korea Food Research Institute (project no. E0121302).

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