Skip to main content
Genome Announcements logoLink to Genome Announcements
. 2015 Oct 8;3(5):e01164-15. doi: 10.1128/genomeA.01164-15

Draft Genome Sequence of Exiguobacterium sp. Strain BMC-KP, an Environmental Isolate from Bryn Mawr, Pennsylvania

Peter Hyson 1,*, Joshua A Shapiro 1, Michelle W Wien 1,
PMCID: PMC4599093  PMID: 26450734

Abstract

Exiguobacterium sp. strain BMC-KP was isolated as part of a student environmental sampling project at Bryn Mawr College, PA. Sequencing of bacterial DNA assembled a 3.32-Mb draft genome. Analysis suggests the presence of genes for tolerance to cold and toxic metals, broad carbohydrate metabolism, and genes derived from phage.

GENOME ANNOUNCEMENT

The genus Exiguobacterium is composed of organisms isolated from a wide range of environments often characterized by extreme conditions, such as heat or cold, high or low pH, or high salinity. The genus was first described by Collins et al. (1) in order to provide a new classification for a Gram-positive, non-spore forming, facultative anaerobic, alkaliphilic bacteria within the Firmicutes. Exiguobacterium species have been isolated from diverse environments, including permafrost (2, 3), soil (4), freshwater microbialites (5), a hyperalkaline spring (6), hot springs (7), plant rhizospheres (8), and glaciers in the Himalayas (9). Exiguobacterium spp. have also been implicated as opportunistic pathogens (10).

Here, we present the draft sequence of Exiguobacterium sp. strain BMC-KP cultured on a nutrient agar plate from swabs of the kitchen, bed, and a backpack in an apartment in Bryn Mawr, PA, as part of an undergraduate environmental sampling lab. The bacterium is Gram positive and appears yellowish orange on nutrient agar. It grows from 2.5 to 43°C and at pH levels from 6 to 10. The bacterium displays gelatinase, caseinase, and starch hydrolysis activities. Based on 16S rRNA gene phylogeny of Bacillales family XII Incertae sedis, Firmicutes, Exiguobacterium sp. BMC-KP falls within group I, which are organisms isolated from cold and temperate habits (11).

DNA was isolated using the Qiagen DNeasy kit. Whole-genome sequencing was performed on an Illumina MiSeq sequencer at the Indiana University Center for Genomics and Bioinformatics, using 300-bp paired-end reads constructed using the Illumina Nextera DNA library preparation kit, yielding 794,481 paired-end reads. Adapter contamination and low-quality sequences were removed using Trimmomatic 0.32.2 (12), and assembly was performed using the SPAdes Assembler 3.5.0 (13). The resulting assembly contigs were filtered for sequences with coverage of at least 40× and length >350 bp, resulting in a 3.32-Mb draft assembly consisting of 17 contigs with an N50 of 236,941 bp and median coverage of 120×.

Analysis using RAST (14) suggests the presence of genes encoding enzymes involved in the metabolism of many carbohydrates, including mannose, glycogen, beta-glucoside, and l-arabinose. The metabolism of l-arabinose was confirmed experimentally. The presence of proteins involved in stress tolerance, including cold shock, cadmium, and multidrug resistance, are also predicted. In addition, the sequence of BMC-KP contains phage DNA.

The genomic sequence of Exiguobacterium sp. BMC-KP allows further investigation of the genetic basis of the adaptation of the Exiguobacterium genus to a wide range of environmental conditions.

Nucleotide sequence accession numbers.

This whole-genome shotgun project has been deposited in DDBJ/ENA/GenBank under the accession no. LGIW00000000; raw reads are available in the NCBI SRA archive under accession no. SRX1093385.

ACKNOWLEDGMENTS

We thank Tamara Davis for advice on DNA isolation and Jeffrey D. Newman and the GCAT-SEEK Consortium (gcatseek.org) for facilitating Illumina sequencing.

This work was supported by the Rosalyn R. Schwartz Teaching Award from Bryn Mawr College (M.W.W.) and startup funds from Bryn Mawr College (J.A.S.).

The funders had no role in the study design, data collection and interpretation, or the decision to submit the work for publication.

Footnotes

Citation Hyson P, Shapiro JA, Wien MW. 2015. Draft genome sequence of Exiguobacterium sp. strain BMC-KP, an environmental isolate from Bryn Mawr, Pennsylvania. Genome Announc 3(5):e1164-15. doi:10.1128/genomeA.01164-15.

REFERENCES

  • 1.Collins MD, Lund BM, Farrow JAE, Schleifer KH. 1983. Chemotaxonomic study of an alkalophilic bacterium, Exiguobacterium aurantiacum gen. nov., sp. nov. J Gen Microbiol 129:2037–2042. doi: 10.1099/00221287-129-7-2037. [DOI] [Google Scholar]
  • 2.Rodrigues DF, Tiedje JM. 2007. Multi-locus real-time PCR for quantitation of bacteria in the environment reveals Exiguobacterium to be prevalent in permafrost. FEMS Microbiol Ecol 59:489–499. doi: 10.1111/j.1574-6941.2006.00233.x. [DOI] [PubMed] [Google Scholar]
  • 3.Rodrigues DF, Ivanova N, He Z, Huebner M, Zhou J, Tiedje JM. 2008. Architecture of thermal adaptation in an Exiguobacterium sibiricum strain isolated from 3 million year old permafrost: A genome and transcriptome approach. BMC Genomics 9:547. doi: 10.1186/1471-2164-9-547. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Jiang X, Xue Y, Want L, Yu B, Ma Y. 2013. Genome sequence of a novel polymer-grade l-lactate-producing alkaliphile, Exiguobacterium sp. strain 8-11-1. Genome Announc 1(4):e00616-13. doi: 10.1128/genomeA.00616-13. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.White RA III, Grassa CJ, Suttle CA. 2013. Draft genome sequence of Exiguobacterium pavilionensis strain RW-2, with wide thermal, salinity, and pH tolerance, isolated from modern freshwater microbialites. Genome Announc 1(4):e00597-13. doi: 10.1128/genomeA.00597-13. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Cabria GL, Argayosa VB, Lazaro JE, Argayosa AM, Arcilla CA. 2014. Draft genome sequence of haloalkaliphilic Exiguobacterium sp. strain AB2 from Manleluag Ophiolitic Spring, Philippines. Genome Announc 2(4):e00840-14. doi: 10.1128/genomeA.00840-14. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Yumoto I, Hishinuma-Narisawa M, Hirota K, Shingyo T, Takebe F, Nodasaka Y, Matsuyama H, Hara I. 2004. Exiguobacterium oxidotolerans sp. nov., a novel alkaliphile exhibiting high catalase activity. Int J Syst Evol Microbiol 54:2013–2017. doi: 10.1099/ijs.0.63129-0. [DOI] [PubMed] [Google Scholar]
  • 8.Tang J, Zhang Y, Meng H, Xue Z, Ma J. 2013. Complete genome sequence of Exiguobacterium sp. strain MH3, isolated from rhizosphere of Lemna minor. Genome Announc 1(6):e01059-13. doi: 10.1128/genomeA.01059-13. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Chaturvedi P, Shivaji S. 2006. Exiguobacterium indicum sp. nov., a psychrophilic bacterium from the Hamta glacier of the Himalayan mountain ranges of India. Int J Syst Evol Microbiol 56:2765–2770. doi: 10.1099/ijs.0.64508-0. [DOI] [PubMed] [Google Scholar]
  • 10.Keynan Y, Weber G, Sprecher H. 2007. Molecular identification of Exiguobacterium acetylicum as the aetiological agent of bacteraemia. J Med Microbiol 56:563–564. doi: 10.1099/jmm.0.46866-0. [DOI] [PubMed] [Google Scholar]
  • 11.Vishnivetskaya TA, Kathariou S, Tiedje JM. 2009. The Exiguobacterium genus: biodiversity and biogeography. Extremophiles 13:541–555. doi: 10.1007/s00792-009-0243-5. [DOI] [PubMed] [Google Scholar]
  • 12.Bolger AM, Lohse M, Usadel B. 2014. Trimmomatic: a flexible trimmer for Illumina sequence data. Bioinformatics 30:2114–2120. doi: 10.1093/bioinformatics/btu170. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Bankevich A, Nurk S, Antipov D, Gurevich AA, Dvorkin M, Kulikov AS, Lesin VM, Nikolenko SI, Pham S, Prjibelski AD, Pyshkin AV, Sirotkin AV, Vyahhi N, Tesler G, Alekseyev MA, Pevzner PA. 2012. SPAdes: a new genome assembly algorithm and its applications to single-cell sequencing. J Comput Biol 19:455–477. doi: 10.1089/cmb.2012.0021. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.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. 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]

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

RESOURCES