Skip to main content
Genome Announcements logoLink to Genome Announcements
. 2013 Apr 18;1(2):e00135-13. doi: 10.1128/genomeA.00135-13

Genome Sequence of a Freshwater Low-Nucleic-Acid-Content Bacterium, Betaproteobacterium Strain CB

Zhenyu Hao a, Lei Li a, Jie Liu a, Yan Ren b, Lei Wang b, Mark Bartlam c, Thomas Egli d,e,, Yingying Wang a
PMCID: PMC3630399  PMID: 23599288

Abstract

Betaproteobacterium strain CB is a typical minute freshwater bacterium, representing the small-cell bacteria that are numerically dominant in most freshwater environments. The genome of betaproteobacterium CB consists of a circular 2,045,720-bp chromosome, and the information we report will provide insights into the mechanisms underlying its survival and ecological function.

GENOME ANNOUNCEMENT

Low-nucleic-acid-content (LNA) bacteria are widely distributed in aquatic environments and constitute numerically a large fraction of microbial communities (1, 2). Very little is known about these ubiquitous, small bacteria, particularly their ecological functions and metabolic mechanisms (3). Betaproteobacterium strain CB is a typical LNA bacterium possessing a distinctive small biovolume (<0.05 µm3), close to the size limit for free-living cells, and the ability to grow at low nutrient concentrations but not in conventional rich medium. Definitions in the available literature indicate the isolate should be a typical “obligate oligotroph” and an “ultramicrobacterium” (2, 3). The most comprehensive understanding of oligotrophs and ultramicrobacteria comes from the facultative oligotrophic bacterium Sphingopyxis alaskensis (4, 5). However, information on obligate oligotrophic bacteria is very limited. Here we present the whole-genome sequence of betaproteobacterium CB, with the aim of unraveling the mechanisms underlying its survival and ecological function. Strain CB was cultured by an unconventional cultivation approach, namely, using sterilized natural freshwater as a cultivation medium and monitoring growth by flow cytometry (2, 6). The whole betaproteobacterium CB genome was sequenced using Solexa paired-end sequencing technology. Genomic libraries were constructed containing 500-bp paired-end (PE) and 3-kb mate-pair (MP) inserts to generate 1,897,661,000 bp of hybrid data, assembled into 10 large contigs and providing 927.6-fold coverage of the genome. The reads, assembled into 46 contigs utilizing de novo assembly, were used to construct 10 scaffolds. Interscaffold and intrascaffold gaps were filled by sequencing PCR products using an ABI 3730 capillary sequencer. An error rate of less than 1 in a 10-kb sequence was achieved for the complete genome through sequence assembly and quality assessment using the Phred/Phrap/Consed software package (7, 8). The complete sequence was analyzed using Augustus, GlimmerHMM, SNAP, and GeneMark for protein-coding genes, Rbsfinder (http://www.tigr.org) for the ribosomal binding site, and tRNAscan-SE (9) for the tRNA. The functions of predicted protein-coding genes were annotated through comparisons with the NCBI nonredundant (NR) and Swiss-Prot protein databases from the European Bioinformatics Institute.

The genome consists of a circular 2,045,720-bp chromosome having no plasmid, with a G+C value of 46.09%. The chromosome contains 1 16S-23S-5S rRNA operon and 36 tRNA genes. The genome carries 2,112 putative protein-coding genes, encoding 188 transmembrane proteins and 1,924 non-transmembrane proteins. The majority of functional genes are involved in basic metabolism, protein translation, and DNA replication.

Strain CB belongs to the genus Polynucleobacter on the basis of 16S rRNA gene sequencing and genetic comparison with the strain Polynucleobacter sp. QLW-P1DMWA-1 (accession no. NC_009379.1). However, this type of strain is conventionally cultivable on rich media, suggesting that this genus is rather shallow and harbors many physiologically different organisms. In summary, we have sequenced the whole genome of a model LNA obligate oligotrophic ultramicrobacterium. To our knowledge, this first genome sequence for freshwater LNA bacteria will provide new insight into the physiological mechanisms of oligotrophic bacteria and their ecological roles.

Nucleotide sequence accession number.

The draft genome sequence of betaproteobacterium CB (10 large contigs) has been assigned GenBank accession no. CP004348.

ACKNOWLEDGMENTS

This work was supported by the Swiss Federal Institute for Aquatic Science and Technology (Eawag) internal funding (Wave21), the National Science Foundation of China (31000247), and the Specialized Research Fund for the Doctoral Program of Higher Education (20100031120018), China.

Footnotes

Citation Hao Z, Li L, Liu J, Ren Y, Wang L, Bartlam M, Egli T, Wang Y. 2013. Genome sequence of a freshwater low-nucleic-acid-content bacterium, betaproteobacterium strain CB. Genome Announc. 1(2):e00135-13. doi:10.1128/genomeA.00135-13.

REFERENCES

  • 1. Bouvier T, Del Giorgio PA, Gasol JM. 2007. A comparative study of the cytometric characteristics of high and low nucleic-acid bacterioplankton cells from different aquatic ecosystems. Environ. Microbiol. 9:2050–2066 [DOI] [PubMed] [Google Scholar]
  • 2. Wang YY, Hammes FA, Boon N, Chami M, Egli T. 2009. Isolation and characterization of low nucleic acid (LNA)-content bacteria. ISME J. 3:889–902 [DOI] [PubMed] [Google Scholar]
  • 3. Schut F, Prins RA, Gottschal JC. 1997. Oligotrophy and pelagic marine bacteria: facts and fiction. Aquat. Microb. Ecol. 12:177–202 [Google Scholar]
  • 4. Williams TJ, Ertan H, Ting L, Cavicchioli R. 2009. Carbon and nitrogen substrate utilization in the marine bacterium Sphingopyxis alaskensis strain RB2256. ISME J. 3:1036–1052 [DOI] [PubMed] [Google Scholar]
  • 5. Federico ML, Diane M, Torsten T, Williams TJ, Egan S, Rice S, DeMaere MZ, Ting L, Ertan H, Johnson J, Ferriera S, Lapidus A, Anderson I, Kyrpides N, Munk AC, Detter C, Han CS, Brown MV, Robb FT, Kjelleberg S, Cavicchioli R. 2009. The genomic basis of trophic strategy in marine bacteria. Proc. Natl. Acad. Sci. USA 106:15527–15533 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6. Wang YY, Hammes FA, De Roy K, Verstraete W, Boon N. 2010. Past, present and future applications of flow cytometry in aquatic microbiology. Trends Biotechnol. 28:416–424 [DOI] [PubMed] [Google Scholar]
  • 7. Ewing B, Green P. 1998. Base-calling of automated sequencer traces using Phred II. Genome Res. 8:186–194 [PubMed] [Google Scholar]
  • 8. Gordon D, Abajian C, Green P. 1998. Consed: a graphical tool for sequence finishing. Genome Res. 8:195–202 [DOI] [PubMed] [Google Scholar]
  • 9. Lowe TM, Eddy SR. 1997. tRNAscan-SE: a program for improved detection of transfer RNA genes in genomic sequence. Nucleic Acids Res. 25:955–964 [DOI] [PMC free article] [PubMed] [Google Scholar]

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

RESOURCES