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. 2015 Apr 9;3(2):e00251-15. doi: 10.1128/genomeA.00251-15

Complete Genome Sequence of a Novel Bacterium within the Family Rhodocyclaceae That Degrades Polycyclic Aromatic Hydrocarbons

David R Singleton a,, Allison N Dickey b, Elizabeth H Scholl b, Fred A Wright b, Michael D Aitken a
PMCID: PMC4392151  PMID: 25858839

Abstract

A polycyclic aromatic hydrocarbon-degrading bacterium designated strain Ca6, a member of the family Rhodocyclaceae and a representative of the uncharacterized pyrene group 1 (PG1), was isolated and its genome sequenced. The presence of several genes suspected to be associated with PG1 was confirmed, and additional genes for aromatic compound metabolism were detected.

GENOME ANNOUNCEMENT

Polycyclic aromatic hydrocarbons (PAHs) are ubiquitous chemicals that, when concentrated at contaminated sites, can pose a serious threat to human and environmental health. Of particular concern are high-molecular-weight PAHs of four or more aromatic rings that are potentially both more carcinogenic and resistant to microbial degradation than are their low-molecular-weight counterparts (1, 2). A prior stable-isotope probing study with the four-ring PAH pyrene revealed DNA sequences from several groups of uncharacterized proteobacteria (3). One predominant group of sequences within the betaproteobacterial family Rhodocyclaceae, designated pyrene group 1 (PG1), was later also implicated in the degradation of phenanthrene (4). A previously constructed metagenome from a mixed culture dominated by PG1 contained eight different ring-hydroxylating dioxygenase (RHD) genes predicted to code for enzymes involved in the initial step of aerobic PAH metabolism (5). Six of those RHDs heterologously expressed in Escherichia coli demonstrated PAH transformation capabilities (5). We subsequently isolated a member of PG1, designated strain Ca6, and its genome was sequenced.

DNA was extracted from a culture of Ca6 grown with pyrene using a modification of the FastDNA spin kit for soil (MP Biomedicals, Santa Ana, CA). The PacBio RSII platform, utilizing 3 single-molecule real-time (SMRT) cells, was used to acquire the raw sequence reads at the University of North Carolina High-Throughput Sequencing Facility. The reads were de novo assembled into a single contig with SMRT Analysis 2.2 using HGAP3, and the contig was polished using Quiver (6). Significant overlap between the ends indicated that the molecule was circular, and the Minimus2 assembler was used to circularize a split contig (7). Final polishing was performed with Quiver, and the resulting consensus sequence had an accuracy of >99.999%.

The finalized circular contig comprised 2,934,611 bp, with an average coverage of 228×. This chromosome was annotated by both the Department of Energy Joint Genomics Institute (JGI) Integrated Microbial Genomes system and the NCBI Prokaryotic Genome Annotation Pipeline. The JGI annotation predicted 2,902 genes, with 2,847 protein-coding genes, two copies of the rRNA operons, and 45 tRNA genes. The G+C content of the chromosome is 55.14%. The closest described relative is Sulfuritalea hydrogenivorans strain sk43H (94% 16S rRNA gene identity).

The predicted proteins were submitted to AromaDeg, a database for the identification of genes associated with the degradation of aromatic compounds (8). All eight RHD genes previously detected in a metagenome were present in the genome of Ca6. AromaDeg additionally identified four genes potentially associated with benzene or benzoate degradation, three and six putative extradiol dioxygenase genes associated with monocyclic and bicyclic compounds, respectively, two extradiol dioxygenases in the protocatechuate family, and a number of additional Rieske-type proteins.

Strain Ca6 is currently being characterized as belonging to a novel genus and species. Gene sequences highly similar to strain Ca6 have been detected in pristine and contaminated sites worldwide, so this organism represents a possible prominent degrader of hazardous aromatic compounds in both natural and engineered systems.

Nucleotide sequence accession number.

The NCBI-annotated genome of Ca6 was deposited in GenBank under the accession no. CP010554. The JGI-annotated version is available at the DOE JGI-IMG website under the name “Rhodocyclaceae bacterium PG1-Ca6.”

ACKNOWLEDGMENTS

This work was supported by a grant from the National Institute of Environmental Health Sciences (NIEHS) Superfund Research Program (SRP), no. 5 P42ES005948.

We thank members of the UNC-HTSF for their sequencing efforts and George Yuan of Pacific Biosciences for assistance in the assembly of the genome.

Footnotes

Citation Singleton DR, Dickey AN, Scholl EH, Wright FA, Aitken MD. 2015. Complete genome sequence of a novel bacterium within the family Rhodocyclaceae that degrades polycyclic aromatic hydrocarbons. Genome Announc 3(2):e00251-15. doi:10.1128/genomeA.00251-15.

REFERENCES

  • 1.National Toxicology Program 2011. Report on carcinogens, twelfth edition, 2011. National Toxicology Program, U.S. Department of Health and Human Services, Washington, DC. [Google Scholar]
  • 2.U.S. Environmental Protection Agency 2000. A resource for MGP site characterization and remediation. Expedited site characterization and source remediation at former manufactured gas plant sites. EPA-542-R-00-005. U.S. Environmental Protection Agency, Washington, DC. [Google Scholar]
  • 3.Singleton DR, Sangaiah R, Gold A, Ball LM, Aitken MD. 2006. Identification and quantification of uncultivated proteobacteria associated with pyrene degradation in a bioreactor treating PAH-contaminated soil. Environ Microbiol 8:1736–1745. doi: 10.1111/j.1462-2920.2006.01112.x. [DOI] [PubMed] [Google Scholar]
  • 4.Singleton DR, Hunt M, Powell SN, Frontera-Suau R, Aitken MD. 2007. Stable-isotope probing with multiple growth substrates to determine substrate specificity of uncultivated bacteria. J Microbiol Methods 69:180–187. doi: 10.1016/j.mimet.2006.12.019. [DOI] [PubMed] [Google Scholar]
  • 5.Singleton DR, Hu J, Aitken MD. 2012. Heterologous expression of polycyclic aromatic hydrocarbon ring-hydroxylating dioxygenase genes from a novel pyrene-degrading betaproteobacterium. Appl Environ Microbiol 78:3552–3559. doi: 10.1128/AEM.00173-12. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Chin C-S, Alexander DH, Marks P, Klammer AA, Drake J, Heiner C, Clum A, Copeland A, Huddleston J, Eichler EE, Turner SW, Korlach J. 2013. Nonhybrid, finished microbial genome assemblies from long-read SMRT sequencing data. Nat Methods 10:563–569. doi: 10.1038/nmeth.2474. [DOI] [PubMed] [Google Scholar]
  • 7.Sommer DD, Delcher AL, Salzberg SL, Pop M. 2007. Minimus: a fast, lightweight genome assembler. BMC Bioinformatics 8:64. doi: 10.1186/1471-2105-8-64. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Duarte M, Jauregui R, Vilchez-Vargas R, Junca H, Pieper DH. 2014. AromaDeg, a novel database for phylogenomics of aerobic bacterial degradation of aromatics. Database (Oxford) 2014:bau118. doi: 10.1093/database/bau118. [DOI] [PMC free article] [PubMed] [Google Scholar]

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