Abstract
The whole-genome shotgun sequence of Rhodococcus ruber strain Chol-4 is presented here. This organism was shown to be able to grow using many steroids as the sole carbon and energy sources. These sequence data will help us to further explore the metabolic abilities of this versatile degrader.
GENOME ANNOUNCEMENT
Rhodococci are aerobic, catabolically versatile soil bacteria with a high GC content and high levels of mycolic acids in their cell envelopes. They have been used as model organisms for numerous applications in bioremediation and biocatalysis due to their exceptional ability to degrade a broad range of compounds (1–5). Rhodococcus ruber strain Chol-4 was isolated from a sewage sludge sample and it is able to grow in minimal medium supplemented with different steroids as sole carbon sources, such as cholesterol, cholestenone, testosterone, 4-androstene-3,17-dione (AD), 1,4-androstadiene-3,17-dione (ADD), and pregnenolone, among others (6, 7).
In order to get a panoramic view of the genetic complexity and metabolic diversity of this strain, the R. ruber strain Chol-4 genome was sequenced using the Roche/454 GS FLX system and assembled with the Newbler assembler version 2.5p1 software (454 Life Sciences). The whole-genome shotgun (WGS) sequence generated 247,832 reads, 89,687,404 bp, that were assembled into 158 contigs with an N50 length of 83,586 bp, and an average coverage of 16.3 reads/bp. This contig-assembling process generated 5.4 Mb of data with a G+C percentage of 70.6%. When analyzed with the Glimmer software 3.0 version, using all the coding sequences from the already sequenced R. equi, R. erythropolis, R. jostii, and R. opacus, these data revealed 3 rRNA genes, 64 tRNAs genes, and 5,338 putative open reading frames (ORFs).
According to RAST version 4.0 (8) and the Glimmer server, many of these ORFs encode proteins likely involved in the metabolism of different compounds, including amino acids and derivatives (537 ORFs), carbohydrates (472 ORFs), fatty acids/lipids (322 ORFs), proteins (207 ORFs), DNA (110 ORFs), aromatic compounds (100 ORFs), RNA (112 ORFs), sulfur (36 ORFs), phosphorus (33 ORFs), nitrogen (30 ORFs), potassium (20 ORFs), iron (20 ORFs) or secondary metabolic constituents (8 ORFs), among others, while cofactors, vitamins, prosthetic groups, or pigments account for 427 ORFs. The genome also contains 315 ORFs involved in transport, 74 of them being ATP-binding cassette (ABC) transporters (e.g., iron, manganese or molybdate ABC transporters). A total of 104 oxygenase-coding genes acting on aromatic compounds were also identified. This bacterium also contains copper, cobalt, zinc, cadmium, mercuric, arsenic, vancomycin, fluoroquinolone, and beta-lactamase resistance genes.
On the basis of these results, we anticipate that R. ruber strain Chol-4 will display a rich and complex metabolic diversity, far beyond the steroid metabolism we have originally found in this strain.
Nucleotide sequence accession numbers.
This whole-genome shotgun project has been deposited at DDBJ/EMBL/GenBank under the accession number ANGC00000000. The version described in this paper is the first version, ANGC01000000.
ACKNOWLEDGMENTS
L.F.H. was the recipient of a scholarship from the Complutense University of Madrid. This project was funded by the projects BFU2006-15214-C03-02 and BFU2009-11545-C03-02 from the Spanish Ministry of Education and Science
We are very grateful to Jose Luis Garcia (CIB-CSIC) and to Federico Morán (Department of Biochemistry and Molecular Biology I, UCM) for their valuable assistance and expertise.
Footnotes
Citation Fernández de las Heras L, Alonso S, de la Vega de León A, Xavier D, Perera J, Navarro Llorens JM. 2013. Draft genome sequence of the steroid degrader Rhodococcus ruber strain Chol-4. Genome Announc. 1(3):e00215-13. doi:10.1128/genomeA.00215-13.
REFERENCES
- 1. Kobayashi M, Shimizu S. 1998. Metalloenzyme nitrile hydratase: structure, regulation, and application to biotechnology. Nat. Biotechnol. 16:733–736 [DOI] [PubMed] [Google Scholar]
- 2. Plaggenborg R, Overhage J, Loos A, Archer JA, Lessard P, Sinskey AJ, Steinbüchel A, Priefert H. 2006. Potential of Rhodococcus strains for biotechnological vanillin production from ferulic acid and eugenol. Appl. Microbiol. Biotechnol. 72:745–755 [DOI] [PubMed] [Google Scholar]
- 3. van der Geize R, Dijkhuizen L. 2004. Harnessing the catabolic diversity of rhodococci for environmental and biotechnological applications. Curr. Opin. Microbiol. 7:255–261 [DOI] [PubMed] [Google Scholar]
- 4. Vereecke D, Burssens S, Simón-Mateo C, Inzé D, Van Montagu M, Goethals K, Jaziri M. 2000. The Rhodococcus fascians-plant interaction: morphological traits and biotechnological applications. Planta 210:241–251 [DOI] [PubMed] [Google Scholar]
- 5. Martínková L, Uhnáková B, Pátek M, Nesvera J, Kren V. 2009. Biodegradation potential of the genus Rhodococcus. Environ. Int. 35:162–177 [DOI] [PubMed] [Google Scholar]
- 6. Fernández de las Heras L, García Fernández E, Navarro Llorens JM, Perera J, Drzyzga O. 2009. Morphological, physiological, and molecular characterization of a newly isolated steroid-degrading actinomycete, identified as Rhodococcus ruber strain Chol-4. Curr. Microbiol. 59:548–553 [DOI] [PubMed] [Google Scholar]
- 7. Fernández de las Heras L, van der Geize R, Drzyzga O, Perera J, Navarro Llorens JM. 2012. Molecular characterization of three 3-ketosteroid-Δ(1)-dehydrogenase isoenzymes of Rhodococcus ruber strain Chol-4. J. Steroid Biochem. Mol. Biol. 132:271–281 [DOI] [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] [PMC free article] [PubMed] [Google Scholar]