Rhodococcus ruber

This student page has not been curated.

Classification

Domain: Bacteria

Phylum: Actinobacteria

Class: Actinobacteria

Order: Corynbacteriales

Family: Nocardiaceae

Genus: Rhodococcus

Species

NCBI: [1]

Rhodococcus ruber

Description and Significance

Historically, the genus Rhodococcus was first defined by Zopf in 1891. Nocardia rubra, or what is known today as Rhodococcus ruber, was isolated from a soil sludge by Kruse in 1896. However, there were issues with classification due to morphological and staining identification techniques. In 1977, Goodfellow and Alderson did a complete reclassification of the genus Rhodococcus, which resulted in Norcordia rubra being amended as Rhodococcus ruber.

The term Rhodococcus is from the combination of the Greek words “rhodon” and “coccus” meaning “the rose” and “the grain“ respectively. The morphological structure of R. ruber first starts as long rods, then breaks off into short rods and cocci throughout different growth phases. Rhodococcus ruber is a gram positive, non-motile, non-spore forming bacteria.

Figure _: Rhodococcus ruber on a LB agar plate [ ]

Genome Structure

12 genome studies have been reported for the following strains of Rhodococcus ruber: R. ruber str. YC-YT1, R. ruber str. YYL, R. ruber str. P14, R. ruber str. SD3, R. ruber str. R1, R. ruber str. DSM 43338, R. ruber str. P25, R. tuber IEGM 231, R. ruber str. OA1, R. ruber str. BKS 20-38, R. ruber str. Chol-4, and R. ruber str. NCRX 15591.

The genome of Rhodococcus ruber consists of one circular chromosome with an average size of 5.57 Mb. The genome size varies for every strain and larger genome sizes can be attributed to the presence of circular plasmids. The strains of R. ruber that contain plasmids are YC-TC1, YYL, and R1. The average amount of protein coding genes is 4932 and the average G+C content is 70.49%. A high guanine-cytosine content is characteristic of Rhodococcus species to provide DNA stability in varying conditions.

The genome sequences of R. ruber are helpful in identifying the genes necessary for metabolic pathways and cycles that R. ruber employs including the tricarboxylic acid cycle, pentose phosphate pathway, glycolysis, and glujconeogeneis. Additionally, the beta oxidation pathway and alkane degradation pathway are utilized. The genome highlights multiple metabolic gene clusters that are used for degradation of aromatic compounds, steroids, hydrocarbons, and xenobiotic polymers that R. ruber uses for carbon and energy sources. Some strains of R. ruber contain redundant genes which contributes to their versatile metabolic abilities with various nutrient sources.

Cell Structure and Metabolism

Interesting features of cell structure; how it gains energy; what important molecules it produces.

Figure _: Rhodococcus ruber cell wall structure [1]

Ecological Impacts

Habitat; symbiosis; biogeochemical significance; contributions to environment.
If relevant, how does this organism cause disease? Human, animal, plant hosts? Virulence factors, as well as patient symptoms.

References

[1]| Alvarez, H. M. Biology of Rhodococcus; Springer, 2010; Vol. 16.

[2] | Bala

[3] | Farkas

[4] | Finnerty, W. R. The Biology and Genetics of the Genus Rhodococcus. Annual Review of Microbiology 1992, 46, 193–218.

[5] | Gravouil, K.; Ferru-Clément, R.; Colas, S.; Helye, R.; Kadri, L.; Bourdeau, L.; Moumen, B.; Mercier, A.; Ferreira, T. Transcriptomics and Lipidomics of the Environmental Strain Rhodococcus ruber Point out Consumption Pathways and Potential Metabolic Bottlenecks for Polyethylene Degradation. Environmental Science & Technology 2017, 51, 5172–5181.

[6] | Guevara

[7] | Heras, L. F. D. L.; Fernández, E. G.; Llorens, J. M. N.; Perera, J.; Drzyzga, O. Morphological, Physiological, and Molecular Characterization of a Newly Isolated Steroid-Degrading Actinomycete, Identified as Rhodococcus ruber Strain Chol-4. Current Microbiology 2009, 59, 548–553.

[8] | Krivorucho

[9] | Montazer, Z.; Najafi, M. B. H.; Levin, D. B. Challenges with Verifying Microbial Degradation of Polyethylene. Polymers 2020, 12.

[10] | Mor, R.; Sivan, A. Biofilm formation and partial biodegradation of polystyrene by the actinomycete Rhodococcus ruber. Biodegradation 2008, 19, 851–858.

[11]| Santo, M.; Weitsman, R.; Sivan, A. The role of the copper-binding enzyme – laccase – in the biodegradation of polyethylene by the actinomycete Rhodococcus ruber. International Biodeterioration & Biodegradation 2013, 84, 204–210.

[12] | Sivan, A.; Szanto, M.; Pavlov, V. Biofilm development of the polyethylene-degrading bacterium Rhodococcus ruber. Applied Microbiology and Biotechnology 2006, 72, 346–352.

[13] [Organism:noexp | Genome]

Author

Page authored by Hannah von Werder, student of Prof. Jay Lennon at Indiana University.