A Microbial Biorealm page on the genus Roseobacter denitrificans
Higher order taxa
Bacteria, Proteobacteria, Alphaproteobacteria, Rhodobacterales, Rhodobacteraceae, Roseobacter
Roseobacter denitrificans sp. OCh114 (previously called Erythrobacter sp. OCh114)
Description and significance
Roseobacter denitrificans is a purple aerobic anyoxygenic phototrophic (AAP) bacterium that dwells free-living in lakes and ocean surface waters, soils and even near deep sea hydrothermal vents. (1,5) It can be isolated from the surfaces of green seaweeds of the coastal marine sediments in Australia, using proteinase K treatment followed by phenol extraction. (10,2) The first instance of its isolation however, was from the samples collected in aerobic marine environments: thalli of Enteromorpha linza, Porphyra sp., Sargussum horneri; beach sand; and the surface seawater from Aburatsubo Inlet in March and May 1978. (13) Members of the Roseobacter clade are widespread and abundant in such marine environments, having diverse metabolisms. The purple proteobacteria in particular, are the only known organisms to capture light energy to enhance growth requiring the presence of oxygen yet do not produce oxygen themselves. It grows photoautotrophically only at low oxygen levels, while at higher oxygen levels, the photosynthetic apparatus is down-regulated, resulting in chemotrophic growth using organic carbon. (2) The highly adaptive AAPs compose more than 10% of the microbial community in some euphotic upper ocean waters and are potentially major contributors to the fixation of the greenhouse gas CO2. The marine AAP species R. denitrificans grows not only photoheterotrophically in the presence of oxygen and light but also anaerobically in the dark using nitrate or trimethylamine N-oxide as an electron acceptor. It is the most studied AAP for this reason and is one of the main model organisms to study aerobic phototrophic bacteria. (2)
The importances of the bacterium's genome sequence are for the following reasons: 1) The evolutionary genesis of photosynthesis genes - it is a marine bacterium, and so may be representative of the globally huge population of aerobic phototrophic bacteria and help narrow their true evolutionary position by whole genome comparisons; (4,7) 2) Pathways of carbon dioxide fixation and production - in understanding the processes for its autotrophic CO2 production and the key genes involved in AAP CO2 fixation pathways. As the only aerobic phototrophic bacterium capable of anaerobic growth with use of nitrate as a terminal electron acceptor, it can also be used to facilitate subsequent studies of the effects of oxygen on photosynthetic and other metabolic processes; (5,6) 3) Light and oxygen signal transduction in gene expression - offering an opportunity, through bioinformatic approaches, to use the AAP's exaggerated responses to study of both light- and oxygen-responsive pathways and mechanisms that are difficult to study in other species. (3,4,11)
The genome sequence of Roseobacter denitrificans sp OCh 114 was completed in 2006 by a team in Arizona State University as the first AAP sequenced. (12) R. denitrificans contains a circular chromosome of 4,133,097 bp and four plasmids. Nearly half of the genes in the largest plasmid (pTB1) share a high degree of similarity to genes in plasmid pSD25 from Ruegeria sp. isolate PR1b and the Ti plasmid from Agrobacterium tumefaciens strain C58. (8) The conservation of many DNA integration and transfer proteins, plasmid replication proteins, and inverted repeats imply that R. denitrificans plasmid pTB1 may also promote lateral gene transfer. This possibility is especially interesting considering the propensity of R. denitrificans to associate with higher organisms. The genome of R. denitrificans additionally lacks genes that code for known photosynthetic carbon fixation pathways, with most notably missing the genes for Calvin cycle enzymes ribulose bisphosphate carboxylase (RuBisCO) and phosphoribukolkinase. (2)
Nearly 15% of the R. denitrificans genome is dedicated to the construction of transport proteins. Among these transporters are more than 120 genes coding for peptide and amino acid transporters(many branched chain), more than 110 genes coding for sugar and carbohydrate transporters, and more than 70 cation and iron transporters. These help the bacteria to acquire nitrogen other than fixing dinitrogen and allow it to adapt to the uptake of a variety of available carbon sources. (2)
The Complete Genome Sequence of Roseobacter denitrificans Reveals a Mixotrophic Rather than Photosynthetic Metabolism provides a possible explanation of how CO2 is fixated and produced using the complete genome sequence. "Based on the genome sequence of R. denitrificans, we suggest that they fix CO2 mixotrophically by using a sequestration pathway supplemented with additional CO2 provided by CO oxidation and heterotrophic respiration." (2)
Cell structure and metabolism
The bacteria are gram-negative rods motile by means of polar or subpolar flagella, oxidase positive, and catalase positive, and produce a small amount of acids from glucose, fructose, xylose, and the other carbohydrates. As an AAP the bacteria captures light in order to gain energy and grow. The primary photosynthetic pigment of AAPBs is bacteriochlorophyll a. The amount of bacteriochlorophyll a found in Och 114 was 5.5 nmol/mg (dry weight). (13) This cellular bacteriochlorophyll a content is rather low, and the genes coding the enzymes synthesizing bacteriochlorophyll a may not be phenotype-expressed when limited by environmental conditions. (6) Although bacteriochlorophyll a is possesed thus the organism is capable of aerobic photosynthesis; however, it is still unable to grow autotrophically. (14)
R.denitrificans does not rely light energy as the only source for energy though and utilizes many other energy-yielding metabolic pathways that likely helps provide additional energy, in the form of ATP, for the formation of OAA from CO2 and metabolic intermediates. The organism has a broad range of physiological properties and uses a multitude of different carbon sources. Additional energy is gained by the organisms through oxidization of reduced sulfur compounds such as sulfite or thiosulfate. (13,14) Inorganic sulfur oxidation, encoded by the large soxWXYZABCDEF cluster, is a likely source for extra energy production yielding sulfate as environmental output. (2) Additionally R. denitrificans has the ability to process organic phosphates as well as degrade the chemically stable C-P bond-containing phosphonates (despite the fact that a major limiting growth factors in the open ocean is phosphorous availability). Another factor is that the organism lacks N2O reductase thus unable to fix dinitrogen. Yet the reduction of oxidized nitrogen compounds is a significant aspect of the lifestyle of the bacteria. The diversity and adaptibility of R. denitrificans is demonstrated by the other means it acquires nitrogen other than through dinitrogen, and it has a large complement of genes to account for this. (2)
All other aerobic organisms that oxidize CO to CO2 for energy grow autotrophically using the Calvin cycle. Although R. denitrificans has not been shown to oxidize CO in culture, it contains the necessary genes (coxG and coxSML) and has been suggested to likely perform the reaction under proper conditions. (15)
Describe any interactions with other organisms (included eukaryotes), contributions to the environment, effect on environment, etc.
There are no known pathological effects of this bacterium on humans.
Application to Biotechnology
Does this organism produce any useful compounds or enzymes? What are they and how are they used?
Enter summaries of the most recent research here--at least three required
Mixotrophic fixation of CO2
Recent studies suggest that due to genes missing for Calvin cycle enzymes in R. denitrificans yet retained genes for pyruvate-orthophosphate dikinase and phosphoenolpyruvate (PEP) carboxylase, processes similar to plant C4 sequestration, crassulacean acid metabolism, and anaplerotic carbon fixation, coupled with photoheterotrophic energy metabolism, cause the mixotrophic fixation.
by using a sequestration pathway supplemented with additional CO2 provided by CO oxidation and heterotrophic respiration. (2)
1) Fleischman D and Kramer D (1998) Photosynthetic rhizobia. Biochim Biophys Acta 1364: 17-36.
2) Swingley W.D., Sadekar S., Mastrian S.D., Matthies H.J., Hao J., Ramos H., Acharya C.R., Conrad A.L., Taylor H.L., Dejesa L.C., Shah M.K., O'Huallachain M.E., Lince M.T., Blankenship R.E., Beatty J.T., Touchman J.W. ; "The complete genome sequence of Roseobacter denitrificans reveals a mixotrophic rather than photosynthetic metabolism"; J. Bacteriol. 189:683-690 (2007)
4) Candela, M., E. Zaccherini, and D. Zannoni. 2001. Respiratory electron transport and light-induced energy transduction in membranes from the aerobic photosynthetic bacterium Roseobacter denitrificans. Arch. Microbiol. 175:168-177
6) Kolber, Z. S., F. G. Plumley, A. S. Lang, J. T. Beatty, R. E. Blankenship, C. L. VanDover, C. Vetriani, M. Koblizek, C. Rathgeber, and P. G. Falkowski. 2001. Contribution of aerobic photoheterotrophic bacteria to the carbon cycle in the ocean. Science 292:2492-2495
7) Schwarze C, Carluccio AV, Venturoli G & Labahn A (2000) Photo-induced cyclic electron transfer involving cytochrome bc1 complex and reaction center in the obligate aerobic phototroph Roseobacter denitrificans. Eur J Biochem 267: 422–433
8) Goodner, B., G. Hinkle, S. Gattung, N. Miller, M. Blanchard, B. Qurollo, B. S. Goldman, Y. Cao, M. Askenazi, C. Halling, L. Mullin, K. Houmiel, J. Gordon, M. Vaudin, O. Iartchouk, A. Epp, F. Liu, C. Wollam, M. Allinger, D. Doughty, C. Scott, C. Lappas, B. Markelz, C. Flanagan, C. Crowell, J. Gurson, C. Lomo, C. Sear, G. Strub, C. Cielo, and S. Slater. 2001. Genome sequence of the plant pathogen and biotechnology agent Agrobacterium tumefaciens C58. Science 294:2323-2328
14) Sorokin, DY (1995) Sulfitobacter pontiacus gen. nov., sp. nov.—a new heterotrophic bacterium from the Black-Sea, specialized on sulfite oxidation. Microbiology 64: 295–305
15) King, G. M. (2003) Molecular and culture-based analyses of aerobic carbon monoxide oxidizer diversity. Appl. Environ. Microbiol. 69:7257-7265
Edited by George Huang student of Rachel Larsen