Streptomyces coelicolor: Difference between revisions

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==Pathology==
==Pathology==


How does this organism cause disease? Human, animal, plant hosts? Virulence factors, as well as patient symptoms.
''Streptomyces coelicolor'' does not cause disease in humans, plants, or animals. Other ''Streptomyces'' species, however are plant pathogens. For example, ''Streptomyces scabies'' causes potato scabs and ''Streptomyces ipomoeae'' causes disease in sweet potatoes.


Edited by Neena Patel, student of Rachel Larsen at UCSD.
Edited by Neena Patel, student of Rachel Larsen at UCSD.

Revision as of 00:44, 31 May 2007

A Microbial Biorealm page on the genus Streptomyces coelicolor

Classification

Higher order taxa

Domain: Bacteria

Phylum: Actinobacteria

Class: Actinobacteria

Subclass: Actinobacteridae

Order: Actinomycetales

Suborder: Streptomycineae

Family: Streptomycetaceae

Strains: Streptomyces coelicolor A3(2)

(1)NCBI

Edited by Amy Stapp, student of Rachel Larsen at UCSD.

Genus

Genus species: Streptomyces coelicolor

Other Names: Streptothrix coelicolor, Cladothrix coelicolor, Nocardia coelicolor, Actinomyces coelicolor (1) Edited by Amy Stapp, student of Rachel Larsen at UCSD.

Description and significance

Streptomyces coelicolor, a filamentous, high G-C, gram + bacteria, was first dubbed Streptothrix coelicolor in 1908 by R. Muller after he found it on a potato scab. Later, it became known as Streptomyces coelicolor. Streptomyces coelicolor, like the streptomyces genus in general, live in the soil. Streptomyces are responsible for much of the break down of organic material in the soil as well as the “earthy” smell of soil. They also live in colonies and have structural similarities to fungus. Colonies of Streptomyces coelicolor release pigments that are blue/green in alkali and red in acidic conditions, thereby giving the bacterial colonies those colors under the respective conditions.Red Streptomyces.jpg Image courtesy of John Innes Center Bioimaging JIC

Streptomyces colonies producing aerial mycelium, except for the red mutant colonies which are not http://www.jic.bbsrc.ac.uk/SCIENCE/molmicro/Strept.html

Other differentiating characteristics of Streptomyces coelicolor are grayish-yellow aerial mycelium, smooth spores, and no melanoid pigment(2). Streptomyces coelicolor are important bacteria and were sequenced because of their “adaptability to environmental stress”, “source of bioactive molecules for medicine and industry”, and “relat[ion] to human pathogens”(3). Streptomyces coelicolor has a very similar core genome to Mycobacterium tuberculosis and Corynebacterium diphtheriae, as well as some similarity to Mycobacterium leprae, so it can be used to study these disease causing bacteria. The streptomyces genus is responsible for producing a majority of the antibiotics in use today, as well as some immunosuppressants and anti-tumor agents. Streptomyces coelicolor also has an interesting life-cycle that includes differentiation into aerial mycelium and spore formation.

Edited by Amy Stapp, student of Rachel Larsen at UCSD.

Genome structure

Streptomyces coelicolor has one linear chromosome and two plasmids, one that is linear and one that is circular. The linear chromosome was sequenced from overlapping clones of the species, most of which were cosmids, that did not contain the two plasmids. This chromosome contains 8,667,507 base pairs, and was the largest bacterial genome sequenced at the time. (Since then, larger bacterial genomes have been sequenced.) The origin of replication (oriC) is located in the middle of the chromosome, and the ends of the chromosome contain terminal inverted repeats (TIRs). The 5’ terminal ends have proteins that are covalently bonded to them. Replication occurs in both directions leaving a gap in one strand of the new chromosome, which is patched by DNA synthesis. The chromosome is considered to be grouped into three regions – the core and two arms. The core region comprises about half of the chromosome and contains the essential genes for the survival of the organism, like “cell division, DNA replication, transcription, translation and amino-acid biosynthesis” (6). The two arm regions are different lengths, one about 1.5 MB and the other 2.3 MB long, and they code for nonessential functions like "secondary metabolites, hydrolytic exoenzymes, the conservons (conserved operons) and 'gas vesicle' proteins" (6). The SPC1 linear plasmid is 365,023 base pairs long, and is involved coding for some regulator proteins including three Sigma factors and proteins found on spore surfaces among other functions. The 31,317 base pair, circular plasmid, SPC2, has a stability region, replication origin, and transfer region. It has a relatively low copy number.

Edited by Amy Stapp, student of Rachel Larsen at UCSD.

Cell structure and metabolism

Streptomyces coelicolor live in the soil, where nutrient conditions can change dramatically. As a result, this bacteria is capable of living on may different carbon sources including "glycerol, L-arabinose, D-arabitol, D-ribose, D-xylose, L-xylitol, D-fructose, D-galactose, D-gluconate, D-glucose, D-mannitol, D-mannose, L-rhamnose, salicin, cellobiose, lactose, maltose, melibiose, trehalose, acetate, citrate, lactate, malate, pyruvate, succinate, tartrate, propanoate, alanine, asparagine, glutamate, glycine, histidine, isoleucine, leucine, lysine, methionine, proline, serine, threonine, tryptophan, [and] valine"(11). Some of its nitrogen sources are "aspartate, asparagine, glutamate, glutamine, isoleucine, leucine, lysine, praline, [and] valine"(11). Despite Streptomyces coelicolor ability to metabolize so many different food sources, it is only capable of aerobic respiration. The lactate dehydrogenase gene is present in Streptomyces coelicolor genome, so the organism should be able to obtain energy from fermentation, but it does not. Some theories as to why this occurs are that some of the other reactions necessary for survival depend on the presence of oxygen or that the byproducts of anaerobic respiration are toxic to the cells. The presence of nar genes, which code for respiratory nitrate reductaces, indicate that under oxygen limiting conditions, Streptomyces coelicolor should be able to use nitrate as an electron receptor. Researchers have determined that the nar genes are indeed expressed and probably used during growth in standing liquid where oxygen levels fluctuate. Despite these findings, conditions that would allow Streptomyces coelicolor to grow anaerobically in a lab setting have not been found yet. Metabolic changes in Streptomyces coelicolor also affect cell differentiation. For example, mutant strains lacking citA, involved in citrate synthase coding, or some bld genes (discussed below) cannot form aerial mycelium when grown on glucose. Glucose forms acidogenic organic acids which makes the substrate in which the organism grows acidic. Citrate synthase initiates the TCA cycle which is necessary for acid metabolism, which is important in keeping the pH of the substrate at a level that does not prevent growth. Without the citA gene or some of the bld genes, this important ability in impaired and, as such, aerial mycelium and antibiotic production do not occur. When grown on mannitol, which is not acidogenic, aerial hyphae will form even in bld and citA mutants.

Streptomyces have a life cycle similar to that of fungi. The cycle starts with growth of vegetative mycelium from a spore, followed by ariel mycelium, and, then, spores. This complex life style is facilitated by cell differentiation. Instead of two totally separated cells forming after cell division, chains of cells remain linked together to form a branching “mycelium network”(14). Vegetative hyphae, the individual strands that make up the vegetative mycelium, have hydrophilic surfaces, which fit well since they usually grown in a moist region. When not grown in submerged culture, hyphae have an extra cellular matrix of up to 1.5 micrometers wide that surround it. Older hyphae have larger extra cellular layers than newer hyphae. Production of aerial mycelium is coded for in the bld genes of Streptomyces coelicolor. When grown in the presence of glucose, SapB is believed to help aerial mycelium break the surface tension of the liquid they begin growing in and ascend into the air. The surfaces of aerial hyphae, the individual strands that make up the aerial mycelium, are hydrophobic, unlike vegetative hyphae. A fibrous layer also surrounds newly formed aerial hyphae, and is believed to help break surface tension as the hyphae move out of an aqueous substrate and into the air. This fibrous layer is not present in older aerial hyphae, so it is believed to be replaced with a “more organized mosaic layer”(13). Sporulation in Streptomyces coelicolor is controlled by the whi genes. Sporulation begins when indentations at the tips of aerial hyphae begin to appear. These indentations are the place where spores will form. The mosaic of fibers covering the aerial hyphae then form a ring around the indentations. A round spore then forms and is covered in the fibrous mosaic. Mature spores are denoted by surface concavities believed to be caused by metabolic slowing and dehydration.


Edited by Amy Stapp, student of Rachel Larsen at UCSD.

Ecology

Describe any interactions with other organisms (included eukaryotes), contributions to the environment, effect on environment, etc.

Pathology

Streptomyces coelicolor does not cause disease in humans, plants, or animals. Other Streptomyces species, however are plant pathogens. For example, Streptomyces scabies causes potato scabs and Streptomyces ipomoeae causes disease in sweet potatoes.

Edited by Neena Patel, student of Rachel Larsen at UCSD.

Application to Biotechnology

Blue Streptomyces.jpg Image courtesy of John Innes Center Bioimaging JIC

"Colonies of Streptomyces coelicolor secreting blue actinorhodin antibiotic" ("From Mapping to Mining...", John Innes Center) http://www.jic.bbsrc.ac.uk/SCIENCE/molmicro/Strept.html

Current Research

Research is being done to determine how Streptomyces coelicolor use signal transduction pathways to sense changes in their highly variable soil environments, which signals antibiotic and spore production. Link to Researcher's Web-page

The bacterial development of Streptomyces coelicolor is also being studied to determine “the role of specific RNA polymerase holoenzymes controlling development and stress response, global characterisation of spore maturation and germination, cytoskeletal proteins, and chromosome organization during hyphal growth” (9). Link to Researcher's Web-Page

Streptomyces coelicolor is currently the subject of research at the University of Warwick due to its ability to produce prodiginines. These compounds show promise in targeting cancer cells, and a synthetic counterpart to the compound made naturally by Streptomyces coelicolor is in clinical trials as of November 2006.

Streptomyces jewels.jpgImage courtesy of the John Innes Center JIC

"Jewels in the crown of a Streptomyces colony are antibiotic secretions" ("From Mapping to Mining", John Innes Center) http://www.jic.bbsrc.ac.uk/SCIENCE/molmicro/Strept.html

References

(1) "Streptomyces coelicolor A3(2)". NCBI Taxonomy Browser. 29 April 2007. NCBI.

(2) Conn, Jean E. “The Pigment Production of Actinomyces coelicolor and A. violaceus-ruber”. Journal of Bacteriology. 1943. Volume 46. p. 133-149. Link to Article

(3) “From Mapping to Mining the Streptomyces Genome”. John Innes Centre Website. 2001. Link to Article

(4) Thompson, Charles J., Dorris Fink, and Liem D. Nguyen. “Principles of Microbial Alchemy: Insights from the Streptomyces coelicolor Genome Sequence”. Genome Biology 3.7. (2002) Link to Article on PubMed

(5) Kutzner, Hans J and Selman A. Waksman. “Streptomyces coelicolor Muller and Streptomyces violaceoruber Waksman and Curtis, Two Distinctly Different Organisms.” Journal of Bacteriology 78.4 (1959) p. 528-538. Link to Article

(6) Bentley, S.D., K. F. Chater, A.-M. Cerdeño-Tárraga, G. L. Challis , N. R. Thomson, K. D. James, D. E. Harris, M. A. Quail, H. Kieser, D. Harper, A. Bateman, S. Brown, G. Chandra, C. W. Chen, M. Collins, A. Cronin, A. Fraser, A. Goble, J. Hidalgo, T. Hornsby, S. Howarth, C.-H. Huang, T. Kieser, L. Larke, L. Murphy, K. Oliver, S. O'Neil, E. Rabbinowitsch, M.-A. Rajandream, K. Rutherford, S. Rutter, K. Seeger, D. Saunders, S. Sharp, R. Squares, S. Squares, K. Taylor, T. Warren, A. Wietzorrek, J. Woodward, B. G. Barrell, J. Parkhill and D. A. Hopwood. "Complete Genome Sequence of the Model Actinomycete Streptomyces coelicolor A3(2)." Nature. 417. (2002) p. 141-147. Link to Article

(7) Bentley, S. D., S. Brown, L. D. Murphy, D. E. Harris, M. A. Quail, J. Parkhill, B. G. Barrell, J. R. McCormick, R. I. Santamaria, R. Losick, M. Yamasaki, H. Kinashi, C. W. Chen, G. Chandra, D. Jakimowicz, H. M. Kieser, T. Kieser and K. F. Chater. "SPC1, a 356023 bp Linear Plasmid Adapted to the Ecology and Developmental Biology of It's Host, Streptomyces coelicolor." Molecular Microbiology 51.6 (2004) p. 1615-1628.

(8) Haug, Iris, Anke Weissenborn, Dirk Brolle, Stephen Bentley, Tobias Kieser, and Josef Altenbuchner. “Streptomyces Coelicolor A3(2) Plasmid SCP2*: Deductions from the Complete Sequence”. Microbiology 149 (2003). p. 505-513. Link to Article

(9) “Streptomyces: Research.” 30 March 2007. UEA Norwich Website. University of East Anglia. 30 April 2007. http://openwetware.org/wiki/Streptomyces:Research

(10) Stanley, Anna E., Laura J. Walton, Malek Kourdi Zerikly, Christophe Corre and Gregory L. Challis. “Elucidation of the Streptomyces coelicolor pathway to 4-methoxy- 2,29-bipyrrole-5-carboxaldehyde, an intermediate in prodiginine Biosynthesis.” Chemical Communications Articles. (Oct. 2006) RBS Publishing. p. 3981-3983. Link to Article

(11) Borodina, Irina, Preben Krabben, and Jens Nielsen. "Genome-scale Analysis of Streptomyces Coelicolor A3(2) Metabolism". Genome Research. 15 (June 2005) p. 820-828.

(12) Keleman, Gabriella H. and Mark J. Buttner. "Initiation of aerial mycelium formation in Streptomyces". Current Opinion in Microbiology. 1 (1998) p. 656-662.

(13) Del Sol, Ricardo, Ian Armstrong, Chris Wright, and Paul Dyson. “Characterization of Changes to the Cell Surface during the Life Cycle of Streptomyces coelicolor: Atomic Force Microscopy of Living Cells.” (2007) Journal of Bacteriology. 189.6 p. 2219-2225.

(14) “Cell Division and Development of Streptomyces”. Genexpress. 22 Aug. 2002. Scheikunde University Leiden. 29 May 2007. Link to Website

(15) Viollier, Patrick H., Wolfgang Minas, Glenn E. Dale, Marc Folcher, and Charles J. Thompson. "Role of Acid Metabolism in Streptomyces coelicolor Morphological Differentiation and Antibiotic Biosynthesis." (2001) Journal of Bacteriology. 183.10 p. 3184-3192.

(16) van Keulen, G., J. Alderson, J. White and R.G. Sawers. "Nitrate Respiration in the actinomycete Streptomyces coelicolor." (2005) Biochemical Society Transactions. 33.1 p.210 - 212.



Edited by student of Rachel Larsen and Kit Pogliano