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Revision as of 06:52, 24 July 2007
| Streptomyces | |
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| Slide culture of a Streptomyces sp. | |
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| Genus: | Streptomyces Waksman & Henrici 1943
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S. ambofaciens | |
Streptomyces is the largest genus of Actinobacteria, a group of Gram-positive and generally high GC-content bacteria.[1] Streptomycetes are found predominantly in soil and in decaying vegetation, and most produce spores. Streptomycetes are noted for their distinct "earthy" odor which results from production of a volatile metabolite, geosmin.
Streptomycetes are characterised by a complex secondary metabolism.[1] They produce a large number of antibiotics that are in clinical use (Neomycin, Chloramphenicol); the now rarely used streptomycin takes its name directly from Streptomyces. Streptomycetes are infrequent pathogens, though infections in human such as mycetoma can be caused by S. somaliensis and S. sudanensis and in plants such as scabies can be caused by S. caviscabies and S. scabies.
Genomics
The complete genome of one of the strain, "S. coelicolor" A3(2), was published in 2002.[2] At the time, the "S. coelicolor" genome contained the largest number of genes of any bacterium. The genome sequence of S. avermitilis was completed in 2003.[3] This is the first complete genome sequence of the industrial microorganism. Both of these genomes comprise a single chromosome that is linear, unlike most bacterial genomes which comprise a circular chromosome. The genome sequence of S. scabies, a member of the genus with the ability to cause potato scab disease, has been determined at the Wellcome Trust Sanger Institute and is currently in annotation, with publication scheduled for 2007.
Taxonomically, "S. coelicolor" A3(2) belongs to the species of S. violaceoruber and not a validly described separate species; don't mistake S. coelicolor A3(2) for S. coelicolor (Müller) (ATCC 23899).
Biotechnology
In recent years, biotechnology researchers have begun to use Streptomyces spp. for production of recombinant human proteins. Traditionally, Escherichia coli was the species of choice to host eukaryotic genes since it was well understood and easy to work with.[4][5] However, E. coli introduces problems such as incorrect (or lack of) glycosylation and incorrect protein folding, resulting in insolubility and loss of bioactivity of the product.[6] Streptomyces spp. on the other hand have the ability to secrete correctly folded recombinant proteins into the medium after production simplifying the subsequent purification steps. These properties among others make Streptomyces spp. an attractive alternative to other bacteria such as E. coli and Bacillus subtilis[citation needed].
Medicine
Streptomyces is the largest antibiotic producing genus ([1]), producing both antibacterials and antifungals, and also a wide range of other bioactive compounds such as immunosuppressants
Some of the antifungals produced by Streptomyces spp.
- Nystatin (from S. noursei)
- Amphotericin B (from S. nodosus)
- Natamycin (from S. natalensis)
Some of the antibiotics produced by Streptomyces spp.
- Erythromycin (from S. erythreus)
- Neomycin (from S. fradiae)
- Streptomycin (from S. griseus)
- Tetracycline (from S. rimosus)
- Vancomycin (from S. orientalis)
- Rifamycin (from S. mediterranei)
- Chloramphenicol (from S. venezuelae)
Some of the anti-cancer compounds produced by Streptomyces spp.
- Migrastatin (from S. platensis)
References
- ^ a b Madigan M; Martinko J (editors). (2005). Brock Biology of Microorganisms (11th ed. ed.). Prentice Hall. ISBN 0-13-144329-1.
{{cite book}}:|author=has generic name (help);|edition=has extra text (help)CS1 maint: multiple names: authors list (link) - ^ Bentley SD; et al. (2002). "Complete genome sequence of the model actinomycete "Streptomyces coelicolor" A3(2)". Nature. 417: 141–147. PMID 12000953.
{{cite journal}}: Explicit use of et al. in:|author=(help) - ^ Ikeda H; Ishikawa J; Hanamoto A; Shinose M; Kikuchi H; Shiba T; Sakaki Y; Hattori M; Omura S (2003). "Complete genome sequence and comparative analysis of the industrial microorganism Streptomyces avermitilis". Nat. Biotechnol. 21: 526–531. PMID 12692562.
{{cite journal}}: CS1 maint: multiple names: authors list (link) - ^ Brawner M, Poste G, Rosenberg M, Westpheling J (1991). "Streptomyces: a host for heterologous gene expression". Curr Opin Biotechnol. 2 (5): 674–81. PMID 1367716.
{{cite journal}}: CS1 maint: multiple names: authors list (link) - ^ Payne G, DelaCruz N, Coppella S (1990). "Improved production of heterologous protein from Streptomyces lividans". Appl Microbiol Biotechnol. 33 (4): 395–400. PMID 1369282.
{{cite journal}}: CS1 maint: multiple names: authors list (link) - ^ Binnie C, Cossar J, Stewart D (1997). "Heterologous biopharmaceutical protein expression in Streptomyces". Trends Biotechnol. 15 (8): 315–20. PMID 9263479.
{{cite journal}}: CS1 maint: multiple names: authors list (link)
Further reading
- Baumberg S (1991). Genetics and Product Formation in Streptomyces. Kluwer Academic. ISBN 978-0306438851.
- Gunsalus IC (1986). Bacteria: Antibiotic-producing Streptomyces. Academic Press. ISBN 978-0123072092.
- Hopwood DA (2007). Streptomyces in Nature and Medicine: The Antibiotic Makers. Oxford University Press. ISBN 978-0195150667.
See also
- List of world records
- Antimycin A - compound produced by this bacteria used in piscicides.
External links
- S. avermitilis genome homepage (Kitasato Institute for Life Sciences)
- S. avermitilis is the avermectin producer.
- S. coelicolor A3(2) genome homepage (Sanger Institute)
- Streptomyces.org.uk homepage (John Innes Centre)
- ScoDB - the S. coelicolor A3(2) genome annotation server
- Streptomyces Genome Projects from Genomes OnLine Database