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Streptomyces coelicolor genome

Tudor Toma

Genome Biology 2002, 3:spotlight-20020509-01  doi:10.1186/gb-spotlight-20020509-01

The electronic version of this article is the complete one and can be found online at:

Published:9 May 2002

© 2002 BioMed Central Ltd

Research news

Streptomyces coelicolor is a soil-dwelling, filamentous bacterium responsible for producing most of the natural antibiotics used in human and veterinary medicine. In the May 9 Nature, Stephen Bentley and colleagues from The Wellcome Trust Sanger Institute, Cambridge, UK and the John Innes Centre, Norwich, UK, report the complete genome sequence of the model actinomycete S. coelicolor A3(2).

Bentley et al. used an ordered cosmid library to sequence the S. coelicolor genome. They observed that at 8,667,507 base pairs the linear chromosome of this organism has the largest number of genes so far discovered in a bacterium - 7,825 - many located in 20 gene clusters coding for known or predicted secondary metabolites.

"The genome contains an unprecedented proportion of regulatory genes, predominantly those likely to be involved in responses to external stimuli and stresses, and many duplicated gene sets that may represent 'tissue-specific' isoforms operating in different phases of colonial development, a unique situation for a bacterium," wrote the authors.

In addition, there is an ancient synteny between the central 'core' of the chromosome and the whole chromosome of Mycobacterium tuberculosis and Corynebacterium diphtheriae - two other pathogenic actinomycetes.

"The genome sequence will greatly increase our understanding of microbial life in the soil as well as aiding the generation of new drug candidates by genetic engineering" conclude the authors.


  1. [ ] webcite

    Bentley SD, Chater KF, Cerdeño-Tárraga A-M, Challis GL, Thomson NR, James KD, Harris DE, Quail MA, Kieser H, Harper D, et al.: Complete genome sequence of the model actinomycete Streptomyces coelicolor A3(2). Nature 2002, 417:141-147.

  2. [ ] webcite

    The Wellcome Trust Sanger Institute

  3. [ ] webcite

    John Innes Centre