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J. Bacteriol. doi:10.1128/JB.00204-08
Copyright (c) 2008, American Society for Microbiology and/or the Listed Authors/Institutions. All Rights Reserved.

The Genome Sequence of the Streptomycin-Producing Microorganism Streptomyces griseus IFO 13350

Department of Biotechnology, Graduate School of Agriculture and Life Sciences, The University of Tokyo, Bunkyo-ku, Tokyo 113-8657, Japan; Department of Bioactive Molecules, National Institute of Infectious Diseases, Shinjuku-ku, Tokyo 162-8640, Japan; Kitasato Institute for Life Sciences, Kitasato University, Sagamihara-shi, Kanagawa 228-8555, Japan; Department of Computational Biology, Graduate School of Frontier Sciences, The University of Tokyo, Kashiwa-shi, Chiba 277-8561, Japan

^* To whom correspondence should be addressed. Email: hattori{at}k.u-tokyo.ac.jp. asuhori{at}mail.ecc.u-tokyo.ac.jp.

	Abstract

We determined the complete genome sequence of Streptomyces griseus IFO 13350, a soil bacterium producing an antituberculosis agent, streptomycin, which is the first aminoglycoside antibiotic discovered more than 60 years ago. The linear chromosome consists of 8,545,929 base pairs (bp), with an average G+C content of 72.2%, predicting 7138 open reading frames, six ribosomal RNA operons (16S-23S-5S), and 66 tRNA genes. It contains extremely long terminal inverted repeats (TIRs) of 132,910 bp each. The telomere is different in nucleotide sequence and secondary structure consisting of several palindromes with a loop sequence of 5'-GGA-3' from the typical ones conserved among other Streptomyces species. In accordance with the difference, the chromosome has pseudogenes for a conserved terminal protein (Tpg) and telomere-associated protein (Tap), and a novel pair of Tpg and Tap is instead encoded on the TIRs. Comparison with the genomes of two related species, Streptomyces coelicolor A3(2) and Streptomyces avermitilis, clarified not only the characteristics of the S. griseus genome, but also 24 Streptomyces-specific proteins. The S. griseus genome contains 34 gene clusters or genes for biosynthesis of known or unknown secondary metabolites. Transcriptome analysis using a DNA microarray showed that at least four of these clusters, in addition to the streptomycin biosynthesis gene cluster, were activated directly or indirectly by AdpA, which is a central transcriptional activator for secondary metabolism and morphogenesis in the A-factor (a -butyrolactone signaling molecule) regulatory cascade in S. griseus.

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