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Int J Syst Bacteriol 47 (1997), 661-669; DOI 10.1099/00207713-47-3-661
© 1997 Society for General Microbiology
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Inter- and Intraspecific Genetic Analysis of the Genus Saccharomonospora with 16S to 23S Ribosomal DNA (rDNA) and 23S to 5S rDNA Internally Transcribed Spacer Sequences

Jung-Hoon Yoon1,2, Taik Lee Sung2, Sam-Bong Kim1, Michael Goodfellow3 and Yong-Ha Park1,*

1Bioinformatics & Systematics Laboratory, Korean Collection for Type Cultures, Korea Research Institute of Bioscience and Biotechnology, Korea Institute of Science and Technology, Daeduk Science Park, Taejeon, Republic of Korea
2Department of Biological Science, Korea Advanced Institute of Science and Technology, Taejeon, Republic of Korea
3Department of Microbiology, The Medical School, University of Newcastle upon Tyne, Newcastle upon Tyne, NE2 4HH, United Kingdom

* Corresponding author. Phone: 82-42-860-4620. Fax: 82-42-860-4625. E-mail: yhpark{at}gerigw.geri.re.kr.

ABSTRACT

In order to clarify interspecific relationships and to investigate the intraspecific phylogenetic structure of the genus Saccharomonospora, 16S to 23S ribosomal DNA (16S-23S) and 23S to 5S ribosomal DNA (23S-5S) internally transcribed spacers (ITSs) were used for sequence analyses. The 16S-23S and 23S-5S ITSs from 22 Saccharomonospora strains were amplified by PCR and directly sequenced. The average levels of nucleotide similarity of the 16S-23S and 23S-5S ITSs for the four valid species were 87.6% ± 3.9% and 83% ± 2.2%, respectively. For the most part, intraspecific sequence differences were not found in the two ITSs; the only exception was Saccharomonospora glauca K194, which differed from other S. glauca strains by 1 bp in the 23S-5S ITS. The Saccharomonospora viridis strains had a smaller 16S-23S ITS region than the other strains, which may be useful for differentiating these organisms from other Saccharomonospora species. The characteristics of the two ITS regions make them more useful than 16S rRNA sequences as a tool for defining and identifying Saccharomonospora strains. However, Saccharomonospora azurea K161Thad two types of 23S-5S ITSs; rrnB, separated by Xho I digestion, had two additional nucleotides inserted between positions 52 and 55. Most of the 16S-23S and 23S-5S ITS sequences of S. azurea K161Tand strains of "Saccharomonospora caesia" were identical; the only exception was rrnB in S. azurea K161T. The lengths and levels of sequence divergence of the two ITSs of Saccharomonospora sp. strain K180 were different from the lengths and levels of sequence divergence of the ITSs of other species. These findings suggest that a taxonomic revision of the genus Saccharomonospora is necessary. Two trees based on 16S-23S and 23S-5S ITS sequences revealed distinct interspecific relationships in the genus Saccharomonospora.




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