Abstract
A cloned 16S rRNA gene from the extreme thermophilic eubacterium Thermus thermophilus HB8 was used to characterize the in vivo expression of the 16S rRNA genes in this organism by nuclease S1 mapping. The gene represents an isolated transcription unit encoding solely 16S rRNA. Under exponential growth conditions, transcription was initiated at a single promoter, which represents the structural equivalent of Escherichia coli rrn P2 promoters. The promoter-leader region was very similar to the E. coli rrn P2 promoter-leader segment that is responsible for antitermination. The T. thermophilus leader region was approximately 85 nucleotides shorter than its E. coli P2 counterpart. Potential processing intermediates were correlated with a proposed secondary structure of T. thermophilus pre-16S rRNA.
MeSH Terms
Base Sequence
Chromosome Mapping
DNA, Bacterial/genetics
DNA, Ribosomal/genetics
Hydrogen Bonding
Molecular Sequence Data
Nucleic Acid Conformation
Promoter Regions, Genetic
RNA Processing, Post-Transcriptional
RNA, Ribosomal/genetics
RNA, Ribosomal, 16S/genetics,ultrastructure
Regulatory Sequences, Nucleic Acid
Thermus/genetics
Transcription, Genetic
Chemicals
DNA, Bacterial
DNA, Ribosomal
RNA, Ribosomal
RNA, Ribosomal, 16S
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Hartmann R K
Institut für Biochemie, Freie Universität Berlin, Federal Republic of Germany.
Erdmann V A
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