Abstract
A 3 kb genomic fragment containing the nusG gene of Streptomyces coelicolor A3(2) was identified, cloned and sequenced. Sequence analysis revealed 3 complete and 2 truncated open reading frames (ORFs): truncated ORFU (similar to a Bacillus gene encoding a thermostable aspartate aminotransferase)-secE (94 amino acids; 79.0% similarity to Escherichia coli SecE)-nusG (300 amino acids; 73.3% similarity to E. coli NusG)-rplK (144 amino acids; 88.5% similarity to E. coli ribosomal subunit L11)-truncated rplA (similar to E. coli ribosomal subunit L1). The gene organization secE-nusG-rplKA exactly matches that in E. coli. Transcriptional analyses by the primer extension method revealed one transcriptional start site each for secE and nusG, and two sites for rplK. The presence of promoters was also confirmed with the aid of a promoter-probe vector.
MeSH Terms
Amino Acid Sequence
Bacterial Proteins/chemistry,genetics
Base Sequence
Cloning, Molecular
DNA, Bacterial/genetics
Escherichia coli Proteins
Genes, Bacterial
Molecular Sequence Data
Open Reading Frames
Peptide Elongation Factors/chemistry,genetics
Promoter Regions, Genetic
Restriction Mapping
Sequence Analysis, DNA
Streptomyces/genetics
Terminator Regions, Genetic
Transcription Factors/biosynthesis,chemistry,genetics
Transcription, Genetic
Chemicals
Bacterial Proteins
DNA, Bacterial
Escherichia coli Proteins
NusG protein, E coli
Peptide Elongation Factors
Transcription Factors
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Puttikhunt C
Department of Biotechnology, Faculty of Engineering, Osaka University, Japan.
Nihira T
Yamada Y
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